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Links from GEO DataSets

Items: 20

1.

Cardiomyocyte HIPK2 Maintains Basal Cardiac Function via ERK Signaling

(Submitter supplied) Background: Cardiac kinases play a critical role in the development of heart failure, and represent potential tractable therapeutic targets. However, only a very small fraction of the cardiac kinome has been investigated. To identify novel cardiac kinases involved in heart failure, we employed an integrated transcriptomics and bioinformatics analysis and identified Homeodomain-Interacting Protein Kinase 2 (HIPK2) as a novel candidate kinase. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
9 Samples
Download data: CEL
Series
Accession:
GSE136308
ID:
200136308
2.

Gene expression profiles from the cardiac tissue of HIPK2-knockout and Wild Type (WT) mice

(Submitter supplied) We use Affymetrix Gene Chip Array to screen the targets of HIPK2 in heart. Total RNA was extracted from 8-week-old HIPK2-knockout and Wild Type (WT) mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL21163
10 Samples
Download data: TXT
Series
Accession:
GSE169429
ID:
200169429
3.

microRNA profiling of myocardial infarction on a PI3K setting in mouse models

(Submitter supplied) Cardiac hypertrophy can lead to heart failure, and is induced either by physiological stimuli eg postnatal development, chronic exrcise training or pathological stimuli eg pressure or volume overload. This data set looks at microRNA profiles in mouse models to examine whether phosphoinositide 3-kinase (p110 alpha isoform) activity is critical for the maintenance of cardiac function and long term survival in a seeting of heart failure (myocardial infarction). more...
Organism:
Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL8824
24 Samples
Download data: TXT
Series
Accession:
GSE14267
ID:
200014267
4.

Gene profiling of pathological cardiac hypertrophy vs physiological hypertrophy

(Submitter supplied) Cardiac hypertrophy can lead to heart failure, and is induced either by physiological stimuli eg postnatal development, chronic exercise training or pathological stimuli eg pressure or volume overload. Majority of new therapies for heart failure has mixed outcomes. A combined mouse model and oligo-array approach are used to examine whether phosphoinositide 3-kinase (p110-alpha isoform) activity is critical for maintenance of cardiac function and long-term survival in a setting of heart failure. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
24 Samples
Download data: CEL, CHP
Series
Accession:
GSE7487
ID:
200007487
5.

Genome-wide analysis of the TEC-specific Hipk2 gene knockout in mouse medullary thymic epithelial cells (mTECs)

(Submitter supplied) Analysis of the role of Hipk2 in regulating gene expression in medullary thymic epithelial cells. The whole genome gene signatures of purified mTEC subsets (CD80 low, CD80 high) from TEC-specific Hipk2 knockout mice were compared to mating wildtype control mice (floxed, Cre-). Results provide the up- or down-regulated genes, affected by the Hipk2 gene knockout.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17543
8 Samples
Download data: IDAT, TXT
Series
Accession:
GSE63432
ID:
200063432
6.

Systems approach identifies HIPK2 as a critical regulator of kidney tubulointerstitial fibrosis

(Submitter supplied) We used an integrated computational/experimental systems biology approach to identify upstream protein kinases that regulate gene expression changes in kidneys of HIV-1 transgenic mice (Tg26), which have significant tubulo-interstitial fibrosis (TIF) and glomerulosclerosis (GS). We identified the homeo-domain interacting protein kinase 2 (HIPK2) as a key regulator of TIF and GS. HIPK2 was upregulated in kidneys of Tg26 and patients with various kidney diseases. more...
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS4233 GDS4234
Platforms:
GPL1261 GPL6244
24 Samples
Download data: CEL, CHP
Series
Accession:
GSE35226
ID:
200035226
7.
Full record GDS4234

Transgenic model Tg26 of HIV-Associated Nephropathy: kidney cortex

Analysis of kidney cortices from HIV-1 transgenic, FVB/N males and females (Tg26). Tg26 models the renal pathologic changes observed in human disease and is used to study HIV-associated nephropathy (HIVAN) pathogenesis. Results provide insight into the molecular mechanisms underlying HIVAN.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL1261
Series:
GSE35226
12 Samples
Download data: CEL, CHP
8.
Full record GDS4233

Protein kinase HIPK2 overexpression effect on Human Embryonic Kidney cells

Analysis of HEK293 cells transfected with homeo-domain interacting protein kinase 2 (HIPK2) and HIPK2-DN mutant. HIPK2 mediates renal fibrosis in 3 mouse models of renal fibrosis (Tg26, UUO, folic-acidinduced renal fibrosis). Results provide further insight into role of HIPK2 in kidney fibrosis.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 3 genotype/variation sets
Platform:
GPL6244
Series:
GSE35226
12 Samples
Download data: CEL, CHP
9.

