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Invited Review: The role of prion‐like mechanisms in neurodegenerative diseases

https://doi.org/10.1111/nan.12592
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A Neurological Syndrome Associated with Orthostatic Hypotension
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Progressive Supranuclear Palsy
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Alpha‐synuclein RT ‐Qu IC in the CSF of patients with alpha‐synucleinopathies
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Sigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degeneration–motor neuron disease
inferredcites →https://doi.org/10.1002/ana.24066openalex-snapshot
Lewy body extracts from Parkinson disease brains trigger α‐synuclein pathology and neurodegeneration in mice and monkeys
inferredcites →https://doi.org/10.1002/ana.24431openalex-snapshot
Detection of TDP‐43 oligomers in frontotemporal lobar degeneration–TDP
inferredcites →https://doi.org/10.1002/ana.24716openalex-snapshot
Seed‐competent high‐molecular‐weight tau species accumulates in the cerebrospinal fluid of Alzheimer's disease mouse model and human patients
inferredcites →https://doi.org/10.1002/ana.25407openalex-snapshot
Early onset cerebral amyloid angiopathy following childhood exposure to cadaveric dura
inferredcites →https://doi.org/10.1002/ana.25446openalex-snapshot
Seeding variability of different alpha synuclein strains in synucleinopathies
inferredcites →https://doi.org/10.1002/ana.410110607openalex-snapshot
Slowly progressive aphasia without generalized dementia
inferredcites →https://doi.org/10.1002/ana.410220411openalex-snapshot
Tau antisera recognize neurofibrillary tangles in a range of neurodegenerative disorders
inferredcites →https://doi.org/10.1002/mds.27370openalex-snapshot
No evidence of iatrogenic human transmission in autopsy confirmed multiple system atrophy
inferredcites →https://doi.org/10.1007/978-3-642-50703-8openalex-snapshot
Histopathologie des Nervensystems
inferredcites →https://doi.org/10.1007/bf00347853openalex-snapshot
[An unusual hereditary familial disease of the central nervous system].
inferredcites →https://doi.org/10.1007/bf00688244openalex-snapshot
Progressive supranuclear palsy: extensive neuropil threads in addition to neurofibrillary tangles
inferredcites →https://doi.org/10.1007/bf01716575openalex-snapshot
Die Histopathologische Forschung in der Psychiatrie
inferredcites →https://doi.org/10.1007/bf02865827openalex-snapshot
Über eine eigenartige hereditär- familiäre Erkrankung des Zentralnervensystems
inferredcites →https://doi.org/10.1007/bf02866081openalex-snapshot
Über eine eigenartige herdförmige erkrankung des zentralnervensystems (Vorläufige mitteilung)
inferredcites →https://doi.org/10.1007/bf02866241openalex-snapshot
über eigenartige Krankheitsfälle des späteren Alters
inferredcites →https://doi.org/10.1007/bf02866679openalex-snapshot
Betrachtungen über art und ausbreitung des krankhaiten prozesses in einem fall von pickscher atrophie des stirnhirns
inferredcites →https://doi.org/10.1007/bf02870932openalex-snapshot
Über eigenartige erkrankungen des zentralnervensystems mit bemerkenswertem anatomischen befunde
inferredcites →https://doi.org/10.1007/bf02878348openalex-snapshot
Anatomische beiträge zur lehre von der pickschen umschriebenen gro\hirnrinden-atrophie („picksche krankheit“)
inferredcites →https://doi.org/10.1007/bf02892896openalex-snapshot
Klinische und anatomische Untersuchungen über eine eigenartige organische Erkrankung des Zentralnervensystems im Praesenium
inferredcites →https://doi.org/10.1007/s00401-006-0127-zopenalex-snapshot
Staging of Alzheimer disease-associated neurofibrillary pathology using paraffin sections and immunocytochemistry
inferredcites →https://doi.org/10.1007/s00401-013-1089-6openalex-snapshot
Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloid
inferredcites →https://doi.org/10.1007/s00401-013-1231-5openalex-snapshot
Peripheral administration of tau aggregates triggers intracerebral tauopathy in transgenic mice
inferredcites →https://doi.org/10.1007/s00401-014-1339-2openalex-snapshot
Aβ seeds resist inactivation by formaldehyde
inferredcites →https://doi.org/10.1007/s00401-014-1360-5openalex-snapshot
Formaldehyde-fixed brain tissue from spontaneously ill α-synuclein transgenic mice induces fatal α-synucleinopathy in transgenic hosts
inferredcites →https://doi.org/10.1007/s00401-016-1537-1openalex-snapshot
Updated TDP-43 in Alzheimer’s disease staging scheme
inferredcites →https://doi.org/10.1007/s00401-016-1565-xopenalex-snapshot
Dura mater is a potential source of Aβ seeds
inferredcites →https://doi.org/10.1007/s00401-016-1588-3openalex-snapshot
Significant association of cadaveric dura mater grafting with subpial Aβ deposition and meningeal amyloid angiopathy
inferredcites →https://doi.org/10.1007/s00401-016-1644-zopenalex-snapshot
Widespread tau seeding activity at early Braak stages
inferredcites →https://doi.org/10.1007/s00401-017-1670-5openalex-snapshot
Prion disease: experimental models and reality
inferredcites →https://doi.org/10.1007/s00401-017-1692-zopenalex-snapshot
Ultrasensitive and selective detection of 3-repeat tau seeding activity in Pick disease brain and cerebrospinal fluid
inferredcites →https://doi.org/10.1007/s00401-017-1703-0openalex-snapshot
Amyloid-β accumulation in the CNS in human growth hormone recipients in the UK
inferredcites →https://doi.org/10.1007/s00401-017-1762-2openalex-snapshot
MSA prions exhibit remarkable stability and resistance to inactivation
inferredcites →https://doi.org/10.1007/s00401-017-1791-xopenalex-snapshot
Neuropathology of iatrogenic Creutzfeldt–Jakob disease and immunoassay of French cadaver-sourced growth hormone batches suggest possible transmission of tauopathy and long incubation periods for the transmission of Abeta pathology
inferredcites →https://doi.org/10.1007/s00401-018-1822-2openalex-snapshot
Evidence of amyloid-β cerebral amyloid angiopathy transmission through neurosurgery
inferredcites →https://doi.org/10.1007/s00401-018-1828-9openalex-snapshot
Fatal Aβ cerebral amyloid angiopathy 4 decades after a dural graft at the age of 2 years
inferredcites →https://doi.org/10.1007/s00401-018-1848-5openalex-snapshot
Infectious prions do not induce Aβ deposition in an in vivo seeding model
inferredcites →https://doi.org/10.1007/s00401-018-1909-9openalex-snapshot
Nodding syndrome in Uganda is a tauopathy
inferredcites →https://doi.org/10.1007/s00401-018-1947-3openalex-snapshot
