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1 sent after cortical exposure to subarachnoid hemolysate.
2 n, and percent HbA1c (%HbA1c) in human blood hemolysate.
3 the addition of calcium to freshly prepared hemolysates.
4 nt methods for their purification from mouse hemolysates.
5 s pathway in unfractionated beta-thalassemic hemolysates.
6 7% to 96% for 3H-alpha-globin among the four hemolysates.
7 le and rapid, requires only small amounts of hemolysate (30 micrograms of globin), and provides excel
10 e results obtained for %HbA1c in human blood hemolysate are in good agreement with those determined u
11 NEL staining in 10/15 subjects injected with hemolysate as compared to 0/9 subjects injected with sal
12 linical picture so similar, and based on the hemolysates CSAT's, we conclude that HbS-Oman produces p
14 was added to reaction mixtures containing a hemolysate from the blood cells of one of four beta-thal
16 f F-cells or the concentration of HbF in the hemolysate, HbF/F-cell and the proportion of F-cells tha
17 n blot analysis to fractionate and visualize hemolysate hGALT, as well as the human enzyme expressed
18 S]methionine; (ii) preparing globin from the hemolysates; (iii) performing electrophoresis of the glo
21 sion fixation was performed on a subgroup of hemolysate- (n=15) and saline-injected (n=9) animals.
26 trometric analyses of adult peripheral blood hemolysates showed that there are three major alpha glob
28 uscle slightly but significantly better than hemolysate, which may have been due to the absence of ca
29 c acids were incubated with chicken red cell hemolysates, which contain the enzyme CPO, and the produ
30 GSH-dependent dehydroascorbate reduction in hemolysates, which was both direct and enzyme-dependent,
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