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Links from GEO DataSets

Items: 20

1.

Transcriptomic analysis of mouse lung tissue exposed to two multiwalled carbon nanotubes (NRCWE-26 and NM-401)

(Submitter supplied) Multi-walled carbon nanotubes (MWCNTs) are extensively produced and used in composite materials and electronic applications, thus increasing risk of worker and consumer exposure. MWCNTs are an inhomogeneous group of nanomaterials that exist in various lengths, shapes and with different metal compositions, which makes hazard evaluation difficult. However, several studies suggest that length plays an important role in the toxicity induced by MWCNTs. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
139 Samples
Download data: TXT
Series
Accession:
GSE55286
ID:
200055286
2.

Expression profiling of mice exposed to multiwalled carbon nanotubes

(Submitter supplied) Mice were aspirated with multiwalled carbon nanotubes in four doses ranging from 10 µg to 80 µg, plus control, and sacrificed after 1, 7, 28, and 56 days. RNA was extracted from the lungs and expression profilling by microarray was performed.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
160 Samples
Download data: TXT
Series
Accession:
GSE29042
ID:
200029042
3.

Gene expression profiles in rat lung following intratracheal instillation with short size single-wall and multi-wall carbon nanotubes

(Submitter supplied) To further development of our gene expression approach to assess the effects of manufactured nanomaterials at the transcriptional level, we have employed whole genome microarray expression profiling to discuss the differences of the pulmonary and pleural
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL7294
15 Samples
Download data: TXT
Series
Accession:
GSE75148
ID:
200075148
4.

Changes in cholesterol homeostasis and acute phase response following pulmonary exposure to multi-walled carbon nanotubes links carbon nanotube exposure to risk of cardiovascular disease

(Submitter supplied) Adverse lung effects in rodents following pulmonary exposure to multi-walled carbon nanotubes (MWCNT) are well documented. However, systemic effects are less understood. Prospective epidemiological studies have shown increased cardiovascular disease risk after pulmonary exposure to airborne particles, which has led to concerns that inhalation exposure to MWCNT might pose similar risks. We used high-content genomics tools to compare hepatic responses after exposure to a short, entangled MWCNT to the hepatic responses after exposure to a long, stiffer MWCNT at the global transcriptomic level. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
60 Samples
Download data: TXT
Series
Accession:
GSE61366
ID:
200061366
5.

Inhaled multi-walled carbon nanotubes-induced gene expression profile in rat lung

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL22740
144 Samples
Download data: TXT
Series
Accession:
GSE113532
ID:
200113532
6.

Inhaled multi-walled carbon nanotubes-induced gene expression profile in rat lung (NM-403)

(Submitter supplied) In this work we study the pulmonary toxicological properties of carbon nanotubes using molecular toxicological approache. For this, we exposed Sprague Dawley rats by nose-only inhalation 6 hours/day, 5 days/week for 4 weeks. Lung samples have been collected up to 180 days after the end of exposure and transcriptomics analysis were performed.
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL22740
72 Samples
Download data: TXT
Series
Accession:
GSE113531
ID:
200113531
7.

Inhaled multi-walled carbon nanotubes-induced gene expression profile in rat lung (NM-401)

(Submitter supplied) In this work we study the pulmonary toxicological properties of carbon nanotubes using molecular toxicological approache. For this, we exposed Sprague Dawley rats by nose-only inhalation 6 hours/day, 5 days/week for 4 weeks. Lung samples have been collected up to 180 days after the end of exposure and transcriptomics analysis were performed.
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL22740
72 Samples
Download data: TXT
Series
Accession:
GSE113528
ID:
200113528
8.

Multiwalled carbon nanotube-induced pulmonary inflammatory and fibrotic responses and genomic changes following aspiration exposure in mice: A 1-year postexposure study.

(Submitter supplied) Pulmonary exposure to multiwalled carbon nanotubes (MWCNT) induces an inflammatory and rapid fibrotic response, although the long-term signaling mechanisms are unknown. The aim of this study was to examine the effects of 1, 10, 40, or 80 µg MWCNT administered by pharyngeal aspiration on bronchoalveolar lavage (BAL) fluid for polymorphonuclear cell (PMN) infiltration, lactate dehydrogenase (LDH) activity, and lung histopathology for inflammatory and fibrotic responses in mouse lungs 1 mo, 6 mo, and 1 yr postexposure. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17400
139 Samples
Download data: CEL
Series
Accession:
GSE112780
ID:
200112780
9.

Gene expression profiles in rat lung following intratracheal instillation with impurity-free single-wall carbon nanotubes

(Submitter supplied) To further development of our gene expression approach to assess the effects of manufactured nanomaterials at the transcriptional level, we have employed whole genome microarray expression profiling as a discovery platform to identify genes with the potential to distinguish characterization of physicochemical properties of impurity-free single-wall carbon nanotubes (SWCNTs). We have prepared two types of dispersed the SWCNTs, namely relatively small bundles and a short linear shape (CNT-1) and large bundles and a long linear shape (CNT-2), and attempted to characterize time-dependent changes in the gene expression of lung tissues until 90 days after intratracheal instillation with SWCNTs suspensions at 0.4 mg injected dose per rat.
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL7294
15 Samples
Download data: TXT
Series
Accession:
GSE61483
ID:
200061483
10.

Gene expression profiles in rat alveolar macrophages exposure to impurity-free single-wall carbon nanotubes

(Submitter supplied) To further development of our gene expression approach to assess the effects of manufactured nanomaterials at the transcriptional level, we have employed whole genome microarray expression profiling as a discovery platform to identify genes with the potential to distinguish characterization of physicochemical properties of impurity-free single-wall carbon nanotubes (SWCNTs), namely, relatively small bundles and a short linear shape (CNT-1) and large bundles and a long linear shape (CNT-2).
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL7294
3 Samples
Download data: TAR
Series
Accession:
GSE61319
ID:
200061319
11.

