Retrolinkin, a membrane protein, plays an important role in retrograde axonal transport
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Calcium tips the balance: a microtubule plus end to lattice binding switch operates in the carboxyl terminus of BPAG1n4.Retrolinkin cooperates with endophilin A1 to mediate BDNF-TrkB early endocytic trafficking and signaling from early endosomesRetrolinkin recruits the WAVE1 protein complex to facilitate BDNF-induced TrkB endocytosis and dendrite outgrowthTransmembrane protein 108 is required for glutamatergic transmission in dentate gyrusHerpesvirus tegument protein pUL37 interacts with dystonin/BPAG1 to promote capsid transport on microtubules during egress.Dystonin/BPAG1 promotes plus-end-directed transport of herpes simplex virus 1 capsids on microtubules during entry.Untethering the nuclear envelope and cytoskeleton: biologically distinct dystonias arising from a common cellular dysfunctionNeuronal dystonin isoform 2 is a mediator of endoplasmic reticulum structure and function.Microtubule stability, Golgi organization, and transport flux require dystonin-a2-MAP1B interaction.Spectraplakins: master orchestrators of cytoskeletal dynamics.Disruption in the autophagic process underlies the sensory neuropathy in dystonia musculorum mice.Loss of the transcription factor Meis1 prevents sympathetic neurons target-field innervation and increases susceptibility to sudden cardiac deathCytoplasmic dynein could be key to understanding neurodegeneration.Cytoplasmic dynein.One gene but different proteins and diseases: the complexity of dystonin and bullous pemphigoid antigen 1.Transgenic expression of neuronal dystonin isoform 2 partially rescues the disease phenotype of the dystonia musculorum mouse model of hereditary sensory autonomic neuropathy VI.Cellular and molecular mechanisms regulating neuronal growth by brain-derived neurotrophic factor.BPAG1a and b associate with EB1 and EB3 and modulate vesicular transport, Golgi apparatus structure, and cell migration in C2.7 myoblasts.A multi-hit hypothesis of bullous pemphigoid and associated neurological disease: Is HLA-DQB1*03:01, a potential link between immune privileged antigen exposure and epitope spreading?Lysosomal compromise and brain dysfunction: examining the role of neuroaxonal dystrophy.A SxIP motif interaction at the microtubule plus end is important for processive retrograde axonal transport.
P2860
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P2860
Retrolinkin, a membrane protein, plays an important role in retrograde axonal transport
description
2007 nî lūn-bûn
@nan
2007 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2007年の論文
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2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Retrolinkin, a membrane protein, plays an important role in retrograde axonal transport
@ast
Retrolinkin, a membrane protein, plays an important role in retrograde axonal transport
@en
type
label
Retrolinkin, a membrane protein, plays an important role in retrograde axonal transport
@ast
Retrolinkin, a membrane protein, plays an important role in retrograde axonal transport
@en
prefLabel
Retrolinkin, a membrane protein, plays an important role in retrograde axonal transport
@ast
Retrolinkin, a membrane protein, plays an important role in retrograde axonal transport
@en
P2093
P2860
P356
P1476
Retrolinkin, a membrane protein, plays an important role in retrograde axonal transport
@en
P2093
Chengbiao Wu
Jia-Jia Liu
Jianqing Ding
Prasanthi Bhagavatula
William C Mobley
Yanmin Yang
P2860
P304
P356
10.1073/PNAS.0602222104
P407
P50
P577
2007-02-07T00:00:00Z