Ursodeoxycholic Acid

ATP binding cassette subfamily B member 4 ; Homo sapiens







12 Article(s)
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Pub. Year
#Total Relationships
1 33915153 ATP8B1, ABCB11, and ABCB4 Genes Defects: Novel Mutations Associated with Cholestasis with Different Phenotypes and Outcomes. 2021 Sep 1
2 34098996 Maternal bile acid profile and subtype analysis of intrahepatic cholestasis of pregnancy. 2021 Jun 7 1
3 30449124 Expanding the mutational spectrum of the ABCB4 gene in inherited adult cholestatic liver disorders with four novel pathogenic variants. 2019 Jan 1
4 26256905 Reversal of advanced fibrosis after long-term ursodeoxycholic acid therapy in a patient with residual expression of MDR3. 2015 Sep-Oct 1
5 25544413 LPAC syndrome associated with deletion of the full exon 4 in a ABCB4 genetic mutation in a patient with hepatitis C. 2014 Dec 4
6 24034919 [Effects of ursodeoxycholic acid on mRNA expression of MDR3 and FXR in infants with cholestatic hepatitis]. 2013 Sep 3
7 22343912 Chinese children with chronic intrahepatic cholestasis and high γ-glutamyl transpeptidase: clinical features and association with ABCB4 mutations. 2012 Aug 1
8 21119540 Clinical features and genotype-phenotype correlations in children with progressive familial intrahepatic cholestasis type 3 related to ABCB4 mutations. 2011 Jan 1
9 20034695 Liver disease associated with canalicular transport defects: current and future therapies. 2010 Feb 1
10 19273348 Liver diseases related to MDR3 (ABCB4) gene deficiency. 2009 Jan 1 8
11 17786139 MDR3 mutations associated with intrahepatic and gallbladder cholesterol cholelithiasis: an update. 2007 Jul-Sep 1
12 11745043 Role of multidrug resistance 3 deficiency in pediatric and adult liver disease: one gene for three diseases. 2001 Nov 1