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2 addition of 1 mM furosemide (frusemide), but was potentiated by 1 mM 4,4'-diisothiocyanatostilbene-2,
5 ighly correlated with glucose concentration, being potentiated by 15 mM but abolished in its absence,
8 (2+) channel blocker nicardipine (2 muM) and was potentiated by 8-pCPT-2'-O-Me-cAMP-AM at concentrati
12 weaker inhibitory activity inherent in uORF2 is potentiated by a sub-optimal nucleotide context surro
13 e HHcy- and HG-induced mu-calpain activation was potentiated by a combination of HHcy and HG in the m
14 hic factor (GDNF) to increase cocaine intake was potentiated by a deletion that abolished its HS bind
16 RGCs to regenerate their axons; this effect was potentiated by a low molecular weight factor that is
17 independent of G(1) exit and, surprisingly, was potentiated by a mutation that prevents EID-1 bindin
18 direct mechanism involves local ACh release, is potentiated by acetylcholinesterase inhibitors and bl
20 gnalling via a G-protein-coupled receptor to be potentiated by action potential waveforms and small a
24 de that a Ca2+-activated K+ current in HUVEC is potentiated by activation of a Gi/Go-coupled receptor
25 ther hand, NMDA-stimulated [14C]GABA release was potentiated by activation of group I metabotropic re
26 m signal caused by activation of native KARs was potentiated by activation of group I mGlu receptors.
27 th flies and in human cells, SoxN repression is potentiated by adding ectopic Tcf, suggesting that So
28 Activation of phospholipase C by convulxin was potentiated by ADP acting through the P2Y12 receptor
31 lcium (Ca(2+)(o))-sensing receptor (CaR) can be potentiated by allosteric activators including calcim
32 ensory nerve discharges evoked by distention were potentiated by alpha,beta-methylene adenosine 5'-tr
33 the EPSCs evoked by dorsal root stimulation were potentiated by alphabetam-ATP as well as by the ect
35 man alpha4beta2 neuronal nicotinic receptors are potentiated by an estrogen steroid, 17beta-estradiol
37 an EGF-sensitive signaling pathway that can be potentiated by an aberrant activity or expression of
38 was absent in mGlu5 knock-out (KO) mice and was potentiated by an A2A antagonist KW-6002 [(E)-1,3-di
41 dent induction of Ca(2+) release by FXa that was potentiated by APS-IgG and SLE/APS- IgG compared to
43 rt here that PGC-1alpha coactivator activity is potentiated by arginine methylation by protein argini
50 of Met by InlB has previously been shown to be potentiated by binding of glycosaminoglycans to the G
51 ls results in degranulation, a response that is potentiated by binding of stem cell factor (SCF) to i
53 catalyzed depalmitoylation of palmitoyl-eNOS is potentiated by Ca(2+)-calmodulin (CaM), a key alloste
54 tion, whereas IP(3)-evoked Ca(2+) liberation was potentiated by Ca(2+) entry during action potentials
56 feedback mechanism of the Ca(2+) entry that is potentiated by cAMP in sources where AC5 is commonly
58 us to choose a cytotoxic drug whose activity is potentiated by cellular thiols with enhanced specific
60 contrast, CPA-evoked TRPC5 channel activity was potentiated by chelerythrine, and inhibited by PDBu,
62 m-negative cells and that this concentration is potentiated by chromosomal lesions resulting from the
65 adhesion-independent cell cycle progression was potentiated by coexpressing Skp2 with cyclin D1 but
71 urine tumors and clinical tumor explants can be potentiated by combining the uCendR peptide with tumo
72 ed the stage of intracellular infection that is potentiated by comparing the wild-type and T2SS mutan
74 ference for the drug-paired environment that was potentiated by concurrent intravenous (iv) administr
75 cute lung injury, alveolar fibrin deposition is potentiated by consistent changes in endogenous coagu
76 ons of capsaicin and moderate heat, however, were potentiated by conversion of PtdIns(4,5)P2 to PtdIn
80 by NMDA receptors that include NR2B subunits are potentiated by D(1)/D(5) receptor activation, wherea
