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Epidermal growth factor receptor and HER-3 restrict cell response to sorafenib in hepatocellular carcinoma cells

Journal of hepatology, 2012-07, Vol.57 (1), p.108-115

2012

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Characterization of a novel ABCC2 mutation in infantile Dubin Johnson syndrome

Clinica chimica acta, 2021-07, Vol.518, p.43-50

2021

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Portal myofibroblasts promote vascular remodeling underlying cirrhosis formation through the release of microparticles

Hepatology (Baltimore, Md.), 2015-03, Vol.61 (3), p.1041-1055

2015

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Dubin-Johnson syndrome and intrahepatic cholestasis of pregnancy in a Sri Lankan family: a case report

BMC research notes, 2017-09, Vol.10 (1), p.487-487, Article 487

2017

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Genotype‐phenotype relationships in the low‐phospholipid‐associated cholelithiasis syndrome: A study of 156 consecutive patients

Hepatology (Baltimore, Md.), 2013-09, Vol.58 (3), p.1105-1110

2013

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Correction to: Dubin-Johnson syndrome and intrahepatic cholestasis of pregnancy in a Sri Lankan family: a case report

BMC research notes, 2017-10, Vol.10 (1), p.492-492, Article 492

2017

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Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome

Nature genetics, 2005-09, Vol.37 (9), p.1003-1007

2005

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A homozygous ABCB4 mutation causing an LPAC syndrome evolves into cholangiocarcinoma

Clinica chimica acta, 2019-08, Vol.495, p.598-605

2019

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W1858 A Novel ABCB4 Mutation Associated with Cholelithiasis and Contraceptive Pill Related Cholestasis

Gastroenterology (New York, N.Y. 1943), 2008, Vol.134 (4), p.A-839-A-839

2008

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Genetic contribution of ABCC2 to Dubin‐Johnson syndrome and inherited cholestatic disorders

Liver international, 2020-01, Vol.40 (1), p.163-174

2020

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Phenotypic variability in Tunisian PFIC3 patients harboring a complex genotype with a differential clinical outcome of UDCA treatment

Clinica chimica acta, 2018-11, Vol.486, p.122-128

2018

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Functional defect of variants in the adenosine triphosphate–binding sites of ABCB4 and their rescue by the cystic fibrosis transmembrane conductance regulator potentiator, ivacaftor (VX‐770)

Hepatology (Baltimore, Md.), 2017-02, Vol.65 (2), p.560-570

2017

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Genetic factors of susceptibility and of severity in primary biliary cirrhosis

Journal of hepatology, 2008-12, Vol.49 (6), p.1038-1045

2008

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Low-phospholipid-associated cholelithiasis syndrome: Prevalence, clinical features, and comorbidities

JHEP reports, 2021-04, Vol.3 (2), p.100201-100201, Article 100201

2021

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LPAC syndrome associated with deletion of the full exon 4 in a ABCB4 genetic mutation in a patient with hepatitis C

Revista española de enfermedades digestivas, 2014-12, Vol.106 (8), p.544-547

2014

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NF-κB transcription factor induces drug resistance through MDR1 expression in cancer cells

Oncogene, 2003-01, Vol.22 (1), p.90-97

2003

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Nationwide French Study of RET Variants Detected from 2003 to 2013 Suggests a Possible Influence of Polymorphisms as Modifiers

Thyroid (New York, N.Y.), 2017-12, Vol.27 (12), p.1511-1522

2017

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Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders

Blood, 2006-07, Vol.108 (1), p.346-352

2006

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ABCB4 variant is associated with hepatobiliary MR abnormalities in people with low-phospholipid-associated cholelithiasis syndrome

JHEP reports, 2022-11, Vol.4 (11), p.100590, Article 100590

2022

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ABCB4 Heterozygous Gene Mutations Associated With Fibrosing Cholestatic Liver Disease in Adults

Gastroenterology (New York, N.Y. 1943), 2008-07, Vol.135 (1), p.131-141

2008

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Defects in Gallbladder Emptying and Bile Acid Homeostasis in Mice With Cystic Fibrosis Transmembrane Conductance Regulator Deficiencies

Gastroenterology (New York, N.Y. 1943), 2012-06, Vol.142 (7), p.1581-1591.e6

2012

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Comparison of in silico prediction and experimental assessment of ABCB4 variants identified in patients with biliary diseases

The international journal of biochemistry & cell biology, 2017-08, Vol.89, p.101-109

2017

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Aspects of liver pathology in adult patients with MDR3/ABCB4 gene mutations

Virchows Archiv : an international journal of pathology, 2012-03, Vol.460 (3), p.291-298

2012

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Phosphorylation of ABCB4 impacts its function: Insights from disease‐causing mutations

Hepatology (Baltimore, Md.), 2014-08, Vol.60 (2), p.610-621

2014

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Connecting dysbiosis, bile-acid dysmetabolism and gut inflammation in inflammatory bowel diseases

Epidermal growth factor receptor and HER-3 restrict cell response to sorafenib in hepatocellular carcinoma cells

Characterization of a novel ABCC2 mutation in infantile Dubin Johnson syndrome

Portal myofibroblasts promote vascular remodeling underlying cirrhosis formation through the release of microparticles

Dubin-Johnson syndrome and intrahepatic cholestasis of pregnancy in a Sri Lankan family: a case report

Genotype‐phenotype relationships in the low‐phospholipid‐associated cholelithiasis syndrome: A study of 156 consecutive patients

Correction to: Dubin-Johnson syndrome and intrahepatic cholestasis of pregnancy in a Sri Lankan family: a case report

Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome

A homozygous ABCB4 mutation causing an LPAC syndrome evolves into cholangiocarcinoma

W1858 A Novel ABCB4 Mutation Associated with Cholelithiasis and Contraceptive Pill Related Cholestasis

Genetic contribution of ABCC2 to Dubin‐Johnson syndrome and inherited cholestatic disorders

Phenotypic variability in Tunisian PFIC3 patients harboring a complex genotype with a differential clinical outcome of UDCA treatment

Functional defect of variants in the adenosine triphosphate–binding sites of ABCB4 and their rescue by the cystic fibrosis transmembrane conductance regulator potentiator, ivacaftor (VX‐770)

Genetic factors of susceptibility and of severity in primary biliary cirrhosis

Low-phospholipid-associated cholelithiasis syndrome: Prevalence, clinical features, and comorbidities

LPAC syndrome associated with deletion of the full exon 4 in a ABCB4 genetic mutation in a patient with hepatitis C

NF-κB transcription factor induces drug resistance through MDR1 expression in cancer cells

Nationwide French Study of RET Variants Detected from 2003 to 2013 Suggests a Possible Influence of Polymorphisms as Modifiers

Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders

ABCB4 variant is associated with hepatobiliary MR abnormalities in people with low-phospholipid-associated cholelithiasis syndrome

ABCB4 Heterozygous Gene Mutations Associated With Fibrosing Cholestatic Liver Disease in Adults

Defects in Gallbladder Emptying and Bile Acid Homeostasis in Mice With Cystic Fibrosis Transmembrane Conductance Regulator Deficiencies

Comparison of in silico prediction and experimental assessment of ABCB4 variants identified in patients with biliary diseases

Aspects of liver pathology in adult patients with MDR3/ABCB4 gene mutations

Phosphorylation of ABCB4 impacts its function: Insights from disease‐causing mutations

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