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SCI Abstract
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Genetic and clinical characteristics of cranial nerve schwannoma harboring fusion gene
The SH3PXD2A-HTRA1 fusion gene has recently been identified in a subset of schwannomas, but its frequency and clinical sig...
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Alpha synuclein-mediated cytoskeletal dysfunction impairs myelination in human oligodendrocytes
Oligodendroglial alpha-synuclein (aSyn) deposits are a key feature in the atypical parkinsonian disorder, multiple system ...
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In silico purification improves DNA methylation-based classification rates of pediatric low-grade gliomas
DNA methylation-based classification using the Heidelberg Classifier is a state-of-the-art data-driven method for molecula...
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Reversible tau hyperphosphorylation in hibernation: a blood biomarker and brain tissue study
Tau hyperphosphorylation, a key neuropathological feature of tauopathies such as Alzheimer’s disease (AD), also occu...
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Expansion of the spectrum of tumors diagnosed as myxopapillary ependymomas
Both spinal ependymomas (SPE) and myxopapillary ependymomas (MPE) exhibit a character...
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Evolution of pilocytic astrocytoma to diffuse leptomeningeal glioneuronal tumor (DLGNT): bridging two distinct tumor types
DCM and JC receive support from the St. Jude Comprehensive Cancer Center (NCI grant P30CA021765) and American Lebanese Syr...
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Impact of APOE on cerebrovascular lipid profile in Alzheimer’s disease
Disturbances within the cerebrovascular system substantially contribute to the pathogenesis of age-related cognitive impai...
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Tumor-associated macrophages in meningiomas: a novel biomarker for poor survival outperforming the benefits of T cells
Tumor-associated macrophages (TAMs) represent the main immune cell population in various brain malignancies, but there is ...
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Primary age-related tauopathy
Primary age-related tauopathy (PART) was proposed in 2014 as a neuropathological term to describe patients with Alzheimer&...
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Molecular characterization and clinical features of diffuse midline glioma in the pediatric precision oncology registry INFORM
Diffuse midline glioma (DMG; a subtype of pediatric high-grade glioma) is a fatal disease in children, due to the localiza...
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Genetic and proteomic analysis identifies BAG3 as an amyloid-responsive regulator of neuronal proteostasis
The autophagy–lysosome pathway (ALP) and the ubiquitin–proteasome system (UPS) are the primary protein degrada...
Acta Neuropathologica
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LRRK2 kinase-mediated accumulation of lysosome-associated phospho-Rabs in tauopathies and synucleinopathies
Parkinson’s disease (PD) pathogenic mutations in leucine-rich repeat kinase 2 (LRRK2) are associated with endolysoso...
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Brain-derived 5-hydroxymethylcytosine epigenetic scores are related to Alzheimer’s disease pathology and cognitive decline
Cytosine modifications play critical roles in gene regulation and disease pathogenesis. Elucidating novel epigenetic contr...
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Alpha-synuclein deposition patterns in Alzheimer’s disease: association with cortical amyloid beta and variable tau load
Alpha-synuclein (α-syn) deposits are common in around half of the Alzheimer’s disease (AD) cases. While direct ...
Acta Neuropathologica
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Spatial protein profiling reveals active roles for astrocytes in the chronic active lesion core during multiple sclerosis
Chronic active lesions are a manifestation of multiple sclerosis (MS) and have been associated with disease progression. W...
Acta Neuropathologica
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Intracellular trafficking SNARE protein, syntaxin-6, modifies prion cellular phenotypes and risk of disease development in vivo
Increased expression of syntaxin-6, a SNARE protein involved in intracellular protein trafficking, is a proposed genetic r...
Acta Neuropathologica
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PolyGR-containing aggregates link with pathology and clinical features of Alzheimer’s disease
Alzheimer’s disease is the most common form of dementia; however, its molecular mechanisms are not fully understood....
Acta Neuropathologica
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Co-infection with two α-synuclein strains reveals novel synergistic interactions
In synucleinopathies, the protein α-synuclein misfolds into Lewy bodies (LBs) in patients with Lewy body disease (LBD...
Acta Neuropathologica
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MSH2, MSH6, MLH1, and PMS2 immunohistochemistry as highly sensitive screening method for DNA mismatch repair deficiency syndromes in pediatric high-grade glioma
Pediatric high-grade glioma (pedHGG) can occur as first manifestation of cancer predisposition syndromes resulting from pa...
Acta Neuropathologica
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IDH-mutant astrocytomas with primitive neuronal component have a distinct methylation profile and a higher risk of leptomeningeal spread
IDH-mutant astrocytomas are diffuse gliomas that are defined by characteristic mutations in IDH1 or IDH2 and do not have c...
Acta Neuropathologica
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Somatic variants in leading to defects in N-glycosylation in mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE)
Mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE) is a new histopathological...
Acta Neuropathologica
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fusion driver in primary central nervous system malignancy: case report
Andreiuolo F, Varlet P, Tauziède-Espariat A, Jünger ST, Dörner E et al (2019) Childhood supratentorial ependymomas with YA...
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Perivascular glial reactivity is a feature of phosphorylated tau lesions in chronic traumatic encephalopathy
Chronic traumatic encephalopathy (CTE), a neurodegenerative disease associated with repetitive head injuries, is character...
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A novel fusion that potentially expands the concept of supratentorial ependymoma, fusion-positive
Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4....
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Brain tissue metal concentrations and Alzheimer’s disease neuropathology in total joint arthroplasty patients versus controls
We examined whether total joint arthroplasty (TJA) is associated with increased metal accumulation in the brain and histop...
Acta Neuropathologica
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Microglia aggregates define distinct immune and neurodegenerative niches in Alzheimer's disease hippocampus
In Alzheimer’s disease (AD), microglia form distinct cellular aggregates that play critical roles in disease progres...
Acta Neuropathologica
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A quantitative Lewy-fold-specific alpha-synuclein seed amplification assay as a progression marker for Parkinson’s disease
Misfolded α-synuclein (αSyn) is the hallmark of α-synucleinopathies such as Parkinson’s disease (PD),...
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Evidence of COMT dysfunction in the olfactory bulb in Parkinson’s disease
Hyposmia is one of the most prevalent non-motor symptoms of Parkinson’s disease and antecedes motor dysfunction by u...
Acta Neuropathologica
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Parkinson-like wild-type superoxide dismutase 1 pathology induces nigral dopamine neuron degeneration in a novel murine model
Atypical wild-type superoxide dismutase 1 (SOD1) protein misfolding and deposition occurs specifically within the degenera...
Acta Neuropathologica
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Human brain tissue with MOGHE carrying somatic variants reveal aberrant protein expression and protein loss in the white matter
Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Epilepsy (MOGHE) is a recently described di...
Acta Neuropathologica
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