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Cited by in CrossRef
For: Sun HZ, Shi H, Zhang SC, Shen XZ. Novel mutation in a Chinese patient with progressive familial intrahepatic cholestasis type 3. World J Gastroenterol 2015; 21(2): 699-703 [PMID: 25593501 DOI: 10.3748/wjg.v21.i2.699]
URL: https://www.wjgnet.com/1007-9327/full/v21/i2/699.htm
Number Citing Articles
1
雅萍 赵. Effects of Combined Treatment with Transmentil and Ursofalk on Liver Function and Perinatal Prognosis in Pregnant Women with Intrahepatic Cholestasis of PregnancyNursing Science 2019; 8(06): 404 doi: 10.12677/NS.2019.86074
2
Fei Qiao, Feng Ren, Weiting Lu, Haoran Yang, Guiling Mo, Shuangshuang Wang, Lina Liu, Xiangtao Xu. A female of progressive familial intrahepatic cholestasis type 3 caused by heterozygous mutations of ABCB4 gene and her cirrhosis improved after treatment of ursodeoxycholic acid: a case reportBMC Medical Genomics 2023; 16(1) doi: 10.1186/s12920-023-01602-y
3
Mona Fathy, Manal Kamal, Marwa Al-Sharkawy, Hanaa Al-Karaksy, Nora Hassan. Molecular characterization of exons 6, 8 and 9 of ABCB4 gene in children with Progressive Familial Intrahepatic Cholestasis type 3Biomarkers 2016; 21(7): 573 doi: 10.3109/1354750X.2016.1166264
4
Zhaoyue Wang, Fan Yang, Jianshe Wang, Xiong Ma. A Novel Mutation of ABCB4 in Progressive Familial Intrahepatic Cholestasis 3Journal of Clinical Gastroenterology 2016; 50(4): 353 doi: 10.1097/MCG.0000000000000474
5
Kan He, Lining Cai, Qin Shi, Hao Liu, Thomas F. Woolf. Inhibition of MDR3 Activity in Human Hepatocytes by Drugs Associated with Liver InjuryChemical Research in Toxicology 2015; 28(10): 1987 doi: 10.1021/acs.chemrestox.5b00201
6
Zhenping Wu, Siying Zhang, Lunli Zhang, Ming Li. Novel ABCB4 mutation in a Chinese female patient with progressive familial intrahepatic cholestasis type 3: a case reportDiagnostic Pathology 2020; 15(1) doi: 10.1186/s13000-020-00955-7
7
Rong Chen, Feng-Xia Yang, Yan-Fang Tan, Mei Deng, Hua Li, Yi Xu, Wen-Xian Ouyang, Yuan-Zong Song. Clinical and genetic characterization of pediatric patients with progressive familial intrahepatic cholestasis type 3 (PFIC3): identification of 14 novel ABCB4 variants and review of the literaturesOrphanet Journal of Rare Diseases 2022; 17(1) doi: 10.1186/s13023-022-02597-y