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本文引用的文献

1
A mitochondrial etiology of neurodegenerative diseases: evidence from Parkinson's disease.神经退行性疾病的线粒体病因：来自帕金森病的证据。
Ann N Y Acad Sci. 2008 Dec;1147:1-20. doi: 10.1196/annals.1427.001.
2
Large-scale chemical dissection of mitochondrial function.线粒体功能的大规模化学剖析
Nat Biotechnol. 2008 Mar;26(3):343-51. doi: 10.1038/nbt1387. Epub 2008 Feb 24.
3
A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations.线粒体疾病的小鼠模型揭示了针对严重线粒体DNA突变的种系选择。
Science. 2008 Feb 15;319(5865):958-62. doi: 10.1126/science.1147786.
4
Strong purifying selection in transmission of mammalian mitochondrial DNA.哺乳动物线粒体DNA传递过程中的强烈纯化选择。
PLoS Biol. 2008 Jan;6(1):e10. doi: 10.1371/journal.pbio.0060010.
5
Small molecule activators of SIRT1 as therapeutics for the treatment of type 2 diabetes.作为治疗2型糖尿病的疗法的SIRT1小分子激活剂。
Nature. 2007 Nov 29;450(7170):712-6. doi: 10.1038/nature06261.
6
Genetic basis for correction of very-long-chain acyl-coenzyme A dehydrogenase deficiency by bezafibrate in patient fibroblasts: toward a genotype-based therapy.苯扎贝特对患者成纤维细胞中极长链酰基辅酶A脱氢酶缺乏症的纠正作用的遗传基础：迈向基于基因型的治疗
Am J Hum Genet. 2007 Dec;81(6):1133-43. doi: 10.1086/522375. Epub 2007 Oct 29.
7
A second generation human haplotype map of over 3.1 million SNPs.一张包含超过310万个单核苷酸多态性的第二代人类单倍型图谱。
Nature. 2007 Oct 18;449(7164):851-61. doi: 10.1038/nature06258.
8
Prevalence of mitochondrial DNA disease in adults.成人线粒体DNA疾病的患病率。
Ann Neurol. 2008 Jan;63(1):35-9. doi: 10.1002/ana.21217.
9
Mitochondrial DNA haplogroups and age-related maculopathy.线粒体DNA单倍群与年龄相关性黄斑病变
Arch Ophthalmol. 2007 Sep;125(9):1235-40. doi: 10.1001/archopht.125.9.1235.
10
A common mitochondrial haplogroup is associated with elevated total serum IgE levels.一种常见的线粒体单倍群与血清总IgE水平升高有关。
J Allergy Clin Immunol. 2007 Aug;120(2):351-8. doi: 10.1016/j.jaci.2007.05.029.

Mitochondria as chi.

作者信息

Wallace Douglas C

机构信息

Center for Molecular and Mitochondrial Medicine and Genetics, Department of Ecology and Evolutionary Biology, University of California, Irvine, California 92697-3940, USA.

出版信息

Genetics. 2008 Jun;179(2):727-35. doi: 10.1534/genetics.104.91769.

DOI:10.1534/genetics.104.91769
PMID:18558648
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2429869/
Abstract
摘要