OTX2 loss causes rod differentiation defect in CRX-associated congenital blindness-Reference-Cited by-同舟云学术

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OTX2 loss causes rod differentiation defect in CRX-associated congenital blindness

Published:2014-01-02 Issue:2 Volume:124 Page:631-643
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Roger Jerome E.,Hiriyanna Avinash,Gotoh Norimoto,Hao Hong,Cheng Debbie F.,Ratnapriya Rinki,Kautzmann Marie-Audrey I.,Chang Bo,Swaroop Anand

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference60 articles.

1. Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait

2. The Marshall M. Parks memorial lecture: making sense of early-onset childhood retinal dystrophies--the clinical phenotype of Leber congenital amaurosis

3. Leber congenital amaurosis: Genes, proteins and disease mechanisms

4. De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis

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1. Retinal primary cilia and their dysfunction in retinal neurodegenerative diseases: beyond ciliopathies;Molecular Medicine;2024-07-26

2. Molecular basis of CRX/DNA recognition and stoichiometry at the Ret4 response element;Structure;2024-07

3. Transcriptional precision in photoreceptor development and diseases – Lessons from 25 years of CRX research;Frontiers in Cellular Neuroscience;2024-02-13

4. CRX haploinsufficiency compromises photoreceptor precursor translocation and differentiation in human retinal organoids;Stem Cell Research & Therapy;2023-12-05

5. Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms;eLife;2023-11-14

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