Neurofilament dynamics and involvement in neurological disorders. - Wikidata - awgldk - TriplyDB

Neurofilament dynamics and involvement in neurological disorders.

Neurofilament dynamics and involvement in neurological disorders.

http://www.wikidata.org/entity/Q38310624

about

Effects of obesogenic diet and estradiol on dorsal raphe gene expression in old female macaques Plasma neurofilament light chain predicts progression in progressive supranuclear palsy Neurobiology of axonal transport defects in motor neuron diseases: Opportunities for translational research?Cytoskeleton as a Target of Quinolinic Acid Neurotoxicity: Insight from Animal Models.Junctions in human health and inherited disease.Neurofilament light protein in CSF and blood is associated with neurodegeneration and disease severity in Huntington's disease R6/2 mice.Diagnostic and Prognostic Biomarkers in Amyotrophic Lateral Sclerosis: Neurofilament Light Chain Levels in Definite Subtypes of Disease.Effect of Vitamin D in HN9.10e Embryonic Hippocampal Cells and in Hippocampus from MPTP-Induced Parkinson's Disease Mouse Model.Effects of GnRH on Neurite Outgrowth, Neurofilament and Spinophilin Proteins Expression in Cultured Spinal Cord Neurons of Rat Embryos.Absence of NEFL in patient-specific neurons in early-onset Charcot-Marie-Tooth neuropathy.The proteome of neurofilament-containing protein aggregates in blood.

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P2860

Neurofilament dynamics and involvement in neurological disorders.

http://www.wikidata.org/entity/Q38310624

description

2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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2015年论文

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2015年论文

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name

Neurofilament dynamics and involvement in neurological disorders.

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Neurofilament dynamics and involvement in neurological disorders.

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Neurofilament dynamics and involvement in neurological disorders.

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Cell and Tissue Research

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Neurofilament dynamics and involvement in neurological disorders.

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P2093

Heather D Durham

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Michael Tibshirani

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P2860

ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

Identification of novel NPRAP/δ-catenin-interacting proteins and the direct association of NPRAP with dynamin 2

NF-M is an essential target for the myelin-directed "outside-in" signaling cascade that mediates radial axonal growth

Charcot-Marie-Tooth disease type 2E, a disorder of the cytoskeleton

Effects of Charcot-Marie-Tooth-linked mutations of the neurofilament light subunit on intermediate filament formation

Encoding and transducing the synaptic or extrasynaptic origin of NMDA receptor signals to the nucleus

Nesprin-3 regulates endothelial cell morphology, perinuclear cytoskeletal architecture, and flow-induced polarization

A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene.

Increased monomerization of mutant HSPB1 leads to protein hyperactivity in Charcot-Marie-Tooth neuropathy

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s00441-014-2082-7

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609-620

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scholarly article

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10.1007/S00441-014-2082-7

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3

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360

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Benoit J Gentil

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