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Study Search Results Table
Title
PMID
PMCID
Public Release Type
Publication Year
DOI
Study Acronym
Request ID(s)
Public Release Origin
A genome-wide association study identifies THBS2 as a candidate modifier of liver disease severity in Alagille syndromeConference Presentation2014PROBEContributing Study
A molecular signature of biliary atresia highly distinct from other cholestatic diseases at diagnosisConference Presentation2011PROBEContributing Study
A multi-center analysis of outcome at 24 months of age in children with biliary atresia in the United StatesConference Presentation2004PROBEContributing Study
A multi-institutional study of interobserver agreement on the histologic diagnosis of biliary obstruction in liver biopsies of cholestatic infants less than six months of ageConference Presentation2006BARC, PROBEContributing Study
A multicenter study of the outcome of biliary atresia in the United States, 1997 to 2000.16647406Journal200610.1016/j.jpeds.2005.12.054BARC, PROBEContributing Study
A new defect in beta-oxidation presenting as sudden liver failureConference Presentation2005PROBEContributing Study
A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiencyConference Presentation2005PROBEContributing Study
A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency.17564966PMC1950923Journal200710.1086/519219PROBEContributing Study
A prospective multi-centered investigation of vitamin supplementation in infants with biliary atresia: interim analysis from the Biliary Atresia Research Consortium (BARC)Conference Presentation2009PROBEContributing Study
A toxin that induces biliary atresia causes disruption of microtubules and loss of primary ciliaConference Presentation2012PROBEContributing Study
Acyl-CoA dehydrogenases: Dynamic history of protein family evolution.19639238PMC4136416Journal200910.1007/s00239-009-9263-0PROBEContributing Study
Analysis of gene mutations in children with cholestasis of undefined etiology.20683201PMC4090691Journal201010.1097/MPG.0b013e3181dffe8fPROBEContributing Study
Baseline Analysis of a Young α-1-Antitrypsin Deficiency Liver Disease Cohort Reveals Frequent Portal Hypertension.25651489PMC4692167Journal201510.1097/MPG.0000000000000753PROBE, LOGICContributing Study
Baseline Ultrasound and Clinical Correlates in Children with Cystic Fibrosis.26254836PMC4586395Journal201510.1016/j.jpeds.2015.06.062PROBEContributing Study
Baseline analysis of the largest reported cohort of children and young adults with Alpha-1-Antitrypsin deficiency liver disease reveals a significant burden of portal hypertension without jaundiceConference Presentation2012PROBEContributing Study
Bile salt kinetics in children with genetic cholestasis and bile diversion therapyConference Presentation2012PROBEContributing Study
Biliary Atresia Research Consortium (BARC).15057888Journal200410.1002/hep.20185BARC, PROBEContributing Study
Biliary Atresia Research Consortium (BARC): NIH-funded network to advance knowledge and improve care and outcomes in biliary atresiaConference Presentation2006BARC, PROBEContributing Study
Biliary atresia screening: why, when, and how?19403487PMC3881183Journal200910.1542/peds.2008-3108PROBEContributing Study
Biliary atresia: will blocking inflammation tame the disease?21226614PMC4096311Journal201110.1146/annurev-med-042909-093734PROBEContributing Study
Childhood Liver Disease Research and Education Network (ChiLDREN)Conference Presentation2010PROBEContributing Study
Cholangiocyte cilia are abnormal in syndromic and non-syndromic biliary atresia.22301700PMC3341539Journal201210.1038/modpathol.2011.212PROBEContributing Study
Circulating microRNA is a biomarker of biliary atresia.22732895PMC3459263Journal201210.1097/MPG.0b013e318264e648PROBEContributing Study
Clinical and demographic features of three major biliary atresia phenotypes in the BARC studyConference Presentation2008BARC, PROBEContributing Study
