Expression of PRPF31 and TFPT : regulation in health and retinal disease

Author： Rose Anna M. Shah Amna Z. Waseem Naushin H. Chakarova Christina F. Alfano Giovanna Coussa Razek G. Ajlan Radwan Koenekoop Robert K. Bhattacharya Shomi S.

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.21, Iss.18, 2012-09, pp. : 4126-4137

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

Disease mechanism for retinitis pigmentosa (RP11) caused by mutations in the splicing factor gene PRPF31

By Deery E.C.

Human Molecular Genetics, Vol. 11, Iss. 25, 2002-12 ,pp. : 3209-3219

Oxford University Press

Access to resources Recommend Favorite

Two trans -acting eQTLs modulate the penetrance of PRPF31 mutations

By Frio Thomas Rio Civic Natacha Ransijn Adriana Beckmann Jacques S. Rivolta Carlo

Human Molecular Genetics, Vol. 17, Iss. 20, 2008-10 ,pp. : 3154-3165

Oxford University Press

Access to resources Recommend Favorite

Expression profiling of the developing and mature Nrl −/− mouse retina: identification of retinal disease candidates and transcriptional regulatory targets of Nrl

By Yoshida Shigeo

Human Molecular Genetics, Vol. 13, Iss. 14, 2004-07 ,pp. : 1487-1503

Oxford University Press

Access to resources Recommend Favorite

Regulation of retinal progenitor expansion by Frizzled receptors: implications for microphthalmia and retinal coloboma

By Liu Chunqiao Bakeri Hirva Li Tiansen Swaroop Anand

Human Molecular Genetics, Vol. 21, Iss. 8, 2012-04 ,pp. : 1848-1860

Oxford University Press

Access to resources Recommend Favorite

Regulation of IL-8 and IL-1 expression in Crohn's disease associated NOD2/CARD15 mutations

By Li Jing

Human Molecular Genetics, Vol. 13, Iss. 16, 2004-08 ,pp. : 1715-1725

Oxford University Press

Access to resources Recommend Favorite