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Biochimica Et Biophysica Acta|February 18, 2005
Purification and cDNA cloning of luxuriosin, a novel antibacterial peptide with Kunitz domain from the longicorn beetle, Acalolepta luxuriosaKenjiro Ueda, Ayaka Saito, Morikazu Imamura, et al.Pathogens (Basel, Switzerland)|July 9, 2020
Inactivation of Scrapie Prions by the Electrically Charged Disinfectant CAC-717Akikazu Sakudo, Yoshifumi Iwamaru, Koichi Furusaki, et al.Microbiology and Immunology|November 11, 2024
Lack of Evidence for Transmission of Atypical H-Type Bovine Spongiform Encephalopathy Prions (H-BSE Prions) by Intracranial and Oral Challenges to Nonhuman PrimatesHiroaki Shibata, Fumiko Ono, Yuko Sato, et al.Journal of Virology|January 14, 2011
Glycosylphosphatidylinositol anchor-dependent stimulation pathway required for generation of baculovirus-derived recombinant scrapie prion proteinMorikazu Imamura, Nobuko Kato, Miyako Yoshioka, et al.Microbiology and Immunology|October 15, 2013
Different antigenicities of the N-terminal region of cellular and scrapie prion proteinsYuko Ushiki-Kaku, Yoshifumi Iwamaru, Kentaro Masujin, et al.Plos One|December 25, 2013
Insect cell-derived cofactors become fully functional after proteinase K and heat treatment for high-fidelity amplification of glycosylphosphatidylinositol-anchored recombinant scrapie and BSE prion proteinsMorikazu Imamura, Nobuko Kato, Hiroyuki Okada, et al.Insect Biochemistry and Molecular Biology|November 11, 2008
Construction of a piggyBac-based enhancer trap system for the analysis of gene function in silkworm Bombyx moriKeiro Uchino, Hideki Sezutsu, Morikazu Imamura, et al.International Journal of Molecular Sciences|November 13, 2021
Ethanolamine Is a New Anti-Prion CompoundKeiji Uchiyama, Hideyuki Hara, Junji Chida, et al.Emerging Infectious Diseases|April 30, 2025
Administration of L-Type Bovine Spongiform Encephalopathy to Macaques to Evaluate Zoonotic PotentialMorikazu Imamura, Ken'ichi Hagiwara, Minoru Tobiume, et al.Veterinary Research|June 25, 2011
Experimental H-type bovine spongiform encephalopathy characterized by plaques and glial- and stellate-type prion protein depositsHiroyuki Okada, Yoshifumi Iwamaru, Morikazu Imamura, et al.Pageof 7