Extensive spontaneous plasticity of corticospinal projections after primate spinal cord injury
about
A Review on Locomotor Training after Spinal Cord Injury: Reorganization of Spinal Neuronal Circuits and Recovery of Motor FunctionMotor cortex electrical stimulation augments sprouting of the corticospinal tract and promotes recovery of motor functionCorticospinal reorganization after spinal cord injuryRestoration of sensorimotor functions after spinal cord injuryRole of Direct vs. Indirect Pathways from the Motor Cortex to Spinal Motoneurons in the Control of Hand DexterityTranslational spinal cord injury research: preclinical guidelines and challengesA Unilateral Cervical Spinal Cord Contusion Injury Model in Non-Human Primates (Macaca mulatta).Derivation of multivariate syndromic outcome metrics for consistent testing across multiple models of cervical spinal cord injury in ratsRat models of spinal cord injury: from pathology to potential therapiesSyndromics: a bioinformatics approach for neurotrauma researchComparison of functional recovery of manual dexterity after unilateral spinal cord lesion or motor cortex lesion in adult macaque monkeys.Multimodal exercises simultaneously stimulating cortical and brainstem pathways after unilateral corticospinal lesion.Combined SCI and TBI: recovery of forelimb function after unilateral cervical spinal cord injury (SCI) is retarded by contralateral traumatic brain injury (TBI), and ipsilateral TBI balances the effects of SCI on paw placementTopological data analysis for discovery in preclinical spinal cord injury and traumatic brain injury.Effects of bone marrow stromal cell transplantation through CSF on the subacute and chronic spinal cord injury in rats.Cortical innervation of the hypoglossal nucleus in the non-human primate (Macaca mulatta)The Irvine, Beatties, and Bresnahan (IBB) Forelimb Recovery Scale: An Assessment of Reliability and Validity.A reassessment of whether cortical motor neurons die following spinal cord injury.Thoracic rat spinal cord contusion injury induces remote spinal gliogenesis but not neurogenesis or gliogenesis in the brainSingle collateral reconstructions reveal distinct phases of corticospinal remodeling after spinal cord injury.Corticospinal sprouting differs according to spinal injury location and cortical origin in macaque monkeys.Harnessing neuroplasticity for clinical applications.mRNA-Seq and microRNA-Seq whole-transcriptome analyses of rhesus monkey embryonic stem cell neural differentiation revealed the potential regulators of rosette neural stem cells.Unconstrained three-dimensional reaching in rhesus monkeysAberrant crossed corticospinal facilitation in muscles distant from a spinal cord injury.Inosine enhances axon sprouting and motor recovery after spinal cord injury.Complement protein C1q modulates neurite outgrowth in vitro and spinal cord axon regeneration in vivo.Motor cortex maturation is associated with reductions in recurrent connectivity among functional subpopulations and increases in intrinsic excitabilityUnilateral pyramidotomy of the corticospinal tract in rats for assessment of neuroplasticity-inducing therapies.Leveraging biomedical informatics for assessing plasticity and repair in primate spinal cord injury.Recovery from chronic spinal cord contusion after Nogo receptor intervention.Characterization of long descending premotor propriospinal neurons in the spinal cordReorganization of corticospinal tract fibers after spinal cord injury in adult macaques.Biomaterial bridges enable regeneration and re-entry of corticospinal tract axons into the caudal spinal cord after SCI: Association with recovery of forelimb functionAnimal models of neurologic disorders: a nonhuman primate model of spinal cord injury.Changes in descending motor pathway connectivity after corticospinal tract lesion in macaque monkey.Concepts and methods for the study of axonal regeneration in the CNSMotor axonal regeneration after partial and complete spinal cord transectionUsing motor behavior during an early critical period to restore skilled limb movement after damage to the corticospinal system during development.Cellular reactions and compensatory tissue re-organization during spontaneous recovery after spinal cord injury in neonatal mice.
