Autophagy in neurodegenerative disorders: pathogenic roles and therapeutic implications

scientific article published on October 12, 2010

Autophagy in neurodegenerative disorders: pathogenic roles and therapeutic implications is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1016/J.TINS.2010.09.001
P953full work available at URLhttps://europepmc.org/articles/pmc2981680?pdf=render
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20947179/pdf/?tool=EBI
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20947179/?tool=EBI
https://europepmc.org/articles/PMC2981680
https://europepmc.org/articles/PMC2981680?pdf=render
https://api.elsevier.com/content/article/PII:S0166223610001244?httpAccept=text/plain
https://api.elsevier.com/content/article/PII:S0166223610001244?httpAccept=text/xml
https://doi.org/10.1016/j.tins.2010.09.001
P932PMC publication ID2981680
P698PubMed publication ID20947179
P5875ResearchGate publication ID47428764

P50authorM. Flint BealQ67409129
P2093author name stringBobby Thomas
Rebecca Banerjee
P2860cites workInhibition of mTOR by rapamycin abolishes cognitive deficits and reduces amyloid-beta levels in a mouse model of Alzheimer's diseaseQ21136406
ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)Q24294908
PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1Q24297155
PINK1 is recruited to mitochondria with parkin and associates with LC3 in mitophagyQ24299149
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonismQ24309753
Disease-causing mutations in parkin impair mitochondrial ubiquitination, aggregation, and HDAC6-dependent mitophagyQ24311582
Phosphorylation of parkin by Parkinson disease-linked kinase PINK1 activates parkin E3 ligase function and NF-kappaB signalingQ24313304
Parkin is recruited selectively to impaired mitochondria and promotes their autophagyQ24317471
Loss of PINK1 function promotes mitophagy through effects on oxidative stress and mitochondrial fissionQ24320327
Hereditary early-onset Parkinson's disease caused by mutations in PINK1Q24337084
LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processingQ24597817
Molecular interplay between mammalian target of rapamycin (mTOR), amyloid-beta, and Tau: effects on cognitive impairmentsQ24633947
Regulation of neuronal survival factor MEF2D by chaperone-mediated autophagyQ24646352
Rapamycin fed late in life extends lifespan in genetically heterogeneous miceQ24647805
Rapamycin rescues TDP-43 mislocalization and the associated low molecular mass neurofilament instabilityQ24648173
XBP-1 deficiency in the nervous system protects against amyotrophic lateral sclerosis by increasing autophagyQ24655821
Dopamine-modified alpha-synuclein blocks chaperone-mediated autophagyQ24683089
Autophagy fights disease through cellular self-digestionQ27860902
TOR, a central controller of cell growthQ27933354
Chaperone-mediated autophagy markers in Parkinson disease brainsQ28115026
Inhibition of mTOR induces autophagy and reduces toxicity of polyglutamine expansions in fly and mouse models of Huntington diseaseQ28261987
Regulation of intracellular accumulation of mutant Huntingtin by Beclin 1Q28300820
Lysosomal proteolysis and autophagy require presenilin 1 and are disrupted by Alzheimer-related PS1 mutationsQ28506710
The autophagy-related protein beclin 1 shows reduced expression in early Alzheimer disease and regulates amyloid beta accumulation in miceQ28591283
Trinucleotide Repeat DisordersQ29038716
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Impaired degradation of mutant alpha-synuclein by chaperone-mediated autophagyQ29614178
Plasma membrane contributes to the formation of pre-autophagosomal structuresQ29614494
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Autophagosome formation from membrane compartments enriched in phosphatidylinositol 3-phosphate and dynamically connected to the endoplasmic reticulumQ29614500
Autophagy gone awry in neurodegenerative diseasesQ29614849
PINK1 stabilized by mitochondrial depolarization recruits Parkin to damaged mitochondria and activates latent Parkin for mitophagyQ29616005
S-nitrosylation of Drp1 mediates beta-amyloid-related mitochondrial fission and neuronal injuryQ29616550
Autophagy in health and disease: a double-edged swordQ29618103
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Parkinson's disease: from molecular pathways in disease to therapeutic approachesQ33644302
Selective molecular alterations in the autophagy pathway in patients with Lewy body disease and in models of alpha-synucleinopathyQ33670282
Cargo recognition failure is responsible for inefficient autophagy in Huntington's diseaseQ33814719
Rapamycin extends maximal lifespan in cancer-prone miceQ33816255
Mitochondrial dysfunction in the limelight of Parkinson's disease pathogenesisQ33840243
A pivotal role for PINK1 and autophagy in mitochondrial quality control: implications for Parkinson diseaseQ33871331
