Many facets of the peripheral myelin protein PMP22 in myelination and disease.
about
N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-LomPERP, an apoptosis-associated target of p53, is a novel member of the PMP-22/gas3 familyCharcot-Marie-Tooth disease and intracellular trafficA brief review of recent Charcot-Marie-Tooth research and prioritiesPMP22 transgenic dorsal root ganglia cultures show myelin abnormalities similar to those of human CMT1AAssociation of calnexin with mutant peripheral myelin protein-22 ex vivo: a basis for "gain-of-function" ER diseasesPeripheral myelin protein 22 is a constituent of intercellular junctions in epitheliaThe tetraspan protein epithelial membrane protein-2 interacts with beta1 integrins and regulates adhesionCollaboration for rare disease drug discovery researchFunctional and comparative genomics analyses of pmp22 in medaka fishRecommendations to enable drug development for inherited neuropathies: Charcot-Marie-Tooth and Giant Axonal Neuropathy.Charcot-marie-tooth disease and related neuropathies: molecular basis for distinction and diagnosis.Distinct phenotypes associated with increasing dosage of the PLP gene: implications for CMT1A due to PMP22 gene duplication.Transgenic mouse models of CMT1A and HNPP.Identification of novel candidate oncogenes in chromosome region 17p11.2-p12 in human osteosarcoma.Understanding Schwann cell-neurone interactions: the key to Charcot-Marie-Tooth disease?Peripheral myelin protein-22 (PMP22) modulates alpha 6 integrin expression in the human endometriumRewiring integrin-mediated signaling and cellular response with the peripheral myelin protein 22 and epithelial membrane protein 2 components of the tetraspan web.Unveiling of miRNA Expression Patterns in Purkinje Cells During Development.Rapamycin activates autophagy and improves myelination in explant cultures from neuropathic mice.Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease.Exposure at the cell surface is required for gas3/PMP22 To regulate both cell death and cell spreading: implication for the Charcot-Marie-Tooth type 1A and Dejerine-Sottas diseases.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.Modulation of epithelial morphology, monolayer permeability, and cell migration by growth arrest specific 3/peripheral myelin protein 22Glycan-independent role of calnexin in the intracellular retention of Charcot-Marie-tooth 1A Gas3/PMP22 mutants.Amyloid-like Fibrils from an α-Helical Transmembrane Protein.PERIPHERAL MYELIN PROTEIN-22 IS EXPRESSED IN CNS MYELIN.Pathophysiology of HNPP explored using axonal excitability.Role of the peripheral myelin protein 22 N-linked glycan in oligomer stability.Elevated Peripheral Myelin Protein 22, Reduced Mitotic Potential, and Proteasome Impairment in Dermal Fibroblasts from Charcot-Marie-Tooth Disease Type 1A Patients.Distal axonopathy in peripheral nerves of PMP22-mutant mice.Development of early postnatal peripheral nerve abnormalities in Trembler-J and PMP22 transgenic mice.
P2860
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P2860
Many facets of the peripheral myelin protein PMP22 in myelination and disease.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
1998年學術文章
@zh-hant
name
Many facets of the peripheral myelin protein PMP22 in myelination and disease.
@en
Many facets of the peripheral myelin protein PMP22 in myelination and disease.
@nl
type
label
Many facets of the peripheral myelin protein PMP22 in myelination and disease.
@en
Many facets of the peripheral myelin protein PMP22 in myelination and disease.
@nl
prefLabel
Many facets of the peripheral myelin protein PMP22 in myelination and disease.
@en
Many facets of the peripheral myelin protein PMP22 in myelination and disease.
@nl
P2860
P1476
Many facets of the peripheral myelin protein PMP22 in myelination and disease.
@en
P2860
P304
P356
10.1002/(SICI)1097-0029(19980601)41:5<359::AID-JEMT3>3.0.CO;2-L
P577
1998-06-01T00:00:00Z