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1 sponds to the maximum slope of the oxygen-Hb dissociation curve.
2 falo (Bubalus bubalis) chromosome 20 by both dissociation curve analysis and conventional marker scor
3                                    PCR-based dissociation curve analysis decreases both time and reso
4 adapted fluorescence-based real-time PCR and dissociation curve analysis for use as a novel scoring m
5 ) were suitable as cross-species markers for dissociation curve analysis in the buffalo radiation hyb
6                                              Dissociation curve analysis is reliable and efficient fo
7 R applications, including post-amplification dissociation curve analysis, or differentiation of ampli
8 onclusion MR imaging-based oxygen-hemoglobin dissociation curves and oxygen-hemoglobin affinity infor
9 ance (MR) imaging-derived, oxygen-hemoglobin dissociation curves and to map fetal-placental oxygen-he
10            Defined endpoints (Ct values) and dissociation curves are generated for each BV-BJ combina
11 nitial validation studies, the oxyhemoglobin dissociation curve for mouse blood was accurately recrea
12               As proof of principle for this dissociation curve method, we generated new maps of rive
13 oncentrations of NO up to 80 ppm, and oxygen dissociation curves (ODCs) were measured.
14  of amplification was monitored by using the dissociation curve of the amplified product.
15   Overall, we obtained 2,388 association and dissociation curves of 223 unique molecular interactions
16 n associated with a left-shift in the oxygen dissociation curve, profound ascorbate deficiency, and c
17 ty include use of mismatch probes, obtaining dissociation curves rather than single temperature hybri
18    We also obtained sequence data to augment dissociation curve results.
19 ed similar results but shifted the sigmoidal dissociation curves to lower urea concentrations.
20                    While a simple monophasic dissociation curve was obtained at neutral pH, the compl
21        The ability to right-shift the oxygen dissociation curve was retained across the spectrum of m
22 he position of these patients' oxyhemoglobin dissociation curves, we plotted arterial and venous oxyg
23           MR imaging-based oxygen-hemoglobin dissociation curves were constructed by nonlinear least
24 teractions since the initial sections of the dissociation curves were too steep to obtain reasonable
25 on of the MR imaging-based oxygen-hemoglobin dissociation curves with a shorter protocol that exclude
26         We found right-shifted oxyhemoglobin dissociation curves, with pH-corrected p50s ranging from

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