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Cited by in CrossRef
For: Deng BC, Lv S, Cui W, Zhao R, Lu X, Wu J, Liu P. Novel ATP8B1 mutation in an adult male with progressive familial intrahepatic cholestasis. World J Gastroenterol 2012; 18(44): 6504-6509 [PMID: 23197899 DOI: 10.3748/wjg.v18.i44.6504]
URL: https://www.wjgnet.com/1007-9327/full/v18/i44/6504.htm
Number Citing Articles
1
Hamoud Alhebbi, Abdul Ali Peer-Zada, Abdulrahman A. Al‐Hussaini, Sara Algubaisi, Awad Albassami, Nasser AlMasri, Yasir Alrusayni, Ibrahim M. Alruzug, Essa Alharby, Manar A. Samman, Syed Zubair Ayoub, Sateesh Maddirevula, Roy W. A. Peake, Fowzan S. Alkuraya, Sami Wali, Naif A. M. Almontashiri. New paradigms of USP53 disease: normal GGT cholestasis, BRIC, cholangiopathy, and responsiveness to rifampicinJournal of Human Genetics 2021; 66(2): 151 doi: 10.1038/s10038-020-0811-1
2
Thibaud Dieudonné, Sara Abad Herrera, Michelle Juknaviciute Laursen, Maylis Lejeune, Charlott Stock, Kahina Slimani, Christine Jaxel, Joseph A Lyons, Cédric Montigny, Thomas Günther Pomorski, Poul Nissen, Guillaume Lenoir. Autoinhibition and regulation by phosphoinositides of ATP8B1, a human lipid flippase associated with intrahepatic cholestatic disorderseLife 2022; 11 doi: 10.7554/eLife.75272
3
José M. Hermosillo-Sandoval, Adolfo D. Rodríguez-Carrizález, Alejandra G. Miranda-Díaz. Strategies in secondary biliary fibrosisJournal of Biomedical Science and Engineering 2013; 6(08): 10 doi: 10.4236/jbise.2013.68A2002
4
Saleh Althenayyan, Amal AlGhamdi, Mohammed H. AlMuhanna, Esra Hawsa, Dalal Aldeghaither, Jahangir Iqbal, Sameer Mohammad, Mohammad A. Aziz. Modulation of ATP8B1 Gene Expression in Colorectal Cancer Cells Suggest its Role as a Tumor SuppressorCurrent Cancer Drug Targets 2022; 22(7): 577 doi: 10.2174/1568009622666220517092340
5
Eun Sang Rhee, Yu Bin Kim, Sunghee Lee, Seak Hee Oh, Beom Hee Lee, Kyung Mo Kim, Han-Wook Yoo. NovelATP8B1Gene Mutations in a Child with Progressive Familial Intrahepatic Cholestasis Type 1Pediatric Gastroenterology, Hepatology & Nutrition 2019; 22(5): 479 doi: 10.5223/pghn.2019.22.5.479