Literature DB >> 11151425

Heteroplasmy of the A3243G transition of mitochondrial tRNA(Leu(UUR)) in a MELAS case and in a 25-week-old miscarried fetus.

E Cardaioli, G M Fabrizi, G S Grieco, M T Dotti, A Federico.   

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Year:  2000        PMID： 11151425     DOI： 10.1007/s004150070080

Source DB:  PubMed          Journal:  J Neurol        ISSN： 0340-5354            Impact factor:   4.849


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  4 in total

1.  Tissue specific distribution of the 3243A->G mtDNA mutation.

Authors:  A L Frederiksen; P H Andersen; K O Kyvik; T D Jeppesen; J Vissing; M Schwartz
Journal:  J Med Genet       Date:  2006-02-20       Impact factor: 6.318

2.  Prenatal diagnosis of myopathy, encephalopathy, lactic acidosis, and stroke-like syndrome: contribution to understanding mitochondrial DNA segregation during human embryofetal development.

Authors:  C Bouchet; J Steffann; J Corcos; S Monnot; V Paquis; A Rötig; S Lebon; P Levy; G Royer; I Giurgea; N Gigarel; A Benachi; Y Dumez; A Munnich; J P Bonnefont
Journal:  J Med Genet       Date:  2006-05-11       Impact factor: 6.318

3.  Segregation of mtDNA throughout human embryofetal development: m.3243A>G as a model system.

Authors:  Sophie Monnot; Nadine Gigarel; David C Samuels; Philippe Burlet; Laetitia Hesters; Nelly Frydman; René Frydman; Violaine Kerbrat; Benoit Funalot; Jelena Martinovic; Alexandra Benachi; Josué Feingold; Arnold Munnich; Jean-Paul Bonnefont; Julie Steffann
Journal:  Hum Mutat       Date:  2011-01       Impact factor: 4.878

4.  Inherited pathogenic mitochondrial DNA mutations and gastrointestinal stem cell populations.

Authors:  Tianhong Su; John P Grady; Sorena Afshar; Stuart Ac McDonald; Robert W Taylor; Doug M Turnbull; Laura C Greaves
Journal:  J Pathol       Date:  2018-11-05       Impact factor: 7.996
  4 in total

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