Dorfin ubiquitylates mutant SOD1 and prevents mutant SOD1-mediated neurotoxicity (Q34141572)

31 July 2017

Dorfin ubiquitylates mutant SOD1 and prevents mutant SOD1-mediated neurotoxicity (English)

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31 July 2017

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Shigeo Murata

6

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Gen Sobue

9

object named as

Gen Sobue

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31 July 2017

Jun-Ichi Niwa

1

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31 July 2017

Shinsuke Ishigaki

2

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31 July 2017

Nozomi Hishikawa

3

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31 July 2017

Masahiko Yamamoto

4

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31 July 2017

Manabu Doyu

5

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31 July 2017

Keiji Tanaka

7

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31 July 2017

Naoyuki Taniguchi

8

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31 July 2017

language of work or name

English

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publication date

26 July 2002

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Journal of Biological Chemistry

31 July 2017

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31 July 2017

277

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31 July 2017

39

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31 July 2017

36793-36798

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Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

31 July 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Amyotrophic lateral sclerosis. unfolding the toxicity of the misfolded

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Neuropathology of ALS: an overview

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Immunocytochemical and ultrastructural studies of lower motor neurons in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Ubiquitin-immunoreactive intraneuronal inclusions in amyotrophic lateral sclerosis. Morphology, distribution, and specificity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

New pathological findings in amyotrophic lateral sclerosis

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M206559200

New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: inclusions containing SOD1 in neurons and astrocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

A novel centrosomal ring-finger protein, dorfin, mediates ubiquitin ligase activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

A novel transactivation domain in parkin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

The ubiquitin-conjugating enzymes UbcH7 and UbcH8 interact with RING finger/IBR motif-containing domains of HHARI and H7-AP1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Features of the parkin/ariadne-like ubiquitin ligase, HHARI, that regulate its interaction with the ubiquitin-conjugating enzyme, Ubch7

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Parkin suppresses unfolded protein stress-induced cell death through its E3 ubiquitin-protein ligase activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Parkin functions as an E2-dependent ubiquitin- protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

The tyrosine kinase negative regulator c-Cbl as a RING-type, E2-dependent ubiquitin-protein ligase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

RING fingers mediate ubiquitin-conjugating enzyme (E2)-dependent ubiquitination

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Ubiquitin protein ligase activity of IAPs and their degradation in proteasomes in response to apoptotic stimuli

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

21 January 2018

RING for destruction?

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

SCF and Cullin/Ring H2-based ubiquitin ligases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

RING finger proteins: mediators of ubiquitin ligase activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

The lore of the RINGs: substrate recognition and catalysis by ubiquitin ligases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Aggresomes: a cellular response to misfolded proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Formation of high molecular weight complexes of mutant Cu, Zn-superoxide dismutase in a mouse model for familial amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Widespread occurrence of argyrophilic glial inclusions in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Caspase-1 is activated in neural cells and tissue with amyotrophic lateral sclerosis-associated mutations in copper-zinc superoxide dismutase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Formation of granular cytoplasmic aggregates in COS7 cells expressing mutant Cu/Zn superoxide dismutase associated with familial amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Impairment of the ubiquitin-proteasome system by protein aggregation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Ubiquitination of a new form of alpha-synuclein by parkin from human brain: implications for Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Parkin ubiquitinates the alpha-synuclein-interacting protein, synphilin-1: implications for Lewy-body formation in Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Do posttranslational modifications of CuZnSOD lead to sporadic amyotrophic lateral sclerosis?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

CHIP is a chaperone-dependent E3 ligase that ubiquitylates unfolded protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

Intense superoxide dismutase-1 immunoreactivity in intracytoplasmic hyaline inclusions of familial amyotrophic lateral sclerosis with posterior column involvement.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206559200

21 January 2018

Identifiers

DOI

10.1074/JBC.M206559200

1 reference

31 July 2017

1 reference