Next Generation Sequencing Competence Network

Next Generation Sequencing Competence Network

e.g. CCGA
(min 2 characters)

Wolfram S Kunz

Prof.
University of Bonn
Experimental Epileptology and Cognition Research
Sigmund-Freud-Straße 25, 53127 Bonn, Germany
Bonn 53127
+49 228 688529
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Ahmad N, Fazeli W, Schlie?ke S, Lesca G, Gokce-Samar Z, Mekbib KY, Jin SC, Burton J, Hoganson G, Petersen A, Gracie S, Granger L, Bartels E, Oppermann H, Kundishora A, Till M, Milleret-Pignot C, Dangerfield S, Viskochil D, Anderson KJ, Palculict TB, Schnur RE, Wentzensen IM, Tiller GE, Kahle KT, Kunz WS, Burkart S, Simons M, Sticht H, Abou Jamra R, Neuser S. De Novo Variants in RAB11B Cause Various Degrees of Global Developmental Delay and Intellectual Disability in Children. Pediatr Neurol. 2023 Aug 24; 148:164-171. PMID: 37734130.
      Citations:    Fields:    
    2. Ilyas M, Holzwarth D, Ishaq R, Ali Y, Habiba U, Raja AM, Saeed S, Abdullah U, Khan SN, Ullah A, Raja GK, Baig SM, Fazeli W, Kunz WS, Shaiq PA. Whole-Exome sequencing identifies GYS2 biallelic variants in individuals with suspected epilepsy. Seizure. 2023 Jul 27. PMID: 37574425.
      Citations:    Fields:    
    3. Zhang DG, Kunz WS, Lei XJ, Zito E, Zhao T, Xu YC, Wei XL, Lv WH, Luo Z. Selenium Ameliorated Oxidized Fish Oil-Induced Lipotoxicity via the Inhibition of Mitochondrial Oxidative Stress, Remodeling of Usp4-Mediated Deubiquitination, and Stabilization of Ppara. Antioxid Redox Signal. 2023 Jul 06. PMID: 37265154.
      Citations:    Fields:    Translation:Humans
    4. Trombly G, Said AM, Kudin AP, Peeva V, Altm?ller J, Becker K, K?hrer K, Zsurka G, Kunz WS. The Fate of Oxidative Strand Breaks in Mitochondrial DNA. Antioxidants (Basel). 2023 May 12; 12(5). PMID: 37237953; PMCID: PMC10215735.
      Citations: 1     
    5. Ree N, Gostimskaya I, Yurov V, Tanaka M, Popadin K, Shamanskiy V, Mikhailova AA, Tretiakov EO, Ushakova K, Mikhailova AG, Oreshkov S, Knorre DA, Overdevest JB, Lukowski SW, Liou CW, Lin TK, Kunz WS, Reymond A, Mazunin I, Bazykin GA, Fellay J, Khrapko K, Gunbin K. Secondary structure of the human mitochondrial genome affects formation of deletions. BMC Biol. 2023 05 08; 21(1):103. PMID: 37158879; PMCID: PMC10166460.
      Citations:    Fields:    Translation:HumansAnimalsCells
    6. Kar S, Perrelli A, Bali KK, Mastrocola R, Kar A, Khan B, Gand L, Nayak A, Hartmann C, Kunz WS, Samii A, Bertalanffy H, Retta SF. Identification of galectin-3 as a novel potential prognostic/predictive biomarker and therapeutic target for cerebral cavernous malformation disease. Genes Dis. 2024 Jan; 11(1):67-71. PMID: 37588216; PMCID: PMC10425784.
      Citations:    
    7. Tietz AK, Madlener M, Ernst L, Racz A, Baumgartner T, Widman G, Siebenbrodt K, Wickel J, Geis C, Lewerenz J, Bien CG, Kraft A, Zettl U, Ismail FS, Ayzenberg I, Urbanek C, Tauber SC, Mues S, Paliantonis A, Elger CE, Surges R, Quesada CM, Then Bergh F, Becker AJ, Kunz WS, Malter MP, Rosenow F, Leypoldt F, Lieb W, German Network for Research on Autoimmune Encephalitis (GENERATE), Strippel C, Herrera-Rivero M, Witten A, Schroeter C, Nelke C, Golombeck KS, R?ber T, Doppler K, Thaler F, Dik A, Kerin C, R?uber S, Gallus M, Kovac S, Grauer OM, Grimm A, Pr?ss H, Goebels N, Ringelstein M, Menge T, Tackenberg B, Kellinghaus C, S?hs KW, K?rtv?lyessy P, Markewitz R, Sommer C, K?mpfel T, Gross CC, Lerche H, Wellmer J, Wandinger KP, Meyer Zu H?rste G, Wiendl H, Kuhlenb?umer G, Meuth SG, Melzer N, Wendorff M, Degenhardt F, Franke A, Stoll M. A genome-wide association study in autoimmune neurological syndromes with anti-GAD65 autoantibodies. Brain. 2023 03 01; 146(3):977-990. PMID: 35348614; PMCID: PMC9976967.
      Citations: 3     Fields:    Translation:Humans
    8. Zsurka G, Appel MLT, Nastaly M, Hallmann K, Hansen N, Nass D, Baumgartner T, Surges R, Hartmann G, Bartok E, Kunz WS. Loss of the Immunomodulatory Transcription Factor BATF2 in Humans Is Associated with a Neurological Phenotype. Cells. 2023 01 05; 12(2). PMID: 36672163; PMCID: PMC9856319.
      Citations: 1     Fields:    Translation:HumansCells
    9. Zsurka G, Trombly G, Sch?ler S, Blei D, Kunz WS. Functional Assessment of Mitochondrial DNA Maintenance by Depletion and Repopulation Using 2',3'-Dideoxycytidine in Cultured Cells. Methods Mol Biol. 2023; 2615:229-240. PMID: 36807796.
      Citations:    Fields:    Translation:HumansCells
    10. Mikhailova AG, Mikhailova AA, Ushakova K, Tretiakov EO, Iliushchenko D, Shamansky V, Lobanova V, Kozenkov I, Efimenko B, Yurchenko AA, Kozenkova E, Zdobnov EM, Makeev V, Yurov V, Tanaka M, Gostimskaya I, Fleischmann Z, Annis S, Franco M, Wasko K, Denisov S, Kunz WS, Knorre D, Mazunin I, Nikolaev S, Fellay J, Reymond A, Khrapko K, Gunbin K, Popadin K. A mitochondria-specific mutational signature of aging: increased rate of A?>?G substitutions on the?heavy strand. Nucleic Acids Res. 2022 10 14; 50(18):10264-10277. PMID: 36130228; PMCID: PMC9561281.
      Citations: 3     Fields:    Translation:AnimalsCells
    11. Pearl PL, Kunz WS. Lysine Reduction and Cognitive Outcomes in Pyridoxine-Dependent Epilepsy: A New Approach to an Old Disease. Neurology. 2022 Aug 25. PMID: 36008152.
      Citations:    Fields:    Translation:Humans
    12. Gozzelino L, Baldassari S, Licchetta L, Iovino E, Liu YC, Bennett CA, Bennett MF, Damiano JA, Marconi C, Giangregorio T, Magini P, Canafoglia L, Seri M, Tinuper P, Scheffer IE, Bahlo M, Berkovic SF, Hildebrand MS, Kunz WS, Giordano L, Bisulli F, Martini M, Hirsch E, Pippucci T, Kochlamazashvili G, Mackintosh AI, Zsurka G, Kuijpers M, Maritzen T, Norata GD, Baulac S, Haucke V. Defective lipid signalling caused by mutations in PIK3C2B underlies focal epilepsy. Brain. 2022 07 29; 145(7):2313-2331. PMID: 35786744; PMCID: PMC9337808.
      Citations: 5     Fields:    Translation:HumansAnimals
    13. Lesca G, Baumgartner T, Monin P, Kunz WS, De Dominicis A, Specchio N. Genetic causes of rare and common epilepsies: What should the epileptologist know? Eur J Med Genet. 2022 Sep; 65(9):104570. PMID: 35850153.
      Citations:    Fields:    Translation:Humans
    14. McCormack M, Patel S, Stapleton C, Bobbili D, Krause R, Sills GJ, Koeleman BP, Striano P, Zara F, Sander JW, Kunz WS, Stefansson K, Stefansson H, Doherty CP, Heinzen EL, Scheffer IE, Goldstein DB, O'Brien T, Cotter D, Berkovic SF, EpiPGX Consortium, Sisodiya SM, Delanty N, Cavalleri GL, Campbell C, Depondt C, Lerche H. A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam. Epilepsia. 2022 06; 63(6):1563-1570. PMID: 35298028; PMCID: PMC9321556.
      Citations: 6     Fields:    Translation:Humans
    15. Schwarz N, Seiffert S, Pendziwiat M, Rademacher AV, Br?nger T, Hedrich UBS, Augustijn PB, Baier H, Bayat A, Bisulli F, Buono RJ, Bruria BZ, Doyle MG, Guerrini R, Heimer G, Iacomino M, Kearney H, Klein KM, Kousiappa I, Kunz WS, Lerche H, Licchetta L, Lohmann E, Minardi R, McDonald M, Montgomery S, Mulahasanovic L, Oegema R, Ortal B, Papacostas SS, Ragona F, Granata T, Reif PS, Rosenow F, Rothschild A, Scudieri P, Striano P, Tinuper P, Tanteles GA, Vetro A, Zahnert F, Goldberg EM, Zara F, Lal D, May P, Muhle H, Helbig I, Weber Y. Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With KCNC2 Pathogenic Variants. Neurology. 2022 05 17; 98(20):e2046-e2059. PMID: 35314505; PMCID: PMC9162046.
      Citations: 6     Fields:    Translation:Humans
    16. von Wrede R, Schidlowski M, Ivo A, Baumgartner T, Hallmann K, Helmstaedter C, Surges R, Kunz WS, Huppertz HJ, R?ber T, Zsurka G. Large Phenotypic Variation of Individuals from a Family with a Novel ASPM Mutation Associated with Microcephaly, Epilepsy, and Behavioral and Cognitive Deficits. Genes (Basel). 2022 02 25; 13(3). PMID: 35327983; PMCID: PMC8956106.
      Citations: 1     Fields:    Translation:Humans
    17. San Antonio-Arce V, Schulze-Bonhage A, Fauser S, Zacher P, Mayer T, Albers K, Cloppenborg T, Kunz W, Surges R, Syrbe S, Wolking S, Bo?elmann CM, Aparicio J, Weber Y. Genetic testing before epilepsy surgery - An exploratory survey and case collection from German epilepsy centers. Seizure. 2022 Feb; 95:4-10. PMID: 34953286.
      Citations: 2     Fields:    Translation:Humans
    18. Birtel J, von Landenberg C, Gliem M, Gliem C, Reimann J, Kunz WS, Herrmann P, Betz C, Caswell R, Nesbitt V, Kornblum C, Charbel Issa P. Mitochondrial Retinopathy. Ophthalmol Retina. 2022 01; 6(1):65-79. PMID: 34257060.
      Citations: 19     Fields:    Translation:Humans
    19. Stapleton C, McCormack M, Delanty N, Johnson MR, Koeleman BPC, Krause R, Kunz WS, Marson AG, Sander JW, Sills GJ, Striano P, Zara F, Sisodiya SM, Cavalleri GL, Wolking S, Campbell C, Depondt C, Lerche H. Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications. Front Pharmacol. 2021; 12:688386. PMID: 34177598; PMCID: PMC8220970.
      Citations: 4     
    20. McCormack M, Krause R, Krenn M, EpiPGx Consortium, Berkovic S, Cavalleri GL, Delanty N, Johnson MR, Koeleman BPC, Kunz WS, Marson AG, O'Brien TJ, Petrovski S, Sander JW, Sills GJ, Striano P, Zara F, Zimprich F, Sisodiya SM, Wolking S, Moreau C, Depondt C, Lerche H, Girard SL, Cossette P. Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy. Ann Clin Transl Neurol. 2021 07; 8(7):1376-1387. PMID: 34018700; PMCID: PMC8283173.
      Citations: 5     Fields:    Translation:Humans
    21. Sheremet NL, Andreeva NA, Barboni P, Barel O, Bychkov I, Caporali L, Capristo M, Carbonelli M, Cascavilla ML, Charbel Issa P, Freisinger P, Gerber S, Ghezzi D, Heidler J, Hempel M, Heon E, Itkis YS, Javasky E, Kaplan J, Kornblum C, Krylova TD, Kunz WS, La Morgia C, Lamperti C, Malacarne PF, Maresca A, Mayr JA, Meisterknecht J, Nevinitsyna TA, Palombo F, Pode-Shakked B, Shmelkova MS, Tagliavini F, Tzadok M, van der Ven AT, Vignal-Clermont C, Zakharova EY, Zhorzholadze NV, Rozet JM, Carelli V, Tsygankova PG, Wittig I, Stenton SL, Catarino CB, Assouline Z, Berutti R, Graf E, Kopajtich R, Kovacs-Nagy R, Ludwig C, Strom TM, Wagner M, Klopstock T, Prokisch H. Impaired complex I repair causes recessive Leber's hereditary optic neuropathy. J Clin Invest. 2021 03 15; 131(6). PMID: 33465056; PMCID: PMC7954600.
      Citations: 50     Fields:    Translation:HumansCells
    22. Hippen M, Peeva V, Machts J, Schwiecker K, Debska-Vielhaber G, Wiesner RJ, Vielhaber S, Kunz WS, Zsurka G. Novel Pathogenic Sequence Variation m.5789T>C Causes NARP Syndrome and Promotes Formation of Deletions of the Mitochondrial Genome. Neurol Genet. 2022 Apr; 8(2):e660. PMID: 35252560; PMCID: PMC8893589.
      Citations: 2     
    23. Debska-Vielhaber G, Peeva V, Zuschratter W, Walczak J, Schreiber S, Petri S, Machts J, Vogt S, Szczepanowska J, Gellerich FN, Vielhaber S, Kunz WS, Miller I, Hermann A. Impairment of mitochondrial oxidative phosphorylation in skin fibroblasts of SALS and FALS patients is rescued by in vitro treatment with ROS scavengers. Exp Neurol. 2021 05; 339:113620. PMID: 33497646.
      Citations: 12     Fields:    Translation:HumansCells
    24. von Wrede R, Jeub M, Elger CE, von Voss H, Klein HG, Becker AJ, Schoch S, Surges R, Kunz WS, Ari?z I. Novel KCNH1 Mutations Associated with Epilepsy: Broadening the Phenotypic Spectrum of KCNH1-Associated Diseases. Genes (Basel). 2021 01 21; 12(2). PMID: 33494179; PMCID: PMC7909785.
      Citations: 5     Fields:    Translation:HumansCells
    25. Rotko D, Kudin AP, Kulawiak B, Szewczyk A, Kunz WS, Zsurka G. Molecular and Functional Effects of Loss of Cytochrome c Oxidase Subunit 8A. Biochemistry (Mosc). 2021 Jan; 86(1):33-43. PMID: 33705280.
      Citations:    Fields:    Translation:HumansCells
    26. Gellerich FN, Szibor M, Gizatullina Z, Lessmann V, Schwarzer M, Doenst T, Vielhaber S, Kunz WS. Reply to Rutter et al.: The roles of cytosolic and intramitochondrial Ca2+ and the mitochondrial Ca2+-uniporter (MCU) in the stimulation of mammalian oxidative phosphorylation. J Biol Chem. 2020 07 24; 295(30):10507. PMID: 32709761; PMCID: PMC7383391.
      Citations:    Fields:    Translation:AnimalsCells
    27. Rotko D, Kunz WS, Szewczyk A, Kulawiak B. Signaling pathways targeting mitochondrial potassium channels. Int J Biochem Cell Biol. 2020 08; 125:105792. PMID: 32574707.
      Citations: 12     Fields:    Translation:HumansAnimalsCells
    28. Rotko D, Bednarczyk P, Koprowski P, Kunz WS, Szewczyk A, Kulawiak B. Heme is required for carbon monoxide activation of mitochondrial BKCa channel. Eur J Pharmacol. 2020 Aug 15; 881:173191. PMID: 32422186.
