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264 related items for PubMed ID: 14672610

  • 1. A progressive familial intrahepatic cholestasis type 2 mutation causes an unstable, temperature-sensitive bile salt export pump.
    Plass JR, Mol O, Heegsma J, Geuken M, de Bruin J, Elling G, Müller M, Faber KN, Jansen PL.
    J Hepatol; 2004 Jan; 40(1):24-30. PubMed ID: 14672610
    [Abstract] [Full Text] [Related]

  • 2. Phenotypic differences in PFIC2 and BRIC2 correlate with protein stability of mutant Bsep and impaired taurocholate secretion in MDCK II cells.
    Kagawa T, Watanabe N, Mochizuki K, Numari A, Ikeno Y, Itoh J, Tanaka H, Arias IM, Mine T.
    Am J Physiol Gastrointest Liver Physiol; 2008 Jan; 294(1):G58-67. PubMed ID: 17947449
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  • 4. Degradation of the bile salt export pump at endoplasmic reticulum in progressive familial intrahepatic cholestasis type II.
    Wang L, Dong H, Soroka CJ, Wei N, Boyer JL, Hochstrasser M.
    Hepatology; 2008 Nov; 48(5):1558-69. PubMed ID: 18798335
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  • 5. Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis.
    Jansen PL, Strautnieks SS, Jacquemin E, Hadchouel M, Sokal EM, Hooiveld GJ, Koning JH, De Jager-Krikken A, Kuipers F, Stellaard F, Bijleveld CM, Gouw A, Van Goor H, Thompson RJ, Müller M.
    Gastroenterology; 1999 Dec; 117(6):1370-9. PubMed ID: 10579978
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  • 6. Levels of plasma membrane expression in progressive and benign mutations of the bile salt export pump (Bsep/Abcb11) correlate with severity of cholestatic diseases.
    Lam P, Pearson CL, Soroka CJ, Xu S, Mennone A, Boyer JL.
    Am J Physiol Cell Physiol; 2007 Nov; 293(5):C1709-16. PubMed ID: 17855769
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  • 9. Genetic cholestasis, causes and consequences for hepatobiliary transport.
    Jansen PL, Sturm E.
    Liver Int; 2003 Oct; 23(5):315-22. PubMed ID: 14708891
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  • 10. The mechanism of increased biliary lipid secretion in mice with genetic inactivation of bile salt export pump.
    Gooijert KE, Havinga R, Wolters H, Wang R, Ling V, Tazuma S, Verkade HJ.
    Am J Physiol Gastrointest Liver Physiol; 2015 Mar 01; 308(5):G450-7. PubMed ID: 25552583
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  • 11. Short-chain ubiquitination is associated with the degradation rate of a cell-surface-resident bile salt export pump (BSEP/ABCB11).
    Hayashi H, Sugiyama Y.
    Mol Pharmacol; 2009 Jan 01; 75(1):143-50. PubMed ID: 18829893
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  • 12. The role of bile salt export pump mutations in progressive familial intrahepatic cholestasis type II.
    Wang L, Soroka CJ, Boyer JL.
    J Clin Invest; 2002 Oct 01; 110(7):965-72. PubMed ID: 12370274
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  • 13. Bile salt export pump (BSEP/ABCB11): trafficking and sorting disturbances.
    Hayashi H, Sugiyama Y.
    Curr Mol Pharmacol; 2013 Jul 01; 6(2):95-103. PubMed ID: 23876151
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  • 14. Expression and localization of hepatobiliary transport proteins in progressive familial intrahepatic cholestasis.
    Keitel V, Burdelski M, Warskulat U, Kühlkamp T, Keppler D, Häussinger D, Kubitz R.
    Hepatology; 2005 May 01; 41(5):1160-72. PubMed ID: 15841457
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  • 15. Partial external biliary diversion in bile salt export pump deficiency: Association between outcome and mutation.
    Ellinger P, Stindt J, Dröge C, Sattler K, Stross C, Kluge S, Herebian D, Smits SHJ, Burdelski M, Schulz-Jürgensen S, Ballauff A, Schulte Am Esch J, Mayatepek E, Häussinger D, Kubitz R, Schmitt L.
    World J Gastroenterol; 2017 Aug 07; 23(29):5295-5303. PubMed ID: 28839429
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  • 16. Two common PFIC2 mutations are associated with the impaired membrane trafficking of BSEP/ABCB11.
    Hayashi H, Takada T, Suzuki H, Akita H, Sugiyama Y.
    Hepatology; 2005 Apr 07; 41(4):916-24. PubMed ID: 15791618
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  • 17. Functional expression of the canalicular bile salt export pump of human liver.
    Noé J, Stieger B, Meier PJ.
    Gastroenterology; 2002 Nov 07; 123(5):1659-66. PubMed ID: 12404240
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  • 18. Bile salt export pump is highly conserved during vertebrate evolution and its expression is inhibited by PFIC type II mutations.
    Cai SY, Wang L, Ballatori N, Boyer JL.
    Am J Physiol Gastrointest Liver Physiol; 2001 Aug 07; 281(2):G316-22. PubMed ID: 11447010
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  • 19. Autoimmune BSEP disease: disease recurrence after liver transplantation for progressive familial intrahepatic cholestasis.
    Kubitz R, Dröge C, Kluge S, Stross C, Walter N, Keitel V, Häussinger D, Stindt J.
    Clin Rev Allergy Immunol; 2015 Jun 07; 48(2-3):273-84. PubMed ID: 25342496
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  • 20. Differences in presentation and progression between severe FIC1 and BSEP deficiencies.
    Pawlikowska L, Strautnieks S, Jankowska I, Czubkowski P, Emerick K, Antoniou A, Wanty C, Fischler B, Jacquemin E, Wali S, Blanchard S, Nielsen IM, Bourke B, McQuaid S, Lacaille F, Byrne JA, van Eerde AM, Kolho KL, Klomp L, Houwen R, Bacchetti P, Lobritto S, Hupertz V, McClean P, Mieli-Vergani G, Shneider B, Nemeth A, Sokal E, Freimer NB, Knisely AS, Rosenthal P, Whitington PF, Pawlowska J, Thompson RJ, Bull LN.
    J Hepatol; 2010 Jul 07; 53(1):170-8. PubMed ID: 20447715
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