Let There Be Light: Gene and Cell Therapy for Blindness-Reference-Cited by-同舟云学术

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Let There Be Light: Gene and Cell Therapy for Blindness

Published:2016-02 Issue:2 Volume:27 Page:134-147
ISSN:1043-0342
Container-title:Human Gene Therapy
language:en
Short-container-title:Human Gene Therapy

Author:

Dalkara Deniz¹,Goureau Olivier¹,Marazova Katia¹,Sahel José-Alain¹²³

Affiliation:

1. Sorbonne Universités, UPMC Université Paris 06, INSERM, CNRS, Institut de la Vision, France.

2. Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts, DHU Sight Restore, INSERM-DHOS CIC 1423, France.

3. Fondation Ophtalmologique Adolphe de Rothschild, Paris, France.

Publisher

Mary Ann Liebert Inc

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/hum.2015.147

Reference131 articles.

1. Ocular immune privilege: therapeutic opportunities from an experiment of nature

2. A look at autoimmunity and inflammation in the eye

3. Gene Therapy for Blindness

4. Immune responses limit adenovirally mediated gene expression in the adult mouse eye

5. High-Capacity Adenoviral Vectors for Gene Transfer and Somatic Gene Therapy

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3. Introduction to Stargardt Disease;Clinical Trials in Stargardt Disease Treatment;2024

4. Stargardt macular dystrophy and therapeutic approaches;British Journal of Ophthalmology;2023-11-08

5. CRISPR/SaCas9-based gene editing rescues photoreceptor degeneration throughout a rhodopsin-associated autosomal dominant retinitis pigmentosa mouse model;Experimental Biology and Medicine;2023-10

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