Related content

Human retinopathy-associated ciliary protein retinitis pigmentosa GTPase regulator mediates cilia-dependent vertebrate development

By Ghosh Amiya K.   Murga-Zamalloa Carlos A.   Chan Lansze   Hitchcock Peter F.   Swaroop Anand   Khanna Hemant  

Human Molecular Genetics, Vol. 19, Iss. 1, 2010-01 ,pp. : 90-98

Oxford University Press

Access to resources Recommend Favorite

Interaction of retinitis pigmentosa GTPase regulator (RPGR) with RAB8A GTPase: implications for cilia dysfunction and photoreceptor degeneration

By Murga-Zamalloa Carlos A.   Atkins Stephen J.   Peranen Johan   Swaroop Anand   Khanna Hemant  

Human Molecular Genetics, Vol. 19, Iss. 18, 2010-09 ,pp. : 3591-3598

Oxford University Press

Access to resources Recommend Favorite

RPGR transcription studies in mouse and human tissues reveal a retina-specific isoform that is disrupted in a patient with X-linked retinitis pigmentosa

By Kirschner Renate  

Human Molecular Genetics, Vol. 8, Iss. 8, 1999-08 ,pp. : 1571-1578

Oxford University Press

Access to resources Recommend Favorite

Systemic splicing factor deficiency causes tissue-specific defects: a zebrafish model for retinitis pigmentosa

By Linder Bastian   Dill Holger   Hirmer Anja   Brocher Jan   Lee Gek Ping   Mathavan Sinnakaruppan   Bolz Hanno Jrn   Winkler Christoph   Laggerbauer Bernhard   Fischer Utz  

Human Molecular Genetics, Vol. 20, Iss. 2, 2011-01 ,pp. : 368-377

Oxford University Press

Access to resources Recommend Favorite

Epigenetic profiling of somatic tissues from human autopsy specimens identifies tissue- and individual-specific DNA methylation patterns

By Byun Hyang-Min   Siegmund Kimberly D.   Pan Fei   Weisenberger Daniel J.   Kanel Gary   Laird Peter W.   Yang Allen S.  

Human Molecular Genetics, Vol. 18, Iss. 24, 2009-12 ,pp. : 4808-4817

Oxford University Press

Access to resources Recommend Favorite