Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Martin, Paparella"'
Autor:
European Food Safety Authority (EFSA), Kevin M. Crofton, Martin Paparella, Anna Price, Iris Mangas, Laura Martino, Andrea Terron, Antonio Hernández‐Jerez
Publikováno v:
EFSA Journal, Vol 22, Iss 8, Pp n/a-n/a (2024)
Abstract The adverse outcome pathway (AOP) framework serves as a practical tool for organising scientific knowledge that can be used to infer cause–effect relationships between stressor events and toxicity outcomes in intact organisms. However, a m
Externí odkaz:
https://doaj.org/article/c3b3bb85a2de473da5a703e2851b6664
Autor:
EFSA (European Food Safety Authority), Antonio Hernandez‐Jerez, Tamara Coja, Martin Paparella, Anna Price, Jerome Henri, Andreas Focks, Jochem Louisse, Andrea Terron, Marco Binaglia, Irene Munoz Guajardo, Iris Mangas, Lucien Ferreira, Dimitra Kardassi, Chloe De Lentdecker, Tunde Molnar, Giorgia Vianello
Publikováno v:
EFSA Journal, Vol 22, Iss 5, Pp n/a-n/a (2024)
Abstract Acetamiprid is a pesticide active substance with insecticidal action whose approval was renewed by Commission Implementing Regulation (EU) 2018/113. In January 2022, the EFSA PPR Panel published a statement following a request from the Europ
Externí odkaz:
https://doaj.org/article/9ee7b1463abd4f499787c72727b1fe25
Autor:
Miriam N. Jacobs, Jan M. Bult, Kevin Cavanagh, Christophe Chesne, Nathalie Delrue, Jianan Fu, Emma Grange, Ingrid Langezaal, Dominika Misztela, Jenny Murray, Martin Paparella, Gilly Stoddart, Torsten Tonn, Carol Treasure, Masaaki Tsukano, Rosemary Versteegen
Publikováno v:
Frontiers in Toxicology, Vol 5 (2023)
The ethical needs and concerns with use and sourcing of human materials, particularly serum, in OECD in vitro test guidelines were explored in a dedicated international workshop held in 2019. The health-related aspects of the donation procedure, incl
Externí odkaz:
https://doaj.org/article/64e648c9e6894018be64557ad5a4ea22
Autor:
Annamaria Colacci, Raffaella Corvi, Kyomi Ohmori, Martin Paparella, Stefania Serra, Iris Da Rocha Carrico, Paule Vasseur, Miriam Naomi Jacobs
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 6, p 5659 (2023)
The history of the development of the cell transformation assays (CTAs) is described, providing an overview of in vitro cell transformation from its origin to the new transcriptomic-based CTAs. Application of this knowledge is utilized to address how
Externí odkaz:
https://doaj.org/article/112a2adec7324ebfb99852d49052816c
Autor:
Yusuke Oku, Federica Madia, Pierre Lau, Martin Paparella, Timothy McGovern, Mirjam Luijten, Miriam N. Jacobs
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 21, p 12718 (2022)
With recent rapid advancement of methodological tools, mechanistic understanding of biological processes leading to carcinogenesis is expanding. New approach methodologies such as transcriptomics can inform on non-genotoxic mechanisms of chemical car
Externí odkaz:
https://doaj.org/article/033f56b2441f4199aaaf0ffecffd7ef8
Autor:
EFSA Panel on Plant Protection Products and their Residues (EFSA PPR Panel), Antonio Hernández‐Jerez, Paulien Adriaanse, Annette Aldrich, Philippe Berny, Tamara Coja, Sabine Duquesne, Andreas Focks, Marina Marinovich, Maurice Millet, Olavi Pelkonen, Silvia Pieper, Aaldrik Tiktak, Christopher Topping, Anneli Widenfalk, Martin Wilks, Gerrit Wolterink, Kevin Crofton, Susanne Hougaard Bennekou, Martin Paparella, Ioanna Tzoulaki
