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There are 9453 results for: content related to: Hepatotoxicity from anabolic androgenic steroids marketed as dietary supplements: contribution from ATP 8B1/ ABCB 11 mutations?

  1. You have free access to this content
    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

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    Canalicular ABC transporters and liver disease

    The Journal of Pathology

    Volume 226, Issue 2, January 2012, Pages: 300–315, Michael Nicolaou, Edward J Andress, Joseph K Zolnerciks, Peter H Dixon, Catherine Williamson and Kenneth J Linton

    Version of Record online : 1 DEC 2011, DOI: 10.1002/path.3019

  3. A novel mutation within a transmembrane helix of the bile salt export pump (BSEP,ABCB11) with delayed development of cirrhosis

    Liver International

    Volume 33, Issue 10, November 2013, Pages: 1527–1535, Jan Stindt, Philipp Ellinger, Katrin Weissenberger, Carola Dröge, Diran Herebian, Ertan Mayatepek, Bernhard Homey, Stephan Braun, Jan Schulte am Esch, Michael Horacek, Ali Canbay, Lutz Schmitt, Dieter Häussinger and Ralf Kubitz

    Version of Record online : 12 JUN 2013, DOI: 10.1111/liv.12217

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    ATP8B1 and ABCB11 analysis in 62 children with normal gamma-glutamyl transferase progressive familial intrahepatic cholestasis (PFIC): Phenotypic differences between PFIC1 and PFIC2 and natural history

    Hepatology

    Volume 51, Issue 5, May 2010, Pages: 1645–1655, Anne Davit-Spraul, Monique Fabre, Sophie Branchereau, Christiane Baussan, Emmanuel Gonzales, Bruno Stieger, Olivier Bernard and Emmanuel Jacquemin

    Version of Record online : 28 JAN 2010, DOI: 10.1002/hep.23539

  5. Characterization and treatment of persistent hepatocellular secretory failure

    Liver International

    Volume 35, Issue 4, April 2015, Pages: 1478–1488, Remco van Dijk, Andreas E. Kremer, Wouter Smit, Bram van den Elzen, Thomas van Gulik, Dirk Gouma, Johan S. Lameris, Hennie Bikker, Valentine Enemuo, Pieter C. F. Stokkers, Mark Feist, Piter Bosma, Peter L. M. Jansen and Ulrich Beuers

    Version of Record online : 4 JUL 2014, DOI: 10.1111/liv.12603

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    Hepatocellular carcinoma in ten children under five years of age with bile salt export pump deficiency

    Hepatology

    Volume 44, Issue 2, August 2006, Pages: 478–486, A. S. Knisely, Sandra S. Strautnieks, Yvonne Meier, Bruno Stieger, Jane A. Byrne, Bernard C. Portmann, Laura N. Bull, Ludmila Pawlikowska, Banu Bilezikçi, Figen Özçay, Aranka László, László Tiszlavicz, Lynette Moore, Jeremy Raftos, Henrik Arnell, Björn Fischler, Antal Németh, Nikos Papadogiannakis, Joanna Cielecka-Kuszyk, Irena Jankowska, Joanna Pawłowska, Hector Melín-Aldana, Karan M. Emerick, Peter F. Whitington, Giorgina Mieli-Vergani and Richard J. Thompson

    Version of Record online : 26 JUL 2006, DOI: 10.1002/hep.21287

  7. Bile salt export pump deficiency: A de novo mutation in a child compound heterozygous for ABCB11. Laboratory investigation to study pathogenic role and transmission of two novel ABCB11 mutations

    Hepatology Research

    Volume 43, Issue 3, March 2013, Pages: 315–319, Paola Francalanci, Isabella Giovannoni, Manila Candusso, Emanuele Bellacchio and Francesco Callea

    Version of Record online : 26 FEB 2013, DOI: 10.1111/j.1872-034X.2012.01061.x

  8. 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

  9. Successful treatment with 4-phenylbutyrate in a patient with benign recurrent intrahepatic cholestasis type 2 refractory to biliary drainage and bilirubin absorption

    Hepatology Research

    Volume 46, Issue 2, February 2016, Pages: 192–200, Hisamitsu Hayashi, Sotaro Naoi, Yu Hirose, Yusuke Matsuzaka, Ken Tanikawa, Koji Igarashi, Hironori Nagasaka, Masayoshi Kage, Ayano Inui and Hiroyuki Kusuhara

