(Q33851812)

29 July 2017

1 reference

title

The peripheral myelin protein 22 and epithelial membrane protein family (English)

1 reference

29 July 2017

1 reference

1 reference

Jetten AM

1

1 reference

29 July 2017

Suter U

series ordinal

2

1 reference

29 July 2017

publication date

1 January 2000

1 reference

Progress in Molecular Biology and Translational Science

29 July 2017

published in

1 reference

29 July 2017

volume

64

1 reference

29 July 2017

page(s)

97-129

1 reference

Characterization of novel complexes on the cell surface between integrins and proteins with 4 transmembrane domains (TM4 proteins).

29 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Myelin and lymphocyte protein (MAL/MVP17/VIP17) and plasmolipin are members of an extended gene family

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

A growth arrest-specific (gas) gene codes for a membrane protein

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Identification and characterization of a novel squamous cell-associated gene related to PMP22

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Epithelial membrane protein-1, peripheral myelin protein 22, and lens membrane protein 20 define a novel gene family

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Characterization of a tumor-associated gene, a member of a novel family of genes encoding membrane glycoproteins

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Epithelial membrane protein-2 and epithelial membrane protein-3: two novel members of the peripheral myelin protein 22 gene family

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

The human lens fiber-cell intrinsic membrane protein MP19 gene: isolation and sequence analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Peripheral myelin protein 22: facts and hypotheses

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

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/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Retroviral-mediated gene transfer of the peripheral myelin protein PMP22 in Schwann cells: modulation of cell growth

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Coexpression of PMP22 gene with MBP and P0 during de novo myelination and nerve repair

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

The genetics of myelin

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

SR13/PMP-22 expression in rat nervous system, in PC12 cells, and C6 glial cell lines.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Ins and outs of peripheral myelin protein-22: mapping transmembrane topology and intracellular sorting

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Progress in the molecular understanding of hereditary peripheral neuropathies reveals new insights into the biology of the peripheral nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Genetic basis of inherited peripheral neuropathies.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Molecular genetics of Charcot-Marie-Tooth neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Charcot-Marie-Tooth disease: a new paradigm for the mechanism of inherited disease

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Biology and Genetics of Hereditary Motor and Sensory Neuropathies

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

The biology and pathobiology of Schwann cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Pathogenesis of Charcot-Marie-Tooth 1A (CMT1A) neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Hereditary neuropathy with liability to pressure palsies: a patient's point mutation in a mouse model

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Development of onion bulb neuropathy in the Trembler mouse. Comparison with normal nerve maturation

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Hereditary demyelinating neuropathy in the Trembler mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Trembler mouse carries a point mutation in a myelin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Comparison of Trembler and Trembler-J mouse phenotypes: varying severity of peripheral hypomyelination

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

A transgenic rat model of Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

A transgenic mouse model for human hereditary neuropathy with liability to pressure palsies

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

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/10.1016%2FS0079-6603%2800%2964003-5

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/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

cDNA cloning, genomic structure, and chromosome mapping of the human epithelial membrane protein CL-20 gene (EMP1), a member of the PMP22 family

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Isolation and sequence determination of cDNA encoding PMP-22 (PAS-II/SR13/Gas-3) of human peripheral myelin

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Isolation and mapping to 17p12-13 of the human homologous of the murine growth arrest specific Gas-3 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Sequence of human GAS3/PMP22 full-length cDNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Purification of PASII/PMP22--an extremely hydrophobic glycoprotein of PNS myelin membrane

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Purification and partial characterization of two glycoproteins in bovine peripheral nerve myelin membrane

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Genes specifically expressed at growth arrest of mammalian cells

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Regulation of expression of growth arrest-specific genes in mouse fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Long lives for homozygous trembler mutant mice despite virtual absence of peripheral nerve myelin

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Widespread expression of the peripheral myelin protein-22 gene (PMP22) in neural and non-neural tissues during murine development

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Identification and characterization of a cDNA and the structural gene encoding the mouse epithelial membrane protein-1

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Distribution of PASII/PMP22 and connexin 32 proteins in the peripheral nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Ultrastructural distribution of PMP22 in Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Identification of transcriptionally regulated genes after sciatic nerve injury.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Molecular Biology of Axon–Glia Interactions in the Peripheral Nervous System1

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Peripheral myelin protein-22 is expressed in rat and mouse brain and spinal cord motoneurons

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

PMP-22 expression in the central nervous system of the embryonic mouse defines potential transverse segments and longitudinal columns

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

The growth arrest genes gas5, gas6, and CHOP-10 (gadd153) are expressed in the mouse preimplantation embryo

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

HNMP-1: a novel hematopoietic and neural membrane protein differentially regulated in neural development and injury.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Neurons promote the translocation of peripheral myelin protein 22 into myelin

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Human peripheral myelin protein-22 carries the L2/HNK-1 carbohydrate adhesion epitope

