Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Y N, Tokarev"'
Publikováno v:
Blood. 89(6)
Familial and congenital polycythemia, not due to high oxygen affinity hemoglobin or reduced 2,3-diphosphoglycerate in erythrocytes, is common in the Chuvash population of the Russian Federation. Hundreds of individuals appear to be affected in an aut
Publikováno v:
Nouvelle revue francaise d'hematologie. 20(4)
A study of the activity of human erythrocyte G-6-PD has been completed on a great number of normal controls, coming from different regions of the USSR. This study has led to the discovery of a new variant of erythrocytic Gd, which was named "Kremench
Publikováno v:
Nouvelle revue francaise d'hematologie. 20(4)
A study of the activity of human erythrocyte G-6-PD has been completed on a great number of normal controls, coming from different regions of the USSR. This study has led to the discovery of a new variant of erythrocytic Gd, which was named "Kremench
Valency hybrids of hemoglobin in red cells of patients with hereditary enzymopenic methemoglobinemia
Autor:
A P, Andreyeva, M G, Dmitriyeva, A A, Levina, L M, Tsibulskaya, Y G, Kazanetz, I I, Ilyinskaya, I V, Derviz, Y N, Tokarev
Publikováno v:
Acta biologica et medica Germanica. 36(5-6)
Twenty eight patients with hereditary methemoglobinemia have been found and examined. Using the techniques of analytic isoelectrofucossing in polyacrylamide gel and the preparative isoelectrofocussing on a column in sucrose gradient we have managed t
Publikováno v:
Acta biologica et medica Germanica. 36(5-6)
Kinetic and electrophoretic properties were studied in 230--300 fold purified preparations of glucose-6-phosphate dehydrogenase (G-6-PD) from red cells of donors and patients with hemolytic anemia induced by G-6-PD deficiency. In abnormal variant of