ライフサイエンスコーパス: displaceable

1 majority (94%) of the binding was specific (displaceable).

2 heme-iron residues in EcDos must be readily displaceable.

3 hat are metastable, but easily reversible or displaceable.

4 5-HT-displaceable [125I]3beta-(4-iodophenyl)-tropane-2beta-ca

5 lon2 subunit correlated with changes in NMDA-displaceable [(3)H]glutamate binding, and mRNA density c

6 However, picrotoxin displaceable [(35)S]TBPS binding to alpha1beta2gamma2 GA

7 glutamate recognition site by specific NMDA-displaceable [3H]glutamate binding assays.

8 NMDA-displaceable [3H]glutamate binding was markedly increase

9 Imipramine-displaceable 5-[3H]HT binding to intact L-S1 cells was s

10 nabled quantitative assessment of imipramine-displaceable 5-[3H]HT binding to the 5-HT transport syst

11 he interaction of PIB with CAA was not fully displaceable and this may be linked to the apolipoprotei

12 Binding potentials relative to non-displaceable binding (BPND) for [(11)C]carfentanil and i

13 1)C-IMA107 binding potential relative to non-displaceable binding (BPND) were generated from the dyna

14 mal tissues, coupled with the high degree of displaceable binding from both tumors and the normal bra

15 mation of the binding parameters due to high displaceable binding in the reference region.

16 (3)H-MK-6240 showed no displaceable binding in the subcortical regions of human

17 Displaceable binding of (11)C-DASB was found in all brai

18 human erythrocytes, and blocked the glucose-displaceable binding of cytochalasin B to GLUT1 in eryth

19 dies showed that genistein inhibited glucose-displaceable binding of cytochalasin B to GLUT1 in eryth

20 oligand binding analyses showed specific and displaceable binding of MIP-1beta to thymocytes with a K

21 ansporter availability was quantified as non-displaceable binding potential using a kinetic model for

22 learly elevated binding potential (BPND (non-displaceable binding potential)) in temporal lobes, late

23 man Alzheimer's disease brains showed highly displaceable binding to tau-rich regions.

24 In rats, displaceable binding was largely reduced in the cerebell

25 No displaceable binding was observed in self-block studies

26 3, namely, reasonable brain permeability and displaceable binding.

27 confirmed that the brain had specific (i.e., displaceable) binding but could not detect specific bind

28 pectively, and these repressor complexes are displaceable by E2F-1.

29 2 receptors was saturable (KD = 0.15 nM) and displaceable by galanin peptides and analogues in rank o

30 rat KD = 0.98 nM and human KD = 2.23 nM) and displaceable by galanin peptides and analogues in the fo

31 g of [(3)H]38 was fully reversible and fully displaceable by nonpeptide antagonists and the agonist p

32 that [3H]-L-685,458 binding was saturatable, displaceable by peptidomimetic and small molecule gamma-

33 sections (but not WAT) in vitro was high and displaceable by pretreatment with rimonabant.

34 HNF-4alpha with intact F-domain was readily displaceable by S-hexadecyl-CoA, a nonhydrolyzable thioe

35 I binding to TE671 cell homogenates is fully displaceable by the small molecule antagonist d-tubocura

36 C cells at 0.02-20 nM concentrations and was displaceable by TSP-1.

37 which is reversibly bound to this enzyme and displaceable by tyramine, will be an antidepressant whic

38 anism that considers the effect of stable vs displaceable coatings during NP migration in CE is sugge

39 e measured binding potential relative to non-displaceable compartment (BPND) and derived percent redu

40 greater Q(10) (27-37 degrees C) than the non-displaceable component

41 s using positron emission tomography and the displaceable D(2)/D(3) receptor radiotracer [(11)C]raclo

42 s in high yield and purity using selectively displaceable DNA linkers.

43 in these DAT-rich regions was significantly displaceable either by preadministration of citalopram f

44 1,3,4,5)P4, showed specific, PtdIns(3,4,5)P3-displaceable labeling of only alpha-COP.

45 -2-linked [3H]BZDC-IP6 showed efficient, IP6-displaceable labeling of the GST-Syt II-C2B.

46 croM) did not reduce dextromethorphan (1 mM)-displaceable ligand binding.

47 stimate of the volume of distribution of non-displaceable ligand in brain tissue that increased with

48 lls in a dose-dependent, saturable, and self-displaceable manner.

49 Confocal microscopy revealed clear, displaceable membrane labeling of CHO-A(3) cells with 19

50 hodology for the fabrication of controllably displaceable monolayers using a carboxyl-functionalized

51 Highly selective Ins(1,3,4,5)P4-displaceable photocovalent modification of the alpha-COP

52 ment study for the other enantiomer found no displaceable radioactivity in the same group of mice; th

53 The displaceable radioactivity of one enantiomer in the brai

54 nance spectroscopies about the nature of the displaceable residue in the heme-PAS domain of EcDos, i.

55 s a high affinity (K(d) = 30 nM), saturable, displaceable, single binding site specific for progestin

56 Induction of displaceable soluble FN binding correlates with the abil

57 lsilane stationary phases using octanol as a displaceable surface template to control the rate of alk

58 ical for binding, the methionines are easily displaceable to increase the accessibility of these resi

59 se patients with [(18)F]FEM-IMPY showed high displaceable uptake in gray matter and low nonspecific b

60 riments showed that the binding to BVECs was displaceable, was saturable, and yielded a typical bindi

61 ons of high SERT density of monkey brain was displaceable with citalopram except in the putamen and c

62 ulation of [123I]IACFT was nearly completely displaceable with unlabeled CFT (1 mg/kg) but was not af

63 macromolecules was specific, reversible, and displaceable with unlabeled leptin (ED50: 0.73 +/- 0.09

64 binding was specific for progestins and was displaceable, with rapid rates of association and dissoc