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Gene-environment regulation of chamber-specific maturation during hypoxemic perinatal circulatory transition.
Zhao Y, Kang X, Barsegian A, He J, Guzman A, Lau RP, Biniwale R, Wadhra M, Reemtsen B, Garg M, Halnon N, Quintero-Rivera F, Grody WW; UCLA Congenital Heart Defects BioCore Faculty; Van Arsdell G, Nelson SF, Touma M. Zhao Y, et al. Among authors: kang x. J Mol Med (Berl). 2020 Jul;98(7):1009-1020. doi: 10.1007/s00109-020-01933-8. Epub 2020 Jun 12. J Mol Med (Berl). 2020. PMID: 32533200 Free PMC article.
Gene-environment regulatory circuits of right ventricular pathology in tetralogy of fallot.
Zhao Y, Kang X, Gao F, Guzman A, Lau RP, Biniwale R, Wadehra M, Reemtsen B, Garg M, Halnon N, Quintero-Rivera F, Van Arsdell G, Coppola G, Nelson SF, Touma M; UCLA Congenital Heart Defects BioCore Faculty. Zhao Y, et al. Among authors: kang x. J Mol Med (Berl). 2019 Dec;97(12):1711-1722. doi: 10.1007/s00109-019-01857-y. Epub 2019 Dec 13. J Mol Med (Berl). 2019. PMID: 31834445 Free PMC article.
Recessive ciliopathy mutations in primary endocardial fibroelastosis: a rare neonatal cardiomyopathy in a case of Alstrom syndrome.
Zhao Y, Wang LK, Eskin A, Kang X, Fajardo VM, Mehta Z, Pineles S, Schmidt RJ, Nagiel A, Satou G, Garg M, Federman M, Reardon LC, Lee SL, Biniwale R, Grody WW, Halnon N, Khanlou N, Quintero-Rivera F, Alejos JC, Nakano A, Fishbein GA, Van Arsdell GS, Nelson SF, Touma M. Zhao Y, et al. Among authors: kang x. J Mol Med (Berl). 2021 Nov;99(11):1623-1638. doi: 10.1007/s00109-021-02112-z. Epub 2021 Aug 13. J Mol Med (Berl). 2021. PMID: 34387706 Free PMC article.
Case Report: Whole Exome Sequencing Identifies Compound Heterozygous Variants in TSFM Gene Causing Juvenile Hypertrophic Cardiomyopathy.
Yang JO, Shaybekyan H, Zhao Y, Kang X, Fishbein GA, Khanlou N, Alejos JC, Halnon N, Satou G, Biniwale R, Lee H, Van Arsdell G, Nelson SF, Touma M; UCLA Clinical Genomics Center; UCLA Congenital Heart Defects-BioCore Faculty. Yang JO, et al. Among authors: kang x. Front Cardiovasc Med. 2022 Jan 6;8:798985. doi: 10.3389/fcvm.2021.798985. eCollection 2021. Front Cardiovasc Med. 2022. PMID: 35071363 Free PMC article.
Whole-Exome Sequencing Identifies Homozygote Nonsense Variants in LMOD2 Gene Causing Infantile Dilated Cardiomyopathy.
Sono R, Larrinaga TM, Huang A, Makhlouf F, Kang X, Su J, Lau R, Arboleda VA, Biniwale R, Fishbein GA, Khanlou N, Si MS, Satou GM, Halnon N, Ucla Congenital Heart Defects-BioCore Faculty, Van Arsdell GS, Gregorio CC, Nelson S, Touma M. Sono R, et al. Among authors: kang x. Cells. 2023 May 23;12(11):1455. doi: 10.3390/cells12111455. Cells. 2023. PMID: 37296576 Free PMC article.
4,131 results