Molecular cross talk between misfolded proteins in animal models of Alzheimer's and prion diseases - Test2 - elhamkhani - TriplyDB

Molecular cross talk between misfolded proteins in animal models of Alzheimer's and prion diseases

Molecular cross talk between misfolded proteins in animal models of Alzheimer's and prion diseases

http://www.wikidata.org/entity/Q24633202

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The spectrum of disease in chronic traumatic encephalopathy Targeting microglial K(ATP) channels to treat neurodegenerative diseases: a mitochondrial issue Hijacking PrP(c)-dependent signal transduction: when prions impair Aβ clearance Insoluble cellular prion protein and its association with prion and Alzheimer diseases Interaction between prion protein and Aβ amyloid fibrils revisited Cross-seeding of misfolded proteins: implications for etiology and pathogenesis of protein misfolding diseases Genesis of mammalian prions: from non-infectious amyloid fibrils to a transmissible prion disease Novel 5' untranslated region directed blockers of iron-regulatory protein-1 dependent amyloid precursor protein translation: implications for down syndrome and Alzheimer's disease Genetic cross-interaction between APOE and PRNP in sporadic Alzheimer's and Creutzfeldt-Jakob diseases.Pharmacological Modulation of Functional Phenotypes of Microglia in Neurodegenerative Diseases Early-onset formation of parenchymal plaque amyloid abrogates cerebral microvascular amyloid accumulation in transgenic mice.Cellular prion protein expression is not regulated by the Alzheimer's amyloid precursor protein intracellular domain.Prion strain interactions are highly selective.Vascular and metabolic dysfunction in Alzheimer's disease: a review.Identification of PrP sequences essential for the interaction between the PrP polymers and Aβ peptide in a yeast-based assay β-amyloid oligomers and prion protein: Fatal attraction?Amyloid-beta42 interacts mainly with insoluble prion protein in the Alzheimer brain.Aggregation of αSynuclein promotes progressive in vivo neurotoxicity in adult rat dopaminergic neurons Human Microbiome and its Association With Health and Diseases.High-affinity Anticalins with aggregation-blocking activity directed against the Alzheimer β-amyloid peptide.Prion infection promotes extensive accumulation of α-synuclein in aged human α-synuclein transgenic mice.Genomic Characteristics of Genetic Creutzfeldt-Jakob Disease Patients with V180I Mutation and Associations with Other Neurodegenerative Disorders.Traumatic brain injury may increase risk of young onset dementia Promiscuous cross-seeding between bacterial amyloids promotes interspecies biofilms.Amylin-Aβ oligomers at atomic resolution using molecular dynamics simulations: a link between Type 2 diabetes and Alzheimer's disease Bacterial curli protein promotes the conversion of PAP248-286 into the amyloid SEVI: cross-seeding of dissimilar amyloid sequences Exploring the basis of [PIN(+)] variant differences in [PSI(+)] induction The cellular prion protein traps Alzheimer's Aβ in an oligomeric form and disassembles amyloid fibers.Cell-to-cell transmission of non-prion protein aggregates.Cerebral vascular amyloid seeds drive amyloid β-protein fibril assembly with a distinct anti-parallel structure Variant-specific prion interactions: Complicating factors.The amyloid interactome: Exploring protein aggregation.Interaction between pathogenic proteins in neurodegenerative disorders.The amyloid state of proteins in human diseases.Alzheimer's disease Aβ assemblies mediating rapid disruption of synaptic plasticity and memory.Postsynaptic Receptors for Amyloid-β Oligomers as Mediators of Neuronal Damage in Alzheimer's Disease.Prion protein oligomer and its neurotoxicity.Biophysical studies of the amyloid β-peptide: interactions with metal ions and small molecules.Taking advantage of physiological proteolytic processing of the prion protein for a therapeutic perspective in prion and Alzheimer diseases.Prion protein and aging.

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P2860

Molecular cross talk between misfolded proteins in animal models of Alzheimer's and prion diseases

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2010 nî lūn-bûn

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2010 թուականի Մարտին հրատարակուած գիտական յօդուած

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2010 թվականի մարտին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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Molecular cross talk between m ...... Alzheimer's and prion diseases

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Molecular cross talk between m ...... Alzheimer's and prion diseases

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Molecular cross talk between m ...... Alzheimer's and prion diseases

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Molecular cross talk between m ...... Alzheimer's and prion diseases

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Molecular cross talk between m ...... Alzheimer's and prion diseases

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Molecular cross talk between m ...... Alzheimer's and prion diseases

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Molecular cross talk between m ...... Alzheimer's and prion diseases

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Molecular cross talk between m ...... Alzheimer's and prion diseases

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Molecular cross talk between m ...... Alzheimer's and prion diseases

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JNEUROSCI.5924-09.2010

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Journal of Neuroscience

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Molecular cross talk between m ...... Alzheimer's and prion diseases

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Claudio Soto

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Diego Morales-Scheihing

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Joaquin Castilla

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Lisbell D Estrada

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Maria C Jara

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Rodrigo Diaz-Espinoza

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Rodrigo Morales

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P2860

Correlative Memory Deficits, Abeta Elevation, and Amyloid Plaques in Transgenic Mice

Cellular prion protein mediates impairment of synaptic plasticity by amyloid-beta oligomers

Abeta and tau form soluble complexes that may promote self aggregation of both into the insoluble forms observed in Alzheimer's disease

Protein misfolding, functional amyloid, and human disease

Exogenous induction of cerebral beta-amyloidogenesis is governed by agent and host

Common mechanisms of amyloid oligomer pathogenesis in degenerative disease

Proteotoxic stress and inducible chaperone networks in neurodegenerative disease and aging

Aggresomes, inclusion bodies and protein aggregation

A trip to the ER: coping with stress

Cellular prion protein regulates beta-secretase cleavage of the Alzheimer's amyloid precursor protein.

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10.1523/JNEUROSCI.5924-09.2010

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13

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42806578

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20357103

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Alzheimer's disease

Prion protein family

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2859074

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