    Version of Record online : 9 SEP 2015, DOI: 10.1111/hepr.12561

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    Retargeting of bile salt export pump and favorable outcome in children with progressive familial intrahepatic cholestasis type 2

    Hepatology

    Volume 62, Issue 1, July 2015, Pages: 198–206, Sharat Varma, Nicole Revencu, Xavier Stephenne, Isabelle Scheers, Françoise Smets, Ana Beleza-Meireles, Raymond Reding, Tania Roskams and Etienne M. Sokal

    Version of Record online : 12 MAY 2015, DOI: 10.1002/hep.27834

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    Targeted pharmacotherapy in progressive familial intrahepatic cholestasis type 2: Evidence for improvement of cholestasis with 4-phenylbutyrate

    Hepatology

    Volume 62, Issue 2, August 2015, Pages: 558–566, Emmanuel Gonzales, Brigitte Grosse, Brice Schuller, Anne Davit-Spraul, Filomena Conti, Catherine Guettier, Doris Cassio and Emmanuel Jacquemin

    Version of Record online : 8 APR 2015, DOI: 10.1002/hep.27767

  12. 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

  13. Compound heterozygous mutations of ABCB11 responsible for benign recurrent intrahepatic cholestasis

    Journal of Digestive Diseases

    Volume 16, Issue 5, May 2015, Pages: 299–302, Yang Tai, Yan Xie and Cheng Wei Tang

    Version of Record online : 28 MAY 2015, DOI: 10.1111/1751-2980.12227

  14. Paternal isodisomy of chromosome 2 in a child with bile salt export pump deficiency

    Hepatology Research

    Volume 42, Issue 3, March 2012, Pages: 327–331, Isabella Giovannoni, Alessandra Terracciano, Fabrizio Gennari, Ezio David, Paola Francalanci and Filippo M. Santorelli

    Version of Record online : 26 FEB 2012, DOI: 10.1111/j.1872-034X.2011.00925.x

  15. ABCB11 gene mutations in Chinese children with progressive intrahepatic cholestasis and low γ glutamyltransferase

    Liver International

    Volume 30, Issue 6, July 2010, Pages: 809–815, Li-Yan Liu, Zhong-Lin Wang, Xiao-Hong Wang, Qi-Rong Zhu and Jian-She Wang

    Version of Record online : 21 OCT 2009, DOI: 10.1111/j.1478-3231.2009.02112.x

  16. Prenatal diagnosis of progressive familial intrahepatic cholestasis type 2

    Journal of Gastroenterology and Hepatology

    Volume 23, Issue 9, September 2008, Pages: 1390–1393, Szu-Ta Chen, Huey-Ling Chen, Yi-Ning Su, Yu-Jung Liu, Yen-Hsuan Ni, Hong-Yuan Hsu, Chia-Shiang Chu, Nai-Yu Wang and Mei-Hwei Chang

    Version of Record online : 18 AUG 2008, DOI: 10.1111/j.1440-1746.2008.05432.x

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    Cholestasis in a patient with gallstones and a normal gamma-glutamyl transferase

    Hepatology

    Volume 57, Issue 6, June 2013, Pages: 2539–2541, Sheida Moghadamrad, Matteo Montani, Rosemarie Weimann and Andrea De Gottardi

    Version of Record online : 12 JUN 2013, DOI: 10.1002/hep.26344

  18. 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

  19. BSEP (ABCB11)

    Pharmacogenomics of Human Drug Transporters: Clinical Impacts

    Bruno Stieger, Gerd A. Kullak-Ublick, Pages: 295–309, 2013

    Published Online : 15 MAR 2013, DOI: 10.1002/9781118353240.ch13

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    Progressive familial intrahepatic cholestasis: Genetic disorders of biliary transporters

    Journal of Gastroenterology and Hepatology

    Volume 20, Issue 6, June 2005, Pages: 807–817, MATTHEW J HARRIS, DAVID G LE COUTEUR and IRWIN M ARIAS

    Version of Record online : 2 MAR 2005, DOI: 10.1111/j.1440-1746.2005.03743.x