HAND1 loss-of-function mutation contributes to congenital double outlet right ventricle-Reference-Cited by-同舟云学术

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HAND1 loss-of-function mutation contributes to congenital double outlet right ventricle

Published:2017-01-20 Issue:3 Volume:39 Page:711-718
ISSN:1107-3756
Container-title:International Journal of Molecular Medicine
language:en
Short-container-title:

Author:

Li Li,Wang Juan,Liu Xing-Yuan,Liu Hua,Shi Hong-Yu,Yang Xiao-Xiao,Li Ning,Li Yan-Jie,Huang Ri-Tai,Xue Song,Qiu Xing-Biao,Yang Yi-Qing

Publisher

Spandidos Publications

Subject

Genetics,General Medicine

Cited by 19 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. The level of HAND1 controls the specification of multipotent cardiac and extraembryonic progenitors;2024-08-17

2. Novel and deleterious nucleotide variations in the HAND1 gene probably affect miRNA target sites and protein function in pediatric patients with congenital heart disease;Molecular Biology Reports;2024-03-29

3. Prenatal delta-9-tetrahydrocannabinol exposure is associated with changes in rhesus macaque DNA methylation enriched for autism genes;Clinical Epigenetics;2023-07-06

4. Delving into the Molecular World of Single Ventricle Congenital Heart Disease;Current Cardiology Reports;2022-02-26

5. HAND transcription factors cooperatively specify the aorta and pulmonary trunk;Developmental Biology;2021-08

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