      Citations: 14     Fields:    Translation:HumansCells
    29. Schulz H, Nies AT, McCormack M, Schaeffeler E, Auce P, Avbersek A, Klein KM, Krenn M, Weckhuysen S, Consortium E, Cavalleri GL, Delanty N, Johnson MR, Kunz WS, Marson AG, Sander JW, Sills GJ, Striano P, Zara F, Zimprich F, Krause R, Sisodiya S, Schwab M, Sander T, Wolking S, Becker F, M?ller RS, Nikanorova M, Depondt C, Koeleman BP, Weber YG, Lerche H. Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study. Pharmacogenomics. 2020 04; 21(5):325-335. PMID: 32308125.
      Citations: 8     Fields:    Translation:Humans
    30. Moreau C, Nies AT, Schaeffeler E, McCormack M, Auce P, Avbersek A, Krenn M, Nikanorova M, Weckhuysen S, Cavalleri GL, Delanty N, Johnson MR, Koeleman BPC, Kunz WS, Marson AG, Sander JW, Sills GJ, Striano P, Zara F, Zimprich F, Schwab M, Krause R, Sisodiya SM, Cossette P, Girard SL, EpiPGX Consortium, Wolking S, Becker F, M?ller RS, Weber YG, Depondt C, Lerche H. Testing association of rare genetic variants with resistance to three common antiseizure medications. Epilepsia. 2020 04; 61(4):657-666. PMID: 32141622.
      Citations: 11     Fields:    Translation:Humans
    31. Eichhorn L, Beiert T, Knappe V, Nickenig G, Peeva V, Kudin AP, Kunz WS, Schrickel JW, St?ckigt F, Radecke T, Steinmetz M, Berwanger C, Kamm L, Schultheis D, Schl?tzer-Schrehardt U, Clemen CS, Schr?der R. Heart failure after pressure overload in autosomal-dominant desminopathies: Lessons from heterozygous DES-p.R349P knock-in mice. PLoS One. 2020; 15(3):e0228913. PMID: 32126091; PMCID: PMC7053759.
      Citations: 2     Fields:    Translation:HumansAnimals
    32. Szibor M, Gizatullina Z, Gainutdinov T, Endres T, Debska-Vielhaber G, Kunz M, Karavasili N, Hallmann K, Schreiber F, Bamberger A, Schwarzer M, Doenst T, Heinze HJ, Lessmann V, Vielhaber S, Kunz WS, Gellerich FN. Cytosolic, but not matrix, calcium is essential for adjustment of mitochondrial pyruvate supply. J Biol Chem. 2020 04 03; 295(14):4383-4397. PMID: 32094224; PMCID: PMC7135991.
      Citations: 25     Fields:    Translation:AnimalsCells
    33. Subhash S, Kalmbach N, Wegner F, Petri S, Glomb T, Dittrich-Breiholz O, Huang C, Bali KK, Kunz WS, Samii A, Bertalanffy H, Kanduri C, Kar S. Transcriptome-wide Profiling of Cerebral Cavernous Malformations Patients Reveal Important Long noncoding RNA molecular signatures. Sci Rep. 2019 12 03; 9(1):18203. PMID: 31796831; PMCID: PMC6890746.
      Citations: 6     Fields:    Translation:HumansCells
    34. Brenner D, Baumgartner T, von Spiczak S, Lewerenz J, Weis R, Grimmer A, Gaspirova P, Wurster CD, Kunz WS, Wagner J, Minassian BA, Elger CE, Ludolph AC, Biskup S, D?cker D. Genotypes and phenotypes of patients with Lafora disease living in Germany. Neurol Res Pract. 2019; 1. PMID: 32587944; PMCID: PMC7316188.
      Citations: 5     
    35. McCormack M, Slattery L, Walley N, Avbersek A, Novy J, Sinha SR, Radtke R, Doherty C, Auce P, Craig J, Johnson MR, Koeleman BPC, Krause R, Kunz WS, Marson AG, O'Brien TJ, Sander JW, Sills GJ, Stefansson H, Striano P, Zara F, EPIGEN Consortium, EpiPGX Consortium, Sisodiya S, Goldstein D, Cavalleri GL, Delanty N, Heavin SB, Wolking S, Depondt C, Lerche H. Genomic and clinical predictors of lacosamide response in refractory epilepsies. Epilepsia Open. 2019 Dec; 4(4):563-571. PMID: 31819912; PMCID: PMC6885661.
      Citations: 5     Fields:    
    36. Annis S, Fleischmann Z, Khrapko M, Franco M, Wasko K, Woods D, Kunz WS, Ellis P, Khrapko K. Quasi-Mendelian paternal inheritance of mitochondrial DNA: A notorious artifact, or anticipated behavior? Proc Natl Acad Sci U S A. 2019 07 23; 116(30):14797-14798. PMID: 31311874; PMCID: PMC6660754.
      Citations: 10     Fields:    Translation:HumansCells
    37. Silvennoinen K, de Lange N, Zagaglia S, Balestrini S, Androsova G, Wassenaar M, Auce P, Avbersek A, Berghuis B, Campbell E, Coppola A, Francis B, Cavalleri GL, Craig J, Delanty N, Johnson MR, Koeleman BPC, Kunz WS, Marson AG, O'Brien TJ, Sander JW, Sills GJ, Striano P, Zara F, van der Palen J, Krause R, Sisodiya SM, EpiPGX Consortium, Becker F, Wolking S, Lerche H, Depondt C. Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy. Epilepsia Open. 2019 Sep; 4(3):420-430. PMID: 31440723; PMCID: PMC6698679.
      Citations: 15     Fields:    
    38. Hangas A, Goffart S, Blei D, Griffith J, Kunz WS, Torregrosa-Mu?umer R, Zsurka G, Pohjoism?ki JLO. Replication fork rescue in mammalian mitochondria. Sci Rep. 2019 06 19; 9(1):8785. PMID: 31217442; PMCID: PMC6584726.
      Citations: 12     Fields:    Translation:HumansAnimalsCells
    39. Schlapakow E, Peeva V, Jeub M, Wabbels B, Kornblum C, Kunz WS, Zsurka G. Distinct segregation of the pathogenic m.5667G>A mitochondrial tRNAAsn mutation in extraocular and skeletal muscle in chronic progressive external ophthalmoplegia. Neuromuscul Disord. 2019 05; 29(5):358-367. PMID: 30962064.
      Citations: 5     Fields:    Translation:HumansCells
    40. Schulz H, Ruppert AK, Zara F, Madia F, Iacomino M, S Vari M, Balagura G, Minetti C, Striano P, Bianchi A, Marini C, Guerrini R, Kunz WS, Oliver KL, Bellows ST, Mullen SA, Berkovic SF, Scheffer IE, Ozbek U, Hoffmann P, Schramm S, Tsortouktzidis D, Becker AJ, Sander T, Weber YG, Becker F, Lerche H, Kapser C, Schankin CJ, M?ller RS, Caglayan H. No evidence for a BRD2 promoter hypermethylation in?blood leukocytes of Europeans with juvenile myoclonic?epilepsy. Epilepsia. 2019 05; 60(5):e31-e36. PMID: 30719712.
      Citations: 2     Fields:    Translation:HumansCells
    41. Nass RD, Hansen N, Quesada C, Kornblum C, Hermann P, Becker A, Hattingen E, Block W, Steidl E, Elger CE, Surges R, Kunz WS, R?ber T, Zsurka G, G?rtner F. Retinoencephalopathy with occipital lobe epilepsy in an OPA-1 mutation carrier. Seizure. 2019 Mar; 66:1-3. PMID: 30738307.
      Citations:    Fields:    Translation:Humans
    42. Berghuis B, Stapleton C, Sonsma ACM, Hulst J, de Haan GJ, Lindhout D, Demurtas R, EpiPGX Consortium, Krause R, Kunz WS, Zara F, Striano P, Craig J, Auce P, Marson AG, Stefansson H, O'Brien TJ, Johnson MR, Sills GJ, Sisodiya SM, Sander JW, Cavalleri GL, Koeleman BPC, McCormack M, Depondt C, Wolking S, Lerche H. A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine. Epilepsia Open. 2019 Mar; 4(1):102-109. PMID: 30868120; PMCID: PMC6398103.
      Citations: 8     Fields:    
    43. May P, Girard S, Harrer M, Bobbili DR, Schubert J, Wolking S, Becker F, Lachance-Touchette P, Meloche C, Gravel M, Niturad CE, Knaus J, De Kovel C, Toliat M, Polvi A, Iacomino M, Marini C, Thiele H, Jabbari K, Ruppert AK, Jurkowski W, Lal D, Rusconi R, Terragni B, Coombs ID, Reid CA, Striano P, Caglayan H, Siren A, Everett K, Hjalgrim H, Muhle H, Helbig I, Kunz WS, Weber YG, Weckhuysen S, Jonghe P, Sisodiya SM, Nabbout R, Franceschetti S, Coppola A, Vari MS, Baykan B, Ozbek U, Bebek N, Klein KM, Rosenow F, Nguyen DK, Carmant L, Lortie A, Desbiens R, Sills GJ, Auce P, Francis B, Johnson MR, Marson AG, Berghuis B, Sander JW, Avbersek A, McCormack M, Cavalleri GL, Delanty N, Depondt C, Krenn M, Zimprich F, Peter S, Nikanorova M, Kraaij R, van Rooij J, Balling R, Ikram MA, Avanzini G, Schorge S, Petrou S, Mantegazza M, Sander T, LeGuern E, Serratosa JM, Koeleman BPC, Palotie A, Lehesjoki AE, Nothnagel M, Maljevic S, Zara F, Cossette P, Krause R, Lerche H, Epicure Consortium, EuroEPINOMICS CoGIE Consortium, EpiPGX Consortium, Guerrero-L?pez R, Baulac S, Altm?ller J, Cest?le S, M?ller RS, Kasteleijn-Nolst Trenit? D, Dubeau F, Cl?ment JF, Cieuta-Walti C, Uitterlinden AG, N?rnberg P. Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study. Lancet Neurol. 2018 08; 17(8):699-708. PMID: 30033060.
      Citations: 31     Fields:    Translation:Humans
    44. Brainstorm Consortium, Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, Lee PH, Turley P, Grenier-Boley B, Chouraki V, Kamatani Y, Berr C, Letenneur L, Hannequin D, Amouyel P, Vardarajan BN, Reitz C, Goate AM, Huentelman MJ, Kamboh MI, Larson EB, Rogaeva E, St George-Hyslop P, Hakonarson H, Kukull WA, Farrer LA, Barnes LL, Beach TG, Demirci FY, Head E, Hulette CM, Jicha GA, Kauwe JSK, Kaye JA, Leverenz JB, Levey AI, Lieberman AP, Pankratz VS, Poon WW, Quinn JF, Saykin AJ, Schneider LS, Smith AG, Sonnen JA, Stern RA, Van Deerlin VM, Van Eldik LJ, Harold D, Russo G, Rubinsztein DC, Bayer A, Tsolaki M, Proitsi P, Fox NC, Owen MJ, Mead S, Passmore P, Morgan K, Rossor M, Lupton MK, Hoffmann P, Lawlor B, McQuillin A, Al-Chalabi A, Bis JC, Seshadri S, Beiser A, Rice K, van der Lee SJ, De Jager PL, Geschwind DH, Riemenschneider M, Riedel-Heller S, Rotter JI, Ransmayr G, Hyman BT, Cruchaga C, Winsvold B, Palta P, Farh KH, Cuenca-Leon E, Furlotte N, Ligthart L, Terwindt GM, Freilinger T, Ran C, Gordon SD, Borck G, Adams HHH, Wedenoja J, Buring JE, Hrafnsdottir M, Hottenga JJ, Penninx B, Artto V, Kaunisto M, Martin NG, Montgomery GW, Kurki MI, Huang H, Huang J, Sandor C, Webber C, Muller-Myhsok B, Schreiber S, Salomaa V, Loehrer E, Macaya A, Pozo-Rosich P, Hansen T, Werge T, Kaprio J, Metspalu A, Kubisch C, Ferrari MD, Belin AC, van den Maagdenberg AMJM, Zwart JA, Boomsma D, Eriksson N, Olesen J, Chasman DI, Nyholt DR, Avbersek A, Baum L, Berkovic S, Bradfield J, Buono RJ, Catarino CB, De Jonghe P, Dlugos D, Ferraro TN, French J, Hjalgrim H, Jamnadas-Khoda J, Kunz WS, Lerche H, Leu C, Lindhout D, Lo W, Lowenstein D, McCormack M, Molloy A, Ng PW, Oliver K, Privitera M, Radtke R, Ruppert AK, Sander T, Schachter S, Schankin C, Scheffer I, Schoch S, Sisodiya SM, Smith P, Sperling M, Striano P, Surges R, Thomas GN, Visscher F, Whelan CD, Zara F, Heinzen EL, Marson A, Becker F, Stroink H, Zimprich F, Gibbs R, Martinez M, Morris HR, Sharma M, Ryten M, Mok KY, Pulit S, Bevan S, Holliday E, Attia J, Battey T, Boncoraglio G, Thijs V, Chen WM, Mitchell B, Rothwell P, Sharma P, Sudlow C, Markus H, Kourkoulis C, Raffeld M, Silliman S, Boraska Perica V, Thornton LM, Huckins LM, William Rayner N, Lewis CM, Gratacos M, Rybakowski F, Keski-Rahkonen A, Raevuori A, Hudson JI, Reichborn-Kjennerud T, Monteleone P, Karwautz A, Mannik K, Baker JH, O'Toole JK, Trace SE, Davis OSP, Helder SG, Herpertz-Dahlmann B, Danner UN, van Elburg AA, Clementi M, Forzan M, Lissowska J, Hauser J, Tortorella A, Maj M, Gonidakis F, Tziouvas K, Papezova H, Yilmaz Z, Wagner G, Cohen-Woods S, Herms S, Dick DM, Ripatti S, Andreassen OA, Espeseth T, Lundervold AJ, Steen VM, Pinto D, Scherer SW, Aschauer H, Schosser A, Alfredsson L, Padyukov L, Halmi KA, Mitchell J, Strober M, Bergen AW, Kaye W, Szatkiewicz JP, Ramos-Quiroga JA, Haavik J, Zayats T, Johansson S, Williams N, Dempfle A, Rothenberger A, Kuntsi J, Oades RD, Banaschewski T, Franke B, Buitelaar JK, Arias Vasquez A, Doyle AE, Reif A, Lesch KP, Freitag C, Rivero O, Palmason H, Romanos M, Langley K, Rietschel M, Witt SH, Dalsgaard S, Waldman I, Wilmot B, Molly N, Crosbie J, Schachar R, Loo SK, McGough JJ, Medland SE, Robinson E, Weiss LA, Bacchelli E, Bailey A, Bal V, Battaglia A, Bolton P, Cantor R, Dawson G, De Rubeis S, Green A, Klauck SM, Levitt P, Maestrini E, Mane S, De-Luca DM, Parr J, Regan R, Reichenberg A, Sandin S, Vorstman J, Wassink T, Wijsman E, Cook E, Santangelo S, Delorme R, Magalhaes T, Arking D, Schulze TG, Thompson RC, Strohmaier J, Matthews K, Melle I, Morris D, Blackwood D, McIntosh A, Bergen SE, Schalling M, Maaser A, Fischer SB, Fullerton JM, Mayoral F, Schofield PR, Cichon S, Degenhardt F, Schumacher J, Mitchell PB, Gershon ES, Rice J, et al. Analysis of shared heritability in common disorders of the brain. Science. 2018 06 22; 360(6395). PMID: 29930110; PMCID: PMC6097237.
      Citations: 685     Fields:    Translation:Humans
    45. Peeva V, Blei D, Trombly G, Corsi S, Szukszto MJ, Rebelo-Guiomar P, Gammage PA, Kudin AP, Becker C, Minczuk M, Kunz WS, Altm?ller J, Zsurka G. Linear mitochondrial DNA is rapidly degraded by components of the replication machinery. Nat Commun. 2018 04 30; 9(1):1727. PMID: 29712893; PMCID: PMC5928156.
      Citations: 82     Fields:    Translation:HumansCells
    46. Peeva V, Kotlyar A, Kunz WS, Zsurka G. Is There Still Any Role for Oxidative Stress in Mitochondrial DNA-Dependent Aging? Genes (Basel). 2018 Mar 21; 9(4). PMID: 29561808; PMCID: PMC5924517.
      Citations: 32     Fields:    
    47. Augustynek B, Koprowski P, Rotko D, Kunz WS, Szewczyk A, Kulawiak B. Mitochondrial BK Channel Openers CGS7181 and CGS7184 Exhibit Cytotoxic Properties. Int J Mol Sci. 2018 Jan 25; 19(2). PMID: 29370072; PMCID: PMC5855575.
