about
Structure and expression of a novel compact myelin protein - small VCP-interacting protein (SVIP)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.Mechanisms contributing to central excitability changes during hearing loss.Axon physiology.The PMP22 gene and its related diseases.Abnormal junctions and permeability of myelin in PMP22-deficient nerves.Tuning PAK Activity to Rescue Abnormal Myelin Permeability in HNPPPhenotype HNPP (Hereditary Neuropathy With Liability to Pressure Palsies) Induced by Medical ProceduresEvaluation of dermal myelinated nerve fibers in diabetes mellitus.Neuropathy in a human without the PMP22 gene.Niacin-mediated Tace activation ameliorates CMT neuropathies with focal hypermyelination.SP110 and PMP22 polymorphisms are associated with tuberculosis risk in a Chinese-Tibetan population.PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies.Murine therapeutic models for Charcot-Marie-Tooth (CMT) disease.Genetic factors for nerve susceptibility to injuries - lessons from PMP22 deficiencyTritium-labelled alkaloids: Synthesis and applications.Unravelling crucial biomechanical resilience of myelinated peripheral nerve fibres provided by the Schwann cell basal lamina and PMP22.Nano-scale Biophysical and Structural Investigations on Intact and Neuropathic Nerve Fibers by Simultaneous Combination of Atomic Force and Confocal Microscopy.Nonrecurrent PMP22-RAI1 contiguous gene deletions arise from replication-based mechanisms and result in Smith-Magenis syndrome with evident peripheral neuropathy.Pathophysiology of HNPP explored using axonal excitability.Implications of Schwann Cells Biomechanics and Mechanosensitivity for Peripheral Nervous System Physiology and Pathophysiology.Sonographic and electrodiagnostic features of hereditary neuropathy with liability to pressure palsies.A dual role for Integrin α6β4 in modulating Hereditary Neuropathy with liability to Pressure Palsies.Myelin abnormality in Charcot-Marie-Tooth type 4J recapitulates features of acquired demyelination.The Axon-Myelin Unit in Development and Degenerative DiseaseElectrophysiological comparison between males and females in HNPP
P2860
Q24336976-DE6566BF-BDFB-4714-A083-49D007EC4C6CQ28084798-E97FCC1A-AE7F-4707-850D-153A82A40DD3Q30371672-E4407685-B7C7-4C52-8645-6BD51C06086BQ30466850-E31E6024-407B-468A-84B0-C14DFF09AFBDQ34181026-A44F87D1-5592-4CA7-B770-E5C07EB14229Q34316615-E4AF2E81-9651-4E08-8F7E-2A5FF9C35723Q34386936-2692F0D8-B805-42A7-91C7-A4D3F690C547Q36119589-16BBC0A4-1F9C-4865-83EB-A23B71D7DB29Q36926249-D147434C-CD27-4F71-931C-6FF3A195C178Q36957751-84CFFFBD-92DB-4C09-9F75-72C90024F220Q37013290-419ACE5D-249E-4D01-8476-46F3778C766FQ37514807-2C73FA24-1319-4F32-B7F1-AEE5F7F9E9EBQ37662373-71B169FE-C422-4B22-84A4-9B65C5557DF7Q37715520-87331C47-D2E1-43AE-889A-35FAE374F67EQ38007033-3272F86A-C784-4A8D-B951-2CC35A409AD5Q38265513-603D5DDB-AFD4-4C89-B953-BC06AB7545A4Q39077963-B4471496-614D-4FA2-9965-7191EBE9C098Q39271306-E5EF1FE8-5C61-42E7-BCAC-84C0F80D673BQ41599391-EA276977-1177-47F6-BAA6-7D34288997CEQ41643440-F9EA168A-6F53-429D-87EA-BFB7F20B3200Q43631107-BFB8E9F2-F4CB-4967-A3D8-D9C05A2D4BD9Q44714913-B6FAF2F0-43B3-456B-A15F-99401BD34BFAQ46613435-69666DC6-7F8E-4B5E-84D6-3461137CD8F0Q47189843-78C502CA-AB3C-44A0-B9B4-BEA66FE3CB56Q52666734-3231DC09-BA4B-47AC-8F48-9EF5C1C3BFB9Q56000910-0B7F8315-6600-4DD1-8EE4-E25814F9CCF1Q57769431-1DC41469-B2F9-49AE-82C7-31E42B9A8174
P2860
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Conduction block in PMP22 deficiency.
@en
type
label
Conduction block in PMP22 deficiency.
@en
prefLabel
Conduction block in PMP22 deficiency.
@en
P2093
P2860
P50
P1476
Conduction block in PMP22 deficiency
@en
P2093
Heather A O'Malley
Mario Andre Saporta
Ueli Suter
Xuebao Zhang
Yunhong Bai
P2860
P304
P356
10.1523/JNEUROSCI.4264-09.2010
P407
P577
2010-01-01T00:00:00Z