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...

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Detalhes bibliográficos
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
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2009
Assuntos:
Protein Synthesis, Post-Translational Modification, and Degradation
Acesso em linha: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
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