(Q81753891)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15898074%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

title

Intrahepatic cholestasis: summary of an American Association for the Study of Liver Diseases single-topic conference (English)

1 reference

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11 January 2020

main subject

intrahepatic cholestasis

1 reference

2

Jorge A Bezerra

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15898074%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

author name string

William F Balistreri

1

1 reference

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11 January 2020

Peter Jansen

3

1 reference

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11 January 2020

Saul J Karpen

4

1 reference

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11 January 2020

Benjamin L Shneider

5

1 reference

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11 January 2020

Frederick J Suchy

6

1 reference

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11 January 2020

language of work or name

English

0 references

publication date

1 July 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15898074%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15898074%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

volume

42

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15898074%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

issue

1

1 reference

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11 January 2020

page(s)

222-235

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11 January 2020

1 reference

7 January 2021

Intrahepatic cholestasis: order out of chaos.

1 reference

7 January 2021

Bile acid synthetic defects and liver disease: a comprehensive review

1 reference

7 January 2021

Identification of HAX-1 as a protein that binds bile salt export protein and regulates its abundance in the apical membrane of Madin-Darby canine kidney cells

1 reference

7 January 2021

Bile salt transporters: molecular characterization, function, and regulation

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7 January 2021

Mechanisms of biliary lipid secretion and their role in lipid homeostasis

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7 January 2021

Enterohepatic bile salt transporters in normal physiology and liver disease

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7 January 2021

The breast cancer resistance protein protects against a major chlorophyll-derived dietary phototoxin and protoporphyria.

1 reference

7 January 2021

Multidrug resistance-associated protein 4 is up-regulated in liver but down-regulated in kidney in obstructive cholestasis in the rat.

1 reference

7 January 2021

Cellular localization and up-regulation of multidrug resistance-associated protein 3 in hepatocytes and cholangiocytes during obstructive cholestasis in rat liver

1 reference

7 January 2021

Differential Ontogenic Regulation of Basolateral and Canalicular Bile Acid Transport Proteins in Rat Liver

1 reference

7 January 2021

Nuclear receptors and lipid physiology: opening the X-files

1 reference

7 January 2021

Multiple mechanisms of ontogenic regulation of nuclear receptors during rat liver development

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7 January 2021

Ligand-dependent activation of the farnesoid X-receptor directs arginine methylation of histone H3 by CARM1

1 reference

7 January 2021

A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis

1 reference

7 January 2021

A missense mutation in FIC1 is associated with greenland familial cholestasis

1 reference

7 January 2021

A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis

1 reference

7 January 2021

Sequence analysis of bile salt export pump (ABCB11) and multidrug resistance p-glycoprotein 3 (ABCB4, MDR3) in patients with intrahepatic cholestasis of pregnancy

1 reference

7 January 2021

Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11

1 reference

7 January 2021

The wide spectrum of multidrug resistance 3 deficiency: from neonatal cholestasis to cirrhosis of adulthood

1 reference

7 January 2021

A multidrug resistance 3 gene mutation causing cholelithiasis, cholestasis of pregnancy, and adulthood biliary cirrhosis

1 reference

7 January 2021

Mutations in the MDR 3 gene cause progressive familial intrahepatic cholestasis

1 reference

7 January 2021

SRD5B1 (AKR1D1) gene analysis in delta(4)-3-oxosteroid 5beta-reductase deficiency: evidence for primary genetic defect

1 reference

7 January 2021

Molecular genetics of 3beta-hydroxy-Delta5-C27-steroid oxidoreductase deficiency in 16 patients with loss of bile acid synthesis and liver disease

1 reference

7 January 2021

Identification of a new inborn error in bile acid synthesis: mutation of the oxysterol 7alpha-hydroxylase gene causes severe neonatal liver disease

1 reference

7 January 2021

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

1 reference

7 January 2021

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

1 reference

7 January 2021

Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT.

1 reference

7 January 2021

Hepatic basolateral sodium-dependent-bile acid transporter expression in two unusual cases of hypercholanemia and in extrahepatic biliary atresia

1 reference

7 January 2021

Inhibition of human m-epoxide hydrolase gene expression in a case of hypercholanemia

1 reference

7 January 2021

A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome

1 reference

7 January 2021

Copper-induced apical trafficking of ATP7B in polarized hepatoma cells provides a mechanism for biliary copper excretion

1 reference

7 January 2021

Claudin-1 gene mutations in neonatal sclerosing cholangitis associated with ichthyosis: a tight junction disease

1 reference

7 January 2021

A missense mutation (R565W) in cirhin (FLJ14728) in North American Indian childhood cirrhosis

1 reference

7 January 2021

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

1 reference

7 January 2021

The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein

1 reference

7 January 2021

Polyductin, the PKHD1 gene product, comprises isoforms expressed in plasma membrane, primary cilium, and cytoplasm

1 reference

7 January 2021

Biliary dysgenesis in the PCK rat, an orthologous model of autosomal recessive polycystic kidney disease

1 reference

7 January 2021

Molecular characterization of hepatocystin, the protein that is defective in autosomal dominant polycystic liver disease.

