Brian Storrie

Federal Grant PI High Impact

Professor

Last publication 2026 Last refreshed 2026-05-22

faculty

Physiology & Cell Biology, College of Medicine

StorrieBrian@uams.edu

44 h-index 183 pubs 6,593 cited

Biography and Research Information

OverviewAI-generated summary

Brian Storrie is a Professor in the Department of Physiology & Cell Biology at the University of Arkansas for Medical Sciences. His research program focuses on the cellular mechanisms underlying platelet function, particularly in the context of hemostasis and thrombosis. He investigates how platelets are activated, aggregate, and release their granular contents to form thrombi at sites of vascular injury.

Dr. Storrie has received federal funding from the NIH/National Heart Lung and Blood Institute for his work on the structure and function determinants of puncture wound thrombus formation, totaling $624,823. His laboratory utilizes advanced techniques, including 3D electron microscopy and deep learning for ultrastructural analysis, to quantify cellular and organelle packing in platelets. Recent studies have explored the impact of specific proteins, such as serglycin, on platelet cargo packaging and release, and have examined platelet behavior in the context of COVID-19 infection. His work also extends to developing mouse models to study genetic disorders affecting protein glycosylation and bone resorption.

With an h-index of 44 and over 183 publications, Dr. Storrie has a well-established record of research productivity. He actively collaborates with colleagues at the University of Arkansas for Medical Sciences, including Irina D. Pokrovskaya, Kelly K. Ball, Sung W. Rhee, and Michael W. Webb.

Metrics

  • h-index: 44
  • Publications: 183
  • Citations: 6,593

Selected Publications

  • Murine Thrombus Organization Limits Access to High Platelet Activation States While Supporting Platelet Recruitment (2026)
  • BPS2026 – Machine learning analysis of cellular remodeling during occlusive blood clot formation (2026)
  • The Syk inhibitor BI 1002494 impairs thrombus infill in a murine femoral artery occlusion without affecting hemostasis (2025)
  • Uncovering the role of the Hsp40 family member cysteine string protein-α in mouse platelets (2025)
  • Contrasting Effects of Platelet GPVI Deletion Versus Syk Inhibition on Mouse Jugular Vein Puncture Wound Structure (2025)
  • BPS2025 - Machine vision pipeline to elucidate structural underpinnings of blood clot formation (2025)
  • Contrasting Effects of Platelet GPVI Deletion versus Syk Inhibition on Mouse Jugular Vein Puncture Wound Structure (2025)
  • Differential Effects of GPVI Deletion and SYK Inhibition on Thrombus Organization and Platelet Adhesion in a Murine Jugular Puncture Wound Model (2024)
  • Densely Populated Cell and Organelles Segmentation with U-Net Ensembles (2024)
    1 citation DOI OpenAlex
  • Single-Platelet Mapping of Jugular, Puncture-Wound Thrombi Reveals the Spatial Evolution of Platelet Activation (2024)
    1 citation DOI OpenAlex
  • Puncture Wound Hemostasis and Preparation of Samples for Montaged Wide-Area Electron Microscopy Analysis (2024)
    1 citation DOI OpenAlex
  • JoVE Video Dataset (2024)
  • Trained image analysis techniques for characterizing cell phenotype in electron microscopy images of mouse thrombi (2024)
    1 citation DOI OpenAlex
  • Screening for Key Structural Differences in Thrombosis Versus Hemostasis through Single Platelet Analysis (2023)
  • OC 61.4 Manipulating Platelet Secretion to Affect Hemostasis (2023)
    2 citations DOI OpenAlex

View all publications on OpenAlex →

Federal Grants 1 $624,823 total

NIH/National Heart Lung and Blood Institute Contact PI Sep 2021 - Aug 2025

Resubmission: Structure/Function Determinants of Puncture Wound Thrombus Formation

National Heart Lung and Blood Institute $624,823 R01

Research Interests

Research search concentrates on how platelet secretion and aggregation properties structure thrombus formation asd provide structure based therapeutic targets. Much of the research uses volume electronn microscopy as a 3D structural approach to puncture wound thrombi and occlusive clots. Mechanism is approached through the use of mouse genetic knockouts and inhibitory drugs of clinical significance.

Grants & Funding

  • 120 kV FEI Electron Microscope and Supporting Sample Preparation Equipment for Biological Microscopy National Science Foundation Principal Investigator
  • Platelet Exocytosis and Endocytosis in Thrombosis and Immunity NIH/Nat. Heart, Lung & Blood Institute - Pass Through: University of Kentucky Research Foundation Principal Investigator
  • STRUCTURAL ORGANIZATION OF THE MAMMALIAN GOLGI COMPLEX NIH Principal Investigator
  • Structural, Functional,and Molecular Characterization of Platelet alpha-Granule Subpopulations American Heart Association (Midwest Affiliate) Principal Investigator
  • Platelet Exocytosis and Endocytosis in Thrombosis and Immunity NIH/Nat. Heart, Lung & Blood Institute - Pass Through: University of Kentucky Research Foundation Principal Investigator
  • No FP attached UAMS College of Medicine Principal Investigator
  • Storrie EM NSF COM Commitment Acct UAMS College of Medicine Principal Investigator
  • Mechanisms of Golgi Apparatus Protein Recycling NIH Principal Investigator

Collaboration Network

68 Collaborators 14 Institutions 3 Countries

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