Cellular pathology of the human heart in Duchenne muscular dystrophy (DMD): lessons learned from in vitro modeling
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physiology (medical),Clinical Biochemistry,Physiology
Link
https://link.springer.com/content/pdf/10.1007/s00424-021-02589-0.pdf
Reference177 articles.
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2. Abdel Aleem A, Elsaid MF, Chalhoub N, Chakroun A, Mohamed KAS, AlShami R, Kuzu O, Mohamed RB, Ibrahim K, AlMudheki N, Osman O, Ross ME, ELalamy O (2020) Clinical and genomic characteristics of LAMA2 related congenital muscular dystrophy in a patients’ cohort from Qatar. A population specific founder variant. Neuromuscul Disord 30:457–471. https://doi.org/10.1016/j.nmd.2020.03.009
3. Acimovic I, Refaat M, Moreau A, Salykin A, Reiken S, Sleiman Y, Souidi M, Přibyl J, Kajava A, Richard S, Lu J, Chevalier P, Skládal P, Dvořak P, Rotrekl V, Marks A, Scheinman M, Lacampagne A, Meli A (2018) Post-translational modifications and diastolic calcium leak associated to the novel RyR2-D3638A mutation lead to CPVT in patient-specific hiPSC-derived cardiomyocytes. J Clin Med 7:423. https://doi.org/10.3390/jcm7110423
4. Adams ME, Odom GL, Kim MJ, Chamberlain JS, Froehner SC (2018) Syntrophin binds directly to multiple spectrin-like repeats in dystrophin and mediates binding of nNOS to repeats 16–17. Hum Mol Genet 27:2978. https://doi.org/10.1093/HMG/DDY197
5. Adkison LR (ed) (2012) Elsevier’s integrated Review Genetics (3rd edn). Elsevier Saunders, Amsterdam
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1. Special issue on recent progress with hPSC-derived cardiovascular cells for organoids, engineered myocardium, drug discovery, disease models, and therapy;Pflügers Archiv - European Journal of Physiology;2021-06-16
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