      Citations: 10     Fields:    Translation:HumansAnimalsCells
    48. McCormack M, Gui H, Speed D, Wright GEB, Zhang EJ, Secolin R, Yasuda C, Kwok M, Wolking S, Becker F, Rau S, Avbersek A, Heggeli K, Leu C, Depondt C, Sills GJ, Marson AG, Auce P, Brodie MJ, Francis B, Johnson MR, Koeleman BPC, Striano P, Coppola A, Zara F, Kunz WS, Sander JW, Lerche H, Klein KM, Weckhuysen S, Krenn M, Krause R, Shear N, Ross CJD, Delanty N, EPIGEN Consortium;, Pirmohamed M, Carleton BC, Canadian Pharmacogenomics Network for Drug Safety;, Cendes F, Lopes-Cendes I, Liao WP, O'Brien TJ, Sisodiya SM, EpiPGX Consortium;, Cherny S, Kwan P, Baum L, International League Against Epilepsy Consortium on Complex Epilepsies;, Cavalleri GL, Ingason A, Gudmundsson LJ, Stef?nsson K. Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients. Neurology. 2018 01 23; 90(4):e332-e341. PMID: 29288229; PMCID: PMC5798660.
      Citations: 13     Fields:    
    49. Kunz WS, Kov?cs R. Metabolic Epilepsies-Commemorative Issue in Honor of Professor Uwe Heinemann. Int J Mol Sci. 2017 Nov 22; 18(11). PMID: 29165369; PMCID: PMC5713464.
      Citations:    Fields:    Translation:Humans
    50. Kudin AP, Mawasi H, Eisenkraft A, Elger CE, Bialer M, Kunz WS. Mitochondrial Liver Toxicity of Valproic Acid and Its Acid Derivatives Is Related to Inhibition of α-Lipoamide Dehydrogenase. Int J Mol Sci. 2017 Sep 06; 18(9). PMID: 28878165; PMCID: PMC5618561.
      Citations: 10     Fields:    Translation:AnimalsCells
    51. Androsova G, Krause R, Wassenaar M, Auce P, Avbersek A, Berghuis B, Campbell E, Coppola A, Francis B, Cavalleri GL, Craig J, Delanty N, Koeleman BPC, Kunz WS, Marson AG, Sander JW, Sills GJ, Striano P, Zara F, Sisodiya SM, EpiPGX Consortium, Borghei M, Becker F, Wolking S, Lerche H, Depondt C. Comparative effectiveness of antiepileptic drugs in patients with mesial temporal lobe epilepsy with hippocampal sclerosis. Epilepsia. 2017 10; 58(10):1734-1741. PMID: 28857179.
      Citations: 13     Fields:    Translation:Humans
    52. Reid CA, Hallmann K, Tae HS, Phillips AM, Kleefuss-Lie A, Elger C, Perez-Reyes E, Petrou S, Kunz WS, Becker F, Teodorescu G, Weber YG, Lerche H, Maljevic S. Functional variants in HCN4 and CACNA1H may contribute to genetic generalized epilepsy. Epilepsia Open. 2017 09; 2(3):334-342. PMID: 29588962; PMCID: PMC5862120.
      Citations: 10     Fields:    
    53. Kropf S, Kollewe K, Petri S, Dengler R, Kunz WS, Nestor PJ, Schreiber S, Debska-Vielhaber G, Abdulla S, Machts J, Schreiber F, K?rtvelyessy P, K?rner S, Vielhaber S. Peripheral nerve atrophy together with higher cerebrospinal fluid progranulin indicate axonal damage in amyotrophic lateral sclerosis. Muscle Nerve. 2018 02; 57(2):273-278. PMID: 28472860.
      Citations: 9     Fields:    Translation:HumansCells
    54. Reimann J, Lehmann D, Hardy SA, Falkous G, Knowles CV, Jones RL, Kunz WS, Taylor RW, Kornblum C. Camptocormia and shuffling gait due to a novel MT-TV mutation: Diagnostic pitfalls. Neurol Genet. 2017 Jun; 3(3):e147. PMID: 28396884; PMCID: PMC5384303.
      Citations: 2     
    55. Kudin AP, Baron G, Hampel KG, Elger CE, Grote A, Thiele H, Schulz H, Ruppert AK, Sander T, Cheng Q, Kunz WS, Zsurka G, Weber Y, Lerche H, N?rnberg P, Arn?r ES, Schomburg L, Seeher S, Fradejas-Villar N, Schweizer U. Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsy. Free Radic Biol Med. 2017 05; 106:270-277. PMID: 28232204.
      Citations: 15     Fields:    Translation:Humans
    56. Augustynek B, Kunz WS, Szewczyk A. Guide to the Pharmacology of Mitochondrial Potassium Channels. Handb Exp Pharmacol. 2017; 240:103-127. PMID: 27838853.
      Citations: 12     Fields:    Translation:HumansAnimalsCells
    57. Hansen N, Widman G, Hattingen E, Elger CE, Kunz WS. Mesial temporal lobe epilepsy associated with KCNT1 mutation. Seizure. 2017 Feb; 45:181-183. PMID: 28081520.
      Citations: 13     Fields:    Translation:Humans
    58. Winter L, Wittig I, Peeva V, Eggers B, Heidler J, Chevessier F, Kley RA, Barkovits K, Strecker V, Berwanger C, Herrmann H, Marcus K, Kornblum C, Kunz WS, Clemen CS, Schr?der R. Mutant desmin substantially perturbs mitochondrial morphology, function and maintenance in skeletal muscle tissue. Acta Neuropathol. 2016 09; 132(3):453-73. PMID: 27393313; PMCID: PMC4992032.
      Citations: 30     Fields:    Translation:HumansAnimalsCells
    59. Lenk GM, Szymanska K, Rydzanicz M, Walczak A, Bekiesinska-Figatowska M, Stawinski P, Buehring S, Hsu DA, Meisler MH, Ploski R, Debska-Vielhaber G, Vielhaber S, Hallmann K, Kunz WS. Biallelic Mutations of VAC14 in Pediatric-Onset Neurological Disease. Am J Hum Genet. 2016 Jul 07; 99(1):188-94. PMID: 27292112; PMCID: PMC5005439.
      Citations: 32     Fields:    Translation:HumansCells
    60. Lal D, Reinthaler EM, Dejanovic B, May P, Thiele H, Ikram MA, van Duijn CM, Uitterlinden AG, Hofman A, Gruber-Sedlmayr U, Neophytou B, Zara F, Hahn A, Genetic Commission of the Italian League against Epilepsy, EuroEPINOMICS CoGIE Consortium, Gormley P, Cilio MR, Kunz WS, Krause R, Zimprich F, Lemke JR, Sander T, Neubauer BA, Lehesjoki AE, Schwarz G, Riesch E, Steinb?ck H, Becker F, Weber YG, N?rnberg P, Lerche H. Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes. PLoS One. 2016; 11(3):e0150426. PMID: 26990884; PMCID: PMC4798642.
      Citations: 8     Fields:    Translation:HumansCTClinical Trials
    61. Volmering E, Niehusmann P, Peeva V, Grote A, Becker AJ, Schoch S, Elger CE, Kunz WS, Zsurka G, Altm?ller J, N?rnberg P. Neuropathological signs of inflammation correlate with mitochondrial DNA deletions in mesial temporal lobe epilepsy. Acta Neuropathol. 2016 08; 132(2):277-288. PMID: 26993140.
      Citations: 23     Fields:    Translation:HumansCells
    62. Hallmann K, Kudin AP, Kornblum C, Reimann J, Waltz S, Hattingen E, Thiele H, Kopatz J, Neumann H, Kunz WS, Zsurka G, St?ve B, N?rnberg P, R?b C, Voos W. Loss of the smallest subunit of cytochrome c oxidase, COX8A, causes Leigh-like syndrome and epilepsy. Brain. 2016 Feb; 139(Pt 2):338-45. PMID: 26685157.
      Citations: 27     Fields:    Translation:Humans
    63. Kunz WS, Zsurka G. Mitochondrial dysfunction and seizures: the neuronal energy crisis. Lancet Neurol. 2015 Sep; 14(9):956-66. PMID: 26293567.
      Citations: 74     Fields:    Translation:HumansAnimalsCells
    64. Lal D, Pernhorst K, Klein KM, Reif P, Tozzi R, Toliat MR, Winterer G, Neubauer B, Rosenow F, Kunz WS, Kurki MI, Becker AJ, Perucca E, Zara F, Sander T, N?rnberg P, Becker F, Lerche H, Hoffmann P, Weber YG. Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy. Epilepsia. 2015 Sep; 56(9):e129-33. PMID: 26174448.
      Citations: 23     Fields:    Translation:Humans
    65. Lal D, Ruppert AK, Trucks H, Schulz H, de Kovel CG, Sonsma AC, Koeleman BP, Lindhout D, Kunz WS, Surges R, Elger CE, Helbig I, Muhle H, Stephani U, Klein KM, Rosenow F, Neubauer BA, Reinthaler EM, Zimprich F, Feucht M, Hjalgrim H, De Jonghe P, Suls A, Lieb W, Franke A, Schurmann C, Schminke U, EPICURE Consortium, Sander T, Kasteleijn-Nolst Trenit? D, Weber YG, Lerche H, Kapser C, Schankin CJ, Gaus V, Schmitz B, M?ller RS, Strauch K, Gieger C, N?rnberg P. Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies. PLoS Genet. 2015 May; 11(5):e1005226. PMID: 25950944; PMCID: PMC4423931.
      Citations: 44     Fields:    Translation:HumansCells
    66. Peeva V, Zsurka G, Kunz WS, Schrickel JW, Baris OR, Ederer S, Neuhaus JF, von Kleist-Retzow JC, Wunderlich CM, Pal M, Wunderlich FT, Hickethier T, Bunck AC, St?ckigt F, Wiesner RJ. Mosaic Deficiency in Mitochondrial Oxidative Metabolism Promotes Cardiac Arrhythmia during Aging. Cell Metab. 2015 May 05; 21(5):667-77. PMID: 25955204.
      Citations: 45     Fields:    Translation:AnimalsCells
    67. Weckhuysen S, Suls A, Korn-Merker E, Hofmann-Peters A, Cross H, Hallmann K, Elger CE, Kunz WS, Becker F, Schubert J, Gr?ninger S, Sperner J, Madeleyen R, Lerche H, Weber YG. Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet? Epilepsy Res. 2015 Aug; 114:47-51. PMID: 26088884.
      Citations: 2     Fields:    Translation:Humans
    68. Kunz WS, M?ller-H?cker J, Sch?fer S, Krebs S, Blum H, Zsurka G, Prokisch H, Seibel P, Jung A. Oxyphil cell metaplasia in the parathyroids is characterized by somatic mitochondrial DNA mutations in NADH dehydrogenase genes and cytochrome c oxidase activity-impairing genes. Am J Pathol. 2014 Nov; 184(11):2922-35. PMID: 25418474.
      Citations: 8     Fields:    Translation:HumansCells
    69. Hallmann K, Zsurka G, Moskau-Hartmann S, Kirschner J, Korinthenberg R, Ruppert AK, Ozdemir O, Weber Y, Becker F, Lerche H, Elger CE, Thiele H, N?rnberg P, Sander T, Kunz WS. A homozygous splice-site mutation in CARS2 is associated with progressive myoclonic epilepsy. Neurology. 2014 Dec 02; 83(23):2183-7. PMID: 25361775.
      Citations: 31     Fields:    Translation:HumansCells
    70. Salar S, Maslarova A, Lippmann K, Nichtweiss J, Weissberg I, Sheintuch L, Kunz WS, Shorer Z, Friedman A, Heinemann U. Blood-brain barrier dysfunction can contribute to pharmacoresistance of seizures. Epilepsia. 2014 Aug; 55(8):1255-63. PMID: 24995798.
      Citations: 21     Fields:    Translation:Animals
    71. Nicholls TJ, Peeva V, Szczesny RJ, Cysewski D, Reyes A, Kornblum C, Sciacco M, Moggio M, Dziembowski A, Kunz WS, Minczuk M, Zsurka G, Sch?ler S. Linear mtDNA fragments and unusual mtDNA rearrangements associated with pathological deficiency of MGME1 exonuclease. Hum Mol Genet. 2014 Dec 01; 23(23):6147-62. PMID: 24986917; PMCID: PMC4222359.
      Citations: 39     Fields:    Translation:HumansCells
    72. Kukat A, Dogan SA, Edgar D, Mourier A, Maiti P, Mauer J, Becker C, Senft K, Wibom R, Kudin AP, Hultenby K, Rosenkranz S, Ricquier D, Kunz WS, Trifunovic A, Jacoby C, Fl?gel U. Loss of UCP2 attenuates mitochondrial dysfunction without altering ROS production and uncoupling activity. PLoS Genet. 2014 Jun; 10(6):e1004385. PMID: 24945157; PMCID: PMC4063685.
      Citations: 32     Fields:    Translation:AnimalsCells
    73. Augustynek B, Kudin AP, Bednarczyk P, Szewczyk A, Kunz WS. Hemin inhibits the large conductance potassium channel in brain mitochondria: a putative novel mechanism of neurodegeneration. Exp Neurol. 2014 Jul; 257:70-5. PMID: 24792919.
      Citations: 17     Fields:    Translation:HumansAnimalsCells
    74. Dejanovic B, Lal D, Catarino CB, Arjune S, Belaidi AA, Trucks H, Vollmar C, Surges R, Kunz WS, Motameny S, Neubauer BA, Noachtar S, Sander T, Altm?ller J, K?hler A, N?rnberg P, Schwarz G. Exonic microdeletions of the gephyrin gene impair GABAergic synaptic inhibition in patients with idiopathic generalized epilepsy. Neurobiol Dis. 2014 Jul; 67:88-96. PMID: 24561070.
      Citations: 26     Fields:    Translation:HumansCells
    75. Kunz WS, Maggio N, Ot?hal J, Folbergrov? J, Kovacs R. Epileptic focus and alteration of metabolism. Int Rev Neurobiol. 2014; 114:209-43. PMID: 25078504.
      Citations: 8     Fields:    Translation:Humans
    76. Claude J, Linnartz-Gerlach B, Kudin AP, Kunz WS, Neumann H. Microglial CD33-related Siglec-E inhibits neurotoxicity by preventing the phagocytosis-associated oxidative burst. J Neurosci. 2013 Nov 13; 33(46):18270-6. PMID: 24227736; PMCID: PMC3828472.
      Citations: 49     Fields:    Translation:AnimalsCells
    77. Kasperaviciute D, Catarino CB, Matarin M, Leu C, Novy J, Tostevin A, Hessel EV, Hallmann K, Hildebrand MS, Dahl HH, Ryten M, Trabzuni D, Ramasamy A, Alhusaini S, Doherty CP, Dorn T, Steinhoff BJ, Zumsteg D, Duncan S, Eriksson KJ, Kantanen AM, Pandolfo M, Gruber-Sedlmayr U, Schlachter K, Reinthaler EM, Stogmann E, Zimprich F, Smith C, O'Brien TJ, Meng Tan K, Petrovski S, Robbiano A, Paravidino R, Zara F, Striano P, Sperling MR, Buono RJ, Hakonarson H, Costa PP, Silva BM, de Graan PN, Koeleman BP, Becker A, Schoch S, von Lehe M, Reif PS, Rosenow F, Becker F, Weber Y, Lerche H, Buchfelder M, Hamer HM, Kobow K, Coras R, Blumcke I, Scheffer IE, Berkovic SF, Weale ME, UK Brain Expression Consortium, Delanty N, Depondt C, Cavalleri GL, Kunz WS, Sisodiya SM, Leal B, Hansen J, Kr?mer G, K?lvi?inen RK, Th??tre E, Chaves J, da Silva AM, R?ssler K. Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A. Brain. 2013 Oct; 136(Pt 10):3140-50. PMID: 24014518; PMCID: PMC3784283.
      Citations: 72     Fields:    Translation:Humans
    78. Schorlemmer K, Bauer S, Belke M, Hermsen A, Klein KM, Reif PS, Oertel WH, Kunz WS, Knake S, Rosenow F, Strzelczyk A. Sustained seizure remission on perampanel in progressive myoclonic epilepsy (Lafora disease). Epilepsy Behav Case Rep. 2013; 1:118-21. PMID: 25667843; PMCID: PMC4150630.
