Genome-wide RNAi of C. elegans using the hypersensitive rrf-3 strain reveals novel gene functions von Simmer, Femke, Moorman, Celine, van der Linden, Alexander M, Kuijk, Ewart, van den Berghe, Peter V E, Kamath, Ravi S, Fraser, Andrew G, Ahringer, Julie, Plasterk, Ronald H A

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Rab25 and CLIC3 Collaborate to Promote Integrin Recycling from Late Endosomes/Lysosomes and Drive Cancer Progression von Dozynkiewicz, Marta A., Jamieson, Nigel B., MacPherson, Iain, Grindlay, Joan, van den Berghe, Peter V.E., von Thun, Anne, Morton, Jennifer P., Gourley, Charlie, Timpson, Paul, Nixon, Colin, McKay, Colin J., Carter, Ross, Strachan, David, Anderson, Kurt, Sansom, Owen J., Caswell, Patrick T., Norman, Jim C.

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Secreted CLIC3 drives cancer progression through its glutathione-dependent oxidoreductase activity von Hernandez-Fernaud, Juan R., Ruengeler, Elena, Casazza, Andrea, Neilson, Lisa J., Pulleine, Ellie, Santi, Alice, Ismail, Shehab, Lilla, Sergio, Dhayade, Sandeep, MacPherson, Iain R., McNeish, Iain, Ennis, Darren, Ali, Hala, Kugeratski, Fernanda G., Al Khamici, Heba, van den Biggelaar, Maartje, van den Berghe, Peter V.E., Cloix, Catherine, McDonald, Laura, Millan, David, Hoyle, Aoisha, Kuchnio, Anna, Carmeliet, Peter, Valenzuela, Stella M., Blyth, Karen, Yin, Huabing, Mazzone, Massimiliano, Norman, Jim C., Zanivan, Sara

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CLIC3 controls recycling of late endosomal MT1-MMP and dictates invasion and metastasis in breast cancer von Macpherson, Iain R, Rainero, Elena, Mitchell, Louise E, van den Berghe, Peter V E, Speirs, Claire, Dozynkiewicz, Marta A, Chaudhary, Suman, Kalna, Gabriela, Edwards, Joanne, Timpson, Paul, Norman, Jim C

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Human copper transporter 2 is localized in late endosomes and lysosomes and facilitates cellular copper uptake von van den Berghe, Peter V E, Folmer, Dineke E, Malingré, Helga E M, van Beurden, Ellen, Klomp, Adriana E M, van de Sluis, Bart, Merkx, Maarten, Berger, Ruud, Klomp, Leo W J

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New developments in the regulation of intestinal copper absorption von Berghe, Peter V.E. van den, Klomp, Leo W.J

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Reduced expression of ATP7B affected by Wilson disease–causing mutations is rescued by pharmacological folding chaperones 4‐phenylbutyrate and curcumin von van den Berghe, Peter V. E., Stapelbroek, Janneke M., Krieger, Elmar, de Bie, Prim, van de Graaf, Stan F. J., de Groot, Reinoud E. A., van Beurden, Ellen, Spijker, Ellen, Houwen, Roderick H. J., Berger, Ruud, Klomp, Leo W. J.

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The copper-transporting capacity of ATP7A mutants associated with Menkes disease is ameliorated by COMMD1 as a result of improved protein expression von Vonk, Willianne I. M., de Bie, Prim, Wichers, Catharina G. K., van den Berghe, Peter V. E., van der Plaats, Rozemarijn, Berger, Ruud, Wijmenga, Cisca, Klomp, Leo W. J., van de Sluis, Bart

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Folding defects in P‐type ATP 8B1 associated with hereditary cholestasis are ameliorated by 4‐phenylbutyrate von van der Velden, Lieke M., Stapelbroek, Janneke M., Krieger, Elmar, van den Berghe, Peter V. E., Berger, Ruud, Verhulst, Patricia M., Holthuis, Joost C. M., Houwen, Roderick H. J., Klomp, Leo W. J., van de Graaf, Stan F. J.

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Posttranslational regulation of copper transporters von van den Berghe, Peter V. E, Klomp, Leo W. J

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Filamin A stabilizes Fc gamma RI surface expression and prevents its lysosomal routing von Beekman, Jeffrey M, van der Poel, Cees E, van der Linden, Joke A, van den Berg, Debbie L C, van den Berghe, Peter V E, van de Winkel, Jan G J, Leusen, Jeanette H W

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Secreted CLIC3 drives cancer progression through its glutathione-dependent oxidoreductase activity von Hernandez-Fernaud, Juan R, Ruengeler, Elena, Casazza, Andrea, Neilson, Lisa J, Pulleine, Ellie, Santi, Alice, Ismail, Shehab, Lilla, Sergio, Dhayade, Sandeep, MacPherson, Iain R, McNeish, Iain, Ennis, Darren, Ali, Hala, Kugeratski, Fernanda G, Al Khamici, Heba, van den Biggelaar, Maartje, van den Berghe, Peter V.E, Cloix, Catherine, McDonald, Laura, Millan, David, Hoyle, Aoisha, Kuchnio, Anna, Carmeliet, Peter, Valenzuela, Stella M, Blyth, Karen, Yin, Huabing, Mazzone, Max, Norman, Jim C, Zanivan, Sara

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Distinct Wilson’s Disease Mutations in ATP7B Are Associated With Enhanced Binding to COMMD1 and Reduced Stability of ATP7B von de Bie, Prim, van de Sluis, Bart, Burstein, Ezra, van de Berghe, Peter V.E, Muller, Patricia, Berger, Ruud, Gitlin, Jonathan D, Wijmenga, Cisca, Klomp, Leo W.J

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