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1 seases and/or when cell-free Hb is used as a blood substitute.
2 romise for the production of stable Hb-based blood substitute.
3 e blood was replaced with a hemoglobin-based blood substitute.
4 before and after isovolumic replacement with blood substitute.
5 ic blood replacement with a hemoglobin-based blood substitute.
6 lobin (Hb) has been evaluated as a potential blood substitute.
7 alues in the development of hemoglobin-based blood substitutes.
8 rable to that of erythrocytes for developing blood substitutes.
9 f the oxidative toxicity of hemoglobin-based blood substitutes.
14 r the optimal combination of oxygen-carrying blood substitute, colloid, and electrolyte solution for
17 application to the development of potential blood substitutes for the rare Bombay blood type that is
18 pproaches for the development of a synthetic blood substitute has been the engineering of novel mutan
19 ctive effects of cell-free, hemoglobin-based blood substitutes have been appreciated, the systemic ef
22 usion for > 3 hours with a cold asanguineous blood substitute, hypothermosol (HTS) solution, has been
23 iscuss the development and current status of blood substitutes, including hemoglobin-based oxygen car
24 including blood transfusion, erythropoietin, blood substitutes, iron therapy, and minimization of dia
28 directed toward imaging the murine heart, a blood substitute may be applied to various optical diagn
30 oxidation of both recombinant MbO2 and HbO2 blood substitute prototypes without altering O2 affinity
31 two crystal structures of one such potential blood substitute, recombinant (r) Hb(alpha 96Val-->Trp),
33 lopments for the rational design of advanced blood substitutes that aim to address unmet clinical nee
34 of materials have been studied as candidate blood substitutes: the perfluorocarbons, modified hemogl
35 d blood cell transfusion or hemoglobin-based blood substitute therapy, the hemoglobinopathies, malari
37 of whole blood and dilutions of blood with a blood substitute were determined with a spectrophotomete
38 including optimization of the development of blood substitutes where Hb is contained within phospholi
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