Dissecting the sub-structure of the intraflagellar transport complex B

Por Texier, Y, van Reeuwijk, J, Mans, DA, Roepman, R, Boldt, K, Ueffing, M
Publicado em 2012

Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice

Por Boldt, K, Mans, DA, Won, J, van Reeuwijk, J, Texier, Y, Nishina, PM, Roepman, R, Ueffing, M
Publicado em 2012

Scrutinizing ciliopathies by unravelling the ciliary interactome

Por van Reeuwijk, J, Boldt, K, Mans, DA, Texier, Y, van Beersum, SE, Letteboer, SJ, Nguyen, MTT, Ueffing, M, Roepman, R
Publicado em 2012

Differential requirements of ciliogenic/ciliopathy module components in restricting Joubert syndrome-associated Arl13b to a C. elegans Inv-like ciliary compartment

Por Blacque, O, Cevik, S, Clarke, L, Van Wijk, E, Sanders, A, Van Reeuwijk, J, Boldt, K, Ueffing, M, Roepman, R, Kremer, H
Publicado em 2012

Systematic exploration of the ciliary protein landscape by large-scale affinity proteomics

Por Boldt, K, Van Reeuwijk, J, Lu, Q, Koutroumpas, K, Horn, N, Beersum, S Van, Texier, Y, Nguyen, TM, Willer, JR, Katsanis, N, Képès, F, Russell, RB, Ueffing, M, Roepman, R
Publicado no Cilia (2015)

The lebercilin-like protein is embedded in a ciliary protein network and is preferentially expressed in motile cilia

Por Mans, DA, Coene, KLM, Boldt, K, Lamers, IJC, van Reeuwijk, J, Loges, NT, Bolat, E, Franke, L, Hetterschijt, L, Letteboer, SJF, Peters, TA, Omran, H, Cremers, FPM, Ueffing, M, Roepman, R
Publicado em 2012

POMT2 mutations cause α-dystroglycan hypoglycosylation and Walker-Warburg syndrome

Por van Reeuwijk, J, Janssen, M, van den Elzen, C, d Beltran-Valero, Sabatelli, P, Merlini, L, Boon, M, Scheffer, H, Brockington, M, Muntoni, F, Huynen, M, Verrips, A, Walsh, C, Barth, P, Brunner, H, van Bokhoven, H
Publicado em 2005