Alec T. Salminen Data-verified
Affiliation confirmed via AI analysis of OpenAlex, ORCID, and web sources.
ORISE Post-Doctoral Fellow
postdoc
Research Areas
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Biography and Research Information
OverviewAI-generated summary
Alec T. Salminen's research focuses on toxicological studies, particularly concerning dermal absorption and the human skin barrier. He has investigated the efficacy of various artificial skin models and excised human skin for in vitro permeation testing, considering factors such as race and pigmentation. His work also extends to the molecular mechanisms of endothelial cell responses and the development of biosensing technologies, including functionalized silicon membranes for viral particle detection. Salminen has published 19 papers with 459 citations and an h-index of 11. He has collaborated with researchers such as Luísa Camacho, Robert P. Felton, Frederick A. Beland, and Nicole Kleinstreuer, all from the National Center for Toxicological Research.
Metrics
- h-index: 11
- Publications: 19
- Citations: 474
Selected Publications
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P19-17 Use of diverse human skin models in in vitro skin permeation testing of dermatological ingredients (2024)
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Race, pigmentation, and the human skin barrier—considerations for dermal absorption studies (2023)
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Parallel evaluation of alternative skin barrier models and excised human skin for dermal absorption studies in vitro (2023)
Collaboration Network
Top Collaborators
- Parallel evaluation of alternative skin barrier models and excised human skin for dermal absorption studies in vitro
- Race, pigmentation, and the human skin barrier—considerations for dermal absorption studies
- P19-17 Use of diverse human skin models in in vitro skin permeation testing of dermatological ingredients
- Parallel evaluation of alternative skin barrier models and excised human skin for dermal absorption studies in vitro
- Race, pigmentation, and the human skin barrier—considerations for dermal absorption studies
- P19-17 Use of diverse human skin models in in vitro skin permeation testing of dermatological ingredients
- Molecular mechanisms underlying the heterogeneous barrier responses of two primary endothelial cell types to sphingosine-1-phosphate
- Rapid and specific detection of intact viral particles using functionalized microslit silicon membranes as a fouling-based sensor
- Molecular mechanisms underlying the heterogeneous barrier responses of two primary endothelial cell types to sphingosine-1-phosphate
- Rapid and specific detection of intact viral particles using functionalized microslit silicon membranes as a fouling-based sensor
- Molecular mechanisms underlying the heterogeneous barrier responses of two primary endothelial cell types to sphingosine-1-phosphate
- Rapid and specific detection of intact viral particles using functionalized microslit silicon membranes as a fouling-based sensor
- Molecular mechanisms underlying the heterogeneous barrier responses of two primary endothelial cell types to sphingosine-1-phosphate
- Rapid and specific detection of intact viral particles using functionalized microslit silicon membranes as a fouling-based sensor
- Parallel evaluation of alternative skin barrier models and excised human skin for dermal absorption studies in vitro
- P19-17 Use of diverse human skin models in in vitro skin permeation testing of dermatological ingredients
- Parallel evaluation of alternative skin barrier models and excised human skin for dermal absorption studies in vitro
- P19-17 Use of diverse human skin models in in vitro skin permeation testing of dermatological ingredients
- Rapid and specific detection of intact viral particles using functionalized microslit silicon membranes as a fouling-based sensor
- Rapid and specific detection of intact viral particles using functionalized microslit silicon membranes as a fouling-based sensor
- Rapid and specific detection of intact viral particles using functionalized microslit silicon membranes as a fouling-based sensor
- Molecular mechanisms underlying the heterogeneous barrier responses of two primary endothelial cell types to sphingosine-1-phosphate
- Molecular mechanisms underlying the heterogeneous barrier responses of two primary endothelial cell types to sphingosine-1-phosphate
- Molecular mechanisms underlying the heterogeneous barrier responses of two primary endothelial cell types to sphingosine-1-phosphate
- Molecular mechanisms underlying the heterogeneous barrier responses of two primary endothelial cell types to sphingosine-1-phosphate
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