Adam C. Paré Data-verified
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Biography and Research Information
OverviewAI-generated summary
Adam C. Paré's research investigates the molecular and cellular mechanisms underlying embryonic development and tissue organization. He has received significant federal funding from the NIH/National Institute of General Medical Sciences for two grants totaling $748,318. The first grant, for which he is PI, focuses on "Control of epithelial morphology and bioenergetics by Toll receptors during dynamic tissue remodeling." The second grant, also with Paré as PI, aims at "Defining the molecular and cellular bases of tissue compartmentalization."
His laboratory utilizes the model organism *Drosophila melanogaster* to study fundamental biological processes. Recent publications explore advanced imaging techniques, such as expansion microscopy for super-resolution imaging of *Drosophila* embryos, and the characterization of protein roles in cell intercalation and compartment boundary formation. Other work investigates mitochondrial dynamics during convergent extension and methods for characterizing cell morphology and protein localization. Paré also collaborates with researchers at the University of Arkansas at Fayetteville, including Maria Espana-Pena, Jeffrey A. Lewis, Stephanie E. Hood, and Ian Millerschultz, with whom he has co-authored multiple publications.
Paré's scholarship metrics include an h-index of 10, 24 total publications, and 1,108 total citations. His work is characterized by a focus on gene expression regulation, cell polarity, and body patterning, drawing upon expertise in transcription factors and homeodomain proteins. The research also touches upon mitochondrial function and bioenergetics within a developmental context.
Metrics
- h-index: 10
- Publications: 24
- Citations: 1,115
Selected Publications
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Characterizing the role of mitochondrial dynamics during <i>Drosophila</i> convergent extension using NADH fluorescence lifetime imaging (2025)
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Surprising regulatory plasticity for the conserved HOG pathway in diverse Saccharomyces cerevisiae strains (2025)
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Surprising regulatory plasticity for the conserved HOG pathway in diverse <i>Saccharomyces cerevisiae</i> strains (2025)
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Surprising regulatory plasticity for the conserved HOG pathway in diverse Saccharomyces cerevisiae strains (2025)
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Striped Expression of Leucine-Rich Repeat Proteins Coordinates Cell Intercalation and Compartment Boundary Formation in the Early Drosophila Embryo (2023)
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JoVE Video Dataset (2023)
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Methods for Characterizing Cell Morphology and Protein Localization During Development and Regeneration (2023)
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JoVE Video Dataset (2023)
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Using Expansion Microscopy to Physically Enlarge Whole-Mount <em>Drosophila</em> Embryos for Super-Resolution Imaging (2023)
Federal Grants 2 $748,318 total
Defining the molecular and cellular bases of tissue compartmentalization
Collaboration Network
Top Collaborators
- Surprising regulatory plasticity for the conserved HOG pathway in diverse Saccharomyces cerevisiae strains
- Surprising regulatory plasticity for the conserved HOG pathway in diverse <i>Saccharomyces cerevisiae</i> strains
- Surprising regulatory plasticity for the conserved HOG pathway in diverse Saccharomyces cerevisiae strains
- Characterizing the role of mitochondrial dynamics during <i>Drosophila</i> convergent extension using NADH fluorescence lifetime imaging
- Surprising regulatory plasticity for the conserved HOG pathway in diverse Saccharomyces cerevisiae strains
- Surprising regulatory plasticity for the conserved HOG pathway in diverse <i>Saccharomyces cerevisiae</i> strains
- Surprising regulatory plasticity for the conserved HOG pathway in diverse Saccharomyces cerevisiae strains
- Surprising regulatory plasticity for the conserved HOG pathway in diverse Saccharomyces cerevisiae strains
- Surprising regulatory plasticity for the conserved HOG pathway in diverse <i>Saccharomyces cerevisiae</i> strains
- Surprising regulatory plasticity for the conserved HOG pathway in diverse Saccharomyces cerevisiae strains
- Surprising regulatory plasticity for the conserved HOG pathway in diverse Saccharomyces cerevisiae strains
- Surprising regulatory plasticity for the conserved HOG pathway in diverse <i>Saccharomyces cerevisiae</i> strains
- Surprising regulatory plasticity for the conserved HOG pathway in diverse Saccharomyces cerevisiae strains
- Surprising regulatory plasticity for the conserved HOG pathway in diverse Saccharomyces cerevisiae strains
- Surprising regulatory plasticity for the conserved HOG pathway in diverse <i>Saccharomyces cerevisiae</i> strains
- Surprising regulatory plasticity for the conserved HOG pathway in diverse Saccharomyces cerevisiae strains
- Using Expansion Microscopy to Physically Enlarge Whole-Mount <em>Drosophila</em> Embryos for Super-Resolution Imaging
- JoVE Video Dataset
- Using Expansion Microscopy to Physically Enlarge Whole-Mount <em>Drosophila</em> Embryos for Super-Resolution Imaging
- JoVE Video Dataset
- Using Expansion Microscopy to Physically Enlarge Whole-Mount <em>Drosophila</em> Embryos for Super-Resolution Imaging
- JoVE Video Dataset
- Surprising regulatory plasticity for the conserved HOG pathway in diverse Saccharomyces cerevisiae strains
- Surprising regulatory plasticity for the conserved HOG pathway in diverse Saccharomyces cerevisiae strains
- Surprising regulatory plasticity for the conserved HOG pathway in diverse Saccharomyces cerevisiae strains
- Surprising regulatory plasticity for the conserved HOG pathway in diverse Saccharomyces cerevisiae strains
- Striped Expression of Leucine-Rich Repeat Proteins Coordinates Cell Intercalation and Compartment Boundary Formation in the Early Drosophila Embryo
- Surprising regulatory plasticity for the conserved HOG pathway in diverse <i>Saccharomyces cerevisiae</i> strains
- Surprising regulatory plasticity for the conserved HOG pathway in diverse <i>Saccharomyces cerevisiae</i> strains
- Characterizing the role of mitochondrial dynamics during <i>Drosophila</i> convergent extension using NADH fluorescence lifetime imaging
- Characterizing the role of mitochondrial dynamics during <i>Drosophila</i> convergent extension using NADH fluorescence lifetime imaging
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