Literature DB >> 8909383

Maternal inheritance and the evaluation of oxidative phosphorylation diseases.

J M Shoffner1.   

Abstract

Mitochondrial DNA is more susceptible than nuclear DNA to mutations. Mitochondrial mutations have been associated with a range of disorders, some of which can be inherited maternally as well as by mendelian patterns. The oxidative phosphorylation diseases are a group of such disorders characterised by a complex phenotype; the Kearns-Sayre syndrome, for example, can include cardiac abnormalities, diabetes mellitus, cerebellar ataxia, and deafness. An understanding of the genetic and biochemical basis of these disorders will help in the adoption of a systematic approach to their diagnosis and to patient management.

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Year:  1996        PMID: 8909383     DOI: 10.1016/S0140-6736(96)09138-6

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  12 in total

1.  Relaxed replication of mtDNA: A model with implications for the expression of disease.

Authors:  P F Chinnery; D C Samuels
Journal:  Am J Hum Genet       Date:  1999-04       Impact factor: 11.025

Review 2.  Mitochondrial genotype and clinical phenotype.

Authors:  P F Chinnery; D M Turnbull
Journal:  J Inherit Metab Dis       Date:  1998-06       Impact factor: 4.982

3.  Predominant cerebellar volume loss as a neuroradiologic feature of pediatric respiratory chain defects.

Authors:  Fernando Scaglia; Lee-Jun C Wong; Georgirene D Vladutiu; Jill V Hunter
Journal:  AJNR Am J Neuroradiol       Date:  2005-08       Impact factor: 3.825

Review 4.  Mouse models of mitochondrial complex I dysfunction.

Authors:  Michael H Irwin; Kodeeswaran Parameshwaran; Carl A Pinkert
Journal:  Int J Biochem Cell Biol       Date:  2012-08-10       Impact factor: 5.085

5.  A reinterpretation of certain disorders affecting the eye muscles and their tissues.

Authors:  Anuchit Poonyathalang; Sangeeta Khanna; R John Leigh
Journal:  Clin Ophthalmol       Date:  2007-12

Review 6.  Mitochondrial disorders: prevalence, myths and advances.

Authors:  D R Thorburn
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

7.  Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

Authors:  K Majamaa; J S Moilanen; S Uimonen; A M Remes; P I Salmela; M Kärppä; K A Majamaa-Voltti; H Rusanen; M Sorri; K J Peuhkurinen; I E Hassinen
Journal:  Am J Hum Genet       Date:  1998-08       Impact factor: 11.025

8.  A Comparative Proteome Profile of Female Mouse Gonads Suggests a Tight Link between the Electron Transport Chain and Meiosis Initiation.

Authors:  Cong Shen; Mingrui Li; Pan Zhang; Yueshuai Guo; Hao Zhang; Bo Zheng; Hui Teng; Tao Zhou; Xuejiang Guo; Ran Huo
Journal:  Mol Cell Proteomics       Date:  2017-11-20       Impact factor: 5.911

Review 9.  Prerequisites and strategies for prenatal diagnosis of respiratory chain deficiency in chorionic villi.

Authors:  L Niers; L van den Heuvel; F Trijbels; R Sengers; J Smeitink
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

10.  Harvesting candidate genes responsible for serious adverse drug reactions from a chemical-protein interactome.

Authors:  Lun Yang; Jian Chen; Lin He
Journal:  PLoS Comput Biol       Date:  2009-07-24       Impact factor: 4.475

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