Seeding selectivity and ultrasensitive detection of tau aggregate conformers of Alzheimer disease
inferredcites →https://doi.org/10.1007/s00401-018-1953-5openalex-snapshot
Amyloid-β pathology enhances pathological fibrillary tau seeding induced by Alzheimer PHF in vivo
inferredcites →https://doi.org/10.1007/s00401-019-01959-4openalex-snapshot
Multiple system atrophy prions retain strain specificity after serial propagation in two different Tg(SNCA*A53T) mouse lines
inferredcites →https://doi.org/10.1007/s00401-019-02037-5openalex-snapshot
Oral and intravenous transmission of α-synuclein fibrils to mice
inferredcites →https://doi.org/10.1007/s00702-005-0385-2openalex-snapshot
Very long term studies of the seeding of β-amyloidosis in primates
inferredcites →https://doi.org/10.1007/s10072-003-0108-0openalex-snapshot
DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonism
inferredcites →https://doi.org/10.1007/s12035-017-0624-1openalex-snapshot
Prion-Like Seeding of Misfolded α-Synuclein in the Brains of Dementia with Lewy Body Patients in RT-QUIC
inferredcites →https://doi.org/10.1007/s12035-018-1007-yopenalex-snapshot
Detecting Alpha Synuclein Seeding Activity in Formaldehyde-Fixed MSA Patient Tissue by PMCA
inferredcites →https://doi.org/10.1007/s12041-018-0963-3openalex-snapshot
Shared mechanisms among neurodegenerative diseases: from genetic factors to gene networks
inferredcites →https://doi.org/10.1016/0006-291x(84)91209-9openalex-snapshot
Alzheimer's disease and Down's syndrome: Sharing of a unique cerebrovascular amyloid fibril protein
inferredcites →https://doi.org/10.1016/0022-510x(89)90219-0openalex-snapshot
Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome)
inferredcites →https://doi.org/10.1016/0092-8674(86)90662-8openalex-snapshot
Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene
inferredcites →https://doi.org/10.1016/0092-8674(93)90360-3openalex-snapshot
Mice devoid of PrP are resistant to scrapie
inferredcites →https://doi.org/10.1016/0140-6736(91)91612-xopenalex-snapshot
Mis-sense mutation Val→Ile in exon 17 of amyloid precursor protein gene in Japanese familial Alzheimer's disease
inferredcites →https://doi.org/10.1016/0304-3940(90)90829-xopenalex-snapshot
Constant neurofibrillary changes in the neocortex in progressive supranuclear palsy. Basic differences with Alzheimer's disease and aging
inferredcites →https://doi.org/10.1016/j.ajhg.2008.12.010openalex-snapshot
Deleterious Variants of FIG4, a Phosphoinositide Phosphatase, in Patients with ALS
inferredcites →https://doi.org/10.1016/j.ajhg.2011.06.008openalex-snapshot
A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease
inferredcites →https://doi.org/10.1016/j.ajpath.2017.03.011openalex-snapshot
Enhanced Tau Aggregation in the Presence of Amyloid β
inferredcites →https://doi.org/10.1016/j.celrep.2013.06.007openalex-snapshot
Prion-like Properties of Pathological TDP-43 Aggregates from Diseased Brains
inferredcites →https://doi.org/10.1016/j.celrep.2014.02.031openalex-snapshot
Detection of Misfolded Aβ Oligomers for Sensitive Biochemical Diagnosis of Alzheimer’s Disease
inferredcites →https://doi.org/10.1016/j.csbj.2014.09.011openalex-snapshot
Cell-based Models To Investigate Tau Aggregation
inferredcites →https://doi.org/10.1016/j.expneurol.2004.01.031openalex-snapshot
Genotype-phenotype correlations in FTDP-17: does form follow function?
inferredcites →https://doi.org/10.1016/j.mpdhp.2018.11.002openalex-snapshot
Transmissible human proteopathies: an expanding field
inferredcites →https://doi.org/10.1016/j.nbd.2016.08.007openalex-snapshot
In vitro prion-like behaviour of TDP-43 in ALS
inferredcites →https://doi.org/10.1016/j.nbd.2018.01.015openalex-snapshot
Prion-like seeding and nucleation of intracellular amyloid-β
inferredcites →https://doi.org/10.1016/j.neuron.2004.11.005openalex-snapshot
Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology
inferredcites →https://doi.org/10.1016/j.neuron.2011.09.010openalex-snapshot
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
inferredcites →https://doi.org/10.1016/j.neuron.2011.09.011openalex-snapshot
Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
inferredcites →https://doi.org/10.1016/j.neuron.2014.04.047openalex-snapshot
Distinct Tau Prion Strains Propagate in Cells and Mice and Define Different Tauopathies
inferredcites →https://doi.org/10.1016/j.neuron.2014.09.027openalex-snapshot
Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS
inferredcites →https://doi.org/10.1016/j.neuron.2016.09.055openalex-snapshot
Tau Prion Strains Dictate Patterns of Cell Pathology, Progression Rate, and Regional Vulnerability In Vivo
inferredcites →https://doi.org/10.1016/j.neuron.2017.07.025openalex-snapshot
TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics
inferredcites →https://doi.org/10.1016/j.parkreldis.2016.07.011openalex-snapshot
Conjugal parkinsonism – Clinical, pathology and genetic study. No evidence of person-to-person transmission
inferredcites →https://doi.org/10.1016/s0140-6736(61)92008-6openalex-snapshot
ENCEPHALOPATHY IN MICE PRODUCED BY INOCULATION WITH SCRAPIE BRAIN MATERIAL
inferredcites →https://doi.org/10.1016/s0140-6736(66)92031-9openalex-snapshot
EXPERIMENTAL "KURU" IN CHIMPANZEES A Pathological Report
inferredcites →https://doi.org/10.1016/s0140-6736(86)90495-2openalex-snapshot
ALZHEIMER'S DISEASE AND TAU PROTEINS
inferredcites →https://doi.org/10.1016/s0140-6736(86)92134-3openalex-snapshot
DEFECTIVE BRAIN MICROTUBULE ASSEMBLY IN ALZHEIMER'S DISEASE
inferredcites →https://doi.org/10.1016/s0197-4580(02)00065-9openalex-snapshot
Staging of brain pathology related to sporadic Parkinson’s disease
inferredcites →https://doi.org/10.1016/s0304-3940(98)00504-7openalex-snapshot
Filamentous α-synuclein inclusions link multiple system atrophy with Parkinson's disease and dementia with Lewy bodies
inferredcites →https://doi.org/10.1016/s0368-1742(59)80029-1openalex-snapshot
Experimental Production of Scrapie in Goats
inferredcites →https://doi.org/10.1016/s0368-1742(61)80013-1openalex-snapshot
Scrapie Produced Experimentally in Goats With Special Reference To the Clinical Syndrome
inferredcites →https://doi.org/10.1016/s0967-5868(96)90003-xopenalex-snapshot
Iatrogenic Creutzfeldt-Jakob disease and its neurosurgical implications
inferredcites →https://doi.org/10.1038/209794a0openalex-snapshot
Experimental Transmission of a Kuru-like Syndrome to Chimpanzees
inferredcites →https://doi.org/10.1038/214764a0openalex-snapshot
Does the Agent of Scrapie Replicate without Nucleic Acid ?