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

The L2/HNK-1 carbohydrate of neural cell adhesion molecules is involved in cell interactions

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Glycans and the modulation of neural-recognition molecule function.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Occurrence of the HNK-1 epitope (3-sulfoglucuronic acid) in PC12 pheochromocytoma cells, chromaffin granule membranes, and chondroitin sulfate proteoglycans

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

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/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Assignment of the lens intrinsic membrane protein MP19 structural gene to human chromosome 19

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Isolation and characterization of a novel oligodendrocyte-specific protein

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Oligodendrocyte-specific protein (OSP) is a major component of CNS myelin

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Cloning and expression of a major rat lens membrane protein, MP20.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Regional localization of rat peripheral myelin protein 22 (Pmp22) gene to Chromosome 10q22 by FISH

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Localization of growth arrest-specific genes on mouse chromosomes 1, 7, 8, 11, 13, and 16.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Chromosomal mapping of Tmp (Emp1), Xmp (Emp2), and Ymp (Emp3), genes encoding membrane proteins related to Pmp22.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Oct-6 (SCIP/Tst-1) is expressed in Schwann cell precursors, embryonic Schwann cells, and postnatal myelinating Schwann cells: comparison with Oct-1, Krox-20, and Pax-3.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Progesterone synthesis and myelin formation by Schwann cells

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Progesterone stimulates the activity of the promoters of peripheral myelin protein-22 and protein zero genes in Schwann cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Mutation analysis of the nerve specific promoter of the peripheral myelin protein 22 gene in CMT1 disease and HNPP.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Expression of growth arrest-specific (gas) genes in senescent murine cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Influence of elevated expression of rat wild-type PMP22 and its mutant PMP22Trembler on cell growth of NIH3T3 fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Improved culture methods to expand Schwann cells with altered growth behaviour from CMT1A patients

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Fate of Schwann cells in CMT1A and HNPP: evidence for apoptosis

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Schwann cell differentiation in Charcot-Marie-Tooth disease type 1A (CMT1A): normal number of myelinating Schwann cells in young CMT1A patients and neural cell adhesion molecule expression in onion bulbs

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Cloning and regulation of cornifin beta, a new member of the cornifin/spr family. Suppression by retinoic acid receptor-selective retinoids.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Regulation of proliferation-specific and differentiation-specific genes during senescence of human epidermal keratinocyte and mammary epithelial cells

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Many facets of the peripheral myelin protein PMP22 in myelination and disease

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Differentially expressed genes after peripheral nerve injury

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Molecular approaches to nerve regeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Onion bulb neuropathy in the trembler mouse: A model of hypertrophic interstitial neuropathy (Dejerine-Sottas) in man

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Animal models of peripheral neuropathy: The trembler mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Dejerine-Sottas neuropathy in mother and son with same point mutation of PMP22 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

The phenotypic manifestations of chromosome 17p11.2 duplication.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Clinical variability in two pairs of identical twins with the Charcot-Marie-Tooth disease type 1A duplication

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Charcot-Marie-Tooth disease type 1A: morphological phenotype of the 17p duplication versus PMP22 point mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Trisomy 17p associated with Charcot-Marie-Tooth neuropathy type 1A phenotype: evidence for gene dosage as a mechanism in CMT1A

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Hereditary demyelinating neuropathy of infancy. A genetically complex syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

De-novo mutation in hereditary motor and sensory neuropathy type I.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

DNA deletion associated with hereditary neuropathy with liability to pressure palsies

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Origin of the de novo duplication in Charcot — Marie — Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Fine mapping of de novo CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Sex-dependent rearrangements resulting in CMT1A and HNPP.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Clinical, genetic and electrophysiologic correlation in hereditary neuropathy with liability to pressure palsies with involvement of PMP22 gene at chromosome 17p11.2

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Molecular basis of common hereditary motor and sensory neuropathies in humans and in mouse models

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsies

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsies

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Gene dosage effects in hereditary peripheral neuropathy. Expression of peripheral myelin protein 22 in Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies nerve biopsies

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Peripheral myelin protein-22 expression in Charcot-Marie-Tooth disease type 1a sural nerve biopsies

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

PMP22 expression in CMT1a neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Correlation between PMP-22 messenger mRNA expression and phenotype in hereditary neuropathy with liability to pressure palsies

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Underexpression of messenger RNA for peripheral myelin protein 22 in hereditary neuropathy with liability to pressure palsies

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Elevated expression of messenger RNA for peripheral myelin protein 22 in biopsied peripheral nerves of patients with Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

PCR-based strategy for the diagnosis of hereditary neuropathy with liability to pressure palsies and Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Pregnancy after preimplantation genetic diagnosis for Charcot-Marie-Tooth disease type 1A.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Molecular specializations at nodes and paranodes in peripheral nerve

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Molecular genetics of demyelination: new wrinkles on an old membrane

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Expression of growth arrest-specific (Gas) genes in murine keratinocytes: Gas2 is specifically regulated

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Differential expression of two mRNA species indicates a dual function of peripheral myelin protein PMP22 in cell growth and myelination

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Effects of nutrient deprivation and differentiation on the expression of growth-arrest genes (gas and gadd) in F9 embryonal carcinoma cells

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Multiple molecular alterations in mouse lung tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Two new mutants, ‘trembler’ and ‘reeler’, with neurological actions in the house mouse (Mus musculus L.)

