A novel <i>KLF13</i> mutation underlying congenital patent ductus arteriosus and ventricular septal defect, as well as bicuspid aortic valve-Reference-Cited by-同舟云学术

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A novel KLF13 mutation underlying congenital patent ductus arteriosus and ventricular septal defect, as well as bicuspid aortic valve

Published:2022-03-01 Issue:4 Volume:23 Page:
ISSN:1792-0981
Container-title:Experimental and Therapeutic Medicine
language:
Short-container-title:Exp Ther Med

Author:

Abhinav Pradhan¹,Zhang Gao-Feng²,Zhao Cui-Mei³,Xu Ying-Jia²,Wang Juan¹,Yang Yi-Qing²

Affiliation:

1. Department of Cardiology, East Hospital, Tongji University School of Medicine, Shanghai 200120, P.R. China

2. Department of Cardiology, Shanghai Fifth People's Hospital, Fudan University, Shanghai 200240, P.R. China

3. Department of Cardiology, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Immunology and Microbiology (miscellaneous),General Medicine

Reference93 articles.

1. Molecular genetics and complex inheritance of congenital heart disease;Diab;Genes (Basel),2021

2. Focused strategies for defining the genetic architecture of congenital heart defects;Martin;Genes (Basel),2021

3. Heart disease and stroke statistics-2019 update: A report from the American Heart Association;Benjamin;Circulation,2019

4. Changes in inflammation and oxidative stress signalling pathways in coarcted aorta triggered by bicuspid aortic valve and growth in young children;Skeffington;Exp Ther Med,2020

5. Left heart hypoplasia operated using double pulmonary arterial banding with double arterial duct stenting: A case report;Dragomir;Exp Ther Med,2020

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1. KLF13 promotes VSMCs phenotypic dedifferentiation by directly binding to the SM22α promoter;Journal of Cellular Physiology;2024-04-18

2. Is the Cis-Element CACCC-Box a Master Regulatory Element during Cardiovascular Disease? A Bioinformatics Approach from the Perspective of the Krüppel-like Family of Transcription Factors;Life;2024-04-11

3. The kruppel-like factor (KLF) family, diseases, and physiological events;Gene;2024-02

4. Somatic GATA4 mutation contributes to tetralogy of Fallot;Experimental and Therapeutic Medicine;2024-01-08

5. 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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