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Brain Pathology (Zurich, Switzerland)|July 28, 2018
A domain responsible for spontaneous conversion of bank vole prion proteinAtsushi Kobayashi, Yuichi Matsuura, Atsuko Takeuchi, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|July 13, 2021
Potential for transmission of sporadic Creutzfeldt-Jakob disease through peripheral routesAtsushi Kobayashi, Yoshiko Munesue, Taishi Shimazaki, et al.
The Journal of General Virology|November 14, 2019
Eliminating transmissibility of bovine spongiform encephalopathy by dry-heat treatmentYuichi Matsuura, Yukiko Ishikawa, Yuichi Murayama, et al.
The Journal of Biological Chemistry|December 17, 2008
Human prion protein (PrP) 219K is converted to PrPSc but shows heterozygous inhibition in variant Creutzfeldt-Jakob disease infectionMasaki Hizume, Atsushi Kobayashi, Kenta Teruya, et al.
Journal of Virology|April 29, 2004
Treatment of transmissible spongiform encephalopathy by intraventricular drug infusion in animal modelsKatsumi Doh-ura, Kensuke Ishikawa, Ikuko Murakami-Kubo, et al.
Neuroscience Letters|December 19, 2006
Efficient in vitro amplification of a mouse-adapted scrapie prion proteinYuichi Murayama, Miyako Yoshioka, Takashi Yokoyama, et al.
Biochemical and Biophysical Research Communications|March 6, 2007
Prion inactivation by the Maillard reactionKyozo Suyama, Miyako Yoshioka, Mitsugu Akagawa, et al.
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