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Links from GEO DataSets

Items: 20

1.

Expression profiling after ICAP1 or constitutive active NOTCH1 over expression in human umbilical vein endothelial cells

(Submitter supplied) ICAP1 (also known as ITG1BP1) is a protein interaction partner of beta1-integrins and the cerebral cavernous malformation protein 1 (CCM1, also known as KRIT1). In mice Icap1 plays an important role for bone development. The function of ICAP1 in endothelial cells is poorly understood. However, the interactions with beta1-integrins and CCM1 suggest that ICAP1 should play an important role also in endothelial cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6884
6 Samples
Download data: TXT
Series
Accession:
GSE18035
ID:
200018035
2.

Gene expression profile after CCM1 over expression in human umbilical vein endothelial cells

(Submitter supplied) CCM1 (also known as KRIT1) is critical regulator of endothelial cell biology. Mutations in CCM1 can lead to the formation of cerebral cavernous malformations (CCM). CCM lesions are frequent in the human population; however, their pathogenesis is poorly understood. This genome-wide expression analysis is aimed to unravelling novel mechanisms how CCM1 executes its functions in endothelial cells. We used human umbilical vein endothelial cells (HUVEC) as a model system to study CCM1 functions after adenoviral over expression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6104
4 Samples
Download data: TXT
Series
Accession:
GSE18014
ID:
200018014
3.

Jag1-dependent gene expression in human endometrial stromal cells

(Submitter supplied) The goal is to investigate gene regulation in endometrial stromal cells expressing the Notch ligand Jag1.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3571
Platform:
GPL570
6 Samples
Download data: CEL, CHP
Series
Accession:
GSE16906
ID:
200016906
4.
Full record GDS3571

Jag1 expression effect on endometrial stromal cells

Analysis of endometrial stromal cells engineered to have an increased expression of Jag1. Jag1 is a Notch ligand. Results provide insight into the role of Notch signaling in endometrial cells.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent sets
Platform:
GPL570
Series:
GSE16906
6 Samples
Download data: CEL, CHP
DataSet
Accession:
GDS3571
ID:
3571
5.

Response of C2C12-hN1∆ECD to DAPT washout

(Submitter supplied) C2C12 cells expressing constitutively active hN1∆ECD were activated by complete DAPT washout for 1h or 6h, or left in 10 uM DAPT
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
3 Samples
Download data: XLSX
Series
Accession:
GSE72847
ID:
200072847
6.

Coronary arterial development is regulated by a Dll4-Jag1-EphrinB2 signaling cascade

(Submitter supplied) Coronaries are essential for myocardial growth and heart function. Notch is crucial for mouse embryonic angiogenesis, but its role in coronary development remains uncertain. We show Jag1, Dll4 and activated Notch1 receptor expression in sinus venosus (SV) endocardium. Endocardial Jag1 removal blocks SV capillary sprouting, while Dll4 inactivation stimulates excessive capillary growth, suggesting that ligand antagonism regulates coronary primary plexus formation. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
36 Samples
Download data: XLS
Series
Accession:
GSE110614
ID:
200110614
7.

KSHV Manipulates Notch Signaling by Upregulating Dll4 and JAG1 to Alter Cell Cycle Gene Expression in LECs

(Submitter supplied) Kaposi sarcoma is the most common cancer in AIDS patients and is typified by red skin lesions. The disease is caused by the KSHV virus (HHV8) and is recognizable by its distinctive red skin lesions. The lesions are KSHV infected spindle cells, most commonly the lymphatic endothelial and blood vessel endothelial cells (LEC and BEC), plus surrounding stroma. Here we examine KSHVs modulation of Notch signaling using wild-type LEC cells co-cultured with DLL4 and JAG1 expressing LEC cells.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
8 Samples
Download data: CEL
Series
Accession:
GSE16547
ID:
200016547
8.

Sequential ligand-dependent Notch signaling activation regulates valve primordium formation and morphogenesis

(Submitter supplied) Our studies identify a mechanism of signaling crosstalk during valve morphogenesis that sheds light on the origin of congenital heart defects associated with reduced Notch function.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11002
16 Samples
Download data: TXT
Series
Accession:
GSE74556
ID:
200074556
9.

Expression analysis of mouse retinas after treatment with VEGF-A or Dll4-Fc.

(Submitter supplied) Transcriptional profiling of retinas extracted from mouse pups 24 hours after IVT injection (at P8) of 1 microgram VEGFA, 4 micrograms Dll4-Fc, or 4 microgram hFc alone. Goal was to determine the mechanism by which inhibiting Dll4/Notch pathway is vasoprotective during retinal development.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL13397
16 Samples
Download data: TXT
Series
Accession:
GSE28516
ID:
200028516
10.

Comprehensive gene expression analysis in liver tissue following forced activation of Notch1 and Notch2 signaling.

(Submitter supplied) We compared the effects of Notch1 and Notch2 signaling induced by AAV8-mediated forced expression of Notch1 intracellular domain (NICD1) and Notch2 intracellular domain (NICD2), respectively, in the liver. Eight-week-old wild-type male mice were injected intraperitoneally with an NICD1- and/or NICD2-overexpressing AAV8 vector. Efficient AAV8-mediated gene transfer was confirmed by co-expressed green fluorescent protein (GFP) fluorescence in hepatocytes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL21163
11 Samples
Download data: TXT
Series
Accession:
GSE178886
ID:
200178886
11.

