Mutations in the N-terminus of the X-linked retinitis pigmentosa protein RP2 interfere with the normal targeting of the protein to the plasma membrane

By Chapple J. Paul   Hardcastle AlisonJ.  

Human Molecular Genetics, Vol. 9, Iss. 13, 2000-08 ,pp. : 1919-1926

Oxford University Press

Access to resources Recommend Favorite

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

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

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 RP1 gene causing autosomal dominant retinitis pigmentosa

By Bowne Sara J.   Daiger Stephen P.   Hims Matthew M.  

Human Molecular Genetics, Vol. 8, Iss. 11, 1999-10 ,pp. : 2121-2128

Oxford University Press

Access to resources Recommend Favorite