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Cardiac-specific deficiency of 3-hydroxy-3-methylglutaryl coenzyme A lyase in mice causes cardiomyopathy and a distinct pattern of acyl-coenzyme A-related biomarkers.
Yang, Hao; Wang, Youlin; Tang, Marie-Christine; Waters, Paula; Wang, Shupei; Allard, Pierre; Ryan, Robert O; Nuyt, Anne-Monique; Paradis, Pierre; Schiffrin, Ernesto L; Furtos, Alexandra; Mitchell, Grant A.
Afiliação
  • Yang H; Medical Genetics Service, Department of Pediatrics and Research Center, CHU Sainte-Justine and Université de Montréal, Montreal, Québec, Canada.
  • Wang Y; Medical Genetics Service, Department of Pediatrics and Research Center, CHU Sainte-Justine and Université de Montréal, Montreal, Québec, Canada.
  • Tang MC; Département de Chimie, Université de Montréal, Montreal, Québec, Canada.
  • Waters P; Medical Genetics Service, Department of Laboratory Medicine, CHU Sherbrooke and Department of Pediatrics, Université de Sherbrooke, Québec, Canada.
  • Wang S; Medical Genetics Service, Department of Pediatrics and Research Center, CHU Sainte-Justine and Université de Montréal, Montreal, Québec, Canada.
  • Allard P; Biochemical Genetics Laboratory, CHU Sainte-Justine, Montreal, Québec, Canada.
  • Ryan RO; Department of Biochemistry and Molecular Biology, University of Nevada, Reno, Reno, NV, United States.
  • Nuyt AM; Sainte-Justine University Hospital and Research Center, University of Montreal, Montreal, Québec, Canada.
  • Paradis P; Hypertension and Vascular Research Unit, Lady Davis Institute for Medical Research, Sir Mortimer B. Davis-Jewish General Hospital, McGill University, Montréal, Québec, Canada.
  • Schiffrin EL; Hypertension and Vascular Research Unit, Lady Davis Institute for Medical Research, Sir Mortimer B. Davis-Jewish General Hospital, McGill University, Montréal, Québec, Canada.
  • Furtos A; Département de Chimie, Université de Montréal, Montreal, Québec, Canada.
  • Mitchell GA; Medical Genetics Service, Department of Pediatrics and Research Center, CHU Sainte-Justine and Université de Montréal, Montreal, Québec, Canada. Electronic address: grant.mitchell.med@ssss.gouv.qc.ca.
Mol Genet Metab ; 137(3): 257-264, 2022 11.
Article em En | MEDLINE | ID: mdl-36228350
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Erros Inatos do Metabolismo dos Aminoácidos / Cardiomiopatias Tipo de estudo: Etiology_studies Limite: Animals Idioma: En Revista: Mol Genet Metab Assunto da revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Canadá
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Erros Inatos do Metabolismo dos Aminoácidos / Cardiomiopatias Tipo de estudo: Etiology_studies Limite: Animals Idioma: En Revista: Mol Genet Metab Assunto da revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Canadá