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

The murine mutation trembler-J: proof of semidominant expression by use of the linked vestigial tail marker

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Neurological actions caused by the mutant gene Trembler in the house mouse (Mus musculus, L.,) an investigation

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Hereditary neuromyotonia: a mouse model associated with deficiency or increased gene dosage of the PMP22 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Hereditary motor-sensory neuropathy and movement disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Neuromyotonia in hereditary motor neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Hereditary hypertrophic neuropathy in the trembler mouse. Part 1. Histopathological studies: light microscopy

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Development of onion bulb neuropathy in the Tremebler mouse. Morphometric study

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Hereditary hypertrophic neuropathy in the trembler mouse. Part 2. Histopathological studies: electron microscopy

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Schwann cell multiplication in Trembler mice

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

X-ray diffraction study of myelin structure in immature and mutant mice

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Abnormal myelination in transplanted Trembler mouse Schwann cells

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Expression of the exon 1A-containing PMP22 transcript is altered in the trembler mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Expression of the PMP-22 gene in Trembler mutant mice: comparison with the other myelin protein genes

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Pathways of incorporation of fatty acid into glycerolipids of the murine peripheral nervous system in vivo: alterations in the dysmyelinating mutant trembler mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Sphingolipid metabolic disorders in Trembler mouse peripheral nerves in vivo result from an abnormal substrate supply

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Expression of the ceramide galactosyltransferase gene during myelination of the mouse nervous system. Comparison with the genes encoding myelin basic proteins, choline kinase and CTP:phosphocholine cytidylyltransferase

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Cerebroside formation in the peripheral nervous system of normal and Trembler mice

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Modulation of the axonal microtubule cytoskeleton by myelinating Schwann cells

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Altered slow axonal transport and regeneration in a myelin-deficient mutant mouse: the trembler as an in vivo model for Schwann cell-axon interactions

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Local control of axonal properties by Schwann cells: neurofilaments and axonal transport in homologous and heterologous nerve grafts

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Morphogenesis of the node of Ranvier: co-clusters of ankyrin and ankyrin-binding integral proteins define early developmental intermediates.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Hypomyelination alters K+ channel expression in mouse mutants shiverer and Trembler

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Signaling pathways mediating axon--Schwann cell interactions

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

The axonal membrane protein Caspr, a homologue of neurexin IV, is a component of the septate-like paranodal junctions that assemble during myelination

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

A distinct pattern of trophic factor expression in myelin-deficient nerves of Trembler mice: implications for trophic support by Schwann cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

A novel PMP22 point mutation causing HNPP phenotype: studies on nerve xenografts

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Abnormal Schwann cell/axon interactions in the Trembler-J mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Distribution of P0 protein and the myelin-associated glycoprotein in peripheral nerves from Trembler mice

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Myelin-associated glycoprotein and other proteins in Trembler mice

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

An in-frame deletion in peripheral myelin protein-22 gene causes hypomyelination and cell death of the Schwann cells in the new Trembler mutant mice

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Animal models for inherited peripheral neuropathies.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

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/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Correlation between varying levels of PMP22 expression and the degree of demyelination and reduction in nerve conduction velocity in transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

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/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Inducible gene targeting in mice using the Cre/lox system

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Inducible and reversible gene expression with the rtTA system for the study of memory.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Advances in Charcot-Marie-Tooth disease research: cellular function of CMT-related proteins, transgenic animal models, and pathomechanisms. The European CMT Consortium

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Low affinity NGF receptor expression in CMT1A nerve biopsies of different disease stages.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Studies on the effects of altered PMP22 expression during myelination in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Major histocompatibility complex class II expression and macrophage responses in genetically proven Charcot-Marie-Tooth type 1 and hereditary neuropathy with liability to pressure palsies

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

The antibody repertoire in experimental allergic neuritis: evidence for PMP-22 as a novel neuritogen

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Induction of experimental autoimmune neuritis with peripheral myelin protein-22.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

Isolation of transcriptionally regulated sequences associated with neuronal and non-neuronal cell interactions

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

P0 protein in normal, trembler heterozygous/homozygous mice during active PNS myelination

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6603%2800%2964003-5

7 January 2021

10.1016/S0079-6603(00)64003-5

Identifiers

DOI

1 reference

29 July 2017

1 reference