Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Prim de Bie"'
Autor:
Willianne I M Vonk, Paulina Bartuzi, Prim de Bie, Niels Kloosterhuis, Catharina G K Wichers, Ruud Berger, Susan Haywood, Leo W J Klomp, Cisca Wijmenga, Bart van de Sluis
Publikováno v:
PLoS ONE, Vol 6, Iss 12, p e29183 (2011)
Canine copper toxicosis is an autosomal recessive disorder characterized by hepatic copper accumulation resulting in liver fibrosis and eventually cirrhosis. We have identified COMMD1 as the gene underlying copper toxicosis in Bedlington terriers. Al
Externí odkaz:
https://doaj.org/article/e50a1f85e64e48528a1bbc3cc33347cf
Publikováno v:
Translational Andrology and Urology. 8:S448-S456
Uric acid (UA) urolithiasis comprises around 5–10% of all stones and can frequently recur. Due to the fact that UA stones form in acidic urine with a pH
Publikováno v:
Journal of the Endocrine Society
In the Netherlands, the diagnosis of growth hormone deficiency in children follows the Dutch national guidelines for Triage and Diagnosis of Growth Disorders in Children. Initial biochemical evaluation includes an IGF-1 measurement as screening param
Publikováno v:
Point of care, 15(1), 7-10. Lippincott Williams and Wilkins
Autor:
Marion Heckman, Willem van Dam, C. Ağar, An K. Stroobants, Willem J. Schornagel, Bianca Bakker, Auguste Sturk, Prim de Bie, Erik-Jan van den Dool
Publikováno v:
Thrombosis research, 131(4), 357-362. Elsevier Limited
Introduction The Coasys® Plus C (Behnk Elektronik, distributed by Roche Diagnostics) is a coagulation analyzer for small to midsize clinical chemistry laboratories. We performed a laboratory evaluation. Materials and Methods After a familiarization
Autor:
Prim de Bie, Aaron Ciechanover
Publikováno v:
Biochemical and Biophysical Research Communications. 426:49-53
The activity and stability of the E3 ubiquitin ligase RING1B are controlled by the ubiquitin system. Self-ubiquitination of RING1B, generating K6, K27 and K48-based mixed polyubiquitin chains, is a prerequisite for its activity as an E3 ligase for hi
Autor:
Prim de Bie, Willianne I. M. Vonk, Cisca Wijmenga, Ruud Berger, Leo W. J. Klomp, Rozemarijn van der Plaats, Bart van de Sluis, Catharina G.K. Wichers, Peter V. E. van den Berghe
Publikováno v:
Cellular and molecular life sciences, 69(1), 149-163. SPRINGER BASEL AG
Cellular and Molecular Life Sciences
Cellular and Molecular Life Sciences
Menkes disease (MD) is an X-linked recessive disorder characterized by copper deficiency resulting in a diminished function of copper-dependent enzymes. Most MD patients die in early childhood, although mild forms of MD have also been described. A di
Autor:
Elmar Krieger, Ellen A.C.M. van Beurden, Janneke M. Stapelbroek, Peter V. E. van den Berghe, Stan F.J. van de Graaf, Prim de Bie, Ruud Berger, Leo W. J. Klomp, Roderick H. J. Houwen, Ellen Spijker, Reinoud E. A. de Groot
Publikováno v:
Hepatology, 50, 1783-1795
Hepatology, 50, 6, pp. 1783-1795
Hepatology (Baltimore, Md.), 50(6), 1783-1795. John Wiley and Sons Ltd
Hepatology, 50, 6, pp. 1783-1795
Hepatology (Baltimore, Md.), 50(6), 1783-1795. John Wiley and Sons Ltd
Item does not contain fulltext Wilson disease (WD) is an autosomal recessive copper overload disorder of the liver and basal ganglia. WD is caused by mutations in the gene encoding ATP7B, a protein localized to the trans-Golgi network that primarily
Autor:
Niki A. Georgiou, Hans S. L. M. Nottet, B. Sweder van Asbeck, Tjomme van der Bruggen, Joannes J.M. Marx, Christine A. Jansen, Prim de Bie, Maroeska Oudshoorn
Publikováno v:
Antiviral Research. 63:97-106
Alternative targets of attack of the human immunodeficiency virus (HIV) are necessary in light of infection persistence due to onset of resistance after conventional reverse transcriptase and protease inhibitor therapy. We have recently shown that th
Autor:
Leo W. J. Klomp, Cisca Wijmenga, Ruud Berger, Niels J. Kloosterhuis, Bart van de Sluis, Paulina Bartuzi, Willianne I. M. Vonk, Catharina G.K. Wichers, Prim de Bie, Susan Haywood
Publikováno v:
PLoS ONE, 6(12):29183. PUBLIC LIBRARY SCIENCE
PLoS ONE
PLoS ONE, Vol 6, Iss 12, p e29183 (2011)
PLoS ONE
PLoS ONE, Vol 6, Iss 12, p e29183 (2011)
Canine copper toxicosis is an autosomal recessive disorder characterized by hepatic copper accumulation resulting in liver fibrosis and eventually cirrhosis. We have identified COMMD1 as the gene underlying copper toxicosis in Bedlington terriers. Al