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Links from GEO DataSets

Items: 20

1.

The genes regulated by SOX11 in mantle cell lymphoma

(Submitter supplied) The genes regulated by SOX11 in MCL was investigated in MCL cell line Granta 519 by siRNA knock down system. Cells were transfected using the LONZA electroporation system. Results represent cells harvested after 20 hours. Details of the experiment is published in PMID 21124928.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
12 Samples
Download data: CEL, TXT
Series
Accession:
GSE25621
ID:
200025621
2.

High resolution ChIP sequencing reveals novel bindings targets and prognostic role for SOX11 in Mantle cell lymphoma

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL9052 GPL11154
10 Samples
Download data: BIGBED
Series
Accession:
GSE52149
ID:
200052149
3.

High resolution ChIP sequencing reveals novel bindings targets and prognostic role for SOX11 in Mantle cell lymphoma (RNA-Seq)

(Submitter supplied) SOX11 (Sex determining region Y-box 11) expression is specific for MCL as compared to other Non-Hodgkin’s lymphomas. However, the function and direct binding targets of SOX11 in MCL are largely unknown. We used high-resolution ChIP-Seq to identify the direct target genes of SOX11 in a genome-wide, unbiased manner and elucidate its functional significance. Pathway analysis identified WNT, PKA and TGF-beta signaling pathways as significantly enriched by SOX11 target genes. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
6 Samples
Download data: TXT
4.

High resolution ChIP sequencing reveals novel bindings targets and prognostic role for SOX11 in Mantle cell lymphoma (ChIP-Seq)

(Submitter supplied) SOX11 (Sex determining region Y-box 11) expression is specific for MCL as compared to other Non-Hodgkin’s lymphomas. However, the function and direct binding targets of SOX11 in MCL are largely unknown. We used high-resolution ChIP-Seq to identify the direct target genes of SOX11 in a genome-wide, unbiased manner and elucidate its functional significance. Pathway analysis identified WNT, PKA and TGF-beta signaling pathways as significantly enriched by SOX11 target genes. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9052
4 Samples
Download data: BIGBED
Series
Accession:
GSE52146
ID:
200052146
5.

Chip-chip from Z138 MCL cell line with SOX11 antibody

(Submitter supplied) To determine the role of SOX11 in aggressive lymphoid neoplasm, we first investigated direct target genes of this transcription factor using chromatin immunoprecipitation and DNA microarrays (ChIP-chip) in MCL cell lines. Analysis of the exact location of SOX11 binding elements showed that SOX11 interacts with DNA predominantly in the enhancer regions (in 40% of the enriched regions) and intron segments (in 33% of the enriched regions), suggesting that in these genes SOX11 may interact with the general transcriptional machinery and transcriptional co-regulators.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL15114
4 Samples
Download data: PAIR, TXT
Series
Accession:
GSE35021
ID:
200035021
6.

SOX11 Gene Expression Profiling

(Submitter supplied) The neural transcription factor SOX11 is overexpressed in aggressive lymphoid neoplasms mainly in mantle cell lymphoma (MCL), but its functional role in malignant B-cells is unknown. To identify target genes transcriptionally regulated by SOX11 in malignant lymphoid cells, we have used Gene Expression Profiling (GEP) after SOX11 silencing in MCL cell lines.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4801
Platform:
GPL570
4 Samples
Download data: CEL
Series
Accession:
GSE34763
ID:
200034763
7.
Full record GDS4801

Neural transcription factor SOX11 depletion effect on mantle cell lymphoma cell line

Analysis of Z138 mantle cell lymphoma (MCL) cells depleted for the neural transcription factor SOX11. SOX11 is overexpressed in aggressive lymphoid neoplasms mainly in MCL. Results provide insight into the role of SOX11 in the pathogenesis of MCL.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 genotype/variation sets
Platform:
GPL570
Series:
GSE34763
4 Samples
Download data: CEL
DataSet
Accession:
GDS4801
ID:
4801
8.

SOX11-positive and SOX11-knockdown xenograft derived tumor Gene Expression Profilings

(Submitter supplied) The neural transcription factor SOX11 is overexpressed in aggressive lymphoid neoplasms mainly in mantle cell lymphoma (MCL). We have recently demonstrated SOX11 tumorigenic potential in vivo by showing a significant reduction on tumor growth of SOX11-knockdown MCL cells in xenograft experiments, confirming the clinical observations that SOX11 may play an important role in the aggressive behavior of MCL (Vegliante et al., 2013). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
14 Samples
Download data: CEL
Series
Accession:
GSE52892
ID:
200052892
9.

Mantle Cell Lymphoma

(Submitter supplied) Gene expression analyis of primary MCL including IGHV mutated and unmutated cases Gene set analysis was perfomed in MCL samples, comparing IGHV mutated cases vs. IGHV unmutated cases
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4984
Platform:
GPL570
38 Samples
Download data: CEL
Series
Accession:
GSE36000
ID:
200036000
10.
Full record GDS4984

IGHV mutated/unmutated Mantle Cell Lymphoma patients: B cell lymphocytes

Analysis of B cell lymphocytes from Mantle Cell Lymphoma (MCL) patients with unmutated or mutated immunoglobulin heavy chain variable (IGHV) genes. Results provide insight into the effect of IGHV mutational status on MCL clinical features.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL570
Series:
GSE36000
38 Samples
Download data: CEL
11.

