"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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| Year | Major Topic | Minor Topic | Total |
|---|
| 2012 | 2 | 0 | 2 |
| 2013 | 0 | 1 | 1 |
| 2014 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2019 | 4 | 1 | 5 |
| 2023 | 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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Entorhinal cortex epigenome-wide association study highlights four novel loci showing differential methylation in Alzheimer's disease. Alzheimers Res Ther. 2023 05 06; 15(1):92.
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De novo variants in PAK1 lead to intellectual disability with macrocephaly and seizures. Brain. 2019 11 01; 142(11):3351-3359.
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Clinical relevance of H-RAS, K-RAS, and N-RAS mRNA expression in primary breast cancer patients. Breast Cancer Res Treat. 2020 Jan; 179(2):403-414.
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Sensory neuropathy-causing mutations in ATL3 affect ER-mitochondria contact sites and impair axonal mitochondrial distribution. Hum Mol Genet. 2019 02 15; 28(4):615-627.
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Retinoencephalopathy with occipital lobe epilepsy in an OPA-1 mutation carrier. Seizure. 2019 Mar; 66:1-3.
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A disease causing ATLASTIN 3 mutation affects multiple endoplasmic reticulum-related pathways. Cell Mol Life Sci. 2019 Apr; 76(7):1433-1445.
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Sensory-Neuropathy-Causing Mutations in ATL3 Cause Aberrant ER Membrane Tethering. Cell Rep. 2018 05 15; 23(7):2026-2038.
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Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3. Brain. 2014 Mar; 137(Pt 3):683-92.
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Sonography of the median nerve in CMT1A, CMT2A, CMTX, and HNPP. Muscle Nerve. 2013 Mar; 47(3):385-95.
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Mitofusin 2 mutations affect mitochondrial function by mitochondrial DNA depletion. Acta Neuropathol. 2013 Feb; 125(2):245-56.
MeSH information