Loss of Jagged1 in mature endothelial cells causes vascular dysfunction with alterations in smooth muscle phenotypes

(Submitter supplied) Notch signaling is an evolutionarily conserved pathway that functions via direct cell-cell contact. The Notch ligand Jagged1 (Jag1) has been extensively studied in vascular development, particularly for its role in smooth muscle cell maturation. Endothelial cell-expressed Jag1 is essential for blood vessel formation by signaling to nascent vascular smooth muscle cells and promoting their differentiation. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
6 Samples
Download data: CSV
Series
Accession:
GSE209736
ID:
200209736
12.

Endothelial Jagged1 levels and distribution are post-transcriptionally controlled by ZFP36 decay proteins

(Submitter supplied) Vascular morphogenesis requires a delicate gradient of Notch signaling that is controlled, at least in part, by the distribution of ligands (Dll4 and Jagged1). How jagged1 (JAG1) expression is compartmentalized in the vascular plexus remains unclear. Here we showed that Jag1 mRNA is a direct target of zinc finger protein 36 (ZFP36), an RNA-binding protein involved in mRNA decay that we found robustly induced by VEGF. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
24 Samples
Download data: CSV
Series
Accession:
GSE235462
ID:
200235462
13.

Effect of NOTCH-γ-secretase inhibitor LY3039478 therapy on patient derived xenograft (PDX) mouse model of intrahepatic cholangiocarcinoma

(Submitter supplied) Intrahepatic Cholangiocarcinoma (iCCA) is a deadly disease with rising incidence and few treatment options. Recently, aberrant Notch signaling was reported in iCCA carcinogenesis. Specifically, altered expression and/or activation of the receptors Notch1/2 suggests a role for Notch pathway overactivation during iCCA formation and progression. In this study, we examined the effects of Notch inhibition by γ-secretase inhibitor, LY3039478 in human iCCA cell lines and in an excellent patient derived-xenograft (PDX) model. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17586
11 Samples
Download data: CEL, CHP
Series
Accession:
GSE134114
ID:
200134114
14.

Adult epidermal Notch activity induces dermal accumulation of stromal cells

(Submitter supplied) K14NICDER transgenic and wildtype littermate mice were treated with 4OHT for 14 days to activate the transgene Epidermis and dermis preparations from Transgenic and Wild type mice plus whole skin
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
18 Samples
Download data: CEL
Series
Accession:
GSE23782
ID:
200023782
15.

Hypoxia-induced Arterial Differentiation Requires Adrenomedullin and Notch Signaling

(Submitter supplied) Hypoxia (low oxygen) and Notch signaling are two important regulators of vascular development, but how they interact in controlling the choice between arterial and venous fates for endothelial cells during vasculogenesis is less well understood. In this report, we show that hypoxia and Notch signaling intersect in promotion of arterial differentiation. Hypoxia upregulated expression of the Notch ligand Dll4 and increases Notch signaling, in a process requiring the vasoactive hormone adrenomedullin but not endogenous VEGF. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6885
12 Samples
Download data: TXT
Series
Accession:
GSE35894
ID:
200035894
16.

Angiogenesis gene expression upon Notch activation in human vascular smooth muscle cells

(Submitter supplied) VSMCs were cultured on Jag1 or IgG-coated plates as described above. RNA was extracted using RNA isolation kit (Qiagen). Reverse-transcription PCR was done with RNA-to-cDNA kit (Applied Biosystems). cDNA was run on a TaqMan Low-Density Array, human angiogenesis panel (Applied Biosystems , Cat#4378725), amplified on a 7900 HT Fast Real Time PCR system (Applied Biosystems) according to manufacturer’s instructions.
Organism:
Homo sapiens
Type:
Expression profiling by RT-PCR
Platform:
GPL14938
4 Samples
Download data: TXT
Series
Accession:
GSE34024
ID:
200034024
17.

Gene expression analysis of Rip1Tag2 spontaneous tumors treated by sEphB4-Alb or PBS

(Submitter supplied) Rip1Tag2 mice spontaneously develop tumors. Mice were treated with sEphB4-Alb or PBS for 3.5 weeks. RNA was isolated from harvested tumors and subjected to global gene expression analysis.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11033
4 Samples
Download data: TXT
Series
Accession:
GSE24603
ID:
200024603
18.

microRNAs-449 control vertebrate multi-ciliogenesis by repressing Notch signalling

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Xenopus laevis
Type:
Non-coding RNA profiling by array; Expression profiling by array; Non-coding RNA profiling by high throughput sequencing
4 related Platforms
64 Samples
Download data: CEL, TXT
Series
Accession:
GSE22147
ID:
200022147
19.

microRNAs signatures of Xenopus laevis embryo epidermis at stage 11 (non ciliated) and 26 (ciliated) using high throughput sequencing

(Submitter supplied) Epidermis of Xenopus embryos forms a mucociliary epithelium constituted of basal, scattered, secreting and ciliated cells and is histologically similar to human airway mucociliary epithelium. We compared microRNAs signatures of epidermis of Xenopus embryos at stage 11.5 (gastrula, non ciliated epidermis) and at stage 26 (tailbud, ciliated epidermis).
Organism:
Xenopus laevis
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL10484
4 Samples
Download data: XLS
Series
Accession:
GSE22146
ID:
200022146
20.

miRNAs high throughput sequencing profiling of basals cells and columnar cells

(Submitter supplied) The airway mucociliary epithelium is consituted of three main cell types : columnar ciliated plus secretory cells and basal cells. Columnar cells are represented by a great majority of ciliated cells. We used Cell sorting by FACSaria to separate basal cells from ciliated and secreting columnar cells. Then, we performed microRNA high throughput sequencing to investigate the specific signature of microRNA of basal and columnar cells.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL9138
6 Samples
Download data: XLS
Series
Accession:
GSE22145
ID:
200022145
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