(Q36541724)

14 August 2017

1 reference

title

Schwann cells and the pathogenesis of inherited motor and sensory neuropathies (Charcot-Marie-Tooth disease). (English)

1 reference

14 August 2017

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Axel Niemann

2

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Philipp Berger

object named as

Philipp Berger

series ordinal

1

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Ueli Suter

series ordinal

3

object named as

Ueli Suter

1 reference

14 August 2017

1 September 2006

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14 August 2017

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14 August 2017

54

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14 August 2017

4

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14 August 2017

243-257

1 reference

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.

14 August 2017

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

Rho-dependent regulation of cell spreading by the tetraspan membrane protein Gas3/PMP22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

Clinical and histologic findings in autosomal centronuclear myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

Nab proteins are essential for peripheral nervous system myelination

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

Plasma membrane channels formed by connexins: their regulation and functions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

Heterozygous peripheral myelin protein 22-deficient mice are affected by a progressive demyelinating tomaculous neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Analysis of compound heterozygous mice reveals that the Trembler mutation can behave as a gain-of-function allele

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Peripheral myelin protein 22 is in complex with alpha6beta4 integrin, and its absence alters the Schwann cell basal lamina.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

ErbB2 signaling in Schwann cells is mostly dispensable for maintenance of myelinated peripheral nerves and proliferation of adult Schwann cells after injury.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Structure and stability of internodal myelin in mouse models of hereditary neuropathy.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucoma

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Functional gap junctions in the schwann cell myelin sheath

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Neural CAMS and their role in the development and organization of myelin sheaths

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

The structure and regulation of myotubularin phosphatases

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

SIMPLE mutation in demyelinating neuropathy and distribution in sciatic nerve

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Multi-level regulation of myotubularin-related protein-2 phosphatase activity by myotubularin-related protein-13/set-binding factor-2

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Loss of phosphatase activity in myotubularin-related protein 2 is associated with Charcot-Marie-Tooth disease type 4B1.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Membrane association of myotubularin-related protein 2 is mediated by a pleckstrin homology-GRAM domain and a coiled-coil dimerization module

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Expression analysis of the N-Myc downstream-regulated gene 1 indicates that myelinating Schwann cells are the primary disease target in hereditary motor and sensory neuropathy-Lom

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Connexin mutations in X-linked Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Selective defects in channel permeability associated with Cx32 mutations causing X-linked Charcot–Marie–Tooth disease

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Mutations in dynamin 2 cause dominant centronuclear myopathy

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Disruption of Mtmr2 produces CMT4B1-like neuropathy with myelin outfolding and impaired spermatogenesis

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Loss of Mtmr2 phosphatase in Schwann cells but not in motor neurons causes Charcot-Marie-Tooth type 4B1 neuropathy with myelin outfoldings.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Human Connexin 32, a gap junction protein altered in the X-linked form of Charcot-Marie-Tooth disease, is directly regulated by the transcription factor SOX10

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

An animal model for Charcot-Marie-Tooth disease type 4B1.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Peripheral neuropathy associated with mitochondrial disorders: 8 cases and review of the literature

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

The transcription factor Sox10 is a key regulator of peripheral glial development.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Localization and functional roles of PMP22 in peripheral nerves of P0-deficient mice

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

DNA deletion associated with hereditary neuropathy with liability to pressure palsies

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

N-myc down-regulated gene 1 modulates the response of term human trophoblasts to hypoxic injury.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Emerging functions of mammalian mitochondrial fusion and fission

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Alterations in the Arf6-regulated plasma membrane endosomal recycling pathway in cells overexpressing the tetraspan protein Gas3/PMP22.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

The myotubularin family of lipid phosphatases

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

PMP22 carrying the trembler or trembler-J mutation is intracellularly retained in myelinating Schwann cells

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Human diseases reveal novel roles for neural laminins

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Restricted growth of Schwann cells lacking Cajal bands slows conduction in myelinated nerves.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

The gene encoding ganglioside-induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Overloaded endoplasmic reticulum-Golgi compartments, a possible pathomechanism of peripheral neuropathies caused by mutations of the peripheral myelin protein PMP22.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Functional organization of a Schwann cell enhancer.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Altered trafficking of mutant connexin32

