Lysosomal hydrolases of different classes are abnormally distributed in brains of patients with Alzheimer disease
about
Reduced glucocerebrosidase is associated with increased α-synuclein in sporadic Parkinson's diseaseLysosomal processing of amyloid precursor protein to A beta peptides: a distinct role for cathepsin SMild cognitive impairment: pathology and mechanisms.Tau fragmentation, aggregation and clearance: the dual role of lysosomal processingDual roles for autophagy: degradation and secretion of Alzheimer's disease Aβ peptideThe cysteine protease inhibitor, E64d, reduces brain amyloid-β and improves memory deficits in Alzheimer's disease animal models by inhibiting cathepsin B, but not BACE1, β-secretase activityCathepsin D--many functions of one aspartic proteaseCysteine protease inhibitors effectively reduce in vivo levels of brain beta-amyloid related to Alzheimer's diseaseArf6 controls beta-amyloid production by regulating macropinocytosis of the Amyloid Precursor Protein to lysosomesThe human amyloid-beta precursor protein770 mutation V717F generates peptides longer than amyloid-beta-(40-42) and flocculent amyloid aggregates.Comparative proteomics of cerebrospinal fluid in neuropathologically-confirmed Alzheimer's disease and non-demented elderly subjects.Lysosomal NEU1 deficiency affects amyloid precursor protein levels and amyloid-β secretion via deregulated lysosomal exocytosisUpregulation of the genes encoding lysosomal hydrolases, a perforin-like protein, and peroxidases in the brains of mice affected with an experimental prion diseaseOxidative stress and autophagy in the regulation of lysosome-dependent neuron death.Cathepsin deficiency as a model for neuronal ceroid lipofuscinoses.Ubiquitin, lysosomes, and neurodegenerative diseases.Myelin basic protein associates with AβPP, Aβ1-42, and amyloid plaques in cortex of Alzheimer's disease brainMassive accumulation of luminal protease-deficient axonal lysosomes at Alzheimer's disease amyloid plaquesCholesterol accumulation is associated with lysosomal dysfunction and autophagic stress in Npc1 -/- mouse brainAmyloid deposition and advanced age fails to induce Alzheimer's type progression in a double knock-in mouse modelThe ubiquitin-proteasome system and the autophagic-lysosomal system in Alzheimer disease.Widespread activation of calcium-activated neutral proteinase (calpain) in the brain in Alzheimer disease: a potential molecular basis for neuronal degenerationThe Role of Oxidized Cholesterol in Diabetes-Induced Lysosomal Dysfunction in the Brain.Delta-secretase cleaves amyloid precursor protein and regulates the pathogenesis in Alzheimer's diseaseTrafficking of cell surface beta-amyloid precursor protein: retrograde and transcytotic transport in cultured neurons.Single cell gene expression profiling in Alzheimer's disease.Autophagic and lysosomal defects in human tauopathies: analysis of post-mortem brain from patients with familial Alzheimer disease, corticobasal degeneration and progressive supranuclear palsy.Neuronal apoptosis and autophagy cross talk in aging PS/APP mice, a model of Alzheimer's disease.The proteasome: a macromolecular assembly designed to confine proteolysis to a nanocompartment.Activation of asparaginyl endopeptidase leads to Tau hyperphosphorylation in Alzheimer disease.Rapid induction of intraneuronal neurofibrillary tangles in apolipoprotein E-deficient mice.pdf1, a palmitoyl protein thioesterase 1 Ortholog in Schizosaccharomyces pombe: a yeast model of infantile Batten disease.Perturbation of neuronal cobalamin transport by lysosomal enzyme inhibitionProtein homeostasis, aging and Alzheimer's disease.Protein truncation as a common denominator of human neurodegenerative foldopathies.Cysteine cathepsins in neurological disorders.The Role of Cathepsin D in the Pathogenesis of Human Neurodegenerative Disorders.Endo-lysosomal and autophagic dysfunction: a driving factor in Alzheimer's disease?APP and APLP1 are degraded through autophagy in response to proteasome inhibition in neuronal cells.The Alzheimer's β-secretase BACE1 localizes to normal presynaptic terminals and to dystrophic presynaptic terminals surrounding amyloid plaques.
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P248
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P2860
Lysosomal hydrolases of different classes are abnormally distributed in brains of patients with Alzheimer disease
description
1991 nî lūn-bûn
@nan
1991 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Lysosomal hydrolases of differ ...... atients with Alzheimer disease
@ast
Lysosomal hydrolases of differ ...... atients with Alzheimer disease
@en
Lysosomal hydrolases of differ ...... atients with Alzheimer disease
@en-gb
Lysosomal hydrolases of differ ...... atients with Alzheimer disease
@nl
type
label
Lysosomal hydrolases of differ ...... atients with Alzheimer disease
@ast
Lysosomal hydrolases of differ ...... atients with Alzheimer disease
@en
Lysosomal hydrolases of differ ...... atients with Alzheimer disease
@en-gb
Lysosomal hydrolases of differ ...... atients with Alzheimer disease
@nl
prefLabel
Lysosomal hydrolases of differ ...... atients with Alzheimer disease
@ast
Lysosomal hydrolases of differ ...... atients with Alzheimer disease
@en
Lysosomal hydrolases of differ ...... atients with Alzheimer disease
@en-gb
Lysosomal hydrolases of differ ...... atients with Alzheimer disease
@nl
P2093
P2860
P921
P356
P1476
Lysosomal hydrolases of differ ...... atients with Alzheimer disease
@en
P2093
A M Cataldo
E Kominami
P A Paskevich
P2860
P304
10998-1002
P356
10.1073/PNAS.88.24.10998
P407
P577
1991-12-15T00:00:00Z