نتایج جستجو برای: rpgr gene

تعداد نتایج: 1141474  

Journal: :EMBO reports 2015
Eyad Kalawy Fansa Nicola J O'Reilly Shehab Ismail Alfred Wittinghofer

L ee and Seo propose in their article [1] that RPGR binds to PDE6d not with the N-terminal RCC1-like propeller domain but solely with the C-terminus. They show, using an immunoprecipitation experiment, that FLAG-tagged fragments missing the C-terminal CaaX motif of RPGR fail to coimmunoprecipitate together with myc-tagged PDE6d. We have previously shown that the N-terminal 400 residues of RPGR ...

Journal: :Investigative ophthalmology & visual science 2007
Tomas S Aleman Artur V Cideciyan Alexander Sumaroka Sharon B Schwartz Alejandro J Roman Elizabeth A M Windsor Janet D Steinberg Kari Branham Mohammad Othman Anand Swaroop Samuel G Jacobson

PURPOSE To investigate in vivo the retinal microstructure in X-linked retinitis pigmentosa (XLRP) caused by RPGR mutations as a prelude to treatment initiatives for this common form of RP. METHODS Patients with RPGR-XLRP (n = 12; age range, 10-56 years) were studied by optical coherence tomography (OCT) in a wide region of central retina. Overall retinal thickness and outer nuclear layer (ONL...

2014
Liping Yang Xiaobei Yin Lina Feng Debo You Lemeng Wu Ningning Chen Aijun Li Genlin Li Zhizhong Ma

X-linked Retinitis Pigmentosa (XLRP) accounts for 10-20% of all RP cases, and represents the most severe subtype of this disease. Mutations in the Retinitis Pigmentosa GTPase Regulator (RPGR) gene are the most common causes of XLRP, accounting for over 70-75% of all XLRP cases. In this work, we analyzed all the exons of RPGR gene with Sanger sequencing in seven Chinese XLRP families, two of the...

Journal: :Human molecular genetics 2005
Xinrong Lu Mallikarjuna Guruju John Oswald Paulo A Ferreira

The retinitis pigmentosa GTPase regulator (RPGR) protein interacts with the retinitis pigmentosa GTPase regulator interacting protein-1 (RPGRIP1). Genetic lesions in the cognate genes lead to distinct and severe human retinal dystrophies. The biological role of these proteins in retinal function and pathogenesis of retinal diseases is elusive. Here, we present the first physiological assay of t...

2016
Alexander G. Bassuk Andrew Zheng Yao Li Stephen H. Tsang Vinit B. Mahajan

Induced pluripotent stem cells (iPSCs) generated from patient fibroblasts could potentially be used as a source of autologous cells for transplantation in retinal disease. Patient-derived iPSCs, however, would still harbor disease-causing mutations. To generate healthy patient-derived cells, mutations might be repaired with new gene-editing technology based on the bacterial system of clustered ...

2012
Debra A. Thompson Naheed W. Khan Mohammad I. Othman Bo Chang Lin Jia Garrett Grahek Zhijian Wu Suja Hiriyanna Jacob Nellissery Tiansen Li Hemant Khanna Peter Colosi Anand Swaroop John R. Heckenlively

Animal models of human disease are an invaluable component of studies aimed at understanding disease pathogenesis and therapeutic possibilities. Mutations in the gene encoding retinitis pigmentosa GTPase regulator (RPGR) are the most common cause of X-linked retinitis pigmentosa (XLRP) and are estimated to cause 20% of all retinal dystrophy cases. A majority of RPGR mutations are present in ORF...

Journal: :International Ophthalmology Clinics 2021

Georgiou, Michalis MD, PhD; Awadh Hashem, Shaima MBBCh, MRCSed, FICO; Daich Varela, Malena MD; Michaelides, Michel MD(Res), FRCOphthAuthor Information

2017
Preena Tanna Melissa Kasilian Rupert Strauss James Tee Angelos Kalitzeos Sergey Tarima Alexis Visotcky Alfredo Dubra Joseph Carroll Michel Michaelides

Purpose To assess reliability and repeatability of cone density measurements by using confocal and (nonconfocal) split-detector adaptive optics scanning light ophthalmoscopy (AOSLO) imaging. It will be determined whether cone density values are significantly different between modalities in Stargardt disease (STGD) and retinitis pigmentosa GTPase regulator (RPGR)-associated retinopathy. Method...

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