Molecular basis of common hereditary motor and sensory neuropathies in humans and in mouse models.
about
Late-onset neurodegeneration in mice with increased dosage of the proteolipid protein geneTissue-engineered rhesus monkey nerve grafts for the repair of long ulnar nerve defects: similar outcomes to autologous nerve graftsThe anatomy and cell biology of peripheral myelin protein-22.The "CMT rat": peripheral neuropathy and dysmyelination caused by transgenic overexpression of PMP22.Correlation between the histopathologic, genotypic, and phenotypic features of hereditary peripheral neuropathies in childhood.Onion bulb cells in mice deficient for myelin genes share molecular properties with immature, differentiated non-myelinating, and denervated Schwann cells.Role of the peripheral myelin protein 22 N-linked glycan in oligomer stability.Many facets of the peripheral myelin protein PMP22 in myelination and disease.Current concepts of PLP and its role in the nervous system.
P2860
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P2860
Molecular basis of common hereditary motor and sensory neuropathies in humans and in mouse models.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年学术文章
@wuu
1995年学术文章
@zh-cn
1995年学术文章
@zh-hans
1995年学术文章
@zh-my
1995年学术文章
@zh-sg
1995年學術文章
@yue
1995年學術文章
@zh
1995年學術文章
@zh-hant
name
Molecular basis of common here ...... in humans and in mouse models.
@en
Molecular basis of common here ...... in humans and in mouse models.
@nl
type
label
Molecular basis of common here ...... in humans and in mouse models.
@en
Molecular basis of common here ...... in humans and in mouse models.
@nl
prefLabel
Molecular basis of common here ...... in humans and in mouse models.
@en
Molecular basis of common here ...... in humans and in mouse models.
@nl
P2860
P1433
P1476
Molecular basis of common here ...... in humans and in mouse models.
@en
P2093
P2860
P304
P356
10.1111/J.1750-3639.1995.TB00600.X
P577
1995-07-01T00:00:00Z