Clinical research for rare disease: opportunities, challenges, and solutions.19013090PMC3134795Journal200910.1016/j.ymgme.2008.10.003PROBEContributing Study
Clues to the etiology of bile duct injury in biliary atresia.23397531PMC3827890Journal201210.1055/s-0032-1329899PROBEContributing Study
Cross sectional assessment of Quality of Life in biliary atresia patients ages 2-25 yearsConference Presentation2009BARC, PROBEContributing Study
Cross-sectional multi-center analysis of portal hypertension in 163 children with biliary atresiaConference Presentation2010PROBEContributing Study
Cytomegalovirus-specific T-cell reactivity in biliary atresia at the time of diagnosis is associated with deficits in regulatory T cells.22105891PMC3319336Journal201210.1002/hep.24807PROBEContributing Study
DXA Bone Density in Alagille Syndrome Correlates with Fracture History and Degree of CholestasisConference Presentation2015PROBEContributing Study
Defects in bile acid biosynthesis--diagnosis and treatment.16819396Journal200610.1097/01.mpg.0000226386.79483.7bPROBEContributing Study
Dendritic cells regulate natural killer cell activation and epithelial injury in experimental biliary atresia.21957172PMC4006997Journal201110.1126/scitranslmed.3002069PROBEContributing Study
Design and validation of the biliary atresia research consortium histologic assessment system for cholestasis in infancy.21238606PMC3400532Journal201110.1016/j.cgh.2011.01.003BARC, PROBEContributing Study
Development of the Pictorial Preschool Cystic Fibrosis Questionnaire-Revised: Child and Parent ReportConference Presentation2014PROBEContributing Study
Diagnostic imaging in neonatal cholestasis: a multi-center prospective analysisConference Presentation2006BARC, PROBEContributing Study
Differences in presentation and progression between severe FIC1 and BSEP deficiencies.20447715PMC3042805Journal201010.1016/j.jhep.2010.01.034PROBEContributing Study
Directed differentiation of cholangiocytes from human pluripotent stem cells.26167630Journal201510.1038/nbt.3294PROBEContributing Study
Discriminating features of biliary atresia - a prospective multi-centered analysisConference Presentation2007PROBEContributing Study
Early growth failure after portoenterostomy is associated with liver transplantaion or death in infants with biliary atresiaConference Presentation2005BARC, PROBEContributing Study
Efficacy of fat-soluble vitamin supplementation in infants with biliary atresia.22891232PMC3428752Journal201210.1542/peds.2011-1423START, PROBEContributing Study
Evaluation guidelines for suspected mitochondrial hepatopathiesConference Presentation2012PROBEContributing Study
Evaluation guidelines for suspected mitochondrial hepatopathiesConference Presentation2012PROBEContributing Study
Evaluation of the child with suspected mitochondrial liver disease.23783016PMC3810178Journal201310.1097/MPG.0b013e31829ef67aPROBEContributing Study
Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene.23336978PMC3736559Journal201310.1053/j.gastro.2013.01.022PROBEContributing Study
Extrahepatic anomalies in infants with biliary atresia: results of a large prospective North American multicenter study.23703680PMC3844083Journal201310.1002/hep.26512PROBEContributing Study
Extrahepatic cholangiocyte cilia are abnormal in biliary atresia.23609896PMC3696479Journal201310.1097/MPG.0b013e318296e525PROBEContributing Study
FXR response in cholestatic liver diseaseConference Presentation2008PROBEContributing Study
Factors Determining δ-Bilirubin Levels in Infants With Biliary Atresia.25564820PMC4409472Journal201510.1097/MPG.0000000000000690PROBEContributing Study
Foxl1-Cre-marked adult hepatic progenitors have clonogenic and bilineage differentiation potential.21632825PMC3110956Journal201110.1101/gad.2027811PROBEContributing Study
Gene expression signature for biliary atresia and a role for interleukin-8 in pathogenesis of experimental disease.24493287PMC4077977Journal201410.1002/hep.27045PROBEContributing Study
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