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Aug 7, 2017 (publication date) through Oct 12, 2025
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Publication Name
World Journal of Gastroenterology
ISSN
1007-9327
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | 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. Partial external biliary diversion in bile salt export pump deficiency: Association between outcome and mutation. World J Gastroenterol 2017; 23(29): 5295-5303 [PMID: 28839429 DOI: 10.3748/wjg.v23.i29.5295] |
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| URL: | https://www.wjgnet.com/1007-9327/full/v23/i29/5295.htm |
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Tim Kroll, Martin Prescher, Sander H. J. Smits, Lutz Schmitt. Structure and Function of Hepatobiliary ATP Binding Cassette Transporters. Chemical Reviews 2021; 121(9): 5240 doi: 10.1021/acs.chemrev.0c00659
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Henkjan J. Verkade, Antonia Felzen, Verena Keitel, Richard Thompson, Emmanuel Gonzales, Pavel Strnad, Binita Kamath, Saskia van Mil. EASL Clinical Practice Guidelines on genetic cholestatic liver diseases. Journal of Hepatology 2024; 81(2): 303 doi: 10.1016/j.jhep.2024.04.006
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Beatriz Mínguez Rodríguez, Cristina Molera Busoms, Loreto Martorell Sampol, Ruth García Romero, Gemma Colomé Rivero, Javier Martín de Carpi. Heterozygous mutations of ATP8B1, ABCB11 and ABCB4 cause mild forms of Progressive Familial Intrahepatic Cholestasis in a pediatric cohort. Gastroenterología y Hepatología (English Edition) 2022; 45(8): 585 doi: 10.1016/j.gastre.2021.12.004
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Mark Nomden, Folkert Kuipers, Willem S. Lexmond, Tao Gu, Velichka Valcheva, Erik Lindström, Henkjan J. Verkade. Pretreatment serum bile acid composition and predictability of subsequent response to odevixibat in patients with bile salt export pump (BSEP) deficiency. Hepatology 2025; doi: 10.1097/HEP.0000000000001430
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Sarah AF Henkel, Judy H Squires, Mary Ayers, Armando Ganoza, Patrick Mckiernan, James E Squires. Expanding etiology of progressive familial intrahepatic cholestasis. World Journal of Hepatology 2019; 11(5): 450-463 doi: 10.4254/wjh.v11.i5.450
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Genotype correlates with the natural history of severe bile salt export pump deficiency. Journal of Hepatology 2020; 73(1): 84 doi: 10.1016/j.jhep.2020.02.007
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Christoph G.W. Gertzen, Holger Gohlke, Dieter Häussinger, Diran Herebian, Verena Keitel, Ralf Kubitz, Ertan Mayatepek, Lutz Schmitt. The many facets of bile acids in the physiology and pathophysiology of the human liver. Biological Chemistry 2021; 402(9): 1047 doi: 10.1515/hsz-2021-0156
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Beatriz Mínguez Rodríguez, Cristina Molera Busoms, Loreto Martorell Sampol, Ruth García Romero, Gemma Colomé Rivero, Javier Martín de Carpi. Heterozygous mutations of ATP8B1, ABCB11 and ABCB4 cause mild forms of Progressive Familial Intrahepatic Cholestasis in a pediatric cohort. Gastroenterología y Hepatología 2022; 45(8): 585 doi: 10.1016/j.gastrohep.2021.12.005
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Willemien F.J. Hof, Jan Freark de Boer, Henkjan J. Verkade. Emerging drugs for the treatment of progressive familial intrahepatic cholestasis: a focus on phase II and III trials. Expert Opinion on Emerging Drugs 2024; 29(3): 305 doi: 10.1080/14728214.2024.2336986
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Xiaoyang Lu, Lin Liu, Wenya Shan, Limin Kong, Na Chen, Yan Lou, Su Zeng. The Role of the Sodium-taurocholate Co-transporting Polypeptide (NTCP) and Bile Salt Export Pump (BSEP) in Related Liver Disease. Current Drug Metabolism 2019; 20(5): 377 doi: 10.2174/1389200220666190426152830
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Muhammad Imran Sohail, Yaprak Dönmez-Cakil, Dániel Szöllősi, Thomas Stockner, Peter Chiba. The Bile Salt Export Pump: Molecular Structure, Study Models and Small-Molecule Drugs for the Treatment of Inherited BSEP Deficiencies. International Journal of Molecular Sciences 2021; 22(2): 784 doi: 10.3390/ijms22020784
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