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Animal models of myasthenia gravis: utility and limitationsClinical features, pathogenesis, and treatment of myasthenia gravis: a supplement to the Guidelines of the German Neurological SocietyERBB3-mediated regulation of Bergmann glia proliferation in cerebellar lamination.Presynaptic LRP4 promotes synapse number and function of excitatory CNS neuronsFlow Cytofluorimetric Analysis of Anti-LRP4 (LDL Receptor-Related Protein 4) Autoantibodies in Italian Patients with Myasthenia Gravis.Slit2 as a β-catenin/Ctnnb1-dependent retrograde signal for presynaptic differentiation.Neuromuscular junction degeneration in muscle wasting.Lrp4 in astrocytes modulates glutamatergic transmissionSchwann Cells in Neuromuscular Junction Formation and MaintenanceMuscle Fibers Secrete FGFBP1 to Slow Degeneration of Neuromuscular Synapses during Aging and Progression of ALS.A Novel Egr-1-Agrin Pathway and Potential Implications for Regulation of Synaptic Physiology and Homeostasis at the Neuromuscular JunctionA Novel Domain-Specific Mutation in a Sclerosteosis Patient Suggests a Role of LRP4 as an Anchor for Sclerostin in Human Bone.Muscle as a paracrine and endocrine organ.Double Seronegative Myasthenia Gravis with Anti-LRP4 Antibodies Presenting with Dropped Head and Acute Respiratory Insufficiency.Molecular cloning and partial characterization of a low-density lipoprotein receptor-related protein 13 (Lrp13) involved in vitellogenin uptake in the cutthroat trout (Oncorhynchus clarki).Postnatal knockdown of dok-7 gene expression in mice causes structural defects in neuromuscular synapses and myasthenic pathology.Super-Resolution Microscopy Reveals a Nanoscale Organization of Acetylcholine Receptors for Trans-Synaptic Alignment at Neuromuscular SynapsesMuscle Yap Is a Regulator of Neuromuscular Junction Formation and Regeneration.Reduced muscle strength in ether lipid-deficient mice is accompanied by altered development and function of the neuromuscular junction.Clinical and research strategies for limb-girdle congenital myasthenic syndromes.Myasthenia gravis: the role of complement at the neuromuscular junction.A Case Study in the Use of Primary Literature in the Context of Authentic Learning Pedagogy in the Undergraduate Neuroscience Classroom.Induction of Anti-agrin Antibodies Causes Myasthenia Gravis in Mice.Enzymatic Activity of the Scaffold Protein Rapsyn for Synapse Formation.Agrin and low-density lipoprotein-related receptor protein 4 antibodies in amyotrophic lateral sclerosis patients.Muscle-Specific Tyrosine Kinase and Myasthenia Gravis Owing to Other Antibodies.Motoneuron Wnts regulate neuromuscular junction development
P2860
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P2860
description
2014 nî lūn-bûn
@nan
2014 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
LRP4 is critical for neuromuscular junction maintenance
@ast
LRP4 is critical for neuromuscular junction maintenance
@en
LRP4 is critical for neuromuscular junction maintenance
@nl
type
label
LRP4 is critical for neuromuscular junction maintenance
@ast
LRP4 is critical for neuromuscular junction maintenance
@en
LRP4 is critical for neuromuscular junction maintenance
@nl
prefLabel
LRP4 is critical for neuromuscular junction maintenance
@ast
LRP4 is critical for neuromuscular junction maintenance
@en
LRP4 is critical for neuromuscular junction maintenance
@nl
P2093
P2860
P1476
LRP4 is critical for neuromuscular junction maintenance
@en
P2093
Andrew Bowman
Chengyong Shen
Wen-cheng Xiong
Yisheng Lu
P2860
P304
13892-13905
P356
10.1523/JNEUROSCI.1733-14.2014
P407
P577
2014-10-01T00:00:00Z