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Items: 1 to 20 of 275

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.

Hum Mol Genet. 2004 Apr 15;13(8):881-92. Epub 2004 Feb 19.

PMID:
14976163
2.

Intestinal bile salt absorption in Atp8b1 deficient mice.

Groen A, Kunne C, Paulusma CC, Kramer W, Agellon LB, Bull LN, Oude Elferink RP.

J Hepatol. 2007 Jul;47(1):114-22. Epub 2007 Mar 7.

PMID:
17448567
3.

Atp8b1 deficiency in mice reduces resistance of the canalicular membrane to hydrophobic bile salts and impairs bile salt transport.

Paulusma CC, Groen A, Kunne C, Ho-Mok KS, Spijkerboer AL, Rudi de Waart D, Hoek FJ, Vreeling H, Hoeben KA, van Marle J, Pawlikowska L, Bull LN, Hofmann AF, Knisely AS, Oude Elferink RP.

Hepatology. 2006 Jul;44(1):195-204.

PMID:
16799980
4.

Hepatic cytochrome P450 deficiency in mouse models for intrahepatic cholestasis predispose to bile salt-induced cholestasis.

Kunne C, de Graaff M, Duijst S, de Waart DR, Oude Elferink RP, Paulusma CC.

Lab Invest. 2014 Oct;94(10):1103-13. doi: 10.1038/labinvest.2014.102. Epub 2014 Jul 28.

5.

Abcg5/8 independent biliary cholesterol excretion in Atp8b1-deficient mice.

Groen A, Kunne C, Jongsma G, van den Oever K, Mok KS, Petruzzelli M, Vrins CL, Bull L, Paulusma CC, Oude Elferink RP.

Gastroenterology. 2008 Jun;134(7):2091-100. doi: 10.1053/j.gastro.2008.02.097. Epub 2008 Mar 8.

PMID:
18466903
6.

Progressive familial intrahepatic cholestasis type 1.

Paulusma CC, Elferink RP, Jansen PL.

Semin Liver Dis. 2010 May;30(2):117-24. doi: 10.1055/s-0030-1253221. Epub 2010 Apr 26. Review.

PMID:
20422494
7.

Genetic cholestasis, causes and consequences for hepatobiliary transport.

Jansen PL, Sturm E.

Liver Int. 2003 Oct;23(5):315-22. Review.

PMID:
14708891
8.

Severe cholestasis induced by cholic acid feeding in knockout mice of sister of P-glycoprotein.

Wang R, Lam P, Liu L, Forrest D, Yousef IM, Mignault D, Phillips MJ, Ling V.

Hepatology. 2003 Dec;38(6):1489-99.

PMID:
14647060
10.
11.

The lipid flippase heterodimer ATP8B1-CDC50A is essential for surface expression of the apical sodium-dependent bile acid transporter (SLC10A2/ASBT) in intestinal Caco-2 cells.

van der Mark VA, de Waart DR, Ho-Mok KS, Tabbers MM, Voogt HW, Oude Elferink RP, Knisely AS, Paulusma CC.

Biochim Biophys Acta. 2014 Dec;1842(12 Pt A):2378-86. doi: 10.1016/j.bbadis.2014.09.003. Epub 2014 Sep 16.

12.

Targeted inactivation of sister of P-glycoprotein gene (spgp) in mice results in nonprogressive but persistent intrahepatic cholestasis.

Wang R, Salem M, Yousef IM, Tuchweber B, Lam P, Childs SJ, Helgason CD, Ackerley C, Phillips MJ, Ling V.

Proc Natl Acad Sci U S A. 2001 Feb 13;98(4):2011-6. Epub 2001 Feb 6.

13.

Altered hepatobiliary gene expressions in PFIC1: ATP8B1 gene defect is associated with CFTR downregulation.

Demeilliers C, Jacquemin E, Barbu V, Mergey M, Paye F, Fouassier L, Chignard N, Housset C, Lomri NE.

Hepatology. 2006 May;43(5):1125-34.

PMID:
16628629
15.

Defective bile salt biosynthesis and hydroxylation in mice with reduced cytochrome P450 activity.

Kunne C, Acco A, Hohenester S, Duijst S, de Waart DR, Zamanbin A, Oude Elferink RP.

Hepatology. 2013 Apr;57(4):1509-17. doi: 10.1002/hep.26133. Epub 2013 Jan 18.

PMID:
23184615
16.

Progressive familial intrahepatic cholestasis, type 1, is associated with decreased farnesoid X receptor activity.

Chen F, Ananthanarayanan M, Emre S, Neimark E, Bull LN, Knisely AS, Strautnieks SS, Thompson RJ, Magid MS, Gordon R, Balasubramanian N, Suchy FJ, Shneider BL.

Gastroenterology. 2004 Mar;126(3):756-64.

PMID:
14988830
17.

[Childhood cholestasis and bile transporters].

Hierro L, Jara P.

Gastroenterol Hepatol. 2005 Aug-Sep;28(7):388-95. Review. Spanish.

PMID:
16137474
18.

Differential effects of progressive familial intrahepatic cholestasis type 1 and benign recurrent intrahepatic cholestasis type 1 mutations on canalicular localization of ATP8B1.

Folmer DE, van der Mark VA, Ho-Mok KS, Oude Elferink RP, Paulusma CC.

Hepatology. 2009 Nov;50(5):1597-605. doi: 10.1002/hep.23158.

PMID:
19731236
19.

Knockdown of ATP8B1 expression leads to specific downregulation of the bile acid sensor FXR in HepG2 cells: effect of the FXR agonist GW4064.

Martínez-Fernández P, Hierro L, Jara P, Alvarez L.

Am J Physiol Gastrointest Liver Physiol. 2009 May;296(5):G1119-29. doi: 10.1152/ajpgi.90371.2008. Epub 2009 Feb 19.

20.

Bile salt-associated electrolyte secretion. A study following a short-term biliary obstruction in the rat.

Roma MG, Carnovale C, Rodíguez Garay A.

Exp Toxicol Pathol. 1992 Oct;44(6):354-60.

PMID:
1450654

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