Neurons promote the translocation of peripheral myelin protein 22 into myelin (Q57042849)

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6 November 2019

title

Neurons promote the translocation of peripheral myelin protein 22 into myelin (English)

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6 November 2019

9

E M Shooter

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6 November 2019

author name string

S Pareek

1

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6 November 2019

L Notterpek

2

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G J Snipes

3

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R Naef

4

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W Sossin

5

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J Laliberté

6

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S Iacampo

7

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U Suter

8

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R A Murphy

10

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6 November 2019

language of work or name

English

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publication date

1 October 1997

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6 November 2019

published in

Journal of Neuroscience

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6 November 2019

volume

17

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issue

20

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6 November 2019

page(s)

7754-7762

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

6 November 2019

cites work

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

Studies on cultured rat Schwann cells. I. Establishment of purified populations from cultures of peripheral nerve

1 reference

12 December 2020

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

1 reference

12 December 2020

Axonal regulation of Schwann cell integrin expression suggests a role for alpha 6 beta 4 in myelination.

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

Role of axons in the regulation of PO biosynthesis by Schwann cells

1 reference

12 December 2020

Regulation of myelination: Schwann cell transition from a myelin-maintaining state to a quiescent state after permanent nerve transection

1 reference

12 December 2020

Assembly of asparagine-linked oligosaccharides

1 reference

12 December 2020

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

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

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

1 reference

12 December 2020

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

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

Regulation of Myelination: Biosynthesis of the Major Myelin Glycoprotein by Schwann Cells in the Presence and Absence of Myelin Assembly

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

Molecular anatomy and genetics of myelin proteins in the peripheral nervous system

1 reference

12 December 2020

Catabolic regulation of the expression of the major myelin glycoprotein by Schwann cells in culture

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

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

1 reference

12 December 2020

Two pathways for the degradation of the H2 subunit of the asialoglycoprotein receptor in the endoplasmic reticulum

1 reference

12 December 2020

Kin recognition between medial Golgi enzymes in HeLa cells.

1 reference

12 December 2020

Lysosomal delivery of the major myelin glycoprotein in the absence of myelin assembly: posttranslational regulation of the level of expression by Schwann cells

1 reference

12 December 2020

A transgenic rat model of Charcot-Marie-Tooth disease

1 reference

12 December 2020

Axons regulate Schwann cell expression of the major myelin and NGF receptor genes

1 reference

12 December 2020

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

1 reference

12 December 2020

Progesterone synthesis and myelin formation by Schwann cells

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

An alternatively spliced miniexon alters the subcellular fate of the human asialoglycoprotein receptor H2 subunit. Endoplasmic reticulum retention and degradation or cell surface expression.

1 reference

12 December 2020

Isolation and partial characterization of rat CNS axolemma enriched fractions

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

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

1 reference

12 December 2020

Endoplasmic reticulum degradation of a subunit of the asialoglycoprotein receptor in vitro. Vesicular transport from endoplasmic reticulum is unnecessary

1 reference

12 December 2020

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

1 reference

12 December 2020

Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

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

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

1 reference

12 December 2020

Myelin genes: getting the dosage right

1 reference

12 December 2020

Protein measurement with the Folin phenol reagent

1 reference

12 December 2020

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

1 reference

12 December 2020

Role of potentially charged transmembrane residues in targeting proteins for retention and degradation within the endoplasmic reticulum

1 reference

12 December 2020

Trembler mouse carries a point mutation in a myelin gene

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1523/JNEUROSCI.17-20-07754.1997

Identifiers

DOI

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6 November 2019

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6 November 2019

PubMed publication ID

9315897

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