Human esophageal dysplasia (16 cases) vs. esophageal squamous cell carcinoma (59 cases)
Ontology highlight
ABSTRACT: Our aim is to identify frequent genomic aberrations both in ESCC and esophageal dysplasia, and to discover important copy number-driving genes and microRNAs in ESCC. We carried out array-based comparative genomic hybridization (array CGH) on 59 ESCC resection samples and 16 dysplasia biopsy samples. Expression of genes at 11q13.3 was analyzed by real-time PCR and immunohistochemistry (IHC). Integrated analysis was performed to identify genes or microRNAs with copy number-expression correlations. Two group experiment, esophageal dysplasia vs. esophageal squamous cell carcinoma. Biological replicates: 16 dysplasias vs. 59 carcinomas
ORGANISM(S): Homo sapiens
SUBMITTER: Ming-Rong Wang
PROVIDER: E-GEOD-46452 | biostudies-arrayexpress |
REPOSITORIES: biostudies-arrayexpress
ACCESS DATA