The extent of axonal loss in the long tracts in hereditary spastic paraplegia.
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Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegiaSpastic paraplegia mutation N256S in the neuronal microtubule motor KIF5A disrupts axonal transport in a Drosophila HSP modelDelving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosologyProtrudin serves as an adaptor molecule that connects KIF5 and its cargoes in vesicular transport during process formationExome sequencing links corticospinal motor neuron disease to common neurodegenerative disordersMice deficient in the Rab5 guanine nucleotide exchange factor ALS2/alsin exhibit age-dependent neurological deficits and altered endosome traffickingClinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot StudyHereditary spastic paraplegia-associated mutations in the NIPA1 gene and its Caenorhabditis elegans homolog trigger neural degeneration in vitro and in vivo through a gain-of-function mechanismSpastin, atlastin, and ER relocalization are involved in axon but not dendrite regeneration.Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms.Low dose tubulin-binding drugs rescue peroxisome trafficking deficit in patient-derived stem cells in Hereditary Spastic Paraplegia.Congenital bovine spinal dysmyelination is caused by a missense mutation in the SPAST gene.Axon-glial interaction in the CNS: what we have learned from mouse models of Pelizaeus-Merzbacher disease.The effect of HSP-causing mutations in SPG3A and NIPA1 on the assembly, trafficking, and interaction between atlastin-1 and NIPA1Inactivation of the hereditary spastic paraplegia-associated Hspd1 gene encoding the Hsp60 chaperone results in early embryonic lethality in mice.Semicentennial tribute to the ingenious neurobiologist Christfried Jakob (1866-1956). 1. Works from Germany and the first Argentina period, 1891-1913.Mitochondrial fission augments capsaicin-induced axonal degenerationNeuropathy target esterase is required for adult vertebrate axon maintenanceER network formation and membrane fusion by atlastin1/SPG3A disease variants.1-Methyl-4-phenylpyridinium affects fast axonal transport by activation of caspase and protein kinase CHereditary spastic paraplegia-causing mutations in atlastin-1 interfere with BMPRII trafficking.A patient-derived stem cell model of hereditary spastic paraplegia with SPAST mutationsMuscle paresis and passive stiffness: key determinants in limiting function in Hereditary and Sporadic Spastic Paraparesis.Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic ParaplegiaQuantitative and functional analyses of spastin in the nervous system: implications for hereditary spastic paraplegiaElectrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP).Cellular pathways of hereditary spastic paraplegia.Axonal degeneration in Alzheimer's disease: when signaling abnormalities meet the axonal transport system.Modeling Axonal Defects in Hereditary Spastic Paraplegia with Human Pluripotent Stem Cells.Contribution of the Degeneration of the Neuro-Axonal Unit to the Pathogenesis of Multiple Sclerosis.The Hsp60-(p.V98I) mutation associated with hereditary spastic paraplegia SPG13 compromises chaperonin function both in vitro and in vivo.Hereditary spastic paraplegia-linked REEP1 modulates endoplasmic reticulum/mitochondria contacts.The Drosophila KIF1A Homolog unc-104 Is Important for Site-Specific Synapse Maturation.The hereditary spastic paraplegia protein strumpellin: characterisation in neurons and of the effect of disease mutations on WASH complex assembly and function.Unique function of Kinesin Kif5A in localization of mitochondria in axonsREEPing the benefits of an animal model of hereditary spastic paraplegiaEnhanced reticulospinal output in patients with (REEP1) hereditary spastic paraplegia type 31.Pathogenesis of autosomal dominant hereditary spastic paraplegia (SPG6) revealed by a rat model.Brain white matter involvement in hereditary spastic paraplegias: analysis with multiple diffusion tensor indices.Quantitative MRI of the spinal cord and brain in adrenomyeloneuropathy: in vivo assessment of structural changes.
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P2860
The extent of axonal loss in the long tracts in hereditary spastic paraplegia.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh-hant
name
The extent of axonal loss in the long tracts in hereditary spastic paraplegia.
@en
The extent of axonal loss in the long tracts in hereditary spastic paraplegia.
@nl
type
label
The extent of axonal loss in the long tracts in hereditary spastic paraplegia.
@en
The extent of axonal loss in the long tracts in hereditary spastic paraplegia.
@nl
prefLabel
The extent of axonal loss in the long tracts in hereditary spastic paraplegia.
@en
The extent of axonal loss in the long tracts in hereditary spastic paraplegia.
@nl
P2860
P1476
The extent of axonal loss in the long tracts in hereditary spastic paraplegia.
@en
P2093
P2860
P304
P356
10.1111/J.1365-2990.2004.00587.X
P577
2004-12-01T00:00:00Z