inferredcites →https://doi.org/10.1038/31508openalex-snapshot
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
inferredcites →https://doi.org/10.1038/33416openalex-snapshot
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
inferredcites →https://doi.org/10.1038/349704a0openalex-snapshot
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
inferredcites →https://doi.org/10.1038/353844a0openalex-snapshot
Early-onset Alzheimer's disease caused by mutations at codon 717 of the β-amyloid precursor protein gene
inferredcites →https://doi.org/10.1038/362059a0openalex-snapshot
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1038/375754a0openalex-snapshot
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
inferredcites →https://doi.org/10.1038/379339a0openalex-snapshot
Normal host prion protein necessary for scrapie-induced neurotoxicity
inferredcites →https://doi.org/10.1038/aps.2017.28openalex-snapshot
Amyloid beta: structure, biology and structure-based therapeutic development
inferredcites →https://doi.org/10.1038/nature05016openalex-snapshot
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
inferredcites →https://doi.org/10.1038/nature05017openalex-snapshot
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
inferredcites →https://doi.org/10.1038/nature08971openalex-snapshot
Mutations of optineurin in amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1038/nature10353openalex-snapshot
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia
inferredcites →https://doi.org/10.1038/nature11280openalex-snapshot
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1038/nature15369openalex-snapshot
Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy
inferredcites →https://doi.org/10.1038/nature20814openalex-snapshot
Structural variation in amyloid-β fibrils from Alzheimer's disease clinical subtypes
inferredcites →https://doi.org/10.1038/ncb1901openalex-snapshot
Transmission and spreading of tauopathy in transgenic mouse brain
inferredcites →https://doi.org/10.1038/ncomms11253openalex-snapshot
CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia
inferredcites →https://doi.org/10.1038/ncomms5824openalex-snapshot
Full-length TDP-43 forms toxic amyloid oligomers that are present in frontotemporal lobar dementia-TDP patients
inferredcites →https://doi.org/10.1038/ncomms8025openalex-snapshot
A mechanistic model of tau amyloid aggregation based on direct observation of oligomers
inferredcites →https://doi.org/10.1038/ng.3622openalex-snapshot
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1038/ng.3626openalex-snapshot
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1038/ng1001-166openalex-snapshot
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2
inferredcites →https://doi.org/10.1038/ng1332openalex-snapshot
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
inferredcites →https://doi.org/10.1038/ng1609openalex-snapshot
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia
inferredcites →https://doi.org/10.1038/ng1742openalex-snapshot
ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1038/ng1884openalex-snapshot
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
inferredcites →https://doi.org/10.1038/nm.2294openalex-snapshot
Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion
inferredcites →https://doi.org/10.1038/nm.3457openalex-snapshot
Cell-to-cell transmission of pathogenic proteins in neurodegenerative diseases
inferredcites →https://doi.org/10.1038/nm.4443openalex-snapshot
Amyloid-β plaques enhance Alzheimer's brain tau-seeded pathologies by facilitating neuritic plaque tau aggregation
inferredcites →https://doi.org/10.1038/nm1746openalex-snapshot
Lewy bodies in grafted neurons in subjects with Parkinson's disease suggest host-to-graft disease propagation
inferredcites →https://doi.org/10.1038/nm1747openalex-snapshot
Lewy body–like pathology in long-term embryonic nigral transplants in Parkinson's disease
inferredcites →https://doi.org/10.1038/nn.3688openalex-snapshot
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1038/nn.4000openalex-snapshot
Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia
inferredcites →https://doi.org/10.1038/nrn.2016.13openalex-snapshot
A critical appraisal of the pathogenic protein spread hypothesis of neurodegeneration
inferredcites →https://doi.org/10.1038/nrneurol.2017.165openalex-snapshot
Parkinson's disease — the story of an eponym
inferredcites →https://doi.org/10.1038/s41467-018-06548-9openalex-snapshot
Patient-derived frontotemporal lobar degeneration brain extracts induce formation and spreading of TDP-43 pathology in vivo
inferredcites →https://doi.org/10.1038/s41531-019-0076-6openalex-snapshot
Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability
inferredcites →https://doi.org/10.1038/s41586-018-0790-yopenalex-snapshot
Transmission of amyloid-β protein pathology from cadaveric pituitary growth hormone
inferredcites →https://doi.org/10.1038/s41593-018-0294-yopenalex-snapshot
TDP-43 extracted from frontotemporal lobar degeneration subject brains displays distinct aggregate assemblies and neurotoxic effects reflecting disease progression rates
inferredcites →https://doi.org/10.1038/srep11573openalex-snapshot
Transmission of scrapie prions to primate after an extended silent incubation period
inferredcites →https://doi.org/10.1056/nejm195711142572005openalex-snapshot
Degenerative Disease of the Central Nervous System in New Guinea
inferredcites →https://doi.org/10.1056/nejm197403212901220openalex-snapshot
Possible Person-to-Person Transmission of Creutzfeldt-Jakob Disease
inferredcites →https://doi.org/10.1056/nejm198403083101021openalex-snapshot
Some Speculations about Prions, Amyloid, and Alzheimer's Disease
inferredcites →https://doi.org/10.1056/nejm198501103120202openalex-snapshot
Creutzfeldt–Jakob Disease Prion Proteins in Human Brains
inferredcites →https://doi.org/10.1056/nejmc1610003openalex-snapshot
Variant Creutzfeldt–Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129
inferredcites →https://doi.org/10.1073/pnas.0604292103openalex-snapshot
Dissociation of pathological and molecular phenotype of variant Creutzfeldt–Jakob disease in transgenic human prion protein 129 heterozygous mice
inferredcites →https://doi.org/10.1073/pnas.0903200106openalex-snapshot
Induction of cerebral β-amyloidosis: Intracerebral versus systemic Aβ inoculation
inferredcites →https://doi.org/10.1073/pnas.0914128107openalex-snapshot
Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase
inferredcites →https://doi.org/10.1073/pnas.1100976108openalex-snapshot
In vivo demonstration that α-synuclein oligomers are toxic
inferredcites →https://doi.org/10.1073/pnas.1301175110openalex-snapshot
Brain homogenates from human tauopathies induce tau inclusions in mouse brain
inferredcites →https://doi.org/10.1073/pnas.1318268110openalex-snapshot
Transmission of multiple system atrophy prions to transgenic mice
inferredcites →https://doi.org/10.1073/pnas.1321785111openalex-snapshot
Intramuscular injection of α-synuclein induces CNS α-synuclein pathology and a rapid-onset motor phenotype in transgenic mice
inferredcites →https://doi.org/10.1073/pnas.1408900111openalex-snapshot
Serial propagation of distinct strains of Aβ prions from Alzheimer’s disease patients
inferredcites →https://doi.org/10.1073/pnas.1411649111openalex-snapshot
Proteopathic tau seeding predicts tauopathy in vivo
inferredcites →https://doi.org/10.1073/pnas.1514475112openalex-snapshot
Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonism
inferredcites →https://doi.org/10.1073/pnas.1524128113openalex-snapshot
Kinetic model of the aggregation of alpha-synuclein provides insights into prion-like spreading
inferredcites →https://doi.org/10.1073/pnas.1705091114openalex-snapshot
Atomic structure of a toxic, oligomeric segment of SOD1 linked to amyotrophic lateral sclerosis (ALS)
inferredcites →https://doi.org/10.1073/pnas.1713215114openalex-snapshot
Amyloid polymorphisms constitute distinct clouds of conformational variants in different etiological subtypes of Alzheimer’s disease
inferredcites →https://doi.org/10.1073/pnas.72.5.1858openalex-snapshot
A protein factor essential for microtubule assembly.
inferredcites →https://doi.org/10.1073/pnas.83.13.4913openalex-snapshot
Abnormal phosphorylation of the microtubule-associated protein tau (tau) in Alzheimer cytoskeletal pathology.
inferredcites →https://doi.org/10.1073/pnas.90.23.11282openalex-snapshot
Molecular cloning of cDNA encoding an unrecognized component of amyloid in Alzheimer disease.
inferredcites →https://doi.org/10.1073/pnas.90.5.1977openalex-snapshot
Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease.
