"Mutant Proteins" 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.
Proteins produced from GENES that have acquired MUTATIONS.
Descriptor ID |
D050505
|
MeSH Number(s) |
D12.776.602
|
Concept/Terms |
Mutant Proteins- Mutant Proteins
- Proteins, Mutant
- Mutant Protein
- Protein, Mutant
|
Below are MeSH descriptors whose meaning is more general than "Mutant Proteins".
Below are MeSH descriptors whose meaning is more specific than "Mutant Proteins".
This graph shows the total number of publications written about "Mutant Proteins" by people in this website by year, and whether "Mutant Proteins" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
---|
2009 | 0 | 1 | 1 |
2016 | 0 | 1 | 1 |
2018 | 0 | 1 | 1 |
2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Mutant Proteins" by people in Profiles.
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Endocannabinoid dysfunction in neurological disease: neuro-ocular DAGLA-related syndrome. Brain. 2022 10 21; 145(10):3383-3390.
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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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S100A11 plays a role in homologous recombination and genome maintenance by influencing the persistence of RAD51 in DNA repair foci. Cell Cycle. 2016 Oct 17; 15(20):2766-79.
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IGHMBP2 is a ribosome-associated helicase inactive in the neuromuscular disorder distal SMA type 1 (DSMA1). Hum Mol Genet. 2009 Apr 01; 18(7):1288-300.