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Deborah A. Shear

Researcher at Walter Reed Army Institute of Research

Publications -  98
Citations -  3056

Deborah A. Shear is an academic researcher from Walter Reed Army Institute of Research. The author has contributed to research in topics: Traumatic brain injury & Morris water navigation task. The author has an hindex of 28, co-authored 90 publications receiving 2643 citations. Previous affiliations of Deborah A. Shear include Central Michigan University & Emory University.

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Biocompatibility of methylcellulose-based constructs designed for intracerebral gelation following experimental traumatic brain injury.

TL;DR: The use of methylcellulose as a scaffolding material, whose concentration and solvent were varied to manipulate its physical properties, indicates that MC is well suited as a biocompatible injectable scaffold for the repair of defects in the brain.
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Laminin and fibronectin scaffolds enhance neural stem cell transplantation into the injured brain.

TL;DR: Behaviour analyses indicated that mice receiving neural stem cells within the laminin‐based scaffold performed significantly better than untreated mice on a spatial learning task, supporting the notion that functional recovery correlates positively with donor cell survival.
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Progesterone protects against necrotic damage and behavioral abnormalities caused by traumatic brain injury.

TL;DR: Results show that 5 days of postinjury progesterone treatment are needed to reduce significantly the neuropathological and behavioral abnormalities found in a rodent model of TBI.
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Neural progenitor cell transplants promote long-term functional recovery after traumatic brain injury.

TL;DR: Assessment of the long-term survival, migration, differentiation and functional significance of NPCs transplanted into a mouse model of TBI out to 1 year post-transplant concluded that transplanted NPCs survive in the host brain up to 14 months, migrate to the site of injury, enhance motor and cognitive recovery, and may play a role in trophic support following TBI.
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Fibronectin promotes survival and migration of primary neural stem cells transplanted into the traumatically injured mouse brain.

TL;DR: It is suggested that FGF2-responsive NSCs present a promising approach for cellular therapy following trauma and that the transplant location and environment may play an important role in graft survival and integration.