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Ruud Berger

Showing results (31-40 of 71) with videos related to

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The Biochemical Journal|December 6, 2002
The N-terminus of the human copper transporter 1 (hCTR1) is localized extracellularly, and interacts with itselfAdriana E M Klomp, Jenneke A Juijn, Linda T M van der Gun, et al.
Pediatric Research|October 22, 2004
Fic1 is expressed at apical membranes of different epithelial cells in the digestive tract and is induced in the small intestine during postnatal development of miceSaskia W C van Mil, Masja M van Oort, Inge E T van den Berg, et al.
Genome Medicine|December 4, 2012
Assessing the metabolic effects of prednisolone in healthy volunteers using urine metabolic profilingSandrine Ellero-Simatos, Ewa Szymańska, Ton Rullmann, et al.
Molecular Endocrinology (Baltimore, Md.)|February 22, 2007
Impaired peroxisome proliferator-activated receptor gamma function through mutation of a conserved salt bridge (R425C) in familial partial lipodystrophyEllen H Jeninga, Olivier van Beekum, Aalt D J van Dijk, et al.
Kidney International. Supplement|April 16, 2003
Hypertriglyceridemia in patients with chronic renal failure: possible mechanismsBerthil H C M T Prinsen, Monique G M de Sain-van der Velden, Eelco J P de Koning, et al.
Plos One|April 3, 2014
The Copper Metabolism MURR1 domain protein 1 (COMMD1) modulates the aggregation of misfolded protein species in a client-specific mannerWillianne I M Vonk, Vaishali Kakkar, Paulina Bartuzi, et al.
Amino Acids|September 28, 2011
Increased concentrations of both NMDA receptor co-agonists D-serine and glycine in global ischemia: a potential novel treatment target for perinatal asphyxiaSabine A Fuchs, Cacha M P C D Peeters-Scholte, Martina M J de Barse, et al.
Gastroenterology|October 9, 2007
Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7BPrim de Bie, Bart van de Sluis, Ezra Burstein, et al.
Journal of Hepatology|December 4, 2003
Extensive changes in liver gene expression induced by hereditary tyrosinemia type I are not normalized by treatment with 2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione (NTBC)Marjanka C Luijerink, Saskia M M Jacobs, Ellen A C M van Beurden, et al.
Journal of Photochemistry and Photobiology. B, Biology|September 7, 2016
Tracking biochemical changes correlated with ultra-weak photon emission using metabolomicsRosilene Cristina Rossetto Burgos, Kateřina Červinková, Tom van der Laan, et al.
Pageof 8

Showing results (31-40 of 71) with videos related to

Sort By:
Pageof 8
The Biochemical Journal|December 6, 2002
The N-terminus of the human copper transporter 1 (hCTR1) is localized extracellularly, and interacts with itselfAdriana E M Klomp, Jenneke A Juijn, Linda T M van der Gun, et al.
Pediatric Research|October 22, 2004
Fic1 is expressed at apical membranes of different epithelial cells in the digestive tract and is induced in the small intestine during postnatal development of miceSaskia W C van Mil, Masja M van Oort, Inge E T van den Berg, et al.
Genome Medicine|December 4, 2012
Assessing the metabolic effects of prednisolone in healthy volunteers using urine metabolic profilingSandrine Ellero-Simatos, Ewa Szymańska, Ton Rullmann, et al.
Molecular Endocrinology (Baltimore, Md.)|February 22, 2007
Impaired peroxisome proliferator-activated receptor gamma function through mutation of a conserved salt bridge (R425C) in familial partial lipodystrophyEllen H Jeninga, Olivier van Beekum, Aalt D J van Dijk, et al.
Kidney International. Supplement|April 16, 2003
Hypertriglyceridemia in patients with chronic renal failure: possible mechanismsBerthil H C M T Prinsen, Monique G M de Sain-van der Velden, Eelco J P de Koning, et al.
Plos One|April 3, 2014
The Copper Metabolism MURR1 domain protein 1 (COMMD1) modulates the aggregation of misfolded protein species in a client-specific mannerWillianne I M Vonk, Vaishali Kakkar, Paulina Bartuzi, et al.
Amino Acids|September 28, 2011
Increased concentrations of both NMDA receptor co-agonists D-serine and glycine in global ischemia: a potential novel treatment target for perinatal asphyxiaSabine A Fuchs, Cacha M P C D Peeters-Scholte, Martina M J de Barse, et al.
Gastroenterology|October 9, 2007
Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7BPrim de Bie, Bart van de Sluis, Ezra Burstein, et al.
Journal of Hepatology|December 4, 2003
Extensive changes in liver gene expression induced by hereditary tyrosinemia type I are not normalized by treatment with 2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione (NTBC)Marjanka C Luijerink, Saskia M M Jacobs, Ellen A C M van Beurden, et al.
Journal of Photochemistry and Photobiology. B, Biology|September 7, 2016
Tracking biochemical changes correlated with ultra-weak photon emission using metabolomicsRosilene Cristina Rossetto Burgos, Kateřina Červinková, Tom van der Laan, et al.
Pageof 8