Obarzanek-Fojt, M; Favre, B; Huber, M; Ryser, S; Moodycliffe, A M; Wipff, P-J; Hinz, B; Hohl, D (2011). Induction of p38, tumour necrosis factor-α and RANTES by mechanical stretching of keratinocytes expressing mutant keratin 10R156H. British journal of dermatology, 164(1), pp. 125-34. Oxford: Wiley-Blackwell 10.1111/j.1365-2133.2010.10013.x
Full text not available from this repository. (Request a copy)Epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma), characterized by ichthyotic, rippled hyperkeratosis, erythroderma and skin blistering, is a rare autosomal dominant disease caused by mutations in keratin 1 or keratin 10 (K10) genes. A severe phenotype is caused by a missense mutation in a highly conserved arginine residue at position 156 (R156) in K10.
Item Type: |
Journal Article (Original Article) |
|---|---|
Division/Institute: |
04 Faculty of Medicine > Department of Dermatology, Urology, Rheumatology, Nephrology, Osteoporosis (DURN) > Clinic of Dermatology |
UniBE Contributor: |
Favre, Bertrand |
ISSN: |
0007-0963 |
Publisher: |
Wiley-Blackwell |
Language: |
English |
Submitter: |
Factscience Import |
Date Deposited: |
04 Oct 2013 14:21 |
Last Modified: |
05 Dec 2022 14:06 |
Publisher DOI: |
10.1111/j.1365-2133.2010.10013.x |
PubMed ID: |
20804491 |
Web of Science ID: |
000285752000019 |
URI: |
https://boris.unibe.ch/id/eprint/7062 (FactScience: 212211) |
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