Functional characterization of GATA6 genetic variants associated with mild congenital heart defects-Reference-Cited by-同舟云学术

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Functional characterization of GATA6 genetic variants associated with mild congenital heart defects

Published:2023-01 Issue: Volume:641 Page:77-83
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Wu Haoran,Wu Han,He Yuxi,Sun Weiyue,Meng Yuanhui,Wen Bin,Chu Maoping

Funder

Wenzhou Municipal Science and Technology Bureau

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference23 articles.

1. Complex genetics and the etiology of human congenital heart disease;Gelb;Cold Spring Harb Perspect Med,2014

2. Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome;Basson;Nat. Genet.,1997

3. Congenital heart disease caused by mutations in the transcription factor NKX2-5;Schott;Science,1998

4. GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5;Garg;Nature,2003

5. Genomic frontiers in congenital heart disease;Morton;Nat. Rev. Cardiol.,2022

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2. Discovery and functional investigation of BMP4 as a new causative gene for human congenital heart disease;American Journal of Translational Research;2024

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4. Screening and evaluation of TBX20 and CITED2 mutations in children with congenital cardiac septal defects: Correlation with cardiac troponin T and caspase-3;Gene;2023-10

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