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Alternative, noninvasive tissues for quantitative screening of mutant mitochondrial DNA.

作者信息

Wong L J, Lam C W

机构信息

Dept. of Pathol. and Lab. Med., Children's Hosp. Los Angeles, Los Angeles, CA 90027, USA.

出版信息

Clin Chem. 1997 Jul;43(7):1241-3.

PMID:9216465
Abstract
摘要

相似文献

1
Alternative, noninvasive tissues for quantitative screening of mutant mitochondrial DNA.用于定量筛选突变型线粒体DNA的替代性非侵入性组织。
Clin Chem. 1997 Jul;43(7):1241-3.
2
Evaluation of three methods for effective extraction of DNA from human hair.三种从人发中有效提取DNA方法的评估。
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3
Molecular-clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load.一个家系中组织线粒体DNA T8993G突变负荷可变的分子临床相关性
Mol Genet Metab. 2006 Aug;88(4):364-71. doi: 10.1016/j.ymgme.2006.02.001. Epub 2006 Mar 20.
4
Searching for A3243G mitochondrial DNA mutation in buccal mucosa in order to improve the screening of patients with mitochondrial diabetes.
Eur J Endocrinol. 2001 Oct;145(4):541-2. doi: 10.1530/eje.0.1450541.
5
A hair follicle in human cheek mucosa.人类颊黏膜中的一个毛囊。
Proc R Soc Med. 1960 Jul;53(7):527-8. doi: 10.1177/003591576005300708.
6
The clinical evaluation for the mitochondrial DNA detected from hair follicles.对从毛囊中检测到的线粒体DNA进行临床评估。
Clin Chim Acta. 2005 Nov;361(1-2):214-6. doi: 10.1016/j.cccn.2005.05.026.
7
Analysis of mitochondrial DNA point mutation heteroplasmy by ARMS quantitative PCR.通过扩增阻滞突变系统定量PCR分析线粒体DNA点突变异质性
Curr Protoc Hum Genet. 2011 Jan;Chapter 19:Unit 19.6.. doi: 10.1002/0471142905.hg1906s68.
8
Rapid and noninvasive screening of patients with mitochondrial myopathy.线粒体肌病患者的快速无创筛查
Hum Mutat. 1994;4(2):132-5. doi: 10.1002/humu.1380040207.
9
[Single-fiber polymerase chain reaction for detection of mutant mitochondrial DNA].
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10
[Determination of the point of gene mutation in two types of tissue from the aminoglycoside antibiotics induced deaf patients].
Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2001 Apr;15(4):149-51.

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A novel mutation in the mitochondrial tRNA(Ser(AGY)) gene associated with mitochondrial myopathy, encephalopathy, and complex I deficiency.线粒体tRNA(Ser(AGY))基因中的一种新型突变与线粒体肌病、脑病及复合体I缺乏相关。
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Simultaneous detection and quantification of mitochondrial DNA deletion(s), depletion, and over-replication in patients with mitochondrial disease.线粒体疾病患者中线粒体DNA缺失、耗竭和过度复制的同步检测与定量分析。
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Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene.线粒体脑肌病与细胞色素b基因中的终止密码子突变相关的复合物III缺乏症。
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Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.线粒体脑肌病、乳酸酸中毒和卒中样发作的A3243G突变的流行病学:成人人群中该突变的患病率
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