      Citations: 27     
    79. Becker F, Heinen M, Lerche H, Kunz WS, Weber YG, Zsurka G, Gdynia HJ. Mutation in the mitochondrial tRNA(Ile) gene causes progressive myoclonus epilepsy. Seizure. 2013 Jul; 22(6):483-6. PMID: 23601850.
      Citations: 5     Fields:    Translation:HumansCells
    80. Schreiber S, Oldag A, Kornblum C, Kollewe K, Kropf S, Schoenfeld A, Feistner H, Jakubiczka S, Kunz WS, Scherlach C, Tempelmann C, Mawrin C, Dengler R, Schreiber F, Goertler M, Vielhaber S. Sonography of the median nerve in CMT1A, CMT2A, CMTX, and HNPP. Muscle Nerve. 2013 Mar; 47(3):385-95. PMID: 23381770.
      Citations: 23     Fields:    Translation:Humans
    81. Lal D, Trucks H, Hjalgrim H, Koeleman BP, de Kovel CG, Visscher F, Weber YG, Lerche H, Becker F, Schankin CJ, Neubauer BA, Surges R, Kunz WS, Zimprich F, Franke A, Illig T, Ried JS, Leu C, Sander T, EMINet Consortium, EPICURE Consortium, M?ller RS, N?rnberg P. Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy. Epilepsia. 2013 Feb; 54(2):265-71. PMID: 23350840.
      Citations: 34     Fields:    Translation:Humans
    82. Kunz WS, Zsurka G. Mitochondrial involvement in neurodegenerative diseases. IUBMB Life. 2013 Mar; 65(3):263-72. PMID: 23341346.
      Citations: 16     Fields:    Translation:HumansCells
    83. Kornblum C, Nicholls TJ, Haack TB, Peeva V, Danhauser K, Hallmann K, Rorbach J, Iuso A, Wieland T, Sciacco M, Ronchi D, Comi GP, Moggio M, Quinzii CM, DiMauro S, Calvo SE, Mootha VK, Klopstock T, Strom TM, Meitinger T, Minczuk M, Kunz WS, Prokisch H, Sch?ler S, Zsurka G. Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease. Nat Genet. 2013 Feb; 45(2):214-9. PMID: 23313956; PMCID: PMC3678843.
      Citations: 111     Fields:    Translation:HumansCells
    84. Weber YG, Klitten LL, Trucks H, Muhle H, Kunz WS, Mefford HC, Franke A, Kautza M, Wolf P, Dennig D, Schreiber S, Wichmann HE, Ernst JP, Schurmann C, Grabe HJ, Tommerup N, Stephani U, Lerche H, Hjalgrim H, Helbig I, Sander T, EPICURE Consortium, M?ller RS, R?ckert IM. Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy. Epilepsia. 2013 Feb; 54(2):256-64. PMID: 23294455.
      Citations: 30     Fields:    Translation:Humans
    85. Tschampa HJ, Urbach H, Greschus S, Kunz WS, Kornblum C. Neuroimaging characteristics in mitochondrial encephalopathies associated with the m.3243A>G MTTL1 mutation. J Neurol. 2013 Apr; 260(4):1071-80. PMID: 23196335.
      Citations: 18     Fields:    Translation:HumansCells
    86. EPICURE Consortium, EMINet Consortium, Steffens M, Leu C, Ruppert AK, Zara F, Striano P, Robbiano A, Capovilla G, Tinuper P, Gambardella A, Bianchi A, La Neve A, Crichiutti G, de Kovel CG, de Haan GJ, Lindhout D, Gaus V, Schmitz B, Janz D, Weber YG, Becker F, Lerche H, Steinhoff BJ, Kunz WS, Surges R, Elger CE, Muhle H, von Spiczak S, Ostertag P, Helbig I, Stephani U, Hjalgrim H, Dibbens LM, Bellows S, Oliver K, Mullen S, Scheffer IE, Berkovic SF, Everett KV, Gardiner MR, Marini C, Guerrini R, Lehesjoki AE, Siren A, Guipponi M, Malafosse A, Thomas P, Nabbout R, Baulac S, Leguern E, Guerrero R, Serratosa JM, Reif PS, Rosenow F, Feucht M, Zimprich F, Kapser C, Schankin CJ, Suls A, Smets K, De Jonghe P, Jordanova A, Caglayan H, Yapici Z, Yalcin DA, Baykan B, Bebek N, Ozbek U, Gieger C, Wichmann HE, Balschun T, Ellinghaus D, Franke A, Meesters C, Becker T, Wienker TF, Hempelmann A, Schulz H, Leber M, Pauck SM, Trucks H, Toliat MR, Avanzini G, Koeleman BP, Sander T, Kasteleijn-Nolst Trenit? D, Kleefu?-Lie AA, M?ller RS, M?rzinger M, R?schendorf F, N?rnberg P. Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. Hum Mol Genet. 2012 Dec 15; 21(24):5359-72. PMID: 22949513.
      Citations: 61     Fields:    Translation:Humans
    87. Vielhaber S, Debska-Vielhaber G, Peeva V, Schoeler S, Kudin AP, Minin I, Schreiber S, Dengler R, Kollewe K, Zuschratter W, Kornblum C, Kunz WS, Zsurka G. Mitofusin 2 mutations affect mitochondrial function by mitochondrial DNA depletion. Acta Neuropathol. 2013 Feb; 125(2):245-56. PMID: 22926664.
      Citations: 30     Fields:    Translation:HumansCells
    88. Jennissen K, Siegel F, Liebig-Gonglach M, Hermann MR, Kipschull S, van Dooren S, Kunz WS, Pfeifer A, F?ssler R. A VASP-Rac-soluble guanylyl cyclase pathway controls cGMP production in adipocytes. Sci Signal. 2012 Aug 28; 5(239):ra62. PMID: 22932701.
      Citations: 18     Fields:    Translation:AnimalsCells
    89. Helmstaedter C, Mihov Y, Toliat MR, Thiele H, Nuernberg P, Schoch S, Surges R, Elger CE, Kunz WS, Hurlemann R. Genetic variation in dopaminergic activity is associated with the risk for psychiatric side effects of levetiracetam. Epilepsia. 2013 Jan; 54(1):36-44. PMID: 22881836.
      Citations: 23     Fields:    Translation:Humans
    90. Franko A, von Kleist-Retzow JC, Sanchez-Lasheras C, Brodesser S, Krut O, Kunz WS, Wiedermann D, Hoehn M, Moll L, Freude S, Krone W, Schubert M, Wiesner RJ, B?se M, St?hr O. Complete failure of insulin-transmitted signaling, but not obesity-induced insulin resistance, impairs respiratory chain function in muscle. J Mol Med (Berl). 2012 Oct; 90(10):1145-60. PMID: 22411022.
      Citations: 24     Fields:    Translation:AnimalsCells
    91. Kudin AP, Augustynek B, Lehmann AK, Kunz WS, Kov?cs R. The contribution of thioredoxin-2 reductase and glutathione peroxidase to H(2)O(2) detoxification of rat brain mitochondria. Biochim Biophys Acta. 2012 Oct; 1817(10):1901-6. PMID: 22398128.
      Citations: 27     Fields:    Translation:AnimalsCells
    92. Auburger G, Klinkenberg M, Drost J, Marcus K, Morales-Gordo B, Kunz WS, Brandt U, Broccoli V, Reichmann H, Gispert S, Jendrach M. Primary skin fibroblasts as a model of Parkinson's disease. Mol Neurobiol. 2012 Aug; 46(1):20-7. PMID: 22350618; PMCID: PMC3443476.
      Citations: 70     Fields:    Translation:HumansCells
    93. EPICURE Consortium, Leu C, de Kovel CG, Zara F, Striano P, Pezzella M, Robbiano A, Bianchi A, Bisulli F, Coppola A, Giallonardo AT, Beccaria F, Lindhout D, Gaus V, Schmitz B, Janz D, Weber YG, Becker F, Lerche H, Kleefuss-Lie AA, Hallman K, Kunz WS, Elger CE, Muhle H, Stephani U, Hjalgrim H, Mullen S, Scheffer IE, Berkovic SF, Everett KV, Gardiner MR, Marini C, Guerrini R, Lehesjoki AE, Siren A, Nabbout R, Baulac S, Leguern E, Serratosa JM, Rosenow F, Feucht M, Unterberger I, Covanis A, Suls A, Weckhuysen S, Kaneva R, Caglayan H, Turkdogan D, Baykan B, Bebek N, Ozbek U, Hempelmann A, Schulz H, Trucks H, Avanzini G, Koeleman BP, Sander T, Trenit? DK, M?ller RS, R?schendorf F, N?rnberg P. Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies. Epilepsia. 2012 Feb; 53(2):308-18. PMID: 22242659.
      Citations: 16     Fields:    Translation:HumansCells
    94. Becker B, Mihov Y, Scheele D, Kendrick KM, Feinstein JS, Matusch A, Aydin M, Reich H, Urbach H, Oros-Peusquens AM, Shah NJ, Kunz WS, Schlaepfer TE, Zilles K, Maier W, Hurlemann R. Fear processing and social networking in the absence of a functional amygdala. Biol Psychiatry. 2012 Jul 01; 72(1):70-7. PMID: 22218285.
      Citations: 58     Fields:    Translation:Humans
    95. Schormair B, Knauf F, Berthele A, Baron R, Maier C, Treede RD, Binder A, Sommer C, Kunz W, Zimprich F, Heemann U, Pfeufer A, Nowak B, Gieger C, Lichtner P, Trenkwalder C, Oexle K, Winkelmann J, Hopfner F, T?lle TR, Maih?fner C, N?bauer M, K??b S. Novel SCARB2 mutation in action myoclonus-renal failure syndrome and evaluation of SCARB2 mutations in isolated AMRF features. BMC Neurol. 2011 Oct 27; 11:134. PMID: 22032306; PMCID: PMC3222607.
      Citations: 10     Fields:    Translation:HumansCells
    96. Malinska D, Kudin AP, Bejtka M, Kunz WS. Changes in mitochondrial reactive oxygen species synthesis during differentiation of skeletal muscle cells. Mitochondrion. 2012 Jan; 12(1):144-8. PMID: 21782978.
      Citations: 33     Fields:    Translation:AnimalsCells
    97. Otte DM, Sommersberg B, Kudin A, Guerrero C, Albayram O, Filiou MD, Frisch P, Yilmaz O, Drews E, Turck CW, Kunz WS, Beck H, Zimmer A, Bilkei-Gorz? A. N-acetyl cysteine treatment rescues cognitive deficits induced by mitochondrial dysfunction in G72/G30 transgenic mice. Neuropsychopharmacology. 2011 Oct; 36(11):2233-43. PMID: 21716263; PMCID: PMC3176560.
      Citations: 49     Fields:    Translation:HumansAnimals
    98. Kunz WS, Folbergrov? J. Mitochondrial dysfunction in epilepsy. Mitochondrion. 2012 Jan; 12(1):35-40. PMID: 21530687.
      Citations: 58     Fields:    Translation:HumansAnimalsCells
    99. Niehusmann P, Surges R, von Wrede RD, Elger CE, Reimann J, Urbach H, Vielhaber S, Bien CG, Kunz WS, Wellmer J. Mitochondrial dysfunction due to Leber's hereditary optic neuropathy as a cause of visual loss during assessment for epilepsy surgery. Epilepsy Behav. 2011 Jan; 20(1):38-43. PMID: 21145289.
      Citations: 5     Fields:    Translation:HumansCells
    100. Stewart JD, Schoeler S, Sitarz KS, Horvath R, Hallmann K, Pyle A, Yu-Wai-Man P, Taylor RW, Samuels DC, Kunz WS, Chinnery PF. POLG mutations cause decreased mitochondrial DNA repopulation rates following induced depletion in human fibroblasts. Biochim Biophys Acta. 2011 Mar; 1812(3):321-5. PMID: 21138766.
      Citations: 21     Fields:    Translation:HumansCells
    101. Kunz WS, Zsurka G. Mitochondrial dysfunction in neurological disorders with epileptic phenotypes. J Bioenerg Biomembr. 2010 Dec; 42(6):443-8. PMID: 21069442.
      Citations: 7     Fields:    Translation:HumansCells
    102. Kudina T, Peeva V, Hallmann K, Elger CE, Khrapko K, Kunz WS, Zsurka G. Distinct patterns of mitochondrial genome diversity in bonobos (Pan paniscus) and humans. BMC Evol Biol. 2010 Sep 02; 10:270. PMID: 20813043; PMCID: PMC2942848.
      Citations: 14     Fields:    Translation:HumansAnimals
    103. Malinska D, Kulawiak B, Wrzosek A, Kunz WS, Szewczyk A. The cytoprotective action of the potassium channel opener BMS-191095 in C2C12 myoblasts is related to the modulation of calcium homeostasis. Cell Physiol Biochem. 2010; 26(2):235-46. PMID: 20798507.
      Citations: 5     Fields:    Translation:AnimalsCells
    104. Guo X, Popadin KY, Markuzon N, Orlov YL, Kraytsberg Y, Krishnan KJ, Turnbull DM, Kunz WS, Khrapko K, Zsurka G. Repeats, longevity and the sources of mtDNA deletions: evidence from 'deletional spectra'. Trends Genet. 2010 Aug; 26(8):340-3. PMID: 20591530; PMCID: PMC2915442.
      Citations: 22     Fields:    Translation:HumansAnimalsCells
    105. Malinska D, Kulawiak B, Kudin AP, Kovacs R, Huchzermeyer C, Kann O, Szewczyk A, Kunz WS. Complex III-dependent superoxide production of brain mitochondria contributes to seizure-related ROS formation. Biochim Biophys Acta. 2010 Jun-Jul; 1797(6-7):1163-70. PMID: 20211146.
      Citations: 40     Fields:    Translation:AnimalsCells
    106. Zsurka G, Hampel KG, Nelson I, Jardel C, Mirandola SR, Sassen R, Kornblum C, Marcorelles P, Kunz WS, Lavou? S, Lomb?s A. Severe epilepsy as the major symptom of new mutations in the mitochondrial tRNA(Phe) gene. Neurology. 2010 Feb 09; 74(6):507-12. PMID: 20142618.
      Citations: 13     Fields:    Translation:Humans
    107. Malinska D, Mirandola SR, Kunz WS. Mitochondrial potassium channels and reactive oxygen species. FEBS Lett. 2010 May 17; 584(10):2043-8. PMID: 20080090.
      Citations: 33     Fields:    Translation:HumansAnimalsCells
    108. Debska-Vielhaber G, Godlewski MM, Kicinska A, Skalska J, Kulawiak B, Piwonska M, Zablocki K, Kunz WS, Szewczyk A, Motyl T. Large-conductance K+ channel openers induce death of human glioma cells. J Physiol Pharmacol. 2009 Dec; 60(4):27-36. PMID: 20065494.
      Citations: 13     Fields:    Translation:HumansCells
    109. Choma K, Bednarczyk P, Koszela-Piotrowska I, Kulawiak B, Kudin A, Kunz WS, Dolowy K, Szewczyk A. Single channel studies of the ATP-regulated potassium channel in brain mitochondria. J Bioenerg Biomembr. 2009 Aug; 41(4):323-34. PMID: 19821034.
      Citations: 11     Fields:    Translation:AnimalsCells
    110. Gispert S, Ricciardi F, Kurz A, Azizov M, Hoepken HH, Becker D, Voos W, Leuner K, Kudin AP, Kunz WS, Zimmermann A, Roeper J, Wenzel D, Jendrach M, Huber L, Rohrer H, Barrera M, Reichert AS, Chen A, Nussbaum RL, Auburger G, M?ller WE, Garc?a-Arenc?bia M, Fern?ndez-Ruiz J, R?b U. Parkinson phenotype in aged PINK1-deficient mice is accompanied by progressive mitochondrial dysfunction in absence of neurodegeneration. PLoS One. 2009 Jun 03; 4(6):e5777. PMID: 19492057; PMCID: PMC2686165.
      Citations: 152     Fields:    Translation:AnimalsCells
    111. Skalska J, Bednarczyk P, Piwonska M, Kulawiak B, Wilczynski G, Dolowy K, Kudin AP, Kunz WS, Szewczyk A. Calcium ions regulate K? uptake into brain mitochondria: the evidence for a novel potassium channel. Int J Mol Sci. 2009 Mar; 10(3):1104-20. PMID: 19399240; PMCID: PMC2672021.
      Citations: 28     Fields:    Translation:AnimalsCells
    112. Kudin AP, Elger CE, Kunz WS, Zsurka G. Mitochondrial involvement in temporal lobe epilepsy. Exp Neurol. 2009 Aug; 218(2):326-32. PMID: 19268667.
