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Results: 1-12 |
Results: 12
TOWARDS GENE-THERAPY OF MITOCHONDRIAL DISORDERS
Authors: COLLOMBET JM COUTELLE C
Citation: Jm. Collombet et C. Coutelle, TOWARDS GENE-THERAPY OF MITOCHONDRIAL DISORDERS, Molecular medicine today, 4(1), 1998, pp. 31-38
EXPRESSION OF OXIDATIVE-PHOSPHORYLATION GENES IN MUSCLE-CELL CULTURESFROM PATIENTS WITH MITOCHONDRIAL MYOPATHIES
Authors: COLLOMBET JM FAUREVIGNY H MANDON G DUMOULIN R BOISSIER S BERNARD A MOUSSON B STEPIEN G
Citation: Jm. Collombet et al., EXPRESSION OF OXIDATIVE-PHOSPHORYLATION GENES IN MUSCLE-CELL CULTURESFROM PATIENTS WITH MITOCHONDRIAL MYOPATHIES, Molecular and cellular biochemistry, 168(1-2), 1997, pp. 73-85
INTRODUCTION OF PLASMID DNA INTO ISOLATED-MITOCHONDRIA BY ELECTROPORATION
Authors: COLLOMBET JM WHEELER VC VOGEL F COUTELLE C
Citation: Jm. Collombet et al., INTRODUCTION OF PLASMID DNA INTO ISOLATED-MITOCHONDRIA BY ELECTROPORATION, The Journal of biological chemistry, 272(8), 1997, pp. 5342-5347
TIME-COURSE AND REGIONAL EXPRESSION OF C-FOS AND HSP70 IN HIPPOCAMPUSAND PIRIFORM CORTEX FOLLOWING SOMAN-INDUCED SEIZURES
Authors: CROM VB COLLOMBET JM BURCKHART MF FOQUIN A PERNOTMARTINO I RONDOUIN G LALLEMENT G
Citation: Vb. Crom et al., TIME-COURSE AND REGIONAL EXPRESSION OF C-FOS AND HSP70 IN HIPPOCAMPUSAND PIRIFORM CORTEX FOLLOWING SOMAN-INDUCED SEIZURES, Journal of neuroscience research, 45(5), 1996, pp. 513-524
ACCUMULATION OF MITOCHONDRIAL-DNA DELETIONS IN MYOTUBES CULTURED FROMMUSCLES OF PATIENTS WITH MITOCHONDRIAL MYOPATHIES
Authors: COLLOMBET JM MANDON G DUMOULIN R MOUSSON B STEPIEN G
Citation: Jm. Collombet et al., ACCUMULATION OF MITOCHONDRIAL-DNA DELETIONS IN MYOTUBES CULTURED FROMMUSCLES OF PATIENTS WITH MITOCHONDRIAL MYOPATHIES, MGG. Molecular & general genetics, 253(1-2), 1996, pp. 182-188
RECURRENT MYOGLOBINURIA DUE TO CARNITINE PALMITOYLTRANSFERASE-II DEFICIENCY - EXPRESSION OF THE MOLECULAR PHENOTYPE IN CULTURED MUSCLE-CELLS
Authors: VILLARD J FISCHER A MANDON G COLLOMBET JM TARONI F MOUSSON B
Citation: J. Villard et al., RECURRENT MYOGLOBINURIA DUE TO CARNITINE PALMITOYLTRANSFERASE-II DEFICIENCY - EXPRESSION OF THE MOLECULAR PHENOTYPE IN CULTURED MUSCLE-CELLS, Journal of the neurological sciences, 136(1-2), 1996, pp. 178-181
EARLY REGIONAL CHANGES OF GFAP MESSENGER-RNA IN RAT HIPPOCAMPUS AND DENTATE GYRUS DURING SOMAN-INDUCED SEIZURES
Authors: BAILLELECROM V COLLOMBET JM CARPENTIER P BROCHIER G BURCKHART MF FOQUIN A PERNOTMARINO I RONDOUIN G LALLEMENT G
Citation: V. Baillelecrom et al., EARLY REGIONAL CHANGES OF GFAP MESSENGER-RNA IN RAT HIPPOCAMPUS AND DENTATE GYRUS DURING SOMAN-INDUCED SEIZURES, NeuroReport, 7(1), 1995, pp. 365-369
AN ABNORMAL EXERCISE TEST RESPONSE REVEALING A RESPIRATORY-CHAIN COMPLEX-III DEFICIENCY
Authors: MOUSSON B COLLOMBET JM DUMOULIN R CARRIER H FLOCARD F BOUZIDI M GODINOT C MAIRE I MATHIEU M QUARD S
Citation: B. Mousson et al., AN ABNORMAL EXERCISE TEST RESPONSE REVEALING A RESPIRATORY-CHAIN COMPLEX-III DEFICIENCY, Acta neurologica Scandinavica, 91(6), 1995, pp. 488-493
2-KETOGLUTARATE DEHYDROGENASE-DEFICIENCY, A RARE CAUSE OF PRIMARY HYPERLACTATEMIA - REPORT OF A NEW CASE
Authors: GUFFON N LOPEZMEDIAVILLA C DUMOULIN R MOUSSON B GODINOT C CARRIER H COLLOMBET JM DIVRY P MATHIEU M GUIBAUD P
Citation: N. Guffon et al., 2-KETOGLUTARATE DEHYDROGENASE-DEFICIENCY, A RARE CAUSE OF PRIMARY HYPERLACTATEMIA - REPORT OF A NEW CASE, Journal of inherited metabolic disease, 16(5), 1993, pp. 821-830
HUMAN CULTURED MYOBLASTS - A MODEL FOR THE DIAGNOSIS OF MITOCHONDRIALDISEASES
Authors: DUMOULIN R MANDON G COLLOMBET JM BLOND JL CARRIER H GODINOT C FLOCARD F VILLARD J GUIBAUD P MATHIEU M MOUSSON B
Citation: R. Dumoulin et al., HUMAN CULTURED MYOBLASTS - A MODEL FOR THE DIAGNOSIS OF MITOCHONDRIALDISEASES, Journal of inherited metabolic disease, 16(3), 1993, pp. 545-547
INTEREST OF SKIN FIBROBLASTS FOR THE DIAGNOSIS OF CYTOCHROME-C-OXIDASE DEFICIENCY
Authors: COLLOMBET JM ZABOT MT VIDAILHET M MAIRE I ECHENNE B FLOQUET J DUMOULIN R RIMOLDI M MATHIEU M MOUSSON B
Citation: Jm. Collombet et al., INTEREST OF SKIN FIBROBLASTS FOR THE DIAGNOSIS OF CYTOCHROME-C-OXIDASE DEFICIENCY, Pediatrie, 48(4), 1993, pp. 287-295
EXPRESSION OF OXIDATIVE-PHOSPHORYLATION GENES IN MYOBLASTS AND MYOTUBES FROM PATIENTS WITH MITOCHONDRIAL PATHOLOGIES
Authors: STEPIEN G VIGNY H MANDON G DUMOULIN R MOUSSON B COLLOMBET JM
Citation: G. Stepien et al., EXPRESSION OF OXIDATIVE-PHOSPHORYLATION GENES IN MYOBLASTS AND MYOTUBES FROM PATIENTS WITH MITOCHONDRIAL PATHOLOGIES, American journal of human genetics, 53(3), 1993, pp. 158-158
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