Deficiency in the mouse mitochondrial adenine nucleotide translocator isoform 2 gene is associated with cardiac noncompaction.-论文-万方医学网

作者： Jason E,Kokoszka ^[1] ; Katrina G,Waymire ^[2] ; Adrian,Flierl ^[3] ; Katelyn M,Sweeney ^[4] ; Alessia,Angelin ^[4] ; Grant R,MacGregor ^[2] ; Douglas C,Wallace ^[5]

作者单位： Forensic Biology Section, Alabama Department of Forensic Sciences, Annex C, Mobile, AL 36617, United States. ^[1] Department of Developmental and Cell Biology, University of California Irvine, Irvine, CA 92697-2300, United States. ^[2] The Parkinson's Institute, Sunnyvale, CA 94085, United States. ^[3] Center for Mitochondrial and Epigenomic Medicine, Children's Hospital of Philadelphia, Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States. ^[4] Center for Mitochondrial and Epigenomic Medicine, Children's Hospital of Philadelphia, Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States. Electronic address: wallaced1@email.chop.edu. ^[5]

主题词腺嘌呤(Adenine);腺嘌呤核苷酸转运体2(Adenine Nucleotide Translocator 2);动物(Animals);生物转运(Biological Transport);细胞增殖(Cell Proliferation);胚胎, 哺乳动物(Embryo, Mammalian);女(雌)性(Female);基因表达调控, 发育期(Gene Expression Regulation, Developmental);基因, 致死(Genes, Lethal);心脏缺损, 先天性(Heart Defects, Congenital);心力衰竭(Heart Failure);心室(Heart Ventricles);整合酶类(Integrases);男(雄)性(Male);小鼠(Mice);小鼠, 转基因(Mice, Transgenic);线粒体(Mitochondria);线粒体肿胀(Mitochondrial Swelling);肌细胞, 心脏(Myocytes, Cardiac);器官发生(Organogenesis);表型(Phenotype)

DOI 10.1016/j.bbabio.2016.03.026

PMID 27048932

发布时间 2024-03-26

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Deficiency in the mouse mitochondrial adenine nucleotide translocator isoform 2 gene is associated with cardiac noncompaction.

Biochimica et biophysica acta

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Deficiency in the mouse mitochondrial adenine nucleotide translocator isoform 2 gene is associated with cardiac noncompaction.

Biochimica et biophysica acta

相似文献

Biochimica et biophysica acta

相关期刊

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