Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Gilbert J Fournie"'
Autor:
Stanislas Faguer, Nicolas Mayeur, Audrey Casemayou, Anne-Laure Pageaud, Claire Courtellemont, Claire Cartery, Gilbert J Fournie, Joost P Schanstra, Ivan Tack, Jean-Loup Bascands, Dominique Chauveau
Publikováno v:
PLoS ONE, Vol 8, Iss 5, p e63585 (2013)
Epithelial repair following acute kidney injury (AKI) requires epithelial-mesenchyme-epithelial cycling associated with transient re-expression of genes normally expressed during kidney development as well as activation of growth factors and cytokine
Externí odkaz:
https://doaj.org/article/f51641cf8ebd4179868456b3ed466842
Autor:
Sahar Kassem, Guillaume Gaud, Isabelle Bernard, Mehdi Benamar, Anne S Dejean, Roland Liblau, Gilbert J Fournié, Céline Colacios, Bernard Malissen, Abdelhadi Saoudi
Publikováno v:
PLoS Genetics, Vol 12, Iss 7, p e1006185 (2016)
The guanine nucleotide exchange factor Vav1 is essential for transducing T cell antigen receptor signals and therefore plays an important role in T cell development and activation. Our previous genetic studies identified a locus on rat chromosome 9 t
Externí odkaz:
https://doaj.org/article/d8479a9b003e41b78eb0bbad0088f8e1
Autor:
Pierre Cavailles, Pierre Flori, Olivier Papapietro, Cordelia Bisanz, Dominique Lagrange, Ludovic Pilloux, Céline Massera, Sara Cristinelli, Delphine Jublot, Olivier Bastien, Corinne Loeuillet, Delphine Aldebert, Bastien Touquet, Gilbert J Fournié, Marie France Cesbron-Delauw
Publikováno v:
PLoS Pathogens, Vol 10, Iss 4, p e1004005 (2014)
Natural immunity or resistance to pathogens most often relies on the genetic make-up of the host. In a LEW rat model of refractoriness to toxoplasmosis, we previously identified on chromosome 10 the Toxo1 locus that directs toxoplasmosis outcome and
Externí odkaz:
https://doaj.org/article/5de3d38192024b219ccf1961b3380639
Autor:
Marianne Chabod, Christophe Pedros, Lucille Lamouroux, Céline Colacios, Isabelle Bernard, Dominique Lagrange, Daniela Balz-Hara, Jean-Francois Mosnier, Christian Laboisse, Nathalie Vergnolle, Olivier Andreoletti, Marie-Paule Roth, Roland Liblau, Gilbert J Fournié, Abdelhadi Saoudi, Anne S Dejean
Publikováno v:
PLoS Genetics, Vol 8, Iss 1, p e1002461 (2012)
Spontaneous or chemically induced germline mutations, which lead to Mendelian phenotypes, are powerful tools to discover new genes and their functions. Here, we report an autosomal recessive mutation that occurred spontaneously in a Brown-Norway (BN)
Externí odkaz:
https://doaj.org/article/6dcffa93dca04eb58a5784b17141819b