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2 ceptor density corresponding to 1,000-10,000 dpm/mg of tissue; conversely, single-ligand binding, alt
9 had a low binding (mean density, 844 +/- 168 dpm/mg of tissue) with the agonist whereas 12 had a high
10 -1) x min(-1) (19.1 +/- 3.1 vs. 36.5 +/- 7.2 dpm/micromol) glucagon infusions, implying that a greate
11 bis-pyridine adducts of (dpm)Mn(II)(py)(2), (dpm)Fe(II)(py)(2), and (dpm)Co(II)(py)(2) reveal each di
12 tural samples with activities as low as 0.20 dpm above background (2sigma, integration time = 2 hr).
15 2 with the agonist (mean density, 348 +/- 49 dpm/mg of tissue) whereas all cases had a high sst2 bind
17 her (4.50 +/- 0.29 vs. 3.16 +/- 0.21 x 10(5) dpm/ml per 5 h; P < 0.05) in the diabetic subjects than
19 had higher receptor binding (2550.9+/-63.59 dpm/mg) when compared to the PE-Free group (2011.9+/-174
20 5) and phospholipase C (control 478.5 +/- 67 dpm/well, +PDGF 1049.3 +/- 93, n = 4, p = 0.003), while
21 -1) x min(-1) (19.0 +/- 3.9 vs. 41.4 +/- 5.7 dpm/micromol) and 3.0 ng x kg(-1) x min(-1) (19.1 +/- 3.
22 els of V1A receptor binding (2689.93+/-254.8 dpm/mg) compared to the PE group (1907.32+/-136.3 dpm/mg
24 (dpm)Mn(II)(py)(2), (dpm)Fe(II)(py)(2), and (dpm)Co(II)(py)(2) reveal each divalent ion to be high-sp
27 le uptake of EBD and (125)I-labeled insulin (dpm per gram dry tissue) with 0.1-Hz stimulation (n = 6)
28 (SQUID, EPR) of the bis-pyridine adducts of (dpm)Mn(II)(py)(2), (dpm)Fe(II)(py)(2), and (dpm)Co(II)(p
29 Site-specific fat specific activity (SA) (dpm/g lipid) decreased as a function of fat mass in both
32 lly populated ligand-based orbitals from the dpm construct lie above partially filled metal 3d orbita
37 tetrahedral in the solid state, whereas the (dpm)Ni(II)(py)(2) is low-spin and adopts a square-planar
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