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

von Hamza, Iqbal, Schaefer, Mark, Klomp, Leo W. J., Gitlin, Jonathan D.
Veröffentlicht 1999

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

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

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

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

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

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

D-Serine Influences Synaptogenesis in a P19 Cell Model

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

COMMD1 expression is controlled by critical residues that determine XIAP binding

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

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

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

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

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

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

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

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

von 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
Veröffentlicht 2003

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

von 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
Veröffentlicht 2004

Distinct Wilson-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.
Veröffentlicht 2007

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

von 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.
Veröffentlicht 2011

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

von 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
Veröffentlicht 2014

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

von 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
Veröffentlicht 2011

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

von 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.
Veröffentlicht 2007

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

von 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.
Veröffentlicht 2010

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
Veröffentlicht 2011

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

von 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
Veröffentlicht 2008

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

von 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
Veröffentlicht 2000