Distinct origins of dura mater graft-associated Creutzfeldt-Jakob disease: past and future problems

Por Kobayashi, Atsushi, Matsuura, Yuichi, Mohri, Shirou, Kitamoto, Tetsuyuki
Publicado em 2014

PrP(res) deposition in the retina is a common finding of sporadic, familial and iatrogenic Creutzfeldt-Jakob diseases (CJD)

Por Takao, Masaki, Kimura, Hiroaki, Kitamoto, Tetsuyuki, Mihara, Ban
Publicado no Acta Neuropathol Commun (2018)

Marchiafava-Bignami disease with haemophagocytic lymphohistiocytosis as a postoperative complication of cardiac surgery

Por Takei, Kentarou, Motoyoshi, Naotaka, Sakamoto, Kazuhiro, Kitamoto, Tetsuyuki
Publicado no BMJ Case Rep (2019)

Prions food and drug safety /

Por Kitamoto, Tetsuyuki., International Symposium of Prion Diseases for Food and Drug Safety
Publicado em 2005

Heterozygous inhibition in prion infection: The stone fence model

Por Kobayashi, Atsushi, Hizume, Masaki, Teruya, Kenta, Mohri, Shirou, Kitamoto, Tetsuyuki
Publicado em 2009

Species Barrier Prevents an Abnormal Isoform of Prion Protein from Accumulating in Follicular Dendritic Cells of Mice with Creutzfeldt-Jakob Disease

Por Muramoto, Tamaki, Kitamoto, Tetsuyuki, Hoque, Mohammad Zahirul, Tateishi, Jun, Goto, Ikuo
Publicado em 1993

Humanized Knock-In Mice Expressing Chimeric Prion Protein Showed Varied Susceptibility to Different Human Prions

Por Taguchi, Yuzuru, Mohri, Shirou, Ironside, James W., Muramoto, Tamaki, Kitamoto, Tetsuyuki
Publicado em 2003

Critical Significance of the Region between Helix 1 and 2 for Efficient Dominant-Negative Inhibition by Conversion-Incompetent Prion Protein

Por Taguchi, Yuzuru, Mistica, Arla M. A., Kitamoto, Tetsuyuki, Schätzl, Hermann M.
Publicado em 2013

Characterization of Variant Creutzfeldt-Jakob Disease Prions in Prion Protein-humanized Mice Carrying Distinct Codon 129 Genotypes

Por Takeuchi, Atsuko, Kobayashi, Atsushi, Ironside, James W., Mohri, Shirou, Kitamoto, Tetsuyuki
Publicado em 2013

Experimental Verification of a Traceback Phenomenon in Prion Infection

Por Kobayashi, Atsushi, Sakuma, Nobuyuki, Matsuura, Yuichi, Mohri, Shirou, Aguzzi, Adriano, Kitamoto, Tetsuyuki
Publicado em 2010

Co-Occurrence of Types 1 and 2 PrP(res) in Sporadic Creutzfeldt-Jakob Disease MM1

Por Kobayashi, Atsushi, Mizukoshi, Kenta, Iwasaki, Yasushi, Miyata, Hajime, Yoshida, Yasuji, Kitamoto, Tetsuyuki
Publicado em 2011

Pathological progression of genetic Creutzfeldt–Jakob disease with a PrP V180I mutation

Por Akagi, Akio, Iwasaki, Yasushi, Mimuro, Maya, Kitamoto, Tetsuyuki, Yamada, Masahito, Yoshida, Mari
Publicado no Prion (2018)

Interaction of Aluminum with PHFτ in Alzheimer’s Disease Neurofibrillary Degeneration Evidenced by Desferrioxamine-Assisted Chelating Autoclave Method

Por Murayama, Harunobu, Shin, Ryong-Woon, Higuchi, Jun, Shibuya, Satoshi, Muramoto, Tamaki, Kitamoto, Tetsuyuki
Publicado em 1999

Enhanced Antigen Retrieval of Amyloid β Immunohistochemistry: Re-evaluation of Amyloid β Pathology in Alzheimer Disease and Its Mouse Model

Por Kai, Hideaki, Shin, Ryong-Woon, Ogino, Koichi, Hatsuta, Hiroyuki, Murayama, Shigeo, Kitamoto, Tetsuyuki
Publicado em 2012

A patient with spastic paralysis finally diagnosed as V180I genetic Creutzfeldt-Jakob disease 9 years after onset

Por Nomura, Taichi, Iwata, Ikuko, Naganuma, Ryoji, Matsushima, Masaaki, Satoh, Katsuya, Kitamoto, Tetsuyuki, Yabe, Ichiro
Publicado no Prion (2020)

Importance of Neuropathological Diagnosis of Dementia Patients in Family Practice

Por Tanaka, Yukiko, Ikeda, Masaki, Mihara, Ban, Ikeda, Yoshio, Sato, Katsuya, Kitamoto, Tetsuyuki, Takao, Masaki
Publicado no JMA J (2019)

A domain responsible for spontaneous conversion of bank vole prion protein

Por Kobayashi, Atsushi, Matsuura, Yuichi, Takeuchi, Atsuko, Yamada, Masahito, Miyoshi, Ichiro, Mohri, Shirou, Kitamoto, Tetsuyuki
Publicado no Brain Pathol (2018)

Ophthalmic Surgery in Prion Diseases

Por Hamaguchi, Tsuyoshi, Noguchi-Shinohara, Moeko, Nakamura, Yosikazu, Sato, Takeshi, Kitamoto, Tetsuyuki, Mizusawa, Hidehiro, Yamada, Masahito
Publicado em 2007

Construction of recombinant monoclonal antibodies from a chicken hybridoma line secreting specific antibody

Por Nakamura, Naoto, Aoki, Yuri, Horiuchi, Hiroyuki, Furusawa, Shuichi, Yamanaka, Hachiro I., Kitamoto, Tetsuyuki, Matsuda, Haruo
Publicado em 2000

Deciphering the pathogenesis of sporadic Creutzfeldt-Jakob disease with codon 129 M/V and type 2 abnormal prion protein

Por Kobayashi, Atsushi, Iwasaki, Yasushi, Otsuka, Hiroyuki, Yamada, Masahito, Yoshida, Mari, Matsuura, Yuichi, Mohri, Shirou, Kitamoto, Tetsuyuki
Publicado em 2013