ライフサイエンスコーパス: nanomolar concentrations of

1 Gel filtration confirms that nanomolar concentrations of 14C-labeled Abeta-(1-40) and

2 Treatment of naive B cells with nanomolar concentrations of 25-hydroxycholesterol suppre

3 GABA(A) receptors, which are potentiated by nanomolar concentrations of 3alpha-hydroxypregnane neuro

4 Nanomolar concentrations of [3H]BTA-1 did not appear to

5 ecreased proliferation and survival with low nanomolar concentrations of 5-aza-CdR is associated with

6 Strikingly, nanomolar concentrations of a synthetic BID BH3 peptide

7 cultured cholinergic neurons exposed to low nanomolar concentrations of AbetaOs.

8 s in apoptotic cell extracts is abolished by nanomolar concentrations of Ac-DEVD-CHO and micromolar a

9 human airway epithelial cultures respond to nanomolar concentrations of ACT when applied to basolate

10 d Caco-2 cells were exposed basolaterally to nanomolar concentrations of activated MMP-3 or coculture

11 The inhibitory effects were maximal using nanomolar concentrations of activating chemokines, a con

12 Standard curves for nanomolar concentrations of ADP, UDP, GDP, and CDP are s

13 e serum or the same medium supplemented with nanomolar concentrations of all-trans-retinoic acid for

14 r striking evidence that, in neuronal cells, nanomolar concentrations of alpha-tocotrienol, but not a

15 Nanomolar concentrations of amplified DNA labeled with t

16 ge-dependent anion channel, we revealed that nanomolar concentrations of amyloid beta-peptide increas

17 ompared to PLG (KD approximately 800 nM) and nanomolar concentrations of apo(a) (500 nM) inhibited PL

18 in is applicable to any living tissue, where nanomolar concentrations of ATP play a critical role in

19 Cells treated with nanomolar concentrations of bafilomycin A1 were largely

20 gh signal-to-background ratio obtained using nanomolar concentrations of BARAC obviated the need for

21 cell patch-clamp recording we show here that nanomolar concentrations of beta-amyloid peptides specif

22 Treatment with nanomolar concentrations of betaAP(1-40) induced a 75% d

23 A cell-based method for the detection of nanomolar concentrations of bioactive amyloid peptide is

24 id, pH-sensitive aggregation occurred at low nanomolar concentrations of both Abeta1-40 and Abeta1-42

25 e isolated proteins was strongly quenched by nanomolar concentrations of both concanamycin and an ind

26 of action and binding epitopes on CCR5, low nanomolar concentrations of both PRO 140 and RANTES inhi

27 mide generation, capping, and apoptosis, and nanomolar concentrations of C(16)-ceramide restored thes

28 Nanomolar concentrations of C1572 markedly reduced c-MYC

29 At nanomolar concentrations of Ca(2+), ROS-GC1 is activated

30 In one mode, at nanomolar concentrations of Ca(2+), the GCAPs activate t

31 CRM1 switches on the enzyme at nanomolar concentrations of Ca2+ and is linked with phot

32 phatidylinositol 4,5-bisphosphate (PIP2) and nanomolar concentrations of calcium, has been identified

33 In this study, we found that nanomolar concentrations of camptothecin (CPT), a topois

34 Similarly, nanomolar concentrations of cardiotonic steroids such as

35 tion of a three-component mixture containing nanomolar concentrations of cationic rhodamine 6G and an

36 ment of cancer cells with micromolar but not nanomolar concentrations of CCI-779 caused a marked decl

37 Nanomolar concentrations of CCK evoked non-oscillatory C

38 Nanomolar concentrations of celecoxib can inhibit VEGF m

39 Nanomolar concentrations of celecoxib reduced VEGF mRNA

40 Low nanomolar concentrations of CLT inhibited proliferation

41 ly, in a simple format, picoliter volumes of nanomolar concentrations of Co(2+), an environmental pol

42 Nanomolar concentrations of commercially obtained S1P we

43 sodium azide and vanadate and sensitivity to nanomolar concentrations of concanamycin A.

44 ate Alexandrium minutum responds to pico- to nanomolar concentrations of copepodamides with up to a 2

45 However, nanomolar concentrations of copper and zinc sulphides ha

46 Since Cro dimer-operator complexes form at nanomolar concentrations of Cro subunits where free dime

47 the MaxiK channel alpha-subunit resistant to nanomolar concentrations of CTx and IbTx.

