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1 itric oxide synthase (eNOS), produced only a partial inhibition.
2 whereas either treatment alone gives rise to partial inhibition.
3 nocytes with clodronate resulted in a modest partial inhibition.
4 sma from the low-dose group resulted in only partial inhibition.
5 DNA-binding domains of USF1 or USF2 produced partial inhibition.
6 dependent kinases or NADPH oxidases rendered partial inhibition.
7 eutralizing antibody against MCP-1 exhibited partial inhibition.
8 200 microm DMNB-cAMP caused stable but only partial inhibition.
10 at doses up to 5 microm, and exhibited only partial inhibition (50%) of the 26 S ubiquitin-independe
13 binds to an exosite, displays noncompetitive partial inhibition, and is synergistic with a competitiv
14 nists in the cultures themselves led to only partial inhibition (approximately 60%), whereas inclusio
15 inhibitor of the DHDPS reaction that causes partial inhibition (approximately 90%) at saturating con
16 ulfated coumarins suggesting that allosteric partial inhibition arises from catalytic dysfunction of
17 f cAMP-response element-binding protein, yet partial inhibition by a dominant negative cAMP-response
18 t in C-1Sec7 of Ser199 or Pro209 resulted in partial inhibition by BFA, whereas replacement of Gln970
19 ng digitonin permeabilization, compared with partial inhibition by BoNT/A, suggesting the importance
20 Ca2+ andMg2+, pH sensitivity, reversibility, partial inhibition by DIDS and Mn2+) are shared with the
27 d upon expression of SOCS-1 or SOCS-3, while partial inhibition (CIS, SOCS-2) or no inhibition (SOCS-
30 show that Bop1Delta expression results in a partial inhibition in the conversion of the 36S to the 3
33 te cyclase, whereas the other drugs produced partial inhibition, indicating the drugs are inducing sl
34 demonstrate that PERK haploinsufficiency or partial inhibition led to reduced ER stress-induced infl
36 of two E2 per EST subunit suggests that the partial inhibition occurs through binding at an alloster
38 iological, and behavioral effects in mice of partial inhibition of a hippocampal cAMP phosphodiestera
39 gainst a portion of the repeat region caused partial inhibition of AC toxin-induced hemolysis without
41 mmended doses of ACE inhibitors provide only partial inhibition of ACE in chronic heart failure (CHF)
42 homeostasis (Na(+), K(+), Ca(2+)) due to the partial inhibition of active Na(+) and K(+) transport.
44 l lines lacking activating PI3KCA mutations, partial inhibition of Akt signaling synergized with camp
45 rent excitation because it was eliminated by partial inhibition of alpha-amino-3-hydroxy-5-methyl-4-i
47 peptides (25 micro mol/L) and demonstrates a partial inhibition of angiogenesis ( approximately 40%)
49 the activity of the p38 MAPK, provided only partial inhibition of apoptosis and had no effect on nec
52 low extracellular substrate concentrations, partial inhibition of ATP synthesis lowered, whereas sup
53 chromosomes in anaphase is very sensitive to partial inhibition of Aurora kinase activity by ZM447439
54 on of GAG/PG-mediated attachment resulted in partial inhibition of bacterial attachment, suggesting t
55 uding tight binding to actin filament sides, partial inhibition of barbed end elongation, inhibition
57 days in physiologic growth factors achieved partial inhibition of Bcr-Abl and downstream targets p-C
58 Furthermore, we provide evidence that the partial inhibition of beta 2m by antisense RNA results i
62 , a new mutant was obtained that resulted in partial inhibition of both processes and also showed an
63 r adequate forces to drive the process, that partial inhibition of branching and polymerization lead
64 neutrophil infiltration and resulted in only partial inhibition of C-mediated hemolytic activity in v
67 ant conferred resistance to phagocytosis and partial inhibition of C3 deposition on the S. pyogenes s
70 presence of Z-VAD-fmk was associated with a partial inhibition of caspase-8, whereas no effects on c
73 leads to a complete loss of tip growth and a partial inhibition of cell division, resulting in plants
74 ics was used to determine the effects of the partial inhibition of cell wall synthesis on the status
81 of signal recognition particle caused only a partial inhibition of CYP2E1 translation under in vitro
82 ential upon reoxygenation, suggesting that a partial inhibition of cytochrome c oxidase had existed.
