Analysis of cybrids harboring MELAS mutations in the mitochondrial tRNALeu(UUR) gene
- 1 January 1995
- journal article
- research article
- Published by Wiley in Muscle & Nerve
- Vol. 18 (S14) , S119-S123
- https://doi.org/10.1002/mus.880181424
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Topical Review: Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Strokelike Episodes (MELAS): Current ConceptsJournal of Child Neurology, 1994
- 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.Proceedings of the National Academy of Sciences, 1992
- Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes.Molecular and Cellular Biology, 1992
- MELAS: An original case and clinical criteria for diagnosisNeuromuscular Disorders, 1992
- A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1991
- In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria.Molecular and Cellular Biology, 1991
- A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathiesNature, 1990
- Human Cells Lacking mtDNA: Repopulation with Exogenous Mitochondria by ComplementationScience, 1989
- DNA Preparation from Cultured Cells and TissuePublished by Elsevier ,1986
- Sequence and organization of the human mitochondrial genomeNature, 1981