Human Prion Disease and Human Prion Protein Disease (1996)
Kitamoto, Tetsuyuki, Tateishi, Jun, 北本, 哲之, 立石, 潤, キタモト, テツユキ, タテイシ, ジュン
edited by Stanley B. Prusiner
Iwaki, Toru, Iwaki, Akiko, Tateishi, Jun, Goldman, James E., 岩城, 徹, 岩城, 明子, ...
The phenotypic effects of selectively altering the levels of alpha B- crystallin in cultured glial cells were analyzed using sense and antisense approaches. Rat C6 glioma cells and human U-373MG...
Gerstmann-Straussler-Scheinker disease in an Alsatian family: clinical and genetic studies (1992)
Tranchant, C, Doh-ura, K, Warter, J M, Steinmetz, G, Chevalier, Y, Hanauer, A, ...
The clinical progression of Gerstmann-Straussler-Scheinker disease in a family of Alsatian origin is reported. The age of onset and the duration of evolution were variable. The clinical picture...
Tomokane, Naoyuki, Kitamoto, Tetsuyuki, Tateishi, Jun, Sato, Yuji, 北本, 哲之, 立石, 潤, ...
Using a computer-assisted image analyser, an immunohistochemical quantification method of substance P-like immunoreactivity (SPLI) in laminae I + II of spinal dorsal horn was established and applied...
Tateishi, Jun, 立石, 潤, タテイシ, ジュン
Thiamphenicol, rifampicin, amantadine, cytosine arabinoside and isoprinosine were administered to mice which were inoculated with brain tissue containing Creutzfeldt-Jakob disease (CJD). All the mice...