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Biomarkers for the diagnosis and post-Kasai portoenterostomy prognosis of biliary atresia: a systematic review and meta-analysis

Scientific reports, 2021-06, Vol.11 (1), p.11692-11692, Article 11692

2021

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Does the Choice of Suture Materials Affect the Vas Deferens after Hernia Ring Closure in Inguinal Hernia Surgery: An Experimental Study in Rats

Journal of pediatric surgery, 2023-07, Vol.58 (7), p.1301-1305

2023

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Human liver organoid derived intra-hepatic bile duct cells support SARS-CoV-2 infection and replication

Scientific reports, 2022-03, Vol.12 (1), p.5375-5375, Article 5375

2022

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Identification of a HOXD13 mutation in a VACTERL patient

American journal of medical genetics. Part A, 2008-12, Vol.146A (24), p.3181-3185

2008

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Embryology and anatomy of Hirschsprung disease

Seminars in pediatric surgery, 2022-12, Vol.31 (6), p.151227-151227, Article 151227

2022

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Environmental Toxin Biliatresone-Induced Biliary Atresia-like Abnormal Cilia and Bile Duct Cell Development of Human Liver Organoids

Toxins, 2024-03, Vol.16 (3), p.144

2024

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Common genetic variants regulating ADD3 gene expression alter biliary atresia risk

Journal of hepatology, 2013-12, Vol.59 (6), p.1285-1291

2013

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Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanism

EBioMedicine, 2021-09, Vol.71, p.103530-103530, Article 103530

2021

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Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease

Proceedings of the National Academy of Sciences - PNAS, 2009-02, Vol.106 (8), p.2694-2699

2009

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Pathological role of methionine in the initiation and progression of biliary atresia

Frontiers in pediatrics, 2023-09, Vol.11, p.1263836-1263836

2023

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Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2

Human molecular genetics, 2010-07, Vol.19 (14), p.2917-2925

2010

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Genome-wide copy number analysis uncovers a new HSCR gene: NRG3

PLoS genetics, 2012-05, Vol.8 (5), p.e1002687

2012

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Depletion of the IKBKAP ortholog in zebrafish leads to hirschsprung disease-like phenotype

World journal of gastroenterology : WJG, 2015-02, Vol.21 (7), p.2040-2046

2015

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Reducing fibrosis progression of biliary atresia by continuous administration of aducanumab at low dose: A potential treatment

Medical hypotheses, 2022-08, Vol.165, p.110901, Article 110901

2022

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Gene network analysis of candidate loci for human anorectal malformations

PloS one, 2013-08, Vol.8 (8), p.e69142-e69142

2013

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Pathogenesis of Choledochal Cyst: Insights from Genomics and Transcriptomics

Genes, 2022-06, Vol.13 (6), p.1030

2022

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Mutational analysis of SHH and GLI3 in anorectal malformations

Birth defects research. A Clinical and molecular teratology, 2008-09, Vol.82 (9), p.644-648

2008

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Fine mapping of the NRG1 Hirschsprung's disease locus

PloS one, 2011-01, Vol.6 (1), p.e16181

2011

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Current Understanding in the Clinical Characteristics and Molecular Mechanisms in Different Subtypes of Biliary Atresia

International journal of molecular sciences, 2022-04, Vol.23 (9), p.4841

2022

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Transamniotic mesenchymal stem cell therapy for neural tube defects preserves neural function through lesion-specific engraftment and regeneration

Cell death & disease, 2020-07, Vol.11 (7), p.523-523, Article 523

2020

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Identification of cancer-related genes FGFR2 and CEBPB in choledochal cyst via RNA sequencing of patient-derived liver organoids

PloS one, 2023-03, Vol.18 (3), p.e0283737-e0283737

2023

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HOXB5 expression is spatially and temporarily regulated in human embryonic gut during neural crest cell colonization and differentiation of enteric neuroblasts

Developmental dynamics, 2003-09, Vol.228 (1), p.1-10

2003

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Conditional deletion of platelet derived growth factor receptor alpha (Pdgfra) in urorectal mesenchyme causes mesenchyme apoptosis and urorectal developmental anomalies in mice

Cell death and differentiation, 2019-08, Vol.26 (8), p.1396-1410

2019

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Beta-amyloid deposition around hepatic bile ducts is a novel pathobiological and diagnostic feature of biliary atresia

Journal of hepatology, 2020-12, Vol.73 (6), p.1391-1403

2020

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PPAR-γ signaling and IL-5 inhibition together prevent chronic rejection of MHC Class II–mismatched cardiac grafts

The Journal of heart and lung transplantation, 2011-06, Vol.30 (6), p.698-706

2011

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Biomarkers for the diagnosis and post-Kasai portoenterostomy prognosis of biliary atresia: a systematic review and meta-analysis

Does the Choice of Suture Materials Affect the Vas Deferens after Hernia Ring Closure in Inguinal Hernia Surgery: An Experimental Study in Rats

Human liver organoid derived intra-hepatic bile duct cells support SARS-CoV-2 infection and replication

Identification of a HOXD13 mutation in a VACTERL patient

Embryology and anatomy of Hirschsprung disease

Environmental Toxin Biliatresone-Induced Biliary Atresia-like Abnormal Cilia and Bile Duct Cell Development of Human Liver Organoids

Common genetic variants regulating ADD3 gene expression alter biliary atresia risk

Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanism

Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease

Pathological role of methionine in the initiation and progression of biliary atresia

Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2

Genome-wide copy number analysis uncovers a new HSCR gene: NRG3

Depletion of the IKBKAP ortholog in zebrafish leads to hirschsprung disease-like phenotype

Reducing fibrosis progression of biliary atresia by continuous administration of aducanumab at low dose: A potential treatment

Gene network analysis of candidate loci for human anorectal malformations

Pathogenesis of Choledochal Cyst: Insights from Genomics and Transcriptomics

Mutational analysis of SHH and GLI3 in anorectal malformations

Fine mapping of the NRG1 Hirschsprung's disease locus

Current Understanding in the Clinical Characteristics and Molecular Mechanisms in Different Subtypes of Biliary Atresia

Transamniotic mesenchymal stem cell therapy for neural tube defects preserves neural function through lesion-specific engraftment and regeneration

Identification of cancer-related genes FGFR2 and CEBPB in choledochal cyst via RNA sequencing of patient-derived liver organoids

HOXB5 expression is spatially and temporarily regulated in human embryonic gut during neural crest cell colonization and differentiation of enteric neuroblasts

Conditional deletion of platelet derived growth factor receptor alpha (Pdgfra) in urorectal mesenchyme causes mesenchyme apoptosis and urorectal developmental anomalies in mice

Beta-amyloid deposition around hepatic bile ducts is a novel pathobiological and diagnostic feature of biliary atresia

PPAR-γ signaling and IL-5 inhibition together prevent chronic rejection of MHC Class II–mismatched cardiac grafts

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