Indolent MCL identified by genomic and gene expression profiling

(Submitter supplied) Mantle cell lymphoma (MCL) is an aggressive neoplasm with poor outcome. However, some patients have an indolent disease (iMCL) and may not require intensive treatment at initial diagnosis. Diagnostic criteria to recognize these patients are not available. We hypothesized that the analysis of the genetic and expression features of the tumors may help to identify patients with an indolent clinical evolution and provide biomarkers that could be used in the clinical setting.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
55 Samples
Download data: CEL
Series
Accession:
GSE16455
ID:
200016455
12.

Expression profiles of SOX11-positive and SOX11-negative Mantle Cell Lymphoma (MCL) primary samples from lymph node and reactive lymph nodes (RLN).

(Submitter supplied) Gene expression profiles were obtained via Nanostring nCounter Expression Assay (PanCancer Immune Profiling Panel, Nanostring Technologies, Hamburg, Germany). We aimed to obtain the differential immune gene expression comparing the lymph node microenvironment of SOX11-positive and SOX11-negative MCL primary samples and non-neoplastic nodal samples (RLN).
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL25262
20 Samples
Download data: RCC
Series
Accession:
GSE141539
ID:
200141539
13.

CCND2 rearrangements are the most frequent genetic events in Cyclin D1-negative mantle cell lymphoma [Affymetrix]

(Submitter supplied) Cyclin D1-negative mantle cell lymphomas (MCL) are not well characterized, in part due to the difficulties in their recognition. SOX11 has been recently identified as a reliable biomarker of MCL, also expressed in the cyclin D1-negative variant. We investigated 40 lymphomas with MCL morphology and immunophenotype, negative for cyclin D1 expression/t(11;14)(q13;q32) but SOX11-positive. These tumors presented clinically with generalized lymphadenopathy, advanced stage, and had a poor outcome (5-year overall survival 48%). more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array
Platforms:
GPL3720 GPL3718
10 Samples
Download data: CEL, TXT
Series
Accession:
GSE42935
ID:
200042935
14.

CCND2 rearrangements are the most frequent genetic events in Cyclin D1-negative mantle cell lymphoma [Agilent]

(Submitter supplied) Cyclin D1-negative mantle cell lymphomas (MCL) are not well characterized, in part due to the difficulties in their recognition. SOX11 has been recently identified as a reliable biomarker of MCL, also expressed in the cyclin D1-negative variant. We investigated 40 lymphomas with MCL morphology and immunophenotype, negative for cyclin D1 expression/t(11;14)(q13;q32) but SOX11-positive. These tumors presented clinically with generalized lymphadenopathy, advanced stage, and had a poor outcome (5-year overall survival 48%). more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL8736
27 Samples
Download data: TXT
Series
Accession:
GSE42917
ID:
200042917
15.

CCND2 rearrangements are the most frequent genetic events in Cyclin D1-negative mantle cell lymphoma

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array; Genome variation profiling by SNP array
Platforms:
GPL3720 GPL8736 GPL3718
37 Samples
Download data: CEL, TXT
Series
Accession:
GSE42854
ID:
200042854
16.

Identification of SoxC-regulated genes during neurogenesis in the developing spinal cord

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Gallus gallus; Mus musculus
Type:
Expression profiling by array
Platforms:
GPL3213 GPL1261
6 Samples
Download data: CEL
Series
Accession:
GSE106788
ID:
200106788
17.

Identification of SoxC-regulated genes during neurogenesis in the developing spinal cord [chicken]

(Submitter supplied) The HMG-domain containing SoxC transcription factors Sox4 and Sox11 are expressed in the vertebrate central nervous system in neuronal precursors and neuroblasts. They are required during early stages of neurogenesis. Here we perform micorarray analysis to identify genes that are downstream of these SoxC proteins during spinal cord neurogenesis in chicken. The identified genes represent potential direct target genes of Sox4 and Sox11.
Organism:
Gallus gallus
Type:
Expression profiling by array
Platform:
GPL3213
2 Samples
Download data: CEL
Series
Accession:
GSE106787
ID:
200106787
18.

Identification of SoxC-regulated genes during neurogenesis in the developing spinal cord [mouse]

(Submitter supplied) The HMG-domain containing SoxC transcription factors Sox4 and Sox11 are expressed in the vertebrate central nervous system in neuronal precursors and neuroblasts. They are required during early stages of neurogenesis. Here we perform micorarray analysis to identify genes that are downstream of these SoxC proteins during spinal cord neurogenesis in mouse. The identified genes represent potential direct target genes of Sox4 and Sox11.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
4 Samples
Download data: CEL
Series
Accession:
GSE106786
ID:
200106786
19.

Identification of SOX4 novel transcriptional targets.

(Submitter supplied) The SOX4 gene belongs to a family of transcription factors and we previously unveiled SOX4 gene amplification and over-expression in a subset of lung cancers, indicating it may constitute a driver oncogene. Here, we searched for SOX4 transcriptional targets and investigate their involvement in lung development and carcinogenesis. We abrogated SOX4 expression in the NIH-H522 lung cancer cell line, carrying SOX4 amplification and over-expression, using an inducible short-hairpin system. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
4 Samples
Download data: JPG, TXT
Series
Accession:
GSE31612
ID:
200031612
20.

Expression data from superficial zone cells of articular cartilage (SFZ) cells treated with retinoic acid

(Submitter supplied) To identify downstream transcription factors induced by retinoic acid, we stimulated SFZ cells with 10 μM retinoic acid for 24 hours and performed microarray analysis.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
2 Samples
Download data: CEL, CHP
Series
Accession:
GSE107069
ID:
200107069
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