Disruption of pathways regulated by Integrator complex in Galloway–Mowat syndrome due to WDR73 mutations

por Tilley, F. C., Arrondel, C., Chhuon, C., Boisson, M., Cagnard, N., Parisot, M., Menara, G., Lefort, N., Guerrera, I. C., Bole-Feysot, C., Benmerah, A., Antignac, C., Mollet, G.
Publicado 2021

Bacterial ClpB heat-shock protein, an antigen-mimetic of the anorexigenic peptide α-MSH, at the origin of eating disorders

por Tennoune, N, Chan, P, Breton, J, Legrand, R, Chabane, Y N, Akkermann, K, Järv, A, Ouelaa, W, Takagi, K, Ghouzali, I, Francois, M, Lucas, N, Bole-Feysot, C, Pestel-Caron, M, do Rego, J-C, Vaudry, D, Harro, J, Dé, E, Déchelotte, P, Fetissov, S O
Publicado 2014

Identification of human mutations in TRAF3IP1 in patients with nephronophthisis and retinal degeneration

por Becker-Heck, A, Bizet, A, Ryan, R, Krug, P, Filhol, E, Linghu, B, Oakeley, E, Serluca, F, Legendre, F, Dörner, N, Lasbennes, MC, Duca, J, Yang, F, Damask, A, Klickstein, L, Labow, M, Schebesta, M, Bouwmeester, T, Valette, H, Pinson, L, Goubaux, B, Dubot, P, Salomon, R, Antignac, C, Gubler, M, Jeanpierre, C, Chibout, S, Bole-Feysot, C, Nitschké, P, Benmerah, A, Szustakowski, JD, Sailer, AW, Saunier, S, Saint-Mezard, P
Publicado 2015