      Citations: 36     Fields:    Translation:HumansAnimalsCells
    113. Szewczyk A, Jarmuszkiewicz W, Kunz WS. Mitochondrial potassium channels. IUBMB Life. 2009 Feb; 61(2):134-43. PMID: 19165895.
      Citations: 57     Fields:    Translation:HumansAnimalsCells
    114. Otte DM, Filiou MD, Turck CW, Yilmaz O, Holst MI, Schilling K, Abou-Jamra R, Schumacher J, Benzel I, Kunz WS, Beck H, Zimmer A, Bilkei-Gorz? A. Behavioral changes in G72/G30 transgenic mice. Eur Neuropsychopharmacol. 2009 May; 19(5):339-48. PMID: 19189879.
      Citations: 30     Fields:    Translation:HumansAnimals
    115. Frisch C, Angenstein F, Kudin A, Kunz W, Elger CE, Helmstaedter C, H?sch K. Dose-dependent memory effects and cerebral volume changes after in utero exposure to valproate in the rat. Epilepsia. 2009 Jun; 50(6):1432-41. PMID: 19374658.
      Citations: 16     Fields:    Translation:Animals
    116. Malinska D, Kudin AP, Debska-Vielhaber G, Vielhaber S, Kunz WS. Chapter 23 Quantification of superoxide production by mouse brain and skeletal muscle mitochondria. Methods Enzymol. 2009; 456:419-37. PMID: 19348902.
      Citations: 8     Fields:    Translation:AnimalsCells
    117. Kunz WS, Preuss SF, Klussmann JP, Guntinas-Lichius O, Wiesner RJ, Gekeler J, Zsurka G. Clonal expansion of different mtDNA variants without selective advantage in solid tumors. Mutat Res. 2009 Mar 09; 662(1-2):28-32. PMID: 19114048.
      Citations: 3     Fields:    Translation:HumansCells
    118. Boes M, Bauer J, Urbach H, Elger CE, Frank S, Baron M, Zsurka G, Kunz WS, Kornblum C. Proof of progression over time: finally fulminant brain, muscle, and liver affection in Alpers syndrome associated with the A467T POLG1 mutation. Seizure. 2009 Apr; 18(3):232-4. PMID: 18783964.
      Citations: 2     Fields:    Translation:Humans
    119. Baron M, Stewart JD, Kornblum C, Sassen R, Taylor RW, Elger CE, Chinnery PF, Kunz WS, Zsurka G, B?s M. Clonally expanded mitochondrial DNA mutations in epileptic individuals with mutated DNA polymerase gamma. J Neuropathol Exp Neurol. 2008 Sep; 67(9):857-66. PMID: 18716558.
      Citations: 12     Fields:    Translation:Humans
    120. Paus S, Zsurka G, Baron M, Deschauer M, Bamberg C, Klockgether T, Kunz WS, Kornblum C. Apraxia of lid opening mimicking ptosis in compound heterozygosity for A467T and W748S POLG1 mutations. Mov Disord. 2008 Jul 15; 23(9):1286-8. PMID: 18546343.
      Citations: 5     Fields:    Translation:Humans
    121. Ali N, Kunz WS, Kornblum C, Wabbels B, Roggenk?mper P. [Chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome : interdisciplinary diagnosis and therapy]. Ophthalmologe. 2008 Jun; 105(6):550-6. PMID: 18373100.
      Citations: 7     Fields:    Translation:Humans
    122. Wassmann K, Widder JD, Wassmann S, Chen CH, Keuler B, Kudin A, Kunz WS, Nickenig G, Mueller CF. Multidrug resistance protein-1 affects oxidative stress, endothelial dysfunction, and atherogenesis via leukotriene C4 export. Circulation. 2008 Jun 03; 117(22):2912-8. PMID: 18506003.
      Citations: 19     Fields:    Translation:AnimalsCells
    123. Kudin AP, Malinska D, Kunz WS. Sites of generation of reactive oxygen species in homogenates of brain tissue determined with the use of respiratory substrates and inhibitors. Biochim Biophys Acta. 2008 Jul-Aug; 1777(7-8):689-95. PMID: 18510942.
      Citations: 34     Fields:    Translation:AnimalsCells
    124. Skalska J, Piwonska M, Wyroba E, Surmacz L, Wieczorek R, Koszela-Piotrowska I, Zielinska J, Bednarczyk P, Dolowy K, Wilczynski GM, Szewczyk A, Kunz WS. A novel potassium channel in skeletal muscle mitochondria. Biochim Biophys Acta. 2008 Jul-Aug; 1777(7-8):651-9. PMID: 18515063.
      Citations: 25     Fields:    Translation:AnimalsCells
    125. Kulawiak B, Kudin AP, Szewczyk A, Kunz WS. BK channel openers inhibit ROS production of isolated rat brain mitochondria. Exp Neurol. 2008 Aug; 212(2):543-7. PMID: 18572168.
      Citations: 42     Fields:    Translation:AnimalsCells
    126. Konieczny P, Fuchs P, Reipert S, Kunz WS, Fischer I, Paulin D, Wiche G, Ze?ld A, Schr?der R. Myofiber integrity depends on desmin network targeting to Z-disks and costameres via distinct plectin isoforms. J Cell Biol. 2008 May 19; 181(4):667-81. PMID: 18490514; PMCID: PMC2386106.
      Citations: 66     Fields:    Translation:AnimalsCells
    127. Kornblum C, Wiesner RJ, Kunz WS, Zsurka G, Schr?der R. Concerted action of two novel tRNA mtDNA point mutations in chronic progressive external ophthalmoplegia. Biosci Rep. 2008 Apr; 28(2):89-96. PMID: 18384291.
      Citations: 3     Fields:    Translation:HumansCells
    128. Kuznetsov AV, Veksler V, Gellerich FN, Saks V, Margreiter R, Kunz WS. Analysis of mitochondrial function in situ in permeabilized muscle fibers, tissues and cells. Nat Protoc. 2008; 3(6):965-76. PMID: 18536644.
      Citations: 333     Fields:    Translation:HumansAnimalsCells
    129. Baron M, Kudin AP, Kunz WS. Mitochondrial dysfunction in neurodegenerative disorders. Biochem Soc Trans. 2007 Nov; 35(Pt 5):1228-31. PMID: 17956319.
      Citations: 26     Fields:    Translation:HumansCells
    130. Vielhaber S, Niessen HG, Debska-Vielhaber G, Kudin AP, Fendrich R, Willker W, Leibfritz D, Schramm J, Elger CE, Heinze HJ, Kunz WS, Wellmer J, Kaufmann J, Sch?nfeld MA. Subfield-specific loss of hippocampal N-acetyl aspartate in temporal lobe epilepsy. Epilepsia. 2008 Jan; 49(1):40-50. PMID: 17822430.
      Citations: 29     Fields:    Translation:HumansCells
    131. Koszela-Piotrowska I, Choma K, Bednarczyk P, Dolowy K, Szewczyk A, Kunz WS, Malekova L, Kominkova V, Ondrias K. Stilbene derivatives inhibit the activity of the inner mitochondrial membrane chloride channels. Cell Mol Biol Lett. 2007; 12(4):493-508. PMID: 17457523; PMCID: PMC6275615.
      Citations: 3     Fields:    Translation:AnimalsCells
    132. Niessen HG, Debska-Vielhaber G, Sander K, Angenstein F, Ludolph AC, Hilfert L, Willker W, Leibfritz D, Heinze HJ, Kunz WS, Vielhaber S. Metabolic progression markers of neurodegeneration in the transgenic G93A-SOD1 mouse model of amyotrophic lateral sclerosis. Eur J Neurosci. 2007 Mar; 25(6):1669-77. PMID: 17432958.
      Citations: 27     Fields:    Translation:HumansAnimals
    133. Hampel KG, Kudina T, Kornblum C, Kraytsberg Y, Elger CE, Khrapko K, Kunz WS, Zsurka G. Inheritance of mitochondrial DNA recombinants in double-heteroplasmic families: potential implications for phylogenetic analysis. Am J Hum Genet. 2007 Feb; 80(2):298-305. PMID: 17236134; PMCID: PMC1785346.
      Citations: 8     Fields:    Translation:Humans
    134. Lanz K, Wickenhauser C, Kudin AP, Kunz WS, Wiesner RJ, Schauen M, Hornig-Do HT, von Kleist-Retzow JC. Human epidermal keratinocytes accumulate superoxide due to low activity of Mn-SOD, leading to mitochondrial functional impairment. J Invest Dermatol. 2007 May; 127(5):1084-93. PMID: 17185981.
      Citations: 20     Fields:    Translation:HumansCells
    135. Kunz WS, Wiesner RJ, Zsurka G. Mitochondrial DNA damage and the aging process: facts and imaginations. Free Radic Res. 2006 Dec; 40(12):1284-94. PMID: 17090418.
      Citations: 23     Fields:    Translation:HumansAnimalsCells
    136. Hoepken HH, Gispert S, Morales B, Wingerter O, Del Turco D, Nussbaum RL, Brandt U, Deller T, Wirth B, Kudin AP, Kunz WS, Auburger G, M?lsch A, M?ller K, Dr?se S. Mitochondrial dysfunction, peroxidation damage and changes in glutathione metabolism in PARK6. Neurobiol Dis. 2007 Feb; 25(2):401-11. PMID: 17141510.
      Citations: 81     Fields:    Translation:HumansCells
    137. Frisch C, Kudin AP, Elger CE, Kunz WS, Helmstaedter C. Amelioration of water maze performance deficits by topiramate applied during pilocarpine-induced status epilepticus is negatively dose-dependent. Epilepsy Res. 2007 Feb; 73(2):173-80. PMID: 17084066.
      Citations: 12     Fields:    Translation:AnimalsCells
    138. Linnebank M, Lutz H, Jarre E, Vielhaber S, Noelker C, Struys E, Jakobs C, Klockgether T, Evert BO, Kunz WS, W?llner U. Binding of copper is a mechanism of homocysteine toxicity leading to COX deficiency and apoptosis in primary neurons, PC12 and SHSY-5Y cells. Neurobiol Dis. 2006 Sep; 23(3):725-30. PMID: 16876425.
      Citations: 16     Fields:    Translation:HumansAnimalsCells
    139. Niessen HG, Angenstein F, Sander K, Kunz WS, Teuchert M, Ludolph AC, Heinze HJ, Scheich H, Vielhaber S. In vivo quantification of spinal and bulbar motor neuron degeneration in the G93A-SOD1 transgenic mouse model of ALS by T2 relaxation time and apparent diffusion coefficient. Exp Neurol. 2006 Oct; 201(2):293-300. PMID: 16740261.
      Citations: 22     Fields:    Translation:HumansAnimalsCells
    140. Szewczyk A, Skalska J, Glab M, Kulawiak B, Malinska D, Koszela-Piotrowska I, Kunz WS. Mitochondrial potassium channels: from pharmacology to function. Biochim Biophys Acta. 2006 May-Jun; 1757(5-6):715-20. PMID: 16787636.
      Citations: 25     Fields:    Translation:HumansAnimalsCells
    141. Vielhaber S, Kornblum C, Heinze HJ, Elger CE, Kunz WS. Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophies--a comment. Brain. 2005 Dec; 128(Pt 12):E38. PMID: 16311266.
      Citations: 2     Fields:    Translation:HumansCells
    142. Bauduin P, Touraud D, Monduzzi M, Ninham BW, Kunz W, Pinna MC. Hofmeister effects in biology: effect of choline addition on the salt-induced super activity of horseradish peroxidase and its implication for salt resistance of plants. J Phys Chem B. 2005 Sep 01; 109(34):16511-4. PMID: 16853099.
      Citations: 5     Fields:    Translation:Cells
    143. Kraytsberg Y, Kudina T, Kornblum C, Elger CE, Khrapko K, Kunz WS, Zsurka G. Recombination of mitochondrial DNA in skeletal muscle of individuals with multiple mitochondrial DNA heteroplasmy. Nat Genet. 2005 Aug; 37(8):873-7. PMID: 16025113; PMCID: PMC1444756.
      Citations: 21     Fields:    Translation:Humans
    144. Niessen HG, Angenstein F, Vielhaber S, Frisch C, Kudin A, Elger CE, Heinze HJ, Scheich H, Kunz WS. Volumetric magnetic resonance imaging of functionally relevant structural alterations in chronic epilepsy after pilocarpine-induced status epilepticus in rats. Epilepsia. 2005 Jul; 46(7):1021-6. PMID: 16026554.
      Citations: 20     Fields:    Translation:Animals
    145. Skalska J, Debska G, Kunz WS, Szewczyk A. Antidiabetic sulphonylureas activate mitochondrial permeability transition in rat skeletal muscle. Br J Pharmacol. 2005 Jul; 145(6):785-91. PMID: 15895111; PMCID: PMC1576186.
      Citations: 10     Fields:    Translation:AnimalsCells
    146. Kudin AP, Debska-Vielhaber G, Kunz WS. Characterization of superoxide production sites in isolated rat brain and skeletal muscle mitochondria. Biomed Pharmacother. 2005 May; 59(4):163-8. PMID: 15862710.
      Citations: 15     Fields:    Translation:AnimalsCells
    147. Minnerop M, Kornblum C, Joe AY, Tatsch K, Kunz WS, Klockgether T, Reinhardt MJ, W?llner U. Dopamine transporter SPECT in patients with mitochondrial disorders. J Neurol Neurosurg Psychiatry. 2005 Jan; 76(1):118-20. PMID: 15608010; PMCID: PMC1739307.
      Citations: 1     Fields:    Translation:Humans
    148. Kudin AP, Debska-Vielhaber G, Vielhaber S, Elger CE, Kunz WS. The mechanism of neuroprotection by topiramate in an animal model of epilepsy. Epilepsia. 2004 Dec; 45(12):1478-87. PMID: 15571505.
      Citations: 36     Fields:    Translation:AnimalsCells
    149. Zsurka G, Kornblum C, Rudolph J, Wiesner RJ, Elger CE, Kunz WS, Schr?der R. Tissue dependent co-segregation of the novel pathogenic G12276A mitochondrial tRNALeu(CUN) mutation with the A185G D-loop polymorphism. J Med Genet. 2004 Dec; 41(12):e124. PMID: 15591266; PMCID: PMC1735651.
      Citations: 8     Fields:    Translation:Humans
    150. Kunz WS, Klockgether T, Kornblum C, Roggenk?mper P, Schr?der R. [Diagnostic value of mitochondrial DNA analysis in chronic progressive external ophthalmoplegia (CPEO)]. Klin Monbl Augenheilkd. 2004 Dec; 221(12):1057-61. PMID: 15599814.
      Citations: 2     Fields:    Translation:HumansCells
    151. Vielhaber S, Feistner H, Weis J, Kreuder J, Sailer M, Kunz WS, Schr?der JM. Primary carnitine deficiency: adult onset lipid storage myopathy with a mild clinical course. J Clin Neurosci. 2004 Nov; 11(8):919-24. PMID: 15519880.
      Citations: 8     Fields:    Translation:Humans
    152. Okulla T, Kunz WS, Klockgether T, Kornblum C, Schr?der R. Diagnostic value of mitochondrial DNA mutation analysis in juvenile unilateral ptosis. Graefes Arch Clin Exp Ophthalmol. 2005 Apr; 243(4):380-2. PMID: 15864628.
      Citations: 2     Fields:    Translation:HumansCells
    153. Kirches E, Mawrin C, Dietzmann K, Lins H, Wallesch CW, Kunz WS, Wiedemann FR, Winkler-Stuck K. Re-evaluation of the dysfunction of mitochondrial respiratory chain in skeletal muscle of patients with Parkinson's disease. J Neural Transm (Vienna). 2005 Apr; 112(4):499-518. PMID: 15340872.
      Citations: 26     Fields:    Translation:HumansCells
    154. Wiedemann FR, Wallesch CW, Kunz WS, Winkler-Stuck K. Effect of coenzyme Q10 on the mitochondrial function of skin fibroblasts from Parkinson patients. J Neurol Sci. 2004 May 15; 220(1-2):41-8. PMID: 15140604.
      Citations: 24     Fields:    Translation:HumansCells
    155. Kraytsberg Y, Schwartz M, Brown TA, Ebralidse K, Kunz WS, Clayton DA, Vissing J, Khrapko K. Recombination of human mitochondrial DNA. Science. 2004 May 14; 304(5673):981. PMID: 15143273.
