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1                              Remarkably, low nanomolar concentrations of 12(S)-HETE-lysophospholipids
2                 Gel filtration confirms that nanomolar concentrations of 14C-labeled Abeta-(1-40) and
3              Treatment of naive B cells with nanomolar concentrations of 25-hydroxycholesterol suppre
4  GABA(A) receptors, which are potentiated by nanomolar concentrations of 3alpha-hydroxypregnane neuro
5                                              Nanomolar concentrations of [3H]BTA-1 did not appear to
6 ecreased proliferation and survival with low nanomolar concentrations of 5-aza-CdR is associated with
7 nsitivity barrier, allowing us to detect mid-nanomolar concentrations of a drug and a drug metabolite
8                                  Strikingly, nanomolar concentrations of a synthetic BID BH3 peptide
9  cultured cholinergic neurons exposed to low nanomolar concentrations of AbetaOs.
10 s in apoptotic cell extracts is abolished by nanomolar concentrations of Ac-DEVD-CHO and micromolar a
11  human airway epithelial cultures respond to nanomolar concentrations of ACT when applied to basolate
12 d Caco-2 cells were exposed basolaterally to nanomolar concentrations of activated MMP-3 or coculture
13    The inhibitory effects were maximal using nanomolar concentrations of activating chemokines, a con
14  and MMP-9 (~548-2561-fold) and detected low nanomolar concentrations of ADAMTS-5.
15                          Standard curves for nanomolar concentrations of ADP, UDP, GDP, and CDP are s
16 e serum or the same medium supplemented with nanomolar concentrations of all-trans-retinoic acid for
17 r striking evidence that, in neuronal cells, nanomolar concentrations of alpha-tocotrienol, but not a
18                                              Nanomolar concentrations of amplified DNA labeled with t
19 ge-dependent anion channel, we revealed that nanomolar concentrations of amyloid beta-peptide increas
20 ompared to PLG (KD approximately 800 nM) and nanomolar concentrations of apo(a) (500 nM) inhibited PL
21 in is applicable to any living tissue, where nanomolar concentrations of ATP play a critical role in
22                           Cells treated with nanomolar concentrations of bafilomycin A1 were largely
23 gh signal-to-background ratio obtained using nanomolar concentrations of BARAC obviated the need for
24 cell patch-clamp recording we show here that nanomolar concentrations of beta-amyloid peptides specif
25                               Treatment with nanomolar concentrations of betaAP(1-40) induced a 75% d
26     A cell-based method for the detection of nanomolar concentrations of bioactive amyloid peptide is
27 id, pH-sensitive aggregation occurred at low nanomolar concentrations of both Abeta1-40 and Abeta1-42
28 rolimus in the treatment of HGG cells at low nanomolar concentrations of both agents, with a reductio
29 e isolated proteins was strongly quenched by nanomolar concentrations of both concanamycin and an ind
30  of action and binding epitopes on CCR5, low nanomolar concentrations of both PRO 140 and RANTES inhi
31 milar to many other FPR2 agonistic peptides, nanomolar concentrations of both PSMalpha2 and PSMalpha3
32 mide generation, capping, and apoptosis, and nanomolar concentrations of C(16)-ceramide restored thes
33                                              Nanomolar concentrations of C1572 markedly reduced c-MYC
34                                           At nanomolar concentrations of Ca(2+), ROS-GC1 is activated
35                              In one mode, at nanomolar concentrations of Ca(2+), the GCAPs activate t
36               CRM1 switches on the enzyme at nanomolar concentrations of Ca2+ and is linked with phot
37 phatidylinositol 4,5-bisphosphate (PIP2) and nanomolar concentrations of calcium, has been identified
38                 In this study, we found that nanomolar concentrations of camptothecin (CPT), a topois
39                                   Similarly, nanomolar concentrations of cardiotonic steroids such as
40 tion of a three-component mixture containing nanomolar concentrations of cationic rhodamine 6G and an
41 ment of cancer cells with micromolar but not nanomolar concentrations of CCI-779 caused a marked decl
42                                              Nanomolar concentrations of CCK evoked non-oscillatory C
43                                              Nanomolar concentrations of celecoxib can inhibit VEGF m
44                                              Nanomolar concentrations of celecoxib reduced VEGF mRNA
45                                          Low nanomolar concentrations of CLT inhibited proliferation
46 ly, in a simple format, picoliter volumes of nanomolar concentrations of Co(2+), an environmental pol
47                                              Nanomolar concentrations of commercially obtained S1P we
48 sodium azide and vanadate and sensitivity to nanomolar concentrations of concanamycin A.