Publikováno v:
EFSA Journal, Vol 19, Iss 6, Pp n/a-n/a (2021)
Abstract The EFSA Panel on Plant Protection Products and their Residues (PPR) has developed, as a self‐task mandate (EFSA‐Q‐2019‐00100), two adverse outcome pathway (AOP)‐informed integrated approach to testing and assessment (IATA) case st
Externí odkaz:
https://doaj.org/article/8397fe0b6b2e4651adffed71c5cbef22
Autor:
Laura M. Langan, Martin Paparella, Natalie Burden, Lisa Constantine, Luigi Margiotta‐Casaluci, Thomas H. Miller, S. Jannicke Moe, Stewart F. Owen, Alexandra Schaffert, Tiina Sikanen
Data Availability statement: No data has been generated in the writing of this article. However, all articles which have been cited or influenced the summarization outlined are provided in supplementary material on a section-by-section basis. Support
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb55e7d7323dc064ec8026449f991fe1
https://bura.brunel.ac.uk/handle/2438/26151
https://bura.brunel.ac.uk/handle/2438/26151
The induction of vasculature formation is proposed to be a significant mechanism behind the non-genotoxic carcinogenicity of a chemical. The vasculature formation model used in this study is based on the coculture of human primary HUVECs and hASCs. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f59e8ff1ed68ff959a0df983e1582c88
https://trepo.tuni.fi/handle/10024/149372
https://trepo.tuni.fi/handle/10024/149372
Autor:
Marco Corvaro, Paule Vasseur, Monica Vaccari, Annamaria Colacci, Federica Madia, Martin Paparella, Akiyoshi Nishikawa, Nathalie Delrue, Kumiko Ogawa, Norman Ertych, Raffaella Corvi, Miriam N. Jacobs, Kiyomi Ohmori, M. Cecilia Aguila, Mirjam Luijten, Daniel Desaulniers, Anoop Kumar Sharma, Abigail Jacobs
Publikováno v:
Jacobs, M N, Colacci, A, Corvi, R, Vaccari, M, Aguila, M C, Corvaro, M, Delrue, N, Desaulniers, D, Ertych, N, Jacobs, A, Luijten, M, Madia, F, Nishikawa, A, Ogawa, K, Ohmori, K, Paparella, M, Sharma, A K & Vasseur, P 2020, ' Chemical carcinogen safety testing: OECD expert group international consensus on the development of an integrated approach for the testing and assessment of chemical non-genotoxic carcinogens ', Archives of Toxicology, vol. 94, no. 8, pp. 2899-2923 . https://doi.org/10.1007/s00204-020-02784-5
Archives of Toxicology
Archives of Toxicology, Springer Verlag, 2020, 94 (8), pp.2899-2923. ⟨10.1007/s00204-020-02784-5⟩
Archives of Toxicology
Archives of Toxicology, Springer Verlag, 2020, 94 (8), pp.2899-2923. ⟨10.1007/s00204-020-02784-5⟩
While regulatory requirements for carcinogenicity testing of chemicals vary according to product sector and regulatory jurisdiction, the standard approach starts with a battery of genotoxicity tests (which include mutagenicity assays). If any of the
Autor:
Christopher Faßbender, Thomas Braunbeck, Adam Lillicrap, Martin Paparella, Paul M. Thomas, Roman Liska, Kristin Schirmer, Stefan Scholz, Gilly Stoddart, Pascal Bicherel, Scott E. Belanger, Kristin A. Connors, Susanne Walter-Rohde, Marlies Halder
Publikováno v:
ALTEX, 38 (1)
Altex
Altex
Information about acute fish toxicity is routinely required in many jurisdictions for environmental risk assessment of chemicals. This information is typically obtained using a 96-hour juvenile fish test for lethality according to OECD test guideline
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86116784fb6028b6e54171f7d6758491