Literature DB >> 1673015

Mitochondrial leucine tRNA mutation in neurological diseases.

D R Johns, O Hurko.   

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Year:  1991        PMID： 1673015     DOI： 10.1016/0140-6736(91)90272-q

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


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  7 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

Review 2.  Mitochondrial DNA mutations and pathogenesis.

Authors:  E A Schon; E Bonilla; S DiMauro
Journal:  J Bioenerg Biomembr       Date:  1997-04       Impact factor: 2.945

3.  The human mitochondrial transcription termination factor (mTERF) is a multizipper protein but binds to DNA as a monomer, with evidence pointing to intramolecular leucine zipper interactions.

Authors:  P Fernandez-Silva; F Martinez-Azorin; V Micol; G Attardi
Journal:  EMBO J       Date:  1997-03-03       Impact factor: 11.598

4.  Codon-specific translational defect caused by a wobble modification deficiency in mutant tRNA from a human mitochondrial disease.

Authors:  Yohei Kirino; Takehiro Yasukawa; Shigeo Ohta; Shigeo Akira; Kaisuke Ishihara; Kimitsuna Watanabe; Tsutomu Suzuki
Journal:  Proc Natl Acad Sci U S A       Date:  2004-10-11       Impact factor: 11.205

Review 5.  Mitochondrial encephalomyopathies: clinical and molecular analysis.

Authors:  E A Schon; M Hirano; S DiMauro
Journal:  J Bioenerg Biomembr       Date:  1994-06       Impact factor: 2.945

6.  MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts.

Authors:  A Chomyn; A Martinuzzi; M Yoneda; A Daga; O Hurko; D Johns; S T Lai; I Nonaka; C Angelini; G Attardi
Journal:  Proc Natl Acad Sci U S A       Date:  1992-05-15       Impact factor: 11.205

Review 7.  Unique features of animal mitochondrial translation systems. The non-universal genetic code, unusual features of the translational apparatus and their relevance to human mitochondrial diseases.

Authors:  Kimitsuna Watanabe
Journal:  Proc Jpn Acad Ser B Phys Biol Sci       Date:  2010       Impact factor: 3.493
  7 in total

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