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Links from GEO DataSets

Items: 20

1.
Full record GDS2721

Pubertal mammary gland development

Analysis of mammary glands of animals from pre-puberty to post-puberty. Results provide insight into the mechanisms underlying mammary gland development during puberty.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 5 age, 3 development stage sets
Platform:
GPL339
Series:
GSE6453
14 Samples
Download data: CEL
DataSet
Accession:
GDS2721
ID:
2721
2.

Expression microarray analysis of pubertal mouse mammary gland development

(Submitter supplied) The aim was to carry out global analysis of gene expression changes occurring in the normal pubertal mouse mammary gland from the appearance to the regression of terminal end buds. Keywords: developmental time course
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2721
Platform:
GPL339
14 Samples
Download data: CEL
Series
Accession:
GSE6453
ID:
200006453
3.

Novel Estrogen Receptor-{alpha} Binding Sites and Estradiol Target Genes Identified by ChIP Cloning in Breast Cancer.

(Submitter supplied) Estrogen receptor-{alpha} (ER{alpha}) and its ligand estradiol play critical roles in breast cancer growth and are important therapeutic targets for this disease. Using chromatin immunoprecipitation (ChIP)-on-chip, ligand-bound ER{alpha} was recently found to function as a master transcriptional regulator via binding to many cis-acting sites genome-wide. Here, we used an alternative technology (ChIP cloning) and identified 94 ER{alpha} target loci in breast cancer cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3283
Platform:
GPL570
9 Samples
Download data: CEL
Series
Accession:
GSE11506
ID:
200011506
4.
Full record GDS3283

Estradiol effect on breast cancer cell line: time course

Analysis of MCF-7 breast cancer cells treated with estradiol for 3 or 6 hours. Results combined with ChIP experiments to identify estrogen receptor alpha binding sites and estradiol target genes in breast cancer cells.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 agent, 2 time sets
Platform:
GPL570
Series:
GSE11506
9 Samples
Download data: CEL
DataSet
Accession:
GDS3283
ID:
3283
5.

Expression profiling of MCF-7 cells with inducible LMO4 and DN-Clim expression

(Submitter supplied) The nuclear LIM-only protein LMO4 is upregulated in breast cancer, especially estrogen receptor negative tumors, and its overexpression in mice leads to hyperplasia and tumor formation. Here, we show that deletion of LMO4 in the mammary glands of mice leads to impaired lobuloalveolar development due to decreased epithelial cell proliferation. With the goal of discovering potential LMO4-target genes, we also developed a conditional expression system in MCF-7 cells for both LMO4 and a dominant negative (DN) form of its co-regulator, Co-factor of LIM domains (Clim/Ldb/Nli). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS2787 GDS2788 GDS2789
Platforms:
GPL96 GPL97 GPL570
18 Samples
Download data: CEL
Series
Accession:
GSE7382
ID:
200007382
6.
Full record GDS2789

LIM homeobox protein cofactor dominant negative form effect on breast cancer cell line

Analysis of breast cancer MCF-7 cells after the induction of expression of a dominant negative form of the cofactor of LIM domains (CLIM), a co-regulator of the nuclear LIM only protein 4 (LMO4). LMO4 is upregulated in breast cancer. Results provide insight into the role of LMO4 in tumor formation.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 protocol sets
Platform:
GPL570
Series:
GSE7382
6 Samples
Download data: CEL
DataSet
Accession:
GDS2789
ID:
2789
7.
Full record GDS2788

LIM-only protein 4 induction effect on breast cancer cell line (HG-U133B)

Analysis of breast cancer MCF-7 cells following the induction of expression of nuclear LIM-only protein 4 (LMO4). LMO4 is upregulated in breast cancer. Results provide insight into the role of LMO4 in promoting tumor formation.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 protocol sets
Platform:
GPL97
Series:
GSE7382
6 Samples
Download data: CEL
DataSet
Accession:
GDS2788
ID:
2788
8.
Full record GDS2787

LIM-only protein 4 induction effect on breast cancer cell line (HG-U133A)

Analysis of breast cancer MCF-7 cells following the induction of expression of nuclear LIM-only protein 4 (LMO4). LMO4 is upregulated in breast cancer. Results provide insight into the role of LMO4 in promoting tumor formation.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 protocol sets
Platform:
GPL96
Series:
GSE7382
6 Samples
Download data: CEL
DataSet
Accession:
GDS2787
ID:
2787
9.

An estrogen-dependent model of breast cancer created by transformation of normal human mammary epithelial cells

(Submitter supplied) This study was performed to check that ESR1 and BMI1 are biologically active after lentiviral transduction of primary human mammary epithelial cells (HMECs) with lentiviral vectors expressing ESR1 and BMI1 from the human PGK promoter. ESR1 targets like PGR, PRLR and GREB1, but not TFF1 and XBP1, were induced by estradiol in the ESR1-expressing cells. BMI1 targets like BMI1, NEFL and CCND2 were repressed in the BMI1-expressing cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
8 Samples
Download data: CEL
Series
Accession:
GSE6548
ID:
200006548
10.

TFAP2C regulates multiple pathways of estrogen signaling

(Submitter supplied) We were interested in determining what genes might be controlled by TFAP2C and/or TFAP2A, either directly or indirectly through regulation of ER-alpha and potentially other signaling pathways. We performed an microarray analysis in MCF7 cells with elimination of either TFAP2C or TFAP2A. The patterns of gene expression with alteration of TFAP2 activity were compared to changes in expression induced by estrogen exposure. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
6 Samples
Download data: CEL, CHP
Series
Accession:
GSE8640
ID:
200008640
11.

