标题
Second Sphere Interactions in Amyloidogenic Diseases
作者
关键词
-
出版物
CHEMICAL REVIEWS
Volume -, Issue -, Pages -
出版商
American Chemical Society (ACS)
发表日期
2022-04-27
DOI
10.1021/acs.chemrev.1c00941
参考文献
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- Role of Copper Ion in the Pathogenesis of Type 2 Diabetes
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- Identification of the Minimal Copper(II)-Binding α-Synuclein Sequence
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- Intranuclear Degradation of Polyglutamine Aggregates by the Ubiquitin-Proteasome System
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- Phosphorylation of Threonine 3
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- Structural organization of human Cu-transporting ATPases: learning from building blocks
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- Cancer linked to Alzheimer disease but not vascular dementia
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- (2009) C. P. J. Maury ORIGINS OF LIFE AND EVOLUTION OF BIOSPHERES
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- Atomic structures of IAPP (amylin) fusions suggest a mechanism for fibrillation and the role of insulin in the process
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- Secondary Structure of Huntingtin Amino-Terminal Region
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- Protein Misfolding and Neurodegeneration
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- Amyloid β−Cu2+Complexes in both Monomeric and Fibrillar Forms Do Not Generate H2O2Catalytically but Quench Hydroxyl Radicals†
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- Role of Mitochondrial Dysfunction in Insulin Resistance
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- Bioinorganic chemistry of copper and zinc ions coordinated to amyloid-β peptide
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- Neprilysin gene expression requires binding of the amyloid precursor protein intracellular domain to its promoter: implications for Alzheimer disease
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- Islet Amyloid in Type 2 Diabetes, and the Toxic Oligomer Hypothesis
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- Mechanisms of neurodegeneration in Huntington’s disease
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- Protective role of Engrailed in a Drosophila model of Huntington's disease
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- A Common β-Sheet Architecture Underliesin Vitroandin Vivoβ2-Microglobulin Amyloid Fibrils
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- Human Prion Protein (PrP) 219K Is Converted to PrPScbut Shows Heterozygous Inhibition in Variant Creutzfeldt-Jakob Disease Infection
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- Amyloid Precursor Protein Trafficking, Processing, and Function
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- Neuronal cell death in neurodegenerative diseases: recurring themes around protein handling
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- Both Met(109) and Met(112) are utilized for Cu(II) coordination by the amyloidogenic fragment of the human prion protein at physiological pH
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- Amyloid β-Protein Monomer Folding: Free-Energy Surfaces Reveal Alloform-Specific Differences
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- Complex I specific increase in superoxide formation and respiration rate by PrP-null mouse brain mitochondria
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- DNA breakage and induction of DNA damage response proteins precede the appearance of visible mutant huntingtin aggregates
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- Quantification of the Binding Constant of Copper(II) to the Amyloid-Beta Peptide
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- Cu2+Binding Modes of Recombinant α-Synuclein − Insights from EPR Spectroscopy
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- Site-Specific Interactions of Cu(II) with α and β-Synuclein: Bridging the Molecular Gap between Metal Binding and Aggregation
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- The Amyloid-β Peptide of Alzheimer’s Disease Binds CuIin a Linear Bis-His Coordination Environment: Insight into a Possible Neuroprotective Mechanism for the Amyloid-β Peptide
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- Zinc-Amyloid β Interactions on a Millisecond Time-Scale Stabilize Non-fibrillar Alzheimer-Related Species
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- Copper(II) Binding to α-Synuclein, the Parkinson’s Protein
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- Genetic risk factors for variant Creutzfeldt–Jakob disease: a genome-wide association study
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- Generation of goats lacking prion protein
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- Amyloid formation by globular proteins under native conditions
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- Zinc at glutamatergic synapses
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- Molecular structural basis for polymorphism in Alzheimer's -amyloid fibrils
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- Production of Prnp −/− goats by gene targeting in adult fibroblasts
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- Oxidative stress hypothesis in Alzheimer’s disease: a reappraisal
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- Oxidative Stress and Neurotoxicity
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- Effect of Phosphorylation on αB-crystallin: Differences in Stability, Subunit Exchange and Chaperone Activity of Homo and Mixed Oligomers of αB-Crystallin and its Phosphorylation-mimicking Mutant
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- Antioxidant activity related to copper binding of native prion protein
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- Characterization of Copper Interactions with Alzheimer Amyloid β Peptides
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