Protein aggregation and degradation mechanisms in neurodegenerative diseases - Wikidata - thesis-toulmin - TriplyDB

Protein aggregation and degradation mechanisms in neurodegenerative diseases

Protein aggregation and degradation mechanisms in neurodegenerative diseases

http://www.wikidata.org/entity/Q34334363

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Autoubiquitination of the 26S proteasome on Rpn13 regulates breakdown of ubiquitin conjugates Neurodegeneration and microtubule dynamics: death by a thousand cuts Sumoylation of critical proteins in amyotrophic lateral sclerosis: emerging pathways of pathogenesis Motor Dysfunctions and Neuropathology in Mouse Models of Spinocerebellar Ataxia Type 2: A Comprehensive Review A Case for Microtubule Vulnerability in Amyotrophic Lateral Sclerosis: Altered Dynamics During Disease The Glymphatic System: A Beginner's Guide Comparative Meta-Analysis of Transcriptomics Data during Cellular Senescence and In Vivo Tissue Ageing.RNA binding motif protein 3: a potential biomarker in cancer and therapeutic target in neuroprotection.Mechanisms of Parkinson's disease-related proteins in mediating secondary brain damage after cerebral ischemia.Role of Cigarette Smoke-Induced Aggresome Formation in Chronic Obstructive Pulmonary Disease-Emphysema Pathogenesis Misfolded polypeptides are selectively recognized and transported toward aggresomes by a CED complex Heat shock protein 90 in Alzheimer's disease The interplay between autophagy and the ubiquitin-proteasome system in cardiac proteotoxicity Expression profiling of the ubiquitin conjugating enzyme UbcM2 in murine brain reveals modest age-dependent decreases in specific neurons.Identification of novel autophagic Radix Polygalae fraction by cell membrane chromatography and UHPLC-(Q)TOF-MS for degradation of neurodegenerative disease proteins.Differential Contributions of Alcohol and the Nicotine-Derived Nitrosamine Ketone (NNK) to Insulin and Insulin-Like Growth Factor Resistance in the Adolescent Rat Brain.Gene Therapy Models of Alzheimer's Disease and Other Dementias.Hydrodynamic size-based separation and characterization of protein aggregates from total cell lysates.Ubiquilin/Dsk2 promotes inclusion body formation and vacuole (lysosome)-mediated disposal of mutated huntingtin Pharmacological chaperone reshapes the energy landscape for folding and aggregation of the prion protein Defects of mutant DNMT1 are linked to a spectrum of neurological disorders.Proteasome regulates turnover of toxic human amylin in pancreatic cells.Advances in gene therapy technologies to treat retinitis pigmentosa.Umbilical cord mesenchymal stem cells labeled with multimodal iron oxide nanoparticles with fluorescent and magnetic properties: application for in vivo cell tracking.The role of s-nitrosylation and s-glutathionylation of protein disulphide isomerase in protein misfolding and neurodegeneration.Cellular Prion Protein (PrPc) and Hypoxia: True to Each Other in Good Times and in Bad, in Sickness, and in Health The mechanisms of Mallory-Denk body formation are similar to the formation of aggresomes in Alzheimer's disease and other neurodegenerative disorders.Metabolic control of the proteotoxic stress response: implications in diabetes mellitus and neurodegenerative disorders.ER fatalities-The role of ER-mitochondrial contact sites in yeast life and death decisions.Ubiquitin ligase ITCH recruitment suppresses the aggregation and cellular toxicity of cytoplasmic misfolded proteins.Atomic force microscopy as an advanced tool in neuroscience.CK2-An Emerging Target for Neurological and Psychiatric Disorders.Proteinopathy, oxidative stress and mitochondrial dysfunction: cross talk in Alzheimer's disease and Parkinson's disease Cigarette smoke induced autophagy-impairment accelerates lung aging, COPD-emphysema exacerbations and pathogenesis.LTP and memory impairment caused by extracellular Aβ and Tau oligomers is APP-dependent.A Mutation in NPAS3 That Segregates with Schizophrenia in a Small Family Leads to Protein Aggregation.Structural and functional insights into the E3 ligase, RNF126.A cluster of palmitoylated cysteines are essential for aggregation of cysteine-string protein mutants that cause neuronal ceroid lipofuscinosis.CUL2-mediated clearance of misfolded TDP-43 is paradoxically affected by VHL in oligodendrocytes in ALS.Enhanced tau pathology via RanBP9 and Hsp90/Hsc70 chaperone complexes.

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P2860

Protein aggregation and degradation mechanisms in neurodegenerative diseases

http://www.wikidata.org/entity/Q34334363

description

2013 nî lūn-bûn

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2013 թուականի Մարտին հրատարակուած գիտական յօդուած

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2013 թվականի մարտին հրատարակված գիտական հոդված

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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

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2013年論文

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2013年論文

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2013年论文

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name

Protein aggregation and degradation mechanisms in neurodegenerative diseases

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Protein aggregation and degradation mechanisms in neurodegenerative diseases

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Protein aggregation and degradation mechanisms in neurodegenerative diseases

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type

label

Protein aggregation and degradation mechanisms in neurodegenerative diseases

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Protein aggregation and degradation mechanisms in neurodegenerative diseases

@en

Protein aggregation and degradation mechanisms in neurodegenerative diseases

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prefLabel

Protein aggregation and degradation mechanisms in neurodegenerative diseases

@ast

Protein aggregation and degradation mechanisms in neurodegenerative diseases

@en

Protein aggregation and degradation mechanisms in neurodegenerative diseases

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P1433

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P1433

American journal of neurodegenerative disease

P1476

Protein aggregation and degradation mechanisms in neurodegenerative diseases

@en

P2093

Antero Salminen

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

Hilkka Soininen

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

Mari Takalo

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

Mikko Hiltunen

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P2860

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

Identification of ubiquilin, a novel presenilin interactor that increases presenilin protein accumulation

Characterization of ubiquilin 1, an mTOR-interacting protein

Ubiquilin interacts with ubiquitylated proteins and proteasome through its ubiquitin-associated and ubiquitin-like domains

Role of ubiquilin associated with protein-disulfide isomerase in the endoplasmic reticulum in stress-induced apoptotic cell death

The deacetylase HDAC6 regulates aggresome formation and cell viability in response to misfolded protein stress

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

p62, a phosphotyrosine-independent ligand of the SH2 domain of p56lck, belongs to a new class of ubiquitin-binding proteins

The UBL domain of PLIC-1 regulates aggresome formation

p62/SQSTM1 binds directly to Atg8/LC3 to facilitate degradation of ubiquitinated protein aggregates by autophagy

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Annakaisa Haapasalo

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2013-03-08T00:00:00Z

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23516262

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neurodegeneration

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3601466

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