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Links from GEO DataSets

Items: 19

1.

Molecular mechanisms of pulmonary response progression in crystalline silica exposed rats

(Submitter supplied) The capability to detect target organ toxicity as well as to determine the molecular mechanisms underlying such toxicity by employing surrogate biospecimens that can be obtained by a non-invasive or minimally invasive procedure has significant advantage in occupational toxicology. Pulmonary toxicity and global gene expression profile in the lungs, peripheral blood and bronchoalveolar lavage (BAL) cells were determined in rats at 44-weeks following pulmonary exposure to crystalline silica (15 mg/m3, 6-hours/day, 5 days). more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL6101
36 Samples
Download data: TXT
Series
Accession:
GSE41572
ID:
200041572
2.

Pulmonary toxicity and global gene expression changes in response to sub-chronic inhalation exposure to crystalline silica in rats

(Submitter supplied) Occupational exposure to crystalline silica results in serious health effects, most notably, silicosis and cancer. A proper understanding of the mechanism(s) underlying the initiation and progression of silica-induced pulmonary toxicity is critical for the intervention and/or prevention of the adverse health effects associated with crystalline silica exposure. Rats were exposed to crystalline silica by inhalation at a concentration of 15 mg/m3, 6 hours/day, 5 days/week for 3, 6 or 12 weeks. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL6101
36 Samples
Download data: TXT
Series
Accession:
GSE49144
ID:
200049144
3.

Transcriptomics Analysis of Lungs and Peripheral Blood of Crystalline Silica Exposed Rats

(Submitter supplied) Non-invasive or minimally invasive surrogate approaches to detect/predict target organ toxicity have significant practical applications in occupational toxicology. Presently, using a rat model, we have investigated the potential application of peripheral blood transcriptomics as a practical approach to study the mechanisms of silica-induced pulmonary toxicity. Rats were exposed by inhalation to crystalline silica for one week (15 mg/m3, 6-hours/day, 5 days/week). more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL6101
24 Samples
Download data: TXT
Series
Accession:
GSE36208
ID:
200036208
4.

Blood gene expression profile of control and crystalline silica exposed rats

(Submitter supplied) The present research aimed to investigate peripheral blood gene expression profiling as a minimally invasive surrogate approach to study silica-induced pulmonary toxicity. Rats were exposed to crystalline silica by inhalation (15 mg/m3, 6 hours/day, 5 days). Pulmonary damage and blood gene expression profiles were determined at various latency periods (0 - 16 weeks). Silica exposure resulted in pulmonary toxicity and this was evidenced by histological changes in the lungs and elevation of LDH activity, and total protein and albumin contents in the bronchoalveolar lavage fluid (BALF) of the rats. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Datasets:
GDS5197 GDS5198 GDS5199
Platform:
GPL6101
96 Samples
Download data: TXT
Series
Accession:
GSE27023
ID:
200027023
5.
Full record GDS5199

Silica-induced pulmonary toxicity: blood (part III)

Analysis of blood samples from Fischer animals 16 hours following inhalation of crystalline silica at a concentration of 1 mg/m3, 6 h/day for 5 consecutive days. Results provide insight into the utility of blood gene expression profiling to detect pulmonary toxicity induced by silica.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, transformed count, 2 agent sets
Platform:
GPL6101
Series:
GSE27023
12 Samples
Download data
DataSet
Accession:
GDS5199
ID:
5199
6.
Full record GDS5198

Silica-induced pulmonary toxicity: blood (part II)

Analysis of blood samples from Fischer animals 16 hours following inhalation of crystalline silica at a concentration of 2 mg/m3, 6 h/day for 5 consecutive days. Results provide insight into the utility of blood gene expression profiling to detect pulmonary toxicity induced by silica.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, transformed count, 2 agent sets
Platform:
GPL6101
Series:
GSE27023
12 Samples
Download data
DataSet
Accession:
GDS5198
ID:
5198
7.
Full record GDS5197

Silica-induced pulmonary toxicity: blood (part I)

Analysis of blood samples from Fischer animals for up to 16 weeks following inhalation of crystalline silica at a concentration of 15 mg/m3, 6 h/day for 5 consecutive days. Results provide insight into the utility of blood gene expression profiling to detect pulmonary toxicity induced by silica.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, transformed count, 2 agent, 6 time sets
Platform:
GPL6101
Series:
GSE27023
72 Samples
Download data
DataSet
Accession:
GDS5197
ID:
5197
8.