48 The oxidation kinetics of nanomolar concentrations of Cu(I) in NaCl solutions have

49 the usual P2X antagonists but was blocked by nanomolar concentrations of Cu2+ ions.

50 tor binding assay allowed rapid detection of nanomolar concentrations of cyclic imine neurotoxins dir

51 his new receptor is selectively activated by nanomolar concentrations of CysLTs with a rank order pot

52 Both receptors are inhibited by nanomolar concentrations of d-tubocurarine (curare) in a

53 in-coupled receptors (GPCRs) to discriminate nanomolar concentrations of DA and NE.

54 Pharmacokinetic analysis suggests that high nanomolar concentrations of dasatinib can be achieved sa

55 rcoma and Ewing's subset of bone sarcomas at nanomolar concentrations of dasatinib.

56 her suggest that the combined use of UV with nanomolar concentrations of DECA offers an effective che

57 Nanomolar concentrations of decorin promoted down-regula

58 reatment of cultured RBL-2H3 mast cells with nanomolar concentrations of dexamethasone causes dissoci

59 Nanomolar concentrations of dexamethasone suppressed pho

60 These results demonstrate that nanomolar concentrations of dieldrin can stimulate micro

61 The results demonstrate that nanomolar concentrations of dieldrin time- and concentra

62 We show that nanomolar concentrations of dimeric tubulin induce volta

63 Here, we report that nanomolar concentrations of EGCG significantly enhance c

64 Nanomolar concentrations of either 1NMPP1 or 1NaPP1, der

65 Nanomolar concentrations of either GST-p53 or GST-299-39

66 Exposure to nanomolar concentrations of either IL-1beta or IL-6 stim

67 on of A431 squamous carcinoma cell growth by nanomolar concentrations of epidermal growth factor (EGF

68 T3) and STAT5 was abrogated upon exposure to nanomolar concentrations of EXEL-0862.

69 When cultured for 6-10 h in the presence of nanomolar concentrations of exogenous [3H]retinol, both

70 In addition, nanomolar concentrations of exogenous L12 inhibits gonoc

71 ed organic compounds on the determination of nanomolar concentrations of Fe(II) have been compared us

72 Nanomolar concentrations of fibrillar Abeta bound cell-s

73 erase activity that is strongly inhibited by nanomolar concentrations of FK506 or rapamycin, indicati

74 s of single molecules have required pico- to nanomolar concentrations of fluorophore in order to isol

75 carbonic anhydrase to determine picomolar to nanomolar concentrations of free transition metal ions b

76 metals, but the interaction was promoted by nanomolar concentrations of free zinc and copper, and it

77 Nanomolar concentrations of G kinase were found to catal

78 We show herein that nanomolar concentrations of genistein induce ASAH1 trans

79 actions; radical activities corresponding to nanomolar concentrations of H(2)O(2) could be detected.

80 In buffer, nanomolar concentrations of H1 induce bending and loopin

81 he Isd system are required for growth on low nanomolar concentrations of hemoglobin as a sole source

82 n expression is activated by the presence of nanomolar concentrations of Hg2+ in liquid media only wh

83 roglia killed neurons only after exposure to nanomolar concentrations of human A beta 1-40 or human A

84 ciated immunophilin is strongly inhibited by nanomolar concentrations of inositol 1,4, 5-trisphosphat

85 Here, we report that nanomolar concentrations of intraaxonal oligomeric (o)Ab

86 pyrithione (ZnPy), we demonstrate that low, nanomolar concentrations of intracellular Zn(2+) ([Zn(2+

87 In the presence of nanomolar concentrations of isolated HMG box A from HMGB

88 Nanomolar concentrations of KPV inhibit the activation o

89 amp recordings in brain slices to reveal how nanomolar concentrations of KYNA alter synaptic transmis

90 ylgeranylated-Ki4B-Ras in cells treated with nanomolar concentrations of L-778,123, and a mixture of

91 onds and was done in microliter volumes with nanomolar concentrations of labeled nucleotides.

