Functional analysis of cone-rod homeobox (CRX) mutations associated with retinal dystrophy-Reference-Cited by-同舟云学术

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Functional analysis of cone-rod homeobox (CRX) mutations associated with retinal dystrophy

Published:2002-04-15 Issue:8 Volume:11 Page:873-884
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:
Short-container-title:

Author:

Chen S.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/11/8/873/1789547/ddf088.pdf

Cited by 68 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. Clinical, Genetic and Histopathological Characteristics of CRX-associated Retinal Dystrophies;Ophthalmology Retina;2024-08

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

3. Mutational scanning ofCRXclassifies clinical variants and reveals biochemical properties of the transcriptional effector domain;2024-03-27

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

5. Pathogenic variants inCRXhave distinctcis-regulatory effects on enhancers and silencers in photoreceptors;Genome Research;2024-02

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