(Q71396545)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8757248%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

title

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

1 reference

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18 October 2019

0 references

2

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15 May 2020

author name string

J P Magyar

1

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15 May 2020

T Ruelicke

3

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15 May 2020

A Aguzzi

4

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15 May 2020

K Adlkofer

5

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15 May 2020

Z Dembic

6

1 reference

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15 May 2020

J Zielasek

7

1 reference

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15 May 2020

K V Toyka

8

1 reference

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15 May 2020

U Suter

9

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15 May 2020

publication date

1 September 1996

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18 October 2019

published in

Journal of Neuroscience

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15 May 2020

volume

16

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15 May 2020

issue

17

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15 May 2020

page(s)

5351-5360

1 reference

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Expression and functional roles of neural cell surface molecules and extracellular matrix components during development and regeneration of peripheral nerves

15 May 2020

cites work

1 reference

12 December 2020

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

1 reference

12 December 2020

The role of macrophages and eicosanoids in the pathogenesis of experimental allergic neuritis. Serial clinical, electrophysiological, biochemical and morphological observations

1 reference

12 December 2020

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

1 reference

12 December 2020

Charcot-Marie-Tooth Disease Type 1A -- Association with a Spontaneous Point Mutation in the PMP22 Gene

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Biology and Genetics of Hereditary Motor and Sensory Neuropathies

1 reference

12 December 2020

Linkage between axonal ensheathment and basal lamina production by Schwann cells

1 reference

12 December 2020

Disruption of Krox-20 results in alteration of rhombomeres 3 and 5 in the developing hindbrain

1 reference

12 December 2020

Monoclonal antibody to 5-bromo- and 5-iododeoxyuridine: A new reagent for detection of DNA replication

1 reference

12 December 2020

Peripheral myelin protein 22: facts and hypotheses

1 reference

12 December 2020

Detection and processing of peripheral myelin protein PMP22 in cultured Schwann cells

1 reference

12 December 2020

Hereditary demyelinating neuropathy in the Trembler mouse

1 reference

12 December 2020

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

1 reference

12 December 2020

Mice deficient for the myelin-associated glycoprotein show subtle abnormalities in myelin.

1 reference

12 December 2020

Nerve grafts in the Trembler mouse. An electrophysiological and histological study

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I)

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Krox-20 controls myelination in the peripheral nervous system

1 reference

12 December 2020

Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice

1 reference

12 December 2020

DNA deletion associated with hereditary neuropathy with liability to pressure palsies

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Homozygous expression of a dominant gene for charcot-marie-tooth neuropathy

1 reference

12 December 2020

P0 promoter directs expression of reporter and toxin genes to Schwann cells of transgenic mice.

1 reference

12 December 2020

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

1 reference

12 December 2020

Muscle and intramuscular nerve pathology in congenital hypomyelination neuropathy

1 reference

12 December 2020

Axon-regulated expression of a Schwann cell transcript that is homologous to a 'growth arrest-specific' gene

1 reference

12 December 2020

A transgenic rat model of Charcot-Marie-Tooth disease

1 reference

12 December 2020

Evidence for a recessive PMP22 point mutation in Charcot–Marie–Tooth disease type 1A

1 reference

12 December 2020

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

1 reference

12 December 2020

Regulation of tissue-specific expression of alternative peripheral myelin protein-22 (PMP22) gene transcripts by two promoters

1 reference

12 December 2020

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

1 reference

12 December 2020

A myelin protein is encoded by the homologue of a growth arrest-specific gene

1 reference

12 December 2020

Inactivation of the N-CAM gene in mice results in size reduction of the olfactory bulb and deficits in spatial learning.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

12 December 2020

Schwann cell precursors and their development

1 reference

12 December 2020

A combination of PLP and DM20 transgenes promotes partial myelination in the jimpy mouse

1 reference

12 December 2020

Genetic basis of inherited peripheral neuropathies.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Trembler mouse carries a point mutation in a myelin gene

1 reference

12 December 2020

10.1523/JNEUROSCI.16-17-05351.1996

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6578876&resulttype=core&format=json

15 May 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6578876&resulttype=core&format=json

15 May 2020

1 reference