Sort   by:  
 Page size 
UnknownRectal budesonide: A potential game changer after Kasai hepatoportoenterostomy.
Not available
S-EPMC12408950 | biostudies-literature
UnknownCharacteristics of the Gut Microbiome and IL-13/TGF-β1 Mediated Fibrosis in Post-Kasai Cholangitis of Biliary Atresia.
Not available
S-EPMC8630618 | biostudies-literature
UnknownEffect of Kasai procedure on liver transplantation in children with biliary atresia: a systematic review and updated meta-analysis.
Not available
S-EPMC10839284 | biostudies-literature
ProteomicsAssessing Native-Liver Post-Kasai Portoenterostomy for biliary atresia through Stool Proteome Analysis
In this prospective study, we analyzed stool proteomes from four patients with well-controlled conditions, four patients with recurrent cholangitis, and three patients with prolonged jaundice but no cholangitis, all of whom had undergone Kasai portoenterostomy for biliary atresia (BA). The study als...
ORGANISM(S): Homo Sapiens (human) 
2025-09-04 | PXD055756 | JPOST Repository
UnknownCyclooxygenase-2 Inhibitor Reduces Hepatic Stiffness in Pediatric Chronic Liver Disease Patients Following Kasai Portoenterostomy.
Not available
S-EPMC4951465 | biostudies-literature
UnknownThe need for early Kasai portoenterostomy: a Western Pediatric Surgery Research Consortium study.
Not available
S-EPMC8742784 | biostudies-literature
TranscriptomicsDownstream genes regulated by TSHZ2 in MCF-7 cells
To clarify downstream genes regulated by TSHZ2, MCF-7 cells were lentivirally transduced by TSHZ2 and its control LacZ and served their RNA samples for gene expression analysis using AGILENT human 8x60K cDNA microarray. Array analysis of MCF-7 cells expressing either TSHZ2 or LacZ. 1 color method wa...
ORGANISM(S): Homo sapiens 
2016-01-11 | E-GEOD-64351 | biostudies-arrayexpress
UnknownEfficacy and safety of S-1 monotherapy in previously treated elderly patients (aged ≥75 years) with non-small cell lung cancer: A retrospective analysis.
Not available
S-EPMC7529563 | biostudies-literature
GenomicBiomarkers in Transplant Recipients

Biliary atresia causes jaundice and liver failure in newborn children. In this study, single nucleotide polymorphisms were characterized in children with biliary atresia and identified ARF6 as a susceptibility gene for this disease. Knockdown of this gene in zebrafish embryos impaired formation o...

phs000960 | dbGaP
UnknownA phase 2 trial of N-Acetylcysteine in Biliary atresia after Kasai portoenterostomy.
Not available
S-EPMC6542754 | biostudies-literature
Sort   by:  
 Page size