(Q51751501)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134191%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

title

Mutant SOD1 inhibits ER-Golgi transport in amyotrophic lateral sclerosis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134191%20AND%20SRC:MED&resulttype=core&format=json

amyotrophic lateral sclerosis

28 February 2020

main subject

0 references

author

Adam Walker

4

1 reference

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28 February 2020

Julie D Atkin

1

1 reference

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28 February 2020

Bradley J Turner

6

1 reference

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28 February 2020

2

Manal A Farg

1 reference

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28 February 2020

3

Kai Ying Soo

1 reference

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28 February 2020

author name string

Mark Halloran

5

1 reference

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28 February 2020

Phillip Nagley

7

1 reference

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28 February 2020

Malcolm K Horne

8

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28 February 2020

language of work or name

English

0 references

publication date

13 November 2013

1 reference

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Journal of Neurochemistry

28 February 2020

published in

1 reference

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28 February 2020

volume

129

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28 February 2020

issue

1

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28 February 2020

page(s)

190-204

1 reference

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Selective targeting of ER exit sites supports axon development

28 February 2020

cites work

1 reference

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Evidence that all newly synthesized proteins destined for fast axonal transport pass through the Golgi apparatus

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The product of C9orf72, a gene strongly implicated in neurodegeneration, is structurally related to DENN Rab-GEFs

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Sar1 assembly regulates membrane constriction and ER export

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The fluorescence protease protection (FPP) assay to determine protein localization and membrane topology

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Mutations of optineurin in amyotrophic lateral sclerosis

21 January 2018

1 reference

The Cu,Zn superoxide dismutase in neuroblastoma SK-N-BE cells is exported by a microvesicles dependent pathway

21 January 2018

1 reference

Fragmentation of the Golgi apparatus of motor neurons in amyotrophic lateral sclerosis revealed by organelle-specific antibodies

21 January 2018

1 reference

The Golgi apparatus of spinal cord motor neurons in transgenic mice expressing mutant Cu,Zn superoxide dismutase becomes fragmented in early, preclinical stages of the disease

21 January 2018

1 reference

Potential therapeutic uses of BDNF in neurological and psychiatric disorders

21 January 2018

1 reference

A Golgi fragmentation pathway in neurodegeneration

21 January 2018

1 reference

A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis

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

Medial Golgi but not late Golgi glycosyltransferases exist as high molecular weight complexes. Role of luminal domain in complex formation and localization

21 January 2018

1 reference

Specificity of cytoplasmic dynein subunits in discrete membrane-trafficking steps

21 January 2018

1 reference

An early onset progressive motor neuron disorder in Scyl1-deficient mice is associated with mislocalization of TDP-43.

21 January 2018

1 reference

Coordinated lipid transfer between the endoplasmic reticulum and the Golgi complex requires the VAP proteins and is essential for Golgi-mediated transport

21 January 2018

1 reference

Reduced endoplasmic reticulum (ER)-to-Golgi protein trafficking contributes to ER stress in lipotoxic mouse beta cells by promoting protein overload.

21 January 2018

1 reference

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21 January 2018

1 reference

The endoplasmic reticulum and protein trafficking in dendrites and axons

21 January 2018

1 reference

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21 January 2018

1 reference

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

21 January 2018

1 reference

Emergent properties of proteostasis-COPII coupled systems in human health and disease

21 January 2018

1 reference

Optineurin links myosin VI to the Golgi complex and is involved in Golgi organization and exocytosis

21 January 2018

1 reference

A role for motoneuron subtype-selective ER stress in disease manifestations of FALS mice

21 January 2018

1 reference

Progressive motor neuronopathy: a critical role of the tubulin chaperone TBCE in axonal tubulin routing from the Golgi apparatus.

21 January 2018

1 reference

Mutation of Vps54 causes motor neuron disease and defective spermiogenesis in the wobbler mouse

21 January 2018

1 reference

Local unfolding in a destabilized, pathogenic variant of superoxide dismutase 1 observed with H/D exchange and mass spectrometry

21 January 2018

1 reference

Recruitment of mitochondria into apoptotic signaling correlates with the presence of inclusions formed by amyotrophic lateral sclerosis-associated SOD1 mutations.

21 January 2018

1 reference

Proteins of the PDI family: unpredicted non-ER locations and functions

21 January 2018

1 reference

Impaired extracellular secretion of mutant superoxide dismutase 1 associates with neurotoxicity in familial amyotrophic lateral sclerosis

21 January 2018

1 reference

Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis

21 January 2018

1 reference

The endoplasmic reticulum-Golgi pathway is a target for translocation and aggregation of mutant superoxide dismutase linked to ALS.

21 January 2018

1 reference

Protein disulphide isomerase protects against protein aggregation and is S-nitrosylated in amyotrophic lateral sclerosis

21 January 2018

1 reference

Coupling of ER exit to microtubules through direct interaction of COPII with dynactin

21 January 2018

1 reference

Reticulon-4A (Nogo-A) redistributes protein disulfide isomerase to protect mice from SOD1-dependent amyotrophic lateral sclerosis

21 January 2018

1 reference

Growing dendrites and axons differ in their reliance on the secretory pathway

21 January 2018

1 reference

Interaction between familial amyotrophic lateral sclerosis (ALS)-linked SOD1 mutants and the dynein complex

21 January 2018

1 reference

Cell surface relocalization of the endoplasmic reticulum chaperone and unfolded protein response regulator GRP78/BiP.

21 January 2018

1 reference