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Links from GEO DataSets

Items: 12

1.

TEL-AML1 (ETV6-RUNX1) in B-cells and leukemia (part 6)

(Submitter supplied) We identified directly and indirectly regulated target genes utilizing an inducible TEL-AML1 system derived from the murine pro B-cell line BA/F3 and a monoclonal antibody directed against TEL-AML1. By integration of promoter binding identified with ChIP-on-chip, gene expression and protein output through microarray technology and stable labelling of amino acids in cell culture (SILAC), we identified directly and indirectly regulated targets of the TEL-AML1 fusion protein.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
4 Samples
Download data: CEL
Series
Accession:
GSE50735
ID:
200050735
2.

TEL-AML1 (ETV6-RUNX1) in B-cells and leukemia

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by array; Genome binding/occupancy profiling by genome tiling array
4 related Platforms
23 Samples
Download data: CEL, PAIR, TXT
Series
Accession:
GSE50736
ID:
200050736
3.

TEL-AML1 (ETV6-RUNX1) in B-cells and leukemia (part 5)

(Submitter supplied) We identified directly and indirectly regulated target genes utilizing an inducible TEL-AML1 system derived from the murine pro B-cell line BA/F3 and a monoclonal antibody directed against TEL-AML1. By integration of promoter binding identified with ChIP-on-chip, gene expression and protein output through microarray technology and stable labelling of amino acids in cell culture (SILAC), we identified directly and indirectly regulated targets of the TEL-AML1 fusion protein.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13607
6 Samples
Download data: TXT
Series
Accession:
GSE50734
ID:
200050734
4.

TEL-AML1 (ETV6-RUNX1) in B-cells and leukemia (part 4)

(Submitter supplied) We identified directly and indirectly regulated target genes utilizing an inducible TEL-AML1 system derived from the murine pro B-cell line BA/F3 and a monoclonal antibody directed against TEL-AML1. By integration of promoter binding identified with ChIP-on-chip, gene expression and protein output through microarray technology and stable labelling of amino acids in cell culture (SILAC), we identified directly and indirectly regulated targets of the TEL-AML1 fusion protein.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL15448
3 Samples
Download data: PAIR
Series
Accession:
GSE50733
ID:
200050733
5.

TEL-AML1 (ETV6-RUNX1) in B-cells and leukemia (part 3)

(Submitter supplied) We identified directly and indirectly regulated target genes utilizing an inducible TEL-AML1 system derived from the murine pro B-cell line BA/F3 and a monoclonal antibody directed against TEL-AML1. By integration of promoter binding identified with ChIP-on-chip, gene expression and protein output through microarray technology and stable labelling of amino acids in cell culture (SILAC), we identified directly and indirectly regulated targets of the TEL-AML1 fusion protein.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL8943
3 Samples
Download data: PAIR
Series
Accession:
GSE50732
ID:
200050732
6.

TEL-AML1 (ETV6-RUNX1) in B-cells and leukemia (part 2)

(Submitter supplied) We identified directly and indirectly regulated target genes utilizing an inducible TEL-AML1 system derived from the murine pro B-cell line BA/F3 and a monoclonal antibody directed against TEL-AML1. By integration of promoter binding identified with ChIP-on-chip, gene expression and protein output through microarray technology and stable labelling of amino acids in cell culture (SILAC), we identified directly and indirectly regulated targets of the TEL-AML1 fusion protein.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL8943
3 Samples
Download data: PAIR
Series
Accession:
GSE50731
ID:
200050731
7.

TEL-AML1 (ETV6-RUNX1) in B-cells and leukemia (part 1)

(Submitter supplied) We identified directly and indirectly regulated target genes utilizing an inducible TEL-AML1 system derived from the murine pro B-cell line BA/F3 and a monoclonal antibody directed against TEL-AML1. By integration of promoter binding identified with ChIP-on-chip, gene expression and protein output through microarray technology and stable labelling of amino acids in cell culture (SILAC), we identified directly and indirectly regulated targets of the TEL-AML1 fusion protein.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL8943
4 Samples
Download data: PAIR
Series
Accession:
GSE50730
ID:
200050730
8.

Five distinct biological processes and 14 differentially expressed genes characterize TEL/AML1-positive leukemia

(Submitter supplied) Background The t(12;21)(p13;q22) translocation is found in 20 to 25% of cases of childhood B-lineage acute lymphoblastic leukemia (B-ALL). This rearrangement results in the fusion of ETV6 (TEL) and RUNX1 (AML1) genes and defines a relatively uniform category, although only some patients suffer very late relapse. TEL/AML1-positive patients are thus an interesting subgroup to study, and such studies should elucidate the biological processes underlying TEL/AML1 pathogenesis. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1708
33 Samples
Download data: TXT
Series
Accession:
GSE9170
ID:
200009170
9.

TEL-AML1 regulation of survivin and apoptosis via miRNA-494 and miRNA-320a

(Submitter supplied) There is increasing evidence that microRNA and transcription factors interact in an instructive fashion in normal and malignant hematopoiesis. We explored the impact of TEL-AML1 (ETV6-RUNX1), the most common fusion protein in childhood leukemia, on miRNA expression and the leukemic phenotype. Using RNA interference, miRNA expression arrays, and quantitative PCR, we identified miRNA-494 and miRNA-320a to be upregulated upon TEL-AML1 silencing independently of TEL expression. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL10861
2 Samples
Download data: TXT
Series
Accession:
GSE23842
ID:
200023842
10.

Genes regulated in EML1 cells expressing the TEL-AML1 oncogene after 5 and 7 days of treatment with IL7 and FLT3 ligand.

(Submitter supplied) The t(12;21) translocation is the most common genetic rearrangement in childhood acute lymphoblastic leukemia (ALL) and gives rise to the TEL-AML1 fusion gene, which functions as a transcription factor. TEL-AML1 expression in EML1 cells results in an impairment of differentiation along the B-lymphoid lineage.
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS5661
Platform:
GPL11533
12 Samples
Download data: CEL
Series
Accession:
GSE64919
ID:
200064919
11.
Full record GDS5661

Interleukin 7 and FLT-3 ligand effect on EML1 HSPC line expressing acute lymphoblastic leukemia TEL-AML1 fusion protein: time course

Analysis of TEL-AML1 oncogene-expressing hematopoietic stem/progenitor cell line EML1 treated with interleukin 7 (IL7) and FLT3 ligand (FLT3L) for up to 7 days. IL7 and FLT3L treatment induces B-cell differentiation. Results provide insight into the role of TEL-AML1 in early B-cell differentiation.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation, 2 protocol, 3 time sets
Platform:
GPL11533
Series:
GSE64919
12 Samples
Download data: CEL
DataSet
Accession:
GDS5661
ID:
5661
12.

Autophagy driving ETV6-RUNX1 positive leukaemia

(Submitter supplied) This file contains the gene expression data for 654 pediatric acute lymphoblastic leukemia samples
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
654 Samples
Download data: CEL
Series
Accession:
GSE87070
ID:
200087070
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