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In this study, the changes in histology indicated that both types of radiations can induce profibrotic responses.
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Both types of radiation can damage DNA and increase the risk of an astronaut developing cancer.
The final group was exposed to both types of radiation, plus the vacuum.
Effects of both types of radiation on erythropoiesis were also evaluated.
A novel versatile tubular reactor that may use both types of radiation, solar and/or artificial, and different types of suspended or immobilized photocatalysts is proposed.
This finding indicates the potential induction of genomic instability in hematopoietic cells of CBA/CaJ mice by both types of radiation.
In contrast, both types of radiation induced increased MN-PCEs frequencies in irradiated CBA/CaJ mice, but not C57BL/6J mice, at late times post-exposure.
Both types of radiation can cause cellular damage and, in some conditions, induce malignant tumors.
In SQ20B cells, the same treatment inhibited late ceramide production and apoptosis following both types of radiation.
UV-irradiation induced DNA fragmentation in both cell lines, and the combination of both types of radiation led to the largest increases in DNA fragmentation.
Inhibition of caspase activity or ceramide production showed that, for both types of radiation, ceramide is essential for the initiation of early apoptosis in radiosensitive cells and late apoptosis following mitotic catastrophe in radioresistant cells.
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