1 - 25 of
41
results
for author:"Cruaud C."
in Literature Citations
| Evolution of the mitochondrial genome in mammals living at high altitude: new insights from a study of the tribe Caprini (Bovidae, Antilopinae). Hassanin A., Ropiquet A., Couloux A., Cruaud C. J. Mol. Evol. 68:293-310(2009) · UniProtKB (234) |
| RNF213, a new nuclear marker for acanthomorph phylogeny. Li B., Dettai A., Cruaud C., Couloux A., Desoutter-Meniger M., Lecointre G. Mol. Phylogenet. Evol. 50:345-363(2009) · UniProtKB (350) |
| Evolution of the Toxoglossa venom apparatus as inferred by molecular phylogeny of the Terebridae. Holford M., Puillandre N., Terryn Y., Cruaud C., Olivera B., Bouchet P. Mol. Biol. Evol. 26:15-25(2009) · UniProtKB (81) |
| Several deep-sea mussels and their associated symbionts are able to live both on wood and on whale falls. Lorion J., Duperron S., Gros O., Cruaud C., Samadi S. Proc. Biol. Sci. 276:177-185(2009) · UniProtKB (18) |
| Tracing the colonization history of the Indian Ocean scops-owls (Strigiformes: Otus) with further insight into the spatio-temporal origin of the Malagasy avifauna. Fuchs J., Pons J.M., Goodman S.M., Bretagnolle V., Melo M., Bowie R.C., Currie D., Safford R., Virani M.Z., Thomsett S. et al. BMC Evol. Biol. 8:197-197(2008) · UniProtKB (127) |
| Patterns of genetic structure among Hawaiian corals of the genus Pocillopora yield clusters of individuals that are compatible with morphology. Flot J.F., Magalon H., Cruaud C., Couloux A., Tillier S. C. R. Biol. 331:239-247(2008) · UniProtKB (27) |
| Starting to unravel the toxoglossan knot: molecular phylogeny of the "turrids" (Neogastropoda: Conoidea). Puillandre N., Samadi S., Boisselier M.C., Sysoev A.V., Kantor Y.I., Cruaud C., Couloux A., Bouchet P. Mol. Phylogenet. Evol. 47:1122-1134(2008) · UniProtKB (222) |
| Did glacial advances during the Pleistocene influence differently the demographic histories of benthic and pelagic Antarctic shelf fishes?--Inferences from intraspecific mitochondrial and nuclear DNA sequence diversity. Janko K., Lecointre G., Devries A., Couloux A., Cruaud C., Marshall C. BMC Evol. Biol. 7:220-220(2007) · UniProtKB (19) |
| Molecular phylogeny in mytilids supports the wooden steps to deep-sea vents hypothesis. Samadi S., Quemere E., Lorion J., Tillier A., von Cosel R., Lopez P., Cruaud C., Couloux A., Boisselier-Dubayle M.C. C. R. Biol. 330:446-456(2007) · UniProtKB (5) |
| Evolutionary history and biogeography of the drongos (Dicruridae), a tropical Old World clade of corvoid passerines. Pasquet E., Pons J.M., Fuchs J., Cruaud C., Bretagnolle V. Mol. Phylogenet. Evol. 45:158-167(2007) · UniProtKB (79) |
| Complex biogeographic history of the cuckoo-shrikes and allies (Passeriformes: Campephagidae) revealed by mitochondrial and nuclear sequence data. Fuchs J., Cruaud C., Couloux A., Pasquet E. Mol. Phylogenet. Evol. 44:138-153(2007) · UniProtKB (122) |
| Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development. Sanlaville D., Etchevers H.C., Gonzales M., Martinovic J., Clement-Ziza M., Delezoide A.L., Aubry M.C., Pelet A., Chemouny S., Cruaud C. et al. J. Med. Genet. 43:211-217(2006) · Mapped (3) |
| Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A. Abel A., Fonknechten N., Hofer A., Durr A., Cruaud C., Voit T., Weissenbach J., Brice A., Klimpe S., Auburger G. et al. Neurogenetics 5:239-243(2004) · Mapped (5) |
| Genome duplication in the teleost fish Tetraodon nigroviridis reveals the early vertebrate proto-karyotype. Jaillon O., Aury J.-M., Brunet F., Petit J.-L., Stange-Thomann N., Mauceli E., Bouneau L., Fischer C., Ozouf-Costaz C., Bernot A. et al. Nature 431:946-957(2004) · UniProtKB (27,873) |
| Whole genome sequence comparisons and 'full-length' cDNA sequences: a combined approach to evaluate and improve Arabidopsis genome annotation. Castelli V., Aury J.-M., Jaillon O., Wincker P., Clepet C., Menard M., Cruaud C., Quetier F., Scarpelli C., Schaechter V. et al. |
| Mutations in PCSK9 cause autosomal dominant hypercholesterolemia. Abifadel M., Varret M., Rabes J.-P., Allard D., Ouguerram K., Devillers M., Cruaud C., Benjannet S., Wickham L., Erlich D. et al. |
| Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome. Dode C., Levilliers J., Dupont J.-M., De Paepe A., Le Du N., Soussi-Yanicostas N., Coimbra R.S., Delmaghani S., Compain-Nouaille S., Baverel F. et al. |
| 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) |
| 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) |
| Genotype-phenotype analysis in four families with mutations in beta-myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy. Tesson F., Richard P., Charron P., Mathieu B., Cruaud C., Carrier L., Dubourg O., Lautie N., Desnos M., Millaire A. et al. Hum. Mutat. 12:385-392(1998) · UniProtKB (1) |
| Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF). Bernot A., da Silva C., Petit J.-L., Cruaud C., Caloustian C., Castet V., Ahmed-Arab M., Dross C., Dupont M., Cattan D. et al. Hum. Mol. Genet. 7:1317-1325(1998) · UniProtKB (1) |
| 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) |
| Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients. Joutel A., Vahedi K., Corpechot C., Troesch A., Chabriat H., Vayssiere C., Cruaud C., Maciazek J., Weissenbach J., Bousser M.-G. et al. Lancet 350:1511-1515(1997) · UniProtKB (1) |
