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Description
Medulloblastoma encompasses a collection of clinically and molecularly diverse tumor subtypes that together comprise the most common malignant childhood brain tumor. These tumors are thought to arise within the cerebellum, with approximately 25% originating from granule neuron precursor cells (GNPC ...See More
Publication Title
Subtypes of medulloblastoma have distinct developmental origins.
Alternate Accession IDs
E-GEOD-24628Sample Metadata Fields
Specimen part
Description
Medulloblastoma is a malignant childhood brain tumour comprising four discrete subgroups. To identify mutations that drive medulloblastoma we sequenced the entire genomes of 37 tumours and matched normal blood. One hundred and thirty-six genes harbouring somatic mutations in this discovery set wer ...See More
Publication Title
Novel mutations target distinct subgroups of medulloblastoma.
Alternate Accession IDs
E-GEOD-37418Sample Metadata Fields
Sex
Description
Medulloblastoma (MB) is the most common malignant brain tumor in children. Patients whose tumors exhibit overexpression or amplification of the MYC oncogene (c-MYC) usually have an extremely poor prognosis, but there are no animal models of this subtype of the disease. Here we show that cerebellar s ...See More
Publication Title
An animal model of MYC-driven medulloblastoma.
Alternate Accession IDs
E-GEOD-34126Sample Metadata Fields
Specimen part
Description
Recent genomic approaches have suggested the existence of multiple distinct subtypes of medulloblastoma. We studied a large cohort of medulloblastomas to determine how many subgroups of the disease exist, how they differ, and the extent of overlap between subgroups. We determined gene expression p ...See More
Publication Title
Medulloblastoma comprises four distinct molecular variants.
Alternate Accession IDs
E-GEOD-21140Sample Metadata Fields
Sex, Age, Specimen part
Description
Affimetrix Human Gene 1.1 ST Array profiling of 763 primary medullobalstoma samples used for identification of Medullobastoma subtypes
Publication Title
Intertumoral Heterogeneity within Medulloblastoma Subgroups.
Alternate Accession IDs
E-GEOD-85217Sample Metadata Fields
Specimen part
Description
Pediatric medulloblastoma is considered a highly heterogeneous disease, and a new strategy of risk stratification to optimize therapeutic outcomes is required. We aimed to investigate a new risk-stratification approach based on expression profiles of medulloblastoma cohorts. We analyzed gene express ...See More
Publication Title
Prognostic classification of pediatric medulloblastoma based on chromosome 17p loss, expression of MYCC and MYCN, and Wnt pathway activation.
Alternate Accession IDs
E-GEOD-30074Sample Metadata Fields
Sex, Specimen part
Description
Medulloblastoma is the most frequent malignant pediatric brain tumor. Considerable efforts are dedicated to identify markers that help to refine treatment strategies. The activation of the Wnt/beta-catenin pathway occurs in 10-15% of medulloblastomas and has been recently described as a marker for f ...See More
Publication Title
Beta-catenin status in paediatric medulloblastomas: correlation of immunohistochemical expression with mutational status, genetic profiles, and clinical characteristics.
Alternate Accession IDs
E-GEOD-12992Sample Metadata Fields
No sample metadata fields
Description
Affymetrix Human Gene 2.0 ST Array profiling of 9 pairs of matched primary-metastases medulloblastoma samples.
Publication Title
Medulloblastoma subgroups remain stable across primary and metastatic compartments.
Alternate Accession IDs
E-GEOD-63668Sample Metadata Fields
Sex, Age, Specimen part, Subject
Description
These gene expression microarrays were performed as part of a project aiming to integrate quantitative proteomic, gene expression and epigenetic data from the childhood brain tumor medulloblastoma.
Publication Title
Proteomic analysis of Medulloblastoma reveals functional biology with translational potential.
Alternate Accession IDs
E-GEOD-109401Sample Metadata Fields
Sex, Specimen part
Description
Bmi-1 and Mel-18 are close structural homologues that belong to the polycomb group (PcG) of transcriptional regulators of homeotic gene expression in development. They are believed to stably maintain repression of gene expression by altering the state of chromatin at specific promoters. A number of ...See More
Publication Title
Contribution of polycomb homologues Bmi-1 and Mel-18 to medulloblastoma pathogenesis.
Alternate Accession IDs
E-GEOD-7578Sample Metadata Fields
No sample metadata fields