(Q57266990)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23280792%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

title

A novel monoclonal antibody reveals a conformational alteration shared by amyotrophic lateral sclerosis-linked SOD1 mutants (English)

1 reference

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amyotrophic lateral sclerosis

21 February 2020

main subject

0 references

1 reference

1 reference

2

1 reference

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21 February 2020

Kohsuke Takeda

8

1 reference

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21 February 2020

Hideki Nishitoh

12

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21 February 2020

Hidenori Ichijō

13

1 reference

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21 February 2020

author name string

Takao Fujisawa

1

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21 February 2020

Namiko Yamaguchi

3

1 reference

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21 February 2020

Hisae Kadowaki

4

1 reference

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21 February 2020

Naomi Tsuburaya

5

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21 February 2020

Isao Naguro

6

1 reference

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21 February 2020

Atsushi Matsuzawa

7

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21 February 2020

Yuji Takahashi

9

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21 February 2020

Jun Goto

10

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21 February 2020

Shoji Tsuji

11

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21 February 2020

publication date

1 November 2012

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21 February 2020

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21 February 2020

volume

72

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21 February 2020

issue

5

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21 February 2020

page(s)

739-749

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Molecular biology of amyotrophic lateral sclerosis: insights from genetics

21 February 2020

cites work

1 reference

Copper-zinc superoxide dismutase and amyotrophic lateral sclerosis

21 January 2018

1 reference

Copper chaperone for superoxide dismutase is essential to activate mammalian Cu/Zn superoxide dismutase

21 January 2018

1 reference

Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury

21 January 2018

1 reference

Transgenics, toxicity and therapeutics in rodent models of mutant SOD1-mediated familial ALS.

21 January 2018

1 reference

Amyotrophic lateral sclerosis. unfolding the toxicity of the misfolded

21 January 2018

1 reference

Wild-type and mutant SOD1 share an aberrant conformation and a common pathogenic pathway in ALS.

21 January 2018

1 reference

Novel antibodies reveal inclusions containing non-native SOD1 in sporadic ALS patients

21 January 2018

1 reference

Astrocytes from familial and sporadic ALS patients are toxic to motor neurons

21 January 2018

1 reference

Amyotrophic lateral sclerosis is a non-amyloid disease in which extensive misfolding of SOD1 is unique to the familial form

21 January 2018

1 reference

An immunological epitope selective for pathological monomer-misfolded SOD1 in ALS.

21 January 2018

1 reference

Selective association of misfolded ALS-linked mutant SOD1 with the cytoplasmic face of mitochondria.

21 January 2018

1 reference

Unfolded proteins and endoplasmic reticulum stress in neurodegenerative disorders

21 January 2018

1 reference

ALS-linked mutant SOD1 induces ER stress- and ASK1-dependent motor neuron death by targeting Derlin-1.

21 January 2018

1 reference

A membrane protein required for dislocation of misfolded proteins from the ER

21 January 2018

1 reference

A membrane protein complex mediates retro-translocation from the ER lumen into the cytosol

21 January 2018

1 reference

Apoptosis signal-regulating kinase (ASK) 2 functions as a mitogen-activated protein kinase kinase kinase in a heteromeric complex with ASK1

21 January 2018

1 reference

Herp, a new ubiquitin-like membrane protein induced by endoplasmic reticulum stress

21 January 2018

1 reference

IRE1 couples endoplasmic reticulum load to secretory capacity by processing the XBP-1 mRNA

21 January 2018

1 reference

XBP1 mRNA is induced by ATF6 and spliced by IRE1 in response to ER stress to produce a highly active transcription factor

21 January 2018

1 reference

Determination and analysis of the 2 A-structure of copper, zinc superoxide dismutase

21 January 2018

1 reference

Structures of the G85R variant of SOD1 in familial amyotrophic lateral sclerosis

21 January 2018

1 reference

Insights into Lou Gehrig's disease from the structure and instability of the A4V mutant of human Cu,Zn superoxide dismutase

21 January 2018

1 reference

ALS mutants of human superoxide dismutase form fibrous aggregates via framework destabilization

21 January 2018

1 reference

Structural and biophysical properties of metal-free pathogenic SOD1 mutants A4V and G93A

21 January 2018

1 reference

SOD1 and amyotrophic lateral sclerosis: mutations and oligomerization

21 January 2018

1 reference

TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

21 January 2018

1 reference

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

21 January 2018

1 reference

Mutations of optineurin in amyotrophic lateral sclerosis

21 January 2018

1 reference

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

21 January 2018

1 reference

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

21 January 2018

1 reference

Toxic mutants in Charcot's sclerosis

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/ANA.23668

1 reference

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21 February 2020

1 reference