Distal axonopathy in peripheral nerves of PMP22-mutant mice.
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N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-LomTransient auditory nerve demyelination as a new mechanism for hidden hearing loss.Congenital hypomyelinating neuropathy with lethal conduction failure in mice carrying the Egr2 I268N mutation.Determinants of reduced health-related quality of life in pediatric inherited neuropathies.The effect of myelinating Schwann cells on axons.Axonal pathology precedes demyelination in a mouse model of X-linked demyelinating/type I Charcot-Marie Tooth neuropathy.Understanding Schwann cell-neurone interactions: the key to Charcot-Marie-Tooth disease?Comparison of a new pmp22 transgenic mouse line with other mouse models and human patients with CMT1A.Comparison between clinical disabilities and electrophysiological values in Charcot-Marie-Tooth 1A patients with PMP22 duplication.Tuning PAK Activity to Rescue Abnormal Myelin Permeability in HNPPHow do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease?Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease.Molecular mechanisms of inherited demyelinating neuropathies.Neuropathy in a human without the PMP22 gene.Schwann cell influence on motor neuron regeneration accuracy.GJB1-associated X-linked Charcot-Marie-Tooth disease, a disorder affecting the central and peripheral nervous systems.Progressive segregation of unmyelinated axons in peripheral nerves, myelin alterations in the CNS, and cyst formation in the kidneys of myelin and lymphocyte protein-overexpressing mice.c-Jun activation in Schwann cells protects against loss of sensory axons in inherited neuropathy.Bex1 is involved in the regeneration of axons after injury.P(0) glycoprotein overexpression causes congenital hypomyelination of peripheral nerves.Remodeling of motor nerve terminals in demyelinating axons of periaxin-null mice.Acquired neuromyotonia and peripheral neuropathy in a patient with Hodgkin's disease.Selective vulnerability of peripheral nerves in avian riboflavin deficiency demyelinating polyneuropathy.Sonographic and electrodiagnostic features of hereditary neuropathy with liability to pressure palsies.Functional recovery of regenerating motor axons is delayed in mice heterozygously deficient for the myelin protein P(0) gene.Paranodal dysmyelination in peripheral nerves of Trembler mice.Myelin-associated glycoprotein modulates expression and phosphorylation of neuronal cytoskeletal elements and their associated kinases.Axonal damage and demyelination in long-term dorsal root ganglia cultures from a rat model of Charcot-Marie-Tooth type 1A disease.Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data, functional studies of the SH3 recognition motif and correlation between wild-type MED25 and PMP22 RNA levels in CMT1A animal modelsMyelin and Axon Pathology in a Long-Term Study ofPMP22-Overexpressing Mice
P2860
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P2860
Distal axonopathy in peripheral nerves of PMP22-mutant mice.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh
1999年學術文章
@zh-hant
name
Distal axonopathy in peripheral nerves of PMP22-mutant mice.
@en
Distal axonopathy in peripheral nerves of PMP22-mutant mice.
@nl
type
label
Distal axonopathy in peripheral nerves of PMP22-mutant mice.
@en
Distal axonopathy in peripheral nerves of PMP22-mutant mice.
@nl
prefLabel
Distal axonopathy in peripheral nerves of PMP22-mutant mice.
@en
Distal axonopathy in peripheral nerves of PMP22-mutant mice.
@nl
P2093
P2860
P356
P1433
P1476
Distal axonopathy in peripheral nerves of PMP22-mutant mice.
@en
P2093
P2860
P304
P356
10.1093/BRAIN/122.8.1563
P407
P478
122 ( Pt 8)
P577
1999-08-01T00:00:00Z