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Mitochondrial function in children with idiopathic dilated cardiomyopathy.

作者信息

Marin-Garcia J, Goldenthal M J, Ananthakrishnan R, Pierpont M E, Fricker F J, Lipshultz S E, Perez-Atayde A

机构信息

Molecular Cardiology Institute, Highland Park, New Jersey 08904, USA.

出版信息

J Inherit Metab Dis. 1996;19(3):309-12. doi: 10.1007/BF01799259.

DOI:10.1007/BF01799259
PMID:8803773
Abstract
摘要

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1
Mitochondrial function in children with idiopathic dilated cardiomyopathy.特发性扩张型心肌病患儿的线粒体功能
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2
Specific mitochondrial DNA deletions in idiopathic dilated cardiomyopathy.
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Biochem Biophys Res Commun. 2018 Mar 18;497(4):1049-1054. doi: 10.1016/j.bbrc.2018.02.173. Epub 2018 Feb 23.
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The complete sequence of mtDNA genes in idiopathic dilated cardiomyopathy shows novel missense and tRNA mutations.特发性扩张型心肌病中线粒体DNA基因的完整序列显示出新的错义突变和tRNA突变。
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A case of cardiomyopathy showing progression from the hypertrophic to the dilated form: association of Mt8348A-->G mutation in the mitochondrial tRNA(Lys) gene with severe ultrastructural alterations of mitochondria in cardiomyocytes.一例心肌病从肥厚型进展为扩张型的病例：线粒体tRNA（Lys）基因中Mt8348A→G突变与心肌细胞线粒体严重超微结构改变的关联。
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Ventricular remodeling and survival are more favorable for myocarditis than for idiopathic dilated cardiomyopathy in childhood: an outcomes study from the Pediatric Cardiomyopathy Registry.心肌炎患儿的心室重构和存活率优于特发性扩张型心肌病患儿：来自儿科心肌病注册中心的一项结局研究。
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AIDS. 2015 Jan 2;29(1):91-100. doi: 10.1097/QAD.0000000000000499.
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Mitochondrial retention of Opa1 is required for mouse embryogenesis.线粒体中 Opa1 的保留对于小鼠胚胎发生是必需的。
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本文引用的文献

1
Impaired mitochondrial function in idiopathic dilated cardiomyopathy: biochemical and molecular analysis.特发性扩张型心肌病中线粒体功能受损：生化与分子分析
J Card Fail. 1995 Sep;1(4):285-91. doi: 10.1016/1071-9164(95)90003-9.
2
Specific mitochondrial DNA deletions in idiopathic dilated cardiomyopathy.
Cardiovasc Res. 1996 Feb;31(2):306-13.
3
The investigation of respiratory chain disorders in heart using endomyocardial biopsies.利用心内膜心肌活检对心脏呼吸链疾病进行研究。
J Inherit Metab Dis. 1993;16(3):541-4. doi: 10.1007/BF00711676.
Int J Exp Pathol. 2000 Dec;81(6):349-72. doi: 10.1046/j.1365-2613.2000.00186.x.
4
Absence of cardiac toxicity of zidovudine in infants.齐多夫定在婴儿中无心脏毒性。
N Engl J Med. 2001 Feb 8;344(6):458. doi: 10.1056/NEJM200102083440613.
5
Biochemical and molecular basis for mitochondrial cardiomyopathy in neonates and children.
J Inherit Metab Dis. 2000 Sep;23(6):625-33. doi: 10.1023/a:1005638231195.
6
Mitochondrial disease in superoxide dismutase 2 mutant mice.超氧化物歧化酶2突变小鼠中的线粒体疾病
Proc Natl Acad Sci U S A. 1999 Feb 2;96(3):846-51. doi: 10.1073/pnas.96.3.846.
7
Human mitochondrial function during cardiac growth and development.心脏生长发育过程中的人类线粒体功能。
Mol Cell Biochem. 1998 Feb;179(1-2):21-6. doi: 10.1023/a:1006839831141.
8
Cardiac mitochondrial dysfunction and DNA depletion in children with hypertrophic cardiomyopathy.肥厚型心肌病患儿的心脏线粒体功能障碍与DNA耗竭
J Inherit Metab Dis. 1997 Sep;20(5):674-80. doi: 10.1023/a:1005322409330.
9
The mitochondrial A3243G mutation presenting as severe cardiomyopathy.表现为严重心肌病的线粒体A3243G突变。
J Med Genet. 1997 Jul;34(7):607-9. doi: 10.1136/jmg.34.7.607.
4
Alterations of the mitochondrial respiratory chain in human dilated cardiomyopathy.
Eur Heart J. 1990 Jun;11(6):509-16. doi: 10.1093/oxfordjournals.eurheartj.a059743.
5
Diseases of the mitochondrial DNA.
Annu Rev Biochem. 1992;61:1175-212. doi: 10.1146/annurev.bi.61.070192.005523.