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Links from GEO DataSets

Items: 20

1.
Full record GDS679

Osteogenesis induced by bone morphogenic protein 2

Response of calvarial MC3T3-1b cells to osteogenic stimulus (beta-glycerophosphate (GP), ascorbic acid (AA) and bone morphogenic protein 2 (BMP-2)) for 0, 1 and 3 days. Notch, Wnt and TGF-β signaling pathways are activated in osteogenesis.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 3 growth protocol, 3 time sets
Platform:
GPL81
Series:
GSE1131
15 Samples
Download data
DataSet
Accession:
GDS679
ID:
679
2.

Osteoblast differentiation experiment: BMP-2 induced osteogenesis in mouse MC3T3 cell line

(Submitter supplied) MC3T3 cells clone 1b were grown in alpha-MEM with 10% fetal calf serum (FCS, Gibco), 1% penicilin/streptomycin (Pen/Strep) and 1% L-Glutamine (L-Glu). For differentiation experiment, cells were seeded on 6 cm dishes (3x105cells/dish in 5 ml medium) and grownt to confluence for 3 days at 37C / 5% CO2. Cells were then stimulated with osteogenic stimulus (10 mM beta-glycerophosphate (GP, Sigma), 50 µM ascorbic acid (AA, Wako) and 1 mg/ml BMP-2 (Novartis)), or with 10mM GP alone for 1 or 3 days. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS679
Platform:
GPL81
15 Samples
Download data
Series
Accession:
GSE1131
ID:
200001131
3.

Expression profiling of BMP9-stimulated mesenchymal stem cells

(Submitter supplied) To identify potential target genes regulated by BMP9 in MSCs, we used microarray to profile expression patterns of BMP9- vs. GFP-stimulated MSCs.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL339
6 Samples
Download data: CEL
Series
Accession:
GSE48882
ID:
200048882
4.

Mouse hypoxia

(Submitter supplied) Vascular disruption following bony injury results in a hypoxic gradient within the wound microenvironment. Nevertheless, the effects of low oxygen tension on osteogenic precursors remain to be fully elucidated. In the present study, we investigated in vitro osteoblast and mesenchymal stem cell differentiation following exposure to 21% O(2) (ambient oxygen), 2% O(2) (hypoxia), and <0.02% O(2) (anoxia). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL2635
2 Samples
Download data
Series
Accession:
GSE2951
ID:
200002951
5.

Effect of histone deacetylase inhibitors on osteoblast gene expression

(Submitter supplied) Background: Osteoblast differentiation requires the coordinated stepwise expression of multiple genes. Histone deacetylase inhibitors (HDIs) accelerate the osteoblast differentiation process by blocking the activity of histone deacetylases (HDACs), which alter gene expression by modifying chromatin structure. We previously demonstrated that HDIs and HDAC3 shRNAs accelerate matrix mineralization and the expression of osteoblast maturation genes (e.g. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS3002
Platform:
GPL1261
15 Samples
Download data: CEL
Series
Accession:
GSE9247
ID:
200009247
6.
Full record GDS3002

Histone deacetylase inhibitors effect on osteoblast differentiation

Analysis of MC3T3-E1 preosteoblasts treated with the histone deacetylase inhibitor (HDI) trichostatin A, MS-275, or valproic acid for 18 hours under osteogenic conditions. HDIs accelerate osteoblast maturation. Results provide insight into molecular mechanisms underlying osteoblast differentiation.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 4 agent sets
Platform:
GPL1261
Series:
GSE9247
15 Samples
Download data: CEL
7.

CTL-OA-OP human IT PF Bone - CompuGen H19K microarray study

(Submitter supplied) Aims of study: (1) To identify systemic differences in osteoarthritic (OA) bone that contribute to OA pathogenesis. (2) Identify novel osteoporotic (OP) bone-related disease genes. Study involved comparison of trabecular bone extracted from the intertrochanteric (IT) region of the proximal femur (PF) from OA, OP and normal/control (CTL) individuals. Bone was obtained from OA and OP individuals at surgery for total hip replacement and from CTL individuals at autopsy. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5391
39 Samples
Download data
Series
Accession:
GSE8406
ID:
200008406
8.

HEY1-NCOA2 expression induces mesenchymal chondrosarcoma interacting with Runx2 [single-cell RNA-seq]

(Submitter supplied) Mesenchymal chondrosarcoma is a high-grade malignant neoplasm characterized by biphasic growth of poorly differentiated small round cells and well differentiated cartilage. Mesenchymal chondrosarcoma affects adolescents and young adults, and the HEY1-NCOA2 fusion gene is causally associated with most cases. Here we generate a mouse model for mesenchymal chondrosarcoma by introducing HEY1-NCOA2 into mouse embryonic chondrogenic progenitors (eSZ) followed by subcutaneous transplantation into nude mice. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21626
1 Sample
Download data: CSV
Series
Accession:
GSE198662
ID:
200198662
9.

HEY1-NCOA2 interacts with RUNX2 to induce mesenchymal chondrosarcoma

(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:
GPL16417 GPL11180
46 Samples
Download data: CEL, TDF
Series
Accession:
GSE163588
ID:
200163588
10.

HEY1-NCOA2 interacts with RUNX2 to induce mesenchymal chondrosarcoma [ChIP-seq]

(Submitter supplied) Mesenchymal chondrosarcoma is a high-grade malignant neoplasm characterized by biphasic growth of poorly differentiated small round cells and well differentiated cartilage. Mesenchymal chondrosarcoma affects adolescents and young adults, and the HEY1-NCOA2 fusion gene is causally associated with most cases. Here we generate a mouse model for mesenchymal chondrosarcoma by introducing HEY1-NCOA2 into mouse embryonic chondrogenic progenitors followed by subcutaneous transplantation into nude mice. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16417
11 Samples
Download data: TDF
Series
Accession:
GSE163585
ID:
200163585
11.