inferredcites →https://doi.org/10.1073/pnas.93.23.13148openalex-snapshot
Normal host prion protein (PrP C ) is required for scrapie spread within the central nervous system
inferredcites →https://doi.org/10.1073/pnas.95.11.6469openalex-snapshot
α-Synuclein in filamentous inclusions of Lewy bodies from Parkinson’s disease and dementia with Lewy bodies
inferredcites →https://doi.org/10.1074/jbc.ac117.001037openalex-snapshot
TAR DNA-binding protein 43 (TDP-43) liquid–liquid phase separation is mediated by just a few aromatic residues
inferredcites →https://doi.org/10.1074/jbc.m115.652693openalex-snapshot
Tau Trimers Are the Minimal Propagation Unit Spontaneously Internalized to Seed Intracellular Aggregation
inferredcites →https://doi.org/10.1074/jbc.ra118.004471openalex-snapshot
Parkinson’s disease and multiple system atrophy have distinct α-synuclein seed characteristics
inferredcites →https://doi.org/10.1074/jbc.ra118.005889openalex-snapshot
Detection of TAR DNA-binding protein 43 (TDP-43) oligomers as initial intermediate species during aggregate formation
inferredcites →https://doi.org/10.1074/jbc.ra118.007222openalex-snapshot
The role of liquid–liquid phase separation in aggregation of the TDP-43 low-complexity domain
inferredcites →https://doi.org/10.1080/19336896.2015.1123371openalex-snapshot
Distinct prion-like strains of amyloid beta implicated in phenotypic diversity of Alzheimer's disease
inferredcites →https://doi.org/10.1086/421054openalex-snapshot
DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4)
inferredcites →https://doi.org/10.1086/425287openalex-snapshot
A Mutation in the Vesicle-Trafficking Protein VAPB Causes Late-Onset Spinal Muscular Atrophy and Amyotrophic Lateral Sclerosis
inferredcites →https://doi.org/10.1093/bmb/66.1.185openalex-snapshot
Bovine spongiform encephalopathy (BSE) and its epidemiology
inferredcites →https://doi.org/10.1093/brain/104.3.559openalex-snapshot
CREUTZFELDT-JAKOB DISEASE VIRUS ISOLATIONS FROM THE GERSTMANN-STRÄUSSLER SYNDROME
inferredcites →https://doi.org/10.1093/brain/awl076openalex-snapshot
Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion protein
inferredcites →https://doi.org/10.1093/brain/awp214openalex-snapshot
A new subtype of frontotemporal lobar degeneration with FUS pathology
inferredcites →https://doi.org/10.1093/brain/awu138openalex-snapshot
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement
inferredcites →https://doi.org/10.1093/brain/awv006openalex-snapshot
Rapidly progressive Alzheimer’s disease features distinct structures of amyloid-β
inferredcites →https://doi.org/10.1093/brain/awv235openalex-snapshot
Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years
inferredcites →https://doi.org/10.1093/brain/aww187openalex-snapshot
Hyperphosphorylated tau in patients with refractory epilepsy correlates with cognitive decline: a study of temporal lobe resections
inferredcites →https://doi.org/10.1093/brain/awx370openalex-snapshot
Hot-spot KIF5A mutations cause familial ALS
inferredcites →https://doi.org/10.1093/brain/awz078openalex-snapshot
The debated toxic role of aggregated TDP-43 in amyotrophic lateral sclerosis: a resolution in sight?
inferredcites →https://doi.org/10.1093/brain/awz099openalex-snapshot
Limbic-predominant age-related TDP-43 encephalopathy (LATE): consensus working group report
inferredcites →https://doi.org/10.1093/brain/awz104openalex-snapshot
Temporal evolution of microglia and α-synuclein accumulation following foetal grafting in Parkinson’s disease
inferredcites →https://doi.org/10.1093/hmg/ddv239openalex-snapshot
Subcellular localization and RNAs determine FUS architecture in different cellular compartments
inferredcites →https://doi.org/10.1096/fj.201901897ropenalex-snapshot
Liquid‐liquid phase separation and fibrillation of the prion protein modulated by a high‐affinity DNA aptamer
inferredcites →https://doi.org/10.1097/00005053-191306000-00001openalex-snapshot
A CASE OF ALZHEIMERʼS DISEASE WITH UNUSUAL NEUROLOGICAL DISTURBANCES
inferredcites →https://doi.org/10.1097/00005053-192304000-00072openalex-snapshot
HISTOPATHOLOGIE DES NERVENSYSTEMS
inferredcites →https://doi.org/10.1098/rstb.2008.0068openalex-snapshot
A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea
inferredcites →https://doi.org/10.1101/cshperspect.a023499openalex-snapshot
Bioassays and Inactivation of Prions
inferredcites →https://doi.org/10.1111/j.1471-4159.2009.06324.xopenalex-snapshot
Seeding induced by α‐synuclein oligomers provides evidence for spreading of α‐synuclein pathology
inferredcites →https://doi.org/10.1111/j.1749-6632.1993.tb23057.xopenalex-snapshot
Experimental Induction of β‐Amyloid Plaques and Cerebral Angiopathy in Primatesa
inferredcites →https://doi.org/10.1111/nan.12592openalex-snapshot
Invited Review: The role of prion‐like mechanisms in neurodegenerative diseases
inferredcites →https://doi.org/10.1111/neup.12270openalex-snapshot
Neuropathological and biochemical criteria to identify acquired Creutzfeldt‐Jakob disease among presumed sporadic cases
inferredcites →https://doi.org/10.1126/science.1062097openalex-snapshot
Formation of Neurofibrillary Tangles in P301L Tau Transgenic Mice Induced by Aβ42 Fibrils
inferredcites →https://doi.org/10.1126/science.1096284openalex-snapshot
Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1
inferredcites →https://doi.org/10.1126/science.1134108openalex-snapshot
Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis
inferredcites →https://doi.org/10.1126/science.1138718openalex-snapshot
A General Model of Prion Strains and Their Pathogenicity
inferredcites →https://doi.org/10.1126/science.1154584openalex-snapshot
TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
inferredcites →https://doi.org/10.1126/science.1165942openalex-snapshot
Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6
inferredcites →https://doi.org/10.1126/science.1194516openalex-snapshot
Peripherally Applied Aβ-Containing Inoculates Induce Cerebral β-Amyloidosis
inferredcites →https://doi.org/10.1126/science.1227157openalex-snapshot
Pathological α-Synuclein Transmission Initiates Parkinson-like Neurodegeneration in Nontransgenic Mice
inferredcites →https://doi.org/10.1126/science.1925564openalex-snapshot
A mutation in the Amyloid Precursor Protein Associated with Hereditary Alzheimer's Disease
inferredcites →https://doi.org/10.1126/science.276.5321.2045openalex-snapshot
Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease
inferredcites →https://doi.org/10.1126/science.6801762openalex-snapshot
Novel Proteinaceous Infectious Particles Cause Scrapie
inferredcites →https://doi.org/10.1126/science.7638622openalex-snapshot
Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus
inferredcites →https://doi.org/10.1126/scitranslmed.aad9157openalex-snapshot
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1126/scitranslmed.aaf6953openalex-snapshot
Nodding syndrome may be an autoimmune reaction to the parasitic worm Onchocerca volvulus
inferredcites →https://doi.org/10.1128/jvi.69.6.3584-3596.1995openalex-snapshot
Cloning and characterization of a novel cellular protein, TDP-43, that binds to human immunodeficiency virus type 1 TAR DNA sequence motifs
inferredcites →https://doi.org/10.1136/jnnp.2005.070805openalex-snapshot
Alzheimer-type neuropathology in a 28 year old patient with iatrogenic Creutzfeldt-Jakob disease after dural grafting
inferredcites →https://doi.org/10.1136/jnnp.32.1.28openalex-snapshot
Orthostatic hypotension and nicotine sensitivity in a case of multiple system atrophy.
