Familial cholestasis: progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis and intrahepatic cholestasis of pregnancy.
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Primary sclerosing cholangitis: diagnosis and treatmentRecent developments in the specific dermatoses of pregnancyGenetics and Molecular Modeling of New Mutations of Familial Intrahepatic Cholestasis in a Single Italian CenterEarly Diagnosis of ABCB11 Spectrum Liver Disorders by Next Generation SequencingPregnancy and ABCB4 gene mutation: risk of recurrent cholelithiasis.Mutational analysis of ATP8B1 in patients with chronic pancreatitis.The Features of GGT in Patients with ATP8B1 or ABCB11 Deficiency Improve the Diagnostic Efficiency.ATP8B1-mediated spatial organization of Cdc42 signaling maintains singularity during enterocyte polarization.Endoscopic nasobiliary drainage improves jaundice attack symptoms in benign recurrent intrahepatic cholestasis: A case report.A perspective on efflux transport proteins in the liverUpregulation of PDZK1 by Calculus Bovis Sativus May Play an Important Role in Restoring Biliary Transport Function in Intrahepatic Cholestasis.ATP11C targets basolateral bile salt transporter proteins in mouse central hepatocytes.Benign recurrent intrahepatic cholestasis: review and long-term follow-up of five cases.Update on dermatoses of pregnancy.Effect of drug transporter pharmacogenetics on cholestasis.Autoimmune BSEP disease: disease recurrence after liver transplantation for progressive familial intrahepatic cholestasis.miR-33 controls the expression of biliary transporters, and mediates statin- and diet-induced hepatotoxicitySteroidal scaffolds as FXR and GPBAR1 ligands: from chemistry to therapeutical application.A Comprehensive Review of Progressive Familial Intrahepatic Cholestasis (PFIC): Genetic Disorders of Hepatocanalicular Transporters.Successful treatment with 4-phenylbutyrate in a patient with benign recurrent intrahepatic cholestasis type 2 refractory to biliary drainage and bilirubin absorption.Cellular localization and biochemical analysis of mammalian CDC50A, a glycosylated β-subunit for P4 ATPases.Exon-skipping and mRNA decay in human liver tissue: molecular consequences of pathogenic bile salt export pump mutations.Bile salt export pump-reactive antibodies form a polyclonal, multi-inhibitory response in antibody-induced bile salt export pump deficiency.An expanded role for heterozygous mutations of ABCB4, ABCB11, ATP8B1, ABCC2 and TJP2 in intrahepatic cholestasis of pregnancy.Benign Recurrent Intrahepatic Cholestasis in a Young Adult.Analysis of mutations of MDR3 exons 9 and 23 in infants with parenteral nutrition-associated cholestasis.Intrahepatic cholestasis in two omani siblings associated with a novel homozygous ATP8B1 mutation, c.379C>G (p.L127V).Bile salt export pump deficiency: A de novo mutation in a child compound heterozygous for ABCB11. Laboratory investigation to study pathogenic role and transmission of two novel ABCB11 mutations.Monitoring bile acid transport in single living cells using a genetically encoded Förster resonance energy transfer sensor.Treatment of pruritus with Prometheus dialysis and absorption system in a patient with benign recurrent intrahepatic cholestasis.Diagnosis and prognosis of early-onset intrahepatic cholestasis of pregnancy: a prospective study.Analysis of aberrant pre-messenger RNA splicing resulting from mutations in ATP8B1 and efficient in vitro rescue by adapted U1 small nuclear RNA.Characterization and treatment of persistent hepatocellular secretory failureDecreased gallbladder emptying in dogs with biliary sludge or gallbladder mucocele
P2860
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P2860
Familial cholestasis: progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis and intrahepatic cholestasis of pregnancy.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on October 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Familial cholestasis: progress ...... atic cholestasis of pregnancy.
@en
Familial cholestasis: progress ...... atic cholestasis of pregnancy.
@nl
type
label
Familial cholestasis: progress ...... atic cholestasis of pregnancy.
@en
Familial cholestasis: progress ...... atic cholestasis of pregnancy.
@nl
prefLabel
Familial cholestasis: progress ...... atic cholestasis of pregnancy.
@en
Familial cholestasis: progress ...... atic cholestasis of pregnancy.
@nl
P2093
P1476
Familial cholestasis: progress ...... patic cholestasis of pregnancy
@en
P2093
Janneke M Stapelbroek
Leo W J Klomp
Roderick H J Houwen
Wendy L van der Woerd
P304
P356
10.1016/J.BPG.2010.07.010
P577
2010-10-01T00:00:00Z