Telomere shortening is a hallmark of genetic cardiomyopathies

This study demonstrates that significantly shortened telomeres are a hallmark of cardiomyocytes (CMs) from individuals with end-stage hypertrophic cardiomyopathy (HCM) or dilated cardiomyopathy (DCM) as a result of heritable defects in cardiac proteins critical to contractile function. Positioned at...

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Detalles Bibliográficos
Autores principales: Chang, Alex C. Y., Chang, Andrew C. H., Kirillova, Anna, Sasagawa, Koki, Su, Willis, Weber, Gerhard, Lin, Jue, Termglinchan, Vittavat, Karakikes, Ioannis, Seeger, Timon, Dainis, Alexandra M., Hinson, John T., Seidman, Jonathan, Seidman, Christine E., Day, John W., Ashley, Euan, Wu, Joseph C., Blau, Helen M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2018
Materias:
Biological Sciences
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6140486/
https://www.ncbi.nlm.nih.gov/pubmed/30150400
http://dx.doi.org/10.1073/pnas.1714538115

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6140486/
https://www.ncbi.nlm.nih.gov/pubmed/30150400
http://dx.doi.org/10.1073/pnas.1714538115

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