Exp Gerontol. 2010 Feb 18. [Epub ahead of print]
Torgovnick A, Schiavi A, Testi R, Ventura N.
Department of Experimental Medicine and Biochemical Sciences, University of Rome "Tor Vergata", Rome, Italy.
Keywords: aging, degenerative disorders, mitochondrial deterioration, cellular damage accumulation, mitochondrial dysfunction, electron transport chain, p53/cep-1, frataxin, Friedreich's ataxia, antioxidant glutathione-S-transferase, therapeutic approaches.
Tuesday, February 23, 2010
Repeat instability as the basis for human diseases and as a potential target for therapy
Nature Reviews Molecular Cell Biology 11, 165-170 (March 2010) | doi:10.1038/nrm2854
Arturo López Castel1, John D. Cleary1,2 & Christopher E. Pearson1,2
1. Arturo López Castel, John D. Cleary and Christopher E. Pearson are at the Program of Genetics & Genome Biology, The Hospital for Sick Children, 101 College Avenue, East Tower 15-312, TMDT Toronto, Ontario, Canada, M5G 1L7.
2. John D. Cleary and Christopher E. Pearson are also at the Department of Molecular Genetics, University of Toronto, Canada.
Keywords: Expansions of repetitive DNA sequences, neurological, neuromuscular diseases, DNA replication, repair, recombination, transcription, epigenetics, therapeutic strategies,Huntington's disease (HD), myotonic dystrophy (DM1), fragile X syndrome type A (FRAXA), Friedreich's ataxia (FRDA), spinocerebellar ataxias (SCAs)
Arturo López Castel1, John D. Cleary1,2 & Christopher E. Pearson1,2
1. Arturo López Castel, John D. Cleary and Christopher E. Pearson are at the Program of Genetics & Genome Biology, The Hospital for Sick Children, 101 College Avenue, East Tower 15-312, TMDT Toronto, Ontario, Canada, M5G 1L7.
2. John D. Cleary and Christopher E. Pearson are also at the Department of Molecular Genetics, University of Toronto, Canada.
Keywords: Expansions of repetitive DNA sequences, neurological, neuromuscular diseases, DNA replication, repair, recombination, transcription, epigenetics, therapeutic strategies,Huntington's disease (HD), myotonic dystrophy (DM1), fragile X syndrome type A (FRAXA), Friedreich's ataxia (FRDA), spinocerebellar ataxias (SCAs)
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