"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 |
|---|
| 2008 | 1 | 1 | 2 |
| 2011 | 0 | 1 | 1 |
| 2018 | 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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The vermiform appendix impacts the risk of developing Parkinson's disease. Sci Transl Med. 2018 10 31; 10(465).
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Mutant HSP70 reverses autoimmune depigmentation in vitiligo. Sci Transl Med. 2013 Feb 27; 5(174):174ra28.
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Aspartate?112 is the selectivity filter of the human voltage-gated proton channel. Nature. 2011 Oct 23; 480(7376):273-7.
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An angiotensin I-converting enzyme mutation (Y465D) causes a dramatic increase in blood ACE via accelerated ACE shedding. PLoS One. 2011; 6(10):e25952.
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Angiotensin I-converting enzyme Gln1069Arg mutation impairs trafficking to the cell surface resulting in selective denaturation of the C-domain. PLoS One. 2010 May 03; 5(5):e10438.
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Angiotensin I-converting enzyme mutation (Trp1197Stop) causes a dramatic increase in blood ACE. PLoS One. 2009 Dec 14; 4(12):e8282.
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Specific residues of RUNX2 are obligatory for formation of BMP2-induced RUNX2-SMAD complex to promote osteoblast differentiation. Cells Tissues Organs. 2009; 189(1-4):133-7.
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Luminal Ca2+ regulation of single cardiac ryanodine receptors: insights provided by calsequestrin and its mutants. J Gen Physiol. 2008 Apr; 131(4):325-34.