Characterization of an Arabidopsis mutant deficient in the non-phosphorylating of GAPN gene.

(Submitter supplied) Non-phosphorylating glyceraldehyde-3-phosphate dehydrogenase (GAPN) is a conserved protein found in higher plants. In photosynthetic cells, the enzyme is involved in a shuttle transfer mechanism to export NADPH from the chloroplast to the cytosol. In this work, we demonstrate that GAPN gene express in leaves and roots at similar levels; showing the highest level of expression in flowers. To investigate the role of this enzyme in different plant tissues, we characterized a mutant from Arabidopsis thaliana having an insertion at the GAPN gene locus. more...
Organism:
Arabidopsis thaliana
Type:
Expression profiling by array
Platform:
GPL1941
3 Samples
Download data
Series
Accession:
GSE3539
ID:
200003539
10.

Distinct Gene Expression Profiles in Adult Mouse Heart Following Targeted MAP Kinase Activation

(Submitter supplied) Three major MAP kinase signaling cascades, ERK, p38 and JNK, play significant roles in the development of cardiac hypertrophy and heart failure in response to external stress and neural/hormonal stimuli. In order to study the specific function of each MAP kinase branch in adult heart, we have generated three transgenic mouse models with cardiac specific and temporally regulated expression of activated mutants of Ras, MKK3 and MKK7, which are selective upstream activators for ERK, p38 and JNK, respectively. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS1306
Platform:
GPL1261
36 Samples
Download data
Series
Accession:
GSE3530
ID:
200003530
11.
Full record GDS1306

MAP kinase activation effect on heart: time course

Analysis of adult hearts after induction of activated transgene mutants of Ras, MKK3, or MKK7, which are specific upstream activators of the MAP kinases ERK, p38, and JNK respectively. Hearts examined at various time points up to 4 weeks following each transgene induction using tamoxifen.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 gender, 4 genotype/variation, 3 time sets
Platform:
GPL1261
Series:
GSE3530
36 Samples
Download data
DataSet
Accession:
GDS1306
ID:
1306
12.

Microarray gene expression profiling of transgenic mice with myocardium-specific over-expression of fatty acid synthase (FASN)

(Submitter supplied) The fatty acid synthase (FASN) is the major fat synthesizing enzyme. FASN is an indispensable enzyme because mice with genetic deletion of Fasn are not viable. Apart from its physiological function, previous studies indicated that FASN could also exert a pathophysiological role, in the heart, because patients with heart failure showed up-reguation of FASN. To investigate the in vivo function of FASN up-regulation in the heart, we generated mice with myocardium-specific expression of FASN under control of the alpha-MHC promoter. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
6 Samples
Download data: CEL, CHP
Series
Accession:
GSE49351
ID:
200049351
13.

Microarray gene expression profiling of heart failure induced in apolipoprotein E-deficient mice by treatment with rosiglitazone

(Submitter supplied) The anti-diabetic drug and agonist of the peroxisome proliferator-activated receptor gamma (Pparg), rosiglitazone, was recently withdrawn in many countries because the drug use was associated with an increased risk of heart failure. To investigate underlying pathomechanisms, we chose 6-month-old apolipoprotein E (apoE)-deficient mice, which are prone to atherosclerosis and insulin resistance, and thereby mimic the risk profile of patients with cardiovascular disease. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
6 Samples
Download data: CEL, CHP
Series
Accession:
GSE28031
ID:
200028031
14.