P2860
Q26746911-583715BE-D2F8-475C-87CE-669B85B7AD04Q26823836-F28D125C-E645-4B59-9810-E522C5D76A7DQ26828054-32172123-1C06-41B8-AD10-6361403A1C1FQ26999051-AFD04009-4D9E-42BA-BFDF-738D45461472Q27013788-FCC358C4-4DD2-42E1-B322-806A031A7AD1Q27025285-09883C44-E127-4DF1-96D3-D0B5188EA89EQ27307173-2BD720F2-ED0C-4DBF-8E95-59E4F15C7A63Q27333128-E075BE84-94C0-4507-A855-C7C4EB7582CFQ28071816-E3FAD6BF-E361-45EC-B093-E35772E7290CQ28741573-BDFB9797-062B-4152-AE76-DFBE5A47A23AQ30541640-836A4B15-5439-46D8-BF5C-B6CC7F6DAAC6Q30560776-74BBFB4F-CEF6-4679-A39A-9897B5BFEA31Q30670369-9E631E33-B88F-45DA-BAF2-83E522B1BF3DQ31004909-F23AA122-5A09-45C8-851B-D2221CF8A0E1Q31139130-FFD52816-6A80-4AED-B698-CA828C24DBCEQ33268549-E11A46C2-8A59-4151-99AF-C769C2447C82Q33851031-76BC2605-C0C8-426A-8685-F2B1235180CFQ33913692-C209BD7F-C639-488B-B2BB-A4DBB27A567EQ33933379-4897A20C-4854-4227-AEBC-9C7042E12FE1Q34146099-F433A4B0-4B61-477A-A519-3C0A0C6D15F3Q34162701-0ECE77BD-0613-4846-B184-8E871AEB8898Q34177415-21EBE1D6-D724-40F8-AF29-623EA2825FAFQ34331161-05C94D29-3801-4283-A700-EFCA7FA6E67CQ34561249-922CCE7D-7F25-4802-9A5F-5190C11A50B4Q35022935-DA655122-FF1A-4827-A9A4-C5F3D8E2CCF6Q35061418-BB3774F1-781A-4975-AE1C-7D62BCD0C4ECQ35164094-247114EC-EC2D-49CB-B034-DA2B5F515C54Q35187485-EE1823A3-8DFE-4E4C-A636-9168288E80C4Q35414846-D68C1B2C-05BD-4D72-8A1A-0915308D8F90Q35567343-02538730-7998-4112-A628-2BB4792B6C88Q35616151-42CD9996-7459-45E9-B8C6-BEB713F66334Q35744572-ABA48601-28B9-4713-9D24-B77CB1533EBBQ35804198-CAB9BB86-569F-4BAC-B8EF-F54DE14C02B4Q35911446-0068CC51-5951-4957-93FE-9D532F55867EQ35913779-89D57DD1-0155-45F7-8C9E-245B7ECA5891Q36054186-1EA109C7-E68D-4311-9BF4-4E110D3E5B49Q36070952-2EA4D086-1764-442B-B177-2FC8D355C799Q36124800-36CB3B6D-9B6E-4576-9DD0-C58967AA906DQ36174503-0BB95990-8AEA-4869-B034-1B8838F6E716Q36235917-7A77CEA5-6D78-454F-84D8-8418292EA723
P2860
Extensive spontaneous plasticity of corticospinal projections after primate spinal cord injury
description
2010 nî lūn-bûn
@nan
2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Extensive spontaneous plastici ...... ter primate spinal cord injury
@ast
Extensive spontaneous plastici ...... ter primate spinal cord injury
@en
type
label
Extensive spontaneous plastici ...... ter primate spinal cord injury
@ast
Extensive spontaneous plastici ...... ter primate spinal cord injury
@en
prefLabel
Extensive spontaneous plastici ...... ter primate spinal cord injury
@ast
Extensive spontaneous plastici ...... ter primate spinal cord injury
@en
P2093
P2860
P50
P356
P1433
P1476
Extensive spontaneous plastici ...... ter primate spinal cord injury
@en
P2093
Darren M Miller
Devin L Jindrich
Ephron S Rosenzweig
John H Brock
Leif A Havton
Mark H Tuszynski
Michael S Beattie
Roland R Roy
Sarah C Strand
V Reggie Edgerton
P2860
P2888
P304
P356
10.1038/NN.2691
P407
P577
2010-11-14T00:00:00Z