Area of research
Surgery · Pulmonary and Respiratory Medicine
Research interest
Research interests include Pediatric Hepatobiliary Diseases and Treatments, Gallbladder and Bile Duct Disorders, Congenital Anomalies and Fetal Surgery, and Intestinal Malrotation and Obstruction Disorders.
RNA m6A methylation regulates CDH6 to promote epithelial-to-mesenchymal transition in cholangiocytes of biliary atresia.
Single-cell transcription reveals hepatocyte-to-cholangiocyte reprogramming and biliary gene profile in biliary atresia.
LncRNA MEG9 Promotes Inflammation and Liver Fibrosis Through S100A9 in Biliary Atresia.
Development and validation of a minimally invasive diagnostic model for biliary atresia using artificial intelligence.
CXCL6 Is a Novel Biliary Marker and a Downstream Target of MMP7 in Biliary Atresia.
Serum FGF19 combined with GGT and other biomarkers predicted native liver survival following Kasai portoenterostomy in early biliary atresia.
Clinical Course and Outcome of COVID-19 in Children With Biliary Atresia: A Retrospective Study.
Progress in Biomarkers Related to Biliary Atresia.
Serum matrix metalloproteinase-7 for discriminating biliary atresia: a diagnostic accuracy and validation study.
Analysis of false reasons based on the artificial intelligence RRCART model to identify frozen sections of lymph nodes in breast cancer
NLRP3 inflammasome activation promotes liver inflammation and fibrosis in experimental biliary atresia.
Incidence and outcome of biliary atresia in Shanghai, China from 2015 to 2016: a cohort study.
Intestinal fibrosis in aganglionic segment of Hirschsprung's disease revealed by single-cell RNA sequencing.
Effect of Adjuvant Steroid Therapy in Type 3 Biliary Atresia: A Single-Center, Open-Label, Randomized Controlled Trial.
Integrative analysis implicates the significance of m6A in the liver fibrosis of biliary atresia by regulating THY1.
Biliatresone: progress in biliary atresia study.
Single-cell and spatial transcriptomics reveal the fibrosis-related immune landscape of biliary atresia.
Characteristics of SOX9-positive progenitor-like cells during cholestatic liver regeneration in biliary atresia.
Preventive effect of prophylactic intravenous antibiotics against cholangitis in biliary atresia: a randomized controlled trial.
Epidemiological characteristics and risk factors of biliary atresia: a case-control study.
Protocol for a diagnostic accuracy study to develop diagnosis algorithm for biliary atresia using MMP-7 (DIABA-7 study): a study recruiting from Chinese Biliary Atresia Collaborative Network
Gut microbial profile in biliary atresia: a case-control study.
The synthetic toxin biliatresone causes biliary atresia in mice.
Modelling liver cancer initiation with organoids derived from directly reprogrammed human hepatocytes
Modelling liver cancer initiation with organoids derived from directly reprogrammed human hepatocytes.
Serum MMP-7 in the Diagnosis of Biliary Atresia.
Risk factors and prognostic effects of cholangitis after Kasai procedure in biliary atresia patients: A retrospective clinical study.
Reoperation after Ladd's procedure in the neonatal period.
Clinical characteristics and prognosis of adrenocortical tumors in children.
Correlation between hepatic oxidative damage and clinical severity and mitochondrial gene sequencing results in biliary atresia.