81 ings revealed that striatal inputs to the EP were potentiated by D1LRs whereas pallidal inputs to the
82 BA postsynaptic currents, GABAergic currents are potentiated by DAMGO after chronic morphine treatmen
83 Extracellular polyphosphate accumulation is potentiated by decreased nutrient levels, potentially
84 pic and signaling responses to the VEGF that were potentiated by decreased transcription of VEGF rece
86 The cytotoxicity of the catecholic estrogens was potentiated by depletion of intracellular glutathion
89 t the activation of the DBH promoter by Arix is potentiated by dHAND via a mechanism independent of a
90 polarization-activated cation (HCN) channels is potentiated by direct binding of cAMP to a cytoplasmi
92 arguments suggest that channel opening must be potentiated by downstream changes in channel activati
94 d by a dynein-independent pathway that could be potentiated by dynactin disruption, consistent with a
97 s suggest that the neural fixation circuitry is potentiated by engaging stationary objects, and inter
99 acetylcholine (ACh) receptor antagonists and was potentiated by eserine, an inhibitor of acetylcholin
101 r-alpha (TNF-alpha) cytotoxicity is shown to be potentiated by ethanol exposure in vitro in the human
102 evant to brain function, and its actions can be potentiated by ethanol; thus, NFKB1 is an excellent c
107 ecies ortholog with high homology to rTRPV1, is potentiated by extracellular protons and magnesium, e
108 mmune cells by extracellular alpha-synuclein is potentiated by extracellular vesicles, possibly by fa
109 onse of ovarian cancer cells to pitavastatin is potentiated by farnesyl diphosphate synthase inhibito
112 rane-proximal external region (MPER) of gp41 were potentiated by FcgammaRI and, to a lesser extent, b
115 of phospholipase C-coupled receptor agonists is potentiated by G(i)-coupled receptors (eg, adenosine
119 GABAA receptor-mediated tonic current, which is potentiated by H2O2, might contribute to H2O2-induced
122 rotease nexin II (K(i) approximately 450 pM) is potentiated by heparin (K(I) approximately 30 pM).
123 e zipper transcription factor whose activity is potentiated by herbicide-induced xenobiotic stress.
127 The induction of apoptosis by ER stress was potentiated by HO inhibition, whereas it was prevent
129 ssion of inwardly rectifying currents, which were potentiated by hyperpolarizing prepulses and inhibi
130 S-nitrosylation of NMDARs by NitroMemantine is potentiated by hypoxia and thereby directed at ischem
133 s is mediated by CD40-CD40L interactions and is potentiated by IL-4 and inhibited by both IL-10 and I
134 ing, whereas IgG1 class switch recombination was potentiated by IL-21 in the context of limited IL-4.
135 tion of NRT2.1 expression and nitrate uptake is potentiated by increased carbon photoassimilate (sucr
138 nostilbene-2,2'-disulphonic acid (DIDS), and was potentiated by inhibiting astrocytic conversion of g
144 nsulin-induced AKT and FoxO1 phosphorylation were potentiated by inhibition of Sirt1 in a cultured hy
153 alpha(2)M*-stimulated cells, and this effect is potentiated by isobutylmethylxanthine, dibutyryl-cAMP
155 The ability of LND to promote cell death was potentiated by its suppression of the pentose phosph
156 rences for EtOH-paired locations (CPPs) that are potentiated by iv heroin and whose acquisition and e
157 the plasma membrane P2X4, the lysosomal P2X4 was potentiated by ivermectin but insensitive to suramin
158 The GABAergic synapses of gamma2(+/-) mice were potentiated by ketamine in parallel but only in the
159 embranes is the fourth activation event, and is potentiated by kinase domain mutations (e.g., H1047R)
160 licated in auditory fear conditioning, which are potentiated by learning, enter a labile state after
162 tional activity of endogenous sea urchin TCF is potentiated by LiCl treatment, which vegetalizes embr
163 the hormones insulin and proopiomelanocortin is potentiated by lineage-specific homeodomain proteins.
