Unknown,Transcriptomics,Genomics,Proteomics

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Comprehensive gene expression profile of human livers from patients with biliary atresia at the time of diagnosis and the corresponding disease and normal controls


ABSTRACT: Liver biopsy samples were obtained from 64 infants with biliary atresia at the time of intraoperative cholangiogram. Liver biopsy samples were obtained from 14 age-matched infants with other causes of intrahepatic cholestasis, and from 7 deceased-donor children. GeneChip® Human Gene 1.0 ST Array (Affymetrix, CA) were used to screen mRNAs whose expression was specifically regulated in the livers from patients with biliary atresia. Gene expression profiling: Liver biopsy samples obtained from infantas with other causes of intrahepatic cholestasis were served as diseased control. Liver tissue obtained from deceased-donor children were served as normal control. A molecular signataure of biliary atresia at the time of diagnosis was identified by comparing hepatic gene expression profile from biliary atresia to those from diseased and normal controls. This dataset is part of the TransQST collection.

ORGANISM(S): Homo sapiens

SUBMITTER: Jorge Bezerra 

PROVIDER: E-GEOD-46960 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Gene expression signature for biliary atresia and a role for interleukin-8 in pathogenesis of experimental disease.

Bessho Kazuhiko K   Mourya Reena R   Shivakumar Pranavkumar P   Walters Stephanie S   Magee John C JC   Rao Marepalli M   Jegga Anil G AG   Bezerra Jorge A JA  

Hepatology (Baltimore, Md.) 20140527 1


<h4>Unlabelled</h4>Biliary atresia (BA) is a progressive fibroinflammatory obstruction of extrahepatic bile ducts that presents as neonatal cholestasis. Due to the overlap in clinical, biochemical, and histological features with other causes of cholestasis, the diagnosis requires an intraoperative cholangiogram. Thus, we determined whether diseased livers express a gene expression signature unique to BA. Applying stringent statistical analysis to a genome-wide liver expression platform of 64 inf  ...[more]

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