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Links from GEO DataSets

Items: 20

1.

Genomic and transcriptomic analysis of medulloblastoma

(Submitter supplied) Identification of transcriptomic and genomic changes by RNA-seq, ATAC-seq and low coverage WGS in mouse and human tumor cells
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Genome variation profiling by high throughput sequencing
Platforms:
GPL16791 GPL17021
33 Samples
Download data: BED, BW, CSV, TXT
Series
Accession:
GSE145921
ID:
200145921
2.

An Animal Model of Myc-driven medulloblastoma

(Submitter supplied) 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 stem cells expressing Myc and mutant Trp53 (p53) generate aggressive tumors following orthotopic transplantation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4478
Platform:
GPL1261
19 Samples
Download data: CEL
Series
Accession:
GSE34126
ID:
200034126
3.
Full record GDS4478

MYC-driven medulloblastoma model

Analysis of Myc/DNp53-infected tumors derived from stem cells or progenitors, uninfected stem cells, and patched tumor cells. Cerebellar stem cells expressing Myc and mutant Trp53 generate tumors similar to MYC-driven medulloblastoma (MB). Results provide insight into transformation to MB tumor.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 4 cell type, 3 genotype/variation, 4 other sets
Platform:
GPL1261
Series:
GSE34126
19 Samples
Download data: CEL
4.

Combined MYC and TP53 defects emerge at medulloblastoma relapse and define rapidly progressive, therapeutically targetable disease

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array; Genome variation profiling by genome tiling array
Platforms:
GPL6885 GPL13534
88 Samples
Download data: IDAT
Series
Accession:
GSE62626
ID:
200062626
5.

Combined MYC and TP53 defects emerge at medulloblastoma relapse and define rapidly progressive, therapeutically targetable disease [gene expression]

(Submitter supplied) We undertook a comprehensive clinical and biological investigation of serial medulloblastoma biopsies obtained at diagnosis and relapse. Combined MYC gene family amplifications and P53 pathway defects commonly emerged at relapse, and all patients in this molecular group died of rapidly progressive disease post-relapse. To study this genetic interaction, we investigated a transgenic model of MYCN-driven medulloblastoma and found spontaneous development of Trp53 inactivating mutations. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6885
48 Samples
Download data: IDAT, TXT
Series
Accession:
GSE62625
ID:
200062625
6.

Methylation data from presentation and relapsed medulloblastoma tumour samples

(Submitter supplied) We undertook a comprehensive clinical and biological investigation of serial medulloblastoma biopsies obtained at diagnosis and relapse. Combined MYC gene family amplifications and P53 pathway defects commonly emerged at relapse, and all patients in this molecular group died of rapidly progressive disease post-relapse. To study this genetic interaction, we investigated a transgenic model of MYCN-driven medulloblastoma and found spontaneous development of Trp53 inactivating mutations. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
40 Samples
Download data: CSV
Series
Accession:
GSE62618
ID:
200062618
7.

ARF suppression by MYC but not MYCN confers increased malignancy of Group 3 medulloblastoma

(Submitter supplied) Group 3 medulloblastoma (MB) carries the worst prognosis of the four molecular subgroups of MB. MYC amplifications represent the most common genetic alteration in Group 3 MB. By specifically driving MYC in hindbrain cells using a Tet-OFF system, we established a novel murine model of MB (GMYC) that accurately recapitulates human Group 3 MB. GMYC tumours develop with 60-70% penetrance, without p53 mutations, and are monoclonal as revealed by multicolour cell fate tracing. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL27583 GPL16331
32 Samples
Download data: TXT
Series
Accession:
GSE139240
ID:
200139240
8.

Remodeling Group 3 medulloblastoma: MYC overexpression alone transforms progenitors of astrocytes and granule neurons in the postnatal cerebellum

(Submitter supplied) Group 3 medulloblastoma is often associated with MYC amplification or overexpression, while whether MYC overexpression alone is sufficient to induce tumorigenesis is unknown and the cell type(s) which can be transformed by MYC is unclear. Here, by generating a new mouse model, we demonstrated that overexpression of Myc alone is sufficient to transform astrocyte progenitors and granule neuron progenitors (GNP) in the early postnatal cerebellum following orthotopic transplantation. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
21 Samples
Download data: TXT
Series
Accession:
GSE114760
ID:
200114760
9.

The miR-17/92 Polycistron Is Up-regulated in Sonic Hedgehog-Driven Medulloblastomas and Induced by N-myc in Sonic Hedgehog–Treated Cerebellar Neural Precursors

(Submitter supplied) Medulloblastoma is the most common malignant pediatric brain tumor, and mechanisms underlying its development are poorly understood. We identified recurrent amplification of the miR-17/92 polycistron proto-oncogene in 6% of pediatric medulloblastomas by high-resolution single-nucleotide polymorphism genotyping arrays and subsequent interphase fluorescence in situ hybridization on a human medulloblastoma tissue microarray. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5175
90 Samples
Download data: CEL
Series
Accession:
GSE21166
ID:
200021166
10.

A mouse model of the most aggressive subgroup of human medulloblastoma

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL11180 GPL1261
79 Samples
Download data: CEL
Series
Accession:
GSE33201
ID:
200033201
11.

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
12.

