Abnormal myelination in transplanted Trembler mouse Schwann cells.
about
PMP22 transgenic dorsal root ganglia cultures show myelin abnormalities similar to those of human CMT1AP0 (protein zero) mutation S34C underlies instability of internodal myelin in S63C mice.Schwann cell-axon interactions in Charcot-Marie-Tooth disease.Regulation of myelin-specific gene expression. Relevance to CMT1.Trembler as a mouse model of CMT1A?Axonal pathology precedes demyelination in a mouse model of X-linked demyelinating/type I Charcot-Marie Tooth neuropathy.Molecular genetics and neuropathology of Charcot-Marie-Tooth disease type 1A.Rat Nasal Respiratory Mucosa-Derived Ectomesenchymal Stem Cells Differentiate into Schwann-Like Cells Promoting the Differentiation of PC12 Cells and Forming Myelin In Vitro.Reinnervation of the tibialis anterior following sciatic nerve crush injury: a confocal microscopic study in transgenic miceImmunoreactive myelin basic proteins are not detected when shiverer mutant Schwann cells and fibroblasts are co-cultured with normal neurons.Heterophilic binding of L1 on unmyelinated sensory axons mediates Schwann cell adhesion and is required for axonal survival.Molecular mechanisms of inherited demyelinating neuropathies.Biochemical characterization of protein quality control mechanisms during disease progression in the C22 mouse model of CMT1A.Local regulation of neurofilament transport by myelinating cells.Myelin restoration: progress and prospects for human cell replacement therapies.Inherited neuromuscular diseases in the mouse. A review of the literature.Absence of myelin basic protein from glial cell lines and cultures.The Schwann cell: a reappraisal of its role in the peripheral nervous system.Involvement of peripheral and central nerves in murine dystrophy.Inherited muscle and nerve diseases in mice: a tabulation with commentary.Hereditary disorders of motor and sensory neurons in the mouse.Axon-Schwann cell relationships in neuropathies of mutant mice.Characterization and developmental changes of UDP-galactose-ceramide galactosyl transferase in a rat CNS axolemma-enriched fraction. Differences and similarities of the enzyme associated with the microsomal and myelin fractions.Animal models for inherited peripheral neuropathies.Myelination of mouse axons by Schwann cells transplanted from normal and abnormal human nerves.Molecular basis of common hereditary motor and sensory neuropathies in humans and in mouse models.Many facets of the peripheral myelin protein PMP22 in myelination and disease.Paranodal dysmyelination in peripheral nerves of Trembler mice.
P2860
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P2860
Abnormal myelination in transplanted Trembler mouse Schwann cells.
description
1977 nî lūn-bûn
@nan
1977年の論文
@ja
1977年論文
@yue
1977年論文
@zh-hant
1977年論文
@zh-hk
1977年論文
@zh-mo
1977年論文
@zh-tw
1977年论文
@wuu
1977年论文
@zh
1977年论文
@zh-cn
name
Abnormal myelination in transplanted Trembler mouse Schwann cells.
@en
type
label
Abnormal myelination in transplanted Trembler mouse Schwann cells.
@en
prefLabel
Abnormal myelination in transplanted Trembler mouse Schwann cells.
@en
P2093
P356
P1433
P1476
Abnormal myelination in transplanted Trembler mouse Schwann cells.
@en
P2093
P2888
P356
10.1038/265073A0
P407
P577
1977-01-01T00:00:00Z
P6179
1028571589