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Links from GEO DataSets

Items: 20

1.
Full record GDS4471

Medulloblastomas in children

Analysis of medulloblastomas from children ages 3 to 16 years. Medulloblastoma is a malignant childhood brain tumor comprising four discrete subgroups. Results provide insights into pathogenesis of medulloblastoma and highlight targets for therapeutic development.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 6 disease state, 2 gender, 4 other sets
Platform:
GPL570
Series:
GSE37418
76 Samples
Download data: CEL
2.

Novel mutations target distinct subgroups of medulloblastoma.

(Submitter supplied) 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 were sequenced in an additional 56 medulloblastomas. Recurrent mutations were detected in 41 genes not yet implicated in medulloblastoma: several target distinct components of the epigenetic machinery in different disease subgroups, e.g., regulators of H3K27 and H3K4 trimethylation in subgroup-3 and 4 (e.g., KDM6A and ZMYM3), and CTNNB1-associated chromatin remodellers in WNT-subgroup tumours (e.g., SMARCA4 and CREBBP). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4471
Platform:
GPL570
76 Samples
Download data: CEL
Series
Accession:
GSE37418
ID:
200037418
3.

A mouse model of the most aggressive subgroup of human medulloblastoma [HT_MG-430_PM]

(Submitter supplied) A series of mouse models designed to mimic pediatric medulloblastoma types in humans were tested by microarray and compared to published human medulloblastoma data
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11180
15 Samples
Download data: CEL
Series
Accession:
GSE33200
ID:
200033200
4.

Microarray-based DNA methylation profiles of primary medulloblastomas

(Submitter supplied) Identification of novel molecular subgroups Background: International consensus recognises four medulloblastoma molecular subgroups - WNT, SHH, Group 3 and Group 4 - each defined by their characteristic genome-wide transcriptomic and DNA methylomic profiles. Subgroups harbor distinct clinico-pathological and molecular features, underpin current disease sub-classification and initial subgroup-directed therapies are underway in clinical trials (i.e. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
428 Samples
Download data: IDAT, TXT
Series
Accession:
GSE93646
ID:
200093646
5.

Disease-associated KBTBD4 mutations in medulloblastoma elicit neomorphic ubiquitylation activity to promote CoREST degradation

(Submitter supplied) E3 ubiquitin ligases of the Cullin RING Ligase (CRL) family assemble into multiprotein complexes to diversify substrate adaptors and ensure selectivity in substrate engagement for degradation. Here we show a novel mechanism whereby mutations in substrate adaptors can drive neo-substrate degradation in cancer. KBTBD4 is a CRL3 substrate adaptor harbouring recurrent indel mutations in a subset of non-WNT/non-SHH medulloblastomas. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
24 Samples
Download data: XLS
Series
Accession:
GSE197240
ID:
200197240
6.

Genomics of medulloblastoma identifies four distinct molecular variants

(Submitter supplied) 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 profiles and DNA copy number aberrations for 103 primary medulloblastomas. Bioinformatic tools were used for class discovery of medulloblastoma subgroups based on the most informative genes in the dataset. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5175
103 Samples
Download data: CEL
Series
Accession:
GSE21140
ID:
200021140
7.

SMARCA4/Brg1 Coordinates Genetic and Epigenetic Networks Underlying Shh-type Medulloblastoma Development

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: BED, TXT
Series
Accession:
GSE69674
ID:
200069674
8.

SMARCA4/Brg1 Coordinates Genetic and Epigenetic Networks Underlying Shh-type Medulloblastoma Development [ChIP-Seq]

(Submitter supplied) Medulloblastoma could be classified into four subtypes: Wnt, Shh, Group 3, and Group 4. Subtypes of medulloblastoma have distinct epigenetic properties. We report that a chromatin regulator SMARCA4/Brg1 controls a transcriptional program that specifically required for Shh-type medulloblastoma identity and proliferation. We show that Brg1 deletion significantly inhibited tumor formation and progression in a mouse medulloblastoma model. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
2 Samples
Download data: BED
Series
Accession:
GSE69673
ID:
200069673
9.

SMARCA4/Brg1 Coordinates Genetic and Epigenetic Networks Underlying Shh-type Medulloblastoma Development [gene expression]

(Submitter supplied) Medulloblastoma could be classified into four subtypes: Wnt, Shh, Group 3, and Group 4. Subtypes of medulloblastoma have distinct epigenetic properties. We report that a chromatin regulator SMARCA4/Brg1 controls a transcriptional program that specifically required for Shh-type medulloblastoma identity and proliferation. We show that Brg1 deletion significantly inhibited tumor formation and progression in a mouse medulloblastoma model. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
2 Samples
Download data: TXT
Series
Accession:
GSE69672
ID:
200069672
10.