49 ate Alexandrium minutum responds to pico- to nanomolar concentrations of copepodamides with up to a 2
50                                     However, nanomolar concentrations of copper and zinc sulphides ha
51   Since Cro dimer-operator complexes form at nanomolar concentrations of Cro subunits where free dime
52 the MaxiK channel alpha-subunit resistant to nanomolar concentrations of CTx and IbTx.
53                    The oxidation kinetics of nanomolar concentrations of Cu(I) in NaCl solutions have
54 the usual P2X antagonists but was blocked by nanomolar concentrations of Cu2+ ions.
55 tor binding assay allowed rapid detection of nanomolar concentrations of cyclic imine neurotoxins dir
56 his new receptor is selectively activated by nanomolar concentrations of CysLTs with a rank order pot
57              Both receptors are inhibited by nanomolar concentrations of d-tubocurarine (curare) in a
58 in-coupled receptors (GPCRs) to discriminate nanomolar concentrations of DA and NE.
59  Pharmacokinetic analysis suggests that high nanomolar concentrations of dasatinib can be achieved sa
60 rcoma and Ewing's subset of bone sarcomas at nanomolar concentrations of dasatinib.
61 her suggest that the combined use of UV with nanomolar concentrations of DECA offers an effective che
62                                              Nanomolar concentrations of decorin promoted down-regula
63 reatment of cultured RBL-2H3 mast cells with nanomolar concentrations of dexamethasone causes dissoci
64                                              Nanomolar concentrations of dexamethasone suppressed pho
65               These results demonstrate that nanomolar concentrations of dieldrin can stimulate micro
66                 The results demonstrate that nanomolar concentrations of dieldrin time- and concentra
67                                 We show that nanomolar concentrations of dimeric tubulin induce volta
68                         Here, we report that nanomolar concentrations of EGCG significantly enhance c
69                                              Nanomolar concentrations of either 1NMPP1 or 1NaPP1, der
70                                              Nanomolar concentrations of either GST-p53 or GST-299-39
71                                  Exposure to nanomolar concentrations of either IL-1beta or IL-6 stim
72 on of A431 squamous carcinoma cell growth by nanomolar concentrations of epidermal growth factor (EGF
73 T3) and STAT5 was abrogated upon exposure to nanomolar concentrations of EXEL-0862.
74  When cultured for 6-10 h in the presence of nanomolar concentrations of exogenous [3H]retinol, both
75                                 In addition, nanomolar concentrations of exogenous L12 inhibits gonoc
76 ed organic compounds on the determination of nanomolar concentrations of Fe(II) have been compared us
77                                              Nanomolar concentrations of fibrillar Abeta bound cell-s
78 erase activity that is strongly inhibited by nanomolar concentrations of FK506 or rapamycin, indicati
79 s of single molecules have required pico- to nanomolar concentrations of fluorophore in order to isol
80 carbonic anhydrase to determine picomolar to nanomolar concentrations of free transition metal ions b
81  metals, but the interaction was promoted by nanomolar concentrations of free zinc and copper, and it
82                                              Nanomolar concentrations of G kinase were found to catal
83                          We show herein that nanomolar concentrations of genistein induce ASAH1 trans
84 range (1.6 nM to 1 muM) and was sensitive to nanomolar concentrations of glucose with a very low limi
85 actions; radical activities corresponding to nanomolar concentrations of H(2)O(2) could be detected.
86                                   In buffer, nanomolar concentrations of H1 induce bending and loopin
87 he Isd system are required for growth on low nanomolar concentrations of hemoglobin as a sole source
88 n expression is activated by the presence of nanomolar concentrations of Hg2+ in liquid media only wh
89 roglia killed neurons only after exposure to nanomolar concentrations of human A beta 1-40 or human A
90 sceptible to blockage by other species, even nanomolar concentrations of impurity metals in solution
91 ciated immunophilin is strongly inhibited by nanomolar concentrations of inositol 1,4, 5-trisphosphat
92                         Here, we report that nanomolar concentrations of intraaxonal oligomeric (o)Ab
93  pyrithione (ZnPy), we demonstrate that low, nanomolar concentrations of intracellular Zn(2+) ([Zn(2+
94                           In the presence of nanomolar concentrations of isolated HMG box A from HMGB
95                                              Nanomolar concentrations of KPV inhibit the activation o
96 amp recordings in brain slices to reveal how nanomolar concentrations of KYNA alter synaptic transmis
97 ylgeranylated-Ki4B-Ras in cells treated with nanomolar concentrations of L-778,123, and a mixture of
98 onds and was done in microliter volumes with nanomolar concentrations of labeled nucleotides.
