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Microbiology and Immunology|January 1, 1991
Practical methods for chemical inactivation of Creutzfeldt-Jakob disease pathogenJ Tateishi, T Tashima, T KitamotoThe Journal of General Virology|December 1, 1989
Organ distribution of proteinase-resistant prion protein in humans and mice with Creutzfeldt-Jakob diseaseT Kitamoto, S Mohri, J TateishiArchives of Pathology & Laboratory Medicine|October 1, 1986
Histochemical classification of systemic amyloid fibril proteins. Alkaline guanidine methodT Tashima, T Kitamoto, J TateishiActa Neuropathologica|January 1, 1991
Immunoreactivity of cerebral amyloidosis is enhanced by protein denaturation treatmentsR Doi-Yi, T Kitamoto, J TateishiActa Neuropathologica|January 1, 1991
Modified tau is present in younger nondemented persons: a study of subcortical nuclei in Alzheimer's disease and progressive supranuclear palsyR W Shin, T Kitamoto, J TateishiAnnals of Neurology|July 1, 1988
Gerstmann-Sträussler-Scheinker disease: immunohistological and experimental studiesJ Tateishi, T Kitamoto, H Hashiguchi, et al.The American Journal of Pathology|June 1, 1992
The sequential development of abnormal prion protein accumulation in mice with Creutzfeldt-Jakob diseaseT Muramoto, T Kitamoto, J Tateishi, et al.The American Journal of Pathology|November 1, 1993
Accumulation of abnormal prion protein in mice infected with Creutzfeldt-Jakob disease via intraperitoneal route: a sequential studyT Muramoto, T Kitamoto, J Tateishi, et al.Brain Research|December 25, 1992
Successful transmission of Creutzfeldt-Jakob disease from human to mouse verified by prion protein accumulation in mouse brainsT Muramoto, T Kitamoto, J Tateishi, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1991
Immunohistochemical quantification of substance P in spinal dorsal horns of patients with multiple system atrophyN Tomokane, T Kitamoto, J Tateishi, et al.Pageof 28