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TranscriptomicsComparison of enchondromas with controls (growth plate and cartilage)
Ollier disease is a rare, non-hereditary disorder which is characterized by the presence of multiple enchondromas (EC), benign cartilaginous neoplasms arising within the medulla of the bone, with an asymmetric distribution. The risk of malignant transformation towards central chondrosarcoma (CS) is ...
ORGANISM(S): Homo sapiens 
2011-08-25 | E-GEOD-22855 | biostudies-arrayexpress
TranscriptomicsGenome-wide analysis of Ollier disease: Is it all in the genes?
This SuperSeries is composed of the following subset Series: GSE22855: Comparison of enchondromas with controls (growth plate and cartilage) GSE22984: Affymetrix SNP6.0 on Ollier disease-related tumors Refer to individual Series
ORGANISM(S): Homo sapiens 
2011-08-25 | E-GEOD-22965 | biostudies-arrayexpress
TranscriptomicsAffymetrix SNP6.0 on Ollier disease-related tumors
Mutations in the PTH1R gene were reported but these mutations are limited to a small subgroup of patients. The etiology of Ollier disease is unknown. We therefore undertook genome-wide copy number and loss of heterozygosity (LOH) analysis using Affymetrix SNP 6.0 arrays on 37 tumors of 28 Ollier pat...
ORGANISM(S): Homo sapiens 
2011-08-26 | E-GEOD-22984 | biostudies-arrayexpress
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