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Links from GEO DataSets

Items: 20

1.

Expression data of Wnt3a stimulated K562 cells after CXXC5 overexpression or knockdown

(Submitter supplied) CXXC5 inhibits the canonical Wnt signaling pathway Impact of CXXC5 on Wnt stimulated gene expression in K562 cells
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL571
12 Samples
Download data: CEL, CHP
Series
Accession:
GSE67060
ID:
200067060
2.

Genes regulated after knock-down of Pirin in U937 cells

(Submitter supplied) Pirin (PIR) is a putative transcriptional regulator whose expression is silenced in cells bearing the AML1/ETO and PML/RAR leukemogenic fusion proteins and is significantly repressed in a large proportion of acute myeloid leukemias. PIR expression increases during in vitro myeloid differentiation of primary hematopoietic precursor cells, and ablation of PIR in the U937 myelomonocytic cell line or in murine primary hematopoietic precursor cells results in impairment of terminal myeloid differentiation. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS5254
Platform:
GPL570
4 Samples
Download data: CEL
Series
Accession:
GSE16798
ID:
200016798
3.
Full record GDS5254

Pirin depletion effect on myelomonocytic cell line

Analysis of U937 myelomonocytic cells depleted for Pirin. Pirin is silenced in cells with the acute myeloid leukemia-1 eight-twenty-one and promyelocytic leukemia/retinoic acid receptor leukemogenic fusion proteins. Results provide insight into the role of Pirin in myeloid differentiation.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 protocol sets
Platform:
GPL570
Series:
GSE16798
4 Samples
Download data: CEL
DataSet
Accession:
GDS5254
ID:
5254
4.

Chromatin accessibility, p300 and histone acetylation define PML-RARalpha- and AML1-ETO-binding sites

(Submitter supplied) Chromatin accessibility is a key determinant of cell-type-specific gene expression. Here, we have investigated the chromatin architecture of different acute myeloid leukemia (AML) cells and the changes in accessibility when NB4 (APL) cells undergo the process of differentiation.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9052
25 Samples
Download data: BED, WIG
Series
Accession:
GSE30254
ID:
200030254
5.

RUNX1 mutated cases in acute myeloid leukemia share a distinct biological subgroup and are associated with inferior outcome. Results of the AML Study Group (AMLSG).

(Submitter supplied) PURPOSE: To evaluate frequency, biological features and clinical relevance of RUNX1 mutations in acute myeloid leukemia (AML). PATIENTS AND METHODS: Diagnostic samples from 945 patients (18 to 60 years) were analyzed for RUNX1 mutations. In a subset of cases (n=269) microarray gene expression analysis was performed. RESULTS: Fifty-nine RUNX1 mutations were identified in 53 of 945 (5.6%) cases, predominantly in exons 3 (n=11), 4 (n=10) and 8 (n=23). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
9 related Platforms
269 Samples
Download data
Series
Accession:
GSE23312
ID:
200023312
6.

Altered miRNA and gene expression in acute myeloid leukemia with complex karyotype identify networks of prognostic relevance

(Submitter supplied) Recently, the p53-miR-34a network was identified to play an important role in tumorigenesis. As in acute myeloid leukemia with complex karyotype (CK-AML) TP53 alterations are the most common known molecular lesion, we further analyzed the p53-miR-34a axis in CK-AML with known TP53 status. Clinically, low miR-34a expression and TP53 alterations predicted for chemotherapy resistance and inferior outcome. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
12 Samples
Download data: CEL
Series
Accession:
GSE39730
ID:
200039730
7.

Long non-coding RNA HOXB-AS3 promotes myeloid cell proliferation and its higher expression is an adverse prognostic marker in myeloid malignancies [MDS_normal]

(Submitter supplied) The mononucleated cells were collected from the bone marrow samples of MDS patients and healthy controls. We compared the expressions between MDS patients and the healthy controls.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17586
320 Samples
Download data: CEL
Series
Accession:
GSE114869
ID:
200114869
8.

Long non-coding RNA HOXB-AS3 promotes myeloid cell proliferation and its higher expression is an adverse prognostic marker in myeloid malignancies [AML_normal]

(Submitter supplied) The mononucleated cells were collected from the bone marrow samples of AML patients and healthy controls. We compared the expressions between AML patients and the healthy controls.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17586
214 Samples
Download data: CEL
Series
Accession:
GSE114868
ID:
200114868
9.

HOXB-AS3 expressions promote cell proliferation

(Submitter supplied) We knock down HOXB-AS3 with shRNA in OCI/AML3 cell line to investigate the downstream pathways of HOXB-AS3 in the cell proliferation.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17586
4 Samples
Download data: CEL
Series
Accession:
GSE114823
ID:
200114823
10.

Gene expression profiles of mono- and biallelic CEBPA mutations in cytogenetically normal AML

(Submitter supplied) Purpose: CEBPA mutations are found as either biallelic (biCEBPA) or monoallelic (moCEBPA). We set out to explore whether the kind of CEBPA mutation is of prognostic relevance in cytogenetically normal AML (CN-AML). Patients and Methods: 467 homogeneously treated CN-AML patients were subdivided into moCEBPA, biCEBPA and wildtype (wt) CEBPA patients. The subgroups were analyzed for clinical parameters and for additional mutations in the NPM1, FLT3 and MLL genes. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL8289
61 Samples
Download data: CEL
Series
Accession:
GSE15210
ID:
200015210
11.

