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Chemokine-driven transmigration of monocytes into the subendothelial space is a fundamental and rate- limiting process in atherogenesis. Our preliminary data show that this process is dysregulated by metabolic stress and that increased monocyte responsiveness to chemokines appears to accelerate atherosclerotic plaque development. We have now uncovered a novel thiol redox-sensitive mechanism in monocytes that upon dysregulation by metabolic disorders, 'primes' and transforms monocytes into a hyper-chemotactic pro- atherogenic phenotype.

UT Health San Antonio
Asmis, Reto H.R.

This study is a prospective, multi-center, proof of principle, phase I human safety study (n=12) evaluating the sequential treatments of the Avance Nerve Graft, a commercially available decellularized processed peripheral nerve allograft, with autologous Bone Marrow Aspirate Concentrate (BMAC), a source of stem cells, for the repair of peripheral nerve injuries of up to 7 cm in length.

Brooke Army Medical Center
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