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P209L mutation in Bag3 does not cause cardiomyopathy in mice.
Fang X, Bogomolovas J, Zhou PS, Mu Y, Ma X, Chen Z, Zhang L, Zhu M, Veevers J, Ouyang K, Chen J. Fang X, et al. Among authors: chen z, chen j. Am J Physiol Heart Circ Physiol. 2019 Feb 1;316(2):H392-H399. doi: 10.1152/ajpheart.00714.2018. Epub 2018 Nov 30. Am J Physiol Heart Circ Physiol. 2019. PMID: 30499714 Free PMC article.
Homozygous G650del nexilin variant causes cardiomyopathy in mice.
Liu C, Spinozzi S, Feng W, Chen Z, Zhang L, Zhu S, Wu T, Fang X, Ouyang K, Evans SM, Chen J. Liu C, et al. Among authors: chen z, chen j. JCI Insight. 2020 Aug 20;5(16):e138780. doi: 10.1172/jci.insight.138780. JCI Insight. 2020. PMID: 32814711 Free PMC article.
Cardiolipin Remodeling Defects Impair Mitochondrial Architecture and Function in a Murine Model of Barth Syndrome Cardiomyopathy.
Zhu S, Chen Z, Zhu M, Shen Y, Leon LJ, Chi L, Spinozzi S, Tan C, Gu Y, Nguyen A, Zhou Y, Feng W, Vaz FM, Wang X, Gustafsson AB, Evans SM, Kunfu O, Fang X. Zhu S, et al. Among authors: chen z. Circ Heart Fail. 2021 Jun;14(6):e008289. doi: 10.1161/CIRCHEARTFAILURE.121.008289. Epub 2021 Jun 15. Circ Heart Fail. 2021. PMID: 34129362 Free PMC article.
PTPMT1 Is Required for Embryonic Cardiac Cardiolipin Biosynthesis to Regulate Mitochondrial Morphogenesis and Heart Development.
Chen Z, Zhu S, Wang H, Wang L, Zhang J, Gu Y, Tan C, Dhanani M, Wever E, Wang X, Xie B, Wang S, Huang L, van Kampen AHC, Liu J, Han Z, Patel HH, Vaz FM, Fang X, Chen J, Ouyang K. Chen Z, et al. Among authors: chen j. Circulation. 2021 Aug 3;144(5):403-406. doi: 10.1161/CIRCULATIONAHA.121.054768. Epub 2021 Aug 2. Circulation. 2021. PMID: 34339306 Free PMC article. No abstract available.
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