Cloning of the human NADH: ubiquinone oxidoreductase subunit B13: localization to chromosome 7q32 and identification of a pseudogene on 11p15.

Suppr

超能文献

作者信息

Russell M W, du Manoir S, Collins F S, Brody L C

机构信息

Department of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor 48109, USA.

出版信息

Mamm Genome. 1997 Jan;8(1):60-1. doi: 10.1007/s003359900350.

DOI:10.1007/s003359900350

PMID:9021153

Abstract

摘要

相似文献

Cloning of the human NADH: ubiquinone oxidoreductase subunit B13: localization to chromosome 7q32 and identification of a pseudogene on 11p15.

Mamm Genome. 1997 Jan;8(1):60-1. doi: 10.1007/s003359900350.

Molecular cloning and characterization of the active human mitochondrial NADH:ubiquinone oxidoreductase 24-kDa gene (NDUFV2) and its pseudogene.

Genomics. 1995 Apr 10;26(3):461-6. doi: 10.1016/0888-7543(95)80163-g.

Chromosomal localization of the human gene encoding the 51-kDa subunit of mitochondrial complex I (NDUFV1) to 11q13.

Genomics. 1993 Nov;18(2):435-9. doi: 10.1006/geno.1993.1493.

The human mitochondrial NADH: ubiquinone oxidoreductase 51-kDa subunit maps adjacent to the glutathione S-transferase P1-1 gene on chromosome 11q13.

Genomics. 1992 Dec;14(4):1116-8. doi: 10.1016/s0888-7543(05)80144-2.

The nuclear-encoded human NADH:ubiquinone oxidoreductase NDUFA8 subunit: cDNA cloning, chromosomal localization, tissue distribution, and mutation detection in complex-I-deficient patients.

Hum Genet. 1998 Nov;103(5):557-63. doi: 10.1007/s004390050869.

A human cDNA encoding the homologue of NADH: ubiquinone oxidoreductase subunit B13.

Biochim Biophys Acta. 1997 Feb 7;1350(2):115-8. doi: 10.1016/s0167-4781(96)00208-4.

Identification and primary structure of five human NADH-ubiquinone oxidoreductase subunits.

Biochem Biophys Res Commun. 1997 Dec 18;241(2):589-94. doi: 10.1006/bbrc.1997.7707.

The human NADH: ubiquinone oxidoreductase NDUFS5 (15 kDa) subunit: cDNA cloning, chromosomal localization, tissue distribution and the absence of mutations in isolated complex I-deficient patients.

J Inherit Metab Dis. 1999 Feb;22(1):19-28. doi: 10.1023/a:1005434912463.

Molecular cloning of the rat NADH:ubiquinone oxidoreductase subunit and its up-regulation in the facial muscle after denervation: detected by means of differential display.

Neurol Res. 1996 Aug;18(4):329-36. doi: 10.1080/01616412.1996.11740431.

Molecular cloning and characterization of the human mitochondrial NADH:oxidoreductase 10-kDa gene (NDUFV3).

Genomics. 1997 Oct 15;45(2):434-7. doi: 10.1006/geno.1997.4930.

引用本文的文献

Role of NAD(+), Oxidative Stress, and Tryptophan Metabolism in Autism Spectrum Disorders.

Int J Tryptophan Res. 2013 Jul 21;6(Suppl 1):15-28. doi: 10.4137/IJTR.S11355. Print 2013.

本文引用的文献

The human B22 subunit of the NADH-ubiquinone oxidoreductase maps to the region of chromosome 8 involved in branchio-oto-renal syndrome.

Genomics. 1996 Jul 1;35(1):6-10. doi: 10.1006/geno.1996.0316.

The murine homolog of the human breast and ovarian cancer susceptibility gene Brca1 maps to mouse chromosome 11D.

Hum Genet. 1996 Feb;97(2):256-9. doi: 10.1007/BF02265277.

Rapid cDNA sequencing (expressed sequence tags) from a directionally cloned human infant brain cDNA library.

Nat Genet. 1993 Aug;4(4):373-80. doi: 10.1038/ng0893-373.

A dinucleotide repeat polymorphism at the ribosomal protein S6 (RPS6) gene.

Hum Mol Genet. 1993 Oct;2(10):1749. doi: 10.1093/hmg/2.10.1749-a.

Preparation and screening of an arrayed human genomic library generated with the P1 cloning system.

Proc Natl Acad Sci U S A. 1994 Mar 29;91(7):2629-33. doi: 10.1073/pnas.91.7.2629.

An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs.

Nucleic Acids Res. 1987 Oct 26;15(20):8125-48. doi: 10.1093/nar/15.20.8125.

Molecular defects of NADH-ubiquinone oxidoreductase (complex I) in mitochondrial diseases.

J Bioenerg Biomembr. 1988 Jun;20(3):365-82. doi: 10.1007/BF00769638.

Congenital deficiency of two polypeptide subunits of the iron-protein fragment of mitochondrial complex I.

J Clin Invest. 1987 Feb;79(2):463-7. doi: 10.1172/JCI112834.

Molecular basis of mitochondrial myopathies: polypeptide analysis in complex-I deficiency.

Lancet. 1988 Mar 5;1(8584):500-3. doi: 10.1016/s0140-6736(88)91296-2.

Abnormalities of the electron transport chain in idiopathic Parkinson's disease.

Ann Neurol. 1989 Dec;26(6):719-23. doi: 10.1002/ana.410260606.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验