Petra A. Jackson
Copenhagen, Denmark
Last Updated: 09/26/2026
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Found 26 publications
Corrigendum to "MWCNTs of different physicochemical properties cause similar inflammatory responses, but differences in transcriptional and histological markers of fibrosis in mouse lungs" [Toxicol. Appl. Pharmacol., 284 (2015) 16-32].
Journal: Toxicology and applied pharmacology
Published: June 18, 2018
Physicochemical predictors of Multi-Walled Carbon Nanotube-induced pulmonary histopathology and toxicity one year after pulmonary deposition of 11 different Multi-Walled Carbon Nanotubes in mice.
Journal: Basic & clinical pharmacology & toxicology
Published: June 11, 2018
Airway exposure to multi-walled carbon nanotubes disrupts the female reproductive cycle without affecting pregnancy outcomes in mice.
Journal: Particle and fibre toxicology
Published: December 23, 2016
Multi-walled carbon nanotube-physicochemical properties predict the systemic acute phase response following pulmonary exposure in mice.
Journal: PloS one
Published: December 21, 2016
Surface modification does not influence the genotoxic and inflammatory effects of TiO2 nanoparticles after pulmonary exposure by instillation in mice.
Journal: Mutagenesis
Published: September 24, 2016
Epoxy composite dusts with and without carbon nanotubes cause similar pulmonary responses, but differences in liver histology in mice following pulmonary deposition.
Journal: Particle and fibre toxicology
Published: February 02, 2016
DNA strand breaks, acute phase response and inflammation following pulmonary exposure by instillation to the diesel exhaust particle NIST1650b in mice.
Journal: Mutagenesis
Published: March 16, 2015
A perspective on the developmental toxicity of inhaled nanoparticles.
Journal: Reproductive toxicology (Elmsford, N.Y.)
Published: March 13, 2015
Last Updated: 09/26/2026