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There are 15140 results for: content related to: Canalicular ABC transporters and liver disease

  1. You have full text access to this OnlineOpen article
    miR-33 controls the expression of biliary transporters, and mediates statin- and diet-induced hepatotoxicity

    EMBO Molecular Medicine

    Volume 4, Issue 9, September 2012, Pages: 882–895, Ryan M. Allen, Tyler J. Marquart, Carolyn J. Albert, Frederick J. Suchy, David Q.-H. Wang, Meenakshisundaram Ananthanarayanan, David A. Ford and Ángel Baldán

    Version of Record online : 5 JUL 2012, DOI: 10.1002/emmm.201201228

  2. You have free access to this content
    Molecular mechanistic explanation for the spectrum of cholestatic disease caused by the S320F variant of ABCB4

    Hepatology

    Volume 59, Issue 5, May 2014, Pages: 1921–1931, Edward J. Andress, Michael Nicolaou, Marta R. Romero, Sandhia Naik, Peter H. Dixon, Catherine Williamson and Kenneth J. Linton

    Version of Record online : 1 APR 2014, DOI: 10.1002/hep.26970

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    A mutation in the canalicular phospholipid transporter gene, ABCB4, is associated with cholestasis, ductopenia, and cirrhosis in adults

    Hepatology

    Volume 48, Issue 4, October 2008, Pages: 1157–1166, Daniel Gotthardt, Heiko Runz, Verena Keitel, Christine Fischer, Christa Flechtenmacher, Michael Wirtenberger, Karl Heinz Weiss, Sandra Imparato, Annika Braun, Kari Hemminki, Wolfgang Stremmel, Franz Rüschendorf, Adolf Stiehl, Ralf Kubitz, Barbara Burwinkel, Peter Schirmacher, A. S. Knisely, Johannes Zschocke and Peter Sauer

    Version of Record online : 19 JUN 2008, DOI: 10.1002/hep.22485

  4. Inheritable Cholestatic Disorders

    The Liver: Biology and Pathobiology, Fifth Edition

    Paul Gissen, A. S. Knisely, Pages: 659–679, 2009

    Published Online : 6 OCT 2009, DOI: 10.1002/9780470747919.ch42

  5. Bile Secretion and Cholestasis

    Textbook of Gastroenterology

    Steven A. Weinman, Sajid Jalil, Pages: 401–428, 2009

    Published Online : 17 FEB 2009, DOI: 10.1002/9781444303254.ch16

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    A missense mutation in ABCB4 gene involved in progressive familial intrahepatic cholestasis type 3 leads to a folding defect that can be rescued by low temperature

    Hepatology

    Volume 49, Issue 4, April 2009, Pages: 1218–1227, Jean-Louis Delaunay, Anne-Marie Durand-Schneider, Danièle Delautier, Alegna Rada, Julien Gautherot, Emmanuel Jacquemin, Tounsia Aït-Slimane and Michèle Maurice

    Version of Record online : 8 DEC 2008, DOI: 10.1002/hep.22775

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    The Arabidopsis concentration-dependent influx/efflux transporter ABCB4 regulates cellular auxin levels in the root epidermis

    The Plant Journal

    Volume 69, Issue 4, February 2012, Pages: 640–654, Martin Kubeš, Haibing Yang, Gregory L. Richter, Yan Cheng, Ewa Młodzińska, Xia Wang, Joshua J. Blakeslee, Nicola Carraro, Jan Petrášek, Eva Zažímalová, Klára Hoyerová, Wendy Ann Peer and Angus S. Murphy

    Version of Record online : 16 NOV 2011, DOI: 10.1111/j.1365-313X.2011.04818.x

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

    Hepatology

    Volume 50, Issue 5, November 2009, Pages: 1597–1605, Dineke E. Folmer, Vincent A. van der Mark, Kam S. Ho-Mok, Ronald P.J. Oude Elferink and Coen C. Paulusma

    Version of Record online : 7 JUL 2009, DOI: 10.1002/hep.23158

  9. Receptor for activated C-kinase 1 regulates the cellular localization and function of ABCB4

    Hepatology Research

    Volume 39, Issue 11, November 2009, Pages: 1091–1107, Yuki Ikebuchi, Tappei Takada, Kousei Ito, Takashi Yoshikado, Naohiko Anzai, Yoshikatsu Kanai and Hiroshi Suzuki

    Version of Record online : 6 AUG 2009, DOI: 10.1111/j.1872-034X.2009.00544.x

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    Diseases of intramembranous lipid transport

    FEBS Letters

    Volume 580, Issue 23, October 09, 2006, Pages: 5500–5509, Coen C. Paulusma and Ronald P.J. Oude Elferink

