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R P Elferink

Showing results (11-20 of 24) with videos related to

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Journal of Lipid Research|December 20, 1999
The role of different P-glycoproteins in hepatobiliary secretion of fluorescently labeled short-chain phospholipidsC M Frijters, C J Tuijn, R Ottenhoff, et al.
The Journal of Clinical Investigation|November 5, 1998
Class III P-glycoproteins mediate the formation of lipoprotein X in the mouseR P Elferink, R Ottenhoff, J van Marle, et al.
Gastroenterology|August 1, 1991
Cell type-dependent effect of phospholipid and cholesterol on bile salt cytotoxicityA L Velardi, A K Groen, R P Elferink, et al.
Carcinogenesis|April 27, 2001
Mrp2-deficiency in the rat impairs biliary and intestinal excretion and influences metabolism and disposition of the food-derived carcinogen 2-amino-1-methyl-6-phenylimidazoC G Dietrich, D R de Waart, R Ottenhoff, et al.
Gastroenterology|December 28, 1999
Postprandial chylomicron formation and fat absorption in multidrug resistance gene 2 P-glycoprotein-deficient miceP J Voshol, D M Minich, R Havinga, et al.
Hepatology (Baltimore, Md.)|September 1, 1996
Influence of dietary calcium phosphate on the disposition of bilirubin in rats with unconjugated hyperbilirubinemiaC N Van Der Veere, B Schoemaker, C Bakker, et al.
Gastroenterology|September 29, 1999
Sulindac is excreted into bile by a canalicular bile salt pump and undergoes a cholehepatic circulation in ratsU Bolder, N V Trang, L R Hagey, et al.
Journal of Hepatology|April 3, 2001
Dietary cholesterol does not normalize low plasma cholesterol levels but induces hyperbilirubinemia and hypercholanemia in Mdr2 P-glycoprotein-deficient miceP J Voshol, N R Koopen, J M de Vree, et al.
Gastroenterology|July 1, 1996
Effects of Ursodeoxycholate and cholate feeding on liver disease in FVB mice with a disrupted mdr2 P-glycoprotein geneC M Van Nieuwkerk, R P Elferink, A K Groen, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 1, 1992
Mechanisms of inherited deficiencies of multiple UDP-glucuronosyltransferase isoforms in two patients with Crigler-Najjar syndrome, type IP J Bosma, J R Chowdhury, T J Huang, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Journal of Lipid Research|December 20, 1999
The role of different P-glycoproteins in hepatobiliary secretion of fluorescently labeled short-chain phospholipidsC M Frijters, C J Tuijn, R Ottenhoff, et al.
The Journal of Clinical Investigation|November 5, 1998
Class III P-glycoproteins mediate the formation of lipoprotein X in the mouseR P Elferink, R Ottenhoff, J van Marle, et al.
Gastroenterology|August 1, 1991
Cell type-dependent effect of phospholipid and cholesterol on bile salt cytotoxicityA L Velardi, A K Groen, R P Elferink, et al.
Carcinogenesis|April 27, 2001
Mrp2-deficiency in the rat impairs biliary and intestinal excretion and influences metabolism and disposition of the food-derived carcinogen 2-amino-1-methyl-6-phenylimidazoC G Dietrich, D R de Waart, R Ottenhoff, et al.
Gastroenterology|December 28, 1999
Postprandial chylomicron formation and fat absorption in multidrug resistance gene 2 P-glycoprotein-deficient miceP J Voshol, D M Minich, R Havinga, et al.
Hepatology (Baltimore, Md.)|September 1, 1996
Influence of dietary calcium phosphate on the disposition of bilirubin in rats with unconjugated hyperbilirubinemiaC N Van Der Veere, B Schoemaker, C Bakker, et al.
Gastroenterology|September 29, 1999
Sulindac is excreted into bile by a canalicular bile salt pump and undergoes a cholehepatic circulation in ratsU Bolder, N V Trang, L R Hagey, et al.
Journal of Hepatology|April 3, 2001
Dietary cholesterol does not normalize low plasma cholesterol levels but induces hyperbilirubinemia and hypercholanemia in Mdr2 P-glycoprotein-deficient miceP J Voshol, N R Koopen, J M de Vree, et al.
Gastroenterology|July 1, 1996
Effects of Ursodeoxycholate and cholate feeding on liver disease in FVB mice with a disrupted mdr2 P-glycoprotein geneC M Van Nieuwkerk, R P Elferink, A K Groen, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 1, 1992
Mechanisms of inherited deficiencies of multiple UDP-glucuronosyltransferase isoforms in two patients with Crigler-Najjar syndrome, type IP J Bosma, J R Chowdhury, T J Huang, et al.
Pageof 3