about
Interaction of tau protein with the dynactin complexNeuronal cotransport of glycine receptor and the scaffold protein gephyrinUNC-16 (JIP3) Acts Through Synapse-Assembly Proteins to Inhibit the Active Transport of Cell Soma Organelles to Caenorhabditis elegans Motor Neuron Axons.A motor neuron disease-associated mutation in p150Glued perturbs dynactin function and induces protein aggregation.Optically resolving individual microtubules in live axons.Single-molecule imaging of NGF axonal transport in microfluidic devices.Automated image analysis for tracking cargo transport in axonsThe ALS disease protein TDP-43 is actively transported in motor neuron axons and regulates axon outgrowth.Relay of retrograde synaptogenic signals through axonal transport of BMP receptors.Ndel1-derived peptides modulate bidirectional transport of injected beads in the squid giant axon.Functional studies of individual myosin molecules.Neuromuscular junction defects in mice with mutation of dynein heavy chain 1.Animal models of Kennedy disease.Distal spinal and bulbar muscular atrophy caused by dynactin mutation.Unraveling the genetics of distal hereditary motor neuronopathies.Doxycycline reduces fibril formation in a transgenic mouse model of AL amyloidosis.The G59S mutation in p150(glued) causes dysfunction of dynactin in mice.RNA processing defects associated with diseases of the motor neuronRetrograde axonal transport and motor neuron disease.Action in the axon: generation and transport of signaling endosomes.Cytoplasmic dynein heavy chain: the servant of many mastersA model system to study transport of self-assembled cargos.Axonal transport defects in neurodegenerative diseases.Disruption of axonal transport in motor neuron diseases.LIS1 and DCX: Implications for Brain Development and Human Disease in Relation to Microtubules.Keeping Neuronal Cargoes on the Right Track: New Insights into Regulators of Axonal Transport.Interaction between familial amyotrophic lateral sclerosis (ALS)-linked SOD1 mutants and the dynein complex.A perspective on neuronal cell death signaling and neurodegeneration.Hereditary spastic paraplegia: clinical genomics and pharmacogenetic perspectives
P2860
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P2860
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Motor neurons rely on motor proteins.
@ast
Motor neurons rely on motor proteins.
@en
type
label
Motor neurons rely on motor proteins.
@ast
Motor neurons rely on motor proteins.
@en
prefLabel
Motor neurons rely on motor proteins.
@ast
Motor neurons rely on motor proteins.
@en
P1476
Motor neurons rely on motor proteins.
@en
P2093
Erika L F Holzbaur
P304
P356
10.1016/J.TCB.2004.03.009
P577
2004-05-01T00:00:00Z