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Association of calnexin with mutant peripheral myelin protein-22 ex vivo: a basis for "gain-of-function" ER diseases

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Studies on the mechanisms of autophagy: formation of the autophagic vacuole

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

The myelinated axon is dependent on the myelinating cell for support and maintenance: molecules involved.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Neuregulins: versatile growth and differentiation factors in nervous system development and human disease

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Apoptotic phenotype induced by overexpression of wild-type gas3/PMP22: its relation to the demyelinating peripheral neuropathy CMT1A.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Transient expression of the neurofilament proteins NF-L and NF-M by Schwann cells is regulated by axonal contact

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Conditional disruption of beta 1 integrin in Schwann cells impedes interactions with axons

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Laminins and their receptors in Schwann cells and hereditary neuropathies

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Characterization of the muscle involvement in dynamin 2-related centronuclear myopathy.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Glycan-independent role of calnexin in the intracellular retention of Charcot-Marie-tooth 1A Gas3/PMP22 mutants

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Emerging role for autophagy in the removal of aggresomes in Schwann cells.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Alterations in degradative pathways and protein aggregation in a neuropathy model based on PMP22 overexpression

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Impaired proteasome activity and accumulation of ubiquitinated substrates in a hereditary neuropathy model

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Control of myelination in Schwann cells: a Krox20 cis-regulatory element integrates Oct6, Brn2 and Sox10 activities

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Distinct disease mechanisms in peripheral neuropathies due to altered peripheral myelin protein 22 gene dosage or a Pmp22 point mutation

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Peripheral demyelination and neuropathic pain behavior in periaxin-deficient mice

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

A novel Gypsy founder mutation, p.Arg1109X in the CMT4C gene, causes variable peripheral neuropathy phenotypes

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Peripheral myelin protein 22 kDa and protein zero: domain specific trans-interactions

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Connexin 32 promoter P2 mutations: a mechanism of peripheral nerve dysfunction

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Glial membranes at the node of Ranvier prevent neurite outgrowth

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Peripheral neuropathy

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

NDRG1 interacts with APO A-I and A-II and is a functional candidate for the HDL-C QTL on 8q24.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Mutation screening of the N-myc downstream-regulated gene 1 (NDRG1) in patients with Charcot-Marie-Tooth Disease

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Construction of a mouse model of Charcot-Marie-Tooth disease type 1A by pronuclear injection of human YAC DNA.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Congenital hypomyelinating neuropathy, central dysmyelination, and Waardenburg-Hirschsprung disease: phenotypes linked by SOX10 mutation

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Identification of a new Pmp22 mouse mutant and trafficking analysis of a Pmp22 allelic series suggesting that protein aggregates may be protective in Pmp22-associated peripheral neuropathy

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

The POU proteins Brn-2 and Oct-6 share important functions in Schwann cell development

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

The origin and development of glial cells in peripheral nerves

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

The peripheral myelin protein 22 and epithelial membrane protein family

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Identification of multiple proteins expressed in murine embryos as binding partners for the WW domains of the ubiquitin-protein ligase Nedd4

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Dominant intermediate Charcot-Marie-Tooth type C maps to chromosome 1p34-p35

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Neural crest stem cells undergo multilineage differentiation in developing peripheral nerves to generate endoneurial fibroblasts in addition to Schwann cells

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Curcumin treatment abrogates endoplasmic reticulum retention and aggregation-induced apoptosis associated with neuropathy-causing myelin protein zero-truncating mutants.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Regulation of myotubularin-related (MTMR)2 phosphatidylinositol phosphatase by MTMR5, a catalytically inactive phosphatase

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

The Pleckstrin Homology Domains of Dynamin Isoforms Require Oligomerization for High Affinity Phosphoinositide Binding

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Myelin protein zero: mutations in the cytoplasmic domain interfere with its cellular trafficking

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Myotubularins, a large disease-associated family of cooperating catalytically active and inactive phosphoinositides phosphatases

