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.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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2004 | 1 | 0 | 1 | 2007 | 0 | 1 | 1 | 2012 | 1 | 0 | 1 | 2015 | 1 | 1 | 2 | 2017 | 1 | 0 | 1 | 2018 | 1 | 1 | 2 | 2019 | 1 | 0 | 1 | 2020 | 0 | 1 | 1 | 2021 | 1 | 1 | 2 |
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Below are the most recent publications written about "Vacuolar Proton-Translocating ATPases" by people in Profiles.
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Wilson ZN, Buysse D, West M, Ahrens D, Odorizzi G. Vacuolar H+-ATPase dysfunction rescues intralumenal vesicle cargo sorting in yeast lacking PI(3,5)P2 or Doa4. J Cell Sci. 2021 08 01; 134(15).
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Pin F, Prideaux M, Huot JR, Essex AL, Plotkin LI, Bonetto A, Bonewald LF. Non-bone metastatic cancers promote osteocyte-induced bone destruction. Cancer Lett. 2021 11 01; 520:80-90.
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Wu JJ, Cai A, Greenslade JE, Higgins NR, Fan C, Le NTT, Tatman M, Whiteley AM, Prado MA, Dieriks BV, Curtis MA, Shaw CE, Siddique T, Faull RLM, Scotter EL, Finley D, Monteiro MJ. ALS/FTD mutations in UBQLN2 impede autophagy by reducing autophagosome acidification through loss of function. Proc Natl Acad Sci U S A. 2020 06 30; 117(26):15230-15241.
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Graner M. V-ATPase expression in gliomas-Not your grandparents' proton pump. EBioMedicine. 2019 Mar; 41:13-14.
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Wilson ZN, Scott AL, Dowell RD, Odorizzi G. PI(3,5)P2 controls vacuole potassium transport to support cellular osmoregulation. Mol Biol Cell. 2018 07 15; 29(13):1718-1731.
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Gstrein T, Edwards A, Pristoupilov? A, Leca I, Breuss M, Pilat-Carotta S, Hansen AH, Tripathy R, Traunbauer AK, Hochstoeger T, Rosoklija G, Repic M, Landler L, Str?neck? V, D?rnberger G, Keane TM, Zuber J, Adams DJ, Flint J, Honzik T, Gut M, Beltran S, Mechtler K, Sherr E, Kmoch S, Gut I, Keays DA. Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans. Nat Neurosci. 2018 02; 21(2):207-217.
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Zhang C, Lai MB, Khandan L, Lee LA, Chen Z, Junge HJ. Norrin-induced Frizzled4 endocytosis and endo-lysosomal trafficking control retinal angiogenesis and barrier function. Nat Commun. 2017 07 04; 8:16050.
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Lee JH, McBrayer MK, Wolfe DM, Haslett LJ, Kumar A, Sato Y, Lie PP, Mohan P, Coffey EE, Kompella U, Mitchell CH, Lloyd-Evans E, Nixon RA. Presenilin 1 Maintains Lysosomal Ca(2+) Homeostasis via TRPML1 by Regulating vATPase-Mediated Lysosome Acidification. Cell Rep. 2015 Sep 01; 12(9):1430-44.
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Zhu H, Sewell AK, Han M. Intestinal apical polarity mediates regulation of TORC1 by glucosylceramide in C. elegans. Genes Dev. 2015 Jun 15; 29(12):1218-23.
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Gheorghe G, Galambos C, Jain S, Krishnamurti L, Jaffe R. A novel TCIRG1 gene mutation leads to severe osteopetrosis with altered content of monocytes/macrophages in several organs. Pediatr Dev Pathol. 2012 Mar-Apr; 15(2):156-9.
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