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Cited by in CrossRef
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]
URL: https://www.wjgnet.com/1007-9327/full/v23/i29/5295.htm
Number Citing Articles
1
Sarah AF Henkel, Judy H Squires, Mary Ayers, Armando Ganoza, Patrick Mckiernan, James E Squires. Expanding etiology of progressive familial intrahepatic cholestasisWorld Journal of Hepatology 2019; 11(5): 450-463 doi: 10.4254/wjh.v11.i5.450
2
Genotype correlates with the natural history of severe bile salt export pump deficiencyJournal of Hepatology 2020; 73(1): 84 doi: 10.1016/j.jhep.2020.02.007
3
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 liverBiological Chemistry 2021; 402(9): 1047 doi: 10.1515/hsz-2021-0156
4
Tim Kroll, Martin Prescher, Sander H. J. Smits, Lutz Schmitt. Structure and Function of Hepatobiliary ATP Binding Cassette TransportersChemical Reviews 2021; 121(9): 5240 doi: 10.1021/acs.chemrev.0c00659
5
Meng-yu Zhang, Jie-ping Wang, Kai He, Xian-ming Xia. Bsep expression in hilar cholangiocarcinoma of rat modelScientific Reports 2021; 11(1) doi: 10.1038/s41598-021-82636-z
6
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 cohortGastroenterología y Hepatología 2022; 45(8): 585 doi: 10.1016/j.gastrohep.2021.12.005
7
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 trialsExpert Opinion on Emerging Drugs 2024;  doi: 10.1080/14728214.2024.2336986
8
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 cohortGastroenterología y Hepatología (English Edition) 2022; 45(8): 585 doi: 10.1016/j.gastre.2021.12.004
9
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 DiseaseCurrent Drug Metabolism 2019; 20(5): 377 doi: 10.2174/1389200220666190426152830
10
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 DeficienciesInternational Journal of Molecular Sciences 2021; 22(2): 784 doi: 10.3390/ijms22020784