Mutation update of transcription factor genes FOXE3 , HSF4 , MAF , and PITX3 causing cataracts and other developmental ocular defects-Reference-Cited by-同舟云学术

Mutation update of transcription factor genes FOXE3 , HSF4 , MAF , and PITX3 causing cataracts and other developmental ocular defects

Published:2018-01-16 Issue:4 Volume:39 Page:471-494
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Anand Deepti¹,Agrawal Smriti A.¹,Slavotinek Anne²,Lachke Salil A.¹³^ORCID

Affiliation:

1. Department of Biological Sciences; University of Delaware; Newark Delaware

2. Department of Pediatrics; Division of Genetics; University of California; UCSF Benioff, Children's Hospital; San Francisco California

3. Center for Bioinformatics and Computational Biology; University of Delaware; Newark Delaware

Funder

University of Delaware Research Foundation, Inc. Strategic Initiatives

National Eye Institute

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.23395/fullpdf

Reference129 articles.

1. Compound mouse mutants of bZIP transcription factors Mafg and Mafk reveal a regulatory network of non-crystallin genes associated with cataract;Agrawal;Human Genetics,2015

2. Pitx3 directly regulates Foxe3 during early lens development;Ahmad;International Journal of Developmental Biology,2013

3. Heat shock factors: Integrators of cell stress, development and lifespan;Akerfelt;Nature Reviews Molecular Cell Biology,2010

4. Novel recessive BFSP2 and PITX3 mutations: Insights into mutational mechanisms from consanguineous populations;Aldahmesh;Genetics in Medicine,2011

5. Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma;Ali;Molecular Vision,2010

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