De Novo ARID1B mutations cause growth delay associated with aberrant Wnt/β–catenin signaling-Reference-Cited by-同舟云学术

De Novo ARID1B mutations cause growth delay associated with aberrant Wnt/β–catenin signaling

Published:2020-03-03 Issue:5 Volume:41 Page:1012-1024
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Liu Xiaomin¹,Hu Guorui¹,Ye Jun¹,Ye Bin²,Shen Nan³,Tao Yue³,Zhang Xia¹,Fan Yanjie¹,Liu Huili¹,Zhang Zhigang²,Fang Danfeng²,Gu Xuefan¹^ORCID,Mo Xi³^ORCID,Yu Yongguo¹^ORCID

Affiliation:

1. Department of Pediatric Endocrinology/Genetics, Xinhua Hospital, Shanghai Institute for Pediatric ResearchShanghai Jiao Tong University School of Medicine Shanghai China

2. Department of Pediatric Internal Medicine, Taizhou Central HospitalTaizhou University Hospital Taizhou China

3. The Laboratory of Pediatric Infectious Diseases, Pediatric Translational Medicine Institute, Shanghai Children's Medical CenterShanghai Jiao Tong University School of Medicine Shanghai China

Funder

National Natural Science Foundation of China

Shanghai Shen Kang Hospital Development Center

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.23990

Reference34 articles.

1. The chromatin remodelling factor Brg-1 interacts with beta-catenin to promote target gene activation

2. Arid1b haploinsufficient mice reveal neuropsychiatric phenotypes and reversible causes of growth impairment