Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Matsuura, Ryoji"'
Publikováno v:
Quintessence International; Jun1989, Vol. 20 Issue 6, p435-437, 3p
Autor:
Ushiroyama, Takahisa, Tanigawa, Yoshinori, Tsuchiya, Mikako, Matsuura, Ryoji, Ueki, Minoru, Sugimoto, Osamu, Shimoyama, Makoto
Publikováno v:
European Journal of Biochemistry; 8/15/85, Vol. 151 Issue 1, p173-177, 5p
Autor:
Tsuchiya, Mikako, Tanigawa, Yoshinori, Ushiroyama, Takahisa, Matsuura, Ryoji, Shimoyama, Makoto
Publikováno v:
European Journal of Biochemistry; 2/15/85, Vol. 147 Issue 1, p33-40, 8p
Autor:
Matsuura, Ryoji, Kishi, Takamasa, Okahata, Hiroyasu, Kobayashi, Masao, Tanabe, Akio, Sakura, Nobuo, Sawano, Kunihiko, Usui, Tomofusa
Publikováno v:
Hiroshima Journal of Medical Sciences. 32(2):173-178
Several functions of polymorphonuclear leukocytes (PMNL) were examined in two siblings with glucose-6-phosphate dehydrogenase (G6PD) deficiency. In spite of marked depression of G6PD activity of PMNL, the patients had no susceptibility to bacterial i
Publikováno v:
Hiroshima Journal of Medical Sciences. 33(2):173-177
The activation of NADPH oxidase on the plasma membranes of polymorphonuclear leukocytes (PMNL) follows the change of membrane potential. It is thought that the activation of NADPH oxidase is disturbed in the PMNL of patients with chronic granulomatou
Autor:
Matsuura, Ryoji
Publikováno v:
Hiroshima Journal of Medical Sciences. 30(3):229-236
Superoxide anion release from polymorphonuclear leukocytes stimulated by concanavalin A was markedly enhanced by the simultaneous addition of cytochalasin A at concentrations of 2×10-8 to 4×10-7M. These concentrations of cytochalasin A did not affe
Publikováno v:
Hiroshima Journal of Medical Sciences. 33(2):173-177
The activation of NADPH oxidase on the plasma membranes of polymorphonuclear leukocytes (PMNL) follows the change of membrane potential. It is thought that the activation of NADPH oxidase is disturbed in the PMNL of patients with chronic granulomatou
Publikováno v:
Hiroshima Journal of Medical Sciences. 31(2):133-135
An 8-year-old boy with familial hypokalemic periodic paralysis is described. Twenty eight cases of periodic paralysis under 15 years of age were collected from the Japanese literature and reviewed. Serum potassium concentrations during an attack of p