      Citations: 85     Fields:    Translation:HumansCells
    156. Kunz WS, Bimpong-Buta NY, Kudin AP, Elger CE. The role of mitochondria in epilepsy: implications for neurodegenerative diseases. Toxicol Mech Methods. 2004; 14(1-2):19-23. PMID: 20021117.
      Citations: 2     Fields:    
    157. Knobloch J, Kunz W, Michel A. P19: a female and tissue specifically expressed gene in Schistosoma mansoni, regulated by pairing with the male. Parasitology. 2003 Dec; 127(Pt 6):519-24. PMID: 14700187.
      Citations: 4     Fields:    Translation:AnimalsCells
    158. Kudin AP, Bimpong-Buta NY, Vielhaber S, Elger CE, Kunz WS. Characterization of superoxide-producing sites in isolated brain mitochondria. J Biol Chem. 2004 Feb 06; 279(6):4127-35. PMID: 14625276.
      Citations: 181     Fields:    Translation:HumansAnimalsCells
    159. Vielhaber S, Kudin AP, Kudina TA, Stiller D, Scheich H, Schoenfeld A, Feistner H, Heinze HJ, Elger CE, Kunz WS. Hippocampal N-acetyl aspartate levels do not mirror neuronal cell densities in creatine-supplemented epileptic rats. Eur J Neurosci. 2003 Oct; 18(8):2292-300. PMID: 14622190.
      Citations: 6     Fields:    Translation:AnimalsCells
    160. Kuznetsov AV, Kunz WS, Saks V, Usson Y, Mazat JP, Letellier T, Gellerich FN, Margreiter R. Cryopreservation of mitochondria and mitochondrial function in cardiac and skeletal muscle fibers. Anal Biochem. 2003 Aug 15; 319(2):296-303. PMID: 12871725.
      Citations: 26     Fields:    Translation:HumansAnimalsCells
    161. Vielhaber S, Kudin A, Winkler K, Wiedemann F, Feistner H, Heinze HJ, Elger CE, Kunz WS, Schr?der R. Is there mitochondrial dysfunction in amyotrophic lateral sclerosis skeletal muscle? Ann Neurol. 2003 May; 53(5):686-7; author reply 687-8. PMID: 12731009.
      Citations: 2     Fields:    Translation:HumansCells
    162. Goudeau B, Simon MC, Fischer D, Eggermann T, Clemen CS, Li Z, Reimann J, Xue Z, Zerres K, van der Ven PF, Kunz WS, Vicart P, Schr?der R, Rudnik-Sch?neborn S, F?rst DO. On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondria. Hum Mol Genet. 2003 Mar 15; 12(6):657-69. PMID: 12620971.
      Citations: 33     Fields:    Translation:HumansCells
    163. Vielhaber S, Von Oertzen JH, Kudin AF, Schoenfeld A, Menzel C, Biersack HJ, Kral T, Elger CE, Kunz WS. Correlation of hippocampal glucose oxidation capacity and interictal FDG-PET in temporal lobe epilepsy. Epilepsia. 2003 Feb; 44(2):193-9. PMID: 12558573.
      Citations: 26     Fields:    Translation:HumansCells
    164. Reimann J, Kunz WS, Vielhaber S, Kappes-Horn K, Schr?der R. Mitochondrial dysfunction in myofibrillar myopathy. Neuropathol Appl Neurobiol. 2003 Feb; 29(1):45-51. PMID: 12581339.
      Citations: 12     Fields:    Translation:HumansCells
    165. Khrapko K, Nekhaeva E, Kraytsberg Y, Kunz W. Clonal expansions of mitochondrial genomes: implications for in vivo mutational spectra. Mutat Res. 2003 Jan 28; 522(1-2):13-9. PMID: 12517407.
      Citations: 15     Fields:    Translation:HumansAnimalsCells
    166. Kunz WS. Different metabolic properties of mitochondrial oxidative phosphorylation in different cell types--important implications for mitochondrial cytopathies. Exp Physiol. 2003 Jan; 88(1):149-54. PMID: 12525863.
      Citations: 24     Fields:    Translation:HumansAnimalsCells
    167. Schauseil-Zipf U, Michalk DV, Kunz WS, von Kleist-Retzow JC. Mitochondrial diseases--an expanding spectrum of disorders and affected genes. Exp Physiol. 2003 Jan; 88(1):155-66. PMID: 12525864.
      Citations: 4     Fields:    Translation:HumansAnimalsCells
    168. Varlamov DA, Kudin AP, Vielhaber S, Sassen R, Becker A, Kunz D, Haug K, Rebstock J, Heils A, Elger CE, Kunz WS, Schr?der R. Metabolic consequences of a novel missense mutation of the mtDNA CO I gene. Hum Mol Genet. 2002 Aug 01; 11(16):1797-805. PMID: 12140182.
      Citations: 15     Fields:    Translation:HumansAnimalsCells
    169. Kunz WS. The role of mitochondria in epileptogenesis. Curr Opin Neurol. 2002 Apr; 15(2):179-84. PMID: 11923632.
      Citations: 24     Fields:    Translation:HumansCells
    170. Kudin AP, Kudina TA, Seyfried J, Vielhaber S, Beck H, Elger CE, Kunz WS. Seizure-dependent modulation of mitochondrial oxidative phosphorylation in rat hippocampus. Eur J Neurosci. 2002 Apr; 15(7):1105-14. PMID: 11982622.
      Citations: 51     Fields:    Translation:AnimalsCells
    171. Kunz D, Winkler K, Elger CE, Kunz WS. Functional imaging of mitochondrial redox state. Methods Enzymol. 2002; 352:135-50. PMID: 12125342.
      Citations: 8     Fields:    Translation:HumansCells
    172. Vielhaber S, Kaufmann J, Kanowski M, Sailer M, Feistner H, Tempelmann C, Elger CE, Heinze HJ, Kunz WS. Effect of creatine supplementation on metabolite levels in ALS motor cortices. Exp Neurol. 2001 Dec; 172(2):377-82. PMID: 11716561.
      Citations: 13     Fields:    Translation:HumansCells
    173. Schechtman D, Winnen R, Tarrab-Hazdai R, Ram D, Shinder V, Grevelding CG, Kunz W, Arnon R. Expression and immunolocalization of the 14-3-3 protein of Schistosoma mansoni. Parasitology. 2001 Dec; 123(Pt 6):573-82. PMID: 11814044.
      Citations: 12     Fields:    Translation:AnimalsCells
    174. Vielhaber S, Winkler K, Weis S, Sailer M, Feistner H, Heinze HJ, Kunz WS, Schr?der R, Schr?der JM. Defective mitochondrial oxidative phosphorylation in myopathies with tubular aggregates originating from sarcoplasmic reticulum. J Neuropathol Exp Neurol. 2001 Nov; 60(11):1032-40. PMID: 11706933.
      Citations: 4     Fields:    Translation:HumansCells
    175. Kunz WS. Control of oxidative phosphorylation in skeletal muscle. Biochim Biophys Acta. 2001 Mar 01; 1504(1):12-9. PMID: 11239481.
      Citations: 13     Fields:    Translation:HumansAnimalsCells
    176. Kunz WS, Scott CS, Gressner AM, Kunz D. Automated CD61 immunoplatelet analysis of thrombocytopenic samples. Br J Haematol. 2001 Mar; 112(3):584-92. PMID: 11260058.
      Citations:    Fields:    Translation:HumansCells
    177. Kunz W, Grevelding CG, Kapp K, Sch?ssler P. Identification, isolation and characterization of a Fyn-like tyrosine kinase from Schistosoma mansoni. Parasitology. 2001 Mar; 122(Pt 3):317-27. PMID: 11289068.
      Citations: 7     Fields:    Translation:HumansAnimalsCells
    178. Debska G, May R, Kicinska A, Szewczyk A, Elger CE, Kunz WS. Potassium channel openers depolarize hippocampal mitochondria. Brain Res. 2001 Feb 16; 892(1):42-50. PMID: 11172747.
      Citations: 30     Fields:    Translation:AnimalsCells
    179. Schwarz CS, Evert BO, Seyfried J, Schaupp M, Kunz WS, Vielhaber S, Klockgether T, W?llner U. Overexpression of bcl-2 results in reduction of cytochrome c content and inhibition of complex I activity. Biochem Biophys Res Commun. 2001 Feb 02; 280(4):1021-7. PMID: 11162629.
      Citations: 3     Fields:    Translation:AnimalsCells
    180. Kunz W, Horny HP, Einsele H, B?hm P. Adult Gaucher disease in association with primary malignant bone tumors. Cancer. 2001 Feb 01; 91(3):457-62. PMID: 11169926.
      Citations: 5     Fields:    Translation:Humans
    181. Heils A, Haug K, Kunz WS, Fernandez G, Horvath S, Rebstock J, Propping P, Elger CE. Interleukin-1beta gene polymorphism and susceptibility to temporal lobe epilepsy with hippocampal sclerosis. Ann Neurol. 2000 Dec; 48(6):948-50. PMID: 11117556.
      Citations: 11     Fields:    Translation:Humans
    182. Kunz WS, Kudin AP, Vielhaber S, Zuschratter W, Schramm J, Beck H, Elger CE, Bl?mcke I. Mitochondrial complex I deficiency in the epileptic focus of patients with temporal lobe epilepsy. Ann Neurol. 2000 Nov; 48(5):766-73. PMID: 11079540.
      Citations: 74     Fields:    Translation:Humans
    183. Kunz WS, Gressner AM, Kunz D, H?ffkes H. Standardized flow cytometric method for the accurate determination of platelet counts in patients with severe thrombocytopenia. Cytometry. 2000 Oct 15; 42(5):284-9. PMID: 11025486.
      Citations: 1     Fields:    Translation:Humans
    184. Kunz WS, Kudin A, Vielhaber S, Elger CE, Attardi G, Villani G. Flux control of cytochrome c oxidase in human skeletal muscle. J Biol Chem. 2000 Sep 08; 275(36):27741-5. PMID: 10869362.
      Citations: 29     Fields:    Translation:HumansCells
    185. Vielhaber S, Kunz D, Winkler K, Wiedemann FR, Kirches E, Feistner H, Heinze HJ, Elger CE, Schubert W, Kunz WS. Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis. Brain. 2000 Jul; 123 ( Pt 7):1339-48. PMID: 10869047.
      Citations: 86     Fields:    Translation:HumansCellsCTClinical Trials
    186. Soldner F, Kunz WS, Schulz JB, Klockgether T, Kovar KA, Seyfried J, W?llner U. Effect of 1-methyl-4-phenylpyridinium on glutathione in rat pheochromocytoma PC 12 cells. Neurochem Int. 2000 May; 36(6):489-97. PMID: 10762085.
      Citations: 10     Fields:    Translation:AnimalsCells
    187. Vielhaber S, Wiedemann FR, Kornblum C, Papassotiropoulos A, Broich P, Zierz S, Elger CE, Reichmann H, Seibel P, Klockgether T, Kunz WS, Schr?der R. New insights into the metabolic consequences of large-scale mtDNA deletions: a quantitative analysis of biochemical, morphological, and genetic findings in human skeletal muscle. J Neuropathol Exp Neurol. 2000 May; 59(5):353-60. PMID: 10888364.
      Citations: 12     Fields:    Translation:HumansCells
    188. Wiedemann FR, Vielhaber S, Elger CE, Kunz WS, Schr?der R. Evaluation of methods for the determination of mitochondrial respiratory chain enzyme activities in human skeletal muscle samples. Anal Biochem. 2000 Mar 01; 279(1):55-60. PMID: 10683230.
      Citations: 11     Fields:    Translation:HumansAnimalsCells
    189. Herrmann M, Ebert AD, Galazky I, Wunderlich MT, Kunz WS, Huth C. Neurobehavioral outcome prediction after cardiac surgery: role of neurobiochemical markers of damage to neuronal and glial brain tissue. Stroke. 2000 Mar; 31(3):645-50. PMID: 10700498.
      Citations: 40     Fields:    Translation:HumansCells
    190. Vielhaber S, Kudin A, Elger CE, Kunz WS, Schr?der R. Muscle fibres: applications for the study of the metabolic consequences of enzyme deficiencies in skeletal muscle. Biochem Soc Trans. 2000 Feb; 28(2):159-64. PMID: 10816119.
      Citations: 5     Fields:    Translation:HumansCells
    191. Kicinska A, D bska G, Kunz W, Szewczyk A. Mitochondrial potassium and chloride channels. Acta Biochim Pol. 2000; 47(3):541-51. PMID: 11310958.
      Citations: 5     Fields:    Translation:HumansAnimalsCells
    192. Feistner H, Schneider W, Weis J, Kunz WS, Vielhaber S. Mitochondrial complex I deficiency in a female with multiplex arthrogryposis congenita. Pediatr Neurol. 2000 Jan; 22(1):53-6. PMID: 10669207.
      Citations:    Fields:    Translation:HumansCells
    193. Kudin A, Vielhaber S, Beck H, Elger CE, Kunz WS. Quantitative investigation of mitochondrial function in single rat hippocampal slices: a novel application of high-resolution respirometry and laser-excited fluorescence spectroscopy. Brain Res Brain Res Protoc. 1999 Dec; 4(3):329-34. PMID: 10592342.
      Citations: 2     Fields:    Translation:AnimalsCells
    194. Winkler K, Kirches E, Kunz D, Feistner H, Elger CE, Ludolph AC, Riepe MW, Kunz WS, Vielhaber S, B?chner M. Visualization of defective mitochondrial function in skeletal muscle fibers of patients with sporadic amyotrophic lateral sclerosis. J Neurol Sci. 1999 Oct 31; 169(1-2):133-9. PMID: 10540022.
      Citations: 42     Fields:    Translation:HumansCells
    195. Winkler K, Vielhaber S, Michael M, Warich-Kirches M, von Bossanyi P, Plate I, Kunz WS, Szibor R, Feistner H, Dietzmann K, Kirches E. Mitochondrial tRNA(Cys) mutation A5823G in a patient with motor neuron disease and temporal lobe epilepsy. Pathobiology. 1999 Jul-Aug; 67(4):214-8. PMID: 10738184.
      Citations: 3     Fields:    Translation:HumansCells
    196. Kunz WS, Goussakov IV, Beck H, Elger CE. Altered mitochondrial oxidative phosphorylation in hippocampal slices of kainate-treated rats. Brain Res. 1999 May 01; 826(2):236-42. PMID: 10224301.
      Citations: 14     Fields:    Translation:AnimalsCells
    197. Kunz WS, Kuznetsov AV, Clark JF, Tracey I, Elger CE. Metabolic consequences of the cytochrome c oxidase deficiency in brain of copper-deficient Mo(vbr) mice. J Neurochem. 1999 Apr; 72(4):1580-5. PMID: 10098864.
      Citations: 10     Fields:    Translation:AnimalsCells
    198. Ridgers I, Johnston DA, Rollinson D, Kunz W, Grevelding CG, Kampk?tter A. Schistosoma mansoni: cloning and characterization of the Ras homologue. Exp Parasitol. 1999 Mar; 91(3):280-3. PMID: 10072330.
      Citations: 1     Fields:    Translation:HumansAnimalsCells
    199. Wiedemann FR, Winkler K, Lins H, Wallesch CW, Kunz WS. Detection of respiratory chain defects in cultivated skin fibroblasts and skeletal muscle of patients with Parkinson's disease. Ann N Y Acad Sci. 1999; 893:426-9. PMID: 10672282.
      Citations: 13     Fields:    Translation:HumansCells
    200. Saks VA, Veksler VI, Kuznetsov AV, Kay L, Sikk P, Tiivel T, Tranqui L, Olivares J, Winkler K, Wiedemann F, Kunz WS. Permeabilized cell and skinned fiber techniques in studies of mitochondrial function in vivo. Mol Cell Biochem. 1998 Jul; 184(1-2):81-100. PMID: 9746314.
      Citations: 138     Fields:    Translation:HumansAnimalsCells
    201. Doenhoff M, Kunz W, Grevelding CG, Quack T. Schistosoma mansoni: the varying occurrence of repetitive elements in different strains shows sex-specific polymorphisms. Exp Parasitol. 1998 Jun; 89(2):222-7. PMID: 9635446.
      Citations: 6     Fields:    Translation:AnimalsCells
    202. Winkler K, Wiedemann FR, von Bossanyi P, Dietzmann K, Kunz WS, Kuznetsov AV. Impaired mitochondrial oxidative phosphorylation in skeletal muscle of the dystrophin-deficient mdx mouse. Mol Cell Biochem. 1998 Jun; 183(1-2):87-96. PMID: 9655182.
