Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3-Reference-Cited by-同舟云学术

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Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3

Published:2014-06 Issue:6 Volume:134 Page:1752-1754
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Eytan Ori,Fuchs-Telem Dana,Mevorach Baruch,Indelman Margarita,Bergman Reuven,Sarig Ofer,Goldberg Ilan,Adir Noam,Sprecher Eli

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference19 articles.

1. The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling;Arnold;Bioinformatics,2006

2. Activation of transient receptor potential vanilloid-3 inhibits human hair growth;Borbiro;J Invest Dermatol,2011

3. Olmsted syndrome in twins;Cambiaghi;Arch Dermatol,1995

4. TRP channel regulates EGFR signaling in hair morphogenesis and skin barrier formation;Cheng;Cell,2010

5. 2-aminoethoxydiphenyl borate activates and sensitizes the heat-gated ion channel TRPV3;Chung;J Neurosci,2004

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