Clarin-1, Encoded by the Usher Syndrome III Causative Gene, Forms a Membranous Microdomain: POSSIBLE ROLE OF CLARIN-1 IN ORGANIZING THE ACTIN CYTOSKELETON

Clarin-1 is the protein product encoded by the gene mutated in Usher syndrome III. Although the molecular function of clarin-1 is unknown, its primary structure predicts four transmembrane domains similar to a large family of membrane proteins that include tetraspanins. Here we investigated the role...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Tian, Guilian, Zhou, Yun, Hajkova, Dagmar, Miyagi, Masaru, Dinculescu, Astra, Hauswirth, William W., Palczewski, Krzysztof, Geng, Ruishuang, Alagramam, Kumar N., Isosomppi, Juha, Sankila, Eeva-Marja, Flannery, John G., Imanishi, Yoshikazu
Format: Artigo
Sprog:Inglês
Udgivet: American Society for Biochemistry and Molecular Biology 2009
Fag:
Protein Synthesis, Post-Translational Modification, and Degradation
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2707243/
https://ncbi.nlm.nih.gov/pubmed/19423712
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M109.003160
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker