 Keratins, Type II
"Keratins, Type II" 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 keratin subtype that includes keratins that are generally larger and less acidic that TYPE I KERATINS. Type II keratins combine with type I keratins to form keratin filaments.
| Descriptor ID |
D053531
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| MeSH Number(s) |
D05.750.078.593.450.600 D12.776.220.475.450.600 D12.776.860.607.650
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| Concept/Terms |
Keratins, Type II- Keratins, Type II
- Type II Keratins
- Keratins, Basic
- Basic Keratins
- Type II Intermediate Filament Proteins
- Type II Keratin
- Keratin, Type II
- Keratin, Type 2
- Type 2 Keratin
- Keratins, Type 2
- Type 2 Keratins
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Below are MeSH descriptors whose meaning is more general than "Keratins, Type II".
Below are MeSH descriptors whose meaning is more specific than "Keratins, Type II".
This graph shows the total number of publications written about "Keratins, Type II" by people in this website by year, and whether "Keratins, Type II" 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 |
|---|
| 2007 | 1 | 0 | 1 | | 2011 | 1 | 0 | 1 |
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Below are the most recent publications written about "Keratins, Type II" by people in Profiles.
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Shah K, Ansar M, Mughal ZU, Khan FS, Ahmad W, Ferrara TM, Spritz RA. Recessive progressive symmetric erythrokeratoderma results from a homozygous loss-of-function mutation of KRT83 and is allelic with dominant monilethrix. J Med Genet. 2017 03; 54(3):186-189.
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Infante C, Ponce M, Asensio E, Zerolo R, Manchado M. Molecular characterization of a novel type II keratin gene (sseKer3) in the Senegalese sole (Solea senegalensis): Differential expression of keratin genes by salinity. Comp Biochem Physiol B Biochem Mol Biol. 2011 Sep; 160(1):15-23.
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Chen J, Jaeger K, Den Z, Koch PJ, Sundberg JP, Roop DR. Mice expressing a mutant Krt75 (K6hf) allele develop hair and nail defects resembling pachyonychia congenita. J Invest Dermatol. 2008 Feb; 128(2):270-9.
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