Molecular insights into the progression of crystalline silica-induced pulmonary toxicity in rats

(Submitter supplied) Identification of molecular target(s) and mechanism(s) of silica-induced pulmonary toxicity is important for the intervention and/or prevention of diseases associated with occupational exposure to crystalline silica. Rats were exposed to crystalline silica by inhalation (15 mg/m3, 6 h/day, 5 days) and global gene expression profile was determined in the lungs by microarray analysis at 1, 2, 4, 8, and 16 weeks following termination of silica exposure. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL6101
60 Samples
Download data: TXT
Series
Accession:
GSE32147
ID:
200032147
9.

Mechanisms of crystalline silica-induced pulmonary toxicity revealed by global gene expression profiling

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Rattus norvegicus
Type:
Expression profiling by array
Platforms:
GPL6947 GPL6101
80 Samples
Download data
Series
Accession:
GSE30216
ID:
200030216
10.

Mechanisms of crystalline silica-induced pulmonary toxicity revealed by global gene expression profiling (A549 cells dataset 5)

(Submitter supplied) A proper understanding of the mechanisms underlying crystalline silica-induced pulmonary toxicity has implications in the management and potential prevention of the adverse health effects associated with silica exposure including silicosis, cancer and several auto-immune diseases. Human lung type II epithelial cells and rat lungs exposed to crystalline silica were employed as experimental models to determine global gene expression changes in order to understand the molecular mechanisms underlying silica-induced pulmonary toxicity. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6947
10 Samples
Download data: TXT
Series
Accession:
GSE30215
ID:
200030215
11.

Mechanisms of crystalline silica-induced pulmonary toxicity revealed by global gene expression profiling (A549 cells dataset 4)

(Submitter supplied) A proper understanding of the mechanisms underlying crystalline silica-induced pulmonary toxicity has implications in the management and potential prevention of the adverse health effects associated with silica exposure including silicosis, cancer and several auto-immune diseases. Human lung type II epithelial cells and rat lungs exposed to crystalline silica were employed as experimental models to determine global gene expression changes in order to understand the molecular mechanisms underlying silica-induced pulmonary toxicity. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6947
10 Samples
Download data: TXT
Series
Accession:
GSE30214
ID:
200030214
12.

Mechanisms of crystalline silica-induced pulmonary toxicity revealed by global gene expression profiling (A549 cells dataset 3)

(Submitter supplied) A proper understanding of the mechanisms underlying crystalline silica-induced pulmonary toxicity has implications in the management and potential prevention of the adverse health effects associated with silica exposure including silicosis, cancer and several auto-immune diseases. Human lung type II epithelial cells and rat lungs exposed to crystalline silica were employed as experimental models to determine global gene expression changes in order to understand the molecular mechanisms underlying silica-induced pulmonary toxicity. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6947
10 Samples
Download data: TXT
Series
Accession:
GSE30213
ID:
200030213
13.

Mechanisms of crystalline silica-induced pulmonary toxicity revealed by global gene expression profiling (A549 cells dataset 2)

(Submitter supplied) A proper understanding of the mechanisms underlying crystalline silica-induced pulmonary toxicity has implications in the management and potential prevention of the adverse health effects associated with silica exposure including silicosis, cancer and several auto-immune diseases. Human lung type II epithelial cells and rat lungs exposed to crystalline silica were employed as experimental models to determine global gene expression changes in order to understand the molecular mechanisms underlying silica-induced pulmonary toxicity. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6947
20 Samples
Download data: TXT
Series
Accession:
GSE30200
ID:
200030200
14.

