Carlos T. Moraes
Carlos T. Moraes
Professor of Neurology
Verified email at - Homepage
Cited by
Cited by
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome
CT Moraes, S DiMauro, M Zeviani, A Lombes, S Shanske, AF Miranda, ...
New England Journal of Medicine 320 (20), 1293-1299, 1989
Deletions of mitochondrial DNA in Kearns‐Sayre syndrome
M Zeviani, CT Moraes, S DiMauro, H Nakase, E Bonilla, EA Schon, ...
Neurology 38 (9), 1339-1339, 1988
Glycolytic oligodendrocytes maintain myelin and long-term axonal integrity
U Fünfschilling, LM Supplie, D Mahad, S Boretius, AS Saab, J Edgar, ...
Nature 485 (7399), 517-521, 2012
Increased muscle PGC-1α expression protects from sarcopenia and metabolic disease during aging
T Wenz, SG Rossi, RL Rotundo, BM Spiegelman, CT Moraes
Proceedings of the National Academy of Sciences 106 (48), 20405-20410, 2009
mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases.
CT Moraes, S Shanske, HJ Tritschler, JR Aprille, F Andreetta, E Bonilla, ...
American journal of human genetics 48 (3), 492, 1991
Mitochondrial encephalomyopathies
S DiMauro, CT Moraes
Archives of Neurology 50 (11), 1197-1208, 1993
A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA
EA Schon, R Rizzuto, CT Moraes, H Nakase, M Zeviani, S DiMauro
Science 244 (4902), 346-349, 1989
Depletion of muscle mitochondrial DNA in AIDS patients with zidovudine-induced myopathy
E Arnaudo, S Shanske, S DiMauro, EA Schon, CT Moraes, M Dalakas
The Lancet 337 (8740), 508-510, 1991
MELAS: clinical features, biochemistry, and molecular genetics
E Ciafaloni, E Ricci, S Shanske, CT Moraes, G Silvestri, M Hirano, ...
Annals of Neurology: Official Journal of the American Neurological …, 1992
The Qo site of the mitochondrial complex III is required for the transduction of hypoxic signaling via reactive oxygen species production
EL Bell, TA Klimova, J Eisenbart, CT Moraes, MP Murphy, GRS Budinger, ...
The Journal of cell biology 177 (6), 1029-1036, 2007
Cloning of an Endangered Species (Bos gaurus) Using Interspecies Nuclear Transfer
RP Lanza, JB Cibelli, F Diaz, CT Moraes, PW Farin, CE Farin, CJ Hammer, ...
Cloning 2 (2), 79-90, 2000
Respiratory complex III is required to maintain complex I in mammalian mitochondria
R Acı́n-Pérez, MP Bayona-Bafaluy, P Fernández-Silva, ...
Molecular cell 13 (6), 805-815, 2004
Reactive oxygen species and mitochondrial diseases
IG Kirkinezos, CT Moraes
Seminars in cell & developmental biology 12 (6), 449-457, 2001
Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA
S Mita, R Rizzuto, CT Moraes, S Shanske, E Arnaudo, GM Fabrizi, Y Koga, ...
Nucleic acids research 18 (3), 561-567, 1990
Titrating the effects of mitochondrial complex I impairment in the cell physiology
A Barrientos, CT Moraes
Journal of Biological Chemistry 274 (23), 16188-16197, 1999
Generation of histocompatible tissues using nuclear transplantation
RP Lanza, HY Chung, JJ Yoo, PJ Wettstein, C Blackwell, N Borson, ...
Nature biotechnology 20 (7), 689-696, 2002
RETRACTED: Activation of the PPAR/PGC-1α Pathway Prevents a Bioenergetic Deficit and Effectively Improves a Mitochondrial Myopathy Phenotype
T Wenz, F Diaz, BM Spiegelman, CT Moraes
Cell metabolism 8 (3), 249-256, 2008
Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy
M Sciacco, E Bonilla, EA Schon, S DiMauro, CT Moraes
Human molecular genetics 3 (1), 13-19, 1994
Specific elimination of mutant mitochondrial genomes in patient-derived cells by mitoTALENs
SR Bacman, SL Williams, M Pinto, S Peralta, CT Moraes
Nature medicine 19 (9), 1111-1113, 2013
A new mtDNA mutation in the tRNA (Lys) gene associated with myoclonic epilepsy and ragged-red fibers (MERRF).
G Silvestri, CT Moraes, S Shanske, SJ Oh, S DiMauro
American journal of human genetics 51 (6), 1213, 1992
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