10
results
for author:"Samson D."
in Literature Citations
| Mechanisms of evolution in Rickettsia conorii and R. prowazekii. Ogata H., Audic S., Renesto-Audiffren P., Fournier P.-E., Barbe V., Samson D., Roux V., Cossart P., Weissenbach J., Claverie J.-M. et al. Science 293:2093-2098(2001) · UniProtKB (1,372) |
| The complete genome sequence of the murine respiratory pathogen Mycoplasma pulmonis. Chambaud I., Heilig R., Ferris S., Barbe V., Samson D., Galisson F., Moszer I., Dybvig K., Wroblewski H., Viari A. et al. Nucleic Acids Res. 29:2145-2153(2001) · UniProtKB (778) |
| Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia). Nicole S., Davoine C.-S., Topaloglu H., Cattolico L., Barral D., Beighton P., Ben-Hamida C., Hammouda H., Cruaud C., White P.S. et al. Nat. Genet. 26:480-483(2000) · UniProtKB (1) |
| Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia. Fonknechten N., Mavel D., Byrne P., Davoine C.-S., Cruaud C., Bonsch D., Samson D., Coutinho P., Hutchinson M., McMonagle P. et al. Hum. Mol. Genet. 9:637-644(2000) · UniProtKB (1) |
| Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. Hazan J., Fonknechten N., Mavel D., Paternotte C., Samson D., Artiguenave F., Davoine C.-S., Cruaud C., Durr A., Wincker P. et al. Nat. Genet. 23:296-303(1999) · UniProtKB (2) |
| A transcriptional map of the FMF region. Bernot A., Heilig R., Clepet C., Smaoui N., Da Silva C., Petit J.-L., Devaud C., Chiannilkulchai N., Fizames C., Samson D. et al. Genomics 50:147-160(1998) · UniProtKB (3) |
| Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1. Abdelhak S., Kalatzis V., Heilig R., Compain S., Samson D., Vincent C., Levi-Acobas F., Cruaud C., le Merrer M., Mathieu M. et al. Hum. Mol. Genet. 6:2247-2255(1997) · UniProtKB (1) |
| A candidate gene for familial Mediterranean fever. Bernot A., Clepet C., Dasilva C., Devaud C., Petit J.-L., Caloustian C., Cruaud C., Samson D., Pulcini F., Weissenbach J. et al. Nat. Genet. 17:25-31(1997) · UniProtKB (3) |
| A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family. Abdelhak S., Kalatzis V., Heilig R., Compain S., Samson D., Vincent C., Weil D., Cruaud C., Sahly I., Leibovici M. et al. |
| Genes for the neuronal immunoglobulin domain cell adhesion molecules neurofascin and Nr-CAM map to mouse chromosomes 1 and 12 and homologous human chromosomes. Burmeister M., Ren Q., Makris G.J., Samson D., Bennett V. Mamm. Genome 7:558-559(1996) · Mapped (27) |