inferredcites →https://doi.org/10.1136/vr.80.1.2openalex-snapshot
The possible nature of the transmissible agent of scrapie
inferredcites →https://doi.org/10.1146/annurev-neuro-071714-033828openalex-snapshot
Neurodegenerative Diseases: Expanding the Prion Concept
inferredcites →https://doi.org/10.1155/2013/704546openalex-snapshot
PrionsEx Vivo: What Cell Culture Models Tell Us about Infectious Proteins
inferredcites →https://doi.org/10.1159/000131165openalex-snapshot
Dégénérescences nigro-striées et cerebello-nigro-striées; pp. 219–232
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What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4980156openalex-extracted
The Intrinsic Connectivity between the Default Mode and Dorsal Attention Networks Is a Marker of Alzheimer's Pathology Burden Independent of Cognitive Reserve
inferred← citeshttps://doi.org/10.1001/jama.2023.14445openalex-snapshot
Intracerebral Hemorrhage Among Blood Donors and Their Transfusion Recipients
inferred← citeshttps://doi.org/10.1002/advs.202500320openalex-snapshot
Nanoplasmonic Infrared Microarray Sensor Enabling Structural Protein Biomarker‐Based Drug Screening for Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.1002/advs.76119openalex-snapshot
TDP‐43 Aggregation: The Healthy‐Toxic Balance of the Prion‐Like Domain
inferred← citeshttps://doi.org/10.1002/mabi.202200489openalex-snapshot
How Single Site Mutations Can Help Understanding Structure Formation of Amyloid β1−40
inferred← citeshttps://doi.org/10.1002/pro.70535openalex-snapshot
Scalable assay to identify inhibitors of prion‐like propagation of protein misfolding as potential therapeutics for neurodegeneration
inferred← citeshttps://doi.org/10.1002/vms3.522openalex-snapshot
Elevated temperatures accelerate the formation of toxic amyloid fibrils of hen egg‐white lysozyme
inferred← citeshttps://doi.org/10.1007/978-3-030-66830-3_12openalex-snapshot
Neurodegenerative Disorders
inferred← citeshttps://doi.org/10.1007/978-3-032-18296-8_3openalex-snapshot
Preclinical Models of Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.1007/978-981-99-2423-3_3openalex-snapshot
Protein–Protein Interactions in Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.1007/978-981-99-7731-4_12openalex-snapshot
The Potential of Curcumin and Its Applications in Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.1007/s00115-024-01644-2openalex-snapshot
Klinik und Diagnostik humaner spongiformer Enzephalopathien: ein Update
inferred← citeshttps://doi.org/10.1007/s00401-020-02153-7openalex-snapshot
Prevalence in Britain of abnormal prion protein in human appendices before and after exposure to the cattle BSE epizootic
inferred← citeshttps://doi.org/10.1007/s00401-021-02312-4openalex-snapshot
Transmissible α-synuclein seeding activity in brain and stomach of patients with Parkinson’s disease
inferred← citeshttps://doi.org/10.1007/s00441-022-03683-0openalex-snapshot
Mechanisms of prion-induced toxicity
inferred← citeshttps://doi.org/10.1007/s00701-021-04751-0openalex-snapshot
Follow-up study of a patient with early onset cerebral amyloid angiopathy following childhood cadaveric dural graft
inferred← citeshttps://doi.org/10.1007/s11011-024-01369-wopenalex-snapshot
The connection between gut microbiota and its metabolites with neurodegenerative diseases in humans
inferred← citeshttps://doi.org/10.1007/s11357-023-00950-yopenalex-snapshot
Hawaiian native herb Mamaki prevents dementia by ameliorating neuropathology and repairing neurons in four different mouse models of neurodegenerative diseases
inferred← citeshttps://doi.org/10.1007/s11655-025-3936-4openalex-snapshot
Dihuang Yinzi Regulates cAMP/PKA/CREB-BDNF to Improve Synaptic Plasticity in APP/PS1 Mice: A Study Based on Brain Metabolomics
inferred← citeshttps://doi.org/10.1007/s12031-021-01944-1openalex-snapshot
Intercellular Propagation and Aggregate Seeding of Mutant Ataxin-1
inferred← citeshttps://doi.org/10.1007/s12275-023-00070-4openalex-snapshot
Prions in Microbes: The Least in the Most
inferred← citeshttps://doi.org/10.1007/s40473-026-00320-wopenalex-snapshot
The Role of Protein Aggregation in Neurodegenerative Diseases: Molecular Mechanisms and Therapeutic Targets
inferred← citeshttps://doi.org/10.1016/b978-0-12-819460-7.00141-9openalex-snapshot
Cofactors and Coenzymes | Cysteamine
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2020.07.003openalex-snapshot
One or more β-amyloid(s)? New insights into the prion-like nature of Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.bbr.2026.116455openalex-snapshot
Extracellular vesicles in neurodegenerative diseases: A new frontier in diagnosis and therapy
inferred← citeshttps://doi.org/10.1016/j.biopha.2025.118758openalex-snapshot
Anti-prion drugs reduce endoplasmic reticulum stress and protect human dopaminergic neurons from death
inferred← citeshttps://doi.org/10.1016/j.bmc.2021.116462openalex-snapshot
Histamine H3 receptor antagonists with peptidomimetic (keto)piperazine structures to inhibit Aβ oligomerisation
inferred← citeshttps://doi.org/10.1016/j.ebiom.2025.105605openalex-snapshot
Extracellular vesicles: new horizons in neurodegeneration
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e31624openalex-snapshot
Genetic variability of FOXP2 and its targets CNTNAP2 and PRNP in frontotemporal dementia: A pilot study in a southern Italian population
inferred← citeshttps://doi.org/10.1016/j.jare.2021.09.005openalex-snapshot
Interplay of gut microbiota and oxidative stress: Perspective on neurodegeneration and neuroprotection
inferred← citeshttps://doi.org/10.1016/j.jhin.2020.10.018openalex-snapshot
Alpha-synuclein seeds of Parkinson's disease show high prion-exceeding resistance to steam sterilization
inferred← citeshttps://doi.org/10.1016/j.jmb.2021.167222openalex-snapshot
The Nt17 Domain and its Helical Conformation Regulate the Aggregation, Cellular Properties and Neurotoxicity of Mutant Huntingtin Exon 1
inferred← citeshttps://doi.org/10.1016/j.mcpro.2023.100629openalex-snapshot
Methods to Discover and Validate Biofluid-Based Biomarkers in Neurodegenerative Dementias
inferred← citeshttps://doi.org/10.1016/j.nbd.2020.104973openalex-snapshot
Genetic risk factors for Creutzfeldt-Jakob disease
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2022.104679openalex-snapshot
Modeling neurodegenerative disorders in zebrafish
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2025.106194openalex-snapshot
The cerebellum in frontotemporal dementia: From neglected bystander to potential neuromodulatory target. A narrative review
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2020.07.030openalex-snapshot
Delay of gCJD aggravation in sick TgMHu2ME199K mice by combining NPC transplantation and Nano-PSO administration
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2025.121509openalex-snapshot
The intrinsic connectivity between the default mode and dorsal attention networks is an independent fMRI biomarker of Alzheimer's disease pathology burden
inferred← citeshttps://doi.org/10.1016/j.neuron.2024.05.012openalex-snapshot
Cryo-EM structures of pathogenic fibrils and their impact on neurodegenerative disease research
inferred← citeshttps://doi.org/10.1016/j.ro.2026.150989openalex-snapshot
Imaging of Central Nervous System Disorders of Protein Folding
inferred← citeshttps://doi.org/10.1016/j.rvsc.2025.105916openalex-snapshot
Gut microbiota alterations linked to classical scrapie in sheep
inferred← citeshttps://doi.org/10.1016/j.talanta.2023.125134openalex-snapshot
Ultrasensitive electrochemical detection of amyloid-beta oligomers using double amplification strategy by MXene substrate and covalent organic framework-based probe
inferred← citeshttps://doi.org/10.1016/j.xcrm.2022.100636openalex-snapshot
Quantification and targeting of elusive neurotoxic amyloid oligomers
inferred← citeshttps://doi.org/10.1016/s1474-4422(21)00379-3openalex-snapshot
Safe laboratory management of prions and proteopathic seeds
inferred← citeshttps://doi.org/10.1017/9781108989855.018openalex-snapshot
Pathology in Parkinson’s Disease
inferred← citeshttps://doi.org/10.1021/acs.chemrev.4c00280openalex-snapshot
Residue-Specific Incorporation of Noncanonical Amino Acids in Auxotrophic Hosts: Quo Vadis?
