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Detection and quantification of mitochondrial DNA deletions.

作者信息

Soong N W, Arnheim N

机构信息

Department of Gene Therapy, University of Southern California, Los Angeles 90033, USA.

出版信息

Methods Enzymol. 1996;264:421-31. doi: 10.1016/s0076-6879(96)64038-5.

DOI:10.1016/s0076-6879(96)64038-5
PMID:8965714
Abstract
摘要

相似文献

1
Detection and quantification of mitochondrial DNA deletions.
Methods Enzymol. 1996;264:421-31. doi: 10.1016/s0076-6879(96)64038-5.
2
Characterisation of repeat and palindrome elements in patients harbouring single deletions of mitochondrial DNA.线粒体DNA单缺失患者中重复和回文元件的特征分析
J Med Genet. 2003 Jul;40(7):e86. doi: 10.1136/jmg.40.7.e86.
3
A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA.直接重复序列是人类线粒体DNA大规模缺失的热点区域。
Science. 1989 Apr 21;244(4902):346-9. doi: 10.1126/science.2711184.
4
mtDNA deletions in Kearns-Sayre.
Neurology. 1990 Aug;40(8):1322-3. doi: 10.1212/wnl.40.8.1322-a.
5
Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.与线粒体DNA缺失相关的自发性凯-赛综合征/慢性进行性眼外肌麻痹加综合征：一种滑链复制模型和代谢疗法。
Proc Natl Acad Sci U S A. 1989 Oct;86(20):7952-6. doi: 10.1073/pnas.86.20.7952.
6
Tandem direct duplications of mitochondrial DNA in mitochondrial myopathy: analysis of nucleotide sequence and tissue distribution.线粒体肌病中线粒体DNA的串联直接重复：核苷酸序列与组织分布分析
Nucleic Acids Res. 1989 Dec 25;17(24):10223-9. doi: 10.1093/nar/17.24.10223.
7
Detection and characterization of mitochondrial DNA rearrangements in Pearson and Kearns-Sayre syndromes by long PCR.通过长链聚合酶链反应检测和鉴定Pearson综合征及Kearns-Sayre综合征中的线粒体DNA重排
Hum Genet. 1997 Oct;100(5-6):643-50. doi: 10.1007/s004390050567.
8
Kearns-Sayre syndrome case presenting a mitochondrial DNA deletion with unusual direct repeats and a rudimentary RNAase mitochondrial ribonucleotide processing target sequence.卡恩斯-塞尔综合征病例，呈现出线粒体DNA缺失，伴有异常的直接重复序列和一个基本的核糖核酸酶线粒体核糖核苷酸加工靶序列。
Genomics. 1993 Apr;16(1):256-8. doi: 10.1006/geno.1993.1170.
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3.1-kb deletion of mitochondrial DNA in a patient with Kearns-Sayre syndrome.一名患有卡恩斯-塞尔综合征患者的线粒体DNA发生3.1千碱基缺失。
Acta Neuropathol. 1995;90(2):126-9. doi: 10.1007/BF00294310.
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[Nucleotide mapping and a kinetic model of a heteroplasmic deletion of 4,666 base pairs from mitochondrial DNA in the Kearns-Sayre syndrome].[核苷酸图谱绘制及卡恩斯-塞尔综合征中线粒体DNA 4666个碱基对异质性缺失的动力学模型]
C R Acad Sci III. 1989;309(10):403-7.

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Mitochondrial DNA levels in Huntington disease leukocytes and dermal fibroblasts.
亨廷顿舞蹈病患者白细胞和皮肤成纤维细胞中的线粒体DNA水平
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Association of large scale 4977-bp "common" deletions in sperm mitochondrial DNA with asthenozoospermia and oligoasthenoteratozoospermia.精子线粒体DNA中4977-bp“常见”大片段缺失与弱精子症和少弱畸精子症的关联。
J Hum Reprod Sci. 2016 Jan-Mar;9(1):35-40. doi: 10.4103/0974-1208.178635.
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Mitochondrial DNA common deletion is not associated with thyroid, breast and colorectal tumors in Turkish patients.线粒体 DNA 常见缺失与土耳其患者的甲状腺、乳腺和结直肠肿瘤无关。
Genet Mol Biol. 2010 Jan;33(1):1-4. doi: 10.1590/S1415-47572009005000102. Epub 2010 Mar 1.
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Spectrum of mitochondrial DNA deletions within the common deletion region induced by low levels of UVB irradiation of human keratinocytes in vitro.体外低水平紫外线B照射人角质形成细胞诱导的常见缺失区域内线粒体DNA缺失谱
Gene. 2009 Jul 1;440(1-2):23-7. doi: 10.1016/j.gene.2009.03.019. Epub 2009 Apr 2.
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Correlation of the 4977 bp mitochondrial DNA deletion with human sperm dysfunction.4977碱基对线粒体DNA缺失与人类精子功能障碍的相关性。
BMC Res Notes. 2009 Feb 4;2:18. doi: 10.1186/1756-0500-2-18.
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Patterns of persistent DNA damage associated with sun exposure and the glutathione S-transferase M1 genotype in melanoma patients.黑色素瘤患者中与阳光暴露及谷胱甘肽S-转移酶M1基因型相关的持续性DNA损伤模式。
Photochem Photobiol. 2009 Jan-Feb;85(1):379-86. doi: 10.1111/j.1751-1097.2008.00455.x.