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Circulation. Arrhythmia and Electrophysiology|June 29, 2026
Decreasing Microtubule Detyrosination Improves Cardiac Mechanics and Sodium Channel Function in Arrhythmogenic CardiomyopathyGiovanna Nasilli, Xianming Lin, Pamela Swiatlowska, et al.
Cell Communication and Signaling : CCS|May 7, 2026
In vitro modeling of renal injury-induced cardiac effects using human iPSC-derived organoidsBeatrice Gabbin, James Gallant, Fangchen Liu, et al.
Materials Today. Bio|October 9, 2023
Heart and kidney organoids maintain organ-specific function in a microfluidic systemBeatrice Gabbin, Viviana Meraviglia, Maricke L Angenent, et al.
The New England Journal of Medicine|July 28, 2010
Patient-specific induced pluripotent stem-cell models for long-QT syndromeAlessandra Moretti, Milena Bellin, Andrea Welling, et al.
Biomaterials|March 16, 2015
Functional maturation of human pluripotent stem cell derived cardiomyocytes in vitro--correlation between contraction force and electrophysiologyMarcelo C Ribeiro, Leon G Tertoolen, Juan A Guadix, et al.
Nature Biotechnology|July 21, 2015
Expansion and patterning of cardiovascular progenitors derived from human pluripotent stem cellsMatthew J Birket, Marcelo C Ribeiro, Arie O Verkerk, et al.
Journal of the American Heart Association|July 26, 2017
Switch From Fetal to Adult <i>SCN5A</i> Isoform in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction Disease-Causing MutationChristiaan C Veerman, Isabella Mengarelli, Elisabeth M Lodder, et al.
The EMBO Journal|November 12, 2013
Isogenic human pluripotent stem cell pairs reveal the role of a KCNH2 mutation in long-QT syndromeMilena Bellin, Simona Casini, Richard P Davis, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 3, 2014
Recessive cardiac phenotypes in induced pluripotent stem cell models of Jervell and Lange-Nielsen syndrome: disease mechanisms and pharmacological rescueMiao Zhang, Cristina D'Aniello, Arie O Verkerk, et al.
Cell Death & Disease|December 7, 2023
Human frataxin, the Friedreich ataxia deficient protein, interacts with mitochondrial respiratory chainDavide Doni, Federica Cavion, Marco Bortolus, et al.
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