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R P Elferink

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Gastroenterology Clinics of North America|April 13, 1999
The mechanism of biliary lipid secretion and its defectsR P Elferink, A K Groen
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 1, 1997
Hepatic canalicular membrane 1: The role of mdr2 P-glycoprotein in hepatobiliary lipid transportR P Elferink, G N Tytgat, A K Groen
Journal of Theoretical Biology|October 7, 1996
Control analysis of biliary lipid secretionA K Groen, R P Elferink, J M Tager
FEBS Letters|July 29, 1996
A mutation which disrupts the hydrophobic core of the signal peptide of bilirubin UDP-glucuronosyltransferase, an endoplasmic reticulum membrane protein, causes Crigler-Najjar type IIJ Seppen, E Steenken, D Lindhout, et al.
The Journal of Clinical Investigation|August 1, 1989
Hepatobiliary transport of glutathione and glutathione conjugate in rats with hereditary hyperbilirubinemiaR P Elferink, R Ottenhoff, W Liefting, et al.
The American Journal of Physiology|September 1, 1995
Impaired hepatocanalicular organic anion transport in endotoxemic ratsH Roelofsen, B Schoemaker, C Bakker, et al.
Molecular Pharmacology|April 18, 2001
Increased bioavailability of the food-derived carcinogen 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine in MRP2-deficient ratsC G Dietrich, D R de Waart, R Ottenhoff, et al.
Hepatology (Baltimore, Md.)|June 1, 1995
Redistribution of canalicular organic anion transport activity in isolated and cultured rat hepatocytesH Roelofsen, C T Bakker, B Schoemaker, et al.
The American Journal of Physiology|September 1, 1993
Preserved organic anion transport in mutant TR- rats with a hepatobiliary secretion defectP L Jansen, J W van Klinken, M van Gelder, et al.
The Journal of Clinical Investigation|April 1, 1990
Immunochemical analysis of uridine diphosphate-glucuronosyltransferase in four patients with the Crigler-Najjar syndrome type IH H van Es, B G Goldhoorn, M Paul-Abrahamse, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Gastroenterology Clinics of North America|April 13, 1999
The mechanism of biliary lipid secretion and its defectsR P Elferink, A K Groen
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 1, 1997
Hepatic canalicular membrane 1: The role of mdr2 P-glycoprotein in hepatobiliary lipid transportR P Elferink, G N Tytgat, A K Groen
Journal of Theoretical Biology|October 7, 1996
Control analysis of biliary lipid secretionA K Groen, R P Elferink, J M Tager
FEBS Letters|July 29, 1996
A mutation which disrupts the hydrophobic core of the signal peptide of bilirubin UDP-glucuronosyltransferase, an endoplasmic reticulum membrane protein, causes Crigler-Najjar type IIJ Seppen, E Steenken, D Lindhout, et al.
The Journal of Clinical Investigation|August 1, 1989
Hepatobiliary transport of glutathione and glutathione conjugate in rats with hereditary hyperbilirubinemiaR P Elferink, R Ottenhoff, W Liefting, et al.
The American Journal of Physiology|September 1, 1995
Impaired hepatocanalicular organic anion transport in endotoxemic ratsH Roelofsen, B Schoemaker, C Bakker, et al.
Molecular Pharmacology|April 18, 2001
Increased bioavailability of the food-derived carcinogen 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine in MRP2-deficient ratsC G Dietrich, D R de Waart, R Ottenhoff, et al.
Hepatology (Baltimore, Md.)|June 1, 1995
Redistribution of canalicular organic anion transport activity in isolated and cultured rat hepatocytesH Roelofsen, C T Bakker, B Schoemaker, et al.
The American Journal of Physiology|September 1, 1993
Preserved organic anion transport in mutant TR- rats with a hepatobiliary secretion defectP L Jansen, J W van Klinken, M van Gelder, et al.
The Journal of Clinical Investigation|April 1, 1990
Immunochemical analysis of uridine diphosphate-glucuronosyltransferase in four patients with the Crigler-Najjar syndrome type IH H van Es, B G Goldhoorn, M Paul-Abrahamse, et al.
Pageof 3