Expression patterns of the aquaporin gene family during renal development: influence of genetic variability

por Parreira, Kleber S., Debaix, Huguette, Cnops, Yvette, Geffers, Lars, Devuyst, Olivier
Publicado 2009

Involvement of TRPC in the abnormal calcium influx observed in dystrophic (mdx) mouse skeletal muscle fibers

por Vandebrouck, Clarisse, Martin, Dominique, Schoor, Monique Colson-Van, Debaix, Huguette, Gailly, Philippe
Publicado 2002

Hepsin-mediated Processing of Uromodulin is Crucial for Salt-sensitivity and Thick Ascending Limb Homeostasis

por Olinger, Eric, Lake, Jennifer, Sheehan, Susan, Schiano, Guglielmo, Takata, Tomoaki, Tokonami, Natsuko, Debaix, Huguette, Consolato, Francesco, Rampoldi, Luca, Korstanje, Ron, Devuyst, Olivier
Publicado 2019

Regulation of Macrophage Motility by the Water Channel Aquaporin-1: Crucial Role of M0/M2 Phenotype Switch

por Tyteca, Donatienne, Nishino, Tomoya, Debaix, Huguette, Van Der Smissen, Patrick, N'Kuli, Francisca, Hoffmann, Delia, Cnops, Yvette, Rabolli, Virginie, van Loo, Geert, Beyaert, Rudi, Huaux, François, Devuyst, Olivier, Courtoy, Pierre J.
Publicado 2015

Impaired autophagy bridges lysosomal storage disease and epithelial dysfunction in the kidney

por Festa, Beatrice Paola, Chen, Zhiyong, Berquez, Marine, Debaix, Huguette, Tokonami, Natsuko, Prange, Jenny Ann, Hoek, Glenn van de, Alessio, Cremonesi, Raimondi, Andrea, Nevo, Nathalie, Giles, Rachel H., Devuyst, Olivier, Luciani, Alessandro
Publicado 2018

Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression

por Trudu, Matteo, Janas, Sylvie, Lanzani, Chiara, Debaix, Huguette, Schaeffer, Céline, Ikehata, Masami, Citterio, Lorena, Demaretz, Sylvie, Trevisani, Francesco, Ristagno, Giuseppe, Glaudemans, Bob, Laghmani, Kamel, Dell’Antonio, Giacomo, Loffing, Johannes, Rastaldi, Maria P., Manunta, Paolo, Devuyst, Olivier, Rampoldi, Luca
Publicado 2013

Impaired mitophagy links mitochondrial disease to epithelial stress in methylmalonyl-CoA mutase deficiency

por Luciani, Alessandro, Schumann, Anke, Berquez, Marine, Chen, Zhiyong, Nieri, Daniela, Failli, Mario, Debaix, Huguette, Festa, Beatrice Paola, Tokonami, Natsuko, Raimondi, Andrea, Cremonesi, Alessio, Carrella, Diego, Forny, Patrick, Kölker, Stefan, Diomedi Camassei, Francesca, Diaz, Francisca, Moraes, Carlos T., Di Bernardo, Diego, Baumgartner, Matthias R., Devuyst, Olivier
Publicado 2020

Author Correction: Impaired mitophagy links mitochondrial disease to epithelial stress in methylmalonyl-CoA mutase deficiency

por Luciani, Alessandro, Schumann, Anke, Berquez, Marine, Chen, Zhiyong, Nieri, Daniela, Failli, Mario, Debaix, Huguette, Festa, Beatrice Paola, Tokonami, Natsuko, Raimondi, Andrea, Cremonesi, Alessio, Carrella, Diego, Forny, Patrick, Kölker, Stefan, Camassei, Francesca Diomedi, Diaz, Francisca, Moraes, Carlos T., Di Bernardo, Diego, Baumgartner, Matthias R., Devuyst, Olivier
Publicado 2020