Cardiomyopathy phenotypes in human-induced pluripotent stem cell-derived cardiomyocytes-a systematic review

作者: Thomas Eschenhagen , Lucie Carrier

DOI: 10.1007/S00424-018-2214-0

关键词:

摘要: … published data allow the definition of an in vitro HCM/DCM hiPSC-CM phenotype. The data … on HCM/DCM dysfunction and pathophysiology. Relatively consistent findings in HCM not …

参考文章(108)
Alan Colman, Hung-Fat Tse, Chung-Wah Siu, Yee-Ki Lee, Jenny Chung-Yee Ho, Wing-Hon Lai, Yau-Chi Chan, Kwong-Man Ng, Lai-Yung Wong, Ka-Wing Au, Yee-Man Lau, Jinqiu Zhang, Kenneth Weijian Lay, Modeling of lamin A/C mutation premature cardiac aging using patient-specific induced pluripotent stem cells Aging (Albany NY). ,vol. 4, pp. 803- 822 ,(2012) , 10.18632/AGING.100503
Haodi Wu, Jaecheol Lee, Ludovic G. Vincent, Qingtong Wang, Mingxia Gu, Feng Lan, Jared M. Churko, Karim I. Sallam, Elena Matsa, Arun Sharma, Joseph D. Gold, Adam J. Engler, Yang K. Xiang, Donald M. Bers, Joseph C. Wu, Epigenetic Regulation of Phosphodiesterases 2A and 3A Underlies Compromised β-Adrenergic Signaling in an iPSC Model of Dilated Cardiomyopathy. Cell Stem Cell. ,vol. 17, pp. 89- 100 ,(2015) , 10.1016/J.STEM.2015.04.020
Ahmed A. Alfares, Melissa A. Kelly, Gregory McDermott, Birgit H. Funke, Matthew S. Lebo, Samantha B. Baxter, Jun Shen, Heather M. McLaughlin, Eugene H. Clark, Larry J. Babb, Stephanie W. Cox, Steven R. DePalma, Carolyn Y. Ho, J. G. Seidman, Christine E. Seidman, Heidi L. Rehm, Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity Genetics in Medicine. ,vol. 17, pp. 880- 888 ,(2015) , 10.1038/GIM.2014.205
Giulia Mearini, Doreen Stimpel, Elisabeth Krämer, Birgit Geertz, Ingke Braren, Christina Gedicke-Hornung, Guillaume Précigout, Oliver J Müller, Hugo A Katus, Thomas Eschenhagen, Thomas Voit, Luis Garcia, Stéphanie Lorain, Lucie Carrier, Repair of Mybpc3 mRNA by 5′-trans-splicing in a Mouse Model of Hypertrophic Cardiomyopathy Molecular therapy. Nucleic acids. ,vol. 2, ,(2013) , 10.1038/MTNA.2013.31
Giulia Mearini, Doreen Stimpel, Birgit Geertz, Florian Weinberger, Elisabeth Krämer, Saskia Schlossarek, Julia Mourot-Filiatre, Andrea Stoehr, Alexander Dutsch, Paul J. M. Wijnker, Ingke Braren, Hugo A. Katus, Oliver J. Müller, Thomas Voit, Thomas Eschenhagen, Lucie Carrier, Mybpc3 gene therapy for neonatal cardiomyopathy enables long-term disease prevention in mice Nature Communications. ,vol. 5, pp. 5515- ,(2014) , 10.1038/NCOMMS6515
E. Rosalie Witjas-Paalberends, Nicoletta Piroddi, Kelly Stam, Sabine J. van Dijk, Vasco Sequeira Oliviera, Claudia Ferrara, Beatrice Scellini, Mark Hazebroek, Folkert J. ten Cate, Marjon van Slegtenhorst, Cris dos Remedios, Hans W.M Niessen, Chiara Tesi, Ger J.M. Stienen, Stephane Heymans, Michelle Michels, Corrado Poggesi, Jolanda van der Velden, Mutations in MYH7 reduce the force generating capacity of sarcomeres in human familial hypertrophic cardiomyopathy Cardiovascular Research. ,vol. 99, pp. 432- 441 ,(2013) , 10.1093/CVR/CVT119
A. A. T. Geisterfer-Lowrance, M. Christe, D. A. Conner, J. S. Ingwall, F. J. Schoen, C. E. Seidman, J. G. Seidman, A Mouse Model of Familial Hypertrophic Cardiomyopathy Science. ,vol. 272, pp. 731- 734 ,(1996) , 10.1126/SCIENCE.272.5262.731
Cheryl Dambrot, Stefan R. Braam, Leon G. J. Tertoolen, Matthew Birket, Douwe E. Atsma, Christine L. Mummery, Serum supplemented culture medium masks hypertrophic phenotypes in human pluripotent stem cell derived cardiomyocytes Journal of Cellular and Molecular Medicine. ,vol. 18, pp. 1509- 1518 ,(2014) , 10.1111/JCMM.12356
Ioannis Karakikes, Francesca Stillitano, Mathieu Nonnenmacher, Christos Tzimas, Despina Sanoudou, Vittavat Termglinchan, Chi-Wing Kong, Stephanie Rushing, Jens Hansen, Delaine Ceholski, Fotis Kolokathis, Dimitrios Kremastinos, Alexandros Katoulis, Lihuan Ren, Ninette Cohen, Johannes M.I.H. Gho, Dimitrios Tsiapras, Aryan Vink, Joseph C. Wu, Folkert W. Asselbergs, Ronald A. Li, Jean-Sebastien Hulot, Evangelia G. Kranias, Roger J. Hajjar, Correction of human phospholamban R14del mutation associated with cardiomyopathy using targeted nucleases and combination therapy Nature Communications. ,vol. 6, pp. 6955- 6955 ,(2015) , 10.1038/NCOMMS7955