Resultats de la cerca - Kitamoto, Tetsuyuki

Distinct origins of dura mater graft-associated Creutzfeldt-Jakob disease: past and future problems per Kobayashi, Atsushi, Matsuura, Yuichi, Mohri, Shirou, Kitamoto, Tetsuyuki

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PrP(res) deposition in the retina is a common finding of sporadic, familial and iatrogenic Creutzfeldt-Jakob diseases (CJD) per Takao, Masaki, Kimura, Hiroaki, Kitamoto, Tetsuyuki, Mihara, Ban

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Marchiafava-Bignami disease with haemophagocytic lymphohistiocytosis as a postoperative complication of cardiac surgery per Takei, Kentarou, Motoyoshi, Naotaka, Sakamoto, Kazuhiro, Kitamoto, Tetsuyuki

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Heterozygous inhibition in prion infection: The stone fence model per Kobayashi, Atsushi, Hizume, Masaki, Teruya, Kenta, Mohri, Shirou, Kitamoto, Tetsuyuki

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Humanized Knock-In Mice Expressing Chimeric Prion Protein Showed Varied Susceptibility to Different Human Prions per Taguchi, Yuzuru, Mohri, Shirou, Ironside, James W., Muramoto, Tamaki, Kitamoto, Tetsuyuki

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Species Barrier Prevents an Abnormal Isoform of Prion Protein from Accumulating in Follicular Dendritic Cells of Mice with Creutzfeldt-Jakob Disease per Muramoto, Tamaki, Kitamoto, Tetsuyuki, Hoque, Mohammad Zahirul, Tateishi, Jun, Goto, Ikuo

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Critical Significance of the Region between Helix 1 and 2 for Efficient Dominant-Negative Inhibition by Conversion-Incompetent Prion Protein per Taguchi, Yuzuru, Mistica, Arla M. A., Kitamoto, Tetsuyuki, Schätzl, Hermann M.

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Characterization of Variant Creutzfeldt-Jakob Disease Prions in Prion Protein-humanized Mice Carrying Distinct Codon 129 Genotypes per Takeuchi, Atsuko, Kobayashi, Atsushi, Ironside, James W., Mohri, Shirou, Kitamoto, Tetsuyuki

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Experimental Verification of a Traceback Phenomenon in Prion Infection per Kobayashi, Atsushi, Sakuma, Nobuyuki, Matsuura, Yuichi, Mohri, Shirou, Aguzzi, Adriano, Kitamoto, Tetsuyuki

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Co-Occurrence of Types 1 and 2 PrP(res) in Sporadic Creutzfeldt-Jakob Disease MM1 per Kobayashi, Atsushi, Mizukoshi, Kenta, Iwasaki, Yasushi, Miyata, Hajime, Yoshida, Yasuji, Kitamoto, Tetsuyuki

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Pathological progression of genetic Creutzfeldt–Jakob disease with a PrP V180I mutation per Akagi, Akio, Iwasaki, Yasushi, Mimuro, Maya, Kitamoto, Tetsuyuki, Yamada, Masahito, Yoshida, Mari

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Early Diagnosis of V180I Genetic Creutzfeldt-Jakob Disease at the Preserved Cognitive Function Stage per Suzuki, Yutaro, Sugiyama, Atsuhiko, Muto, Mayumi, Satoh, Katsuya, Kitamoto, Tetsuyuki, Kuwabara, Satoshi

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Interaction of Aluminum with PHFτ in Alzheimer’s Disease Neurofibrillary Degeneration Evidenced by Desferrioxamine-Assisted Chelating Autoclave Method per Murayama, Harunobu, Shin, Ryong-Woon, Higuchi, Jun, Shibuya, Satoshi, Muramoto, Tamaki, Kitamoto, Tetsuyuki

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Enhanced Antigen Retrieval of Amyloid β Immunohistochemistry: Re-evaluation of Amyloid β Pathology in Alzheimer Disease and Its Mouse Model per Kai, Hideaki, Shin, Ryong-Woon, Ogino, Koichi, Hatsuta, Hiroyuki, Murayama, Shigeo, Kitamoto, Tetsuyuki

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A patient with spastic paralysis finally diagnosed as V180I genetic Creutzfeldt-Jakob disease 9 years after onset per Nomura, Taichi, Iwata, Ikuko, Naganuma, Ryoji, Matsushima, Masaaki, Satoh, Katsuya, Kitamoto, Tetsuyuki, Yabe, Ichiro

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Importance of Neuropathological Diagnosis of Dementia Patients in Family Practice per Tanaka, Yukiko, Ikeda, Masaki, Mihara, Ban, Ikeda, Yoshio, Sato, Katsuya, Kitamoto, Tetsuyuki, Takao, Masaki

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A domain responsible for spontaneous conversion of bank vole prion protein per Kobayashi, Atsushi, Matsuura, Yuichi, Takeuchi, Atsuko, Yamada, Masahito, Miyoshi, Ichiro, Mohri, Shirou, Kitamoto, Tetsuyuki

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Ophthalmic Surgery in Prion Diseases per Hamaguchi, Tsuyoshi, Noguchi-Shinohara, Moeko, Nakamura, Yosikazu, Sato, Takeshi, Kitamoto, Tetsuyuki, Mizusawa, Hidehiro, Yamada, Masahito

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Construction of recombinant monoclonal antibodies from a chicken hybridoma line secreting specific antibody per Nakamura, Naoto, Aoki, Yuri, Horiuchi, Hiroyuki, Furusawa, Shuichi, Yamanaka, Hachiro I., Kitamoto, Tetsuyuki, Matsuda, Haruo

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Deciphering the pathogenesis of sporadic Creutzfeldt-Jakob disease with codon 129 M/V and type 2 abnormal prion protein per Kobayashi, Atsushi, Iwasaki, Yasushi, Otsuka, Hiroyuki, Yamada, Masahito, Yoshida, Mari, Matsuura, Yuichi, Mohri, Shirou, Kitamoto, Tetsuyuki

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