Inherited retinal diseases: Linking genes, disease-causing variants, and relevant therapeutic modalities.

Schneider, Nina; Sundaresan, Yogapriya; Gopalakrishnan, Prakadeeswari; Beryozkin, Avigail; Hanany, Mor; Levanon, Erez Y; Banin, Eyal; Ben-Aroya, Shay; Sharon, Dror

Schneider, Nina; Sundaresan, Yogapriya; Gopalakrishnan, Prakadeeswari; Beryozkin, Avigail; Hanany, Mor; Levanon, Erez Y; Banin, Eyal; Ben-Aroya, Shay; Sharon, Dror.

Afiliação

Schneider N; Department of Ophthalmology, Hadassah Medical Center, Faculty of Medicine, The Hebrew University of Jerusalem, 91120, Israel.
Sundaresan Y; Department of Ophthalmology, Hadassah Medical Center, Faculty of Medicine, The Hebrew University of Jerusalem, 91120, Israel.
Gopalakrishnan P; Department of Ophthalmology, Hadassah Medical Center, Faculty of Medicine, The Hebrew University of Jerusalem, 91120, Israel.
Beryozkin A; Department of Ophthalmology, Hadassah Medical Center, Faculty of Medicine, The Hebrew University of Jerusalem, 91120, Israel.
Hanany M; Department of Ophthalmology, Hadassah Medical Center, Faculty of Medicine, The Hebrew University of Jerusalem, 91120, Israel.
Levanon EY; The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat Gan, 5290002, Israel.
Banin E; Department of Ophthalmology, Hadassah Medical Center, Faculty of Medicine, The Hebrew University of Jerusalem, 91120, Israel.
Ben-Aroya S; The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat Gan, 5290002, Israel.
Sharon D; Department of Ophthalmology, Hadassah Medical Center, Faculty of Medicine, The Hebrew University of Jerusalem, 91120, Israel. Electronic address: dror.sharon1@mail.huji.ac.il.

Prog Retin Eye Res ; 89: 101029, 2022 07.

Article em En | MEDLINE | ID: mdl-34839010

Assuntos

Doenças Retinianas; Distrofias Retinianas; Estudos de Associação Genética; Humanos; Mutação; Linhagem; Retina; Doenças Retinianas/genética; Doenças Retinianas/terapia; Distrofias Retinianas/genética

Palavras-chave

CRISPR-Cas; DNA editing; Disease-causing variant; Gene; Gene therapy; Genotype-phenotype correlation; Inherited retinal diseases; RNA editing; Retinal degeneration; Retinitis pigmentosa; Translational read-through

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Retinianas / Distrofias Retinianas Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

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