Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene. - Wikidata - awgldk - TriplyDB

Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene.

Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene.

http://www.wikidata.org/entity/Q34323617

about

Zebrafish: an important tool for liver disease research Pathogenesis of biliary atresia: defining biology to understand clinical phenotypes Elevated glypican-1 expression is associated with an unfavorable prognosis in pancreatic ductal adenocarcinoma.Recent advances in the pathogenesis and management of biliary atresia The Role of ARF6 in Biliary Atresia.Alagille Syndrome Mimicking Biliary Atresia in Early Infancy.Methylation Microarray Studies Highlight PDGFA Expression as a Factor in Biliary Atresia Identification and expression analysis of zebrafish glypicans during embryonic development.Replication of a GWAS signal in a Caucasian population implicates ADD3 in susceptibility to biliary atresia.Association between rs17095355 polymorphism on 10q24 and susceptibility to biliary atresia: a meta-analysis.Genome-wide association studies in biliary atresia.Alterations in mandibular morphology associated with glypican 1 and glypican 3 gene mutations.Achondroplasia and Biliary Atresia: A Rare Association and Review of Literature.Loss of a Candidate Biliary Atresia Susceptibility Gene, add3a, Causes Biliary Developmental Defects in Zebrafish.Loss of cilia causes embryonic lung hypoplasia, liver fibrosis, and cholestasis in the talpid3 ciliopathy mutant.The Sea Lamprey as an Etiological Model for Biliary Atresia.Newborn screening for biliary atresia in the United States.Association of polymorphism in the VEGFA gene 3'-UTR +936T/C with susceptibility to biliary atresia in a Southern Chinese Han population.EVI1 modulates oncogenic role of GPC1 in pancreatic carcinogenesis.Hedgehog signalling in liver pathophysiology.Embryonic cholecystitis and defective gallbladder contraction in the Sox17-haploinsufficient mouse model of biliary atresia.Using zebrafish to model liver diseases-Where do we stand?BILIARY ATRESIA: Clinical and Research Challenges for the 21st Century.Aortic coarctation and carotid artery aneurysm in a patient with Hardikar syndrome: Cardiovascular implications for affected individuals.A patient with Simpson-Golabi-Behmel syndrome, biliary cirrhosis and successful liver transplantation.A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1

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Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene.

http://www.wikidata.org/entity/Q34323617

description

2013 nî lūn-bûn

@nan

2013 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի հունվարին հրատարակված գիտական հոդված

@hy

2013年の論文

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2013年論文

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2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

name

Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene.

@ast

Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene.

@en

Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene.

@nl

type

label

Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene.

@ast

Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene.

@en

Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene.

@nl

prefLabel

Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene.

@ast

Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene.

@en

Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene.

@nl

P1433

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P356

J.GASTRO.2013.01.022

P1433

Gastroenterology

P1476

Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene

@en

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Barbara A Haber

http://www.w3.org/2001/XMLSchema#string

Ellen A Tsai

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Hakon Hakonarson

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Melissa Leyva-Vega

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Nancy B Spinner

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Randolph P Matthews

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Shuang Cui

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P2860

Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization

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

Pregnancy-specific glycoprotein 1 induces endothelial tubulogenesis through interaction with cell surface proteoglycans

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

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants

A genome-wide association study of autism reveals a common novel risk locus at 5p14.1

Haploinsufficiency of the mouse Forkhead Box f1 gene causes defects in gall bladder development

Glypican-3 modulates BMP- and FGF-mediated effects during renal branching morphogenesis

Glypican-3 inhibits Hedgehog signaling during development by competing with patched for Hedgehog binding

P304

1107-1115.e3

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scholarly article

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10.1053/J.GASTRO.2013.01.022

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P433

5

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144

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Marcella Devoto

Joseph Glessner

Steven F Eauclaire

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2013-01-18T00:00:00Z

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234822273

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23336978

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3736559

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