Rchr
J-GLOBAL ID:202101007723531339   Update date: May. 08, 2024

hamasaki hideomi

ハマサキ ヒデオミ | hamasaki hideomi
Affiliation and department:
Research field  (1): Anatomy
Research theme for competitive and other funds  (1):
  • 2022 - 2025 Wide-area, high-resolution digital image analysis for neurodegenerative diseases
Papers (27):
  • Sachiko Koyama, Kaoru Yagita, Hideomi Hamasaki, Hideko Noguchi, Masahiro Shijo, Kosuke Matsuzono, Kei-Ichiro Takase, Keita Kai, Shin-Ichi Aishima, Kyoko Itoh, et al. Novel method for classification of prion diseases by detecting PrPres signal patterns from formalin-fixed paraffin-embedded samples. Prion. 2024. 18. 1. 40-53
  • Hiroyuki Honda, Motoi Yoshimura, Hajime Arahata, Kaoru Yagita, Shoko Sadashima, Hideomi Hamasaki, Masahiro Shijo, Sachiko Koyama, Hideko Noguchi, Naokazu Sasagasako. Mutated FUS in familial amyotrophic lateral sclerosis involves multiple hnRNPs in the formation of neuronal cytoplasmic inclusions. Journal of Neuropathology & Experimental Neurology. 2023. 82. 3. 231-241
  • Hideko Noguchi, Sachiko Koyama, Kaoru Yagita, Masahiro Shijo, Kosuke Matsuzono, Hideomi Hamasaki, Takaaki Kanemaru, Tsuyoshi Okamoto, Keita Kai, Shinichi Aishima, et al. Silence of resident microglia in GPI anchorless prion disease and activation of microglia in Gerstmann-Sträussler-Scheinker disease and sporadic Creutzfeldt-Jakob disease. Journal of Neuropathology & Experimental Neurology. 2022. 82. 1. 38-48
  • Hamasaki H, Maeda N, Sasagasako N, Honda H, Shijo M, Mori SI, Yagita K, Arahata H, Iwaki T. Neuropathology of classic myotonic dystrophy type 1 is characterized by both early initiation of primary age-related tauopathy of the hippocampus and unique 3-repeat tauopathy of the brainstem. Journal of neuropathology and experimental neurology. 2022
  • Kaoru Yagita, Hideko Noguchi, Sachiko Koyama, Hideomi Hamasaki, Takashi Komori, Shinichi Aishima, Takayuki Kosaka, Mitsuharu Ueda, Yoshihiro Komohara, Akihiro Watanabe, et al. Chronological Changes in the Expression Pattern of Hippocampal Prion Proteins During Disease Progression in Sporadic Creutzfeldt-Jakob Disease MM1 Subtype. Journal of neuropathology and experimental neurology. 2022. 81. 11. 900-909
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