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Anne-Catherine Heuskin

Researcher at Université de Namur

Publications -  29
Citations -  663

Anne-Catherine Heuskin is an academic researcher from Université de Namur. The author has contributed to research in topics: Linear energy transfer & Cell killing. The author has an hindex of 13, co-authored 25 publications receiving 426 citations. Previous affiliations of Anne-Catherine Heuskin include Lawrence Berkeley National Laboratory.

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Roadmap for metal nanoparticles in radiation therapy: current status, translational challenges, and future directions.

TL;DR: This roadmap outlines the potential roles of metallic nanoparticles in the field of radiation therapy and covers contributions from experts in these topics summarizing their view of the current status and challenges, as well as expected advancements in technology to address these challenges.
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Gold Nanoparticles as a Potent Radiosensitizer: A Transdisciplinary Approach from Physics to Patient

TL;DR: The current state of knowledge is reviewed by addressing how gold nanoparticles exert their radiosensitizing effects from a transdisciplinary perspective and the current and future challenges to go towards a successful clinical translation of this promising therapeutic approach.
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Gateway to genetic exchange? DNA double‐strand breaks in the bdelloid rotifer Adineta vaga submitted to desiccation

TL;DR: Interestingly, when investigating the influence of UV‐A and UV‐B exposure on the genomic integrity of desiccated bdelloids, it was observed that these natural radiations also caused important DNA DSBs, suggesting that the genome is not protected during the desiccation stage but that the repair mechanisms are extremely efficient in these intriguing organisms.
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Proton irradiation orchestrates macrophage reprogramming through NFκB signaling.

TL;DR: It is shown that M1 macrophages (THP-1 cell line) were more resistant to proton irradiation than unpolarized (M0) and M2macrophages, which correlated with differential DNA damage detection, and propton irradiation-induced macrophage reprogramming from M2 to a mixed M1/M2 phenotype is suggested.