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Items: 1 to 20 of 84

1.
Full record GDS5318

Drug efflux transporter ABCB5 knockdown effect on G3361 melanoma cells

Analysis of pigmented melanoma G3361 cell line following ABCB5 ablation. ABCB5 [ATP-binding cassette, subfamily B (MDR/TAP), member 5] is a drug efflux transporter shown to be highly overexpressed in diverse human cancers. Results provide insight into the role of ABCB5 in melanoma.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 protocol sets
Platform:
GPL571
Series:
GSE38290
6 Samples
Download data: CEL, EXP, TXT
2.
Full record GDS5317

Drug efflux transporter ABCB5 knockdown effect on A375 melanoma cells

Analysis of nonpigmented melanoma A375 cell line following ABCB5 ablation. ABCB5 [ATP-binding cassette, subfamily B (MDR/TAP), member 5] is a drug efflux transporter shown to be highly overexpressed in diverse human cancers. Results provide insight into the role of ABCB5 in melanoma.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 protocol sets
Platform:
GPL571
Series:
GSE38290
6 Samples
Download data: CEL, EXP, TXT
3.
Full record GDS5286

Monocyte-derived dendritic cells from young and aged donors

Comparison of dendritic cells (DCs) from young (20 to 27 years) and aged (77 to 87 years) donors. DCs are antigen-presenting cells important in initiating and regulating innate and adaptive immune responses. Results provide insight into the molecular basis of the decline in DC function with age.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 age sets
Platform:
GPL571
Series:
GSE58015
9 Samples
Download data: CEL
4.
Full record GDS5669

WHO grade IV primary glioblastoma of long-term survivors

Analysis of 7 patients with glioblastoma (GBM) treated at Memorial Sloan-Kettering Cancer Center, with survival > 48 months. These long-term survivors (LTSs) represent proneural, neural, classical, and mesenchymal subtypes of GBM. Results provide insight into molecular characteristics of GBM LTSs.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 4 disease state, 7 individual, 7 time sets
Platform:
GPL571
Series:
GSE54077
7 Samples
Download data: CEL
5.
Full record GDS5445

E3 ubiquitin ligase PARK2 depletion effect on SF539 glioma cell line

Analysis of SF539 glioma cells depleted for PARK2. PARK2 is an E3 ubiquitin ligase. Results provide insight into the role of PARK2 in the coordinate control of cyclins in cell cycle regulation and tumor suppression.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 3 agent sets
Platform:
GPL571
Series:
GSE50864
6 Samples
Download data: CEL
6.
Full record GDS5444

E3 ubiquitin ligase PARK2 depletion effect on SNB19 glioma cell line

Analysis of SNB19 glioma cells depleted for PARK2. PARK2 is an E3 ubiquitin ligase. Results provide insight into the role of PARK2 in the coordinate control of cyclins in cell cycle regulation and tumor suppression.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 3 agent sets
Platform:
GPL571
Series:
GSE50864
6 Samples
Download data: CEL
7.
Full record GDS5635

Chlamydia Type III secretion effector TepP-deficient mutant infection of endocervical epithelial cells in vitro

Analysis of A2EN endocervical epithelial cells infected with a Chlamydia trachomatis mutant strain lacking type III secretion effector TepP (Ct875) or its complemented counterpart for 4hr. Results provide insight into the impact of effector protein TepP on the host cell molecular response.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 3 infection sets
Platform:
GPL571
Series:
GSE54336
6 Samples
Download data: CEL
8.
Full record GDS4897

Skeletal muscle of patients with inherited insulin resistance

Analysis of muscle from patients with a mutation (Arg1174Gln) in the tyrosine kinase domain of the insulin receptor gene (INSR). This mutation is associated with inherited insulin resistance. Results provide insight into molecular mechanisms underlying insulin resistance in skeletal muscle.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 genotype/variation sets
Platform:
GPL571
Series:
GSE36297
16 Samples
Download data: CEL
DataSet
Accession:
GDS4897
ID:
4897
9.
Full record GDS5076

PIAS1 SUMO ligase depletion effect on breast cancer cell line

Analysis of MDA-MB231 breast cancer cells depleted for PIAS1. PIAS1 is a SUMO ligase. Results provide insight into the role of PIAS1 in breast tumorigenesis.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 growth protocol, 2 protocol sets
Platform:
GPL571
Series:
GSE44024
4 Samples
Download data: CEL, CHP
10.
Full record GDS4875

Proliferator-activated receptor gamma agonist rosiglitazone effect on extravillous cytotrophoblasts in vitro

Analysis of EVCTs isolated from first trimester placenta and treated with rosiglitazone, a PPARγ agonist. EVCT invasion into the uterus is critical for placental and fetal development. Results provide insight into the molecular basis of PPARγ-mediated regulation of EVCT invasion in vitro.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent sets
Platform:
GPL571
Series:
GSE28426
10 Samples
Download data: CEL
11.
Full record GDS5339

Endometriosis: ectopic and eutopic endometrium

Analysis of ectopic endometria and eutopic endometria from endometriosis patients. Endometriosis is characterized by the presence of endometrial tissue at extra-uterine sites. Results provide insight into the molecular mechanisms underlying endometriosis pathogenesis.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 disease state, 3 tissue sets
Platform:
GPL571
Series:
GSE25628
22 Samples
Download data: CEL
DataSet
Accession:
GDS5339
ID:
5339
12.
Full record GDS4891

