"Keratin-5" 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-14 in the internal stratified EPITHELIUM. Mutations in the gene for keratin-5 are associated with EPIDERMOLYSIS BULLOSA SIMPLEX.
Descriptor ID |
D053555
|
MeSH Number(s) |
D05.750.078.593.450.600.500 D12.776.220.475.450.600.500 D12.776.860.607.650.500
|
Concept/Terms |
Keratin-5- Keratin-5
- Keratin 5
- Cytokeratin-5
- Cytokeratin 5
|
Below are MeSH descriptors whose meaning is more general than "Keratin-5".
Below are MeSH descriptors whose meaning is more specific than "Keratin-5".
This graph shows the total number of publications written about "Keratin-5" by people in this website by year, and whether "Keratin-5" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
---|
2006 | 0 | 1 | 1 |
2007 | 0 | 1 | 1 |
2010 | 1 | 0 | 1 |
2011 | 1 | 0 | 1 |
2012 | 1 | 0 | 1 |
2019 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Keratin-5" by people in Profiles.
-
Mast cell activation in Dowling-Degos disease. Br J Dermatol. 2019 12; 181(6):1312-1314.
-
Galli-Galli disease is an acantholytic variant of Dowling-Degos disease: additional genetic evidence in a German family. J Am Acad Dermatol. 2012 Jun; 66(6):e250-1.
-
[Galli-Galli disease. Clinical and histopathological investigation using a case series of 18 patients]. Hautarzt. 2011 Nov; 62(11):842-51.
-
Systematic mutation screening of KRT5 supports the hypothesis that Galli-Galli disease is a variant of Dowling-Degos disease. Br J Dermatol. 2010 Jul; 163(1):197-200.
-
Identification of a keratin-associated protein with a putative role in vesicle transport. Eur J Cell Biol. 2007 Dec; 86(11-12):827-39.
-
Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease. Am J Hum Genet. 2006 Mar; 78(3):510-9.