Literature DB >> 8487499

Tissue distribution of mutant mitochondrial DNA in mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).

Y Shoji1, W Sato, K Hayasaka, G Takada.   

Abstract

We analysed the distribution of mutant mitochondrial DNA (mtDNA) with A-to-G substitution mutation of tRNA(Leu)(UUR) in various autopsied tissues from a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS). There was no significant difference in the proportion (76-86%) of mutant mtDNA in many tissues, except in the lung and spleen. Unequal partitioning of mtDNA in somatic cells appears less prominent than that in germ cells.

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Year:  1993        PMID: 8487499     DOI: 10.1007/bf00711311

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  10 in total

1.  Genetic analysis of three pedigrees of mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)

Authors:  W Sato; K Hayasaka; K Komatsu; Y Sawaishi; K Sakemi; Y Shoji; G Takada
Journal:  Am J Hum Genet       Date:  1992-03       Impact factor: 11.025

2.  Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation.

Authors:  Y Goto; S Horai; T Matsuoka; Y Koga; K Nihei; M Kobayashi; I Nonaka
Journal:  Neurology       Date:  1992-03       Impact factor: 9.910

3.  Widespread tissue distribution of a tRNALeu(UUR) mutation in the mitochondrial DNA of a patient with MELAS syndrome.

Authors:  E Ciafaloni; E Ricci; S Servidei; S Shanske; G Silvestri; G Manfredi; E A Schon; S DiMauro
Journal:  Neurology       Date:  1991-10       Impact factor: 9.910

4.  A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

Authors:  Y Goto; I Nonaka; S Horai
Journal:  Nature       Date:  1990-12-13       Impact factor: 49.962

5.  Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction.

Authors:  J Hayashi; S Ohta; A Kikuchi; M Takemitsu; Y Goto; I Nonaka
Journal:  Proc Natl Acad Sci U S A       Date:  1991-12-01       Impact factor: 11.205

6.  A specific point mutation in the mitochondrial genome of Caucasians with MELAS.

Authors:  C Enter; J Müller-Höcker; S Zierz; G Kurlemann; D Pongratz; C Förster; B Obermaier-Kusser; K D Gerbitz
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

7.  Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome.

Authors:  S G Pavlakis; P C Phillips; S DiMauro; D C De Vivo; L P Rowland
Journal:  Ann Neurol       Date:  1984-10       Impact factor: 10.422

8.  Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy.

Authors:  T Ozawa; M Yoneda; M Tanaka; K Ohno; W Sato; H Suzuki; M Nishikimi; M Yamamoto; I Nonaka; S Horai
Journal:  Biochem Biophys Res Commun       Date:  1988-08-15       Impact factor: 3.575

9.  Mitochondrial encephalomyopathies with the mutation of the mitochondrial tRNA(Leu(UUR)) gene.

Authors:  K Inui; H Fukushima; H Tsukamoto; M Taniike; M Midorikawa; J Tanaka; T Nishigaki; S Okada
Journal:  J Pediatr       Date:  1992-01       Impact factor: 4.406

10.  MELAS: clinical features, biochemistry, and molecular genetics.

Authors:  E Ciafaloni; E Ricci; S Shanske; C T Moraes; G Silvestri; M Hirano; S Simonetti; C Angelini; M A Donati; C Garcia
Journal:  Ann Neurol       Date:  1992-04       Impact factor: 10.422

  10 in total
  2 in total

1.  Neuroradiological features of six kindreds with MELAS tRNA(Leu) A2343G point mutation: implications for pathogenesis.

Authors:  C M Sue; D S Crimmins; Y S Soo; R Pamphlett; C M Presgrave; N Kotsimbos; M J Jean-Francois; E Byrne; J G Morris
Journal:  J Neurol Neurosurg Psychiatry       Date:  1998-08       Impact factor: 10.154

2.  Heteroplasmy and Copy Number in the Common m.3243A>G Mutation-A Post-Mortem Genotype-Phenotype Analysis.

Authors:  Leila Motlagh Scholle; Stephan Zierz; Christian Mawrin; Claudia Wickenhauser; Diana Lehmann Urban
Journal:  Genes (Basel)       Date:  2020-02-18       Impact factor: 4.096

  2 in total

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