inferred← citeshttps://doi.org/10.1021/acsbiomaterials.6c00290openalex-snapshot
Nanotheranostics for Alzheimer’s Disease: The Rising Promise of Fluorescent Carbon Dots
inferred← citeshttps://doi.org/10.1021/acschemneuro.5c00085openalex-snapshot
Soluble N-Terminal Domain of the Prion Protein Interferes with Fibrillization of α-Synuclein to Form Off-Pathway Assemblies that Lack Cellular Seeding Activity
inferred← citeshttps://doi.org/10.1021/acschemneuro.5c00236openalex-snapshot
Mechanisms of Alpha-Synuclein-Seeded Aggregation in Neurons Revealed by Fluorescence Lifetime Imaging
inferred← citeshttps://doi.org/10.1021/acsnutrsci.6c00006openalex-snapshot
Protective Effects of Erinacine A against Neuro 2a Cell Death Induced by Endoplasmic Reticulum Stress and Amyloid-Beta Aggregates
inferred← citeshttps://doi.org/10.1021/jasms.2c00332openalex-snapshot
Structural Proteomic Profiling of Cerebrospinal Fluids to Reveal Novel Conformational Biomarkers for Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1038/s41467-024-44945-5openalex-snapshot
Heterotypic interactions can drive selective co-condensation of prion-like low-complexity domains of FET proteins and mammalian SWI/SNF complex
inferred← citeshttps://doi.org/10.1038/s41556-026-01871-6openalex-snapshot
Glucosylceramide-induced ectosomes propagate pathogenic α-synuclein in Parkinson’s disease
inferred← citeshttps://doi.org/10.1038/s41598-022-08528-yopenalex-snapshot
Disrupted connectivity in the olfactory bulb-entorhinal cortex-dorsal hippocampus circuit is associated with recognition memory deficit in Alzheimer’s disease model
inferred← citeshttps://doi.org/10.1039/d4an01402bopenalex-snapshot
Proximity hybridization-triggered cascade amplification for label-free SERS detection of Alzheimer's amyloid-β oligomers
inferred← citeshttps://doi.org/10.1080/10985549.2025.2481054openalex-snapshot
Investigating the Aggregation and Prionogenic Properties of Human Cancer-Related Proteins
inferred← citeshttps://doi.org/10.1080/12298093.2024.2322211openalex-snapshot
A Story Between s and S: [Het-s] Prion of the Fungus Podospora anserina
inferred← citeshttps://doi.org/10.1080/14737175.2025.2526113openalex-snapshot
Contemporary perspectives in cerebral amyloid angiopathy
inferred← citeshttps://doi.org/10.1093/gigascience/giag059openalex-snapshot
Cell type transcriptomic modules reveal shared molecular mechanisms in Alzheimer’s and Parkinson’s disease
inferred← citeshttps://doi.org/10.1101/2021.07.18.452825openalex-snapshot
Common molecular mechanisms underlie the transfer of alpha-synuclein, Tau and huntingtin and modulate spontaneous activity in neuronal cells
inferred← citeshttps://doi.org/10.1101/2023.04.12.536623openalex-snapshot
Heterotypic interactions in the dilute phase can drive co-condensation of prion-like low-complexity domains of FET proteins and mammalian SWI/SNF complex
inferred← citeshttps://doi.org/10.1101/2025.02.17.638647openalex-snapshot
Cell type transcriptomics reveal shared genetic mechanisms in Alzheimer’s and Parkinson’s disease
inferred← citeshttps://doi.org/10.1101/2025.08.17.670564openalex-snapshot
Regional Patterns of Neurodegeneration in a Mouse Model of Proteinopathy
inferred← citeshttps://doi.org/10.1103/16f3-t125openalex-snapshot
Experimental electronic modeling of focal and progressive brain lesion processes using a network of single-transistor chaotic oscillators
inferred← citeshttps://doi.org/10.1111/cns.70056openalex-snapshot
Olfactory bulb stimulation mitigates Alzheimer's‐like disease progression
inferred← citeshttps://doi.org/10.1155/2023/6687264openalex-snapshot
The Prion Basis of Progressive Neurodegenerative Disorders
inferred← citeshttps://doi.org/10.1161/strokeaha.123.042583openalex-snapshot
Seed to Bleed: Iatrogenic Cerebral Amyloid Angiopathy
inferred← citeshttps://doi.org/10.1161/strokeaha.124.049279openalex-snapshot
Proteinopathies and the Neurodegenerative Aftermath of Stroke: Potential Biomarkers and Treatment Targets
inferred← citeshttps://doi.org/10.1177/1877718x261461375openalex-snapshot
Structural biology of alpha-synuclein amyloid filaments: Implications in synucleinopathies
inferred← citeshttps://doi.org/10.1186/s12974-023-02751-8openalex-snapshot
TGF-β1 signalling in Alzheimer’s pathology and cytoskeletal reorganization: a specialized Tau perspective
inferred← citeshttps://doi.org/10.1186/s13041-021-00864-wopenalex-snapshot
Neuronal excitatory-to-inhibitory balance is altered in cerebral organoid models of genetic neurological diseases
inferred← citeshttps://doi.org/10.1186/s40035-024-00461-6openalex-snapshot
Peripheral proteinopathy in neurodegenerative diseases
inferred← citeshttps://doi.org/10.1186/s40478-020-00990-xopenalex-snapshot
Towards an improved early diagnosis of neurodegenerative diseases: the emerging role of in vitro conversion assays for protein amyloids
inferred← citeshttps://doi.org/10.1186/s40478-021-01120-xopenalex-snapshot
Prion-induced photoreceptor degeneration begins with misfolded prion protein accumulation in cones at two distinct sites: cilia and ribbon synapses
inferred← citeshttps://doi.org/10.12703/b/9-6openalex-snapshot
Recent advances in understanding and treatment of Parkinson’s disease
inferred← citeshttps://doi.org/10.1364/boe.545580openalex-snapshot
Optical, contact-free assessment of brain tissue stiffness and neurodegeneration
inferred← citeshttps://doi.org/10.1371/journal.pone.0272736openalex-snapshot
Network diffusion model predicts neurodegeneration in limb-onset Amyotrophic Lateral Sclerosis
inferred← citeshttps://doi.org/10.17879/freeneuropathology-2020-2813openalex-snapshot
Multiple system atrophy - a clinicopathological update
inferred← citeshttps://doi.org/10.17879/freeneuropathology-2020-3025openalex-snapshot
Aβ plaques
inferred← citeshttps://doi.org/10.17879/freeneuropathology-2020-3050openalex-snapshot
Neuropathology of the Alzheimer's continuum: an update
inferred← citeshttps://doi.org/10.18388/abp.2020_5679openalex-snapshot
The engineered peptide construct NCAM1-Aβ inhibits fibrillization of the human prion protein (PrP)
inferred← citeshttps://doi.org/10.20944/preprints202302.0461.v1openalex-snapshot
The Case For Including Neuroprotective Factors in Sporadic Creutzfeldt-Jakob Questionnaires
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3331103/v1openalex-snapshot
Colonoscopy does not increase the risk of Parkinson’s disease
inferred← citeshttps://doi.org/10.2139/ssrn.5401595openalex-snapshot
The Intrinsic Connectivity between the Default Mode and Dorsal Attention Networks is an Independent fMRI Biomarker of Alzheimer's Disease Pathology Burden
inferred← citeshttps://doi.org/10.2174/1567205017666201203124341openalex-snapshot
Identification of Somatic Mutations in Dementia-related Genes in Cancer Patients
inferred← citeshttps://doi.org/10.26599/bsa.2026.905010openalex-snapshot
Towards unified multimodal cross-scale modelling of neurodegenerative diseases
inferred← citeshttps://doi.org/10.3233/jpd-223183openalex-snapshot
Disease-Modifying Therapies for Multiple System Atrophy: Where Are We in 2022?