A mouse model of the most aggressive subgroup of human medulloblastoma [Mouse430_2]

(Submitter supplied) Mouse models of medulloblastoma are compared to human subgroups through microarray expression and other measures
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
64 Samples
Download data: CEL
Series
Accession:
GSE33199
ID:
200033199
13.

Genetic alterations in mouse medulloblastomas and generation of tumors from cerebellar grunule neuron precursors

(Submitter supplied) Mice lacking p53 and one or two alleles of the cyclin D-dependent kinase inhibitor p18Ink4c are prone to medulloblastoma development. The tumor frequency is increased by exposing postnatal animals to ionizing radiation at a time when their cerebella are developing. In irradiated mice engineered to express a floxed p53 allele and a Nestin-Cre transgene, tumor development can be restricted to the brain. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL339 GPL340
10 Samples
Download data: CEL
Series
Accession:
GSE6463
ID:
200006463
14.

Single-cell RNA-seq Reveals a Developmental Hierarchy and Oncogenic Networks for Initiation of Medulloblastoma

(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
30 Samples
Download data: FPKM_TRACKING, MTX, TSV, TXT, WIG
Series
Accession:
GSE120974
ID:
200120974
15.

Single-cell RNA-seq Reveals a Developmental Hierarchy and Oncogenic Networks for Initiation of Medulloblastoma [RNA-Seq]

(Submitter supplied) By utilizing single-cell analysis at different stages of tumorigenesis, we demonstrated a developmental hierarchy of dynamic progenitor pools in murine sonic hedgehog-(SHH) MBs. We identified Olig2+ progenitors as transit-amplifying cells during initial tumorigenic phases. These cells are quiescent stem-like progenitors in full-blown tumors but enriched in therapy-resistant as well as recurrent medulloblastomas. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
16 Samples
Download data: FPKM_TRACKING
Series
Accession:
GSE120973
ID:
200120973
16.

Single-cell RNA-seq Reveals a Developmental Hierarchy and Oncogenic Networks for Initiation of Medulloblastoma [Drop-Seq]

(Submitter supplied) By utilizing single-cell analysis at different stages of tumorigenesis, we demonstrated a developmental hierarchy of dynamic progenitor pools in murine sonic hedgehog-(SHH) MBs. We identified Olig2+ progenitors as transit-amplifying cells during initial tumorigenic phases. These cells are quiescent stem-like progenitors in full-blown tumors but enriched in therapy-resistant as well as recurrent medulloblastomas. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
2 Samples
Download data: TXT
Series
Accession:
GSE120972
ID:
200120972
17.

Single-cell RNA-seq Reveals a Developmental Hierarchy and Oncogenic Networks for Initiation of Medulloblastoma [ChIP-Seq]

(Submitter supplied) By utilizing single-cell analysis at different stages of tumorigenesis, we demonstrated a developmental hierarchy of dynamic progenitor pools in murine sonic hedgehog-(SHH) MBs. We identified Olig2+ progenitors as transit-amplifying cells during initial tumorigenic phases. These cells are quiescent stem-like progenitors in full-blown tumors but enriched in therapy-resistant as well as recurrent medulloblastomas. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
9 Samples
Download data: WIG
Series
Accession:
GSE120968
ID:
200120968
18.

Single-cell RNA-seq Reveals a Developmental Hierarchy and Oncogenic Networks for Initiation of Medulloblastoma [ATAC-Seq]

(Submitter supplied) By utilizing single-cell analysis at different stages of tumorigenesis, we demonstrated a developmental hierarchy of dynamic progenitor pools in murine sonic hedgehog-(SHH) MBs. We identified Olig2+ progenitors as transit-amplifying cells during initial tumorigenic phases. These cells are quiescent stem-like progenitors in full-blown tumors but enriched in therapy-resistant as well as recurrent medulloblastomas. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
2 Samples
Download data: WIG
Series
Accession:
GSE120967
ID:
200120967
19.

Single-cell RNA-seq Reveals a Developmental Hierarchy and Oncogenic Networks for Initiation of Medulloblastoma [10x Genomics Chromium]

(Submitter supplied) By utilizing single-cell analysis at different stages of tumorigenesis, we demonstrated a developmental hierarchy of dynamic progenitor pools in murine sonic hedgehog-(SHH) MBs. We identified Olig2+ progenitors as transit-amplifying cells during initial tumorigenic phases. These cells are quiescent stem-like progenitors in full-blown tumors but enriched in therapy-resistant as well as recurrent medulloblastomas. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
1 Sample
Download data: MTX, TSV
Series
Accession:
GSE120966
ID:
200120966
20.

Dormant SOX9-positive cells facilitate MYC-driven recurrence of medulloblastoma

(Submitter supplied) Tumor recurrence is a slow biological process involving therapy resistance, immune escape and metastasis and is the leading cause of death in medulloblastoma, the most frequent malignant pediatric brain tumor. By studying paired primary-recurrent patient samples and patient-derived xenografts we identified significant accumulation of SOX9-positive cells in relapses and metastases. They exist as rare, quiescent cells in Group 3 and Group 4 patients that constitute two thirds of medulloblastoma. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL16331 GPL24247
44 Samples
Download data: TXT
Series
Accession:
GSE162080
ID:
200162080
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