Interaction of the copper chaperone HAH1 with the Wilson disease protein is essential for copper homeostasis

di Hamza, Iqbal, Schaefer, Mark, Klomp, Leo W. J., Gitlin, Jonathan D.
Pubblicazione 1999

Cu,Zn Superoxide Dismutase Maturation and Activity Are Regulated by COMMD1

di Vonk, Willianne I. M., Wijmenga, Cisca, Berger, Ruud, van de Sluis, Bart, Klomp, Leo W. J.
Pubblicazione 2010

Clusterin (Apolipoprotein J), a Molecular Chaperone That Facilitates Degradation of the Copper-ATPases ATP7A and ATP7B

di Materia, Stephanie, Cater, Michael A., Klomp, Leo W. J., Mercer, Julian F. B., La Fontaine, Sharon
Pubblicazione 2011

Clusterin and COMMD1 Independently Regulate Degradation of the Mammalian Copper ATPases ATP7A and ATP7B

di Materia, Stephanie, Cater, Michael A., Klomp, Leo W. J., Mercer, Julian F. B., La Fontaine, Sharon
Pubblicazione 2012

D-Serine Influences Synaptogenesis in a P19 Cell Model

di Fuchs, Sabine A., Roeleveld, Martin W., Klomp, Leo W. J., Berger, Ruud, de Koning, Tom J.
Pubblicazione 2012

COMMD1 expression is controlled by critical residues that determine XIAP binding

di Maine, Gabriel N., Mao, Xicheng, Muller, Patricia A., Komarck, Christine M., Klomp, Leo W.J., Burstein, Ezra
Pubblicazione 2009

Biochemical characterization and subcellular localization of human copper transporter 1 (hCTR1).

di Klomp, Adriana E M, Tops, Bastiaan B J, Van Denberg, Inge E T, Berger, Ruud, Klomp, Leo W J
Pubblicazione 2002

Transcription Factor Sp1 Plays an Important Role in the Regulation of Copper Homeostasis in Mammalian Cells

di Song, Im-Sook, Chen, Helen H. W., Aiba, Isamu, Hossain, Anwar, Liang, Zheng D., Klomp, Leo W. J., Kuo, Macus Tien
Pubblicazione 2008

Characterization of COMMD protein–protein interactions in NF-κB signalling

di de Bie, Prim, van de Sluis, Bart, Burstein, Ezra, Duran, Karen J., Berger, Ruud, Duckett, Colin S., Wijmenga, Cisca, Klomp, Leo W. J.
Pubblicazione 2006

The N-terminus of the human copper transporter 1 (hCTR1) is localized extracellularly, and interacts with itself.

di Klomp, Adriana E M, Juijn, Jenneke A, van der Gun, Linda T M, van den Berg, Inge E T, Berger, Ruud, Klomp, Leo W J
Pubblicazione 2003

A novel role for XIAP in copper homeostasis through regulation of MURR1

di Burstein, Ezra, Ganesh, Lakshmanan, Dick, Robert D, van De Sluis, Bart, Wilkinson, John C, Klomp, Leo W J, Wijmenga, Cisca, Brewer, George J, Nabel, Gary J, Duckett, Colin S
Pubblicazione 2004

Distinct Wilson-disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B

di 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.
Pubblicazione 2007

Increased concentrations of both NMDA receptor co-agonists d-serine and glycine in global ischemia: a potential novel treatment target for perinatal asphyxia

di Fuchs, Sabine A., Peeters-Scholte, Cacha M. P. C. D., de Barse, Martina M. J., Roeleveld, Martin W., Klomp, Leo W. J., Berger, Ruud, de Koning, Tom J.
Pubblicazione 2011

The Copper Metabolism MURR1 Domain Protein 1 (COMMD1) Modulates the Aggregation of Misfolded Protein Species in a Client-Specific Manner

di Vonk, Willianne I. M., Kakkar, Vaishali, Bartuzi, Paulina, Jaarsma, Dick, Berger, Ruud, Hofker, Marten H., Klomp, Leo W. J., Wijmenga, Cisca, Kampinga, Harm H., van de Sluis, Bart
Pubblicazione 2014

Liver-Specific Commd1 Knockout Mice Are Susceptible to Hepatic Copper Accumulation

di Vonk, Willianne I. M., Bartuzi, Paulina, de Bie, Prim, Kloosterhuis, Niels, Wichers, Catharina G. K., Berger, Ruud, Haywood, Susan, Klomp, Leo W. J., Wijmenga, Cisca, van de Sluis, Bart
Pubblicazione 2011

Human copper transporter 2 is localized in late endosomes and lysosomes and facilitates cellular copper uptake

di vandenBerghe, Peter V. E., Folmer, Dineke E., Malingré, Helga E. M., vanBeurden, Ellen, Klomp, Adriana E. M., vandeSluis, Bart, Merkx, Maarten, Berger, Ruud, Klomp, Leo W. J.
Pubblicazione 2007

Heteromeric Interactions Required for Abundance and Subcellular Localization of Human CDC50 Proteins and Class 1 P(4)-ATPases

di van der Velden, Lieke M., Wichers, Catharina G. K., van Breevoort, Adriana E. D., Coleman, Jonathan A., Molday, Robert S., Berger, Ruud, Klomp, Leo W. J., van de Graaf, Stan F. J.
Pubblicazione 2010

The copper-transporting capacity of ATP7A mutants associated with Menkes disease is ameliorated by COMMD1 as a result of improved protein expression

di 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
Pubblicazione 2011

ELEVATED GLUTATHIONE LEVELS CONFER CELLULAR SENSITIZATION TO CISPLATIN TOXICITY BY UPREGULATION OF COPPER TRANSPORTER HCTR1

di Chen, Helen H. W., Song, Im-Sook, Hossain, Anwar, Choi, Min-Koo, Yamane, Yoshiaki, Liang, Zheng D., Lu, Jia, Wu, Lily Y-H, Siddik, Zahid H., Klomp, Leo W. J., Savaraj, Niramol, Tien, Kuo Macus
Pubblicazione 2008

Molecular Characterization of 3-Phosphoglycerate Dehydrogenase Deficiency—a Neurometabolic Disorder Associated with Reduced L-Serine Biosynthesis

di Klomp, Leo W. J., de Koning, Tom J., Malingré, Helga E. M., van Beurden, Ellen A. C. M., Brink, Miny, Opdam, Frans L., Duran, Marinus, Jaeken, Jaak, Pineda, Merce, van Maldergem, Lionel, Poll-The, Bwee Tien, van den Berg, Inge E. T., Berger, Ruud
Pubblicazione 2000