Masato Hasegawa


Ontology type: schema:Person     


Person Info

NAME

Masato

SURNAME

Hasegawa

Publications in SciGraph latest 50 shown

  • 2018-12 Potent prion-like behaviors of pathogenic α-synuclein and evaluation of inactivation methods in ACTA NEUROPATHOLOGICA COMMUNICATIONS
  • 2018-12 Mutations in bassoon in individuals with familial and sporadic progressive supranuclear palsy-like syndrome in SCIENTIFIC REPORTS
  • 2017-12 Propagation of pathological α-synuclein in marmoset brain in ACTA NEUROPATHOLOGICA COMMUNICATIONS
  • 2017-12 Desulfation of Heparan Sulfate by Sulf1 and Sulf2 Is Required for Corticospinal Tract Formation in SCIENTIFIC REPORTS
  • 2017-12 Accumulation of multiple neurodegenerative disease-related proteins in familial frontotemporal lobar degeneration associated with granulin mutation in SCIENTIFIC REPORTS
  • 2017-12 TDP-43 stabilises the processing intermediates of mitochondrial transcripts in SCIENTIFIC REPORTS
  • 2017 Molecular Biology of Dementia with Lewy Bodies in DEMENTIA WITH LEWY BODIES
  • 2016-12 Chorea as a clinical feature of the basophilic inclusion body disease subtype of fused-in-sarcoma-associated frontotemporal lobar degeneration in ACTA NEUROPATHOLOGICA COMMUNICATIONS
  • 2016-12 Calcium dysregulation contributes to neurodegeneration in FTLD patient iPSC-derived neurons in SCIENTIFIC REPORTS
  • 2016-12 Quantitative and combinatory determination of in situ phosphorylation of tau and its FTDP-17 mutants in SCIENTIFIC REPORTS
  • 2016-12 Pathological tau deposition in Motor Neurone Disease and frontotemporal lobar degeneration associated with TDP-43 proteinopathy in ACTA NEUROPATHOLOGICA COMMUNICATIONS
  • 2016-11 Exposure to bacterial endotoxin generates a distinct strain of α-synuclein fibril in SCIENTIFIC REPORTS
  • 2016-10 Inositol Hexakisphosphate Kinase 2 Promotes Cell Death in Cells with Cytoplasmic TDP-43 Aggregation in MOLECULAR NEUROBIOLOGY
  • 2016-09 Mass spectrometric analysis of accumulated TDP-43 in amyotrophic lateral sclerosis brains in SCIENTIFIC REPORTS
  • 2016-02 Biochemical classification of tauopathies by immunoblot, protein sequence and mass spectrometric analyses of sarkosyl-insoluble and trypsin-resistant tau in ACTA NEUROPATHOLOGICA
  • 2015-06 Extracellular association of APP and tau fibrils induces intracellular aggregate formation of tau in ACTA NEUROPATHOLOGICA
  • 2014-12 Brain distribution of dipeptide repeat proteins in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72 in ACTA NEUROPATHOLOGICA COMMUNICATIONS
  • 2014-12 Pathological alpha-synuclein propagates through neural networks in ACTA NEUROPATHOLOGICA COMMUNICATIONS
  • 2014-12 Tau accumulation in the nucleus accumbens in tangle-predominant dementia in ACTA NEUROPATHOLOGICA COMMUNICATIONS
  • 2014-11 Concomitant accumulation of α-synuclein and TDP-43 in a patient with corticobasal degeneration in JOURNAL OF NEUROLOGY
  • 2014-02 3R and 4R tau isoforms in paired helical filaments in Alzheimer’s disease in ACTA NEUROPATHOLOGICA
  • 2013-12 A longitudinal study on α-synuclein in blood plasma as a biomarker for Parkinson's disease in SCIENTIFIC REPORTS
  • 2013-12 Dipeptide repeat proteins are present in the p62 positive inclusions in patients with frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72 in ACTA NEUROPATHOLOGICA COMMUNICATIONS
  • 2013-12 Extensive deamidation at asparagine residue 279 accounts for weak immunoreactivity of tau with RD4 antibody in Alzheimer’s disease brain in ACTA NEUROPATHOLOGICA COMMUNICATIONS
  • 2011-12 C-Jun N-terminal kinase controls TDP-43 accumulation in stress granules induced by oxidative stress in MOLECULAR NEURODEGENERATION
  • 2011-11 Molecular Dissection of TDP-43 Proteinopathies in JOURNAL OF MOLECULAR NEUROSCIENCE
  • 2010-12 Effect of topographical distribution of α-synuclein pathology on TDP-43 accumulation in Lewy body disease in ACTA NEUROPATHOLOGICA
  • 2010-07 Phosphorylated TDP-43 pathology and hippocampal sclerosis in progressive supranuclear palsy in ACTA NEUROPATHOLOGICA
  • 2009-11 Plasma phosphorylated-TDP-43 protein levels correlate with brain pathology in frontotemporal lobar degeneration in ACTA NEUROPATHOLOGICA
  • 2009-09 TDP-43 in ubiquitinated inclusions in the inferior olives in frontotemporal lobar degeneration and in other neurodegenerative diseases: a degenerative process distinct from normal ageing in ACTA NEUROPATHOLOGICA
  • 2009-08 TDP-43 pathology in familial British dementia in ACTA NEUROPATHOLOGICA
  • 2009-02 Accumulation of phosphorylated TDP-43 in brains of patients with argyrophilic grain disease in ACTA NEUROPATHOLOGICA
  • 2009-02 Phosphorylated TDP-43 in Alzheimer’s disease and dementia with Lewy bodies in ACTA NEUROPATHOLOGICA
  • 2006-09 Corticobasal degeneration with focal, massive tau accumulation in the subcortical white matter astrocytes in ACTA NEUROPATHOLOGICA
  • 2005-10 Four-repeat tau-positive Pick body-like inclusions are distinct from classic Pick bodies in ACTA NEUROPATHOLOGICA
  • 2004-04 Accumulation of phosphorylated α-synuclein in the brain and peripheral ganglia of patients with multiple system atrophy in ACTA NEUROPATHOLOGICA
  • 2002-02 α-Synuclein is phosphorylated in synucleinopathy lesions in NATURE CELL BIOLOGY
  • 2002 Biochemical Analysis of Tau and α-Synuclein in Neurodegenerative Diseases in MAPPING THE PROGRESS OF ALZHEIMER’S AND PARKINSON’S DISEASE
  • 2001-03 Co-localization of α-synuclein and phosphorylated tau in neuronal and glial cytoplasmic inclusions in a patient with multiple system atrophy of long duration in ACTA NEUROPATHOLOGICA
  • 2001 Tau mutations altering splicing of tau exon 10 in japanese frontotemporal dementia in NEUROSCIENTIFIC BASIS OF DEMENTIA
  • 2000-01 Juvenile-onset generalized neuroaxonal dystrophy (Hallervorden-Spatz disease) with diffuse neurofibrillary and Lewy body pathology in ACTA NEUROPATHOLOGICA
  • 1996-10 Assembly of microtubule-associated protein tau into Alzheimer-like filaments induced by sulphated glycosaminoglycans in NATURE
  • 1994-08 Neuronal and glial tau-positive inclusions in diverse neurologic diseases share common phosphorylation characteristics in ACTA NEUROPATHOLOGICA
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