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69 documents classés par :  Date de publication, production Titre du document Nom du 1er auteur Type de publication Date de dépôt

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The PRMT1 methyltransferase is a binding partner of HBx and a negative regulator of hepatitis B virus transcription Benhenda S., Ducroux A., Rivière L., Ward M., Dion S., Hantz O., Protzer U., Michel M., Benkirane M., Semmes O. et al J. Virol. 87, 8 (2013) 4360-4371 [hal-00817739 - version 1]

Hyperthermia stimulates HIV-1 replication. Roesch F., Meziane O., Kula A., Nisole S., Porrot F., Anderson I., Mammano F., Fassati A., Marcello A., Benkirane M. et al PLoS Pathogens 8, 7 (2012) e1002792 [hal-00723104 - version 1]

Nxnl2 splicing results in dual functions in neuronal cell survival and maintenance of cell integrity. Jaillard C., Mouret A., Niepon M.-L., Clérin E., Yang Y., Lee-Rivera I., Aït-Ali N., Millet-Puel G., Cronin T., Sedmak T. et al Human Molecular Genetics 21, 10 (2012) 2298-311 [inserm-00675213 - version 1]

Permanent genetic resources added to Molecular Ecology Resources database 1 December 2011 - 31 January 2012. Arias M.C., Arnoux E., Bell J. J., Bernadou A., Bino G., Blatrix R., Bourguet D., Carrea C., Clamens A.-L., Cunha H. A. et al Molecular Ecology Resources 12, 3 (2012) 570-572 [hal-00687667 - version 1]

Insertion site preference of Mu, Tn5, and Tn7 transposons. Green B., Bouchier C., Fairhead C., Craig N., Cormack B. Mobile DNA 3, 1 (2012) 3 [pasteur-00675691 - version 1]

Systemic delivery of allogenic muscle stem cells induces long-term muscle repair and clinical efficacy in duchenne muscular dystrophy dogs. Rouger K., Larcher T., Dubreil L., Deschamps J.-Y., Le Guiner C., Jouvion G., Delorme B., Lieubeau B., Carlus M., Fornasari B. et al American Journal of Pathology 179, 5 (2011) 2501-18 [inserm-00712818 - version 1]

SAMHD1 is the dendritic- and myeloid-cell-specific HIV-1 restriction factor counteracted by Vpx. Laguette N., Sobhian B., Casartelli N., Ringeard M., Chable-Bessia C., Segeral E., Yatim A., Emiliani S., Schwartz O., Benkirane M. Nature 474, 7353 (2011) 654-7 [hal-00616451 - version 1]

Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis. Bonnet C., Grati M., Marlin S., Levilliers J., Hardelin J.-P., Parodi M., Niasme-Grare M., Zelenika D., Délépine M., Feldmann D. et al Orphanet Journal of Rare Diseases 6, 1 (2011) 21 [pasteur-00663885 - version 1]

Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability. Pagan C., Botros H. Goubran, Poirier K., Dumaine A., Jamain S., Moreno S., de Brouwer A., Van Esch H., Delorme R., Launay J.-M. et al BMC Medical Genetics 12, 1 (2011) 17 [inserm-00610655 - version 1]

Prevalence of SOS-mediated control of integron integrase expression as an adaptive trait of chromosomal and mobile integrons Cambray G., Sanchez-Alberola N., Campoy S., Guerin E., Da Re S., González-Zorn B., Ploy M.-C., Barbé J., Mazel D., Erill I. Mobile DNA 2, 1 (2011) 6 [inserm-00598347 - version 1]