      Citations: 91     Fields:    Translation:HumansAnimalsCells
    203. Winkler K, Warich-Kirches M, Szibor R, Wien F, Kunz WS, von Bossanyi P, Bajaj PK, Dietzmann K, Kirches EJ. mtDNA depletion and impairment of mitochondrial function in a case of a multisystem disorder including severe myopathy. J Inherit Metab Dis. 1998 Jun; 21(4):400-8. PMID: 9700597.
      Citations: 1     Fields:    Translation:Humans
    204. Kuznetsov AV, Mayboroda O, Kunz D, Winkler K, Schubert W, Kunz WS. Functional imaging of mitochondria in saponin-permeabilized mice muscle fibers. J Cell Biol. 1998 Mar 09; 140(5):1091-9. PMID: 9490722; PMCID: PMC2132706.
      Citations: 35     Fields:    Translation:AnimalsCells
    205. Finken-Eigen M, Michel A, Grevelding CG, Kunz W, Sch?ssler P, K?hrer K. A female-specific cDNA sequence of Schistosoma mansoni encoding an amidase that is expressed in the gastrodermis. Parasitology. 1998 Feb; 116 ( Pt 2):131-7. PMID: 9509022.
      Citations:    Fields:    Translation:AnimalsCells
    206. Kunz WS, Wiedemann FR. Oxygen dependence of flux control of cytochrome c oxidase -- implications for mitochondrial diseases. FEBS Lett. 1998 Jan 23; 422(1):33-5. PMID: 9475164.
      Citations: 3     Fields:    Translation:AnimalsCells
    207. Winkler K, Kuznetsov AV, Bartels C, Vielhaber S, Feistner H, Kunz WS, Wiedemann FR. Impairment of mitochondrial function in skeletal muscle of patients with amyotrophic lateral sclerosis. J Neurol Sci. 1998; 156(1):65-72. PMID: 9559989.
      Citations: 86     Fields:    Translation:HumansCells
    208. Wiedemann FR, Winkler K, Kunz WS, Kuznetsov AV. Use of saponin-permeabilized muscle fibers for the diagnosis of mitochondrial diseases. Biofactors. 1998; 7(3):221-3. PMID: 9568252.
      Citations: 4     Fields:    Translation:HumansCells
    209. Winkler K, Kuznetsov AV, Lins H, Kirches E, Wallesch CW, Kunz WS. Detection of mitochondrial defects by laser fluorimetry. Mol Cell Biochem. 1997 Sep; 174(1-2):97-100. PMID: 9309672.
      Citations: 2     Fields:    Translation:HumansCells
    210. Kunz W, Finken-Eigen M. Schistosoma mansoni: gene structure and localization of a homologue to cysteine protease ER 60. Exp Parasitol. 1997 May; 86(1):1-7. PMID: 9149235.
      Citations: 4     Fields:    Translation:AnimalsCells
    211. Winkler K, Kirches E, Lins H, Feistner H, Kunz WS, Kuznetsov AV. Application of inhibitor titrations for the detection of oxidative phosphorylation defects in saponin-skinned muscle fibers of patients with mitochondrial diseases. Biochim Biophys Acta. 1997 Apr 12; 1360(2):142-50. PMID: 9128179.
      Citations: 13     Fields:    Translation:HumansCells
    212. Luley C, Winkler K, Lins H, Kunz WS, Kunz D. Flow cytometric detection of mitochondrial dysfunction in subpopulations of human mononuclear cells. Anal Biochem. 1997 Mar 15; 246(2):218-24. PMID: 9073359.
      Citations: 6     Fields:    Translation:HumansCells
    213. Grevelding CG, Kunz W, Sch?ssler P. Cloning and characterization of elongation factor 1-alpha of Schistosoma mansoni. Parasitol Res. 1997; 83(2):206-8. PMID: 9039706.
      Citations: 1     Fields:    Translation:HumansAnimalsCells
    214. Grevelding CG, Kampk?tter A, Hollmann M, Sch?fer U, Kunz W. Direct PCR on fruitflies and blood flukes without prior DNA isolation. Nucleic Acids Res. 1996 Oct 15; 24(20):4100-1. PMID: 8918821; PMCID: PMC146205.
      Citations: 2     Fields:    Translation:Animals
    215. Clark JF, Winkler K, Kunz WS, Kuznetsov AV. Increase of flux control of cytochrome c oxidase in copper-deficient mottled brindled mice. J Biol Chem. 1996 Jan 05; 271(1):283-8. PMID: 8550574.
      Citations: 11     Fields:    Translation:AnimalsCells
    216. Kuznetsov AV, Lins H, Kirches E, von Bossanyi P, Dietzmann K, Frank B, Feistner H, Kunz WS, Winkler K. Laser-excited fluorescence studies of mitochondrial function in saponin-skinned skeletal muscle fibers of patients with chronic progressive external ophthalmoplegia. Biochim Biophys Acta. 1995 Dec 12; 1272(3):181-4. PMID: 8541350.
      Citations: 7     Fields:    Translation:HumansCells
    217. Michel A, Kunz W, Menrath M. A female-specific cDNA sequence of Schistosoma mansoni encoding a mucin-like protein that is expressed in the epithelial cells of the reproductive duct. Parasitology. 1995 Nov; 111 ( Pt 4):477-83. PMID: 11023412.
      Citations: 8     Fields:    Translation:AnimalsCells
    218. Gohr LG, Sommer G, Kunz W, Grevelding CG, Sch?ssler P. Combined isolation of nucleic acids and protein from small amounts of tissue. Trends Genet. 1995 Oct; 11(10):378-9. PMID: 7482759.
      Citations:    Fields:    Translation:Animals
    219. Ghoneim H, Resto M, Klinkert MQ, Kunz W, Michel A. Sequence, characterization and localization of a cysteine proteinase cathepsin L in Schistosoma mansoni. Mol Biochem Parasitol. 1995 Jul; 73(1-2):7-18. PMID: 8577349.
      Citations: 16     Fields:    Translation:HumansAnimalsCells
    220. Gellerich FN, Kunz WS, Wisniewski E. Distribution of flux control among the enzymes of mitochondrial oxidative phosphorylation in calcium-activated saponin-skinned rat musculus soleus fibers. Eur J Biochem. 1995 Jun 01; 230(2):549-54. PMID: 7607228.
      Citations: 7     Fields:    Translation:AnimalsCells
    221. Luley C, Fritz S, Bohnensack R, Winkler K, Kunz WS, Wallesch CW, Kunz D. Oxygraphic evaluation of mitochondrial function in digitonin-permeabilized mononuclear cells and cultured skin fibroblasts of patients with chronic progressive external ophthalmoplegia. Biochem Mol Med. 1995 Apr; 54(2):105-11. PMID: 8581354.
      Citations: 3     Fields:    Translation:HumansCells
    222. Belikova Y, Kuznetsov AV, Gellerich FN, Schild L, Neumann HW, Kunz WS, Khuchua Z. Caffeine and Ca2+ stimulate mitochondrial oxidative phosphorylation in saponin-skinned human skeletal muscle fibers due to activation of actomyosin ATPase. Biochim Biophys Acta. 1994 Dec 30; 1188(3):373-9. PMID: 7803452.
      Citations: 6     Fields:    Translation:HumansCells
    223. Gellerich FN, Schild L, Kunz W. Contribution to control of mitochondrial oxidative phosphorylation by supplement of reducing equivalents. Biochem Med Metab Biol. 1994 Jun; 52(1):65-75. PMID: 7917469.
      Citations: 3     Fields:    Translation:AnimalsCells
    224. Gellerich FN, Ulrich J, Kunz W. Unusual properties of mitochondria from the human term placenta are caused by alkaline phosphatase. Placenta. 1994 Apr; 15(3):299-310. PMID: 8066053.
      Citations: 1     Fields:    Translation:HumansCells
    225. Gellerich FN, Kapischke M, Kunz W, Neumann W, Kuznetsov A, Brdiczka D, Nicolay K. The influence of the cytosolic oncotic pressure on the permeability of the mitochondrial outer membrane for ADP: implications for the kinetic properties of mitochondrial creatine kinase and for ADP channelling into the intermembrane space. Mol Cell Biochem. 1994 Apr-May; 133-134:85-104. PMID: 7808467.
      Citations: 15     Fields:    Translation:HumansAnimalsCells
    226. Sobek A, Symmons P, Kunz W, Finken M. Characterization of the complete protein disulfide isomerase gene of Schistosoma mansoni and identification of the tissues of its expression. Mol Biochem Parasitol. 1994 Mar; 64(1):135-44. PMID: 8078516.
      Citations: 8     Fields:    Translation:HumansAnimalsCells
    227. Kuznetsov AV, Winkler K, Gellerich FN, Neuhof S, Neumann HW, Kunz WS. Measurement of fluorescence changes of NAD(P)H and of fluorescent flavoproteins in saponin-skinned human skeletal muscle fibers. Anal Biochem. 1994 Feb 01; 216(2):322-7. PMID: 8179187.
      Citations: 11     Fields:    Translation:HumansCells
    228. Kuznetsov AV, Schulze W, Eichhorn K, Schild L, Striggow F, Bohnensack R, Neuhof S, Grasshoff H, Neumann HW, Gellerich FN, Kunz WS. Functional characterization of mitochondrial oxidative phosphorylation in saponin-skinned human muscle fibers. Biochim Biophys Acta. 1993 Aug 16; 1144(1):46-53. PMID: 8347661.
      Citations: 33     Fields:    Translation:HumansAnimalsCells
    229. Gellerich FN, Kunz WS. Quantification of the content of fluorescent flavoproteins in mitochondria from liver, kidney cortex, skeletal muscle, and brain. Biochem Med Metab Biol. 1993 Aug; 50(1):103-10. PMID: 8373630.
      Citations: 32     Fields:    Translation:AnimalsCells
    230. Kuznetsov AV, Gellerich FN, Kunz WS. Mitochondrial oxidative phosphorylation in saponin-skinned human muscle fibers is stimulated by caffeine. FEBS Lett. 1993 May 24; 323(1-2):188-90. PMID: 8495738.
      Citations: 8     Fields:    Translation:HumansCells
    231. Kunz WS, Gellerich FN, Wisniewski E. Phosphate affects the distribution of flux control among the enzymes of oxidative phosphorylation in rat skeletal muscle mitochondria. J Biol Chem. 1993 May 05; 268(13):9343-6. PMID: 8486629.
      Citations: 17     Fields:    Translation:AnimalsCells
    232. Hoeltke HJ, Ettl I, Finken M, West S, Kunz W. Multiple nucleic acid labeling and rainbow detection. Anal Biochem. 1992 Nov 15; 207(1):24-31. PMID: 1489097.
      Citations: 4     Fields:    Translation:AnimalsCells
    233. Krinelke L, Gellerich FN, Kunz WS. Glutamine affects glutamate metabolism in isolated rat kidney cortex mitochondria. Biochim Biophys Acta. 1992 Jun 19; 1100(3):329-31. PMID: 1351747.
      Citations:    Fields:    Translation:AnimalsCells
    234. Kunz WS, Augustin W, Noack H. Evaluation of a procedure for the simultaneous determination of oxidized and reduced pyridine nucleotides and adenylates in organic phenol extracts from mitochondria. Anal Biochem. 1992 Apr; 202(1):162-5. PMID: 1621979.
      Citations: 14     Fields:    Translation:AnimalsCells
    235. Hirzmann J, Preis D, Symmons P, Kunz W, Dietzel J. Ferritins of Schistosoma mansoni: sequence comparison and expression in female and male worms. Mol Biochem Parasitol. 1992 Feb; 50(2):245-54. PMID: 1741011.
      Citations: 16     Fields:    Translation:AnimalsCells
    236. Kunz WS, Halangk W. Use of NAD(P)H and flavoprotein fluorescence signals to characterize the redox state of pyridine nucleotides in epididymal bull spermatozoa. Biochim Biophys Acta. 1991 Feb 08; 1056(3):273-8. PMID: 2001381.
      Citations: 2     Fields:    Translation:AnimalsCells
    237. Scholz W, Wolf A, Kunz W, Willenbrock R, Steffen C. Effect of orotic acid on the generation of reactive oxygen and on lipid peroxidation in rat liver. Toxicology. 1991 Feb; 66(2):197-212. PMID: 2014518.
      Citations:    Fields:    Translation:AnimalsCells
    238. Kunz WS, Davis EJ. Control of reversible intracellular transfer of reducing potential. Arch Biochem Biophys. 1991 Jan; 284(1):40-6. PMID: 1824912.
      Citations: 3     Fields:    Translation:AnimalsCells
    239. Kunz WS. Application of the theory of steady-state flux control to mitochondrial beta-oxidation. Biomed Biochim Acta. 1991; 50(12):1143-57. PMID: 1668635.
      Citations: 7     Fields:    Translation:AnimalsCells
    240. Kunz WS, Bohnensack R, Gellerich FN. Estimation of flux control coefficients from inhibitor titrations by non-linear regression. FEBS Lett. 1990 Nov 12; 274(1-2):167-70. PMID: 2253770.
      Citations: 24     Fields:    Translation:AnimalsCells
    241. Kunz W, West S, Schr?der J. A multiple-staining procedure for the detection of different DNA fragments on a single blot. Anal Biochem. 1990 Nov 01; 190(2):254-8. PMID: 1705397.
      Citations: 9     Fields:    Translation:Animals
    242. Gellerich FN, Schild L, Kunz W, Bohnensack R. The function of the adenine nucleotide translocator in the control of oxidative phosphorylation. Biochim Biophys Acta. 1990 Jul 25; 1018(2-3):182-4. PMID: 2168208.
      Citations: 2     Fields:    Translation:AnimalsCells
    243. Kunz WS, Krinelke L. [Characterization of surface fluorescence signals of isolated perfused rat kidney]. Biomed Biochim Acta. 1990; 49(11):1119-30. PMID: 2094217.
      Citations: 1     Fields:    Translation:AnimalsCells
    244. Schild L, Kunz W, Sch?nfeld P. Long-chain fatty acids act as protonophoric uncouplers of oxidative phosphorylation in rat liver mitochondria. Biochim Biophys Acta. 1989 Dec 07; 977(3):266-72. PMID: 2556180.
      Citations: 14     Fields:    Translation:AnimalsCells
    245. Wojtczak AB, Geelen MJ, Kunz W, Wojtczak L, Sch?nfeld P. On the mechanism of the so-called uncoupling effect of medium- and short-chain fatty acids. Biochim Biophys Acta. 1988 Dec 07; 936(3):280-8. PMID: 3196710.
      Citations: 7     Fields:    Translation:AnimalsCells
    246. Gellerich FN, Schild L, Kunz W, Sch?nfeld P. Kinetic limitations in the overall reaction of mitochondrial oxidative phosphorylation accounting for flux-dependent changes in the apparent delta GexP/delta mu H+ ratio. FEBS Lett. 1988 Jun 06; 233(1):17-21. PMID: 2898384.
      Citations: 6     Fields:    Translation:AnimalsCells
    247. Kunz WS. Evaluation of electron-transfer flavoprotein and alpha-lipoamide dehydrogenase redox states by two-channel fluorimetry and its application to the investigation of beta-oxidation. Biochim Biophys Acta. 1988 Jan 20; 932(1):8-16. PMID: 3337800.
      Citations: 15     Fields:    Translation:AnimalsCells
    248. Halangk W, Dietz H, Bohnensack R, Kunz W. Regulation of oxidative phosphorylation in mitochondria of epididymal bull spermatozoa. Biochim Biophys Acta. 1987 Aug 12; 893(1):100-8. PMID: 3607041.
      Citations:    Fields:    Translation:AnimalsCells
    249. Kunz W, Opatz K, Finken M, Symmons P. Sequences of two genomic fragments containing an identical coding region for a putative egg-shell precursor protein of Schistosoma mansoni. Nucleic Acids Res. 1987 Jul 24; 15(14):5894. PMID: 3615210; PMCID: PMC306038.
      Citations: 4     Fields:    Translation:AnimalsCells
    250. Gellerich FN, Schlame M, Bohnensack R, Kunz W. Dynamic compartmentation of adenine nucleotides in the mitochondrial intermembrane space of rat-heart mitochondria. Biochim Biophys Acta. 1987 Feb 11; 890(2):117-26. PMID: 3801462.
