Cellular GDNF delivery promotes growth of motor and dorsal column sensory axons after partial and complete spinal cord transections and induces remyelination. (Q38911887)

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English	Cellular GDNF delivery promotes growth of motor and dorsal column sensory axons after partial and complete spinal cord transections and induces remyelination.	scientific article

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20 December 2019

Cellular GDNF delivery promotes growth of motor and dorsal column sensory axons after partial and complete spinal cord transections and induces remyelination (English)

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20 December 2019

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20 December 2019

Mark H. Tuszynski

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Mark H Tuszynski

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20 December 2019

The Journal of Comparative Neurology

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20 December 2019

GDNF prevents degeneration and promotes the phenotype of brain noradrenergic neurons in vivo

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A distinct subgroup of small DRG cells express GDNF receptor components and GDNF is protective for these neurons after nerve injury.

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The glial cell line-derived neurotrophic factor family receptor components are differentially regulated within sensory neurons after nerve injury.

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Influence of the axotomy to cell body distance in rat rubrospinal and spinal motoneurons: differential regulation of GAP-43, tubulins, and neurofilament-M

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Truncated soluble Nogo receptor binds Nogo-66 and blocks inhibition of axon growth by myelin.

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BDNF and NT-3, but not NGF, prevent axotomy-induced death of rat corticospinal neurons in vivo

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The survival-promoting effect of glial cell line-derived neurotrophic factor on axotomized corticospinal neurons in vivo is mediated by an endogenous brain-derived neurotrophic factor mechanism.

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Complete and long-term rescue of lesioned adult motoneurons by lentiviral-mediated expression of glial cell line-derived neurotrophic factor in the facial nucleus.

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Nogo receptor mRNA expression in intact and regenerating CNS neurons

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Brain-derived neurotrophic factor stimulates hindlimb stepping and sprouting of cholinergic fibers after spinal cord injury.

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Transplants of fibroblasts genetically modified to express BDNF promote axonal regeneration from supraspinal neurons following chronic spinal cord injury

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Neurotrophin-4 (NT-4) and glial cell line-derived neurotrophic factor (GDNF) promote the survival of corticospinal motor neurons of neonatal rats in vitro

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BDNF and NT-4/5 prevent atrophy of rat rubrospinal neurons after cervical axotomy, stimulate GAP-43 and Talpha1-tubulin mRNA expression, and promote axonal regeneration.

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Identifiers

10.1002/CNE.10934

1 reference

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20 December 2019

1 reference

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14608602%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

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