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69 documents classés par : 
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Origin and evolution of DNA topoisomerases.
Forterre P., Gribaldo S., Gadelle D., Serre M.-C.
Biochimie 89, 4 (2007) 427-46 [hal-00194416 - version 1]
SAGE analysis of mosquito salivary gland transcriptomes during Plasmodium invasion.
Rosinski-Chupin I., Briolay J., Brouilly P., Perrot S., Gomez S. M., Chertemps T., Roth C. W., Keime C., Gandrillon O., Couble P. et al
Cellular Microbiology 9, 3 (2007) 708-24 [hal-00176474 - version 1]
fulltext access Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
Durand C. M., Betancur C., Boeckers T. M., Bockmann J., Chaste P., Fauchereau F., Nygren G., Rastam M., Gillberg I. C., Anckarsäter H. et al
Nat Genet 39, 1 (2007) 25-7 [inserm-00126175 - version 2]
Mutation in the Trapalpha/Ssr1 gene, encoding translocon-associated protein alpha, results in outflow tract morphogenetic defects.
Mesbah K., Camus A., Babinet C., Barra J.
Mol Cell Biol 26, 20 (2006) 7760-71 [hal-00106274 - version 1]
Evolutionary insights into the high worldwide prevalence of MBL2 deficiency alleles.
Verdu P., Barreiro L. B., Patin E., Gessain A., Cassar O., Kidd J. R., Kidd K. K., Behar D. M., Froment A., Heyer E. et al
Human Molecular Genetics 15, 17 (2006) 2650-8 [hal-00090493 - version 1]
Towards a crucial role for DC-SIGN in tuberculosis and beyond.
Neyrolles O., Gicquel B., Quintana-Murci L.
Trends in Microbiology 14, 9 (2006) 383-7 [hal-00090497 - version 1]
fulltext access No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control subjects.
Delorme R., Durand C. M., Betancur C., Wagner M., Ruhrmann S., Grabe H.-J., Nygren G., Gillberg C., Leboyer M., Bourgeron T. et al
Biological psychiatry 60, 2 (2006) 202-3 [inserm-00124742 - version 1]
Sub-Saharan African coding sequence variation and haplotype diversity at the NAT2 gene.
Patin E., Harmant C., Kidd K. K., Kidd J., Froment A., Mehdi S. Q., Sica L., Heyer E., Quintana-Murci L.
Human Mutation 27, 7 (2006) 720 [hal-00090583 - version 1]
Horizontal transfer of a virulence operon to the ancestor of Mycobacterium tuberculosis.
Rosas-Magallanes V., Deschavanne P., Quintana-Murci L., Brosch R., Gicquel B., Neyrolles O.
Molecular Biology and Evolution 23, 6 (2006) 1129-35 [hal-00090585 - version 1]
The NEMO mutation creating the most-upstream premature stop codon is hypomorphic because of a reinitiation of translation.
Puel A., Reichenbach J., Bustamante J., Ku C.-L., Feinberg J., Döffinger R., Bonnet M., Filipe-Santos O., Beaucoudrey L. D., Durandy A. et al
Am J Hum Genet 78, 4 (2006) 691-701 [inserm-00142391 - version 1]