"Adenosine Triphosphatases" 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 group of enzymes which catalyze the hydrolysis of ATP. The hydrolysis reaction is usually coupled with another function such as transporting Ca(2+) across a membrane. These enzymes may be dependent on Ca(2+), Mg(2+), anions, H+, or DNA.
| Descriptor ID |
D000251
|
| MeSH Number(s) |
D08.811.277.040.025
|
| Concept/Terms |
DNA-Dependent Adenosinetriphosphatases- DNA-Dependent Adenosinetriphosphatases
- Adenosinetriphosphatases, DNA-Dependent
- DNA Dependent Adenosinetriphosphatases
- ATPase, DNA-Dependent
- ATPase, DNA Dependent
- DNA-Dependent ATPase
- DNA Dependent ATPase
|
Below are MeSH descriptors whose meaning is more general than "Adenosine Triphosphatases".
Below are MeSH descriptors whose meaning is more specific than "Adenosine Triphosphatases".
This graph shows the total number of publications written about "Adenosine Triphosphatases" by people in this website by year, and whether "Adenosine Triphosphatases" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 1 | 0 | 1 |
| 1999 | 1 | 0 | 1 |
| 2001 | 1 | 0 | 1 |
| 2003 | 1 | 0 | 1 |
| 2006 | 1 | 0 | 1 |
| 2008 | 0 | 1 | 1 |
| 2009 | 0 | 1 | 1 |
| 2012 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2017 | 0 | 1 | 1 |
| 2019 | 1 | 0 | 1 |
| 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Adenosine Triphosphatases" by people in Profiles.
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BCL7A-containing SWI/SNF/BAF complexes modulate mitochondrial bioenergetics during neural progenitor differentiation. EMBO J. 2022 Dec 01; 41(23):e110595.
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Moyamoya angiopathy in PHACE syndrome not associated with RNF213 variants. Childs Nerv Syst. 2019 07; 35(7):1231-1237.
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Stroke in Ehlers-Danlos Syndrome Kyphoscoliotic Type: Dissection or Vasculitis? Pediatr Neurol. 2017 Sep; 74:92-96.
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PEX6 is Expressed in Photoreceptor Cilia and Mutated in Deafblindness with Enamel Dysplasia and Microcephaly. Hum Mutat. 2016 Feb; 37(2):170-4.
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Mutations in SRCAP, encoding SNF2-related CREBBP activator protein, cause Floating-Harbor syndrome. Am J Hum Genet. 2012 Feb 10; 90(2):308-13.
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IGHMBP2 is a ribosome-associated helicase inactive in the neuromuscular disorder distal SMA type 1 (DSMA1). Hum Mol Genet. 2009 Apr 01; 18(7):1288-300.
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Analysis of mitochondrial function in situ in permeabilized muscle fibers, tissues and cells. Nat Protoc. 2008; 3(6):965-76.
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Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase. Nat Genet. 2006 Oct; 38(10):1184-91.
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Comparative sequence and expression analyses of four mammalian VPS4 genes. Gene. 2003 Feb 13; 305(1):47-59.
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Mammalian cells express two VPS4 proteins both of which are involved in intracellular protein trafficking. J Mol Biol. 2001 Sep 21; 312(3):469-80.
MeSH information
