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Contact Info

Mark Raymond Buckley, Ph.D. Department of Biomedical Engineering University of Rochester work Box 270168 Rochester, NY 14627-0168 office: Goergen Hall 317 p 585-276-4195 f Buckley

Recent Publications

    • Dunkman AA
    • Buckley MR
    • Mienaltowski MJ
    • Adams SM
    • Thomas SJ
    • Satchell L
    • Kumar A
    • Pathmanathan L
    • Beason DP
    • Iozzo RV
    • Birk DE
    • Soslowsky LJ
    (2013 Jan). Decorin expression is important for age-related changes in tendon structure and mechanical properties. - Matrix biology : journal of the International Society for Matrix Biology. .
    • Chandler EM
    • Seo BR
    • Califano JP
    • Andresen Eguiluz RC
    • Lee JS
    • Yoon CJ
    • Tims DT
    • Wang JX
    • Cheng L
    • Mohanan S
    • Buckley MR
    • Cohen I
    • Nikitin AY
    • Williams RM
    • Gourdon D
    • Reinhart-King CA
    • Fischbach C
    (2012 Jun 19). Implanted adipose progenitor cells as physicochemical regulators of breast cancer. - Proceedings of the National Academy of Sciences of the United States of America. .
  • (2012 May). Insights into interstitial flow, shear stress, and mass transport effects on ECM heterogeneity in bioreactor-cultivated engineered cartilage hydrogels. - Biomechanics and modeling in mechanobiology. .
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Mark Raymond Buckley

Photo of Mark Buckley
  • Assistant Professor

    • Biomedical Engineering

Buckley Lab

Research Overview

Tendon, ligament, cartilage and many other soft biological tissues serve predominantly mechanical functions. However, unlike steel, concrete and other elastic solids, these structurally complex materials exhibit a history- and time-dependent response to loading (i.e., viscoelasticity) that must be characterized in order to predict in vivo deformations and understand loss of mechanical function in the pathological state. Our lab is interested in evaluating changes in soft tissue viscoelastic properties across multiple length scales during processes including exercise, aging, injury and disease and identifying the specific biological and structural factors responsible for these alterations. To characterize viscoelasticity at the tissue, matrix and cellular levels, we combine simultaneous high-speed microscopy, force measurement and control of deformation on live tissue explants. Using our findings, we seek to devise strategies for assessing the efficacy of treatments or diagnosing damage based on viscoelastic measurements.