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

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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

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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

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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

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The retinitis pigmentosa protein RP2 links pericentriolar vesicle transport between the Golgi and the primary cilium

By Evans R. Jane   Schwarz Nele   Nagel-Wolfrum Kerstin   Wolfrum Uwe   Hardcastle Alison J.   Cheetham Michael E.  

Human Molecular Genetics, Vol. 19, Iss. 7, 2010-04 ,pp. : 1358-1367

Oxford University Press

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