Targeted deletion of Crb1/Crb2 in the optic vesicle models key features of leber congenital amaurosis 8-Reference-Cited by-同舟云学术

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Targeted deletion of Crb1/Crb2 in the optic vesicle models key features of leber congenital amaurosis 8

Published:2019-09 Issue:2 Volume:453 Page:141-154
ISSN:0012-1606
Container-title:Developmental Biology
language:en
Short-container-title:Developmental Biology

Author:

Cho Seo-Hee,Nahar Ankur,Kim Ji Hyang,Lee Matthew,Kozmik Zbynek,Kim Seonhee

Funder

National Institutes of Health

Curing Retinal Blindness Foundation

Shriners Hospitals for Children Research

Czech Ministry of Education, Youth and Sports

Publisher

Elsevier BV

Subject

Cell Biology,Developmental Biology,Molecular Biology

Reference78 articles.

1. Human CRB1-associated retinal degeneration: comparison with the rd8 Crb1-mutant mouse model;Aleman;Investig. Ophthalmol. Vis. Sci.,2011

2. Genetic characterization and disease mechanism of retinitis pigmentosa; current scenario;Ali;3 Biotech,2017

3. Microarray and morphological analysis of early postnatal CRB2 mutant retinas on a pure C57BL/6J genetic background;Alves;PLoS One,2013

4. Targeted ablation of Crb2 in photoreceptor cells induces retinitis pigmentosa;Alves;Hum. Mol. Genet.,2014

5. The CRB1 and adherens junction complex proteins in retinal development and maintenance;Alves;Prog. Retin. Eye Res.,2014

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Perturbed cell cycle phase-dependent positioning and nuclear migration of retinal progenitors along the apico-basal axis underlie global retinal disorganization in the LCA8-like mouse model;Developmental Biology;2024-09

2. Genotype-phenotype associations in CRB1 bi-allelic patients: a novel mutation, a systematic review and meta-analysis;BMC Ophthalmology;2024-04-15

3. Genotype-Phenotype of CRB1-Associated Early-Onset Retinal Dystrophy: Novel Insights on Retinal Architecture and Therapeutic Window for Clinical Trials;Investigative Opthalmology & Visual Science;2024-03-11

4. Bi-allelic variations in CRB2, encoding the crumbs cell polarity complex component 2, lead to non-communicating hydrocephalus due to atresia of the aqueduct of sylvius and central canal of the medulla;Acta Neuropathologica Communications;2023-02-20

5. Clinical and Therapeutic Evaluation of the Ten Most Prevalent CRB1 Mutations;Biomedicines;2023-01-27

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