Mechanisms of crystalline silica-induced pulmonary toxicity revealed by global gene expression profiling (A549 cells dataset 1)

(Submitter supplied) A proper understanding of the mechanisms underlying crystalline silica-induced pulmonary toxicity has implications in the management and potential prevention of the adverse health effects associated with silica exposure including silicosis, cancer and several auto-immune diseases. Human lung type II epithelial cells and rat lungs exposed to crystalline silica were employed as experimental models to determine global gene expression changes in order to understand the molecular mechanisms underlying silica-induced pulmonary toxicity. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6947
10 Samples
Download data: TXT
Series
Accession:
GSE30180
ID:
200030180
15.

Mechanisms of crystalline silica-induced pulmonary toxicity revealed by global gene expression profiling (rat lungs)

(Submitter supplied) A proper understanding of the mechanisms underlying crystalline silica-induced pulmonary toxicity has implications in the management and potential prevention of the adverse health effects associated with silica exposure including silicosis, cancer and several auto-immune diseases. Human lung type II epithelial cells and rat lungs exposed to crystalline silica were employed as experimental models to determine global gene expression changes in order to understand the molecular mechanisms underlying silica-induced pulmonary toxicity. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL6101
20 Samples
Download data: TXT
Series
Accession:
GSE30178
ID:
200030178
16.

Tobacco smoke exposure exacerbates silica-induced pulmonary toxicity in rats

(Submitter supplied) Previous studies have shown that smoking induces oxidative stress and inflammation, known factors that coincide with the development and progression of silicosis. Nevertheless, the precise role of cigarette smoke exposure in silicosis and the underlying mechanisms are not clearly understood. Therefore, the objective of the present study was to determine the effect of smoking, if any, on silica-induced pulmonary response and the underlying mechanisms. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18694
24 Samples
Download data: TXT
Series
Accession:
GSE136945
ID:
200136945
17.

Lung response to multi-walled carbon nanotube exposure in rats.

(Submitter supplied) The projected increase in the production and use of nanomaterials is expected to result in a corresponding increase in human exposure, potentially resulting in significant morbidity and mortality. Currently, the lung toxicity of multi-walled carbon nanotubes (MWCNT), a prototype nanomaterial, was investigated in a rat model. The rats were exposed by whole-body inhalation to air (controls) or MWCNT (6 hours/day, 3 days) to result in cumulative doses of 180, 90, 45, 22.5, or 11.25 mg/m3. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18694
60 Samples
Download data: CSV
Series
Accession:
GSE148869
ID:
200148869
18.

Lung response to crystalline nanocellulose exposure in rats

(Submitter supplied) Crystalline nanocellulose (CNC) is an emerging nanomaterial with multiple commercial and industrial applications. Occupational exposure to CNC during the production and/or use of products containing the nanomaterial potentially resulting in adverse health effects among workers is possible. Therefore, there is an immediate need to determine the toxicity potential of CNC. Rats were exposed to either air or CNC (20 mg/m^3, 6 hours/day, 5 days/week, 14 days) and lung toxicity was determined one day following termination of the exposures. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18694
12 Samples
Download data: CSV
Series
Accession:
GSE150567
ID:
200150567
19.

Biological effects of inhaled hydraulic fracturing sand dust in rats

(Submitter supplied) The pulmonary inflammatory response to inhalation exposure to fracking sand dust (FSD) was investigated in a rat model. Adult male Sprague-Dawley rats were exposed by whole-body inhalation to air or an aerosol of FSD at concentrations of 10 or 30 mg/m3, 6 hours/day for 4 days. The control and FSD-exposed rats were euthanized at post-exposure time intervals of 1, 7 or 27days and pulmonary inflammatory, cytotoxic and oxidant responses were determined. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18694
64 Samples
Download data: CSV
Series
Accession:
GSE148255
ID:
200148255
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