HEY1-NCOA2 interacts with RUNX2 to induce mesenchymal chondrosarcoma [Array]

(Submitter supplied) Mesenchymal chondrosarcoma is a high-grade malignant neoplasm characterized by biphasic growth of poorly differentiated small round cells and well differentiated cartilage. Mesenchymal chondrosarcoma affects adolescents and young adults, and the HEY1-NCOA2 fusion gene is causally associated with most cases. Here we generate a mouse model for mesenchymal chondrosarcoma by introducing HEY1-NCOA2 into mouse embryonic chondrogenic progenitors followed by subcutaneous transplantation into nude mice. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11180
35 Samples
Download data: CEL
Series
Accession:
GSE163291
ID:
200163291
12.

Nodal points and complexity of Notch-Ras signal integration

(Submitter supplied) Metazoans utilize a handful of highly conserved signaling pathways to create a signaling backbone that governs all stages of development, by providing spatial and temporal cues that influence gene expression. How these few signals have such a versatile developmental action is of significance to evolution, development, and disease. Their versatility likely depends upon the larger-scale network they form through integration. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by array
Platform:
GPL72
24 Samples
Download data: CEL
Series
Accession:
GSE11203
ID:
200011203
13.

A time series study on BMP6 induced osteoblast differentiation of human mesenchymal stem cells (hMSC)

(Submitter supplied) BMP6 mediated osteoblast differentiation plays a key role in skeletal development and bone disease. Unfortunately, the signaling pathways regulated by BMP6 are largely uncharacterized due to both a lack of data and the complexity of the response. To better characterize the signaling pathways responsive to BMP6, we conducted a time series microarray study to track BMP6 induced osteoblast differentiation and mineralization.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13303
26 Samples
Download data: CEL
Series
Accession:
GSE28074
ID:
200028074
14.

Temporal Gene Expression Profiling during Rat Femoral Marrow Ablation-Induced Intramembranous Bone Regeneration

(Submitter supplied) Enhanced understanding of differential gene expression and biological pathways associated with distinct phases of intramembranous bone regeneration following femoral marrow ablation surgery will improve future advancements regarding osseointegration of joint replacement implants, biomaterials design, and bone tissue engineering. A rat femoral marrow ablation model was performed and genome-wide microarray data were obtained from samples at 1, 3, 5, 7, 10, 14, 28, and 56 days post-ablation, with intact bones serving as controls at Day 0. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL1355
27 Samples
Download data: CEL
Series
Accession:
GSE22321
ID:
200022321
15.

Comparision of expression profile between wild-type and Slc39a13 knockout chondrocytes

(Submitter supplied) In order to explore molecules whose expression is controlled by Slc39a13, we investigated gene expression profiling of primary chondrocyte isolated from wild-type and Slc39a13 knockout mice. Keywords: knockout vs wild-type
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS3485
Platform:
GPL1261
6 Samples
Download data: CEL, CHP
Series
Accession:
GSE10556
ID:
200010556
16.

Comparision of expression profile between wild-type and Slc39a13 knockout osteoblasts

(Submitter supplied) In order to explore molecules whose expression is controlled by Slc39a13, we investigated gene expression profiling of primary osteoblast isolated from wild-type and Slc39a13 knockout mice. Keywords: knockout vs wild-type
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
2 Samples
Download data: CEL, CHP
Series
Accession:
GSE10555
ID:
200010555
17.
Full record GDS3485

Zinc transporter SLC39A13 deficiency effect on chondrocytes

Analysis of chondrocytes lacking the zinc transporter SLC39A13. Zinc is an essential trace element that is abundant in connective tissues. Results provide insight into the role of zinc in connective tissues.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation sets
Platform:
GPL1261
Series:
GSE10556
6 Samples
Download data: CEL, CHP
18.

KB001b:Gene expression profiling of the growth plate of large and small breed dogs provides new insights in endochondral bone formation

(Submitter supplied) The regeneration of bone in large bone defects remains a challenge in orthopaedics. It may be possible that the difference in the adult height of mammals, and hence in endochondral bone formation, can serve to identify targets for bone regeneration. In line with this hypothesis, the intra-species disparity in adult height of Great Danes and Miniature Poodles was investigated at a transcriptional level. more...
Organism:
Canis lupus familiaris
Type:
Expression profiling by array
Platform:
GPL15184
22 Samples
Download data: TXT
Series
Accession:
GSE53277
ID:
200053277
19.

UB/OC-1 differentiation

(Submitter supplied) This study explores the profiles of genes expressed during conditional differentiation of inner ear hair cell precursors in vitro. The cell line UB/OC-1 was derived from mouse embryonic organs of Corti (Rivolta et al, Proc. R. Soc. Lond. B 265: 1595-1603, 1998) and it can be induced to differentiate upon a temperature shift. The study has been replicated in two separate populations of cells, named Exp A and Exp B. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Datasets:
GDS45 GDS51
Platforms:
GPL75 GPL76
32 Samples
Download data
Series
Accession:
GSE36
ID:
200000036
20.
Full record GDS51

Cochlear hair cell line differentiation time course (Mu11K-B)

Gene expression profile of differentiation of inner ear hair cell precursors in vitro. A conditionally immortal cell line derived from the mouse cochlea, UB/OC-1, examined from 0 to 14 days.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 12 time sets
Platform:
GPL76
Series:
GSE36
16 Samples
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