      Citations: 24     Fields:    Translation:AnimalsCells
    251. Petzold D, Fischer HD, Kunz W, Wustmann C. [ATP-metabolizing enzymes in suspensions of isolated coupled rat brain mitochondria]. Biomed Biochim Acta. 1987; 46(5):331-40. PMID: 3663204.
      Citations:    Fields:    Translation:AnimalsCells
    252. Wustmann C, Petzold D, Kunz W, Fischer HD. Respiratory function of rat brain mitochondria after hypobaric hypoxia and piracetam treatment. Biomed Biochim Acta. 1987; 46(7):635-8. PMID: 3426574.
      Citations:    Fields:    Translation:AnimalsCells
    253. Kunz W, Gellerich FN. Cause and consequences of dynamic compartmentation of adenine nucleotides in the mitochondrial intermembrane space in respect to exchange of energy rich phosphates between cytosol and mitochondria. Biomed Biochim Acta. 1987; 46(8-9):S545-8. PMID: 3435511.
      Citations: 6     Fields:    Translation:AnimalsCells
    254. Kunz WS. Spectral properties of fluorescent flavoproteins of isolated rat liver mitochondria. FEBS Lett. 1986 Jan 20; 195(1-2):92-6. PMID: 3753688.
      Citations: 20     Fields:    Translation:AnimalsCells
    255. Kunz WS, Kunz W. Contribution of different enzymes to flavoprotein fluorescence of isolated rat liver mitochondria. Biochim Biophys Acta. 1985 Sep 06; 841(3):237-46. PMID: 4027266.
      Citations: 54     Fields:    Translation:AnimalsCells
    256. Halangk W, Bohnensack R, Kunz W. Interdependence of mitochondrial ATP production and extramitochondrial ATP utilization in intact spermatozoa. Biochim Biophys Acta. 1985 Jul 17; 808(2):316-22. PMID: 3848331.
      Citations: 5     Fields:    Translation:AnimalsCells
    257. Buchmann A, Kuhlmann W, Schwarz M, Kunz W, Wolf CR, Moll E, Friedberg T, Oesch F. Regulation and expression of four cytochrome P-450 isoenzymes, NADPH-cytochrome P-450 reductase, the glutathione transferases B and C and microsomal epoxide hydrolase in preneoplastic and neoplastic lesions in rat liver. Carcinogenesis. 1985 Apr; 6(4):513-21. PMID: 3921270.
      Citations: 23     Fields:    Translation:AnimalsCells
    258. Sch?fer M, Kunz W. rDNA in Locusta migratoria is very variable: two introns and extensive restriction site polymorphisms in the spacer. Nucleic Acids Res. 1985 Feb 25; 13(4):1251-66. PMID: 2987820; PMCID: PMC341070.
      Citations: 1     Fields:    Translation:AnimalsCells
    259. Kamensky Y, Konstantinov AA, Kunz WS, Surkov S. Effects of bc1-site electron transfer inhibitors on the absorption spectra of mitochondrial cytochromes b. FEBS Lett. 1985 Feb 11; 181(1):95-9. PMID: 2982656.
      Citations: 5     Fields:    Translation:AnimalsCells
    260. Hartung KJ, Jung K, Minda R, Kunz W. Mitochondrial respiratory function as indicator of the ischemic injury of the rat kidney. Biomed Biochim Acta. 1985; 44(10):1435-43. PMID: 4084249.
      Citations: 3     Fields:    Translation:AnimalsCells
    261. Halangk W, Bohnensack R, Frank K, Kunz W. Effect of various substrates on mitochondrial and cellular energy state of intact spermatozoa. Biomed Biochim Acta. 1985; 44(3):411-20. PMID: 4004841.
      Citations: 6     Fields:    Translation:AnimalsCells
    262. Kunz WS, Konstantinov A. Cytochrome b reduction by hexaammineruthenium in mitochondria and submitochondrial particles. Evidence for heme b-562 localization at the M-side of the mitochondrial membrane. FEBS Lett. 1984 Sep 17; 175(1):100-4. PMID: 6479328.
      Citations: 2     Fields:    Translation:AnimalsCells
    263. Kunz WS, Konstantinov A, Tsofina L, Liberman EA. Localization of a ferricyanide-reactive site of cytochrome b-c1 complex, possibly of cytochrome b or ubisemiquinone, at the outer face of submitochondrial particles. FEBS Lett. 1984 Jul 09; 172(2):261-6. PMID: 6086391.
      Citations: 1     Fields:    Translation:AnimalsCells
    264. Petzold D, Kunz W, Sch?nfeld P. Influence of octanoate on the rate of oxidative phosphorylation and the associated extramitochondrial ATP/ADP ratios studied with isolated rat liver mitochondria oxidizing pyruvate. Biomed Biochim Acta. 1984; 43(10):1055-65. PMID: 6525184.
      Citations:    Fields:    Translation:AnimalsCells
    265. Kunz WS, Konstantinov AA. Effect of b-c1-site inhibitors on the midpoint potentials of mitochondrial cytochromes b. FEBS Lett. 1983 May 08; 155(2):237-40. PMID: 6303845.
      Citations: 2     Fields:    Translation:AnimalsCells
    266. Gellerich FN, Bohnensack R, Kunz W. Control of mitochondrial respiration. The contribution of the adenine nucleotide translocator depends on the ATP- and ADP-consuming enzymes. Biochim Biophys Acta. 1983 Feb 17; 722(2):381-91. PMID: 6301555.
      Citations: 17     Fields:    Translation:AnimalsCells
    267. Kunz WS, Konstantinov A. Energy-linked spectral shift of ferrocytochrome b in beef heart submitochondrial particles. FEBS Lett. 1983 Feb 07; 152(1):53-6. PMID: 6840277.
      Citations:    Fields:    Translation:AnimalsCells
    268. Tager JM, Wanders RJ, Groen AK, Kunz W, Bohnensack R, Letko G, Duszynski J, Wojtczak L, K?ster U, B?hme G. Control of mitochondrial respiration. FEBS Lett. 1983 Jan 10; 151(1):1-9. PMID: 6337871.
      Citations: 44     Fields:    Translation:AnimalsCells
    269. Bohnensack R, Kunz W, Sch?nfeld P, B?hme G. Influence of the beta-hydroxybutyrate/acetoacetate ratio on the redox states of mitochondrial NAD(P) and cytochrome c systems, extramitochondrial ATP/ADP ratio and the respiration of isolated liver mitochondria in the resting state. Biomed Biochim Acta. 1983; 42(1):3-13. PMID: 6309158.
      Citations:    Fields:    Translation:AnimalsCells
    270. Hartung KJ, Kunz W, B?hme G. Involvement of intramitochondrial adenine nucleotides and inorganic phosphate in oxidative phosphorylation of extramitochondrially added adenosine-5'-diphosphate. Biomed Biochim Acta. 1983; 42(1):15-26. PMID: 6224484.
      Citations: 1     Fields:    Translation:AnimalsCells
    271. Markefski M, Kunz W, Zinchenko VP. Role of substrates in Sr2+-induced oscillations of ionic fluxes in rat liver mitochondria. Biochim Biophys Acta. 1982 Mar 16; 679(3):444-51. PMID: 7066310.
      Citations:    Fields:    Translation:AnimalsCells
    272. Letko G, Bohnensack R, Pohl K, Kunz W, K?ster U, B?hme G. Interrelationship between oxidative energy transformation and energy consumption at mitochondrial and cellular levels. Acta Biol Med Ger. 1982; 41(9):735-50. PMID: 6299035.
      Citations: 1     Fields:    Translation:AnimalsCells
    273. Bohnensack R, Kunz W, B?hme G, Sch?nfeld P, K?ster U. Interrelationships between hydrogen-supplying reactions, respiration rate and extramitochondrial adenine nucleotide pattern. Physiol Bohemoslov. 1982; 31(2):159-68. PMID: 6212956.
      Citations:    Fields:    Translation:AnimalsCells
    274. Duszynski J, Bogucka K, Letko G, Kunz W, Wojtczak L, K?ster U. Relationship between the energy cost of ATP transport and ATP synthesis in mitochondria. Biochim Biophys Acta. 1981 Sep 14; 637(2):217-23. PMID: 7295709.
      Citations: 10     Fields:    Translation:AnimalsCells
    275. Letko G, Kunz W, Duszynsky J, Bogucka K, Wojtczak L, K?ster U. Influence of different energy drains on the interrelationship between the rate of respiration, proton-motive force and adenine nucleotide patterns in isolated mitochondria. Biochim Biophys Acta. 1981 Jun 12; 636(1):32-8. PMID: 7284343.
      Citations: 4     Fields:    Translation:AnimalsCells
    276. Kunz W, Bohnensack R, Letko G, B?hme G, K?ster U, Sch?nfeld P. Relations between extramitochondrial and intramitochondrial adenine nucleotide systems. Arch Biochem Biophys. 1981 Jun; 209(1):219-29. PMID: 6456693.
      Citations: 8     Fields:    Translation:AnimalsCells
    277. Kitta D, Schwarz M, Tennekes HA, Uehleke H, Kunz W. Covalent binding of CCl4-intermediates to reduced pyridine nucleotides in mouse liver. Adv Exp Med Biol. 1981; 136 Pt A:769-77. PMID: 7344492.
      Citations:    Fields:    Translation:AnimalsCells
    278. Letko G, Duszynski J, Kunz W, K?ster U. Investigation of the dependence of the intramitochondrial [ATP]/[ADP] ratio on the respiration rate. Biochim Biophys Acta. 1980 Dec 03; 593(2):196-203. PMID: 7236631.
      Citations: 5     Fields:    Translation:AnimalsCells
    279. Renkawitz-Pohl R, Gl?tzer KH, Kunz W. Characterization of cloned ribosomal DNA from Drosophila hydei. Nucleic Acids Res. 1980 Oct 24; 8(20):4593-611. PMID: 6255425; PMCID: PMC324373.
      Citations: 27     Fields:    Translation:AnimalsCells
    280. Kunz W, Lyr H, B?hme G, Sch?nfeld P, K?ster U. The multifunctional actions of beta-thujaplicin on the oxidative energy transformations as a consequence of its lipophilic and chelating properties. Acta Biol Med Ger. 1980; 39(11-12):1153-63. PMID: 6787824.
      Citations: 1     Fields:    Translation:AnimalsCells
    281. Laib RJ, Bolt HM, Kunz W, St?ckle G. Vinyl chloride and trichloroethylene: comparison of alkylating effects of metabolites and induction of preneoplastic enzyme deficiencies in rat liver. J Cancer Res Clin Oncol. 1979 Jun 08; 94(2):139-47. PMID: 157359.
      Citations: 9     Fields:    Translation:AnimalsCells
    282. Bohnensack R, Kunz W. Mathematical model of regulation of oxidative phosphorylation in intact mitochondria. Acta Biol Med Ger. 1978; 37(1):97-112. PMID: 706931.
      Citations:    Fields:    Translation:Cells
    283. Reichert M, Schaller H, Kunz W, Gerber G. The dependence on the extramitochondrial ATP/ADP-ratio of the oxidative phosphorylation in mitochondria isolated by a new procedure from rat skeletal muscle. Acta Biol Med Ger. 1978; 37(8):1167-76. PMID: 749453.
      Citations: 2     Fields:    Translation:AnimalsCells
    284. Bohnensack R, Kunz W, K?ster U. Control of oxidative phosphorylation by the extra-mitochondrial ATP/ADP ratio. Biochim Biophys Acta. 1976 Aug 13; 440(2):391-402. PMID: 952975.
      Citations: 12     Fields:    Translation:AnimalsCells
    285. Lenartowicz E, Winter C, Kunz W, Wojtczak AB. The inhibition of isocitrate oxidation by palmitoyl-l-carnitine and palmitoyl-C0 A in rat liver mitochondria. Eur J Biochem. 1976 Aug 01; 67(1):137-44. PMID: 183951.
      Citations: 1     Fields:    Translation:AnimalsCells
    286. Schewe T, Rapoport S, Kunz W, B?hme G. [Action site of the systemic fungicide carboxin in the respiratory chain]. Acta Biol Med Ger. 1973; 31(1):73-86. PMID: 4774673.
      Citations:    Fields:    Translation:AnimalsCells
    287. Lutze G, Liese W, Kunz W. FEBS Lett. 1972 Aug 01; 24(2):189-192. PMID: 11946669.
      Citations: 1     Fields:    
    288. Steinbrecht I, Kunz W. [Determination of oxydated and reduced pyridine nucleotides in human and rabbit blood using the polarographic cycling method]. Acta Biol Med Ger. 1972; 29(4):495-507. PMID: 4405795.
      Citations: 1     Fields:    Translation:HumansAnimalsCells
    289. Bohnensack R, Kunz W. [Investigation of the penetration of oxaloacetate into rat liver mitochondria]. Biochim Biophys Acta. 1971 Jan 12; 226(1):33-41. PMID: 4323696.
      Citations: 1     Fields:    Translation:AnimalsCells
    290. Liese W, Jung K, Kunz W, David H. [Enzyme and electron microscopy studies on the preparation of membranes from rat liver mitochondria]. Acta Biol Med Ger. 1971; 27(3):477-98. PMID: 4336793.
      Citations:    Fields:    Translation:AnimalsCells
    291. Lutze G, Liese W, Kunz W. FEBS Lett. 1970 Oct 05; 10(3):133-135. PMID: 11945376.
      Citations:    Fields:    
    292. Steinbrecht I, Kunz W. [Use of "cycling" technic for random quantitative determination of the degree of reduction of NAD and NADP system in rat liver mitochondria with continuous recording of the measurements]. Acta Biol Med Ger. 1970; 25(5):731-47. PMID: 4399840.
      Citations: 8     Fields:    Translation:AnimalsCells
    293. Kunz W, B?hme G. [A simple registering single beam fluorometer for recording of redox changes in mitochondrial pyridine nucleotides]. Acta Biol Med Ger. 1969; 22(3):643-51. PMID: 4391413.
      Citations: 1     Fields:    Translation:AnimalsCells
    294. Kunz W, Klossek P. [On the energy-linked ion translocation through the mitochondrial membrane]. Acta Biol Med Ger. 1967; 19(5):766-79. PMID: 5589680.
      Citations:    Fields:    Translation:AnimalsCells
    295. KUNZ W, BOEHME G. [STUDIES ON COMPARTMENTATION OF ATP IN THE MITOCHONDRIA FROM THE RAT LIVER AND ASCITES TUMOR CELLS]. Acta Biol Med Ger. 1965; 14:250-8. PMID: 14315561.
      Citations: 1     Fields:    Translation:AnimalsCells
    296. KUNZ W, BOEHME G. [ON THE PREPARATION AND FUNCTIONAL PROPERTIES OF MITOCHONDRIA OF EHRLICH ASCITES CARCINOMA IN THE MOUSE]. Acta Biol Med Ger. 1964; 13:865-82. PMID: 14335765.
      Citations:    Fields:    Translation:AnimalsCells
    297. KUNZ W, MUELLER E, SIESS M. [The distribution of 2,6-bis (diethanolamino)-4,8-dipiperidino-pyrimido-(5,4-d)pyrimidine in organs and in the myocardial cells of rats and mice]. Arzneimittelforschung. 1963 Mar; 13:179-85. PMID: 13927400.
      Citations: 3     Fields:    Translation:Animals
    298. KUNZ W. [POLAROGRAPHIC STUDIES ON THE EFFECT OF OXALOACETATE ON SUCCINATE OXIDATION BY INTACT LIVER MITOCHONDRIA]. Hoppe Seylers Z Physiol Chem. 1963; 334:128-40. PMID: 14136703.
      Citations:    Fields:    Translation:AnimalsCells
    299. KUNZ W. [On the kinetics of choline oxidation by isolated liver mitochondria]. Acta Biol Med Ger. 1962; 9:674-81. PMID: 13927399.
      Citations:    Fields:    Translation:Cells
    300. KUNZ W, KAISER G. [On the interaction of oleic acid, serum albumin and calcium ions with liver mitochondria]. Hoppe Seylers Z Physiol Chem. 1961 Oct 25; 326:17-24. PMID: 14460633.
      Citations:    Fields:    Translation:HumansCells
    301. IZZO JL, CRUMP SL, KUNZ W. A clinical comparison of modified insulins. J Clin Invest. 1950 Nov; 29(11):1514-27. PMID: 14794780; PMCID: PMC436200.
      Citations: 4     Fields:    Translation:Humans

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