Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta
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Charcot-Marie-Tooth-linked mutant GARS is toxic to peripheral neurons independent of wild-type GARS levelsEndogenous Nmnat2 is an essential survival factor for maintenance of healthy axonsPathways and genes differentially expressed in the motor cortex of patients with sporadic amyotrophic lateral sclerosisThe novel protein KBP regulates mitochondria localization by interaction with a kinesin-like proteinExome sequencing identifies a DYNC1H1 mutation in a large pedigree with dominant axonal Charcot-Marie-Tooth diseasePhosphoproteomic Analysis of the Mouse Brain Cytosol Reveals a Predominance of Protein Phosphorylation in Regions of Intrinsic Sequence DisorderCellular localization, oligomerization, and membrane association of the hereditary spastic paraplegia 3A (SPG3A) protein atlastinBPAG1n4 is essential for retrograde axonal transport in sensory neuronsMutations in the neurofilament light gene linked to Charcot-Marie-Tooth disease cause defects in transportA novel hook-related protein family and the characterization of hook-related protein 1Protein interaction analysis of senataxin and the ALS4 L389S mutant yields insights into senataxin post-translational modification and uncovers mutant-specific binding with a brain cytoplasmic RNA-encoded peptideThe early onset dystonia protein torsinA interacts with kinesin light chain 1Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.Dominant intermediate Charcot-Marie-Tooth type C maps to chromosome 1p34-p35Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementiaDominant intermediate Charcot-Marie-Tooth neuropathy maps to chromosome 19p12-p13.2.Polarized axonal surface expression of neuronal KCNQ channels is mediated by multiple signals in the KCNQ2 and KCNQ3 C-terminal domainsThe kinesin KIF1C and microtubule plus ends regulate podosome dynamics in macrophages.Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesisRat kinesin light chain 3 associates with spermatid mitochondriaA kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouseMapping of Charcot-Marie-Tooth disease type 1C to chromosome 16p identifies a novel locus for demyelinating neuropathiesCargos and genes: insights into vesicular transport from inherited human diseaseMissense mutation in the tubulin-specific chaperone E (Tbce) gene in the mouse mutant progressive motor neuronopathy, a model of human motoneuron diseaseThe progressive nature of Wallerian degeneration in wild-type and slow Wallerian degeneration (WldS) nervesCytoskeleton Molecular Motors: Structures and Their Functions in NeuronThe Roles of Microtubule-Based Transport at Presynaptic Nerve TerminalsCollective dynamics of processive cytoskeletal motorsMolecular motor proteins and amyotrophic lateral sclerosisCharcot-Marie-Tooth disease and intracellular trafficAxonal transport: cargo-specific mechanisms of motility and regulationExtracellular and Intracellular Signaling for Neuronal PolarityTracking individual secretory vesicles during exocytosis reveals an ordered and regulated process.The Microtubule Regulatory Protein Stathmin Is Required to Maintain the Integrity of Axonal Microtubules in DrosophilaEnergetic and dynamic: how mitochondria meet neuronal energy demandsThe Caenorhabditis elegans Kinesin-3 motor UNC-104/KIF1A is degraded upon loss of specific binding to cargoAxonal Transport and Neurodegeneration: How Marine Drugs Can Be Used for the Development of TherapeuticsAutophagosome dynamics in neurodegeneration at a glanceAssociation of the kinesin motor KIF1A with the multimodular protein liprin-alpha
P2860
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P2860
Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta
description
2001 nî lūn-bûn
@nan
2001 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta
@ast
Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta
@en
Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta
@nl
type
label
Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta
@ast
Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta
@en
Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta
@nl
prefLabel
Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta
@ast
Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta
@en
Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta
@nl
P2093
P3181
P1433
P1476
Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta
@en
P2093
N Hirokawa
T Nakagawa
P304
P3181
P356
10.1016/S0092-8674(01)00363-4
P407
P577
2001-06-01T00:00:00Z