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Links from GEO DataSets

Items: 17

1.

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
2.

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
3.
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
4.

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
5.
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
6.

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
7.

Progesterone Receptor Targetome in the Mammary Gland

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL1261 GPL9250
16 Samples
Download data: CEL, WIG
Series
Accession:
GSE42888
ID:
200042888
8.

Progesterone receptor ChIP-seq within the mouse mammary gland

(Submitter supplied) Progesterone (P) acting through its cognate nuclear receptors (PRs) plays an essential role in driving pregnancy-associated branching morphogenesis of the mammary gland. However, the fundamental mechanisms, including global cistromic and acute genomic transcriptional responses that are required to elicit active branching morphogenesis in response to P, have not been elucidated. We used chromatin immunoprecipitation followed by deep sequencing (ChIP-seq) to identify P-regulated genes that directly recruit PRs in the mouse mammary gland after acute P treatment.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9250
4 Samples
Download data: WIG
Series
Accession:
GSE42887
ID:
200042887
9.

Progesterone receptor-dependent gene signatures in the mouse mammary gland after acute progesterone treatment

(Submitter supplied) Progesterone (P) acting through its cognate nuclear receptors (PRs) plays an essential role in driving pregnancy-associated branching morphogenesis of the mammary gland. However, the fundamental mechanisms, including global cistromic and acute genomic transcriptional responses that are required to elicit active branching morphogenesis in response to P, have not been elucidated. We used microarray analysis to identify global gene expression signatures that are acutely regulated by PRs in the mouse mammary gland after acute P treatment.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
12 Samples
Download data: CEL
Series
Accession:
GSE42858
ID:
200042858
10.

Global mammary luminal cells gene expression data from C451A-ERα and WT female mice treated by E2 or E2+Pg during 21 days.

(Submitter supplied) We used microarrays to detail the global programme of gene expression in mammary luminal cells C451A-ERα and WT female mice treated by E2 0.01 MG and E2 0.01 MG +Pg 1.5 MG during 21 days.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL21163
19 Samples
Download data: TXT
Series
Accession:
GSE142297
ID:
200142297
11.

caArray_green-00030: 2-methoxyestradiol (2ME2) induces mammary gland differentiation through amphiregulin-EGFR mediated signaling

(Submitter supplied) 2-methoxyestradiol (2ME2) induces mammary gland differentiation through amphiregulin-EGFR mediated signaling: molecular distinctions from the mammary gland of pregnant mice.High levels of 2ME2 are observed in the late stages of pregnancy. We investigated the role of 2ME2 on normal mammary gland development. Large scale gene expression assays were performed using Affymetrix GeneChips in pursuit of detailed molecular basis. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL81 GPL1261
55 Samples
Download data: CEL, XLS
Series
Accession:
GSE70048
ID:
200070048
12.

Gene expression of RonTK-/- mammary glands compared to RonTK+/+ controls during development

(Submitter supplied) RON WT and RON KO at 5, 6, 7 week virgin mammary glands In the study, we demonstrated that RON regulates mammary gland branching morphogenesis in pubertal development associated with changes in gene expression. Keywords: Pubertal mammary glands
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
18 Samples
Download data: CEL
Series
Accession:
GSE16629
ID:
200016629
13.

Deaf-1 regulated genes in the mouse mammary gland

(Submitter supplied) Microarray analysis was used to compare the gene expression profiles of Deaf-1-transduced mouse mammary epithelial cells (MECs) relative to Deaf-1-deficient MECs.
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS3490
Platform:
GPL1261
4 Samples
Download data: CEL
Series
Accession:
GSE12367
ID:
200012367
14.
Full record GDS3490

Deaf-1 deficiency and overexpression effect on cultured mammary epithelial cells

Analysis of cultured mammary epithelial cells lacking or overexpressing the transcription factor Deaf-1. Deaf-1 is involved in mammary gland development and breast cancer. Results identify target genes of Deaf-1.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 protocol sets
Platform:
GPL1261
Series:
GSE12367
4 Samples
Download data: CEL
15.

Transcriptomal profiling of C57BL/6 wild type and ER-alpha KO mice fetal mammary gland after fetal exposure to Bisphenol A (BPA) and 17alpha-ethynylestradiol (EE2)

(Submitter supplied) To examine whether the BPA-induced morphological alterations of the fetal mouse mammary glands are a) associated with changes in mRNA expression reflecting estrogenic actions and/or b) dependent on the estrogen receptor α (ERα), we compared the transcriptomal effects of BPA and the steroidal estrogen ethinylestradiol (EE2) on fetal mammary tissues of wild type and ERα knock-out mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
36 Samples
Download data: CEL
Series
Accession:
GSE44387
ID:
200044387
16.

Expression data from mammary macrophages isolated from MMTV-iFGFR1 transgenic mice

(Submitter supplied) The goal of this experiment was to profile macrophages from mammary glands isolated from transgenic mice that express inducible FGFR1 in mammary epithelial cells (MMTV-iFGFR1 transgenic mice). The mice were treated with with dimerizer to activates iFGFR1 for 48 hours and 4 weeks to induce mammary hyperplasias. Control mice included non-transgenic littermates treated with dimerizer for the same amount of time.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
8 Samples
Download data: CEL
Series
Accession:
GSE36477
ID:
200036477
17.

Pubertal Ductal Morphogenesis: Isolation and Transcriptome Analysis of the Terminal End Bud.

(Submitter supplied) The terminal end buds (TEB) are the growing part of the ductal mammary epithelium during puberty, which enable the formation of the primary mammary epithelial network. These bulbous end structures are highly proliferative, and this allows the ductal expansion into the mammary fat pad. The TEB comprise of an outer cap cell layer, which include the progenitor cells of the myoepithelium, and the body cells, which are thought to be the progenitors from which the luminal epithelium is formed. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL23018
4 Samples
Download data: CEL
Series
Accession:
GSE94371
ID:
200094371
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Supplemental Content

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