Portal:AOP/Mission
From WikiPathways
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Villeneuve ''et al.'' (2014). Adverse Outcome Pathway (AOP) Development I: Strategies and Principles. ''Toxicological Sciences'' [https://www.ncbi.nlm.nih.gov/pubmed/25466378 PubMed] | Villeneuve ''et al.'' (2014). Adverse Outcome Pathway (AOP) Development I: Strategies and Principles. ''Toxicological Sciences'' [https://www.ncbi.nlm.nih.gov/pubmed/25466378 PubMed] | ||
- | The list of Featured Pathways is not static and can be updated at any time. If you know of a pathway that should be added, please [mailto:marvin.martens@maastrichtuniversity contact Marvin Martens]. | + | The list of Featured Pathways is not static and can be updated at any time. If you know of a pathway that should be added, please [mailto:marvin.martens@maastrichtuniversity.nl contact Marvin Martens]. |
Revision as of 17:15, 6 January 2021
The purpose of this portal is to create a collection of AOPs on the molecular level and facilitating the use of high-throughput transcriptomic data in the AOP framework. The subjects of the first AOPs are linked to the use cases of the EU-ToxRisk program, based on [aopwiki.org AOP-Wiki] entries, and the CIAO project on COVID-19 AOPs.
List of molecular AOPs present in this portal (some are more defined than others):
- Mitochondrial Complex I inhibition leads to liver injury
- Mitochondrial Complex I inhibition leads to parkinsonian motor deficits
- Mitochondrial Complex I inhibition leads to Fanconi syndrome
- Protein alkylation leads to liver fibrosis
- Interaction with lung resident cell membrane components leads to lung fibrosis
- Multiple MIEs lead to liver steatosis
- ACE2 inhibition leads to increased mortality
Basic strategies and principles for general AOPs are described in this paper:
Villeneuve et al. (2014). Adverse Outcome Pathway (AOP) Development I: Strategies and Principles. Toxicological Sciences PubMed
The list of Featured Pathways is not static and can be updated at any time. If you know of a pathway that should be added, please contact Marvin Martens.