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Results: 10

Authors: Djavaheri-Mergny, M Marsac, C Maziere, C Santus, R Michel, L Dubertret, L Maziere, JC
Citation: M. Djavaheri-mergny et al., UV-A irradiation induces a decrease in the mitochondrial respiratory activity of human NCTC 2544 keratinocytes, FREE RAD RE, 34(6), 2001, pp. 583-594

Authors: Pequignot, MO Dey, R Zeviani, M Tiranti, V Godinot, C Poyau, A Sue, C Di Mauro, S Abitbol, M Marsac, C
Citation: Mo. Pequignot et al., Mutations in the SURF1 gene associated with Leigh syndrome and cytochrome c oxidase deficiency, HUM MUTAT, 17(5), 2001, pp. 374-381

Authors: Pequignot, MO Desguerre, I Dey, R Tartari, M Zeviani, M Agostino, A Benelli, C Fouque, F Prip-Buus, C Marchant, D Abitbol, M Marsac, C
Citation: Mo. Pequignot et al., New splicing-site mutations in the SURF1 gene in Leigh syndrome patients, J BIOL CHEM, 276(18), 2001, pp. 15326-15329

Authors: Nandrot, E Dufour, EM Provost, AC Pequignot, MO Bonnel, S Gogat, K Marchant, D Rouillac, C de Conde, BS Bihoreau, MT Shaver, C Dufier, JL Marsac, C Lathrop, M Menasche, M Abitbol, MM
Citation: E. Nandrot et al., Homozygous deletion in the coding sequence of the c-mer gene in RCS rats unravels general mechanisms of physiological cell adhesion and apoptosis, NEUROBIOL D, 7(6), 2000, pp. 586-599

Authors: Zadeh, MS Kolb, JP Geromin, D D'Anna, R Boulmerka, A Marconi, A Dugas, B Marsac, C D'Alessio, P
Citation: Ms. Zadeh et al., Regulation of ICAM-1/CD54 expression on human endothelial cells by hydrogen peroxide involves inducible NO synthase, J LEUK BIOL, 67(3), 2000, pp. 327-334

Authors: Parfait, B Chretien, D Rotig, A Marsac, C Munnich, A Rustin, P
Citation: B. Parfait et al., Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome, HUM GENET, 106(2), 2000, pp. 236-243

Authors: Pinard, JM Marsac, C Barkaoui, E Desguerre, I Birch-Machin, M Reinert, P Ponsot, G
Citation: Jm. Pinard et al., Riboflavin-response Leigh syndrome and leukodystrophy associated to partial succinate dehydrogenase deficiency., ARCH PED, 6(4), 1999, pp. 421-426

Authors: Rouillac, C Aral, B Fouque, F Marchant, D Saudubray, JM Dumez, Y Lindsay, G Abitbol, M Dufier, JL Marsac, C Benelli, C
Citation: C. Rouillac et al., First prenatal diagnosis of defects in the HsPDX1 gene encoding protein X,an additional lipoyl-containing subunit of the human pyruvate dehydrogenase complex, PRENAT DIAG, 19(12), 1999, pp. 1160-1164

Authors: Merad-Saidoune, M Boitier, E Nicole, A Marsac, C Martinou, JC Sola, B Sinet, PM Ceballos-Picot, I
Citation: M. Merad-saidoune et al., Overproduction of Cu/Zn-superoxide dismutase or Bcl-2 prevents the brain mitochondrial respiratory dysfunction induced by glutathione depletion, EXP NEUROL, 158(2), 1999, pp. 428-436

Authors: Fouque, F Marsac, C Benelli, C
Citation: F. Fouque et al., The pyruvate dehydrogenase complex: from molecular organization to clinical issues, M S-MED SCI, 14(12), 1998, pp. 1366-1374
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