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Carlos T. Moraes
Carlos T. Moraes
Professor of Neurology
Verified email at med.miami.edu - Homepage
Title
Cited by
Cited by
Year
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
14432012
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
11881989
Deletions of mitochondrial DNA in Kearns-Sayre syndrome
M Zeviani, CT Moraes, S DiMauro, H Nakase, E Bonilla, EA Schon, ...
Neurology 51 (6), 1525-1525-a, 1998
9801998
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
7922009
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
7271989
Mitochondrial encephalomyopathies
S DiMauro, CT Moraes
Archives of neurology 50 (11), 1197-1208, 1993
7021993
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
7021991
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
6561991
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
6532007
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
6071992
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
5462004
Reactive oxygen species and mitochondrial diseases
IG Kirkinezos, CT Moraes
Seminars in cell & developmental biology 12 (6), 449-457, 2001
5422001
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
4922000
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
4672013
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
4652002
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
4601999
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
4311990
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
3652008
Mitochondrial DNA damage and reactive oxygen species in neurodegenerative disease
N Nissanka, CT Moraes
FEBS letters 592 (5), 728-742, 2018
3612018
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
3371994
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