Mitochondrial damage mediates genotoxicity of arsenic in mammalian cells
LIU, Su-Xian, DAVIDSON, Mercy M, XIUWEI TANG, WALKER, Winsome F, ATHAR, Mohammad, IVANOV, Vladimir, HEI, Tom K
Published in Cancer research (Chicago, Ill.) (15.04.2005)
Published in Cancer research (Chicago, Ill.) (15.04.2005)
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A functionally dominant mitochondrial DNA mutation
Sacconi, Sabrina, Salviati, Leonardo, Nishigaki, Yutaka, Walker, Winsome F., Hernandez-Rosa, Evelyn, Trevisson, Eva, Delplace, Severine, Desnuelle, Claude, Shanske, Sara, Hirano, Michio, Schon, Eric A., Bonilla, Eduardo, De Vivo, Darryl C., DiMauro, Salvatore, Davidson, Mercy M.
Published in Human molecular genetics (15.06.2008)
Published in Human molecular genetics (15.06.2008)
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Evidence for nuclear modifier gene in mitochondrial cardiomyopathy
Davidson, Mercy M, Walker, Winsome F, Hernandez-Rosa, Evelyn, Nesti, Claudia
Published in Journal of molecular and cellular cardiology (01.06.2009)
Published in Journal of molecular and cellular cardiology (01.06.2009)
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Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations
Pallotti, Francesco, Baracca, Alessandra, Hernandez-Rosa, Evelyn, Walker, Winsome F, Solaini, Giancarlo, Lenaz, Giorgio, Melzi D'Eril, Gian Vico, Dimauro, Salvatore, Schon, Eric A, Davidson, Mercy M
Published in Biochemical journal (01.12.2004)
Published in Biochemical journal (01.12.2004)
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The m.3243A>G mtDNA mutation is pathogenic in an in vitro model of the human blood brain barrier
Davidson, Mercy M, Walker, Winsome F, Hernandez-Rosa, Evelyn
Published in Mitochondrion (01.11.2009)
Published in Mitochondrion (01.11.2009)
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Novel cell lines derived from adult human ventricular cardiomyocytes
Davidson, Mercy M., Nesti, Claudia, Palenzuela, Lluis, Walker, Winsome F., Hernandez, Evelyn, Protas, Lev, Hirano, Michio, Isaac, Nithila D.
Published in Journal of molecular and cellular cardiology (01.07.2005)
Published in Journal of molecular and cellular cardiology (01.07.2005)
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Copper supplementation restores cytochrome c oxidase activity in cultured cells from patients with SCO2 mutations
Salviati, Leonardo, Hernandez-Rosa, Evelyn, Walker, Winsome F, Sacconi, Sabrina, DiMauro, Salvatore, Schon, Eric A, Davidson, Mercy M
Published in Biochemical journal (15.04.2002)
Published in Biochemical journal (15.04.2002)
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Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation
Giordano, Carla, Pallotti, Francesco, Walker, Winsome F, Checcarelli, Nicoletta, Musumeci, Olimpia, Santorelli, Filippo, d'Amati, Giulia, Schon, Eric A, DiMauro, Salvatore, Hirano, Michio, Davidson, Mercy M
Published in Biochemical and biophysical research communications (26.04.2002)
Published in Biochemical and biophysical research communications (26.04.2002)
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Analysis of Dystrophin Expression after Activation of Myogenesis in Amniocytes, Chorionic-Villus Cells, and Fibroblasts -- A New Method for Diagnosing Duchenne's Muscular Dystrophy
Sancho, Sara, Mongini, Tiziana, Tanji, Kurenai, Tapscott, Stephen J, Walker, Winsome F, Weintraub, Harold, Miller, A. Dusty, Miranda, Armand F
Published in The New England journal of medicine (23.09.1993)
Published in The New England journal of medicine (23.09.1993)
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Deficient muscle carnitine transport in primary carnitine deficiency
PONS, R, CARROZZO, R, TEIN, I, WALKER, W. F, ADDONIZIO, L. J, RHEAD, W, MIRANDA, A. F, DIMAURO, S, DE VIVO, D. C
Published in Pediatric research (01.11.1997)
Published in Pediatric research (01.11.1997)
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Mitochondrial mobility in differentiating muscle heterokaryons
Walker, Ulrich A, Walker, Winsome F, Miranda, Armand F
Published in Journal of the neurological sciences (22.10.1997)
Published in Journal of the neurological sciences (22.10.1997)
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Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2 , a COX assembly gene
Schon, Eric A, Papadopoulou, Lefkothea C, Sue, Carolyn M, Davidson, Mercy M, Tanji, Kurenai, Nishino, Ichizo, Sadlock, James E, Krishna, Sindu, Walker, Winsome, Selby, Jeanette, Glerum, D. Moira, Coster, Rudy Van, Lyon, Gilles, Scalais, Emmanuel, Lebel, Roger, Kaplan, Paige, Shanske, Sara, De Vivo, Darryl C, Bonilla, Eduardo, Hirano, Michio, DiMauro, Salvatore
Published in Nature genetics (01.11.1999)
Published in Nature genetics (01.11.1999)
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Copper supplementation restores cytochrome c oxidase activity in cultured cells from patients with SCO2 mutations
SALVIATI, Leonardo, HERNANDEZ-ROSA, Evelyn, WALKER, Winsome F., SACCONI, Sabrina, DiMAURO, Salvatore, SCHON, Eric A., DAVIDSON, Mercy M.
Published in Biochemical journal (15.04.2002)
Published in Biochemical journal (15.04.2002)
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