16
results
for author:"Petit E."
in Literature Citations
| Glutathione transferases kappa 1 and kappa 2 localize in peroxisomes and mitochondria, respectively, and are involved in lipid metabolism and respiration in Caenorhabditis elegans. Petit E., Michelet X., Rauch C., Bertrand-Michel J., Terce F., Legouis R., Morel F. FEBS J. 276:5030-5040(2009) · Mapped (2) |
| Progestins induce catalase activities in breast cancer cells through PRB isoform: correlation with cell growth inhibition. Petit E., Courtin A., Kloosterboer H.J., Rostene W., Forgez P., Gompel A. J. Steroid Biochem. Mol. Biol. 115:153-160(2009) · Mapped (10) |
| Cystathionine beta synthase deficiency induces catalase-mediated hydrogen peroxide detoxification in mice liver. Hamelet J., Seltzer V., Petit E., Noll C., Andreau K., Delabar J.M., Janel N. Biochim. Biophys. Acta 1782:482-488(2008) · Mapped (1) |
| TNF receptor I sensitizes neurons to erythropoietin- and VEGF-mediated neuroprotection after ischemic and excitotoxic injury. Taoufik E., Petit E., Divoux D., Tseveleki V., Mengozzi M., Roberts M.L., Valable S., Ghezzi P., Quackenbush J., Brines M. et al. Proc. Natl. Acad. Sci. U.S.A. 105:6185-6190(2008) · Mapped (6) |
| Endocarditis in cattle caused by Bartonella bovis. Maillard R., Petit E., Chomel B., Lacroux C., Schelcher F., Vayssier-Taussat M., Haddad N., Boulouis H.J. Emerging Infect. Dis. 13:1383-1385(2007) · UniProtKB (7) |
| FLIP(L) protects neurons against in vivo ischemia and in vitro glucose deprivation-induced cell death. Taoufik E., Valable S., Muller G.J., Roberts M.L., Divoux D., Tinel A., Voulgari-Kokota A., Tseveleki V., Altruda F., Lassmann H. et al. J. Neurosci. 27:6633-6646(2007) · Mapped (17) |
| Synergistic effects of CoCl(2) and ROCK inhibition on mesenchymal stem cell differentiation into neuron-like cells. Pacary E., Legros H., Valable S., Duchatelle P., Lecocq M., Petit E., Nicole O., Bernaudin M. J. Cell. Sci. 119:2667-2678(2006) · Mapped (3) |
| Expression of the gene encoding the pro-apoptotic BNIP3 protein and stimulation of hypoxia-inducible factor-1alpha (HIF-1alpha) protein following focal cerebral ischemia in rats. Althaus J., Bernaudin M., Petit E., Toutain J., Touzani O., Rami A. Neurochem. Int. 48:687-695(2006) · Mapped (2) |
| Gene and protein characterization of the human glutathione S-transferase kappa and evidence for a peroxisomal localization. Morel F., Rauch C., Petit E., Piton A., Theret N., Coles B., Guillouzo A. J. Biol. Chem. 279:16246-16253(2004) · UniProtKB (1) · Mapped (6) |
| The negative regulator of Gli, Suppressor of fused (Sufu), interacts with SAP18, Galectin3 and other nuclear proteins. Paces-Fessy M., Boucher D., Petit E., Paute-Briand S., Blanchet-Tournier M.F. Biochem. J. 378:353-362(2004) · Mapped (9) |
| Role of Fcgamma receptors IIA, IIIA, and IIIB in susceptibility to rheumatoid arthritis. Radstake T.R., Petit E., Pierlot C., van de Putte L.B., Cornelis F., Barrera P. J. Rheumatol. 30:926-933(2003) · Mapped (4) |
| The DNA sequence and analysis of human chromosome 14. Heilig R., Eckenberg R., Petit J.-L., Fonknechten N., Da Silva C., Cattolico L., Levy M., Barbe V., De Berardinis V., Ureta-Vidal A. et al. Nature 421:601-607(2003) · UniProtKB (543) |
| Association between tumor necrosis factor receptor II and familial, but not sporadic, rheumatoid arthritis: evidence for genetic heterogeneity. European Consortium on Rheumatoid Arthritis Families Arthritis Rheum. 46:2039-2044(2002) · Mapped (7) |
| Normobaric hypoxia induces tolerance to focal permanent cerebral ischemia in association with an increased expression of hypoxia-inducible factor-1 and its target genes, erythropoietin and VEGF, in the adult mouse brain. Bernaudin M., Nedelec A.S., Divoux D., MacKenzie E.T., Petit E., Schumann-Bard P. J. Cereb. Blood Flow Metab. 22:393-403(2002) · Mapped (8) |
| Exclusion of the coding sequence of the doublecortin gene as a susceptibility locus in autistic disorder. Vourc'h P., Petit E., Muh J.P., Andres C., Bienvenu T., Beldjord C., Chelly J., Barthelemy C. Am. J. Med. Genet. 108:164-167(2002) · Mapped (3) |
| Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formation. Hovnanian A., Rochat A., Bodemer C., Petit E., Rivers C.A., Prost C., Fraitag S., Christiano A.M., Uitto J., Lathrop M. et al. Am. J. Hum. Genet. 61:599-610(1997) · UniProtKB (1) |
