"Blotting, Southern" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A method (first developed by E.M. Southern) for detection of DNA that has been electrophoretically separated and immobilized by blotting on nitrocellulose or other type of paper or nylon membrane followed by hybridization with labeled NUCLEIC ACID PROBES.
| Descriptor ID |
D015139
|
| MeSH Number(s) |
E05.196.401.114 E05.301.300.087 E05.601.150
|
| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Blotting, Southern".
Below are MeSH descriptors whose meaning is more specific than "Blotting, Southern".
This graph shows the total number of publications written about "Blotting, Southern" by people in this website by year, and whether "Blotting, Southern" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 0 | 1 | 1 |
| 1997 | 0 | 1 | 1 |
| 1998 | 0 | 2 | 2 |
| 1999 | 0 | 2 | 2 |
| 2000 | 0 | 3 | 3 |
| 2002 | 0 | 1 | 1 |
| 2003 | 0 | 1 | 1 |
| 2004 | 0 | 2 | 2 |
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Below are the most recent publications written about "Blotting, Southern" by people in Profiles.
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[Diagnostic value of mitochondrial DNA analysis in chronic progressive external ophthalmoplegia (CPEO)]. Klin Monbl Augenheilkd. 2004 Dec; 221(12):1057-61.
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Diagnostic value of mitochondrial DNA mutation analysis in juvenile unilateral ptosis. Graefes Arch Clin Exp Ophthalmol. 2005 Apr; 243(4):380-2.
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Reverse transcriptase and reverse splicing activities encoded by the mobile group II intron cobI1 of fission yeast mitochondrial DNA. J Mol Biol. 2003 May 30; 329(2):191-206.
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A novel mutation in the SURF1 gene in a child with Leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency. J Child Neurol. 2002 Mar; 17(3):233-6.
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Flux control of cytochrome c oxidase in human skeletal muscle. J Biol Chem. 2000 Sep 08; 275(36):27741-5.
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A deletion distinct from the classical homologous recombination of juvenile nephronophthisis type 1 (NPH1) allows exact molecular definition of deletion breakpoints. Hum Mutat. 2000 Sep; 16(3):211-23.
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Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis. Brain. 2000 Jul; 123 ( Pt 7):1339-48.
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Mitochondrial tRNA(Cys) mutation A5823G in a patient with motor neuron disease and temporal lobe epilepsy. Pathobiology. 1999 Jul-Aug; 67(4):214-8.
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Schistosoma mansoni: cloning and characterization of the Ras homologue. Exp Parasitol. 1999 Mar; 91(3):280-3.
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Schistosoma mansoni: the varying occurrence of repetitive elements in different strains shows sex-specific polymorphisms. Exp Parasitol. 1998 Jun; 89(2):222-7.
MeSH information