92 The effect of exposure to nanomolar concentrations of lead on several parameters o

93 s, in which cells are transiently exposed to nanomolar concentrations of ligand, ligand capture and r

94 g isolated cells, which are activated by sub-nanomolar concentrations of lipopolysaccharide (LPS).

95 Nanomolar concentrations of LXA(4) analog reduced NF-kap

96 We demonstrate that nanomolar concentrations of MCH strongly activate SLC-1-

97 MCHR2 is specifically activated by nanomolar concentrations of MCH, binds to MCH with high

98 Nanomolar concentrations of MCP-1 induced chemotaxis in

99 osphorylated and internalized in response to nanomolar concentrations of MCP-1.

100 that in MT1/MT2 cultures, physiological (low nanomolar) concentrations of melatonin decrease the acti

101 pores to sense the activity of picomolar to nanomolar concentrations of membrane-active enzymes with

102 switch has been improved from micromolar to nanomolar concentrations of methoxyfenozide.

103 Nanomolar concentrations of methyllycaconitine blocked t

104 treatment of primary astrocyte cultures with nanomolar concentrations of MIP-2 or KC markedly up-regu

105 Treatment with nanomolar concentrations of MIP-2 or KC markedly up-regu

106 Nanomolar concentrations of MPO increased H(2)O(2) micro

107 an wild-type plants to growth retardation by nanomolar concentrations of MTX, and this is associated

108 hat one receptor signaled in response to low nanomolar concentrations of murine JE, whereas the secon

109 In vitro, low nanomolar concentrations of natural ceramide stimulate K

110 In L9'A mice, microinjection of low nanomolar concentrations of nicotine into the preBotC in

111 t are potently activated and desensitized by nanomolar concentrations of nicotine.

112 t might explain the response of RBL cells to nanomolar concentrations of nicotine.

113 Low nanomolar concentrations of nitric oxide activate guanyl

114 ometric probe demonstrated the production of nanomolar concentrations of NO by PBM and THP-1 cells up

115 Low nanomolar concentrations of NO increased intracellular C

116 Previous studies demonstrated that nanomolar concentrations of nocodazole can block cells i

117 this hypothesis by examining the effects of nanomolar concentrations of nocodazole on microtubule dy

118 the stimulation of growth in the presence of nanomolar concentrations of O2.

119 ieve inhibition of gene expression using low nanomolar concentrations of ODN.

120 in phosphatase activity is inhibited by high nanomolar concentrations of okadaic acid and the specifi

121 MEase activity is dramatically inhibited by nanomolar concentrations of okadaic acid, a specific inh

122 present study provides strong evidence that nanomolar concentrations of ONOO- both inhibit leukocyte

123 inhibition of both proteins was achieved at nanomolar concentrations of ONs in normal and breast can

124 Surprisingly, it was found that nanomolar concentrations of ouabain, similar to those ci

125 ivation of PACAP-selective PAC(1) receptors: nanomolar concentrations of PACAP27 and PACAP38 were req

126 Nanomolar concentrations of PCB 95, a NDL congener with

127 ingly, using competitive ELISA, we found low nanomolar concentrations of Pepcans in human plasma and

128 The presence of nanomolar concentrations of peptide in the bathing solut

129 Nanomolar concentrations of peroxynitrite increased the

130 o endogenous ligands but can be activated by nanomolar concentrations of pharmacologically inert, dru

131 Nanomolar concentrations of PLP can then be measured by

132 e to mature human spermatozoa, we found that nanomolar concentrations of progesterone dramatically po

133 ells, iSC cells, or CG4 oligodendrocytes but nanomolar concentrations of prosaptides prevented cell d

134 QD PL caused by the activity of picomolar to nanomolar concentrations of protease were detected as ch

135 ell lines tested, with responses observed at nanomolar concentrations of R115777.

136 heir dimerization in the plasma membrane; at nanomolar concentrations of receptor, both unliganded an

137 these receptors bind to and are activated by nanomolar concentrations of recombinant prokineticins.

138 Surprisingly, GPCR142 was activated by nanomolar concentrations of relaxin-3 but was completely

139 Treatment of cells with low nanomolar concentrations of retinoic acid decreased the

140 Here we present in vivo evidence that low (nanomolar) concentrations of RGD-mimetic alpha(v)beta(3)

141 d for 1.0 x 10(-6) M riboflavin and very low nanomolar concentrations of Rhodamine 6G.

