ライフサイエンスコーパス: the rank order of

1 r complexes was successfully used to predict the rank order of a series of nucleoside monophosphate a

2 nd caspase-8 with similar kinetics, although the rank order of activation was caspase-3 > caspase-9 >

3 varied 20-fold depending on the FXR isoform; the rank order of activation was FXRbeta2 > FXRalpha2 FX

4 lso accepted other acyl-CoAs as primers with the rank order of activity being acetyl-CoA approximatel

5 e binding was blocked by unlabeled LTs, with the rank order of affinities being LTD(4) >> LTE(4) = LT

6 No significant difference was found in the rank order of affinities for a series of thromboxane

7 atidine and carbamylcholine; for epibatidine the rank order of affinities is alphaepsilon > alphagamm

8 lcholine-binding sites on a single receptor; the rank order of affinities is the same for both fetal-

9 Curiously, the rank order of affinities of the compounds at 5-HT2A

10 tive enzyme-linked immunosorbent assay, that the rank order of affinities of TRAIL for the recombinan

11 These results reveal that the rank ordering of affinities for protein-protein inte

12 The rank order of affinity for displacement of [3H]-LSD

13 d measurement of InsP3 binding revealed that the rank order of affinity for InsP3 was type I > type I

14 The rank order of affinity for the agonist DAMGO is as f

15 The rank order of affinity of glucuronidated ezetimibe f

16 The rank order of agonist potency was ATP >/= 2 methylth

17 The rank order of agonist potency, based on inspection o

18 The rank order of agonist preference, UTP>ATP>ATPgammaS,

19 The rank order of agonists as TNF-alpha inhibitors sugge

20 SAR revealed that the rank order of agonists is alkyl glycerol phosphate >

21 The rank order of anionic permeability was: SCN- > I- >

22 In pulldown assays, the rank order of AnkG binding strength is Nav1.2 >> KCN

23 In normal rabbits, the rank order of arterial cholesterol concentrations wa

24 laminin-coated microtiter plate wells, with the rank order of attachment as follows: fibronectin > l

25 100-fold across USPSTF recommendations, and the rank order of benefits varied considerably among pat

26 Notably, the rank order of bile acids as CYP3A4 inducers and acti

27 ructure activity relationship that predicted the rank order of binding affinities for the series of i

28 s of a series of peptide ligands showed that the rank order of binding of the CTR ECD is identical to

29 er of binding of the CTR ECD is identical to the rank order of binding of the full-length CTR, confir

30 The rank order of binding potency for both the human rec

31 be accommodated by the NQO1 active site, and the ranking order of binding energies correlated with th

32 The rank order of biochemical and transcriptomic respons

33 Consistently, the rank-order of blockade of nicotinic acetylcholine re

34 Interestingly, the rank order of CaM binding affinity (gamma > beta > d

35 The rank order of Candida isolates was as follows: Candi

36 The rank order of Candida spp. occurrence was as follows

37 n of radioactivity across brain according to the rank order of CB1 receptor densities.

38 the high-affinity site of K+ channels, with the rank order of decreases being K26A >> W25A > K24A =

39 the SN proteins studied do not correspond to the rank order of denatured ensemble sizes detected by 1

40 Changes in species evenness and the rank order of dominant species are more widespread r

41 The simulations predicted the ranked order of drug sensitivity for indomethacin, a

42 We replicated the rank order of effect sizes for subcortical volumetri

43 The rank order of effect was arginine > glycine > serine

44 The rank order of effectiveness of agonists was approxim

45 ally been distinguished pharmacologically by the rank order of effectiveness of agonists; some prefer

46 The rank order of effectiveness of the 3-substituent was

47 The rank order of effectiveness of these compounds was:

48 The rank order of effects of canonical base pair substit

49 The rank order of effects on toxicity was C1---aldehyde

50 Therefore, the rank order of efficacy in coupling to AC6 is beta(1)

51 The rank order of efficacy to inhibit insulin-stimulated

52 reduced [3H]DAMGO binding in membranes with the rank order of etorphine > DAMGO = beta-endorphin > m

53 The rank order of expression with various tested 3' regi

54 -9 were less potent, as compared with 1, and the rank order of functional potencies correlated with t

55 The rank order of germination was not consistent in all

56 The rank order of HCV virucidal activity of commonly use

57 The peptide helix contents show that the rank order of helix propensities changes with temper

58 e for NPC1L1 in each species correlates with the rank order of in vivo activity with monkey > dog > h

59 ateral hippocampus not experiencing SD, with the rank order of induction as follows: DG > CA3 > CA1.

60 The rank order of inhibition by these compounds was cons

61 treatment was initiated after disease onset, the rank order of inhibitory activity was as follows: th

62 The rank order of inhibitory effectiveness of Abeta(17-3

63 The rank order of inhibitory potency for the remaining 1

64 There are strong similarities between the rank orders of interacting bases in the DNA and the

65 The rank order of internalization efficiencies was the s

66 The rank order of Kiapp values of additional nicotinic l

67 cant, positive correlation was found between the rank orders of L-VSCC activity and of alpha(1D), but

68 ry (ITC), resulting in a good correlation in the rank ordering of ligand affinity.

