"Models, Molecular" 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.
Models used experimentally or theoretically to study molecular shape, electronic properties, or interactions; includes analogous molecules, computer-generated graphics, and mechanical structures.
Descriptor ID |
D008958
|
MeSH Number(s) |
E05.599.595
|
Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Models, Molecular".
Below are MeSH descriptors whose meaning is more specific than "Models, Molecular".
This graph shows the total number of publications written about "Models, Molecular" by people in this website by year, and whether "Models, Molecular" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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1999 | 0 | 1 | 1 |
2000 | 0 | 1 | 1 |
2005 | 0 | 1 | 1 |
2008 | 1 | 1 | 2 |
2009 | 0 | 1 | 1 |
2010 | 0 | 1 | 1 |
2011 | 1 | 2 | 3 |
2012 | 0 | 2 | 2 |
2013 | 1 | 5 | 6 |
2014 | 1 | 2 | 3 |
2015 | 1 | 3 | 4 |
2016 | 0 | 2 | 2 |
2018 | 0 | 3 | 3 |
2019 | 0 | 6 | 6 |
2020 | 0 | 1 | 1 |
2021 | 0 | 2 | 2 |
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Below are the most recent publications written about "Models, Molecular" by people in Profiles.
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Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome. J Am Soc Nephrol. 2021 03; 32(3):580-596.
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Novel KCNH1 Mutations Associated with Epilepsy: Broadening the Phenotypic Spectrum of KCNH1-Associated Diseases. Genes (Basel). 2021 01 21; 12(2).
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Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis. Proc Natl Acad Sci U S A. 2020 06 30; 117(26):15137-15147.
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The recurrent postzygotic pathogenic variant p.Glu47Lys in RHOA causes a novel recognizable neuroectodermal phenotype. Hum Mutat. 2020 03; 41(3):591-599.
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De novo variants in PAK1 lead to intellectual disability with macrocephaly and seizures. Brain. 2019 11 01; 142(11):3351-3359.
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LMO2 activation by deacetylation is indispensable for hematopoiesis and T-ALL leukemogenesis. Blood. 2019 10 03; 134(14):1159-1175.
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Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia. J Hum Genet. 2019 Aug; 64(8):803-813.
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Tautomerism and bioactivities of curcumenol, a common sesquiterpenoid widely existing in edible plants. Food Funct. 2019 Mar 20; 10(3):1288-1294.
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Cycloartane triterpenoids from Actaea vaginata with anti-inflammatory effects in LPS-stimulated RAW264.7 macrophages. Phytochemistry. 2019 Apr; 160:1-10.
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Discovery of the First-in-Class Dual Histone Deacetylase-Proteasome Inhibitor. J Med Chem. 2018 11 21; 61(22):10299-10309.