"Protein-Arginine Deiminases" 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.
A family of ENZYMES that, in the presence of calcium ion, converts ARGININE to CITRULLINE in proteins.
| Descriptor ID |
D000076342
|
| MeSH Number(s) |
D08.811.277.721
|
| Concept/Terms |
Protein-Arginine Deiminases- Protein-Arginine Deiminases
- Deiminases, Protein-Arginine
- Protein Arginine Deiminases
- Protein-L-Arginine Iminohydrolase
- Iminohydrolase, Protein-L-Arginine
- Protein L Arginine Iminohydrolase
- Protein-Arginine Deiminase
- Deiminase, Protein-Arginine
- Protein Arginine Deiminase
- Peptidylarginine Deiminase
- Deiminase, Peptidylarginine
- Peptidylarginine Deiminases
- Deiminases, Peptidylarginine
- Protein-L-Arginine Iminohydrolases
- Iminohydrolases, Protein-L-Arginine
- Protein L Arginine Iminohydrolases
|
Below are MeSH descriptors whose meaning is more general than "Protein-Arginine Deiminases".
Below are MeSH descriptors whose meaning is more specific than "Protein-Arginine Deiminases".
This graph shows the total number of publications written about "Protein-Arginine Deiminases" by people in this website by year, and whether "Protein-Arginine Deiminases" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2016 | 0 | 1 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Protein-Arginine Deiminases" by people in Profiles.
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Variant PADI3 in Central Centrifugal Cicatricial Alopecia. N Engl J Med. 2019 02 28; 380(9):833-841.
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Maternal variants in NLRP and other maternal effect proteins are associated with multilocus imprinting disturbance in offspring. J Med Genet. 2018 07; 55(7):497-504.
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Congenital Anonychia and Uncombable Hair Syndrome: Coinheritance of Homozygous Mutations in RSPO4 and PADI3. J Invest Dermatol. 2017 05; 137(5):1176-1179.
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Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome. Am J Hum Genet. 2016 Dec 01; 99(6):1292-1304.
MeSH information