84 of dominant negative Foxo1 mutant results in partial inhibition of dex/cAMP-induced G6p and Pepck exp
86 h substitutions at either Lys6 or Arg28 show partial inhibition of DNA strand exchange activity, yet
90 otoxicity to TS inhibition and indicate that partial inhibition of dUTPase is a viable therapeutic ap
92 ve inhibitor of p38 MAPK kinase, resulted in partial inhibition of either p38- or strain-activated hB
93 O in xenobiotic oxidation in mammals and the partial inhibition of elevated AO activity by a range of
96 e of N-p-tosyl-L-chloromethyl ketone and the partial inhibition of enzyme activity by diisopropyl flu
99 ydrophobic molecule, diffuses into cells and partial inhibition of FAAH has a pronounced effect upon
101 ically inactive NEP protein also resulted in partial inhibition of FAK phosphorylation and cell migra
102 ced morphological changes and exhibited only partial inhibition of FAK site-specific tyrosine phospho
104 om complete inhibition of bacterial NAGS, to partial inhibition of fish NAGS, to activation of frog a
105 Although treatment with R115777 resulted in partial inhibition of FTase activity in mononuclear cell
107 in vps21Delta and vps27Delta strains caused partial inhibition of glucose-dependent dissociation.
108 found that moderate increases in H2O2 during partial inhibition of glutathione (GSH) peroxidase by me
109 ligonucleotides, or wortmannin resulted in a partial inhibition of GM-CSF-mediated pro-survival activ
110 5R1489E in a wild-type yeast strain caused a partial inhibition of growth which was reversed by overe
111 nding to the erythrocytes is disrupted, only partial inhibition of hemolysis is mediated by TT30 in s
112 iation of the two proteins, and results in a partial inhibition of HGF-mediated activation of c-Met a
115 ketone (z-VAD-fmk), and found that it caused partial inhibition of hydrogen peroxide formation as wel
116 ppaB dependent transcription, which involved partial inhibition of IkappaB and RelA/p65 serine phosph
117 hythmia in human ventricles, and establishes partial inhibition of IKs as a potential anti-arrhythmic
119 Inhibition of either MAPK or PKC resulted in partial inhibition of IL-8-stimulated polymorphonuclear
121 but not wild-type Dicer, also resulted in a partial inhibition of Influenza A virus-but not poliovir
122 naling in SCA2 pathogenesis and suggest that partial inhibition of InsP3-mediated Ca2+ signaling coul
124 hypotheses that in nondiabetic individuals, partial inhibition of insulin secretion with the ATP-sen
127 DP pool was experimentally reduced by either partial inhibition of isoprenoid synthesis pathway by fo
131 r downstream signal of PI3K resulted in only partial inhibition of mechanical stretch-induced prolife
141 ocytes to ouabain concentrations that caused partial inhibition of Na+/K+-ATPase but no loss of viabi
142 We showed before that in cardiac myocytes partial inhibition of Na+/K+-ATPase by nontoxic concentr
143 before that in neonatal rat cardiac myocytes partial inhibition of Na+/K+-ATPase by nontoxic concentr
144 f ouabain, i.e. net influx of Ca2+ caused by partial inhibition of Na+/K+-ATPase, also initiates the
150 Anti-CXCL8 neutralizing antibody induced a partial inhibition of NK cell differentiation, which sug
151 KK45R, but not Akt-AAA, caused a significant partial inhibition of NO production in response to adipo
157 eutralization of TNF functional activity and partial inhibition of other secondary biologic effects o
158 ut not prevent, senescence may be related to partial inhibition of p16 expression, as the Id-1-overex
160 pothesis that OGs are generated in planta by partial inhibition of pathogen-encoded polygalacturonase
164 of the immediate early protein ICP27 causes partial inhibition of pre-mRNA splicing, with the result
165 d ADH/alpha-crystallin were adjusted so that partial inhibition of protein aggregation at 60 degrees
172 concentrations of nine other agents produced partial inhibition of RyR1-mediated Ca(2)(+) release fro
173 , an activator of KATP channels, resulted in partial inhibition of S6K1 phosphorylation by 20 mmol/l
175 t, findings that correlate with the observed partial inhibition of SK-RC-45-induced apoptosis in the
