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

por Hamza, Iqbal, Schaefer, Mark, Klomp, Leo W. J., Gitlin, Jonathan D.
Publicado em 1999

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

por Vonk, Willianne I. M., Wijmenga, Cisca, Berger, Ruud, van de Sluis, Bart, Klomp, Leo W. J.
Publicado em 2010

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

por Materia, Stephanie, Cater, Michael A., Klomp, Leo W. J., Mercer, Julian F. B., La Fontaine, Sharon
Publicado em 2011

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

por Materia, Stephanie, Cater, Michael A., Klomp, Leo W. J., Mercer, Julian F. B., La Fontaine, Sharon
Publicado em 2012

D-Serine Influences Synaptogenesis in a P19 Cell Model

por Fuchs, Sabine A., Roeleveld, Martin W., Klomp, Leo W. J., Berger, Ruud, de Koning, Tom J.
Publicado em 2012

COMMD1 expression is controlled by critical residues that determine XIAP binding

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

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

por Klomp, Adriana E M, Tops, Bastiaan B J, Van Denberg, Inge E T, Berger, Ruud, Klomp, Leo W J
Publicado em 2002

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

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

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

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

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

por 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
Publicado em 2003

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

por 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
Publicado em 2004

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

por 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.
Publicado em 2007

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

por 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.
Publicado em 2011

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

por 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
Publicado em 2014

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

por 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
Publicado em 2011

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

por 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.
Publicado em 2007

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

por 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.
Publicado em 2010

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

por 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
Publicado em 2011

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

por 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
Publicado em 2008

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

por 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
Publicado em 2000