Transcriptomic analysis reveals novel mechanistic insight into murine biological responses to multi-walled carbon nanotubes in lungs and cultured lung epithelia cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
44 Samples
Download data: TXT
Series
Accession:
GSE47000
ID:
200047000
12.

Transcriptomic analysis of cultured lung epithelial cells exposed to multiwalled carbon nanotubes (Mitsui7)

(Submitter supplied) There is great interest in substituting animal with in vitro experimentation in human health risk assessment, but there are rather few comparisons of in vitro and in vivo biological responses to engineered nanomaterials (ENM). We used high-content genomics tools, to compare in vivo pulmonary responses of multiwalled carbon nanotubes (MWCNT) to those in vitro in cultured lung epithelial cells at the global transcriptomic level. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
22 Samples
Download data: TXT
Series
Accession:
GSE46999
ID:
200046999
13.

Transcriptomic analysis of mouse lung tissue exposed to multiwalled carbon nanotubes (Mitsui7)

(Submitter supplied) There is great interest in substituting animal with in vitro experimentation in human health risk assessment, but there are rather few comparisons of in vitro and in vivo biological responses to engineered nanomaterials (ENM). We used high-content genomics tools, to compare in vivo pulmonary responses of multiwalled carbon nanotubes (MWCNT) to those in vitro in cultured lung epithelial cells at the global transcriptomic level. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
22 Samples
Download data: TXT
Series
Accession:
GSE46998
ID:
200046998
14.

Surface modified titanium dioxide nanoparticles induce fibrosis-like changes in lungs at high doses

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
233 Samples
Download data: TXT
Series
Accession:
GSE81570
ID:
200081570
15.

Surface modified titanium dioxide nanoparticles induce fibrosis-like changes in lungs at high doses [set 6]

(Submitter supplied) Previous studies have shown that TiO2NPs induce lung inflammation in mice and have suggested that the degree of inflammation varies with their size and other physical and chemical properties, e.g., shapes, surface modifications and surface charge. It is currently unknown if the observed inflammation in mouse lungs following exposure to TiO2NPs will cause any disease in the long term. This study examined mouse lung responses to six individual TiO2NPs of varying sizes (10, 20 and 300 nm), surface modifications and shapes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
40 Samples
Download data: TXT
Series
Accession:
GSE81569
ID:
200081569
16.

Surface modified titanium dioxide nanoparticles induce fibrosis-like changes in lungs at high doses [set 5]

(Submitter supplied) Previous studies have shown that TiO2NPs induce lung inflammation in mice and have suggested that the degree of inflammation varies with their size and other physical and chemical properties, e.g., shapes, surface modifications and surface charge. It is currently unknown if the observed inflammation in mouse lungs following exposure to TiO2NPs will cause any disease in the long term. This study examined mouse lung responses to six individual TiO2NPs of varying sizes (10, 20 and 300 nm), surface modifications and shapes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
40 Samples
Download data: TXT
Series
Accession:
GSE81568
ID:
200081568
17.

Surface modified titanium dioxide nanoparticles induce fibrosis-like changes in lungs at high doses [set 4]

(Submitter supplied) Previous studies have shown that TiO2NPs induce lung inflammation in mice and have suggested that the degree of inflammation varies with their size and other physical and chemical properties, e.g., shapes, surface modifications and surface charge. It is currently unknown if the observed inflammation in mouse lungs following exposure to TiO2NPs will cause any disease in the long term. This study examined mouse lung responses to six individual TiO2NPs of varying sizes (10, 20 and 300 nm), surface modifications and shapes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
40 Samples
Download data: TXT
Series
Accession:
GSE81567
ID:
200081567
18.

Surface modified titanium dioxide nanoparticles induce fibrosis-like changes in lungs at high doses [set 3]

(Submitter supplied) Previous studies have shown that TiO2NPs induce lung inflammation in mice and have suggested that the degree of inflammation varies with their size and other physical and chemical properties, e.g., shapes, surface modifications and surface charge. It is currently unknown if the observed inflammation in mouse lungs following exposure to TiO2NPs will cause any disease in the long term. This study examined mouse lung responses to six individual TiO2NPs of varying sizes (10, 20 and 300 nm), surface modifications and shapes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
37 Samples
Download data: TXT
Series
Accession:
GSE81566
ID:
200081566
19.

Surface modified titanium dioxide nanoparticles induce fibrosis-like changes in lungs at high doses [set 2]

(Submitter supplied) Previous studies have shown that TiO2NPs induce lung inflammation in mice and have suggested that the degree of inflammation varies with their size and other physical and chemical properties, e.g., shapes, surface modifications and surface charge. It is currently unknown if the observed inflammation in mouse lungs following exposure to TiO2NPs will cause any disease in the long term. This study examined mouse lung responses to six individual TiO2NPs of varying sizes (10, 20 and 300 nm), surface modifications and shapes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
39 Samples
Download data: TXT
Series
Accession:
GSE81565
ID:
200081565
20.

Surface modified titanium dioxide nanoparticles induce fibrosis-like changes in lungs at high doses [set 1]

(Submitter supplied) Previous studies have shown that TiO2NPs induce lung inflammation in mice and have suggested that the degree of inflammation varies with their size and other physical and chemical properties, e.g., shapes, surface modifications and surface charge. It is currently unknown if the observed inflammation in mouse lungs following exposure to TiO2NPs will cause any disease in the long term. This study examined mouse lung responses to six individual TiO2NPs of varying sizes (10, 20 and 300 nm), surface modifications and shapes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
37 Samples
Download data: TXT
Series
Accession:
GSE81564
ID:
200081564
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