Metabolic Maturation Media Improve Physiological Function of Human iPSC-Derived Cardiomyocytes
Dries Feyen(Utrecht University), Wesley L. McKeithan(Sanford Burnham Prebys Medical Discovery Institute), Arne A.N. Bruyneel(Cardiovascular Institute of the South), Sean Spiering(Sanford Burnham Prebys Medical Discovery Institute), Larissa Hörmann(Universität Hamburg), Bärbel Ulmer(Universität Hamburg), Hui Zhang(University of California San Diego), Francesca Briganti(Cardiovascular Institute of the South), Michaela Schweizer(Universität Hamburg), Bence Hegyi(University of California, Davis), Zhandi Liao(University of California, Davis), Risto-Pekka Pölönen(University of California, Davis), Kenneth S. Ginsburg(University of California, Davis), Chi Keung Lam(Cardiovascular Institute of the South), Ricardo Serrano(Cardiovascular Institute of the South), Christine Wahlquist(Sanford Burnham Prebys Medical Discovery Institute), Alexander Kreymerman(Cardiovascular Institute of the South), Michelle M. Vu(Cardiovascular Institute of the South), Prashila Amatya(Cardiovascular Institute of the South), Charlotta Sophie Behrens(Universität Hamburg), Sara Ranjbarvaziri(Cardiovascular Institute of the South), Renée G. C. Maas(Utrecht University), Matthew Greenhaw(Cardiovascular Institute of the South), Daniel Bernstein(Cardiovascular Institute of the South), Joseph C. Wu(Cardiovascular Institute of the South), Donald M. Bers(University of California, Davis), Thomas Eschenhagen(Universität Hamburg), Christian M. Metallo(University of California San Diego), Mark Mercola(Sanford Burnham Prebys Medical Discovery Institute)
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Abstract
channel SCN5A and dilated cardiomyopathy due to a mutation in the RNA splicing factor RBM20. The maturation media should increase the fidelity of hiPSC-CMs as disease models.
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