181 n adipose-specific Rab10 KO female mice, the partial inhibition of stimulated glucose uptake in adipo
182 o effects on GABAA receptors that produces a partial inhibition of T-type Ca2+ current with reasonabl
183 nd functional activity of myosin-5B in vitro Partial inhibition of the actin-activated steady-state A
184 dotHCTnI(R145G) small middle dotHCTnC), only partial inhibition of the actin-tropomyosin-myosin ATPas
187 Nontoxic concentrations of ouabain, causing partial inhibition of the cardiac myocyte Na(+)/K(+)-ATP
190 hydrolase with 100 microM of 5b resulted in partial inhibition of the enzyme without any apparent ch
191 by using antisense oligonucleotides led to a partial inhibition of the Epo-independent proliferation
192 rotection of telomeric DNA was identified by partial inhibition of the expression of GAPDH using smal
195 n merotelic correction is conserved, because partial inhibition of the human kinesin-5 homolog Eg5 us
196 ed to remove CO from solution, there is only partial inhibition of the incorporation of CO(2)-derived
198 ated degranulation in human mast cells and a partial inhibition of the later calcium response at high
200 chondrial dysfunction based upon the chronic partial inhibition of the mitochondrial enzyme cytochrom
202 osolic Ca(2+) increase upon stimulation, and partial inhibition of the plasma membrane Ca(2+)-ATPase,
203 lity-increasing protein (rBPI21) resulted in partial inhibition of the PMNL activation and phagocytos
204 thrombin was correlated quantitatively with partial inhibition of the rate of the thrombin-antithrom
205 n susceptible embryo fibroblasts resulted in partial inhibition of the replication of a flavivirus bu
207 the increase in the SR load was prevented by partial inhibition of the SR Ca(2+) with thapsigargin, c
208 as primarily a consequence of selective and partial inhibition of the synthesis of the linear arabin
210 t for patients with KCNQ2 encephalopathy, as partial inhibition of these channels counteracts the inc
212 videnced by an increase in PARP cleavage and partial inhibition of this effect by the pan-caspase inh
213 em on platelet membranes is supported by the partial inhibition of thrombin-induced Ca2+ influx by wo
215 aB activation by thalidomide correlated with partial inhibition of TNF-induced degradation of an inhi
217 3'-FAM OMe 12-mer oligonucleotide exhibited partial inhibition of trans-activation activity, but thi
219 tion of replication fork velocity but not by partial inhibition of translation or transcription.
221 ng loop failed to inhibit FXIIa but retained partial inhibition of trypsin (Ki = 11.7 +/- 1.2 mum) an
222 on of phosphatidylinositol-3-kinase leads to partial inhibition of tumor angiogenesis, thus demonstra
226 te, to which the binding of Zn(2+) exhibited partial inhibitions of both Cd(2+) and Hg(2+) bindings.
227 hibitor, and a dominant negative PKC exhibit partial inhibition on Wnt-mediated transcriptional activ
228 -pyridine (MPEP) site on mGlu5 but have only partial inhibition or no functional effects on the mGlu5
229 ic rate and substrate binding, implying that partial inhibition or selective inhibition with regard t
230 ; 2), the distance between RyR clusters; 3), partial inhibition or stimulation of SR Ca(2+) pumps; 4)
231 five categories: activation, autoactivation, partial inhibition, substrate inhibition, and biphasic s
233 2 signaling by two distinct mechanisms: by a partial inhibition that is decreased at elevated STAT5b
236 ressing TRPC3, TRPC6, or TRPC7 and that this partial inhibition was observed whether the channels wer
238 However, at higher xanthine concentrations, partial inhibition was seen, suggesting the formation of
240 and 3-isobutyl-1-methylxanthine (970 microM, partial inhibition) were also substantially higher than
241 take phase during MCO of DTT but causes only partial inhibition when added after the reaction is well
242 the cells sampled, 54 of 137 (40%) achieved partial inhibition when tested with 60 msec tones, and t
243 n by SDS, guanidine, heat (55 degrees C), or partial inhibition with DCI, proteasomes still functione
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