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1 and temperature-induced shifts in the oxygen dissociation curve.
2 sponds to the maximum slope of the oxygen-Hb dissociation curve.
3 falo (Bubalus bubalis) chromosome 20 by both dissociation curve analysis and conventional marker scor
5 adapted fluorescence-based real-time PCR and dissociation curve analysis for use as a novel scoring m
6 ) were suitable as cross-species markers for dissociation curve analysis in the buffalo radiation hyb
8 R applications, including post-amplification dissociation curve analysis, or differentiation of ampli
9 onclusion MR imaging-based oxygen-hemoglobin dissociation curves and oxygen-hemoglobin affinity infor
10 and Changeux to simulate whole-blood oxygen dissociation curves and red cell sickling in the absence
11 ance (MR) imaging-derived, oxygen-hemoglobin dissociation curves and to map fetal-placental oxygen-he
12 f metabolic acidosis on the CO(2)-hemoglobin dissociation curve, and then it should be interpreted wi
14 nitial validation studies, the oxyhemoglobin dissociation curve for mouse blood was accurately recrea
19 Overall, we obtained 2,388 association and dissociation curves of 223 unique molecular interactions
20 n associated with a left-shift in the oxygen dissociation curve, profound ascorbate deficiency, and c
21 ty include use of mismatch probes, obtaining dissociation curves rather than single temperature hybri
26 he position of these patients' oxyhemoglobin dissociation curves, we plotted arterial and venous oxyg
28 teractions since the initial sections of the dissociation curves were too steep to obtain reasonable
29 on of the MR imaging-based oxygen-hemoglobin dissociation curves with a shorter protocol that exclude