inferred← citeshttps://doi.org/10.3233/jpd-223516openalex-snapshot
Molecular Mechanisms Mediating the Transfer of Disease-Associated Proteins and Effects on Neuronal Activity
inferred← citeshttps://doi.org/10.3233/jpd-240017openalex-snapshot
Colonoscopy and Subsequent Risk of Parkinson’s Disease
inferred← citeshttps://doi.org/10.3389/fnagi.2020.581374openalex-snapshot
Molecular Chaperones: A Double-Edged Sword in Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.3389/fnagi.2022.874734openalex-snapshot
The Use of Real-Time Quaking-Induced Conversion for the Diagnosis of Human Prion Diseases
inferred← citeshttps://doi.org/10.3389/fnagi.2022.907293openalex-snapshot
Alpha-Synuclein Strain Variability in Body-First and Brain-First Synucleinopathies
inferred← citeshttps://doi.org/10.3389/fncel.2024.1426231openalex-snapshot
New views on the complex interplay between degeneration and autoimmunity in multiple sclerosis
inferred← citeshttps://doi.org/10.3389/fnins.2021.817983openalex-snapshot
New Inroads Into Our Understanding of the Tauopathies, Alzheimer's Disease, and the Contribution of Altered Protein Conformation to Human Neurological Disease
inferred← citeshttps://doi.org/10.3389/fnins.2026.1941231openalex-snapshot
One organelle to rule them all: enhancement of lysosomal activity as a therapeutic modality for protein misfolding neurodegenerative diseases
inferred← citeshttps://doi.org/10.3389/fnut.2025.1673533openalex-snapshot
Linking dietary patterns to Alzheimer's disease biomarkers with network mathematical modeling could enable new approach methodologies in preventative AD research: a narrative interdisciplinary review
inferred← citeshttps://doi.org/10.3389/fvets.2022.824677openalex-snapshot
Genome-Wide Methylation Profiling in the Thalamus of Scrapie Sheep
inferred← citeshttps://doi.org/10.3390/antiox11112287openalex-snapshot
New Insights into the Gut Microbiota in Neurodegenerative Diseases from the Perspective of Redox Homeostasis
inferred← citeshttps://doi.org/10.3390/antiox14070854openalex-snapshot
Modulatory Effects of Urtica dioica on Neurodegenerative Diseases: Unveiling the Latest Findings and Applications Related to Neuroinflammation, Oxidative Stress, and Cognitive Dysfunction
inferred← citeshttps://doi.org/10.3390/bacteria4030042openalex-snapshot
POLETicians in the Mud: Preprokaryotic Organismal Lifeforms Existing Today (POLET) Hypothesis
inferred← citeshttps://doi.org/10.3390/biom10081188openalex-snapshot
C. elegans Models to Study the Propagation of Prions and Prion-Like Proteins
inferred← citeshttps://doi.org/10.3390/biom10091305openalex-snapshot
From Seeds to Fibrils and Back: Fragmentation as an Overlooked Step in the Propagation of Prions and Prion-Like Proteins
inferred← citeshttps://doi.org/10.3390/biom11020207openalex-snapshot
Prion Diseases: A Unique Transmissible Agent or a Model for Neurodegenerative Diseases?
inferred← citeshttps://doi.org/10.3390/biom11050767openalex-snapshot
Green Tea Epigallocatechin-3-gallate (EGCG) Targeting Protein Misfolding in Drug Discovery for Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.3390/biom11071014openalex-snapshot
Prion-Like Proteins in Phase Separation and Their Link to Disease
inferred← citeshttps://doi.org/10.3390/biom12020166openalex-snapshot
Recent Advances in Our Molecular and Mechanistic Understanding of Misfolded Cellular Proteins in Alzheimer’s Disease (AD) and Prion Disease (PrD)
inferred← citeshttps://doi.org/10.3390/biom15040522openalex-snapshot
Iatrogenic Dementia: Providing Insight into Transmissible Subtype of Alzheimer’s Disease, Creutzfeldt–Jakob Disease and Cerebral Amyloid Angiopathy
inferred← citeshttps://doi.org/10.3390/biomedicines10051080openalex-snapshot
C9orf72 Hexanucleotide Repeat Expansion-Related Neuropathology Is Attenuated by Nasal Rifampicin in Mice
inferred← citeshttps://doi.org/10.3390/brainsci14111132openalex-snapshot
Prion-like Spreading of Disease in TDP-43 Proteinopathies
inferred← citeshttps://doi.org/10.3390/cells10092438openalex-snapshot
All Roads Lead to Rome: Different Molecular Players Converge to Common Toxic Pathways in Neurodegeneration
inferred← citeshttps://doi.org/10.3390/cells9081791openalex-snapshot
The Impact of ALS-Associated Genes hnRNPA1, MATR3, VCP and UBQLN2 on the Severity of TDP-43 Aggregation
inferred← citeshttps://doi.org/10.3390/ijms21062108openalex-snapshot
The PERK-Dependent Molecular Mechanisms as a Novel Therapeutic Target for Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.3390/ijms21197020openalex-snapshot
Fused in Sarcoma (FUS) in DNA Repair: Tango with Poly(ADP-ribose) Polymerase 1 and Compartmentalisation of Damaged DNA
inferred← citeshttps://doi.org/10.3390/ijms221810093openalex-snapshot
Is Multiple System Atrophy a Prion-like Disorder?
