The ocular albinism type 1 (OA1) G-protein-coupled receptor functions with MART-1 at early stages of melanogenesis to control melanosome identity and composition

Author： Giordano Francesca   Bonetti Ciro   Surace Enrico M.   Marigo Valeria   Raposo Graa  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.18, Iss.23, 2009-12, pp. : 4530-4545

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Defective intracellular transport and processing of OA1 is a major cause of ocular albinism type 1

By d’Addio Marilena  

Human Molecular Genetics, Vol. 9, Iss. 20, 2000-12 ,pp. : 3011-3018

Oxford University Press

Access to resources Recommend Favorite

Oa1 knock-out: new insights on the pathogenesis of ocular albinism type 1

By Incerti Barbara  

Human Molecular Genetics, Vol. 9, Iss. 19, 2000-11 ,pp. : 2781-2788

Oxford University Press

Access to resources Recommend Favorite

Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin

By Weil Dominique  

Human Molecular Genetics, Vol. 12, Iss. 5, 2003-03 ,pp. : 463-471

Oxford University Press

Access to resources Recommend Favorite

Large-scale Expression and Purification of a G-protein-coupled Receptor for Structure Determination – An Overview

By Grisshammer Reinhard   White Jim   Trinh Loc   Shiloach Joseph  

Journal of Structural and Functional Genomics, Vol. 6, Iss. 2-3, 2005-09 ,pp. : 159-163

Springer Publishing Company

Access to resources Recommend Favorite

Association of a functional 17-estradiol sensitive IL6-174G/C promoter polymorphism with early-onset type 1 diabetes in females

By Kristiansen Ole P.  

Human Molecular Genetics, Vol. 12, Iss. 10, 2003-05 ,pp. : 1101-1110

Oxford University Press

Access to resources Recommend Favorite