165 eceptors to submaximal concentrations of ATP is potentiated by low levels of extracellular zinc.
166 stimulation also evoked release of ATP that was potentiated by low Ca(2+) and inhibited by FFA and G
167 ne dye flux evoked by mechanical stimulation was potentiated by low Ca(2+) and was inhibited by FFA a
176 which serves as a guidance cue for the PGCs, is potentiated by mesodermally restricted HMGCoA-reducta
179 itumour response of mouse CD8(+) T cells can be potentiated by modulating cholesterol metabolism.
180 e-stimulated CFTR-mediated chloride currents are potentiated by MRP4 inhibition, and this potentiatio
181 nhibitory activity in transfected A7r5 cells was potentiated by MSY1, but antagonized by serum respon
184 hat the transcriptional activity of CBP/p300 is potentiated by mycobacterial stimulation of monocytes
185 significant benefits and that its action can be potentiated by nanobubble agents to result in improve
186 nnels, particularly GABA(A) receptors, which are potentiated by nanomolar concentrations of 3alpha-hy
187 potential and calcium channel blockers, and were potentiated by niflumic acid, an anion channel bloc
188 l for learning and memory, has been shown to be potentiated by NO signaling, therefore, a peptidomime
191 for DDB2 by E2F, which does not require but is potentiated by p53, and demonstrate that DDB2 is invo
193 pression of EWS-FLI1 or EWS-ERG fusion genes was potentiated by PARP1 inhibition in ESFT cell lines.
195 LB phosphorylation and SERCA2 activity; this was potentiated by PDE3 inhibition but not by PDE4 inhib
196 2L receptors were blocked by bicuculline and were potentiated by pentobarbital and flunitrazepam.
197 demonstrated that the concatemeric receptors were potentiated by pentobarbital, diazepam, and the neu
198 concentration-dependent GABAR currents that were potentiated by pentobarbital, loreclezole, and lant
199 -gated calcium channels (Ca(v)) 2.2 currents are potentiated by phorbol-12-myristate, 13-acetate (PMA
200 activation, whereas TRPC4/5 channel activity is potentiated by phosphatidylinositol 4,5-bisphosphate
202 glial cells by an IP(3)-dependent mechanism, were potentiated by physiological concentrations of mela
204 ve to PA, we found that only TREK1 and TREK2 are potentiated by PLD2 and that none of these channels
205 , the thapsigargin-induced activation of SOC was potentiated by PMA and abolished by both calphostin
206 nt with Ba(2+) (I(Ba)) as the charge carrier was potentiated by PMA or acetyl-beta-methylcholine (MCh
208 Kinetic analysis shows Arg17 methylation is potentiated by pre-acetylation of Lys18, and this is
210 ggregation and secretion induced by collagen are potentiated by preincubation with thrombopoietin (TP
211 depletion of striatal dopamine, TH, or GABA was potentiated by pretreatment with 1 mg/kg CPX and att
212 IL-6 secretion stimulated by IL-1 in hCBMCs is potentiated by priming with IL-4 and reflects the hig
213 e novo Treg-cell generation in the periphery was potentiated by propionate, another SCFA of microbial
215 luding zinterol, salbutamol, and procaterol, was potentiated by PTX, indicating concurrent G(s) and G
217 be demonstrated by coimmunoprecipitation and was potentiated by Rab5, whose activity is required to r
218 and Mesozoic birds to new ecological niches was potentiated by rapid diversification of feather vane
221 ow evidence that SA-dependent plant defenses are potentiated by RLs following challenge by B. cinerea
222 ulates DNA unwinding by BLM in a manner that is potentiated by RMI1-RMI2, and that the processivity o
223 At submaximal insulin doses, protection was potentiated by rosiglitazone, an insulin-sensitizing
224 t, convulxin-induced dense granule secretion was potentiated by rottlerin but was abolished by Go6976
227 ge induced by selective G(12/13) stimulation was potentiated by SFK inhibitors, which was abolished b
229 rawling and transendothelial migration (TEM) are potentiated by shear stress caused by blood flow.
