Transcriptome studies of inherited dilated cardiomyopathies
Author:
Funder
Mayo Foundation for Medical Education and Research
National Institutes of Health
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
https://link.springer.com/content/pdf/10.1007/s00335-023-09978-z.pdf
Reference99 articles.
1. Abplanalp Wesley Tyler, Tucker Nathan, Dimmeler Stefanie (2022) Single-cell technologies to decipher cardiovascular diseases. Euro Heart J 43(43):4536–4547. https://doi.org/10.1093/eurheartj/ehac095
2. Ahmad F, Seidman JG, Seidman CE (2005) The genetic basis for cardiac remodeling. Annu Rev Genomics Hum Genet 6:185–216. https://doi.org/10.1146/annurev.genom.6.080604.162132
3. Bang ML et al (2001) The complete gene sequence of titin, expression of an unusual≈ 700-kDa titin isoform, and its interaction with obscurin identify a novel Z-line to I-band linking system. Circ Res 89(11):1065–1072. https://doi.org/10.1161/hh2301.100981
4. Belmonte T et al (2020) Peripheral microRNA panels to guide the diagnosis of familial cardiomyopathy. Transl Res 218:1–15. https://doi.org/10.1016/j.trsl.2020.01.003
5. Calderon-Dominguez M et al (2020) Emerging role of microRNAs in dilated cardiomyopathy: Evidence regarding etiology. Transl Res 215:86–101. https://doi.org/10.1016/j.trsl.2019.08.007
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