99                    The effect of exposure to nanomolar concentrations of lead on several parameters o
100 s, in which cells are transiently exposed to nanomolar concentrations of ligand, ligand capture and r
101 g isolated cells, which are activated by sub-nanomolar concentrations of lipopolysaccharide (LPS).
102                                              Nanomolar concentrations of LXA(4) analog reduced NF-kap
103                          We demonstrate that nanomolar concentrations of MCH strongly activate SLC-1-
104           MCHR2 is specifically activated by nanomolar concentrations of MCH, binds to MCH with high
105                                              Nanomolar concentrations of MCP-1 induced chemotaxis in
106 osphorylated and internalized in response to nanomolar concentrations of MCP-1.
107 that in MT1/MT2 cultures, physiological (low nanomolar) concentrations of melatonin decrease the acti
108  pores to sense the activity of picomolar to nanomolar concentrations of membrane-active enzymes with
109  switch has been improved from micromolar to nanomolar concentrations of methoxyfenozide.
110                                              Nanomolar concentrations of methyllycaconitine blocked t
111 treatment of primary astrocyte cultures with nanomolar concentrations of MIP-2 or KC markedly up-regu
112                               Treatment with nanomolar concentrations of MIP-2 or KC markedly up-regu
113                                              Nanomolar concentrations of MPO increased H(2)O(2) micro
114 an wild-type plants to growth retardation by nanomolar concentrations of MTX, and this is associated
115 hat one receptor signaled in response to low nanomolar concentrations of murine JE, whereas the secon
116                                In vitro, low nanomolar concentrations of natural ceramide stimulate K
117          In L9'A mice, microinjection of low nanomolar concentrations of nicotine into the preBotC in
118 t are potently activated and desensitized by nanomolar concentrations of nicotine.
119 t might explain the response of RBL cells to nanomolar concentrations of nicotine.
120                                          Low nanomolar concentrations of nitric oxide activate guanyl
121 ometric probe demonstrated the production of nanomolar concentrations of NO by PBM and THP-1 cells up
122                                          Low nanomolar concentrations of NO increased intracellular C
123           Previous studies demonstrated that nanomolar concentrations of nocodazole can block cells i
124  this hypothesis by examining the effects of nanomolar concentrations of nocodazole on microtubule dy
125 the stimulation of growth in the presence of nanomolar concentrations of O2.
126 ieve inhibition of gene expression using low nanomolar concentrations of ODN.
127 in phosphatase activity is inhibited by high nanomolar concentrations of okadaic acid and the specifi
128  MEase activity is dramatically inhibited by nanomolar concentrations of okadaic acid, a specific inh
129  present study provides strong evidence that nanomolar concentrations of ONOO- both inhibit leukocyte
130  inhibition of both proteins was achieved at nanomolar concentrations of ONs in normal and breast can
131              Surprisingly, it was found that nanomolar concentrations of ouabain, similar to those ci
132 ivation of PACAP-selective PAC(1) receptors: nanomolar concentrations of PACAP27 and PACAP38 were req
133                                              Nanomolar concentrations of PCB 95, a NDL congener with
134 ingly, using competitive ELISA, we found low nanomolar concentrations of Pepcans in human plasma and
135                              The presence of nanomolar concentrations of peptide in the bathing solut
136                                              Nanomolar concentrations of peroxynitrite increased the
137 human hepatocellular cancer cell line cells, nanomolar concentrations of PG substantially diminish TG
138 o endogenous ligands but can be activated by nanomolar concentrations of pharmacologically inert, dru
139                                              Nanomolar concentrations of PLP can then be measured by
140 e to mature human spermatozoa, we found that nanomolar concentrations of progesterone dramatically po
141 ells, iSC cells, or CG4 oligodendrocytes but nanomolar concentrations of prosaptides prevented cell d
142 QD PL caused by the activity of picomolar to nanomolar concentrations of protease were detected as ch
143                                    Moreover, nanomolar concentrations of proteases can be detected vi
144                                              Nanomolar concentrations of PSMalpha2 are recognized by
145 major chromosome 3 peak that is activated by nanomolar concentrations of PZQ.
146 ell lines tested, with responses observed at nanomolar concentrations of R115777.
147 heir dimerization in the plasma membrane; at nanomolar concentrations of receptor, both unliganded an
148 these receptors bind to and are activated by nanomolar concentrations of recombinant prokineticins.
