The role of histone modification and a regulatory single-nucleotide polymorphism (rs2071166) in the Cx43 promoter in patients with TOF
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-017-10756-6.pdf
Reference58 articles.
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2. Wu, Y. et al. Expression of Cx43-related microRNAs in patients with tetralogy of Fallot. World J Pediatr 10, 138–144, doi: 10.1007/s12519-013-0434-0 (2014).
3. Nishii, K., Shibata, Y. & Kobayashi, Y. Connexin mutant embryonic stem cells and human diseases. World J Stem Cells 6, 571–578, doi: 10.4252/wjsc.v6.i5.571 (2014).
4. Salameh, A., Blanke, K. & Daehnert, I. Role of connexins in human congenital heart disease: the chicken and egg problem. Front Pharmacol 4, 70, doi: 10.3389/fphar.2013.00070 (2013).
5. Molica, F., Meens, M. J., Morel, S. & Kwak, B. R. Mutations in cardiovascular connexin genes. Biol Cell 106, 269–293, doi: 10.1111/boc.201400038 (2014).
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