Abnormal junctions and permeability of myelin in PMP22-deficient nerves.
about
Molecular regulators of nerve conduction - Lessons from inherited neuropathies and rodent genetic modelsAfferent Visual Pathway Affection in Patients with PMP22 Deletion-Related Hereditary Neuropathy with Liability to Pressure Palsies.Motor neuron intrinsic and extrinsic mechanisms contribute to the pathogenesis of FUS-associated amyotrophic lateral sclerosis.Poly(ADP-ribosylation) is present in murine sciatic nerve fibers and is altered in a Charcot-Marie-Tooth-1E neurodegenerative model.The homology model of PMP22 suggests mutations resulting in peripheral neuropathy disrupt transmembrane helix packing.PMP22 is critical for actin-mediated cellular functions and for establishing lipid rafts.Tuning PAK Activity to Rescue Abnormal Myelin Permeability in HNPPPhenotype HNPP (Hereditary Neuropathy With Liability to Pressure Palsies) Induced by Medical ProceduresNiacin-mediated Tace activation ameliorates CMT neuropathies with focal hypermyelination.Genetic factors for nerve susceptibility to injuries - lessons from PMP22 deficiencyBarrier function in the peripheral and central nervous system-a review.Unravelling crucial biomechanical resilience of myelinated peripheral nerve fibres provided by the Schwann cell basal lamina and PMP22.Lentivirus-Mediated RNA Interference Targeting RhoA Slacks the Migration, Proliferation, and Myelin Formation of Schwann Cells.Peripheral myelin protein 22 alters membrane architecture.Nano-scale Biophysical and Structural Investigations on Intact and Neuropathic Nerve Fibers by Simultaneous Combination of Atomic Force and Confocal Microscopy.Hereditary neuropathy with liability to pressure palsy (HNPP): report of a family with a new point mutation in PMP22 gene.Biophysical characterization of interactions between the C-termini of peripheral nerve claudins and the PDZ₁ domain of zonula occludens.Implications of Schwann Cells Biomechanics and Mechanosensitivity for Peripheral Nervous System Physiology and Pathophysiology.Influence of Mechanical Stimuli on Schwann Cell Biology.A dual role for Integrin α6β4 in modulating Hereditary Neuropathy with liability to Pressure Palsies.Blood-spinal cord barrier breakdown and pericyte deficiency in peripheral neuropathy.S-Palmitoylation of Junctional Adhesion Molecule C Regulates Its Tight Junction Localization and Cell Migration.Methylglyoxal Disrupts Paranodal Axoglial Junctions via Calpain Activation.Vesicular glutamate release from central axons contributes to myelin damage.Regulation of the neuropathy-associated Pmp22 gene by a distal super-enhancer
P2860
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P2860
Abnormal junctions and permeability of myelin in PMP22-deficient nerves.
description
2014 nî lūn-bûn
@nan
2014 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի փետրվարին 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
Abnormal junctions and permeability of myelin in PMP22-deficient nerves.
@ast
Abnormal junctions and permeability of myelin in PMP22-deficient nerves.
@en
Abnormal junctions and permeability of myelin in PMP22-deficient nerves.
@nl
type
label
Abnormal junctions and permeability of myelin in PMP22-deficient nerves.
@ast
Abnormal junctions and permeability of myelin in PMP22-deficient nerves.
@en
Abnormal junctions and permeability of myelin in PMP22-deficient nerves.
@nl
prefLabel
Abnormal junctions and permeability of myelin in PMP22-deficient nerves.
@ast
Abnormal junctions and permeability of myelin in PMP22-deficient nerves.
@en
Abnormal junctions and permeability of myelin in PMP22-deficient nerves.
@nl
P2093
P2860
P356
P1433
P1476
Abnormal junctions and permeability of myelin in PMP22-deficient nerves.
@en
P2093
Beat A Imhof
Bruce D Carter
Jiasong Guo
Leiming Wang
Sezgi Arpag
Ueli Suter
Xinxia Tian
P2860
P304
P356
10.1002/ANA.24086
P577
2014-02-20T00:00:00Z