"Keratin-1" 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 type II keratin that is found associated with the KERATIN-10 in terminally differentiated epidermal cells such as those that form the stratum corneum. Mutations in the genes that encode keratin-1 have been associated with HYPERKERATOSIS, EPIDERMOLYTIC.
| Descriptor ID |
D053556
|
| MeSH Number(s) |
D05.750.078.593.450.600.100 D12.776.220.475.450.600.100 D12.776.860.607.650.100
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Keratin-1".
Below are MeSH descriptors whose meaning is more specific than "Keratin-1".
This graph shows the total number of publications written about "Keratin-1" by people in this website by year, and whether "Keratin-1" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2014 | 0 | 1 | 1 |
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Below are the most recent publications written about "Keratin-1" by people in Profiles.
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Exceptional aggressiveness of cerebral cavernous malformation disease associated with PDCD10 mutations. Genet Med. 2015 Mar; 17(3):188-196.