Protein aggregation and degradation mechanisms in neurodegenerative diseases
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Autoubiquitination of the 26S proteasome on Rpn13 regulates breakdown of ubiquitin conjugatesNeurodegeneration and microtubule dynamics: death by a thousand cutsSumoylation of critical proteins in amyotrophic lateral sclerosis: emerging pathways of pathogenesisMotor Dysfunctions and Neuropathology in Mouse Models of Spinocerebellar Ataxia Type 2: A Comprehensive ReviewA Case for Microtubule Vulnerability in Amyotrophic Lateral Sclerosis: Altered Dynamics During DiseaseThe Glymphatic System: A Beginner's GuideComparative 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 PathogenesisMisfolded polypeptides are selectively recognized and transported toward aggresomes by a CED complexHeat shock protein 90 in Alzheimer's diseaseThe interplay between autophagy and the ubiquitin-proteasome system in cardiac proteotoxicityExpression 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 huntingtinPharmacological chaperone reshapes the energy landscape for folding and aggregation of the prion proteinDefects 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 HealthThe 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 diseaseCigarette 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.
P2860
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P2860
Protein aggregation and degradation mechanisms in neurodegenerative diseases
description
2013 nî lūn-bûn
@nan
2013 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի մարտին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
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
@nl
type
label
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
@nl
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
@nl
P2093
P2860
P1476
Protein aggregation and degradation mechanisms in neurodegenerative diseases
@en
P2093
Antero Salminen
Hilkka Soininen
Mari Takalo
Mikko Hiltunen
P2860
P577
2013-03-08T00:00:00Z