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Titlebook: Cytoskeleton of the Nervous System; Ralph A. Nixon,Aidong Yuan Book 2011 Springer Science+Business Media, LLC 2011

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Herz-Lungen-Maschine: Anästhesiemanagementne and to organelles, including the nucleus. Within the nucleus, IFs play a ubiquitously important role in structuring the nuclear envelope and help to regulate gene expression. Nuclear IF protein function is mediated through interactions with both large structural proteins and small regulatory prot
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Georg Petroianu,Peter Michael Osswalde place at tyrosine residues, and the dephosphorylation of the modified residues by tau phosphatases. In addition, we will comment on the toxicity of phosphotau in disorders such as Alzheimer’s disease and the development of possible therapies to prevent tau phosphorylation.
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R. Larsen,H. Sonntag,D. Kettler of a single intermediate filament and can now be considered to be a fourth subunit of NF in the adult CNS. Its role as a subunit of CNS NF explains the close relationship of α-internexin with the pathology of CNS diseases associated with NF accumulation.
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https://doi.org/10.1007/978-3-642-28291-1ng evidence for the involvement of neurofilaments in a number of neurodegenerative disorders such as amyotrophic lateral sclerosis, hereditary spastic paraplegia, Charcot–Marie–Tooth disease, and Alzheimer’s disease. Disrupted neurofilament transport is thought to be a common mechanism in some or all of these disorders.
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Intensivbehandlung nach Herzoperationenf neurofilament carboxy terminal phosphorylation in establishing axonal diameter. In this review, the contribution of each neurofilament gene-targeted mouse to our current understanding of the role of neurofilaments and neurofilament phosphorylation in radial axonal growth is discussed.
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https://doi.org/10.1007/978-3-662-52987-4l argue that coordinated activity of these molecular events determines the speed and direction of axon growth, with particular emphasis on how Ca. signals control the driving machinery for growth cone navigation.
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Tau Phosphorylation,e place at tyrosine residues, and the dephosphorylation of the modified residues by tau phosphatases. In addition, we will comment on the toxicity of phosphotau in disorders such as Alzheimer’s disease and the development of possible therapies to prevent tau phosphorylation.
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