Author

V. T.-V. Dao

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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Pharmacology & Toxicology· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Research Focus:protein folding & dynamics· 1 Assay:proteomics· 1

Frequent Co-Authors

H. H. H. W. Schmidt· 2 shared M. H. Elbatreek· 2 shared A. Gödecke· 1 shared A. Güldner· 1 shared A. I. Casas· 1 shared C. Ibarra· 1 shared C. T. Neullens· 1 shared M. Deile· 1 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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2 shared papersPharmacology & Toxicology

H. H. H. W. Schmidt

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2 papers

Recent·Most cited

A non-canonical chemical feedback self-limits nitric oxide-cyclic GMP signaling in health and disease

V. T.-V. Dao, M. H. Elbatreek, M. Deile, P. I. Nedvetsky, A. Güldner, C. Ibarra, A. Gödecke, H. H. H. W. Schmidt

The paper shows NO-cGMP signaling is self-limiting through NO-induced sGC degradation, with implications for disease treatment using apo-sGC activators.

bioRxiv · Feb 6, 2020Pharmacology & Toxicology

Isoform-selective NADPH oxidase inhibitor panel for pharmacological target validation

V. T.-V. Dao, M. H. Elbatreek, S. Altenhöfer, A. I. Casas, M. P. Pachado, C. T. Neullens, U. Knaus, H. H. H. W. Schmidt

The paper demonstrates isoform-selective inhibition of NADPH oxidases (NOX1-NOX5) using advanced inhibitors and validates their efficacy in a human blood-brain barrier model.

bioRxiv · Jul 23, 2019Pharmacology & Toxicology