Comprehensive expression profiling across primary fetal liver terminal erythroid differentiation

(Submitter supplied) Primary murine fetal liver cells were freshly isolated from day e14.5 livers and then sorted for successive differentiation stages by Ter119 and CD71 surface expression (ranging from double-negative CFU-Es to Ter-119 positive enucleated erythrocytes) [Zhang, et al. Blood. 2003 Dec 1; 102(12):3938-46]. RNA isolated from each freshly isolated, stage-sorted population was reverse-transcribed, labelled, and then hybridized onto 3' oligo Affymetrix arrays. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
11 Samples
Download data: CEL, TXT
Series
Accession:
GSE20391
ID:
200020391
15.

Murine fetal liver TER119-negative erythroid precursors: Hipk1 or Hipk2 knockdown versus control

(Submitter supplied) Expression profiling of fetal liver erythroid precursors after either Hipk1 or Hipk2 knockdown by shRNA versus control shRNA
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL8860
4 Samples
Download data: TXT
Series
Accession:
GSE17106
ID:
200017106
16.

Deletion of the Cardiomyocyte Glucocorticoid Receptor Leads to Sexually Dimorphic Changes in Cardiac Gene Expression and Progression to Heart Failure

(Submitter supplied) Background The contribution of glucocorticoids to sexual dimorphism in the heart is essentially unknown. Therefore, we sought to determine the sexually dimorphic actions of glucocorticoid signaling in cardiac function and gene expression. To accomplish this goal, we conducted studies on mice lacking glucocorticoid receptors (GR) in cardiomyocytes (cardioGRKO mouse model). Methods and Results Deletion of cardiomyocyte GR leads to an increase in mortality because of the development of spontaneous cardiac pathology in both male and female mice; however, females are more resistant to GR signaling inactivation in the heart. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
12 Samples
Download data: TXT
Series
Accession:
GSE120573
ID:
200120573
17.

Time-dependent Effects of BRAF-V600E on Cell Cycling, Metabolism, and Function in Engineered Myocardium

(Submitter supplied) Candidate cardiomyocyte (CM) mitogens such as those affecting ERK signaling pathway represent potential targets for functional heart regeneration. We explored whether activating ERK via a constitutively active mutant of BRAF, BRAF-V600E (caBRAF), can induce pro-proliferative effects in neonatal rat engineered cardiac tissues (ECTs). Sustained CM-specific caBRAF expression induced chronic ERK activation, significant tissue growth, deficit in sarcomeres and contractile function, and tissue stiffening, all of which persisted for at least 4 weeks of culture. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL14844
12 Samples
Download data: XLSX
Series
Accession:
GSE193466
ID:
200193466
18.

Comparison of gene expression profiles of neonate rat cardiomyocytes (NRCMs) transfected with LacZ, 23k prolactin (PRL), or 16k PRL.

(Submitter supplied) Recently, it is reported that multiple signaling pathways are involved with the pathogenesis of PPCM. Here, we show that 23k PRL activates PERK signaling.
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18694
9 Samples
Download data: BW
Series
Accession:
GSE169063
ID:
200169063
19.

Comparison of gene expression profiles of hearts in nulloparous (NP) or postpartum (PP) PERK wild type (flx) or PERK cardiac-specific knockout (cko) mice.

(Submitter supplied) Recently, it is reported that multiple signaling pathways are involved with the pathogenesis of PPCM. Here, we show that PERK kockout affect these pathways in postpartum period.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
12 Samples
Download data: BIGWIG
Series
Accession:
GSE168536
ID:
200168536
20.

Differential Myocardial Gene Expression in the Development and Rescue of Murine Heart Failure

(Submitter supplied) Numerous murine models of heart failure (HF) have been described, many of which develop progressive deterioration of cardiac function. We have recently demonstrated that several of these can be "rescued" or prevented by transgenic cardiac expression of a peptide inhibitor of the beta-adrenergic receptor kinase (betaARKct). To uncover genomic changes associated with cardiomyopathy and/or its phenotypic rescue by the betaARKct, oligonucleotide microarray analysis of left ventricular (LV) gene expression was performed in a total of 53 samples, including 12 each of Normal, HF, and Rescue. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Datasets:
GDS411 GDS427
Platforms:
GPL75 GPL76
106 Samples
Download data
Series
Accession:
GSE670
ID:
200000670
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