Calcium-Transporting ATPases
"Calcium-Transporting ATPases" 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.
Cation-transporting proteins that utilize the energy of ATP hydrolysis for the transport of CALCIUM. They differ from CALCIUM CHANNELS which allow calcium to pass through a membrane without the use of energy.
| Descriptor ID |
D000252
|
| MeSH Number(s) |
D08.811.277.040.025.314.250 D12.776.157.530.450.250.500 D12.776.157.530.813.250 D12.776.543.585.450.250.500 D12.776.543.585.813.250
|
| Concept/Terms |
Calcium-Transporting ATPases- Calcium-Transporting ATPases
- ATPases, Calcium-Transporting
- Calcium Transporting ATPases
- Calcium-ATPase
- ATPase, Calcium
- Calcium ATPase
- Adenosinetriphosphatase, Calcium
- Calcium Adenosinetriphosphatase
- Ca(2+)-Transporting ATPase
- Adenosine Triphosphatase, Calcium
- Calcium Adenosine Triphosphatase
- Triphosphatase, Calcium Adenosine
- Ca2+ ATPase
- ATPase, Ca2+
|
Below are MeSH descriptors whose meaning is more general than "Calcium-Transporting ATPases".
Below are MeSH descriptors whose meaning is more specific than "Calcium-Transporting ATPases".
This graph shows the total number of publications written about "Calcium-Transporting ATPases" by people in this website by year, and whether "Calcium-Transporting ATPases" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 1 | 1 | 2 |
| 1997 | 0 | 1 | 1 |
| 1999 | 0 | 2 | 2 |
| 2000 | 0 | 1 | 1 |
| 2002 | 0 | 1 | 1 |
| 2003 | 1 | 0 | 1 |
| 2004 | 0 | 3 | 3 |
| 2005 | 3 | 2 | 5 |
| 2006 | 4 | 0 | 4 |
| 2007 | 1 | 2 | 3 |
| 2014 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
| 2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Calcium-Transporting ATPases" by people in Profiles.
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PMCA4 inhibition does not affect cardiac remodelling following myocardial infarction, but may reduce susceptibility to arrhythmia. Sci Rep. 2021 01 15; 11(1):1518.
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The plasma membrane calcium ATPase 4 signalling in cardiac fibroblasts mediates cardiomyocyte hypertrophy. Nat Commun. 2016 Mar 29; 7:11074.
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Plasma membrane calcium ATPase isoform 4 inhibits vascular endothelial growth factor-mediated angiogenesis through interaction with calcineurin. Arterioscler Thromb Vasc Biol. 2014 Oct; 34(10):2310-20.
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The sarcolemmal calcium pump, alpha-1 syntrophin, and neuronal nitric-oxide synthase are parts of a macromolecular protein complex. J Biol Chem. 2006 Aug 18; 281(33):23341-8.
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[The first genetically supported case of chronic benign pemphigus (Hailey-Hailey disease in Hungary]. Orv Hetil. 2005 Sep 11; 146(37):1933-5.
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Impairment of human sperm motility and viability by quercetin is independent of lipid peroxidation. Andrologia. 2001 Sep; 33(5):277-81.
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An alpha-cardiac myosin heavy chain gene mutation impairs contraction and relaxation function of cardiac myocytes. Am J Physiol. 1999 05; 276(5):H1780-7.
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CREB and its associated proteins act as survival factors for human melanoma cells. J Biol Chem. 1998 Sep 18; 273(38):24884-90.
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Activation of purinergic receptors triggers oscillatory contractions in adult rat ventricular myocytes. Circ Res. 1996 Jul; 79(1):94-102.
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Colocalization of the rat homolog of the von Hippel Lindau (Vhl) gene and the plasma membrane Ca++ transporting ATPase isoform 2 (Atp2b2) gene to rat chromosome bands 4q41.3-->42.1. Cytogenet Cell Genet. 1995; 71(3):253-6.