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Analysis of congenital hypomyelinating Egr2Lo/Lo nerves identifies Sox2 as an inhibitor of Schwann cell differentiation and myelination

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Direct regulation of myelin protein zero expression by the Egr2 transactivator

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Regulation of cholesterol/lipid biosynthetic genes by Egr2/Krox20 during peripheral nerve myelination

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Tamoxifen-inducible glia-specific Cre mice for somatic mutagenesis in oligodendrocytes and Schwann cells

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Recessive, but not dominant, mutations in peripheral myelin protein 22 gene show unique patterns of aggregation and intracellular trafficking.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

WWOX binds the specific proline-rich ligand PPXY: identification of candidate interacting proteins

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Impaired differentiation of Schwann cells in transgenic mice with increased PMP22 gene dosage

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Distinct elements of the peripheral myelin protein 22 (PMP22) promoter regulate expression in Schwann cells and sensory neurons

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

P0-deficient knockout mice as tools to understand pathomechanisms in Charcot-Marie-Tooth 1B and P0-related Déjérine-Sottas syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Immune-mediated components of hereditary demyelinating neuropathies: lessons from animal models and patients

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

https://api.crossref.org/works/10.1002%2FGLIA.20386

1 reference

7 January 2021

Early onset neuropathy in a compound form of Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Connexin32-containing gap junctions in Schwann cells at the internodal zone of partial myelin compaction and in Schmidt-Lanterman incisures

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Axonal neuregulin-1 regulates myelin sheath thickness

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Phosphatidylinositol 3,5-bisphosphate: metabolism and cellular functions

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Mycobacterium bovis Bacillus Calmette-Guerin and its cell wall complex induce a novel lysosomal membrane protein, SIMPLE, that bridges the missing link between lipopolysaccharide and p53-inducible gene, LITAF(PIG7), and estrogen-inducible gene, EET-1

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Aberrant protein trafficking in Trembler suggests a disease mechanism for hereditary human peripheral neuropathies

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Impaired intracellular trafficking is a common disease mechanism of PMP22 point mutations in peripheral neuropathies

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

EGR2 mutations in inherited neuropathies dominant-negatively inhibit myelin gene expression.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Mutations in GDAP1: autosomal recessive CMT with demyelination and axonopathy

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Altered molecular architecture of peripheral nerves in mice lacking the peripheral myelin protein 22 or connexin32

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Pathomechanisms of mutant proteins in Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: new implications for Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Uncoupling of myelin assembly and schwann cell differentiation by transgenic overexpression of peripheral myelin protein 22

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Peripheral myelin protein 22 is a constituent of intercellular junctions in epithelia

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

PMP22 accumulation in aggresomes: implications for CMT1A pathology

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Upregulation of the endosomal-lysosomal pathway in the trembler-J neuropathy.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Ndrg1-deficient mice exhibit a progressive demyelinating disorder of peripheral nerves

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Neurons promote the translocation of peripheral myelin protein 22 into myelin

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Krox-20 inhibits Jun-NH2-terminal kinase/c-Jun to control Schwann cell proliferation and death

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Ascorbic acid treatment corrects the phenotype of a mouse model of Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

GDAP1, the protein causing Charcot-Marie-Tooth disease type 4A, is expressed in neurons and is associated with mitochondria

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Protein zero gene expression is regulated by the glial transcription factor Sox10

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Induced myelination and demyelination in a conditional mouse model of Charcot-Marie-Tooth disease type 1A.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Phenotypic analysis of neurofilament light gene mutations linked to Charcot-Marie-Tooth disease in cell culture models

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

The local differentiation of myelinated axons at nodes of Ranvier

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

The dynamin superfamily: universal membrane tubulation and fission molecules?

