Literature DB >> 1539604

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

W Sato, K Hayasaka, K Komatsu, Y Sawaishi, K Sakemi, Y Shoji, G Takada.   

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Year:  1992        PMID： 1539604      PMCID： PMC1684303     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  13 in total

1.  Mitochondrial leucine tRNA mutation in neurological diseases.

Authors:  D R Johns; O Hurko
Journal:  Lancet       Date:  1991-04-13       Impact factor: 79.321

2.  A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).

Authors:  Y Kobayashi; M Y Momoi; K Tominaga; T Momoi; K Nihei; M Yanagisawa; Y Kagawa; S Ohta
Journal:  Biochem Biophys Res Commun       Date:  1990-12-31       Impact factor: 3.575

3.  Paternal inheritance of mitochondrial DNA in mice.

Authors:  U Gyllensten; D Wharton; A Josefsson; A C Wilson
Journal:  Nature       Date:  1991-07-18       Impact factor: 49.962

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.  Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.

Authors:  J M Shoffner; M T Lott; A M Lezza; P Seibel; S W Ballinger; D C Wallace
Journal:  Cell       Date:  1990-06-15       Impact factor: 41.582

6.  Sequence and organization of the human mitochondrial genome.

Authors:  S Anderson; A T Bankier; B G Barrell; M H de Bruijn; A R Coulson; J Drouin; I C Eperon; D P Nierlich; B A Roe; F Sanger; P H Schreier; A J Smith; R Staden; I G Young
Journal:  Nature       Date:  1981-04-09       Impact factor: 49.962

7.  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

8.  Germline mosaicism and Duchenne muscular dystrophy mutations.

Authors:  E Bakker; C Van Broeckhoven; E J Bonten; M J van de Vooren; H Veenema; W Van Hul; G J Van Ommen; A Vandenberghe; P L Pearson
Journal:  Nature       Date:  1987 Oct 8-14       Impact factor: 49.962

9.  A partial deletion of the muscular dystrophy gene transmitted twice by an unaffected male.

Authors:  B T Darras; U Francke
Journal:  Nature       Date:  1987 Oct 8-14       Impact factor: 49.962

10.  Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

Authors:  M Tanaka; H Ino; K Ohno; T Ohbayashi; S Ikebe; T Sano; T Ichiki; M Kobayashi; Y Wada; T Ozawa
Journal:  Biochem Biophys Res Commun       Date:  1991-01-31       Impact factor: 3.575
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  2 in total

1.  Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) decrease in diastolic left ventricular function assessed by echocardiography.

Authors:  Y Suzuki; K Harada; Y Miura; W Sato; K Hayasaka; K Kawamura; G Takada
Journal:  Pediatr Cardiol       Date:  1993-07       Impact factor: 1.655

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

Authors:  Y Shoji; W Sato; K Hayasaka; G Takada
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982
  2 in total

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