| Natural mutations of the anti-Mullerian hormone type II receptor found in persistent Mullerian duct syndrome affect ligand binding, signal transduction and cellular transport. Belville C., Marechal J.D., Pennetier S., Carmillo P., Masgrau L., Messika-Zeitoun L., Galey J., Machado G., Treton D., Gonzales J. et al.
Hum. Mol. Genet. 18:3002-3013(2009) · Mapped (2) |
| Use of normal modes for structural modeling of proteins: the case study of rat heme oxygenase 1. Marechal J.D., Perahia D.
Eur. Biophys. J. 37:1157-1165(2008) · Mapped (1) |
| Genome characteristics of facultatively symbiotic Frankia sp. strains reflect host range and host plant biogeography. Normand P., Lapierre P., Tisa L.S., Gogarten J.P., Alloisio N., Bagnarol E., Bassi C.A., Berry A.M., Bickhart D.M., Choisne N. et al.
Genome Res. 17:7-15(2007) · UniProtKB (18,286) |
| Why is quinidine an inhibitor of cytochrome P450 2D6? The role of key active-site residues in quinidine binding. McLaughlin L.A., Paine M.J., Kemp C.A., Marechal J.D., Flanagan J.U., Ward C.J., Sutcliffe M.J., Roberts G.C., Wolf C.R.
J. Biol. Chem. 280:38617-38624(2005) · Mapped (18) |
| Characterization of the sodF gene region of Frankia sp. strain ACN14a and complementation of Escherichia coli sod mutant. Marechal J., Santos R., Hammad Y., Alloisio N., Domenach A.M., Normand P.
Can. J. Microbiol. 49:294-300(2003) · UniProtKB (10) |
| Modification of the protein expression pattern induced in the nitrogen-fixing actinomycete Frankia sp. strain ACN14a-tsr by root exudates of its symbiotic host Alnus glutinosa and cloning of the sodF gene. Hammad Y., Marechal J., Cournoyer B., Normand P., Domenach A.M.
Can. J. Microbiol. 47:541-547(2001) · UniProtKB (1) |
| A recA gene phylogenetic analysis confirms the close proximity of Frankia to Acidothermus. Marechal J., Clement B., Nalin R., Gandon C., Orso S., Cvejic J.H., Bruneteau M., Berry A., Normand P.
Int. J. Syst. Evol. Microbiol. 50:781-785(2000) · UniProtKB (7) |
| Mutations of the VHL gene in sporadic renal cell carcinoma: definition of a risk factor for VHL patients to develop an RCC. Gallou C., Joly D., Mejean A., Staroz F., Martin N., Tarlet G., Orfanelli M.T., Bouvier R., Droz D., Chretien Y. et al.
Hum. Mutat. 13:464-475(1999) · UniProtKB (1) |
| Low expression allele alpha LELY of red cell spectrin is associated with mutations in exon 40 (alpha V/41 polymorphism) and intron 45 and with partial skipping of exon 46. Wilmotte R., Marechal J., Morle L., Baklouti F., Philippe N., Kastally R., Kotula L., Delaunay J., Alloisio N.
J. Clin. Invest. 91:2091-2096(1993) · UniProtKB (1) |
| Spectrin Jendouba: an alpha II/31 spectrin variant that is associated with elliptocytosis and carries a mutation distant from the dimer self-association site. Alloisio N., Wilmotte R., Morle L., Baklouti F., Marechal J., Ducluzeau M.-T., Denoroy L., Feo C., Forget B.G., Kastally R. et al.
Blood 80:809-815(1992) · UniProtKB (1) |
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