Browse the latest research summaries in the field of genetics for spinal cord injury patients and caregivers.
Showing 61-70 of 1,773 results
Cell Cycle, 2012 • September 1, 2012
The mammalian target of rapamycin (mTOR) signaling pathway plays an important role in multiple cellular functions, such as cell metabolism, proliferation and survival. SCI involves multiple pathophysi...
KEY FINDING: Inhibition of mTOR reduces cell death in damaged neural tissue following SCI.
Cell Cycle, 2012 • September 15, 2012
The study demonstrates that multipotent, nestin-expressing stem cells are present throughout the hair follicle and that the upper part of the follicle can produce the stem cells in large amounts that ...
KEY FINDING: Nestin-expressing cells are located in all regions of the hair follicle (upper, middle, and lower parts of the vibrissa follicle).
BMC Developmental Biology, 2012 • August 25, 2012
This study investigates positional information during zebrafish caudal fin regeneration by examining bony ray bifurcations after repeated amputations at different locations. The results show that repe...
KEY FINDING: Repeated amputations performed at a long distance from the bifurcation do not change its proximal-distal position in the regenerated fin, while consecutive amputations near the bifurcation induce a positional reset and progressively shift its position distally.
Anat Rec (Hoboken), 2012 • October 1, 2012
This study investigates the tissue-specific signaling requirements for spinal cord and muscle regeneration in Xenopus tadpoles, focusing on the Wnt and Fgf pathways. The results demonstrate that both ...
KEY FINDING: Both spinal cord and muscle regeneration depend on the Wnt-β-catenin and the Fgf pathways.
Int. J. Mol. Sci., 2012 • July 6, 2012
This review summarizes findings on the neuroprotective potential of PACAP in models of different traumatic nerve injuries, highlighting its role in neuronal regeneration. Endogenous PACAP and its rece...
KEY FINDING: Expression of endogenous PACAP and its specific PAC1 receptor is elevated in different parts of the central and peripheral nervous system after traumatic injuries.
EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2011 • June 6, 2011
The study investigated the neuroprotective effects of erythropoietin (EPO) on spinal cord injury (SCI) in rats, focusing on the role of platelet-derived growth factor (PDGF)-B. Results showed that EPO...
KEY FINDING: EPO treatment resulted in a more rapid recovery in SCI rats, as evidenced by higher BBB scores.
Cell Adhesion & Migration, 2012 • November 1, 2012
Two recent studies show that activating integrin signaling in dorsal root ganglion (DRG) neurons renders them able to overcome inhibitory signals, and could possibly lead to new strategies to improve ...
KEY FINDING: Addition of CSPGs to dorsal root ganglion (DRG) cultures resulted in a reduction of activated integrins and growth inhibition. By adding manganese to the cultures, both FAK phosphorylation and growth response was restored, indicating that integrin activation is sufficient to override the inhibitory effects of CSPGs.
CNS Neuroscience & Therapeutics, 2013 • January 1, 2013
This study investigates the mechanism of endoplasmic reticulum (ER) stress–induced apoptosis and the protective action of basic fibroblast growth factor (bFGF) in spinal cord injury (SCI). bFGF admini...
KEY FINDING: ER stress-induced apoptosis is involved in the early stages of spinal cord injury in rats, indicated by increased levels of GRP78, CHOP, and caspase-12.
Journal of Visualized Experiments, 2012 • August 17, 2012
Adult DRG neurons provide a useful system to study axon regeneration due to their ability to regenerate axons robustly after peripheral nerve injury. The in vitro procedure presented enables rapid and...
KEY FINDING: Re-plated neurons extend axons quickly with reduced branching, mimicking the effects of a conditioning lesion.
Molecular Pain, 2012 • November 7, 2012
This study comprehensively maps the expression of Nav1.7, a key sodium channel, within the pain pathways of rat DRG neurons from peripheral skin terminals to central spinal cord terminals. The finding...
KEY FINDING: Nav1.7 is robustly expressed in small diameter DRG neurons, particularly in both peptidergic and non-peptidergic subpopulations.