"GTPase-Activating Proteins" 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.
Proteins that activate the GTPase of specific GTP-BINDING PROTEINS.
Descriptor ID |
D020690
|
MeSH Number(s) |
D12.644.360.325.150 D12.776.476.325.150
|
Concept/Terms |
GTPase-Activating Proteins- GTPase-Activating Proteins
- GTPase Activating Proteins
- GAP Proteins
- GAP Protein
- GTPase-Activating Protein
- GTPase Activating Protein
|
Below are MeSH descriptors whose meaning is more general than "GTPase-Activating Proteins".
Below are MeSH descriptors whose meaning is more specific than "GTPase-Activating Proteins".
This graph shows the total number of publications written about "GTPase-Activating Proteins" by people in this website by year, and whether "GTPase-Activating Proteins" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2000 | 1 | 0 | 1 |
2005 | 1 | 0 | 1 |
2010 | 1 | 0 | 1 |
2012 | 0 | 1 | 1 |
2013 | 0 | 1 | 1 |
2015 | 1 | 0 | 1 |
2016 | 1 | 1 | 2 |
2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "GTPase-Activating Proteins" by people in Profiles.
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Bi-allelic Variants in RALGAPA1 Cause Profound Neurodevelopmental Disability, Muscular Hypotonia, Infantile Spasms, and Feeding Abnormalities. Am J Hum Genet. 2020 02 06; 106(2):246-255.
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Genetic Analysis of 'PAX6-Negative' Individuals with Aniridia or Gillespie Syndrome. PLoS One. 2016; 11(4):e0153757.
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Nocturnal frontal lobe epilepsy caused by a mutation in the GATOR1 complex gene NPRL3. Epilepsia. 2016 Mar; 57(3):e60-3.
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Human-specific gene ARHGAP11B promotes basal progenitor amplification and neocortex expansion. Science. 2015 Mar 27; 347(6229):1465-70.
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The genetic basis of DOORS syndrome: an exome-sequencing study. Lancet Neurol. 2014 Jan; 13(1):44-58.
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Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. Nat Genet. 2012 Dec; 44(12):1341-8.
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Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. Biol Psychiatry. 2010 Aug 15; 68(4):320-8.
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Use of MLL/GRAF fusion mRNA for measurement of minimal residual disease during chemotherapy in an infant with acute monoblastic leukemia (AML-M5). Genes Chromosomes Cancer. 2005 Aug; 43(4):424-6.
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The human GRAF gene is fused to MLL in a unique t(5;11)(q31;q23) and both alleles are disrupted in three cases of myelodysplastic syndrome/acute myeloid leukemia with a deletion 5q. Proc Natl Acad Sci U S A. 2000 Aug 01; 97(16):9168-73.