(Q57650102)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16495463%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

title

Different intracellular pathomechanisms produce diverse Myelin Protein Zero neuropathies in transgenic mice (English)

1 reference

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17 January 2020

3

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17 January 2020

Pietro Fratta

6

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17 January 2020

Stefano C. Previtali

8

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17 January 2020

Daniel A Kirschner

13

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17 January 2020

Angelo Quattrini

16

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17 January 2020

1

Lawrence Wrabetz

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17 January 2020

15

M Laura Feltri

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17 January 2020

4

Gabriele Dati

1 reference

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17 January 2020

14

Albee Messing

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17 January 2020

11

Klaus Toyka

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17 January 2020

author name string

Maurizio D'Antonio

2

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17 January 2020

Elisa Tinelli

5

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17 January 2020

Daniele Imperiale

9

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17 January 2020

Jurgen Zielasek

10

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17 January 2020

Robin L Avila

12

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17 January 2020

language of work or name

English

0 references

publication date

1 February 2006

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17 January 2020

published in

Journal of Neuroscience

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17 January 2020

volume

26

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17 January 2020

page(s)

2358-2368

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17 January 2020

issue

8

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A novel P0 glycoprotein transgene activates expression of lacZ in myelin-forming Schwann cells

17 January 2020

cites work

1 reference

12 December 2020

Loss of distal axons and sensory Merkel cells and features indicative of muscle denervation in hindlimbs of P0-deficient mice

1 reference

12 December 2020

PMP22 accumulation in aggresomes: implications for CMT1A pathology

1 reference

12 December 2020

Genetic analysis of myelin galactolipid function.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Regulation of eukaryotic initiation factor eIF2B.

1 reference

12 December 2020

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

1 reference

12 December 2020

Transcriptional and translational control in the Mammalian unfolded protein response

1 reference

12 December 2020

Molecular analysis in Japanese patients with Charcot-Marie-Tooth disease: DGGE analysis for PMP22, MPZ, and Cx32/GJB1 mutations

1 reference

12 December 2020

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

1 reference

12 December 2020

Disease mechanisms in inherited neuropathies

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12 December 2020

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

1 reference

12 December 2020

Age-dependent changes in the oligosaccharide structure of the major myelin glycoprotein, P0

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

Phenotypic clustering in MPZ mutations

1 reference

12 December 2020

A trip to the ER: coping with stress

1 reference

12 December 2020

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

12 December 2020

XBP1: a link between the unfolded protein response, lipid biosynthesis, and biogenesis of the endoplasmic reticulum.

1 reference

12 December 2020

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

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Endoplasmic reticulum stress modulates the response of myelinating oligodendrocytes to the immune cytokine interferon-gamma

1 reference

12 December 2020

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

1 reference

12 December 2020

Protein zero of peripheral nerve myelin: biosynthesis, membrane insertion, and evidence for homotypic interaction.

1 reference

12 December 2020

Role of myelin Po protein as a homophilic adhesion molecule

1 reference

12 December 2020

Membrane structure in isolated and intact myelins

1 reference

12 December 2020

Membrane interactions in nerve myelin. I. Determination of surface charge from effects of pH and ionic strength on period.

1 reference

12 December 2020

The hypertrophic forms of hereditary motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN type III) in childhood

1 reference

12 December 2020

A C-terminal signal prevents secretion of luminal ER proteins

1 reference

12 December 2020

Compact myelin exists in the absence of basic protein in the shiverer mutant mouse

1 reference

12 December 2020

De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)

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

Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot-Marie-Tooth disease type 1B

1 reference

12 December 2020

Uniform slowing of conduction velocities in Charcot-Marie-Tooth polyneuropathy type 1

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

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

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

Dominant-negative effect on adhesion by myelin Po protein truncated in its cytoplasmic domain

1 reference

12 December 2020

Beta 4 integrin and other Schwann cell markers in axonal neuropathy

1 reference

12 December 2020

Inherited demyelinating peripheral neuropathies: relating myelin packing abnormalities to P0 molecular defects

1 reference

12 December 2020

Myelin Po protein mutated at Cys21 has a dominant-negative effect on adhesion of wild type Po.

1 reference

12 December 2020

10.1523/JNEUROSCI.3819-05.2006

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16495463%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

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17 January 2020

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