142 r membrane (optoporation) in order to inject nanomolar concentrations of rhodamine phalloidin (an imp

143 d for the fluorescence-based quantitation of nanomolar concentrations of ribonucleoside diphosphates

144 The ability to detect sub-nanomolar concentrations of ricin using fluorescently ta

145 .g. 10% bovine calf serum (BCS), neutral pH, nanomolar concentrations of RNA and hrPrP).

146 Direct activation with nanomolar concentrations of ryanodine evoked increases i

147 kemia cells with constitutive Wnt activation nanomolar concentrations of salinomycin down-regulated t

148 Nanomolar concentrations of SDF-1 induced HO-1 in endoth

149 Lack of biological response to nanomolar concentrations of secretin was best explained

150 catalytic oxidation of sulfhydryls even with nanomolar concentrations of selenium.

151 bo1 and Robo2) and that CAD cells respond to nanomolar concentrations of Slit2 by markedly decelerati

152 strong inhibition of osteoblast viability by nanomolar concentrations of sphingosine, but not of cera

153 Nanomolar concentrations of SPP also induced a marked in

154 Nanomolar concentrations of strychnine selectively block

155 At nanomolar concentrations of subunits, assembly can be dr

156 ults show that the organic exudate generates nanomolar concentrations of superoxide and hydrogen pero

157 d that SK channels can be fully activated by nanomolar concentrations of Tb(3+), indicating an appare

158 Low nanomolar concentrations of tetrahydroquinoline (THQ)-ba

159 of antinociceptive agents, is blocked by low nanomolar concentrations of (-)-tetrodotoxin(TTX) but no

160 ding of CA200645 to tauD3 was antagonized by nanomolar concentrations of the A3 antagonist MRS 1220,

161 Exposure of myofibroblasts to nanomolar concentrations of the demethylating agent 5-az

162 pecific antisense inhibition was observed at nanomolar concentrations of the G-clamp S-ONs.

163 4E-binding protein 1 (4E-BP1), is blocked by nanomolar concentrations of the immunosuppressant rapamy

164 Within 40 s of treatment with nanomolar concentrations of the natural or synthetic ver

165 nsitive to atropine but that were blocked by nanomolar concentrations of the nicotinic alpha7 recepto

166 MLO-Y4 and osteoblastic cells were seen with nanomolar concentrations of the peptide hormone calciton

167 rated to picomolar concentrations of WKYMVm, nanomolar concentrations of the peptide were required to

168 at an excited state quenching is possible at nanomolar concentrations of the proteins, while the disa

169 The simultaneous addition of nanomolar concentrations of the RXRalpha ligand (9-cis-r

170 pe plants when incubated in media containing nanomolar concentrations of this antifolate, and vacuola

171 Nanomolar concentrations of this potent multifunctional

172 The approach allows the quantification of nanomolar concentrations of thrombin, and provides assoc

173 differentiation increased in the presence of nanomolar concentrations of thymosin beta4.

174 rium inhibition in the prolonged presence of nanomolar concentrations of tkP3BzPB was nearly 100%.

175 For all lipid mixtures tested, addition of nanomolar concentrations of toxin resulted in an increas

176 Efficient cell killing was possible at nanomolar concentrations of TuBB-9 due to the effective

177 Cholesterol export is inhibited by nanomolar concentrations of U18666A, a cationic sterol.

178 artial deficiency of npc1 or were exposed to nanomolar concentrations of U18666A, both of which lead

179 roteins, which was prevented by inclusion of nanomolar concentrations of unlabeled NAADP or 5N(3)-NAA

180 These chaperone proteins allow sub-nanomolar concentrations of UvrA to load UvrB through >1

181 However, nanomolar concentrations of VEGF/PlGF were able to elici

182 We showed that low nanomolar concentrations of VIP, acting through G(s)-pro

183 urthermore, exposure of endothelial cells to nanomolar concentrations of vorapaxar induces endothelia

184 hSMG-1 kinase activity is inhibited by high nanomolar concentrations of wortmannin (IC(50) = 105 nm)

185 Nanomolar concentrations of wortmannin, 33.3 microm LY29

186 ced in vitro and ex vivo upon treatment with nanomolar concentrations of YM-01.