Biogenesis of γ-secretase early in the secretory pathway

por Kim, Jinoh, Kleizen, Bertrand, Choy, Regina, Thinakaran, Gopal, Sisodia, Sangram S., Schekman, Randy W.
Publicado 2007

The Primary Folding Defect and Rescue of ΔF508 CFTR Emerge during Translation of the Mutant Domain

por Hoelen, Hanneke, Kleizen, Bertrand, Schmidt, Andre, Richardson, John, Charitou, Paraskevi, Thomas, Philip J., Braakman, Ineke
Publicado 2010

Transmembrane Helices 7 and 8 Confer Aggregation Sensitivity to the Cystic Fibrosis Transmembrane Conductance Regulator

por Kleizen, Bertrand, de Mattos, Eduardo, Papaioannou, Olga, Monti, Michele, Tartaglia, Gian Gaetano, van der Sluijs, Peter, Braakman, Ineke
Publicado 2023

Assembly of γ-secretase occurs through stable dimers after exit from the endoplasmic reticulum

por Wouters, Rosanne, Michiels, Christine, Sannerud, Ragna, Kleizen, Bertrand, Dillen, Katleen, Vermeire, Wendy, Ayala, Abril Escamilla, Demedts, David, Schekman, Randy, Annaert, Wim
Publicado 2021

Alteration of protein function by a silent polymorphism linked to tRNA abundance

por Kirchner, Sebastian, Cai, Zhiwei, Rauscher, Robert, Kastelic, Nicolai, Anding, Melanie, Czech, Andreas, Kleizen, Bertrand, Ostedgaard, Lynda S., Braakman, Ineke, Sheppard, David N., Ignatova, Zoya
Publicado 2017

Folding–function relationship of the most common cystic fibrosis–causing CFTR conductance mutants

por van Willigen, Marcel, Vonk, Annelotte M, Yeoh, Hui Ying, Kruisselbrink, Evelien, Kleizen, Bertrand, van der Ent, Cornelis K, Egmond, Maarten R, de Jonge, Hugo R, Braakman, Ineke, Beekman, Jeffrey M, van der Sluijs, Peter
Publicado 2019