The anatomy and cell biology of peripheral myelin protein-22. (Q33787330)

29 July 2017

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title

The anatomy and cell biology of peripheral myelin protein-22. (English)

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29 July 2017

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Snipes GJ

1

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29 July 2017

Orfali W

2

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29 July 2017

Fraser A

3

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29 July 2017

Dickson K

4

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29 July 2017

Colby J

5

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29 July 2017

language of work or name

English

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publication date

1 September 1999

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Annals of the New York Academy of Sciences

29 July 2017

published in

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29 July 2017

volume

883

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29 July 2017

page(s)

143-151

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

29 July 2017

cites work

1 reference

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21 January 2018

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Genes specifically expressed at growth arrest of mammalian cells

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Functional glycoproteins expressed in Schwann cell membrane

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

21 January 2018

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Trembler mouse carries a point mutation in a myelin gene

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A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouse

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Immunoreactivity of PMP-22, P0, and other 19 to 28 kDa glycoproteins in peripheral nerve myelin of mammals and fish with HNK1 and related antibodies

21 January 2018

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

21 January 2018

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Biology and Genetics of Hereditary Motor and Sensory Neuropathies

21 January 2018

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Quality control in the secretory pathway

21 January 2018

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The transient association of ERp57 with N-glycosylated proteins is regulated by glucose trimming

21 January 2018

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Protein folding stability can determine the efficiency of escape from endoplasmic reticulum quality control

21 January 2018

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Inhibition of glucose trimming with castanospermine reduces calnexin association and promotes proteasome degradation of the alpha-subunit of the nicotinic acetylcholine receptor

21 January 2018

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Connexin46 is retained as monomers in a trans-Golgi compartment of osteoblastic cells

21 January 2018

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The neuron-specific kinesin superfamily protein KIF1A is a unique monomeric motor for anterograde axonal transport of synaptic vesicle precursors

21 January 2018

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

21 January 2018

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Ultrastructural PMP22 expression in inherited demyelinating neuropathies

21 January 2018

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

21 January 2018

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10.1111/J.1749-6632.1999.TB08577.X

21 January 2018

Identifiers

DOI

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29 July 2017

1 reference