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Items: 1 to 20 of 978

1.

Real-time quantitative PCR analysis of mice kidney after administration of Lu-177-octreotate, Lu-177-octreotate + A1M and A1M

(Submitter supplied) This work aimed to examine the regulation of apoptosis-related genes in kidney cortex and kindey medulla one and seven days after administration of 177Lu-octreotate with and without A1M and of A1M alone. C57BL/6N mice were injected with either 177Lu-octreotate + PBS, A1M + PBS or 177Lu-octreotate + A1M. Also, a control group was sham-treated with saline. Half of the animals in each treatment and control group were terminated by cardiac puncture one-day post-injection (1 dpi), and the remaining animals were terminated at 7dpi. more...
Organism:
Mus musculus
Type:
Expression profiling by RT-PCR
Platform:
GPL32158
60 Samples
Download data: XLSX
Series
Accession:
GSE200619
ID:
200200619
2.

PEGboIFN-lambda as a FMD preexposure prophylactic and vaccine adjuvant in cattle—ISG and adaptive immunity gene expression

(Submitter supplied) Foot-and-mouth disease (FMD) is a vesicular disease of cloven-hoofed animals with devastating economic implications. The current FMD vaccine, routinely used in enzootic countries, requires at least 7 days to induce protection. However, FMD vaccination is typically not recommended for use in non-enzootic areas, underscoring the need to develop new fast-acting therapies for FMD control during outbreaks. more...
Organism:
Bos taurus
Type:
Expression profiling by RT-PCR
Platform:
GPL34326
112 Samples
Download data: TXT
Series
Accession:
GSE262192
ID:
200262192
3.

Real-time quantitative PCR analysis of ccRCC model rats III

(Submitter supplied) Carcinogen-induced ccRCC rat models of mRNA expression arrays were used to explore genes potentially associated with the destruction of pseudo capsule (PC).
Organism:
Rattus norvegicus
Type:
Expression profiling by RT-PCR
Platform:
GPL34196
6 Samples
Download data: TXT
Series
Accession:
GSE255822
ID:
200255822
4.

Real-time quantitative PCR analysis of ccRCC model rats II

(Submitter supplied) Carcinogen-induced ccRCC rat models of mRNA expression arrays were used to explore genes potentially associated with the destruction of pseudo capsule (PC).
Organism:
Rattus norvegicus
Type:
Expression profiling by RT-PCR
Platform:
GPL34195
6 Samples
Download data: TXT
Series
Accession:
GSE255820
ID:
200255820
5.

Real-time quantitative PCR analysis of ccRCC model rats

(Submitter supplied) Carcinogen-induced ccRCC rat models of mRNA expression arrays were used to explore genes potentially associated with the destruction of pseudo capsule (PC).
Organism:
Rattus norvegicus
Type:
Expression profiling by RT-PCR
Platform:
GPL34194
6 Samples
Download data: TXT
Series
Accession:
GSE255816
ID:
200255816
6.

In vitro aging alters the gene expression and secretome composition of canine adipose-derived mesenchymal stem cells

(Submitter supplied) Canine adipose-derived mesenchymal stem cells (cAD-MSCs) show therapeutic promise for their regenerative potential, particularly in their secretome. However, concerns arise regarding the impact of in vitro cultivation need for storing therapeutic doses, prompting this study to comprehensively explore the impact of in vitro aging on gene expression and secretome composition. The study involved collecting abdominal adipose tissue samples from nine healthy female dogs, from which cAD-MSCs were extracted and cultured. more...
Organism:
Canis lupus familiaris
Type:
Expression profiling by RT-PCR
Platform:
GPL34182
18 Samples
Download data: XLSX
Series
Accession:
GSE255585
ID:
200255585
7.

Real-time quantitative PCR analysis of Tomato stress response

(Submitter supplied) To extract RNA from shoots and roots, 3 weeks old control and treated plants were harvested at 2pm in the greenhouse. Total RNA was extracted using the AccuPrep® Universal RNA extraction kit (Bioneer, Daejeon, Korea) and treated with RNase-free DNase to remove DNA fragments (Qiagen, Hilden, Germany). One microgram of total RNA was used to synthesize cDNA with AccuPower® RT PreMix (Bioneer, Daejeon, Korea). more...
Organism:
Solanum lycopersicum
Type:
Expression profiling by RT-PCR
Platform:
GPL33939
16 Samples
Download data: XLS
Series
Accession:
GSE248090
ID:
200248090
8.

Repositioning the early pathology of type 1 diabetes to the extra-islet vasculature.

(Submitter supplied) Repositioning the early pathology of type 1 diabetes to the extra-islet vasculature.
Organism:
Mus musculus
Type:
Expression profiling by RT-PCR
Download data: CSV, TXT
Series
Accession:
GSE253956
ID:
200253956
9.

Weight loss following Roux-en-Y gastric bypass surgery leads to changes in the expression of several miRNAs and their predicted target genes in skeletal muscle

(Submitter supplied) miRNA profiles were investigated in skeletal muscle in severely obese individuals with or without diabetes before and after Roux-en-Y gastric bypass surgery.
Organism:
Homo sapiens
Type:
Expression profiling by RT-PCR
Platform:
GPL22463
50 Samples
Download data: TXT
Series
Accession:
GSE87131
ID:
200087131
10.

Real Time quantitative PCR analysis of human T cells overexpressing AMPKg2

(Submitter supplied) Human T cells were transduced to overexpress AMPKg2 or an EV control. CD4+ T cells were assessed for expression of TH subset related genes
Organism:
Homo sapiens
Type:
Expression profiling by RT-PCR
Platform:
GPL34054
4 Samples
Download data: TXT
Series
Accession:
GSE252375
ID:
200252375
11.

