Utilization of induced pluripotent stem cells to model the molecular network regulating congenital heart disease
Author:
Affiliation:
1. Stanford Cardiovascular Institute, 240 Pasteur Drive, Room 3200, Palo Alto, CA, 94305, USA
Funder
National Institutes of Health
Propel Postdoctoral Scholars Program
Publisher
Oxford University Press (OUP)
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology
Link
https://academic.oup.com/cardiovascres/advance-article-pdf/doi/10.1093/cvr/cvab373/42102616/cvab373.pdf
Reference12 articles.
1. Patient-specific iPSC-derived cardiomyocytes reveal abnormal regulation of FGF16 in a familial atrial septal defect;Ye;Cardiovasc Res,2021
2. Congenital heart disease in the general population: changing prevalence and age distribution;Marelli;Circulation,2007
3. Socioeconomic mediators of racial and ethnic disparities in congenital heart disease outcomes: a population-based study in California;Peyvandi;J Am Heart Assoc,2018
4. Race and genetics in congenital heart disease: application of iPSCs, omics, and machine learning technologies;Mullen;Front Cardiovasc Med,2021
5. Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics;Pierpont;Circulation,2007
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1. Generation of two induced pluripotent stem cell lines from healthy patients of African American ancestry;Stem Cell Research;2024-04
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