A synergistic dysfunction of mitochondrial fission/fusion dynamics and mitophagy in Alzheimer's diseaseQ34073879
Clearing the brain's amyloid cobwebsQ34099588
A small-molecule scaffold induces autophagy in primary neurons and protects against toxicity in a Huntington disease model.Q34165508
Dynein mutations impair autophagic clearance of aggregate-prone proteinsQ34429194
Inositol and IP3 levels regulate autophagy: biology and therapeutic speculations.Q34552031
Clinical trials for neuroprotection in ALS.Q34618907
Small molecules enhance autophagy and reduce toxicity in Huntington's disease models.Q34626231
Ubiquitination of alpha-synuclein and autophagy in Parkinson's disease.Q34740278
Macroautophagy--a novel Beta-amyloid peptide-generating pathway activated in Alzheimer's diseaseQ36320351
Lithium induces autophagy by inhibiting inositol monophosphataseQ36321015
Chaperone-mediated autophagy in aging and diseaseQ36510519
Does autophagy contribute to cell death?Q36549462
A century-old debate on protein aggregation and neurodegeneration enters the clinicQ36628151
Dynamin-like protein 1 reduction underlies mitochondrial morphology and distribution abnormalities in fibroblasts from sporadic Alzheimer's disease patientsQ36778260
Cell death modalities: classification and pathophysiological implicationsQ36790543
Autophagy, amyloidogenesis and Alzheimer diseaseQ37011121
Amyloid-beta overproduction causes abnormal mitochondrial dynamics via differential modulation of mitochondrial fission/fusion proteinsQ37039531
Autophagy: principles and significance in health and diseaseQ37330775
Cell death pathways in Parkinson's disease: proximal triggers, distal effectors, and final stepsQ37376117
Autophagy, lithium, and amyotrophic lateral sclerosisQ37554121
Coordination of membrane events during autophagy by multiple class III PI3-kinase complexesQ37606853
Chaperone-mediated autophagy in health and diseaseQ37660666
Pathology of protein synthesis and degradation systems in ALS.Q37681655
The small heat shock protein B8 (HspB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS).Q39689378
Novel targets for Huntington's disease in an mTOR-independent autophagy pathwayQ41978909
Sequestosome 1/p62 links familial ALS mutant SOD1 to LC3 via an ubiquitin-independent mechanism.Q42066100
Wild type alpha-synuclein is degraded by chaperone-mediated autophagy and macroautophagy in neuronal cellsQ42423397
Trehalose ameliorates dopaminergic and tau pathology in parkin deleted/tau overexpressing mice through autophagy activationQ42472879
Age at onset in Huntington's disease is modified by the autophagy pathway: implication of the V471A polymorphism in Atg7.Q42941899
Mitochondrial abnormalities in Alzheimer's disease.Q43581697
Raised intracellular glucose concentrations reduce aggregation and cell death caused by mutant huntingtin exon 1 by decreasing mTOR phosphorylation and inducing autophagyQ44406691
α-Synuclein Is Degraded by Both Autophagy and the ProteasomeQ44420467
Harnessing chaperone-mediated autophagy for the selective degradation of mutant huntingtin proteinQ45296862
Huntingtin is cleaved by caspases in the cytoplasm and translocated to the nucleus via perinuclear sites in Huntington's disease patient lymphoblastsQ45296864
Rapamycin alleviates toxicity of different aggregate-prone proteinsQ45299514
Studies on brain biopsies of patients with Huntington's choreaQ45300907
Huntingtin expression stimulates endosomal-lysosomal activity, endosome tubulation, and autophagy.Q45301281
Trehalose, a novel mTOR-independent autophagy enhancer, accelerates the clearance of mutant huntingtin and alpha-synuclein.Q45303665
A stress sensitive ER membrane-association domain in Huntingtin protein defines a potential role for Huntingtin in the regulation of autophagyQ45306898
Mutant huntingtin expression in clonal striatal cells: dissociation of inclusion formation and neuronal survival by caspase inhibition.Q48298684
Mutant ubiquitin and p62 immunoreactivity in cases of combined multiple system atrophy and Alzheimer's disease.Q48304039
Presenilin mutations in familial Alzheimer disease and transgenic mouse models accelerate neuronal lysosomal pathology.Q53263789
Extensive involvement of autophagy in Alzheimer disease: an immuno-electron microscopy study.Q53369656
Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS.Q54792092
The LysosomeQ55037468
Autophagy and amyotrophic lateral sclerosis: The multiple roles of lithiumQ57201203
Altered macroautophagy in the spinal cord of SOD1 mutant miceQ80496792
Increased autophagy in transgenic mice with a G93A mutant SOD1 geneQ80774356
P433issue12
P407language of work or nameEnglishQ1860
P921main subjectautophagyQ288322
neurodegenerationQ1755122
P304page(s)541-549
P577publication date2010-10-12
P1433published inTrends in NeurosciencesQ3538443
P1476titleAutophagy in neurodegenerative disorders: pathogenic roles and therapeutic implications
P478volume33

Reverse relations

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