RT-qPCR analysis in zebrafish Viperin KO fish under VHSV infections

(Submitter supplied) For this experiment, WT and Viperin KO fish were used and fish were injected with either PBS or VHSV and the gene expression was analyzed
Organism:
Danio rerio
Type:
Expression profiling by RT-PCR
Platform:
GPL34003
20 Samples
Download data: TXT
Series
Accession:
GSE250036
ID:
200250036
12.

Real-time quantitative PCR analysis of Nrf2, HO-1, IL-6 and VEGF-A genes in human retinal pigment epithelium (RPE-19) cells

(Submitter supplied) Human RPE-19 cells were treated with either Trolox (50 µg/mL), lutein (10 µg/mL) or gac peel extracts (0-200 µg/mL) for 12, 24, 48 or 72 h before being exposed to 500 µM H2O2 for 24 h prior to RNA collection. Results were presented as the fold change compared to untreated controls ± SEM (n=3), different letters indicated statistical significance at p≤0.05 between different treatments (Analysis by One-way ANOVA with Turkey’s LSD test).
Organism:
Homo sapiens
Type:
Expression profiling by RT-PCR
Platform:
GPL33598
36 Samples
Download data: TXT
Series
Accession:
GSE237892
ID:
200237892
13.

Calprotectin blockade inhibits long-term vascular pathology following peritoneal dialysis-associated bacterial infection.

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by RT-PCR
Platform:
GPL29397
7 Samples
Download data
Series
Accession:
GSE246102
ID:
200246102
14.

Calprotectin blockade inhibits long-term vascular pathology following peritoneal dialysis-associated bacterial infection. [2]

(Submitter supplied) Bacterial infections and the concurrent inflammation have been associated with increased long-term cardiovascular (CV) risk. In patients receiving peritoneal dialysis (PD), bacterial peritonitis is a common occurrence, and each episode further increases late CV mortality risk. However, the underlying mechanism(s) remains to be elucidated before safe and efficient anti-inflammatory interventions can be developed. more...
Organism:
Mus musculus
Type:
Expression profiling by RT-PCR
Platform:
GPL29397
4 Samples
Download data: XLS
Series
Accession:
GSE246101
ID:
200246101
15.

Calprotectin blockade inhibits long-term vascular pathology following peritoneal dialysis-associated bacterial infection. [1]

(Submitter supplied) Bacterial infections and the concurrent inflammation have been associated with increased long-term cardiovascular (CV) risk. In patients receiving peritoneal dialysis (PD), bacterial peritonitis is a common occurrence, and each episode further increases late CV mortality risk. However, the underlying mechanism(s) remains to be elucidated before safe and efficient anti-inflammatory interventions can be developed. more...
Organism:
Mus musculus
Type:
Expression profiling by RT-PCR
Platform:
GPL29397
3 Samples
Download data: XLS
Series
Accession:
GSE246100
ID:
200246100
16.

qPCR gene expression profiling of 84 key genes involved in brain micro-vessel treatment

(Submitter supplied) The Mouse osteogenesis RT² Profiler PCR Array profiles the expression of 84 key genes involved in brain micro-vessel treatment. In this experiment, we established an ex vivo cerebral microvascular model and treated it with PDGF-BB. There are two samples: one is the control group, and the other is the PDGF-BB treated group.
Organism:
Mus musculus
Type:
Expression profiling by RT-PCR
Platform:
GPL33761
2 Samples
Download data: XLSX
Series
Accession:
GSE243144
ID:
200243144
17.

Real-time quantitative PCR analysis of liver tissue from pigs infected experimentally with hepatitis E virus (HEV)

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Sus scrofa
Type:
Expression profiling by RT-PCR
Platforms:
GPL33783 GPL33782 GPL33776
52 Samples
Download data
Series
Accession:
GSE243864
ID:
200243864
18.

Real-time quantitative PCR analysis of liver tissue from pigs infected experimentally with hepatitis E virus (HEV) [pig liver]

(Submitter supplied) We aimed to identify interferon (IFN)-regulated genes that are differentially expressed during HEV infection in swine liver tissues.
Organism:
Sus scrofa
Type:
Expression profiling by RT-PCR
Platform:
GPL33783
8 Samples
Download data: TXT
Series
Accession:
GSE243862
ID:
200243862
19.

Real-time quantitative PCR analysis of human HepaRG cells infected with hepatitis E virus (HEV) [D100 plaque 2]

(Submitter supplied) We aimed to identify interferon (IFN)-regulated genes that are differentially expressed during chronic HEV infection in human hepatocytes, the main site of HEV replication, using HepaRG cells.
Organism:
Homo sapiens
Type:
Expression profiling by RT-PCR
Platform:
GPL33782
12 Samples
Download data: TXT
Series
Accession:
GSE243860
ID:
200243860
20.

Real-time quantitative PCR analysis of human HepaRG cells infected with hepatitis E virus (HEV) [D100 plaque 1]

(Submitter supplied) We aimed to identify interferon (IFN)-regulated genes that are differentially expressed during chronic HEV infection in human hepatocytes, the main site of HEV replication, using HepaRG cells.
Organism:
Homo sapiens
Type:
Expression profiling by RT-PCR
Platform:
GPL33776
12 Samples
Download data: TXT
Series
Accession:
GSE243856
ID:
200243856
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