Identification and functional study of FOXC1 variants in Chinese families with glaucoma-Reference-Cited by-同舟云学术

Identification and functional study of FOXC1 variants in Chinese families with glaucoma

Published:2021-11-06 Issue:2 Volume:188 Page:540-547
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:American J of Med Genetics Pt A

Author:

Wang Xinyao¹²,Liu Xiangyuan¹²,Li Yuying¹²,Yang Bo³,Sun Xuejiao¹²,Yang Peng³,Zhong Zilin¹²,Chen Jianjun¹²^ORCID

Affiliation:

1. Birth Defect Group, Clinical Research Center for Mental Disorders, Shanghai Pudong New Area Mental Health Center, School of Medicine Tongji University Shanghai China

2. Department of Medical Genetics School of Medicine, Tongji University Shanghai China

3. Clinical and Translational Research Center of Shanghai First Maternity and Infant Hospital, Shanghai Key Laboratory of Signaling and Disease Research, School of Life Sciences and Technology Tongji University Shanghai China

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62551

Reference29 articles.

1. FOXC1 Transcriptional Regulation Is Mediated by N- and C-terminal Activation Domains and Contains a Phosphorylated Transcriptional Inhibitory Domain

2. FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A

3. A forkhead gene, FoxE3, is essential for lens epithelial proliferation and closure of the lens vesicle

4. Gene mapping for primary open angle glaucoma

Cited by 1 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. De Novo Mosaic 6p23-p25.3 Tetrasomy Caused by a Small Supernumerary Marker Chromosome Presenting Trisomy Distal 6p Phenotype: A Case Report and Literature Review;Diagnostics;2022-09-24