Vacuolar Proton-Translocating ATPases
"Vacuolar Proton-Translocating 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.
Proton-translocating ATPases that are involved in acidification of a variety of intracellular compartments.
| Descriptor ID |
D025262
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| MeSH Number(s) |
D08.811.277.040.025.325.875 D08.811.913.696.650.150.500.875 D12.776.157.530.450.250.875.500.875 D12.776.543.585.450.250.875.500.875
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| Concept/Terms |
Vacuolar Proton-Translocating ATPases- Vacuolar Proton-Translocating ATPases
- Lysosomal Proton-Translocating ATPases
- ATPases, Lysosomal Proton-Translocating
- Lysosomal Proton Translocating ATPases
- Proton-Translocating ATPases, Lysosomal
- V-Type ATPase
- ATPase, V-Type
- V Type ATPase
- Vacuolar ATPase
- ATPase, Vacuolar
- Vacuolar F(1)F(0) ATPases
- Vacuolar H+-ATPase
- H+-ATPase, Vacuolar
- Vacuolar H+ ATPase
- Vacuolar Membrane H(+)-ATPase
- Lysosomal F(1)F(0) ATPase
- Vacuolar F(1)F(0) ATPase
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Below are MeSH descriptors whose meaning is more general than "Vacuolar Proton-Translocating ATPases".
Below are MeSH descriptors whose meaning is more specific than "Vacuolar Proton-Translocating ATPases".
This graph shows the total number of publications written about "Vacuolar Proton-Translocating ATPases" by people in this website by year, and whether "Vacuolar Proton-Translocating ATPases" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2014 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 3 | 0 | 3 |
| 2018 | 1 | 1 | 2 |
| 2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Vacuolar Proton-Translocating ATPases" by people in Profiles.
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Nsp2 has the potential to be a drug target revealed by global identification of SARS-CoV-2 Nsp2-interacting proteins. Acta Biochim Biophys Sin (Shanghai). 2021 Aug 31; 53(9):1134-1141.
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Prognostic and immunological value of ATP6AP1 in breast cancer: implications for SARS-CoV-2. Aging (Albany NY). 2021 07 06; 13(13):16904-16921.
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Lysosomal ion channels involved in cellular entry and uncoating of enveloped viruses: Implications for therapeutic strategies against SARS-CoV-2. Cell Calcium. 2021 03; 94:102360.
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Hypokalemic Distal Renal Tubular Acidosis. Adv Chronic Kidney Dis. 2018 07; 25(4):303-320.
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Genotype-Phenotype Analysis in Pediatric Patients with Distal Renal Tubular Acidosis. Kidney Blood Press Res. 2018; 43(2):513-521.
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Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects. J Exp Med. 2017 Dec 04; 214(12):3707-3729.
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Nanoparticulate vacuolar ATPase blocker exhibits potent host-targeted antiviral activity against feline coronavirus. Sci Rep. 2017 10 12; 7(1):13043.
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The yeast protein kinase Sch9 adjusts V-ATPase assembly/disassembly to control pH homeostasis and longevity in response to glucose availability. PLoS Genet. 2017 Jun; 13(6):e1006835.
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The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis. Kidney Int. 2017 05; 91(5):1243-1255.
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FK506, an Immunosuppressive Drug, Induces Autophagy by Binding to the V-ATPase Catalytic Subunit A in Neuronal Cells. J Proteome Res. 2017 01 06; 16(1):55-64.