    Version of Record online : 30 JUN 2006, DOI: 10.1016/j.febslet.2006.06.067

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    AASLD Abstracts

    Hepatology

    Volume 56, Issue S1, October 2012, Pages: 191A–1144A,

    Version of Record online : 1 OCT 2012, DOI: 10.1002/hep.26040

  12. The Function of the Canalicular Membrane in Bile Formation and Secretion

    The Liver: Biology and Pathobiology, Fifth Edition

    Ronald P. J. Oude Elferink, Coen C. Paulusma, Pages: 339–348, 2009

    Published Online : 6 OCT 2009, DOI: 10.1002/9780470747919.ch23

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    Missense mutations and single nucleotide polymorphisms in ABCB11 impair bile salt export pump processing and function or disrupt pre-messenger RNA splicing

    Hepatology

    Volume 49, Issue 2, February 2009, Pages: 553–567, Jane A. Byrne, Sandra S. Strautnieks, Gudrun Ihrke, Franco Pagani, A.S. Knisely, Kenneth J. Linton, Giorgina Mieli-Vergani and Richard J. Thompson

    Version of Record online : 14 OCT 2008, DOI: 10.1002/hep.22683

  14. Genetic Cholestatic Diseases

    Textbook of Hepatology: From Basic Science to Clinical Practice, Third Edition

    Juan Rodés, Jean-Pierre Benhamou, Andres T. Blei, Jürg Reichen, Mario Rizzetto, Pages: 1383–1388, 2008

    Published Online : 15 APR 2008, DOI: 10.1002/9780470691861.ch16j

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    Phosphorylation of ABCB4 impacts its function: Insights from disease-causing mutations

    Hepatology

    Volume 60, Issue 2, August 2014, Pages: 610–621, Julien Gautherot, Danièle Delautier, Marie-Anne Maubert, Tounsia Aït-Slimane, Gérard Bolbach, Jean-Louis Delaunay, Anne-Marie Durand-Schneider, Delphine Firrincieli, Véronique Barbu, Nicolas Chignard, Chantal Housset, Michèle Maurice and Thomas Falguières

    Version of Record online : 19 MAY 2014, DOI: 10.1002/hep.27170

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

    Hepatology

    Volume 44, Issue 1, July 2006, Pages: 195–204, Coen C. Paulusma, Annemiek Groen, Cindy Kunne, Kam S. Ho-Mok, Astrid L. Spijkerboer, D. Rudi de Waart, Frans J. Hoek, Heleen Vreeling, Kees A. Hoeben, Jan van Marle, Ludmila Pawlikowska, Laura N. Bull, Alan F. Hofmann, A. S. Knisely and Ronald P. J. Oude Elferink

    Version of Record online : 23 JUN 2006, DOI: 10.1002/hep.21212

  17. Functional defect of variants in the adenosine triphosphate–binding sites of ABCB4 and their rescue by the cystic fibrosis transmembrane conductance regulator potentiator, ivacaftor (VX-770)

    Hepatology

    Volume 65, Issue 2, February 2017, Pages: 560–570, Jean-Louis Delaunay, Alix Bruneau, Brice Hoffmann, Anne-Marie Durand-Schneider, Véronique Barbu, Emmanuel Jacquemin, Michèle Maurice, Chantal Housset, Isabelle Callebaut and Tounsia Aït-Slimane

    Version of Record online : 24 DEC 2016, DOI: 10.1002/hep.28929

  18. Adaptive Regulation of Hepatocyte Transporters in Cholestasis

    The Liver: Biology and Pathobiology, Fifth Edition

    Irwin M. Arias, Pages: 681–702, 2009

    Published Online : 6 OCT 2009, DOI: 10.1002/9780470747919.ch43

  19. Combined features of low phospholipid-associated cholelithiasis and progressive familial intrahepatic cholestasis 3

    Liver International

    Volume 30, Issue 2, February 2010, Pages: 327–331, Raoul Poupon, Véronique Barbu, Patrick Chamouard, Dominique Wendum, Olivier Rosmorduc and Chantal Housset

    Version of Record online : 19 OCT 2009, DOI: 10.1111/j.1478-3231.2009.02148.x

  20. You have free access to this content
    Folding defects in P-type ATP 8B1 associated with hereditary cholestasis are ameliorated by 4-phenylbutyrate

    Hepatology

    Volume 51, Issue 1, January 2010, Pages: 286–296, Lieke M. van der Velden, Janneke M. Stapelbroek, Elmar Krieger, Peter V. E. van den Berghe, Ruud Berger, Patricia M. Verhulst, Joost C. M. Holthuis, Roderick H. J. Houwen, Leo W. J. Klomp and Stan F. J. van de Graaf

    Version of Record online : 4 SEP 2009, DOI: 10.1002/hep.23268