A Deletion in FOXN1 Is Associated with a Syndrome Characterized by Congenital Hypotrichosis and Short Life Expectancy in Birman Cats

por Abitbol, Marie, Bossé, Philippe, Thomas, Anne, Tiret, Laurent
Publicado 2015

A COLQ Missense Mutation in Sphynx and Devon Rex Cats with Congenital Myasthenic Syndrome

por Abitbol, Marie, Hitte, Christophe, Bossé, Philippe, Blanchard-Gutton, Nicolas, Thomas, Anne, Martignat, Lionel, Blot, Stéphane, Tiret, Laurent
Publicado 2015

Transcription analysis in the MeLiM swine model identifies RACK1 as a potential marker of malignancy for human melanocytic proliferation

por Egidy, Giorgia, Julé, Sophia, Bossé, Philippe, Bernex, Florence, Geffrotin, Claudine, Vincent-Naulleau, Silvia, Horak, Vratislav, Sastre-Garau, Xavier, Panthier, Jean-Jacques
Publicado 2008