(Q73382782)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9169527%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9169527%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference

K Adlkofer

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9169527%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

R Frei

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9169527%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

D H Neuberg

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9169527%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

J Zielasek

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9169527%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

K V Toyka

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9169527%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

U Suter

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9169527%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

publication date

1 June 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9169527%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

published in

Journal of Neuroscience

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9169527%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

volume

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9169527%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

issue

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9169527%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

page(s)

4662-4671

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9169527%20AND%20SRC:MED&resulttype=core&format=json

Hereditary compression syndrome of peripheral nerves.

3 November 2019

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

Enhanced expression of the extracellular matrix molecule J1/tenascin in the regenerating adult mouse sciatic nerve

1 reference

12 December 2020

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

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

Long-lasting conduction block in hereditary neuropathy with liability to pressure palsies

1 reference

12 December 2020

Myelin: keeping nerves well wrapped up

1 reference

12 December 2020

Ultrastructural PMP22 expression in inherited demyelinating neuropathies

1 reference

12 December 2020

New functions for gap junctions

1 reference

12 December 2020

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

1 reference

12 December 2020

HEREDITARY NEUROPATHY, WITH LIABILITY TO PRESSURE PALSIES; A CLINICAL AND ELECTROPHYSIOLOGICAL STUDY OF FOUR FAMILIES

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

Recurrent peripheral nerve palsies in a family

1 reference

12 December 2020

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

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

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

1 reference

12 December 2020

Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletion

1 reference

12 December 2020

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

1 reference

12 December 2020

Conduction block in hereditary neuropathy with susceptibility to pressure palsies

1 reference

12 December 2020

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

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

Hereditary neuropathy with liability to pressure palsies. Report of two families and review of the literature

1 reference

12 December 2020

Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination

1 reference

12 December 2020

Tomaculous neuropathy in chromosome 1 Charcot-Marie-Tooth syndrome

1 reference

12 December 2020

A transgenic rat model of Charcot-Marie-Tooth disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Tomaculous neuropathy: a clinical and electrophysiological study in patients with and without 1.5-Mb deletions in chromosome 17p11.2.

1 reference

12 December 2020

The number of Schmidt-Lanterman incisures is more than doubled in shiverer PNS myelin sheaths.

1 reference

12 December 2020

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

1 reference

12 December 2020

1 reference

12 December 2020

Functional abnormalities in P0-deficient mice resemble human hereditary neuropathies linked to P0 gene mutations

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

Genetic and clinical aspects of Charcot-Marie-Tooth's disease

1 reference

12 December 2020

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

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

B4B, a novel growth-arrest gene, is expressed by a subset of progenitor/pre-B lymphocytes negative for cytoplasmic mu-chain.

1 reference

12 December 2020

Crucial role for the myelin-associated glycoprotein in the maintenance of axon-myelin integrity

1 reference

12 December 2020

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

1 reference

12 December 2020

Trembler mouse carries a point mutation in a myelin gene

1 reference

12 December 2020

10.1523/JNEUROSCI.17-12-04662.1997

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9169527%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9169527%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

PubMed publication ID

9169527

1 reference