"GTP Phosphohydrolases" 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.
Enzymes that hydrolyze GTP to GDP. EC 3.6.1.-.
| Descriptor ID |
D020558
|
| MeSH Number(s) |
D08.811.277.040.330
|
| Concept/Terms |
GTP Phosphohydrolases- GTP Phosphohydrolases
- Phosphohydrolases, GTP
- GTPase
- GTPases
- Guanosinetriphosphatases
- Guanosine Triphosphate Phosphohydrolases
- Phosphohydrolases, Guanosine Triphosphate
- Triphosphate Phosphohydrolases, Guanosine
- GTP Phosphohydrolase
- Phosphohydrolase, GTP
|
Below are MeSH descriptors whose meaning is more general than "GTP Phosphohydrolases".
Below are MeSH descriptors whose meaning is more specific than "GTP Phosphohydrolases".
This graph shows the total number of publications written about "GTP Phosphohydrolases" by people in this website by year, and whether "GTP Phosphohydrolases" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 1 | 1 | 2 |
| 1997 | 2 | 0 | 2 |
| 1998 | 2 | 2 | 4 |
| 1999 | 2 | 1 | 3 |
| 2000 | 0 | 1 | 1 |
| 2001 | 0 | 1 | 1 |
| 2002 | 2 | 1 | 3 |
| 2011 | 1 | 0 | 1 |
| 2012 | 1 | 2 | 3 |
| 2013 | 1 | 1 | 2 |
| 2016 | 0 | 1 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 0 | 1 | 1 |
| 2020 | 0 | 1 | 1 |
| 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "GTP Phosphohydrolases" by people in Profiles.
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Ceramide synthase 6 impacts T-cell allogeneic response and graft-versus-host disease through regulating N-RAS/ERK pathway. Leukemia. 2022 07; 36(7):1907-1915.
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Inhibition of RAS: proven and potential vulnerabilities. Biochem Soc Trans. 2020 10 30; 48(5):1831-1841.
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Combined treatment with GSNO and CAPE accelerates functional recovery via additive antioxidant activities in a mouse model of TBI. J Neurosci Res. 2018 12; 96(12):1900-1913.
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Diagnostic Value of RAS Mutations in Indeterminate Thyroid Nodules. Otolaryngol Head Neck Surg. 2017 03; 156(3):472-479.
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Targeting FLT3-ITD signaling mediates ceramide-dependent mitophagy and attenuates drug resistance in AML. Blood. 2016 10 13; 128(15):1944-1958.
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HRES-1/Rab4-mediated depletion of Drp1 impairs mitochondrial homeostasis and represents a target for treatment in SLE. Ann Rheum Dis. 2014 Oct; 73(10):1888-97.
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Emerging roles for intersectin (ITSN) in regulating signaling and disease pathways. Int J Mol Sci. 2013 Apr 10; 14(4):7829-52.
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Panitumumab combined with irinotecan for patients with KRAS wild-type metastatic colorectal cancer refractory to standard chemotherapy: a GERCOR efficacy, tolerance, and translational molecular study. Ann Oncol. 2013 Feb; 24(2):412-419.
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Intersectin (ITSN) family of scaffolds function as molecular hubs in protein interaction networks. PLoS One. 2012; 7(4):e36023.
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Plexins are GTPase-activating proteins for Rap and are activated by induced dimerization. Sci Signal. 2012 Jan 17; 5(207):ra6.