Author

A. F. Rodrigues

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioengineering· 1 Microbiology· 1 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:mouse· 3 Research Focus:host-pathogen & immune response· 2 Assay:proteomics· 2 Organism:human· 1 Assay:metabolomics· 1

Frequent Co-Authors

M. Bader· 2 shared A. A. Peluso· 1 shared A. D. de Kloet· 1 shared A. Esteban-Arranz· 1 shared A. L. Nazarova· 1 shared A. Maifeld· 1 shared A. Nawrocki· 1 shared A. Rauch· 1 shared

Activity by Year

2018-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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2 shared papersPharmacology & Toxicology

M. Bader

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Angiotensin-(1-5) is a Potent Endogenous Angiotensin AT2-Receptor Agonist

I. M. Souza-Silva, A. A. Peluso, K. Elsaafien, A. L. Nazarova, K. B. Assersen, L. Rodrigues-Ribeiro, M. Mohammed, A. F. Rodrigues, A. Nawrocki, L. A. Johansen, P. Jensen, A. D. de Kloet, E. G. Krause, M. DelBorgo, I. Maslov, , U. M. Steckelings

This study identifies angiotensin-(1-5) as a potent endogenous agonist of the AT2-receptor, showing its ability to increase nitric oxide release and lower blood pressure through AT2R-mediated mechanisms.

bioRxiv · Apr 5, 2024 · PreprintPharmacology & Toxicology

Quantifying the impact of gut microbiota on inflammation and hypertensive organ damage

E. G. Avery, H. Bartolomaeus, A. Rauch, C.-Y. Chen, G. N'diaye, U. Loeber, T. U. Bartolomaeus, R. Fritsche-Guenther, A. F. Rodrigues, D. Tsvetkov, M. Todiras, J.-K. Park, L. Marko, A. Maifeld, M. Bader, , N. Wilck

This study quantifies how gut microbiota affects inflammation and organ damage in hypertension using germ-free and colonized mice, finding the kidney is more susceptible to microbial influence.

bioRxiv · Sep 17, 2021Microbiology

Graphene Oxide as 2D Platform for Complexation and Intracellular Delivery of siRNA

I. de Lazaro, S. Vranic, D. Marson, A. F. Rodrigues, M. Buggio, A. Esteban-Arranz, M. Mazza, P. Posocco, K. Kostarelos

This study evaluates graphene oxide as a 2D platform for siRNA delivery without surface modification, showing efficient internalization but limited gene silencing due to rapid siRNA release.

bioRxiv · Dec 4, 2018Bioengineering