231 abundant in young human diploid fibroblasts, is potentiated by signalling through the Ras-Raf-MEK kin
232 on IR-beta-EP release and on cAMP production were potentiated by simultaneous incubation with ethanol
235 demonstrate that trk B receptor activity can be potentiated by small-molecule compounds via the extra
237 eover, termination-dependent destabilization is potentiated by stable secondary structure 3' of the u
238 The influence of p300 on LHbeta promoter is potentiated by steroid receptor co-activator, as well
239 ed by inhibitors of NF-kappaB activation and is potentiated by stimulation with PMA, suggesting that
245 ong-term arsenic exposure on cIMT, which may be potentiated by suboptimal or incomplete arsenic methy
248 hree major classes of bactericidal drugs can be potentiated by targeting bacterial systems that remed
250 ors containing a single functional GABA site are potentiated by the neurosteroid allopregnanolone reg
252 ire antagonist activity, which could further be potentiated by the introduction of an additional basi
253 several receptor-mediated processes and may be potentiated by the up-regulated expression of adhesio
254 s the ARC(Glutamatergic)-->PVH(MC4R) synapse is potentiated by the ARC(POMC) neuron-derived MC4R agon
255 by several of the steroid hormone receptors is potentiated by the Hsp90-associated cochaperone FKBP5
256 g that H(2)O(2)-induced NF-kappaB activation is potentiated by the inhibition of tyrosine phosphatase
258 ibitor staurosporine, and the response to EH is potentiated by the phosphatase inhibitor calyculin A.
260 reatment of a S. aureus mouse burn infection is potentiated by the presence of a LasA-producing P. ae
261 A region except during embryogenesis when it is potentiated by the presence of Phaseolus vulgaris ABI
262 vitro, but in M. tuberculosis, its function is potentiated by the previously identified sulfolipid t
265 P<0.05 versus beta-AR stimulation alone) but was potentiated by the beta(2)-AR-selective antagonist I
267 ial expressions, as the startle-blink reflex was potentiated by the CS(neg) versus both CS(neu) and C
268 with serum stimulated DNA synthesis and this was potentiated by the HO inhibitors, zinc and tin proto
272 /L), and dibutyryl cAMP (5x10(-4) mol/L) and was potentiated by the phosphodiesterase inhibitor 3-iso
274 lation resulting from loss of Apc expression was potentiated by the presence of oncogenic Kras (G12D)
275 rease in endothelial heme oxygenase activity was potentiated by the presence of S-nitrosoglutathione.
277 Shear stress-mediated ERK1/2 activation was potentiated by the voltage-gated sodium channel anta
278 ucosal neurons from healthy volunteers could be potentiated by their pre-incubation with histamine; t
284 -2-induced Syk and PLCgamma2 phosphorylation is potentiated by TxA2 and that TxA2 plays a critical ro
286 s decreased the UIC2 reactivity; this effect was potentiated by vanadate, a nucleotide-trapping agent
289 ed excitatory and inhibitory synaptic inputs were potentiated by visual experience and E/I remained c
291 elial cell migration stimulated by VEGF(121) was potentiated by vitronectin to a greater extent than
292 rents in SNc dopamine neurons, both of which were potentiated by VU0238429 and absent in M5 knock-out
293 necessary for the formation of a GABAAR that is potentiated by widely used anxiolytics, anticonvulsan
294 Mac-1-dependent activation of NF-kappaB was potentiated by wild-type, and attenuated by dominant
298 n a Na(+)-free medium; the sustained plateau was potentiated by zinc or increasing extracellular pH.