(Q39152094)

9 September 2017

title

Prions disturb post-Golgi trafficking of membrane proteins (English)

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9 September 2017

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1 reference

Keiji Uchiyama

1

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9 September 2017

Naomi Muramatsu

2

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9 September 2017

Masashi Yano

3

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9 September 2017

Takeshi Usui

4

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9 September 2017

Hironori Miyata

5

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9 September 2017

Suehiro Sakaguchi

6

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9 September 2017

language of work or name

English

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publication date

1 January 2013

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9 September 2017

published in

Nature Communications

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9 September 2017

volume

4

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9 September 2017

page(s)

1846

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https://scigraph.springernature.com/pub.10.1038/ncomms2873

9 September 2017

exact match

0 references

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Mice devoid of PrP are resistant to scrapie

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Fragmentation of the Golgi apparatus in neurodegenerative diseases and cell death

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

A Golgi fragmentation pathway in neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Proteasome inhibitors promote the sequestration of PrPSc into aggresomes within the cytosol of prion-infected CAD neuronal cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Visualization of prion infection in transgenic mice expressing green fluorescent protein-tagged prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

A transmembrane form of the prion protein in neurodegenerative disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Transmissible and genetic prion diseases share a common pathway of neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Neurodegenerative illness in transgenic mice expressing a transmembrane form of the prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Insulin and insulin-like growth factor receptors in the nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Insulin and insulin-like growth factor-1 regulate tau phosphorylation in cultured human neurons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Insulin inhibits amyloid beta-induced cell death in cultured human brain pericytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Does insulin dysfunction play a role in Alzheimer's disease?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Insulin and cholesterol pathways in neuronal function, memory and neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Attractin/mahogany/zitter plays a critical role in myelination of the central nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Effects of a brain-engraftable microglial cell line expressing anti-prion scFv antibodies on survival times of mice infected with scrapie prions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

A distinct trans-Golgi network subcompartment for sorting of synaptic and granule proteins in neurons and neuroendocrine cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Characterization of intracellular localization of PrP(Sc) in prion-infected cells using a mAb that recognizes the region consisting of aa 119-127 of mouse PrP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Getting a grip on Thy-1 signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Differential distribution of glutamate receptors in the cochlear nuclei

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Prion protein is necessary for normal synaptic function

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Spongiform degeneration in mahoganoid mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Functional depletion of mahogunin by cytosolically exposed prion protein contributes to neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Inhibition of Golgi apparatus glycosylation causes endoplasmic reticulum stress and decreased protein synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Caspase-12 and endoplasmic reticulum stress mediate neurotoxicity of pathological prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

The disulfide isomerase Grp58 is a protective factor against prion neurotoxicity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Cryo-immunogold electron microscopy for prions: toward identification of a conversion site

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Transport at the recycling endosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

The regulation of endosome-to-Golgi retrograde transport by tethers and scaffolds.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Mutant prion protein expression is associated with an alteration of the Rab GDP dissociation inhibitor alpha (GDI)/Rab11 pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Prion strain-dependent differences in conversion of mutant prion proteins in cell culture

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Dynamin II is involved in endocytosis but not in the formation of transport vesicles from the trans-Golgi network

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Mutants of vesicular stomatitis virus blocked at different stages in maturation of the viral glycoprotein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

A Transmembrane Form of the Prion Protein Is Localized in the Golgi Apparatus of Neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Altered circadian activity rhythms and sleep in mice devoid of prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2873

Mitogenically uncoupled insulin and IGF-I receptors of differentiated human neuroblastoma cells are functional and mediate ligand-induced signals

21 January 2018

1 reference

12 December 2020

In vivo regulation of cell death by embryonic (pro)insulin and the insulin receptor during early retinal neurogenesis.

1 reference

12 December 2020

A mouse prion protein transgene rescues mice deficient for the prion protein gene from purkinje cell degeneration and demyelination

1 reference

12 December 2020

PrP gene dosage determines the timing but not the final intensity or distribution of lesions in scrapie pathology

1 reference

12 December 2020

Accumulation of proteinase K-resistant prion protein (PrP) is restricted by the expression level of normal PrP in mice inoculated with a mouse-adapted strain of the Creutzfeldt-Jakob disease agent

1 reference

12 December 2020

Phosphatidylinositol 3-kinase-mediated regulation of neuronal apoptosis and necrosis by insulin and IGF-I.

1 reference

12 December 2020

Identifiers

DOI

10.1038/NCOMMS2873

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Dimensions Publication ID

9 September 2017

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1014705445

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1 reference