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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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Roles of Enteric Neural Stem Cell Niche and Enteric Nervous System Development in Hirschsprung Disease

International journal of molecular sciences, 2021-09, Vol.22 (18), p.9659

2021

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Proteomic Analysis of the Mode of Antibacterial Action of Silver Nanoparticles

Journal of proteome research, 2006-04, Vol.5 (4), p.916-924

2006

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Silver nanoparticles: partial oxidation and antibacterial activities

Journal of biological inorganic chemistry, 2007-05, Vol.12 (4), p.527-534

2007

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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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The Emerging Genetic Landscape of Hirschsprung Disease and Its Potential Clinical Applications

Frontiers in pediatrics, 2021-08, Vol.9, p.638093-638093

2021

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Immunomodulatory Mechanisms of Mesenchymal Stem Cells and Their Potential Clinical Applications

International journal of molecular sciences, 2022-09, Vol.23 (17), p.10023

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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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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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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Artificial intelligence-based approaches for the detection and prioritization of genomic mutations in congenital surgical diseases

Frontiers in pediatrics, 2023-08, Vol.11, p.1203289-1203289

2023

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Somatic PIK3CA mutations in seven patients with PIK3CA‐related overgrowth spectrum

American journal of medical genetics. Part A, 2017-04, Vol.173 (4), p.978-984

2017

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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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Diagnosis and spectrum of melamine-related renal disease: Plausible mechanism of stone formation in humans

Clinica chimica acta, 2009-04, Vol.402 (1), p.150-155

2009

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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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Actionable secondary findings in 1116 Hong Kong Chinese based on exome sequencing data

Journal of human genetics, 2021-06, Vol.66 (6), p.637-641

2021

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Gold(III) porphyrin complex is more potent than cisplatin in inhibiting growth of nasopharyngeal carcinoma in vitro and in vivo

International journal of cancer, 2009-04, Vol.124 (8), p.1971-1979

2009

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Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease

Scientific reports, 2015-11, Vol.5 (1), p.16473-16473, Article 16473

2015

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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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A Highly Specific BODIPY-Based Fluorescent Probe for the Detection of Hypochlorous Acid

Organic letters, 2008-06, Vol.10 (11), p.2171-2174

2008

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Genetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia

PloS one, 2013-06, Vol.8 (6), p.e66631-e66631

2013

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Genetics of Hirschsprung’s disease

Pediatric surgery international, 2023-02, Vol.39 (1), p.104-104, Article 104

2023

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Correction of Hirschsprung-Associated Mutations in Human Induced Pluripotent Stem Cells Via Clustered Regularly Interspaced Short Palindromic Repeats/Cas9, Restores Neural Crest Cell Function

Gastroenterology (New York, N.Y. 1943), 2017-07, Vol.153 (1), p.139-153.e8

2017

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

Roles of Enteric Neural Stem Cell Niche and Enteric Nervous System Development in Hirschsprung Disease

Proteomic Analysis of the Mode of Antibacterial Action of Silver Nanoparticles

Silver nanoparticles: partial oxidation and antibacterial activities

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

The Emerging Genetic Landscape of Hirschsprung Disease and Its Potential Clinical Applications

Immunomodulatory Mechanisms of Mesenchymal Stem Cells and Their Potential Clinical Applications

Identification of a HOXD13 mutation in a VACTERL patient

Embryology and anatomy of Hirschsprung disease

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

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

Artificial intelligence-based approaches for the detection and prioritization of genomic mutations in congenital surgical diseases

Somatic PIK3CA mutations in seven patients with PIK3CA‐related overgrowth spectrum

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

Diagnosis and spectrum of melamine-related renal disease: Plausible mechanism of stone formation in humans

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

Actionable secondary findings in 1116 Hong Kong Chinese based on exome sequencing data

Gold(III) porphyrin complex is more potent than cisplatin in inhibiting growth of nasopharyngeal carcinoma in vitro and in vivo

Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease

Gene network analysis of candidate loci for human anorectal malformations

A Highly Specific BODIPY-Based Fluorescent Probe for the Detection of Hypochlorous Acid

Genetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia

Genetics of Hirschsprung’s disease

Correction of Hirschsprung-Associated Mutations in Human Induced Pluripotent Stem Cells Via Clustered Regularly Interspaced Short Palindromic Repeats/Cas9, Restores Neural Crest Cell Function

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