Subgroup specific somatic copy number aberrations in the medulloblastoma genome

(Submitter supplied) Medulloblastoma, the most common malignant pediatric brain tumour is currently treated with non-specific cytotoxic therapies including surgery, whole brain radiation, and aggressive chemotherapy. As medulloblastoma exhibits marked intertumoural heterogeneity, with at least four distinct molecular variants, prior attempts to identify targets for therapy have been underpowered due to small samples sizes. more...
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by SNP array; SNP genotyping by SNP array
Platforms:
GPL6801 GPL11532
1382 Samples
Download data: CEL, CHP
Series
Accession:
GSE37385
ID:
200037385
11.

Subgroup specific somatic copy number aberrations in the medulloblastoma genome [gDNA]

(Submitter supplied) Affymetrix SNP6 profiling of 1087 medulloblastoma samples and 10 medulloblastoma cell lines.
Organism:
Homo sapiens
Type:
SNP genotyping by SNP array; Genome variation profiling by SNP array
Platform:
GPL6801
1097 Samples
Download data: CEL, CHP, TXT
Series
Accession:
GSE37384
ID:
200037384
12.

Subgroup specific somatic copy number aberrations in the medulloblastoma genome [mRNA]

(Submitter supplied) Affymetrix Human Gene 1.1 ST Array profiling of 285 primary medulloblastoma samples.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL11532
285 Samples
Download data: CEL
Series
Accession:
GSE37382
ID:
200037382
13.

DDX3X suppresses neural lineage susceptibility to medulloblastoma

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Genome variation profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL21103 GPL24247
270 Samples
Download data
Series
Accession:
GSE147180
ID:
200147180
14.

DDX3X suppresses neural lineage susceptibility to medulloblastoma [RNA-seq]

(Submitter supplied) DDX3X is frequently mutated in the WNT and SHH subtypes of medulloblastoma Ð the commonest malignant childhood brain tumor. But whether DDX3X functions as a medulloblastoma oncogene or tumor suppressor gene is not known. Here we show that Ddx3x regulates hindbrain patterning and development by controlling Hox gene expression and cell stress signaling. In mice predisposed to Wnt or Shh-medulloblastoma Ddx3x sensed oncogenic stress and suppressed tumor formation. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
257 Samples
Download data: CSV
Series
Accession:
GSE147178
ID:
200147178
15.

DDX3X suppresses neural lineage susceptibility to medulloblastoma [DNA-Seq]

(Submitter supplied) DDX3X is frequently mutated in the WNT and SHH subtypes of medulloblastoma Ð the commonest malignant childhood brain tumor. But whether DDX3X functions as a medulloblastoma oncogene or tumor suppressor gene is not known. Here we show that Ddx3x regulates hindbrain patterning and development by controlling Hox gene expression and cell stress signaling. In mice predisposed to Wnt or Shh-medulloblastoma Ddx3x sensed oncogenic stress and suppressed tumor formation. more...
Organism:
Mus musculus
Type:
Genome variation profiling by high throughput sequencing
Platform:
GPL24247
13 Samples
Download data: TXT
Series
Accession:
GSE147069
ID:
200147069
16.

Failure of human rhombic lip differentiation constitutes medulloblastoma

(Submitter supplied) Single-nucleus RNA sequencing was performed on Group 3 medulloblastoma tumorspheres expresssing high vs. low levels of OTX2
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
4 Samples
Download data: TXT
Series
Accession:
GSE200791
ID:
200200791
17.

Medulloblastoma is a differentiation disorder of the human rhombic lip

(Submitter supplied) RNA sequencing was performed on Group 3 medulloblastoma tumorspheres expressing high vs. low levels of OTX2.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
12 Samples
Download data: SF, TXT
18.

Microarray-based DNA methylation profiling of medulloblastoma and normal cerebellum samples

(Submitter supplied) Robust molecular subgrouping and copy-number profiling of medulloblastoma from small amounts of archival tumor material. Validation of patterns identified by whole-genome bisulphite sequencing in a larger cohort.
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
284 Samples
Download data: TXT
Series
Accession:
GSE54880
ID:
200054880
19.

Subtypes of medulloblastoma have distinct developmental origins

(Submitter supplied) 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 (GNPCs) following aberrant activation of the Sonic Hedgehog pathway (hereafter, SHH-subtype). The pathological processes that drive heterogeneity among the other medulloblastoma subtypes are not known, hindering the development of much needed new therapies. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
16 Samples
Download data: CEL
Series
Accession:
GSE24628
ID:
200024628
20.

Downregulation of ARID1B, a tumor-suppressor in the WNT subgroup medulloblastoma, activates multiple oncogenic signaling pathways

(Submitter supplied) About 85% of WNT subgroup medulloblastomas exhibit the loss of one copy of chromosome 6. Loss of function mutations were identified in the ARID1B gene located on chromosome 6 in WNT subgroup tumors suggesting tumor suppressor role for ARID1B in WNT medulloblastomas. The expression of ARID1B was downregulated in the medulloblastoma cell line Daoy using two independent shRNA sequences in a doxycycline-inducible lentiviral vector tet-pLKO-puro and the effect of its downregulation on the gene expression profile was studied by the RNA-seq analysis
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
4 Samples
Download data: TXT
Series
Accession:
GSE163810
ID:
200163810
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