<p>NeuN positive nuclei in spinal cord at 2-, 24-hours and 4 weeks after injury. At 2 hours (2 h), a small number of neurons were visible at the centre of the injury site located mainly in the dorsal horns. By 24 hours (24 h) there had been further loss of neurons up to 2 mm either side of the centre of the injury site. NeuN profiles at 4 weeks (4w) were similar to that at 24 hours indicating that the loss of grey matter neurons occurs within the first 24 hours (see also <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0012021#pone-0012021-g006" target="_blank">Fig. 6</a>).</p
<p><b>A–B</b>. Coronal section in intact spinal cord (A) showed that E2F1 is relatively weak and det...
Cellular mechanisms of secondary damage progression following spinal cord injury remain unclear. We ...
<p>(<b>A</b>) Schematic illustration showing the routes of the cells migrating from the ependymal la...
<p><b>A</b>) Number of NeuN immunoreactive nuclei per section (mean ± SEM) in 10 mm segments centred...
<p>In control animals immunoreactivity is mostly confined to white matter of spinal cord. At 2 hours...
Studies of spinal cord injury using contusion (impact) injury paradigms have shown that neuronal dea...
<p>ΔfosB staining was used to measure the extent of persistent neuronal activation in the spinal cor...
OBJECTIVES Traumatic and non-traumatic spinal cord injury produce neurodegeneration across the en...
It has been shown previously that after spinal cord injury, the loss of grey matter is relatively fa...
The objective of this study was to investigate the influence of the length of the remaining axons on...
To identify cellular and molecular gradients following spinal cord injury (SCI), a rat contusion mod...
OBJECTIVE: To investigate whether gray matter pathology above the level of injury, alongside white m...
<p>Coronal spinal cord sections were analyzed in the parenchyma and around the central canal. (A) Qu...
International audienceFollowing incomplete spinal cord injuries, neonatal mammals display a remarkab...
Cellular mechanisms of secondary damage progression following spinal cord injury remain unclear. We ...
<p><b>A–B</b>. Coronal section in intact spinal cord (A) showed that E2F1 is relatively weak and det...
Cellular mechanisms of secondary damage progression following spinal cord injury remain unclear. We ...
<p>(<b>A</b>) Schematic illustration showing the routes of the cells migrating from the ependymal la...
<p><b>A</b>) Number of NeuN immunoreactive nuclei per section (mean ± SEM) in 10 mm segments centred...
<p>In control animals immunoreactivity is mostly confined to white matter of spinal cord. At 2 hours...
Studies of spinal cord injury using contusion (impact) injury paradigms have shown that neuronal dea...
<p>ΔfosB staining was used to measure the extent of persistent neuronal activation in the spinal cor...
OBJECTIVES Traumatic and non-traumatic spinal cord injury produce neurodegeneration across the en...
It has been shown previously that after spinal cord injury, the loss of grey matter is relatively fa...
The objective of this study was to investigate the influence of the length of the remaining axons on...
To identify cellular and molecular gradients following spinal cord injury (SCI), a rat contusion mod...
OBJECTIVE: To investigate whether gray matter pathology above the level of injury, alongside white m...
<p>Coronal spinal cord sections were analyzed in the parenchyma and around the central canal. (A) Qu...
International audienceFollowing incomplete spinal cord injuries, neonatal mammals display a remarkab...
Cellular mechanisms of secondary damage progression following spinal cord injury remain unclear. We ...
<p><b>A–B</b>. Coronal section in intact spinal cord (A) showed that E2F1 is relatively weak and det...
Cellular mechanisms of secondary damage progression following spinal cord injury remain unclear. We ...
<p>(<b>A</b>) Schematic illustration showing the routes of the cells migrating from the ependymal la...