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European Journal of Human Genetics : EJHG|August 19, 2010
Alternative splice variants of the USH3A gene Clarin 1 (CLRN1)Hanna Västinsalo, Reetta Jalkanen, Astra Dinculescu, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 31, 2008
Downregulation of p22phox in retinal pigment epithelial cells inhibits choroidal neovascularization in miceQiuhong Li, Astra Dinculescu, Zhiying Shan, et al.
The Journal of Biological Chemistry|January 26, 2002
Insertional mutagenesis and immunochemical analysis of visual arrestin interaction with rhodopsinAstra Dinculescu, J Hugh McDowell, Stephanie A Amici, et al.
Advances in Experimental Medicine and Biology|May 4, 2018
Co-Expression of Wild-Type and Mutant S163R C1QTNF5 in Retinal Pigment EpitheliumAstra Dinculescu, Frank M Dyka, Seok-Hong Min, et al.
Plos Genetics|March 11, 2025
The USH3A causative gene clarin1 functions in Müller glia to maintain retinal photoreceptorsHannah J T Nonarath, Samantha L Simpson, Tricia L Slobodianuk, et al.
Investigative Ophthalmology & Visual Science|October 30, 2015
Pathological Effects of Mutant C1QTNF5 (S163R) Expression in Murine Retinal Pigment EpitheliumAstra Dinculescu, Seok-Hong Min, Frank M Dyka, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 11, 2008
High-efficiency transduction of the mouse retina by tyrosine-mutant AAV serotype vectorsHilda Petrs-Silva, Astra Dinculescu, Qiuhong Li, et al.
Human Gene Therapy|June 17, 2015
Stability and Safety of an AAV Vector for Treating RPGR-ORF15 X-Linked Retinitis PigmentosaWen-Tao Deng, Frank M Dyka, Astra Dinculescu, et al.
Frontiers in Neuroscience|July 6, 2017
Gene Therapy in a Large Animal Model of PDE6A-Retinitis PigmentosaFreya M Mowat, Laurence M Occelli, Joshua T Bartoe, et al.
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