Notch and interacting signalling pathways in cardiac development, disease, and regeneration
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Link
http://www.nature.com/articles/s41569-018-0100-2.pdf
Reference209 articles.
1. Garg, V. et al. Mutations in NOTCH1 cause aortic valve disease. Nature 437, 270–274 (2005).
2. Luxan, G. et al. Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy. Nat. Med. 19, 193–201 (2013).
3. Li, L. et al. Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1. Nat. Genet. 16, 243–251 (1997).
4. Oda, T. et al. Mutations in the human Jagged1 gene are responsible for Alagille syndrome. Nat. Genet. 16, 235–242 (1997).
5. Abu-Issa, R. & Kirby, M. L. Heart field: from mesoderm to heart tube. Annu. Rev. Cell Dev. Biol. 23, 45–68 (2007).
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