1 reference

7 January 2021

Abnormal hepatocystin caused by truncating PRKCSH mutations leads to autosomal dominant polycystic liver disease

1 reference

7 January 2021

Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome

1 reference

7 January 2021

Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC-1] and Byler syndrome): evidence for heterogeneity

1 reference

7 January 2021

Characterization of mutations in ATP8B1 associated with hereditary cholestasis

1 reference

7 January 2021

FIC1 disease: a spectrum of intrahepatic cholestatic disorders

1 reference

7 January 2021

A mouse genetic model for familial cholestasis caused by ATP8B1 mutations reveals perturbed bile salt homeostasis but no impairment in bile secretion

1 reference

7 January 2021

Surgical treatment of progressive familial intrahepatic cholestasis: comparison of partial external biliary diversion and ileal bypass

1 reference

7 January 2021

Functional expression of the canalicular bile salt export pump of human liver

1 reference

7 January 2021

Severe cholestasis induced by cholic acid feeding in knockout mice of sister of P-glycoprotein

1 reference

7 January 2021

Homozygous disruption of the murine mdr2 P-glycoprotein gene leads to a complete absence of phospholipid from bile and to liver disease

1 reference

7 January 2021

Progressive familial intrahepatic cholestasis. Genetic basis and treatment

1 reference

7 January 2021

Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases

1 reference

7 January 2021

Jagged1 mutations in alagille syndrome

1 reference

7 January 2021

Mutational analysis of the Jagged 1 gene in Alagille syndrome families

1 reference

7 January 2021

Familial Tetralogy of Fallot caused by mutation in the jagged1 gene

1 reference

7 January 2021

Conditional JAG1 mutation shows the developing heart is more sensitive than developing liver to JAG1 dosage

1 reference

7 January 2021

Inhibition of Jagged-mediated Notch signaling disrupts zebrafish biliary development and generates multi-organ defects compatible with an Alagille syndrome phenocopy

1 reference

7 January 2021

Conversion of biliary system to pancreatic tissue in Hes1-deficient mice

1 reference

7 January 2021

The mouse Forkhead Box m1 transcription factor is essential for hepatoblast mitosis and development of intrahepatic bile ducts and vessels during liver morphogenesis

1 reference

7 January 2021

Transcriptional reprogramming in murine liver defines the physiologic consequences of biliary obstruction

1 reference

7 January 2021

Genetic induction of proinflammatory immunity in children with biliary atresia

1 reference

7 January 2021

Obstruction of extrahepatic bile ducts by lymphocytes is regulated by IFN-gamma in experimental biliary atresia

1 reference

7 January 2021

Biliary atresia and Th1 function: linking lymphocytes and bile ducts: commentary on the article by Mack et al. on page 79.

1 reference

7 January 2021

Biochemistry of arsenic detoxification

1 reference

7 January 2021

Transport and detoxification systems for transition metals, heavy metals and metalloids in eukaryotic and prokaryotic microbes.

1 reference

7 January 2021

Structure-function analysis of the ArsA ATPase: contribution of histidine residues.

1 reference

7 January 2021

Arsenate transport and reduction in the hyper-tolerant fungus Aspergillus sp. P37.

1 reference

7 January 2021

Arsenite transport by mammalian aquaglyceroporins AQP7 and AQP9.

1 reference

7 January 2021

Arsenic trioxide uptake by human and rat aquaglyceroporins

1 reference

7 January 2021

Liver injury in the setting of steatosis: crosstalk between adipokine and cytokine

1 reference

7 January 2021

Liver fibrosis: signals leading to the amplification of the fibrogenic hepatic stellate cell

1 reference

7 January 2021

Enhanced carbon tetrachloride-induced liver fibrosis in mice lacking adiponectin

1 reference

7 January 2021

Adiponectin protects LPS-induced liver injury through modulation of TNF-alpha in KK-Ay obese mice

1 reference

7 January 2021

The enzymes, regulation, and genetics of bile acid synthesis

1 reference

7 January 2021

Delta 4-3-oxosteroid 5 beta-reductase deficiency described in identical twins with neonatal hepatitis. A new inborn error in bile acid synthesis

1 reference

7 January 2021

Liver disease caused by failure to racemize trihydroxycholestanoic acid: gene mutation and effect of bile acid therapy

1 reference

7 January 2021

Mutations in the sterol 27-hydroxylase gene (CYP27A) cause hepatitis of infancy as well as cerebrotendinous xanthomatosis.

1 reference

7 January 2021

Bile acid regulation of hepatic physiology: IV. Bile acids and death receptors

1 reference

7 January 2021

Kupffer cell engulfment of apoptotic bodies stimulates death ligand and cytokine expression

1 reference

7 January 2021

Apoptosis: the nexus of liver injury and fibrosis.

1 reference

7 January 2021

RNA interference targeting Fas protects mice from fulminant hepatitis

1 reference

7 January 2021

The Caspase Inhibitor IDN-6556 Attenuates Hepatic Injury and Fibrosis in the Bile Duct Ligated Mouse

1 reference

7 January 2021

First clinical trial of a novel caspase inhibitor: anti-apoptotic caspase inhibitor, IDN-6556, improves liver enzymes.

1 reference

7 January 2021

Nuclear receptor regulation of hepatic function

1 reference

7 January 2021

Identification of a nuclear receptor for bile acids

1 reference

7 January 2021

Bile acids: natural ligands for an orphan nuclear receptor

1 reference

7 January 2021

Progressive familial intrahepatic cholestasis, type 1, is associated with decreased farnesoid X receptor activity

1 reference

7 January 2021

Endotoxin leads to rapid subcellular re-localization of hepatic RXRalpha: A novel mechanism for reduced hepatic gene expression in inflammation

1 reference

7 January 2021

Hepatoprotection by the farnesoid X receptor agonist GW4064 in rat models of intra- and extrahepatic cholestasis

1 reference

7 January 2021

The nuclear receptor CAR mediates specific xenobiotic induction of drug metabolism

1 reference

7 January 2021

Mapping of the locus for cholestasis-lymphedema syndrome (Aagenaes syndrome) to a 6.6-cM interval on chromosome 15q

1 reference

7 January 2021

A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13

1 reference

7 January 2021

Identifiers

DOI

10.1002/HEP.20729

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15898074%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

1 reference