inferred← citeshttps://doi.org/10.3390/ijms231810241openalex-snapshot
Recent Advances in Prion Inactivation by Plasma Sterilizer
inferred← citeshttps://doi.org/10.3390/ijms232012609openalex-snapshot
Epigenetic Changes in Prion and Prion-like Neurodegenerative Diseases: Recent Advances, Potential as Biomarkers, and Future Perspectives
inferred← citeshttps://doi.org/10.3390/ijms241512134openalex-snapshot
α-Synuclein Strains and Their Relevance to Parkinson’s Disease, Multiple System Atrophy, and Dementia with Lewy Bodies
inferred← citeshttps://doi.org/10.3390/ijms25041991openalex-snapshot
Vulnerability of the Hippocampus to Insults: Links to Blood–Brain Barrier Dysfunction
inferred← citeshttps://doi.org/10.3390/ijms26199816openalex-snapshot
Gene-Exercise Interactions in Amyloid Metabolism and Clearance: Implications for Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3390/ijms27010553openalex-snapshot
Cerebrospinal Fluid Biomarkers in Creutzfeldt–Jakob Disease: Diagnostic Value, Limitations, and Future Multi-Omics Strategies
inferred← citeshttps://doi.org/10.3390/jof8020122openalex-snapshot
Differential Interactions of Molecular Chaperones and Yeast Prions
inferred← citeshttps://doi.org/10.3390/nu16111589openalex-snapshot
New Value of Acorus tatarinowii/gramineus Leaves as a Dietary Source for Dementia Prevention
inferred← citeshttps://doi.org/10.3390/pathogens10010024openalex-snapshot
Inactivation of Prions by Low-Temperature Sterilization Technology Using Vaporized Gas Derived from a Hydrogen Peroxide–Peracetic Acid Mixture
inferred← citeshttps://doi.org/10.3390/pathogens9100819openalex-snapshot
Effect of Nitrogen Gas Plasma Generated by a Fast-Pulsed Power Supply Using a Static Induction Thyristor on Scrapie Prion
inferred← citeshttps://doi.org/10.4014/jmb.2503.03046openalex-snapshot
Yeast Prions: Discovery, Nature, Cellular Manipulation and Implication
inferred← citeshttps://doi.org/10.55418/9781933477435-02openalex-snapshot
Prion Diseases
inferred← citeshttps://doi.org/10.5772/intechopen.101299openalex-snapshot
Tau in Health and Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.6084/m9.figshare.16786651openalex-snapshot
Additional file 10 of Neuronal excitatory-to-inhibitory balance is altered in cerebral organoid models of genetic neurological diseases
inferred← citeshttps://doi.org/10.6084/m9.figshare.16786657openalex-snapshot
Additional file 11 of Neuronal excitatory-to-inhibitory balance is altered in cerebral organoid models of genetic neurological diseases
inferred← citeshttps://doi.org/10.6084/m9.figshare.16786660openalex-snapshot
Additional file 12 of Neuronal excitatory-to-inhibitory balance is altered in cerebral organoid models of genetic neurological diseases
inferred← citeshttps://doi.org/10.6084/m9.figshare.16786663openalex-snapshot
Additional file 13 of Neuronal excitatory-to-inhibitory balance is altered in cerebral organoid models of genetic neurological diseases
inferred← citeshttps://doi.org/10.6084/m9.figshare.16786666openalex-snapshot
Additional file 14 of Neuronal excitatory-to-inhibitory balance is altered in cerebral organoid models of genetic neurological diseases
inferred← citeshttps://doi.org/10.6084/m9.figshare.16786669openalex-snapshot
Additional file 15 of Neuronal excitatory-to-inhibitory balance is altered in cerebral organoid models of genetic neurological diseases
inferred← citeshttps://doi.org/10.6084/m9.figshare.16786672openalex-snapshot
Additional file 16 of Neuronal excitatory-to-inhibitory balance is altered in cerebral organoid models of genetic neurological diseases
inferred← citeshttps://doi.org/10.6084/m9.figshare.16786675openalex-snapshot
Additional file 17 of Neuronal excitatory-to-inhibitory balance is altered in cerebral organoid models of genetic neurological diseases
inferred← citeshttps://doi.org/10.6084/m9.figshare.16786678openalex-snapshot
Additional file 18 of Neuronal excitatory-to-inhibitory balance is altered in cerebral organoid models of genetic neurological diseases
inferred← citeshttps://doi.org/10.6084/m9.figshare.16786681openalex-snapshot
Additional file 19 of Neuronal excitatory-to-inhibitory balance is altered in cerebral organoid models of genetic neurological diseases
inferred← citeshttps://doi.org/10.6084/m9.figshare.16786687openalex-snapshot
Additional file 1 of Neuronal excitatory-to-inhibitory balance is altered in cerebral organoid models of genetic neurological diseases
inferred← citeshttps://doi.org/10.6084/m9.figshare.16786714openalex-snapshot
Additional file 8 of Neuronal excitatory-to-inhibitory balance is altered in cerebral organoid models of genetic neurological diseases
inferred← citeshttps://doi.org/10.6084/m9.figshare.16786717openalex-snapshot
Additional file 9 of Neuronal excitatory-to-inhibitory balance is altered in cerebral organoid models of genetic neurological diseases
inferred← citeshttps://doi.org/10.61173/dfsfgj49openalex-snapshot
Prions and Neurodegenerative Diseases: Mechanisms of Protein Misfolding and Spread
inferred← citeshttps://doi.org/10.70675/41caa2ebzce2bz41f1za34azee35192fd4bbopenalex-snapshot
Implication physio-pathologique de l'axe de signalisation PrPC-ADAM10/17 : des maladies neurodégénératives aux cancers
inferred← citeshttps://doi.org/10.70675/60b353ffz56fcz41a2z9e53zf0d9ac078167openalex-snapshot
Transmission of Alzheimer pathology in murine and primate models : from proteinopathies to neuronal and cognitive impairments
inferred← citeshttps://doi.org/10.70675/68582d99z4406z4ad4zbd76z15927fb63da5openalex-snapshot
Implication de la protéine prion cellulaire dans la neurotoxicité de protéines amyloïdes et de nanoparticules
inferred← citeshttps://doi.org/10.70675/a212ad92z3b22z4eeczb177z417025bff4efopenalex-snapshot
La protéine prion cellulaire : rôles physiologiques et implications croisées dans les maladies neurodégénératives amyloïdes
inferred← citeshttps://doi.org/10.70675/c6d262f3zda3ez4005z96ffzb15b50db412bopenalex-snapshot
Propagation et toxicité de la superoxide dismutase 1 dans la Sclérose Latérale Amyotrophique modélisée par des neurones moteurs dérivés de cellules souches pluripotentes induites
inferred← citeshttps://doi.org/10.7554/elife.100737openalex-snapshot
Simply crushed zizyphi spinosi semen prevents neurodegenerative diseases and reverses age-related cognitive decline in mice
inferred← citeshttps://doi.org/10.7554/elife.100737.1openalex-snapshot
Simply crushed Zizyphi spinosi semen prevents neurodegenerative diseases and reverses age-related cognitive decline in mice
inferred← citeshttps://doi.org/10.7554/elife.100737.2openalex-snapshot
Simply crushed zizyphi spinosi semen prevents neurodegenerative diseases and reverses age-related cognitive decline in mice
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