Liganded retinoic acid X receptor α represses connexin 43 through a potential retinoic acid response element in the promoter region-Reference-Cited by-同舟云学术

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Liganded retinoic acid X receptor α represses connexin 43 through a potential retinoic acid response element in the promoter region

Published:2016-03-18 Issue:1 Volume:80 Page:159-168
ISSN:0031-3998
Container-title:Pediatric Research
language:en
Short-container-title:Pediatr Res

Author:

Gu Ruoyi,Xu Jun,Lin Yixiang,Zhang Jing,Wang Huijun,Sheng Wei,Ma Duan,Ma Xiaojing,Huang Guoying

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

http://www.nature.com/articles/pr201647.pdf

Reference42 articles.

1. Zhao QM, Ma XJ, Ge XL, et al.; Neonatal Congenital Heart Disease screening group. Pulse oximetry with clinical assessment to screen for congenital heart disease in neonates in China: a prospective study. Lancet 2014;384:747–54.

2. Hoffman JIe. The global burden of congenital heart disease. Cardiovasc J Afr 2013;24:141–5.

3. Kathiriya IS, Nora EP, Bruneau BG. Investigating the transcriptional control of cardiovascular development. Circ Res 2015;116:700–14.

4. Nemer M. Genetic insights into normal and abnormal heart development. Cardiovasc Pathol 2008;17:48–54.

5. Salat-Canela C, Sesé M, Peula C, Ramón y Cajal S, Aasen T. Internal translation of the connexin 43 transcript. Cell Commun Signal 2014;12:31.

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1. Retinoic acid reduces the formation of, and acutely modulates, invertebrate electrical synapses;Journal of Neurophysiology;2024-06-01

2. Serine-threonine protein phosphatase regulation of Cx43 dephosphorylation in arrhythmogenic disorders;Cellular Signalling;2021-10

3. DNA methylation at CpG island shore and RXRα regulate NR2F2 in heart tissues of tetralogy of Fallot patients;Biochemical and Biophysical Research Communications;2020-09

4. Association ofCx43rs2071166 polymorphism with an increased risk for atrial septal defect;Cardiology in the Young;2017-12-04

5. The role of histone modification and a regulatory single-nucleotide polymorphism (rs2071166) in the Cx43 promoter in patients with TOF;Scientific Reports;2017-09-05

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