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Links from GEO DataSets

Items: 11

1.
Full record GDS1929

Growth hormone effect on bone: time course

Analysis of femurs and tibias of growth hormone (GH) deficient animals at 6 and 24 hours following treatment with 4 mg/kg body weight GH. Results provide insight into the insulin-like growth factor-I dependent and independent pathways that mediate the action of GH in bone.
Organism:
Mus musculus
Type:
Expression profiling by array, log2 ratio, 2 time sets
Platform:
GPL922
Series:
GSE3689
6 Samples
Download data
2.

Whole genome microarray analysis of growth hormone induced genes in bone

(Submitter supplied) Growth hormone (GH) is important in the development and maintenance of bone; however the IGF-dependent and -independent molecular pathways involved remain to be established. We used microarray analysis to identify genes acutely regulated by GH, in the bones of four week old GH-deficient mice at 6 or 24 hours following a single injection of GH (4 mg/kg body wt) or PBS (n = 6/group). 6,160 genes were differentially expressed at P = 0.05 and 17% of these genes were identified at both time points. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS1929
Platform:
GPL922
6 Samples
Download data
Series
Accession:
GSE3689
ID:
200003689
3.

Short-term growth hormone treatment on the liver and muscle transcriptome in rainbow trout (Oncorhynchus mykiss)

(Submitter supplied) Although studies have established that exogenous growth hormone (GH) treatment stimulates growth in fish, its effects on target tissue gene expression are not well characterized. We assessed the effects Posilac® (Monsanto Co., St. Louis, MO), a recombinant bovine somatotropin, on tissue transcript levels. Transcript abundance was measure in liver and muscle using the GRASP 16 K cDNA microarray. A selection of the genes identified as altered with the microarray, and also transcripts for insulin-like growth factors, growth hormone receptors (GHR) and myostatins were measured by realtime PCR in the liver, muscle, brain, kidney, intestine, stomach, gill and heart. more...
Organism:
Oncorhynchus mykiss; Salmo salar
Type:
Expression profiling by array
Platform:
GPL3976
16 Samples
Download data: TXT
Series
Accession:
GSE8285
ID:
200008285
4.

Bone microarray profiles from the Hybrid Mouse Diversity Panel

(Submitter supplied) Significant advances have been made in the discovery of genes affecting bone mineral density (BMD); however, our understanding of its genetic basis remains incomplete. In the current study, genome-wide association (GWA) and co-expression network analysis was used in the recently described Hybrid Mouse Diversity Panel (HMDP) to identify and functionally characterize novel BMD genes. In the HMDP, a GWA of total body, spinal and femoral BMD revealed four significant associations (-log10P > 5.39) affecting at least one BMD trait on chromosomes (Chrs.) 7, 11, 12 and 17. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6105
149 Samples
Download data: TXT
Series
Accession:
GSE27483
ID:
200027483
5.

Loss of TBX3 enhances pancreatic progenitor generation from human pluripotent stem cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL16791 GPL20301
22 Samples
Download data: BIGWIG
Series
Accession:
GSE180528
ID:
200180528
6.

Loss of TBX3 enhances pancreatic progenitor generation from human pluripotent stem cells [Hepatoblast ATAC-seq]

(Submitter supplied) Tbx3 regulates liver development in the mouse, but it's role in human liver development is unclear. We generated TBX3 knockout pluripotent stem cell lines and found that liver differentiation is also impaired in humans. Interestingly we noted expression of pancreas-specific genes during the liver differentiation in the TBX3 knockout line. To further investigate this phenomenon, we performed ATAC-seq on cells at the hepatoblast stage of the liver differentiation. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20301
4 Samples
Download data: BIGWIG
Series
Accession:
GSE180527
ID:
200180527
7.

Loss of TBX3 enhances pancreatic progenitor generation from human pluripotent stem cells [Hepatoblast RNA-seq]

(Submitter supplied) Tbx3 regulates liver development in the mouse, but it's role in human liver development is unclear. We generated TBX3 knockout pluripotent stem cell lines and found that liver differentiation is also impaired in humans. Interestingly we noted expression of pancreas-specific genes during the liver differentiation in the TBX3 knockout line. To further investigate this phenomenon, we performed RNA-seq on cells at the hepatoblast stage of the liver differentiation. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
6 Samples
Download data: TXT
8.

Loss of TBX3 enhances pancreatic progenitor generation from human pluripotent stem cells [Pancreas RNA-seq]

(Submitter supplied) Tbx3 regulates liver development in the mouse, but it's role in human liver development is unclear. We generated TBX3 knockout pluripotent stem cell lines and found that liver differentiation is also impaired in humans. Interestingly we noted expression of pancreas-specific genes during the liver differentiation in the TBX3 knockout line.To further investigate this phenomenon, we performed RNA-seq on cells from two stages of the pancreatic differentation. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
12 Samples
Download data: TXT
9.

Temporal changes of gene expression in mouse heart, kidney and lung during juvenile growth

(Submitter supplied) Temporal changes of gene expression from 1-wk- to 4-wk and 8-wk-old mouse in heart, kidney and lung. Mammalian somatic growth is rapid in early postnatal life but then slows and eventually ceases in multiple tissues. We hypothesized that there exists a postnatal gene expression program that is common to multiple tissues and is responsible for this coordinate growth deceleration. Consistent with this hypothesis, microarray analysis identified >1600 genes that were regulated with age coordinately in kidney, lung, and heart of juvenile mice, including many genes that regulate proliferation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4316
Platform:
GPL1261
40 Samples
Download data: CEL
Series
Accession:
GSE38754
ID:
200038754
10.
Full record GDS4316

Heart, kidney and lung during juvenile growth

Analysis of heart, kidney, and lung from C57BL/6 males at 1, 4, 8 weeks of age. Mammalian somatic growth is rapid in early postnatal life but slows and eventually ceases in multiple tissues. Results provide insight into molecular events common to multiple tissues that regulate growth deceleration.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 3 time, 3 tissue sets
Platform:
GPL1261
Series:
GSE38754
40 Samples
Download data: CEL
11.

Effects of triiodothyronine on human osteoblast-like cells: novel insights from a global transcriptome analysis

(Submitter supplied) In order to investigate, at the mRNA level, the signaling pathways through which triiodothyronine (T3) affects osteoblast function, human mesenchymal stem cells derived from adipose tissue were subjected to a pre-established osteoinduction protocol, resulting in osteoblast-like cells, which were cultured with or without T3. RNA-Seq was performed using Illumina platform, and differential gene expression was assessed with DESeq2. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
9 Samples
Download data: CSV
Series
Accession:
GSE205678
ID:
200205678
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