DMSO control and DZNep treated MOLM-14 cells

(Submitter supplied) We demonstrated that 3-Deazaneplanocin A (DZNep), a histone methyltransferase inhibitor, induce robust apoptosis in AML cells through increased ROS production and ER stress. We identified a core gene signature including TXNIP, a major redox control molecule which is crucial in DZNep-induced apoptosis.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
4 Samples
Download data: CEL
Series
Accession:
GSE30315
ID:
200030315
12.

Whole-genome DNA methylation profiling of 152 pediatric AML patients

(Submitter supplied) Genome-wide CpG-island methylation profiling on pediatric AML samples was performed to identify specific methylation patterns discriminating particular AML subgroups from the rest of AML samples based on the methylation profile.
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL9767
152 Samples
Download data: TXT
Series
Accession:
GSE100284
ID:
200100284
13.

Gene expression profiling of 35 AML FAB-M0 samples

(Submitter supplied) Ficolled AML-M0 sample gene expression profiles on Affymetrix HGU133Plus2.0 GeneChips. Acute myeloid leukemia (AML) classified as FAB-M0 is defined as a subtype with minimally differentiated morphology. Here we investigated by gene expression (GEP) profiling whether AML-M0 cases should be considered as one or more unique molecular subgroups that discriminates them from other AML patients. By applying GEP and subsequent unsupervised analysis of 35 AML-M0 samples and 253 previously reported AML cases, we demonstrate that AML-M0 cases express a unique signature. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
35 Samples
Download data: CEL
Series
Accession:
GSE17061
ID:
200017061
14.

Expression profile and whole genome SNP data from acute monocytic leukemia patients

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by SNP array; SNP genotyping by SNP array
Platforms:
GPL570 GPL8887 GPL8888
19 Samples
Download data: CEL
Series
Accession:
GSE27244
ID:
200027244
15.

High VEGFC expression is associated with unique gene expression profiles and predicts adverse prognosis in pediatric and adult acute myeloid leukemia.

(Submitter supplied) High VEGFC mRNA expression of AML blasts is related to increased in vitro and in vivo drug resistance. The prognostic significance of VEGFC on long-term outcome and its associated gene expression profiles remain to be defined. We studied the effect of VEGFC on treatment outcome and investigated gene expression profiles associated with VEGFC using microarray data of 525 adult and 100 pediatric AML patients. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
98 Samples
Download data: CEL
Series
Accession:
GSE22056
ID:
200022056
16.

Acute myeloid leukemia samples of samples =< 60yrs on HG-U133 plus 2

(Submitter supplied) The pretreatment karyotype of leukemic blasts is currently the key determinant in therapy decision-making in acute myeloid leukemia (AML). However, approximately fifty percent of AML patients, often carrying a normal karyotype, are currently unclassifiable based these established methods. Gene expression profiling has proven to be valuable for risk stratification of AML. The gene expression profiles of AML samples of two independent cohorts (n=247 and n=214) were determined using Affymetrix U133Plus2.0 GeneChips: all Samples below 4000 are in the training cohort; all Samples higher than 4000 are in the validation cohort. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
537 Samples
Download data: CEL
Series
Accession:
GSE6891
ID:
200006891
17.

The DNA Double-Strand Break Response Is Abnormal in Myeloblasts From Patients With Therapy-Related Acute Myeloid Leukemia

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by genome tiling array
Platforms:
GPL18053 GPL570
44 Samples
Download data: CEL, PAIR
Series
Accession:
GSE53251
ID:
200053251
18.

The DNA Double-Strand Break Response Is Abnormal in Myeloblasts From Patients With Therapy-Related Acute Myeloid Leukemia [NimbleGen]

(Submitter supplied) In order to examine if acquired copy number alterations in DNA repair genes is commonly observed in therapy-related AML, we used this custom built NimbleGen array with dense tiling of probes in 170 DNA repair genes to interrogate paired normal (skin) and tumor (bone marrow) samples.
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL18053
30 Samples
Download data: PAIR
Series
Accession:
GSE53250
ID:
200053250
19.

The DNA Double-Strand Break Response Is Abnormal in Myeloblasts From Patients With Therapy-Related Acute Myeloid Leukemia [Affymetrix]

(Submitter supplied) In order to examine if the upregulation of DNA repair genes on chromosome 8 was associated with the abnormal DSB phenotype observed in trisomy 8 (defined by array CGH or cytogenetics), we compared the mRNA levels of DNA repair genes on chromosome 8 in trisomy 8 t-AML patients versus normal t-AML gammaH2AX responders using gene expression array data.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
14 Samples
Download data: CEL, TXT
Series
Accession:
GSE52478
ID:
200052478
20.

Role of NFATc1 in patients with FLT3-ITD AML

(Submitter supplied) Diagnostic samples of peripheral blood form acute myeloid leukemia were analysed for gene expression differences MLL Munich Leukemia Laboratory
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
325 Samples
Download data: CEL, PDF
Series
Accession:
GSE61804
ID:
200061804
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