Discoid lupus erythematosus and psoriasis skin biopsies

Analysis of discoid lupus erythematosus (DLE) and psoriasis skin samples. DLE is the most common skin manifestation of lupus; psoriasis is the most well-characterized autoimmune skin disease to date. Results provide insight into the molecular mechanisms underlying DLE skin.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 3 disease state, 2 other sets
Platform:
GPL571
Series:
GSE52471
38 Samples
Download data: CEL
13.
Full record GDS4871

Donor lymphocyte infusion effect on bone marrow-infiltrating CD3+ T cells of patients with relapsed chronic myelogenous leukemia

Analysis of marrow-infiltrating CD3+ T cells isolated from relapsed chronic myelogenous leukemia (CML) patients following donor lymphocyte infusion (DLI) therapy. Four patients were DLI-responsive, two were DLI-nonresponsive. Results provide mechanistic insights into DLI response in relapsed CML.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 individual, 2 protocol sets
Platform:
GPL571
Series:
GSE49067
12 Samples
Download data: CEL
14.
Full record GDS4962

Transcription factor ETS fusion EWS/FLI1 knockdown in Ewing sarcoma cell line: time course

Analysis of A673 Ewing Sarcoma cell line for up to 96hrs after inducible EWSR1/FLI1 knockdown. Oncogenic ETS fusions are driver mutations in diverse cancers, including Ewing sarcoma. Results provide insight into the molecular mechanisms underlying ETS-driven tumorigenesis.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 protocol, 6 time sets
Platform:
GPL571
Series:
GSE27524
16 Samples
Download data: CEL
15.
Full record GDS4989

PGC1alpha depletion effect on melanoma cell line

Analysis of A375P melanoma cells depleted for PGC1alpha. PGC1alpha is a transcriptional coactivator that promotes mitochondrial biogenesis and respiration. A375P is a cell line that overexpresses PGC1alpha. Results provide insight into the role of PGC1alpha in melanoma.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 protocol sets
Platform:
GPL571
Series:
GSE36879
8 Samples
Download data: CEL
16.
Full record GDS5154

FAT1 depletion effect on astrocyte and glioma cell lines

Analysis of astrocyte and glioma cells depleted for FAT1. FAT1 encodes a cadherin-like protein. Results provide insight into the role of FAT1 in cancer development.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 3 cell line, 2 cell type, 2 protocol sets
Platform:
GPL571
Series:
GSE40583
18 Samples
Download data: CEL
17.
Full record GDS4353

Cerebral Palsy: skeletal muscle biopsies

Analysis of gracilis and semitendinosus muscle biopsies from pediatric cerebral palsy (CP) patients. Muscles from CP patients are spastic and form contractures limiting range of motion and joint function. Results provide insight into molecular basis of skeletal muscle response to CP.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 disease state, 2 tissue sets
Platform:
GPL571
Series:
GSE31243
40 Samples
Download data: CEL
18.
Full record GDS4597

In vitro model for inflammatory dendritic cells

Analysis of an in vitro model of peptidoglycan-activated monocytes as inflammatory myeloid dendritic cells (DCs). DCs are thought to have an important role in the pathogenesis of inflammatory skin lesions such as psoriasis. Results provide insight into molecular basis of psoriasis pathogenesis.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 5 agent sets
Platform:
GPL571
Series:
GSE42305
15 Samples
Download data: CEL
19.
Full record GDS4401

H9 hESC-derived neural stem cells harboring pathogenic leucine-rich repeat kinase 2 mutation

Analysis of LRRK2 (Gly2019Ser) mutant neural stem cells (NSC) treated with LRRK2 kinase specific inhibitor LRRK2-IN-1. The LRRK2 (G2019S) mutation causes familial Parkinson's disease. Results provide insight into molecular basis of progressive degeneration of NSCs caused by pathogenic LRRK2.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent, 2 genotype/variation sets
Platform:
GPL571
Series:
GSE36321
9 Samples
Download data: CEL
20.
Full record GDS4400

Fibroblast-derived induced pluripotent stem cells harboring pathogenic leucine-rich repeat kinase 2 mutation

Analysis of IPSCs generated from LRRK2 (Gly2019Ser) mutation-bearing patient fibroblasts by cell reprogramming. The LRRK2 (G2019S) mutation causes familial Parkinson's disease (PD). Results provide insight into the molecular mechanisms underlying PD.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 3 cell type, 3 genotype/variation sets
Platform:
GPL571
Series:
GSE33298
14 Samples
Download data: CEL
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db=gds|term=911%201646%201733%201735%202038%202295%202310%202417%202478%202535%202563%202606%202622%202626%202676%202706%202754%202778%202920%202939%203011%203029%203032%203155%203160%203218%203309%203324%203362%203363%203393%203459%203470%203484%203518%203576%203581%203606%203609%203638%203750%203797%203838%203980%204052%204059%204063%204070%204084%204101%204110%204154%204175%204196%204301%204353%204400%204401%204448%204451%204458%204550%204569%204595%204597%204606%204607%204846%204871%204875%204891%204897%204962%204989%205076%205154%205286%205317%205318%205339%205444%205445%205635%205669[uid]|query=1|qty=2|blobid=MCID_665630066c05354989de899c|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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