Generation and characterization of a human induced pluripotent stem cell line heterozygous for a NOTCH1 mutation (NCHi014-A)
Author:
Funder
National Heart Lung and Blood Institute
Publisher
Elsevier BV
Subject
Cell Biology,Developmental Biology,General Medicine
Reference5 articles.
1. Molecular genetic mechanisms of congenital heart disease;Choudhury;Curr. Opin. Genet. Dev.,2022
2. Mutations in NOTCH1 cause aortic valve disease;Garg;Nature,2005
3. Notch and interacting signalling pathways in cardiac development, disease, and regeneration;MacGrogan;Nat. Rev. Cardiol.,2018
4. Overlapping but distinct roles for NOTCH receptors in human cardiovascular disease;Meester;Clin. Genet.,2019
5. Impaired Human Cardiac Cell Development due to NOTCH1 Deficiency;Ye;Circ. Res.,2023
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