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Proceedings of the National Academy of Sciences of the United States of America|October 10, 2009
Functional interchangeability of rod and cone transducin alpha-subunitsWen-Tao Deng, Keisuke Sakurai, Jianwen Liu, et al.
The Journal of Biological Chemistry|May 9, 2009
Clarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeletonGuilian Tian, Yun Zhou, Dagmar Hajkova, et al.
The American Journal of Pathology|November 3, 2022
Distinct Phenotypic Consequences of Pathogenic Mutants Associated with Late-Onset Retinal DegenerationLei Xu, William N Ruddick, Susan N Bolch, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 20, 2005
Prolonged recovery of retinal structure/function after gene therapy in an Rs1h-deficient mouse model of x-linked juvenile retinoschisisSeok H Min, Laurie L Molday, Mathias W Seeliger, et al.
Scientific Reports|October 19, 2017
Modeling and Preventing Progressive Hearing Loss in Usher Syndrome IIIRuishuang Geng, Akil Omar, Suhasini R Gopal, et al.
Investigative Ophthalmology & Visual Science|July 1, 2008
AAV-mediated gene therapy for retinal degeneration in the rd10 mouse containing a recessive PDEbeta mutationJi-Jing Pang, Sanford L Boye, Ashok Kumar, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 9, 2010
Long-term retinal function and structure rescue using capsid mutant AAV8 vector in the rd10 mouse, a model of recessive retinitis pigmentosaJi-jing Pang, Xufeng Dai, Shannon E Boye, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 19, 2013
Cone phosphodiesterase-6α' restores rod function and confers distinct physiological properties in the rod phosphodiesterase-6β-deficient rd10 mouseWen-Tao Deng, Keisuke Sakurai, Saravanan Kolandaivelu, et al.
The Journal of Pathology|October 19, 2019
Clarin-1 expression in adult mouse and human retina highlights a role of Müller glia in Usher syndromeLei Xu, Susan N Bolch, Clayton P Santiago, et al.
Human Gene Therapy|December 1, 2018
Long-Term Effects of Gene Therapy in a Novel Mouse Model of Human <i>MFRP</i>-Associated RetinopathyAnil Chekuri, Bhubanananda Sahu, Venkata Ramana Murthy Chavali, et al.
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