69 However, the rank order of m values of the SN proteins studied do

70 ta111 NmtRs also show clear perturbations in the rank order of metal responsiveness to Ni(II), Co(II)

71 s, while there is a good correlation between the ranking order of mismatches at the 5' end of synapti

72 The rank order of mutagenicity was N-nitrosodimethylamin

73 The rank order of neuroprotective potency was rosuvastat

74 The rank order of opiate ligand efficacies in producing

75 ofiles of the peptides, in general, followed the rank order of peptide entry to the brain with up to

76 The rank order of peptide potency on membrane excitabili

77 The rank order of performance was plasma AcSDKP, urine A

78 Flux for an uncharged solute, mannitol, and the rank order of permeabilities for the alkali metal ca

79 The rank order of photocovalent modification paralleled

80 eneral SAR of the tropanes is maintained and the rank order of potencies based on substitution at the

81 fferences were observed with Galphai2, where the rank order of potencies for both dopamine and norepi

82 The rank order of potencies for dopamine receptor agonis

83 In the wild type fibroblasts, the rank order of potencies for nucleotide-induced Delta

84 The rank order of potencies of inverse agonists to decre

85 The rank ordering of potencies of the nicotinic agonists

86 The rank order of potency (C4 (compound 4) > C3 (compoun

87 otective agent during MNNG incubations, with the rank order of potency being minocycline > doxycyclin

88 The rank order of potency determined for the inhibition

89 The rank order of potency for adenine nucleotides was Bz

90 The rank order of potency for inhibition of catecholamin

91 The rank order of potency for inhibition of tyrosine hyd

92 The rank order of potency for MAP kinase phosphorylation

93 The rank order of potency for nicotinic agonists was as

94 The rank order of potency for six nucleotides was UTP =

95 The rank order of potency for stimulation of PI hydrolys

96 The rank order of potency is [Leu31,Pro34]NPY > or = NPY

97 The rank order of potency of agonists in stimulating the

98 The rank order of potency of agonists was [Nle(10)]NKA(4

99 The rank order of potency of all the 5-HT3 receptor agon

100 The rank order of potency of NAADP, 2',3'-cyclic NAADP a

101 The rank order of potency of nicotinic antagonists in bl

102 scular responses from the PHN by determining the rank order of potency of several NPY-related peptide

103 The rank order of potency of the antagonists in the cell

104 The rank order of potency of the QA ions toward the diff

105 The rank order of potency of these compounds for decreas

106 The rank order of potency of three N-biotinylated peptid

107 The rank order of potency of various agonists in [3H]5'-

108 The rank order of potency to increase fecal pellet outpu

109 hat an alpha(2)AR mediates this response, as the rank order of potency was 5-bromo-N-(4,5-dihydro-1H-

110 The rank order of potency was BD1008 (N-[2-(3, 4-dichlor

111 The rank order of potency was the following: RNPA >> QP

112 The rank order of potency was WIN (IC50=2 nM)>2-AGE (350

113 ectively the frequency of [Ca2+]i spiking in the rank order of potency: CP 54,939 > CP 55,940 > Win 5

114 The rank-order of potency in the cyclic antagonist serie

115 everal different in vitro assays established the rank order of PP1 isoform selection by neurabins to

116 The rank order of preferred DNA sequences also differs,

117 caudoputamen (CP) showed strong agreement in the ranked order of projection intensities between the t

118 The rank order of recognition is different using the P14

119 es increased in a dose-dependent manner with the rank order of responsiveness absolute lymphocyte > m

120 The rank ordering of screening improvements according to

121 The rank ordering of search strategies by information pe

122 ed into three clusters, and the stability of the rank order of severity of symptoms within clusters a

123 The rank order of specific 3beta-(4-[125I]iodophenyl)tro

124 Moreover, the rank-order of substrate cutting is similar in apopto

125 Mucosal lacerations may affect the rank order of susceptibility to HIV but cannot be as

126 The rank order of tachykinin peptides competing for [3H]

127 nations received, and there was no change in the rank order of the 5 most commonly observed physician

128 The rank order of the extent of damage in the three gene

129 This model predicted the rank order of the four data sets described previousl

130 The rank order of the relative contribution of HIV/AIDS

131 ss of agonists was approximately the same as the rank order of their binding affinities to the mu rec

132 ta > alpha) does not directly correlate with the rank order of their CaM dependence for autophosphory

133 by each beta4 splice variant correlated with the rank order of their nuclear-targeting properties (be

134 ordinal utility of the available options and the rank ordering of their cached values, thereby provid

135 possible fitness landscapes on the basis of the rank ordering of their genotypic fitness values.

136 s functional or nonfunctional by correlating the rank ordering of these hybrids based on their activi

137 The results show that the rank order of this series of agonists was different

138 The comparison of the rank order of tissue telomere lengths within individ

139 The rank order of tolerogenic activity in the Lewis rat

140 The rank order of uptake was striatum > neocortical regi

141 ole drugs against Mtb H37Rv were determined, the rank order of which correlated well with Kd values f