149       Surprisingly, GPCR142 was activated by nanomolar concentrations of relaxin-3 but was completely
150                  Treatment of cells with low nanomolar concentrations of retinoic acid decreased the
151   Here we present in vivo evidence that low (nanomolar) concentrations of RGD-mimetic alpha(v)beta(3)
152 d for 1.0 x 10(-6) M riboflavin and very low nanomolar concentrations of Rhodamine 6G.
153 r membrane (optoporation) in order to inject nanomolar concentrations of rhodamine phalloidin (an imp
154 d for the fluorescence-based quantitation of nanomolar concentrations of ribonucleoside diphosphates
155                    The ability to detect sub-nanomolar concentrations of ricin using fluorescently ta
156 .g. 10% bovine calf serum (BCS), neutral pH, nanomolar concentrations of RNA and hrPrP).
157                       Direct activation with nanomolar concentrations of ryanodine evoked increases i
158 kemia cells with constitutive Wnt activation nanomolar concentrations of salinomycin down-regulated t
159                                              Nanomolar concentrations of SDF-1 induced HO-1 in endoth
160               Lack of biological response to nanomolar concentrations of secretin was best explained
161 catalytic oxidation of sulfhydryls even with nanomolar concentrations of selenium.
162 bo1 and Robo2) and that CAD cells respond to nanomolar concentrations of Slit2 by markedly decelerati
163 strong inhibition of osteoblast viability by nanomolar concentrations of sphingosine, but not of cera
164                                              Nanomolar concentrations of SPP also induced a marked in
165                                              Nanomolar concentrations of strychnine selectively block
166                                           At nanomolar concentrations of subunits, assembly can be dr
167 ults show that the organic exudate generates nanomolar concentrations of superoxide and hydrogen pero
168 d that SK channels can be fully activated by nanomolar concentrations of Tb(3+), indicating an appare
169                                          Low nanomolar concentrations of tetrahydroquinoline (THQ)-ba
170 of antinociceptive agents, is blocked by low nanomolar concentrations of (-)-tetrodotoxin(TTX) but no
171 ding of CA200645 to tauD3 was antagonized by nanomolar concentrations of the A3 antagonist MRS 1220,
172                Exposure of myofibroblasts to nanomolar concentrations of the demethylating agent 5-az
173 pecific antisense inhibition was observed at nanomolar concentrations of the G-clamp S-ONs.
174 4E-binding protein 1 (4E-BP1), is blocked by nanomolar concentrations of the immunosuppressant rapamy
175 we demonstrate that clinically relevant, low nanomolar concentrations of the L-type channel inhibitor
176                Within 40 s of treatment with nanomolar concentrations of the natural or synthetic ver
177 nsitive to atropine but that were blocked by nanomolar concentrations of the nicotinic alpha7 recepto
178 MLO-Y4 and osteoblastic cells were seen with nanomolar concentrations of the peptide hormone calciton
179 rated to picomolar concentrations of WKYMVm, nanomolar concentrations of the peptide were required to
180 at an excited state quenching is possible at nanomolar concentrations of the proteins, while the disa
181                 The simultaneous addition of nanomolar concentrations of the RXRalpha ligand (9-cis-r
182 pe plants when incubated in media containing nanomolar concentrations of this antifolate, and vacuola
183                                              Nanomolar concentrations of this potent multifunctional
184    The approach allows the quantification of nanomolar concentrations of thrombin, and provides assoc
185 differentiation increased in the presence of nanomolar concentrations of thymosin beta4.
186 rium inhibition in the prolonged presence of nanomolar concentrations of tkP3BzPB was nearly 100%.
187   For all lipid mixtures tested, addition of nanomolar concentrations of toxin resulted in an increas
188       Efficient cell killing was possible at nanomolar concentrations of TuBB-9 due to the effective
189           Cholesterol export is inhibited by nanomolar concentrations of U18666A, a cationic sterol.
190 artial deficiency of npc1 or were exposed to nanomolar concentrations of U18666A, both of which lead
191 roteins, which was prevented by inclusion of nanomolar concentrations of unlabeled NAADP or 5N(3)-NAA
192           These chaperone proteins allow sub-nanomolar concentrations of UvrA to load UvrB through >1
193                                     However, nanomolar concentrations of VEGF/PlGF were able to elici
194                           We showed that low nanomolar concentrations of VIP, acting through G(s)-pro
195 urthermore, exposure of endothelial cells to nanomolar concentrations of vorapaxar induces endothelia
196  hSMG-1 kinase activity is inhibited by high nanomolar concentrations of wortmannin (IC(50) = 105 nm)
197                                              Nanomolar concentrations of wortmannin, 33.3 microm LY29
198 ced in vitro and ex vivo upon treatment with nanomolar concentrations of YM-01.

 
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