Elferink RP - Search Results

1

A mouse genetic model for familial cholestasis caused by ATP8B1 mutations reveals perturbed bile salt homeostasis but no impairment in bile secretion.

Pawlikowska L, Groen A, Eppens EF, Kunne C, Ottenhoff R, Looije N, Knisely AS, Killeen NP, Bull LN, Elferink RP, Freimer NB. Pawlikowska L, et al. Among authors: elferink rp. Hum Mol Genet. 2004 Apr 15;13(8):881-92. doi: 10.1093/hmg/ddh100. Epub 2004 Feb 19. Hum Mol Genet. 2004. PMID: 14976163

2

Strain background modifies phenotypes in the ATP8B1-deficient mouse.

Shah S, Sanford UR, Vargas JC, Xu H, Groen A, Paulusma CC, Grenert JP, Pawlikowska L, Sen S, Elferink RP, Bull LN. Shah S, et al. Among authors: elferink rp. PLoS One. 2010 Feb 1;5(2):e8984. doi: 10.1371/journal.pone.0008984. PLoS One. 2010. PMID: 20126555 Free PMC article.

3

Activity of the bile salt export pump (ABCB11) is critically dependent on canalicular membrane cholesterol content.

Paulusma CC, de Waart DR, Kunne C, Mok KS, Elferink RP. Paulusma CC, et al. Among authors: elferink rp. J Biol Chem. 2009 Apr 10;284(15):9947-54. doi: 10.1074/jbc.M808667200. Epub 2009 Feb 19. J Biol Chem. 2009. PMID: 19228692 Free PMC article.

4

The mechanism of biliary lipid secretion and its defects.

Elferink RP, Groen AK. Elferink RP, et al. Gastroenterol Clin North Am. 1999 Mar;28(1):59-74, vi. doi: 10.1016/s0889-8553(05)70043-1. Gastroenterol Clin North Am. 1999. PMID: 10198778 Review.

5

Hepatic canalicular membrane 1: The role of mdr2 P-glycoprotein in hepatobiliary lipid transport.

Elferink RP, Tytgat GN, Groen AK. Elferink RP, et al. FASEB J. 1997 Jan;11(1):19-28. doi: 10.1096/fasebj.11.1.9034162. FASEB J. 1997. PMID: 9034162 Review.

6

Class III P-glycoproteins mediate the formation of lipoprotein X in the mouse.

Elferink RP, Ottenhoff R, van Marle J, Frijters CM, Smith AJ, Groen AK. Elferink RP, et al. J Clin Invest. 1998 Nov 1;102(9):1749-57. doi: 10.1172/JCI3597. J Clin Invest. 1998. PMID: 9802889 Free PMC article.

7

Effects of Ursodeoxycholate and cholate feeding on liver disease in FVB mice with a disrupted mdr2 P-glycoprotein gene.

Van Nieuwkerk CM, Elferink RP, Groen AK, Ottenhoff R, Tytgat GN, Dingemans KP, Van Den Bergh Weerman MA, Offerhaus GJ. Van Nieuwkerk CM, et al. Among authors: elferink rp. Gastroenterology. 1996 Jul;111(1):165-71. doi: 10.1053/gast.1996.v111.pm8698195. Gastroenterology. 1996. PMID: 8698195

8

Control analysis of biliary lipid secretion.

Groen AK, Elferink RP, Tager JM. Groen AK, et al. Among authors: elferink rp. J Theor Biol. 1996 Oct 7;182(3):427-36. doi: 10.1006/jtbi.1996.0183. J Theor Biol. 1996. PMID: 8944177

9

The role of different P-glycoproteins in hepatobiliary secretion of fluorescently labeled short-chain phospholipids.

Frijters CM, Tuijn CJ, Ottenhoff R, Zegers BN, Groen AK, Elferink RP. Frijters CM, et al. Among authors: elferink rp. J Lipid Res. 1999 Nov;40(11):1950-8. J Lipid Res. 1999. PMID: 10552998 Free article.

10

Hepatobiliary transport of glutathione and glutathione conjugate in rats with hereditary hyperbilirubinemia.

Elferink RP, Ottenhoff R, Liefting W, de Haan J, Jansen PL. Elferink RP, et al. J Clin Invest. 1989 Aug;84(2):476-83. doi: 10.1172/JCI114189. J Clin Invest. 1989. PMID: 2760197 Free PMC article.

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