The impact of mitochondrial tRNA mutations on the amount of ATP synthase differs in the brain compared to other tissues-Reference-Cited by-同舟云学术

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The impact of mitochondrial tRNA mutations on the amount of ATP synthase differs in the brain compared to other tissues

Published:2008-05 Issue:5 Volume:1782 Page:317-325
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Fornuskova Daniela,Brantova Olga,Tesarova Marketa,Stiburek Lukas,Honzik Tomas,Wenchich Laszlo,Tietzeova Evzenie,Hansikova Hana,Zeman Jiri

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference42 articles.

1. The molecular basis for tissue specificity of the oxidative phosphorylation deficiencies in patients with mutations in the mitochondrial translation factor EFG1;Antonicka;Hum. Mol. Genet.,2006

2. Mitochondrial transcription and its regulation in mammalian cells;Asin-Cayuela;Trends Biochem. Sci.,2007

3. The mitochondrial genome: structure, transcription, translation and replication;Taanman;Biochim. Biophys. Acta,1999

4. G8363A mutation in the mitochondrial DNA transfer ribonucleic acidLys gene: another cause of Leigh syndrome;Shtilbans;J. Child Neurol.,2000

5. Myoclonus epilepsy associated with ragged-red fibers: a G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA(Lys) in two families;Ozawa;Muscle Nerve,1997

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