The X-linked retinitis pigmentosa protein RP2 facilitates G protein traffic

By Schwarz Nele   Novoselova Tatiana V.   Wait Robin   Hardcastle Alison J.   Cheetham Michael E.  

Human Molecular Genetics, Vol. 21, Iss. 4, 2012-02 ,pp. : 863-873

Oxford University Press

Access to resources Recommend Favorite

Localization in the human retina of the X-linked retinitis pigmentosa protein RP2, its homologue cofactor C and the RP2 interacting protein Arl3

By Cheetham M.E.  

Human Molecular Genetics, Vol. 11, Iss. 24, 2002-09 ,pp. : 3065-3074

Oxford University Press

Access to resources Recommend Favorite

Mutations in the X-linked RP2 gene cause intracellular misrouting and loss of the protein

By Schwahn U.   Paland N.   Techritz S.   Lenzner S.   Berger W.  

Human Molecular Genetics, Vol. 10, Iss. 11, 2001-05 ,pp. : 1177-1183

Oxford University Press

Access to resources Recommend Favorite

Mapping of X-linked progressive retinal atrophy (XLPRA), the canine homolog of retinitis pigmentosa 3 (RP3)

By Zeiss Caroline J.   Ray Kunal   Acland Gregory M.   Aguirre Gustavo D.  

Human Molecular Genetics, Vol. 9, Iss. 4, 2000-03 ,pp. : 531-537

Oxford University Press

Access to resources Recommend Favorite

The retinitis pigmentosa protein RP2 interacts with polycystin 2 and regulates cilia-mediated vertebrate development

By Hurd Toby   Zhou Weibin   Jenkins Paul   Liu Chia-Jen   Swaroop Anand   Khanna Hemant   Martens Jeffrey   Hildebrandt Friedhelm   Margolis Ben  

Human Molecular Genetics, Vol. 19, Iss. 22, 2010-11 ,pp. : 4330-4344

Oxford University Press

Access to resources Recommend Favorite