Veerman, C. C., I. Mengarelli, E. M. Lodder, G. Kosmidis, M. Bellin, M. Zhang, S. Dittmann, K. Guan, A. A. M. Wilde, E. Schulze-Bahr, B. Greber, C. R. Bezzina and A. O. Verkerk: Switch From Fetal to Adult SCN5A Isoform in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction Disease-Causing Mutation. In: J am Heart Assoc 6, 7 (2017).
url: https://www.ncbi.nlm.nih.gov/pubmed/28739862
Marczenke, M., I. Piccini, I. Mengarelli, J. Fell, A. Ropke, G. Seebohm, A. O. Verkerk and B. Greber: Cardiac Subtype-Specific Modeling of Kv1.5 Ion Channel Deficiency Using Human Pluripotent Stem Cells. In: Front Physiol 8, (2017).
url: https://www.ncbi.nlm.nih.gov/pubmed/28729840
Greber, B., A. O. Verkerk, G. Seebohm, C. L. Mummery and M. Bellin: Reply to Christ et al.: LQT1 and JLNS phenotypes in hiPSC-derived cardiomyocytes are due to KCNQ1 mutations. In: Proc Natl Acad Sci u S A 112, 16, (2015).
url: http://www.ncbi.nlm.nih.gov/pubmed/25795241
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