Examining the Role of Cone-expressed RPE65 in Mouse Cone Function by Alexander V. Kolesnikov, Peter H. Tang, Vladimir J. Kefalov

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Carrier frequency and incidence estimation of RPE65-associated inherited retinal diseases in East Asian population by population database-based analysis by Eun Hye Cho, Jong Eun Park, Taeheon Lee, Kyeongsu Ha, Chang-Seok Ki

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Seven novel variants expand the spectrum of RPE65-related Leber congenital amaurosis in the Chinese population by Zilin Zhong, Feng Rong, Yinghui Dai, Alakezi Yibulayin, Lin Zeng, Jian Liao, Liefeng Wang, Zhihua Huang, Zhenping Zhou, Jianjun Chen

Subjects: “…RPE65…”
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A Gene Scan Study of RPE65 in Chinese Patients with Leber Congenital Amaurosis by Jing Liu, Juan Bu

Subjects: “…Leber Congenital Amaurosis; Mutation; RPE65…”
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Mutation in the RPE65 gene causing hereditary retinal dystrophy in the Briard dogs: application of a new detection method by R. Bechyňová, J. Dostál, A. Stratil, F. Jílek, P. Horák

Subjects: “…rpe65 gene…”
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Frequency of RPE65 Gene Mutation in Patients with Hereditary Retinal Dystrophy by Neslihan Sinim Kahraman, Ayşe Öner, Yusuf Özkul, Munis Dündar

Subjects: “…rpe65 gene…”
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Predicting potentially pathogenic effects of hRPE65 missense mutations: a computational strategy based on molecular dynamics simulations by Giulio Poli, Ivana Barravecchia, Gian Carlo Demontis, Andrea Sodi, Alessandro Saba, Stanislao Rizzo, Marco Macchia, Tiziano Tuccinardi

Subjects: “…RPE65…”
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RPE65-associated inherited retinal diseases: consensus recommendations for eligibility to gene therapy by Andrea Sodi, Sandro Banfi, Francesco Testa, Michele Della Corte, Ilaria Passerini, Elisabetta Pelo, Settimio Rossi, Francesca Simonelli, Italian IRD Working Group

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A Virtual Reality Orientation and Mobility Test for Inherited Retinal Degenerations: Testing a Proof-of-Concept After Gene Therapy by Aleman TS, Miller AJ, Maguire KH, Aleman EM, Serrano LW, O'Connor KB, Bedoukian EC, Leroy BP, Maguire AM, Bennett J

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An in silico toolbox for the prediction of the potential pathogenic effects of missense mutations in the dimeric region of hRPE65 by Giulio Poli, Gian Carlo Demontis, Andrea Sodi, Alessandro Saba, Stanislao Rizzo, Marco Macchia, Tiziano Tuccinardi

Subjects: “…RPE65…”
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Generation and Characterization of Induced Pluripotent Stem Cells and Retinal Organoids From a Leber’s Congenital Amaurosis Patient With Novel RPE65 Mutations by Guilan Li, Guanjie Gao, Panfeng Wang, Xiaojing Song, Ping Xu, Bingbing Xie, Tiancheng Zhou, Guangjin Pan, Fuhua Peng, Qingjiong Zhang, Jian Ge, Xiufeng Zhong

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Light deprivation reduces the severity of experimental diabetic retinopathy by Christina Thebeau, Sheng Zhang, Alexander V. Kolesnikov, Vladimir J. Kefalov, Clay F. Semenkovich, Rithwick Rajagopal

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Cas9-targeted-based long-read sequencing for genetic screening of RPE65 locus by Cristina Rodilla, Cristina Rodilla, Gonzalo Núñez-Moreno, Gonzalo Núñez-Moreno, Gonzalo Núñez-Moreno, Yolanda Benitez, Yolanda Benitez, Raquel Romero, Raquel Romero, Raquel Romero, Lidia Fernández-Caballero, Lidia Fernández-Caballero, Pablo Mínguez, Pablo Mínguez, Pablo Mínguez, Marta Corton, Marta Corton, Carmen Ayuso, Carmen Ayuso

Subjects: “…RPE65 gene…”
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A Korean Patient With Leber Congenital Amaurosis and a Homozygous RPE65 Variant Originating From a Paternal Uniparental Isodisomy by Hane Lee, Dongseok Moon, Rin Khang, Go Hun Seo, Chang Ki Yoon, Un Chul Park, Kyu Hyung Park, Eun Kyoung Lee

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A Comprehensive Study of the Retinal Phenotype of Rpe65-Deficient Dogs by Matthew J Annear, Freya M Mowat, Laurence M Occelli, Alexander J Smith, Paul G Curran, James W Bainbridge, Robin R Ali, Simon M Petersen-Jones

Subjects: “…Rpe65…”
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Enhancing Understanding of the Visual Cycle by Applying CRISPR/Cas9 Gene Editing in Zebrafish by Rebecca Ward, Husvinee Sundaramurthi, Husvinee Sundaramurthi, Husvinee Sundaramurthi, Valeria Di Giacomo, Breandán N. Kennedy

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A decision making algorithm for inherited retinal dystrophies, caused by biallelic mutations in the RPE65 gene, in the clinical practice of an ophthalmologist by E. I. Saidasheva, V. V. Kadyshev, V. V. Brzheskiy, N. A. Malinovskaya, K. K. Shefer

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Cost-effectiveness of voretigene neparvovec in the treatment of patients with inherited retinal disease with RPE65 mutation in Switzerland by Arjun Bhadhuri, Daniel Dröschel, Mike Guldimann, Claudia Jetschgo, Judit Banhazi, Matthias Schwenkglenks, C. Simone Sutherland

Subjects: “…RPE65…”
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Prospects for the diagnosis and gene therapy of inherited retinal dystrophies caused by biallelic mutations in the RPE65 gene by V. V. Neroev, L. A. Katargina, V. V. Kadyshev, I. V. Zolnikova, S. I. Kutsev

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A novel RPE65 variant p.(Ala391Asp) in Leber congenital amaurosis: a case report and literature review in Japan by Natsuki Higa, Takaaki Hayashi, Takaaki Hayashi, Kei Mizobuchi, Maki Iwasa, Shingo Kubota, Kazuki Kuniyoshi, Shuhei Kameya, Hiroyuki Kondo, Mineo Kondo, Tadashi Nakano

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