His main research concerns Pathology, Molecular biology, Biochemistry, Alpha-synuclein and Phosphorylation. His Molecular biology study integrates concerns from other disciplines, such as Epitope, Exon, Cytoplasmic inclusion and Proteinase K. His Biochemistry research includes elements of Tau protein and Cell biology.
His studies deal with areas such as Fibril, Dementia with Lewy bodies, Human brain, Genetically modified mouse and Atrophy as well as Alpha-synuclein. His Dementia with Lewy bodies research includes themes of Immunoelectron microscopy and Synuclein. In his study, Activator and Downregulation and upregulation is strongly linked to Kinase, which falls under the umbrella field of Phosphorylation.
His primary areas of investigation include Pathology, Cell biology, Phosphorylation, Frontotemporal lobar degeneration and Biochemistry. His study in Pathology concentrates on Tauopathy, Corticobasal degeneration, Progressive supranuclear palsy, Dementia and Dementia with Lewy bodies. His Dementia with Lewy bodies research incorporates themes from α synuclein, Synucleinopathies and Atrophy.
He combines subjects such as Fibril, In vitro, Ubiquitin and Alpha-synuclein with his study of Cell biology. His Phosphorylation research incorporates elements of Molecular biology and Antibody. His Frontotemporal lobar degeneration study also includes
Masato Hasegawa mainly focuses on Cell biology, Pathology, Tauopathy, Neuroscience and Neurodegeneration. His research integrates issues of In vitro, α synuclein, Pathogenesis and Alpha-synuclein in his study of Cell biology. His Pathology study is mostly concerned with Frontotemporal lobar degeneration, Autopsy, Pathological, Substantia nigra and Gliosis.
His studies in Tauopathy integrate themes in fields like Progressive supranuclear palsy, Corticobasal degeneration, Dementia, Parkinsonism and Gene isoform. His study explores the link between Neuroscience and topics such as Amyotrophic lateral sclerosis that cross with problems in Cerebellum and Tau pathology. His Protein aggregation research is multidisciplinary, relying on both Fibril, Ubiquitin and Phosphorylation.
Cell biology, Neurodegeneration, Protein aggregation, In vitro and Neuroscience are his primary areas of study. His Cell biology research is multidisciplinary, incorporating perspectives in Cell culture, Dopaminergic, Neurotransmission and Alpha-synuclein. His research in Neurodegeneration tackles topics such as Phenotype which are related to areas like Axoplasmic transport, Frontotemporal lobar degeneration, Amyloid, Amyotrophic lateral sclerosis and Parkinson's disease.
His In vitro research includes themes of Fibril and In vivo. His research integrates issues of Ubiquitin, Amyloid β, Disease, Biochemistry of Alzheimer's disease and Amyloidosis in his study of Neuroscience. Dementia is a subfield of Pathology that Masato Hasegawa explores.
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α-Synuclein in filamentous inclusions of Lewy bodies from Parkinson’s disease and dementia with Lewy bodies
M G Spillantini;R A Crowther;R Jakes;M Hasegawa.
Proceedings of the National Academy of Sciences of the United States of America (1998)
TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Tetsuaki Arai;Masato Hasegawa;Haruhiko Akiyama;Kenji Ikeda.
Biochemical and Biophysical Research Communications (2006)
Assembly of microtubule-associated protein tau into Alzheimer-like filaments induced by sulphated glycosaminoglycans
M. Goedert;R. Jakes;M. G. Spillantini;M. G. Spillantini;M. Hasegawa.
Nature (1996)
Prion-like spreading of pathological α-synuclein in brain
Masami Masuda-Suzukake;Takashi Nonaka;Masato Hosokawa;Takayuki Oikawa.
Brain (2013)
PROLINE-DIRECTED AND NON-PROLINE-DIRECTED PHOSPHORYLATION OF PHF-TAU
Maho Morishima-Kawashima;Masato Hasegawa;Koji Takio;Masami Suzuki.
Journal of Biological Chemistry (1995)
Tau proteins with FTDP-17 mutations have a reduced ability to promote microtubule assembly
Masato Hasegawa;Michael J Smith;Michel Goedert.
FEBS Letters (1998)
Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Masato Hasegawa;Tetsuaki Arai;Takashi Nonaka;Fuyuki Kametani.
Annals of Neurology (2008)
Inhibition of Heparin-induced Tau Filament Formation by Phenothiazines, Polyphenols, and Porphyrins
Sayuri Taniguchi;Nobuyuki Suzuki;Masami Masuda;Shin-ichi Hisanaga.
Journal of Biological Chemistry (2005)
Drug screening for ALS using patient-specific induced pluripotent stem cells.
Naohiro Egawa;Shiho Kitaoka;Kayoko Tsukita;Motoko Naitoh.
Science Translational Medicine (2012)
Phosphorylated α-Synuclein Is Ubiquitinated in α-Synucleinopathy Lesions
Masato Hasegawa;Hideo Fujiwara;Takashi Nonaka;Koichi Wakabayashi.
Journal of Biological Chemistry (2002)
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