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Links from GEO DataSets

Items: 7

1.

Imatinib effects on CD34+ cells

(Submitter supplied) purified CD34+ cells from bone marrow of imatinib-treated patients were compared to those of healthy donors Keywords = CML Keywords = CD34+ cells Keywords = imatinib Keywords: ordered
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS838
Platform:
GPL201
14 Samples
Download data: CEL
Series
Accession:
GSE1418
ID:
200001418
2.
Full record GDS838

Imatinib effects on chronic myelogenous leukemia CD34+ cells

Comparison of purified bone marrow CD34+ cells from imatinib-treated chronic myelogenous leukemia (CML) patients and healthy donors.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 agent sets
Platform:
GPL201
Series:
GSE1418
14 Samples
Download data: CEL
DataSet
Accession:
GDS838
ID:
838
3.

Gene expression of CML CD34+ cells during Imatinib therapy

(Submitter supplied) Imatinib has become the current standard therapy for patients with chronic myelogenous leukaemia (CML). For a better understanding of the Imatinib-related molecular effects in vivo, we assessed gene expression profiles of Philadelphia Chromosome positive (Ph+) CD34+ cells from peripheral blood of 6 patients with de novo CML in chronic phase. After 7 days of treatment with Imatinib the Ph+ CD34+ cells were reassessed to look for changes in the transcriptome. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3518
Platform:
GPL571
12 Samples
Download data: CEL, CHP
Series
Accession:
GSE12211
ID:
200012211
4.
Full record GDS3518

Chronic myelogenous leukemia response to imatinib: Philadelphia chromosome positive CD34+ cells

Analysis of Philadelphia chromosome-positive CD34+ cells of chronic myelogenous leukemia patients treated with imatinib. The anti-cancer drug imatinib is a selective bcr-abl tyrosine kinase inhibitor. Results provide insight into the molecular events affected by bcr-abl inhibition through imatinib.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent, 6 individual sets
Platform:
GPL571
Series:
GSE12211
12 Samples
Download data: CEL, CHP
DataSet
Accession:
GDS3518
ID:
3518
5.

BCR/ABL1-Dependent Transcriptional Response Reveals Enrichment for Genes Involved in Negative Feedback Regulation

(Submitter supplied) Philadelphia (Ph) chromosome-positive leukemia is characterized by the BCR/ABL1 fusion protein that affects a wide range of signal transduction pathways. The knowledge about its downstream target genes is, however, still quite limited. To identify novel BCR/ABL1-regulated genes we used global gene expression profiling of several Ph-positive and Ph-negative cell lines treated with imatinib. Following imatinib treatment, the Ph-positive cells showed decreased growth, viability, and reduced phosphorylation of BCR/ABL1 and STAT5. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4861
72 Samples
Download data: GPR
Series
Accession:
GSE10283
ID:
200010283
6.

Imatinib therapy of chronic myeloid leukemia restores the expression levels of key genes for DNA damage and cell cycle progression

(Submitter supplied) Background: Chronic myeloid leukemia (CML) is a malignant clonal disorder of the hematopoietic system caused by the expression of the BCR/ABL fusion oncogene. It is well known that CML cells are genetically unstable. However, the mechanisms by which these cells acquire genetic alterations are poorly understood. Imatinib mesylate (IM) is the standard therapy for newly diagnosed CML patients. IM targets the oncogenic kinase activity of BCR-ABL. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4869
Platform:
GPL570
27 Samples
Download data: CEL
Series
Accession:
GSE33075
ID:
200033075
7.
Full record GDS4869

Imatinib mesylate effect on bone marrow hematopoietic cells of chronic myeloid leukemia patients

Analysis of bone marrow hematopoietic cells in chronic myeloid leukemia (CML) patients one month after imatinib mesylate (IM) therapy. CML is caused by expression of the BCR/ABL fusion oncogene. Results provide insight into the molecular consequences of IM blockade of oncoprotein Bcr-Abl in CML.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 10 age, 10 gender, 10 individual, 3 protocol sets
Platform:
GPL570
Series:
GSE33075
27 Samples
Download data: CEL
DataSet
Accession:
GDS4869
ID:
4869
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