In: Neuroscience, 2012, vol. 27, p. 271–282
In adult macaque monkeys subjected to an incomplete spinal cord injury (SCI), corticospinal (CS) fibers are rarely observed to grow in the lesion territory. This situation is little affected by the application of an anti-Nogo-A antibody which otherwise fosters the growth of CS fibers rostrally and caudally to the lesion. However, when using the Sternberger monoclonal-incorporated antibody 32...
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In: Cortex, 2012, p. -
In the context of an autologous cell transplantation study, a unilateral biopsy of cortical tissue was surgically performed from the right dorsolateral prefrontal cortex (dlPFC) in two intact adult macaque monkeys (dlPFC lesioned group), together with the implantation of a chronic chamber providing access to the left motor cortex. Three other monkeys were subjected to the same chronic chamber...
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Thèse de doctorat : Université de Fribourg, 2008 ; Nr. 1592.
After injury to the adult central nervous system (CNS), permanent deficits remain to a large part due to limited cell renewal, axonal regeneration and reestablishment of functional connectivity. Evidence indicate that the lack of axonal regeneration is partly due to the myelin-associated inhibitory factor Nogo-A. A therapeutical strategy to overcome this inhibition is to prevent the neurite...
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In: BMC Neuroscience, 2009, vol. 10, p. 155
Background Polymicrogyria is a malformation of the cerebral cortex often resulting in epilepsy or mental retardation. It remains unclear whether this pathology affects the structure and function of the corticospinal (CS) system. The anatomy and histology of the brain of one macaque monkey exhibiting a spontaneous polymicrogyria (PMG monkey) were examined and compared to the brain of normal...
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In: European Journal of Neuroscience, 2009, vol. 29, no. 5, p. 983 - 996
In rodents and nonhuman primates subjected to spinal cord lesion, neutralizing the neurite growth inhibitor Nogo-A has been shown to promote regenerative axonal sprouting and functional recovery. The goal of the present report was to re-examine the data on the recovery of the primate manual dexterity using refined behavioral analyses and further statistical assessments, representing secondary...
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In: BMC Neuroscience, 2008, vol. 9, no. 1, p. 5
Background: After unilateral cervical cord lesion at the C7/C8 border interrupting the dorsolateral funiculus in adult monkeys, neutralization of Nogo-A using a specific monoclonal antibody promoted sprouting of corticospinal (CS) axons rostral and caudal to the lesion and, in parallel, improved functional recovery. In monkeys lesioned but not treated with the anti-Nogo-A antibody, the CS neurons...
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In: Nature Medicine, 2007, vol. 13, no. 5, p. 561 - 566
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In: The Journal of Comparative Neurology, 2007, vol. 502, no. 4, p. 644 - 659
After injury, regrowth of axons in mammalian adult central nervous system is highly limited. However, in monkeys subjected to unilateral cervical lesion (C7-C8 level), neutralization of an important neurite outgrowth inhibitor, Nogo-A, stimulated axonal sprouting caudal to the lesion, accompanied by enhanced functional recovery of manual dexterity, compared with lesioned monkeys treated with a...
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In: Molecular and Cellular Neuroscience, 2006, vol. 32, no. 1-2, p. 161-173
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In: Nature Medicine
In rodents, after spinal lesion, neutralizing the neurite growth inhibitor Nogo-A promotes axonal sprouting and functional recovery. To evaluate this treatment in primates, 12 monkeys were subjected to cervical lesion. Recovery of manual dexterity and sprouting of corticospinal axons were enhanced in monkeys treated with Nogo-A– specific antibody as compared to monkeys treated with control...
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