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Epitope-tagged P(0) glycoprotein causes Charcot-Marie-Tooth-like neuropathy in transgenic mice.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

The phosphoinositide-3-phosphatase MTMR2 associates with MTMR13, a membrane-associated pseudophosphatase also mutated in type 4B Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Ubiquitination and endocytosis of plasma membrane proteins: role of Nedd4/Rsp5p family of ubiquitin-protein ligases

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Modulation of epithelial morphology, monolayer permeability, and cell migration by growth arrest specific 3/peripheral myelin protein 22

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

The temporospatial expression of peripheral myelin protein 22 at the developing blood-nerve and blood-brain barriers

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Pathology of a mouse mutation in peripheral myelin protein P0 is characteristic of a severe and early onset form of human Charcot-Marie-Tooth type 1B disorder

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Aggresome formation in neuropathy models based on peripheral myelin protein 22 mutations

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

NT-3 promotes nerve regeneration and sensory improvement in CMT1A mouse models and in patients

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

SIMPLE mutations in Charcot-Marie-Tooth disease and the potential role of its protein product in protein degradation

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Unique role of dystroglycan in peripheral nerve myelination, nodal structure, and sodium channel stabilization

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Central Nervous System Involvement in Hereditary Neuropathy With Liability to Pressure Palsies

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Regulation of Schwann cell proliferation and apoptosis in PMP22-deficient mice and mouse models of Charcot-Marie-Tooth disease type 1A.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Transgenic expression of human connexin32 in myelinating Schwann cells prevents demyelination in connexin32-null mice

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Connexin32-null mice develop demyelinating peripheral neuropathy

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathy

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot-Marie-Tooth neuropathy type 4B2/11p15.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

A transgenic rat model of Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Therapeutic administration of progesterone antagonist in a model of Charcot-Marie-Tooth disease (CMT-1A).

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Phenotypic differences between peripheral myelin protein-22 (PMP22) and myelin protein zero (P0) mutations associated with Charcot-Marie-Tooth-related diseases

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Crystal structure of the extracellular domain from P0, the major structural protein of peripheral nerve myelin

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Mechanisms of axon ensheathment and myelin growth

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Specific disruption of a schwann cell dystrophin-related protein complex in a demyelinating neuropathy

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

SIMPLE interacts with NEDD4 and TSG101: evidence for a role in lysosomal sorting and implications for Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Peripheral neuropathies caused by mutations in the myelin protein zero

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Phenotypic clustering in MPZ mutations

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Characterization of a novel peripheral nervous system myelin protein (PMP-22/SR13)

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

The unfolded protein response modulates disease severity in Pelizaeus-Merzbacher disease.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Association of N-myc downregulated gene 1 with heat-shock cognate protein 70 in mast cells

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouse

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Disease mechanisms in inherited neuropathies

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Biology and Genetics of Hereditary Motor and Sensory Neuropathies

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Trembler mouse carries a point mutation in a myelin gene

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Charcot-Marie-Tooth disease and related hereditary polyneuropathies: molecular diagnostics determine aspects of medical management

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Conditional, floxed allele of the Krox20 gene.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Periaxin mutations cause a broad spectrum of demyelinating neuropathies.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Neuregulin-1 type III determines the ensheathment fate of axons

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Dynamin 2 binds gamma-tubulin and participates in centrosome cohesion

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Differential aggregation of the Trembler and Trembler J mutants of peripheral myelin protein 22

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Krox-20 controls myelination in the peripheral nervous system

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Altered expression of ion channel isoforms at the node of Ranvier in P0-deficient myelin mutants.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Claudins and epithelial paracellular transport

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

From stem cells to neurons and glia: a Soxist's view of neural development

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

PTEN and myotubularin phosphatases: from 3-phosphoinositide dephosphorylation to disease

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Different Intracellular Pathomechanisms Produce Diverse Myelin Protein Zero Neuropathies in Transgenic Mice

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

P(0) glycoprotein overexpression causes congenital hypomyelination of peripheral nerves

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Schwann cell myelination requires timely and precise targeting of P(0) protein

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Emerging pathways for hereditary axonopathies

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20386

7 January 2021

Identifiers

DOI

10.1002/GLIA.20386

1 reference

release_2x57l3ciirb7bjmogo3xwnan2y

14 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/2x57l3ciirb7bjmogo3xwnan2y

24 November 2022

mapped directly with Wikidata item

PubMed ID

16856148

1 reference

PubMed ID

16856148