Amyotrophic lateral sclerosis (ALS)-associated VAPB-P56S inclusions represent an ER quality control compartment - Wikidata - wikimedia - TriplyDB

Amyotrophic lateral sclerosis (ALS)-associated VAPB-P56S inclusions represent an ER quality control compartment

Amyotrophic lateral sclerosis (ALS)-associated VAPB-P56S inclusions represent an ER quality control compartment

http://www.wikidata.org/entity/Q41874848

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Golgi Fragmentation in ALS Motor Neurons. New Mechanisms Targeting Microtubules, Tethers, and Transport Vesicles Autophagy and Neurodegeneration: Insights from a Cultured Cell Model of ALS Protein Quality Control and the Amyotrophic Lateral Sclerosis/Frontotemporal Dementia Continuum Clinical and genetic diversity of SMN1-negative proximal spinal muscular atrophies Vapb/Amyotrophic lateral sclerosis 8 knock-in mice display slowly progressive motor behavior defects accompanying ER stress and autophagic response.VAMP-associated Proteins (VAP) as Receptors That Couple Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Proteostasis with Lipid Homeostasis.Gain-of-function mutations in the ALS8 causative gene VAPB have detrimental effects on neurons and muscles.Cellular Signature of SIL1 Depletion: Disease Pathogenesis due to Alterations in Protein Composition Beyond the ER Machinery.The ALS-linked E102Q mutation in Sigma receptor-1 leads to ER stress-mediated defects in protein homeostasis and dysregulation of RNA-binding proteins.Cellular Chaperones As Therapeutic Targets in ALS to Restore Protein Homeostasis and Improve Cellular Function ALS-Associated Endoplasmic Reticulum Proteins in Denervated Skeletal Muscle: Implications for Motor Neuron Disease Pathology.Autophagy as a common pathway in amyotrophic lateral sclerosis.ER Dynamics and Derangement in Neurological Diseases.

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Amyotrophic lateral sclerosis (ALS)-associated VAPB-P56S inclusions represent an ER quality control compartment

http://www.wikidata.org/entity/Q41874848

description

2013 nî lūn-bûn

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

2013年论文

@zh

2013年论文

@zh-cn

name

Amyotrophic lateral sclerosis ...... ER quality control compartment

@en

type

label

Amyotrophic lateral sclerosis ...... ER quality control compartment

@en

prefLabel

Amyotrophic lateral sclerosis ...... ER quality control compartment

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Acta neuropathologica communications

P1476

Amyotrophic lateral sclerosis ...... ER quality control compartment

@en

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Casper C Hoogenraad

http://www.w3.org/2001/XMLSchema#string

Dick Jaarsma

http://www.w3.org/2001/XMLSchema#string

Elize D Haasdijk

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Jan A Post

http://www.w3.org/2001/XMLSchema#string

Karin Vocking

http://www.w3.org/2001/XMLSchema#string

Marijn Kuijpers

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Vera van Dis

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Molecular cloning and characterization of mammalian homologues of vesicle-associated membrane protein-associated (VAMP-associated) proteins

TEB4 is a C4HC3 RING finger-containing ubiquitin ligase of the endoplasmic reticulum

The ALS8 protein VAPB interacts with the ER-Golgi recycling protein YIF1A and regulates membrane delivery into dendrites

VAPB interacts with the mitochondrial protein PTPIP51 to regulate calcium homeostasis

Characterization of amyotrophic lateral sclerosis-linked P56S mutation of vesicle-associated membrane protein-associated protein B (VAPB/ALS8)

Characterization of the properties of a novel mutation in VAPB in familial amyotrophic lateral sclerosis

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

The amyotrophic lateral sclerosis 8 protein VAPB is cleaved, secreted, and acts as a ligand for Eph receptors

BAP31 interacts with Sec61 translocons and promotes retrotranslocation of CFTRDeltaF508 via the derlin-1 complex

A conserved ER targeting motif in three families of lipid binding proteins and in Opi1p binds VAP

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24

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scholarly article

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10.1186/2051-5960-1-24

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1

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Martin Harterink

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2013-06-12T00:00:00Z

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257885180

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1036754401

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amyotrophic lateral sclerosis

quality control

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3893532

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