异质性小鼠中缺失的线粒体DNA分子的序列分析 - Suppr

Suppr

超能文献

Sequence analysis of a deleted mitochondrial DNA molecule in heteroplasmic mice.

作者信息

Nelson I, Gerasimov S, Marsac C, Lestienne P, Boursot P

机构信息

INSERM U75, CHU, Necker-Enfants Malades, Paris, France.

出版信息

Mamm Genome. 1993 Nov;4(11):680-3. doi: 10.1007/BF00360907.

DOI:10.1007/BF00360907

PMID:8281018

Abstract

摘要

相似文献

Sequence analysis of a deleted mitochondrial DNA molecule in heteroplasmic mice.异质性小鼠中缺失的线粒体DNA分子的序列分析

Mamm Genome. 1993 Nov;4(11):680-3. doi: 10.1007/BF00360907.

Specific detection of deleted mitochondrial DNA by in situ hybridization using a chimera probe.使用嵌合探针通过原位杂交对缺失的线粒体DNA进行特异性检测。

Biochim Biophys Acta. 1996 Sep 11;1308(3):215-21. doi: 10.1016/0167-4781(96)00104-2.

Rapid mapping of mitochondrial dna deletions by large-fragment PCR.

Trends Genet. 1996 Apr;12(4):131-2.

Molecular instability in the COII-tRNA(Lys) intergenic region of the human mitochondrial genome: multiple origins of the 9-bp deletion and heteroplasmy for expanded repeats.人类线粒体基因组COII - tRNA(Lys)基因间隔区的分子不稳定性：9碱基缺失的多个起源及重复序列扩增的异质性

Philos Trans R Soc Lond B Biol Sci. 1998 Jun 29;353(1371):955-65. doi: 10.1098/rstb.1998.0260.

Rapid detection of mitochondrial deletions by long-distance polymerase chain reaction.

Eur J Pediatr. 1995 Dec;154(12):996. doi: 10.1007/BF01958647.

Direct sequencing of deleted mitochondrial DNA in myopathic patients.

Biochem Biophys Res Commun. 1989 Oct 16;164(1):156-63. doi: 10.1016/0006-291x(89)91696-3.

Cochlear mitochondrial DNA3867bp deletion in aged mice.老年小鼠耳蜗线粒体DNA 3867bp缺失

Chin Med J (Engl). 2002 Sep;115(9):1390-3.

A topoisomerase II cleavage site is associated with a novel mitochondrial DNA deletion.一种拓扑异构酶II切割位点与一种新的线粒体DNA缺失相关。

Hum Genet. 1995 Jan;95(1):75-81. doi: 10.1007/BF00225079.

Mitochondrial DNA copy number and mitochondrial DNA deletion in adult and senescent rats.成年和衰老大鼠的线粒体DNA拷贝数及线粒体DNA缺失

Mutat Res. 1992 Sep;275(3-6):181-93. doi: 10.1016/0921-8734(92)90022-h.

Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?肌病与大规模线粒体DNA重复和缺失的关联：何者具有致病性？

Ann Neurol. 1997 Aug;42(2):180-8. doi: 10.1002/ana.410420208.

本文引用的文献

Mitochondrial diseases: genotype versus phenotype.线粒体疾病：基因型与表型

Trends Genet. 1993 Apr;9(4):128-33. doi: 10.1016/0168-9525(93)90207-x.

Sequence and gene organization of mouse mitochondrial DNA.小鼠线粒体DNA的序列与基因组织

Cell. 1981 Oct;26(2 Pt 2):167-80. doi: 10.1016/0092-8674(81)90300-7.

Listing of stocks and strains of mice in the genus Mus derived from the feral state.源自野生状态的小家鼠属小鼠品系和种群列表。

Curr Top Microbiol Immunol. 1986;127:373-95. doi: 10.1007/978-3-642-71304-0_45.

Mitotic segregation of mitochondrial DNAs in human cell hybrids and expression of chloramphenicol resistance.线粒体DNA在人类细胞杂种中的有丝分裂分离及氯霉素抗性的表达。

Somat Cell Mol Genet. 1986 Jan;12(1):41-9. doi: 10.1007/BF01560726.

Length variation and heteroplasmy are frequent in mitochondrial DNA from parthenogenetic and bisexual lizards (genus Cnemidophorus).孤雌生殖和两性生殖的鞭尾蜥属蜥蜴的线粒体DNA中经常出现长度变异和异质性。

Genetics. 1985 Aug;110(4):689-707. doi: 10.1093/genetics/110.4.689.

Kearns-Sayre syndrome with muscle mitochondrial DNA deletion.伴有肌肉线粒体DNA缺失的卡恩斯-塞尔综合征

Lancet. 1988 Apr 16;1(8590):885. doi: 10.1016/s0140-6736(88)91632-7.

Studies of sequence heterogeneity of mitochondrial DNA from rat and mouse tissues: evidence for an increased frequency of deletions/additions with aging.大鼠和小鼠组织线粒体DNA序列异质性的研究：衰老过程中缺失/插入频率增加的证据。

Mech Ageing Dev. 1988 Jun;43(3):279-93. doi: 10.1016/0047-6374(88)90037-1.

Heteroplasmy in mice with deletion of a large coding region of mitochondrial DNA.

Mol Biol Evol. 1987 Jan;4(1):46-55. doi: 10.1093/oxfordjournals.molbev.a040421.

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies.线粒体肌病患者肌肉线粒体DNA的缺失

Nature. 1988 Feb 25;331(6158):717-9. doi: 10.1038/331717a0.

Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome.卡恩斯-塞尔综合征中异质性线粒体DNA缺失的定位

Nucleic Acids Res. 1989 Oct 25;17(20):8117-24. doi: 10.1093/nar/17.20.8117.

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验