(Q45304146)

11 December 2017

VCP/p97 in abnormal protein aggregates, cytoplasmic vacuoles, and cell death, phenotypes relevant to neurodegeneration (English)

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11 December 2017

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Hirabayashi M

1

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11 December 2017

Inoue K

2

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11 December 2017

Tanaka K

3

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11 December 2017

Nakadate K

4

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11 December 2017

Ohsawa Y

5

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11 December 2017

Kamei Y

6

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11 December 2017

Popiel AH

7

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11 December 2017

Sinohara A

8

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11 December 2017

Iwamatsu A

9

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11 December 2017

Kimura Y

10

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11 December 2017

Uchiyama Y

11

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11 December 2017

Hori S

12

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11 December 2017

Kakizuka A

13

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11 December 2017

1 October 2001

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Cell Death & Differentiation

11 December 2017

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11 December 2017

8

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11 December 2017

977-984

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11 December 2017

10

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https://scigraph.springernature.com/pub.10.1038/sj.cdd.4400907

11 December 2017

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cites work

Protein precipitation: a common etiology in neurodegenerative disorders?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Reexamination of granulovacuolar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Huntingtin localization in brains of normal and Huntington's disease patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Submicroscopic immunodetection of PrP in the brain of a patient with a new-variant of Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Transgenic mice in the study of polyglutamine repeat expansion diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Modeling human neurodegenerative diseases in Drosophila: on a wing and a prayer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Structure and replication of yeast prions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Role of the chaperone protein Hsp104 in propagation of the yeast prion-like factor [psi+]

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Aggregation of huntingtin in yeast varies with the length of the polyglutamine expansion and the expression of chaperone proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Polyglutamine aggregates alter protein folding homeostasis in Caenorhabditis elegans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Hsp104, Hsp70, and Hsp40: a novel chaperone system that rescues previously aggregated proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

N-ethylmaleimide-sensitive fusion protein: a trimeric ATPase whose hydrolysis of ATP is required for membrane fusion

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Structure and conformational changes in NSF and its membrane receptor complexes visualized by quick-freeze/deep-etch electron microscopy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Crystal structure of the amino-terminal domain of N-ethylmaleimide-sensitive fusion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Proteasome inhibition leads to a heat-shock response, induction of endoplasmic reticulum chaperones, and thermotolerance

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Neuropathological changes in two lines of mice carrying a transgene for mutant human Cu,Zn SOD, and in mice overexpressing wild type human SOD: a model of familial amyotrophic lateral sclerosis (FALS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Interactions of the chaperone Hsp104 with yeast Sup35 and mammalian PrP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Triggering of neuronal cell death by accumulation of activated SEK1 on nuclear polyglutamine aggregations in PML bodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Each Domain of theN-Ethylmaleimide-sensitive Fusion Protein Contributes to Its Transport Activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

New order from neurological disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

Properties of the endosomal-lysosomal system in the human central nervous system: disturbances mark most neurons in populations at risk to degenerate in Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400907

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.CDD.4400907

1 reference

Dimensions Publication ID

11 December 2017

1050801713

0 references

Fatcat ID

release_p3gfjf7cnjepngzz4lyfu6whj4

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/p3gfjf7cnjepngzz4lyfu6whj4

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference