Katsumi Doh‐ura

Lysosomotropic Agents and Cysteine Protease Inhibitors Inhibit Scrapie-Associated Prion Protein Accumulation

Katsumi Doh‐ura, Toru Iwaki, Byron Caughey · Journal of Virology · 2000 · 313 citations · Full text

Protein Function, Biochemistry, Natural Sciences +13

Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease

Tetsuyuki Kitamoto, Tamaki Muramoto, Satoshi Mohri et al. · Journal of Virology · 1991 · 289 citations · Full text

Creutzfeldt-jakob Disease, Immunodeficiencies, Immunology +18

Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease.

Tetsuyuki Kitamoto, R W Shin, Katsumi Doh‐ura et al. · PubMed · 1992 · 270 citations · Full text

Pro→Leu change at position 102 of prinon protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome

Katsumi Doh‐ura, Jun Tateishi, Hiroyuki Sasaki et al. · Biochemical and Biophysical Research Communications · 1989 · 265 citations

Position 102, Prinon Protein, Mendelian Disorder +10

Genomic organization of the human amyloid beta-protein precursor gene

Shun-ichi Yoshikai, Hiroyuki Sasaki, Katsumi Doh‐ura et al. · Gene · 1990 · 255 citations

Genomic Organization, Alzheimer's Disease, Protein Folding +4