Estrogen-responsive genes in the parenchyma and fat pad of the bovine mammary gland by microarray analysis

(Submitter supplied) Characterizing estrogen-responsive genes is an essential step towards fully understanding mechanisms of estrogen action during mammary gland development and function. To catalogue these genes, sixteen prepubertal heifers were used in a 2 x 2 factorial with ovarian status (intact or ovariectomized) as the first factor and estrogen treatment as the second (control or estradiol). Heifers were ovariectomized at approximately 4.5 months of age and estrogen treatments were initiated one month later. more...
Organism:
Bos taurus
Type:
Expression profiling by array
Platform:
GPL3711
32 Samples
Download data: CEL
Series
Accession:
GSE4054
ID:
200004054
12.

The gene expression program of the developing mammary gland

(Submitter supplied) The developing mammary gland contains distinct microenvironments that perform specialized functions for branching and ductal invasion. These microenvironments include the terminal end buds (TEBs) at the tips of invading primary ducts and the more differentiated proximal ducts that give rise to side branches. We have devised a novel microarray approach to identify genes that are expressed in the epithelium and stroma of these distinct microenvironments. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2115
Platform:
GPL2660
12 Samples
Download data
Series
Accession:
GSE2988
ID:
200002988
13.
Full record GDS2115

Developing mammary gland: terminal end buds and ducts

Comparison of terminal end buds (TEBs) and ducts from 5-week-old mammary glands. TEBs and ducts perform specialized functions for ductal invasion and branching. Results provide insight into the epithelial-stromal crosstalk that drives mammary morphogenesis.
Organism:
Mus musculus
Type:
Expression profiling by array, log2 ratio, 2 tissue sets
Platform:
GPL2660
Series:
GSE2988
12 Samples
Download data
14.

Estrogen Receptor alpha ChIP-Seq in mouse mammary gland

(Submitter supplied) Estrogen Receptor is a key transcriptional regulator in mammary gland development and breast cancer. In this study, we have mapped the Estrogen Receptor chromatin binding patterns in healthy mouse mammary gland
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
2 Samples
Download data: BED, TXT
Series
Accession:
GSE43415
ID:
200043415
15.

Cyclin D1 determines estrogen dependent signaling in human breast cancer cell line MCF7

(Submitter supplied) The CCND1 gene, which is frequently overexpressed in cancers, encodes the regulatory subunit of a holoenzyme that phosphorylates the retinoblastoma protein (pRb). It is known that cyclin D1 regulates ERα transactivation using heterologous reporter systems, the significance of this observation to E2 dependent gene activation is unknow. E2 stimulated MCF7 cells treated with cyclin D1 siRNA in order to analyze the genes regulated by estradiol in a cyclin D1 dependent manner. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
8 Samples
Download data: CEL
Series
Accession:
GSE48989
ID:
200048989
16.

Cyclin D1 determines estrogen depependent signaling in mouse mammary gland.

(Submitter supplied) Ovariectomized virgin Ccnd1-/- and Ccnd1+/+ mice (5 weeks of age) were allowed to recuperate for 2 weeks. The mice were assigned to either replacement pellets containing E2 (0.75 mg, 60-day release) or pellet containing placebo. Mice were sacrificed at day 7 after pellet implantation. RNA extracted from mammary glands (3 each group) was labeled and used to probe Affymetrix 430_2.0 arrays.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
12 Samples
Download data: CEL
Series
Accession:
GSE48884
ID:
200048884
17.

Profile of estrogen-responsive genes in an estrogen-specific mammary gland outgrowth model

(Submitter supplied) Both ovarian and pituitary hormones are required for the pubertal development of the mouse mammary gland. Estradiol directs ductal elongation and branching within the adipose stroma of the adolescent mouse mammary gland, while progesterone leads to tertiary branching and alveolar development. The purpose of this investigation was to identify the estrogen-responsive genes that are associated with estrogen-stimulated ductal elongation and branching in the mouse mammary gland in the absence of other ovarian hormones. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL891
16 Samples
Download data: TIFF, TXT
Series
Accession:
GSE4647
ID:
200004647
18.

Estrogen receptor-depended gene signatures and ER binding sites in the mouse mammary gland after acute estradiol treatment

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL17021
7 Samples
Download data: BED, WIG
Series
Accession:
GSE130032
ID:
200130032
19.

Estrogen receptor-depended gene signatures in the mouse mammary gland after acute estradiol treatment (RNA-Seq)

(Submitter supplied) Estrogen receptor α (ERα) is the major driving transcription factor in normal mammary gland development as well as breast cancer initiation and progression.However,the fundamental mechanisms,including global cistromic and genomic transcriptional responses that are required to elicit mammary epithelial cell proliferation in response to estradiol, have not been elucidated. We used RNA-seq analysis to identify global gene expression signatures that are acutely regulated by estroegn receptors in the mouse mammary gland after acute estradiol treatment.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: WIG
Series
Accession:
GSE130031
ID:
200130031
20.

The Genomic Landscape of Estrogen Receptor α Binding Sites in Mouse Mammary Gland

(Submitter supplied) Estrogen receptor α (ERα) is the major driving transcription factor in normal mammary gland development as well as breast cancer initiation and progression.However,the fundamental mechanisms,including global cistromic and genomic transcriptional responses that are required to elicit mammary epithelial cell proliferation in response to ERα, have not been elucidated. We used chromatin immunoprecipitation followed by deep sequencing (ChIP-seq) to identify estrogen regulated genes that directly recruit ERα in the WT mouse mammary gland
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
3 Samples
Download data: BED
Series
Accession:
GSE129847
ID:
200129847
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