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1 IC patients had human immunodefiency virus (HIV)/AIDS, c
2 IC performance metrics (sensitivity, specificity, positi
3 IC(50) variability (25/75 percentiles) differed for drug
4 IC(50) was determined to be 460 nM.
5 ICs showed differential sensitivity to positive and nega
7 ad exquisite selectivity toward both IRAK-1 (IC(50) = 24 nm) and IRAK-4 (IC(50) = 20 nm), with only m
8 inst HOCl (IC(50) = 0.79 ug/mL) and O(2)(-) (IC(50) = 12.92 ug/mL) without toxicity on intestinal cel
10 otent lead compound [compound 14 (ARN-21934) IC(50) = 2 muM for inhibition of DNA relaxation, as comp
11 SAR studies on the initial hit, compound 4 (IC(50) = 257 nM), resulted in several highly potent inhi
12 ard both IRAK-1 (IC(50) = 24 nm) and IRAK-4 (IC(50) = 20 nm), with only minimal TAK1-inhibiting activ
14 he evaluation of Michaelis-Menten and EC(50)/IC(50) kinetic parameters, as well as the results of hig
17 ndent block of the AQP1 ion current by 5HMF (IC(50) 0.43 mM), 5NFA (IC(50) 1.2 mM), and 5AMF (IC(50)
18 ion current by 5HMF (IC(50) 0.43 mM), 5NFA (IC(50) 1.2 mM), and 5AMF (IC(50) ~3 mM) but no inhibitio
19 yl]-1H-pyrazol-1-yl}methyl)benzonitrile (73, IC(50) = 12 nM) and 4-({5-[4-chloro-1-(2H-indazol-6-yl)-
22 lized acid-secreting A-intercalated cells (A-ICs) in the kidney using both imaging and functional stu
24 pound 15 showed improved anti-HAdV activity (IC(50) = 0.27 muM), significantly decreased cytotoxicity
25 hich exhibit potent in vitro HDAC8 activity (IC(50) = 66, 23, and 66 nM, respectively) and up to 410-
28 .9-fold higher than protein binding-adjusted IC(90) (PA-IC(90)) of LPV for HIV-1 (140 ng/mL) followin
30 been discovered with high binding affinity (IC(50) values of 67-84 nM) and good selectivity over oth
35 e, we introduce a novel platform that allows IC-FPOP to occur in a sterile incubation system complete
39 toheptaoside (<50% inhibition) than amylose (IC(50): epigallocatechin gallate = 20.41 +/- 0.25 uM, qu
41 d considerably improved potency, reaching an IC(50) value up to 100-fold lower than an inhibitor that
44 ibition of DNA relaxation, as compared to an IC(50) = 120 muM for the anticancer drug etoposide] with
45 st potent azaindole 45 inhibits SHP2 with an IC(50) = 0.031 muM in an enzymatic assay and with an IC(
47 nyl-mediated block of hERG channels, with an IC(50) at pH 8.4 being 7-fold lower than that at pH 7.4.
51 led the juvenile form of F. hepatica with an IC(50) of 3 uM, better than the reference drug triclaben
53 id (LCA) inhibits NAPE-PLD activity (with an IC(50) of 68 mum), but LCA is also a highly potent ligan
54 tracellular vestibule of the channel with an IC(50) of 72 nM and greater than 200-fold selectivity ov
59 nase activity of mutant c-KIT(D816V) with an IC(50) value that is 9-fold more potent than the sunitin
60 lpB-DnaK bichaperone system in vitro with an IC(50)~5 muM and suppressed the growth of cultured Esche
63 depth, ACD (SRC = 0.64, SPCC(2) = 0.19) and IC (SRC = -0.26, SPCC(2) = 0.041) were the strongest det
65 the complexes, NMR titration experiments and IC(50) measurements reveal the molecular basis underlyin
66 with the percent inhibition being lower and IC(50) being higher for the edited GluA2(R) relative to
67 ng connectivity patterns, while the anterior IC connectivity was distinct, suggesting two major funct
68 tibody fused with alkaline phosphatase (anti-IC-HT2 scFv-ALP) which is able to produce an electroacti
69 s-associated protein with nanomolar apparent IC(50) values, and reduce TEAD target gene expression.
75 rall cure (resolution of signs of candidemia/IC + mycological eradication) at day 14 (primary endpoin
77 The prevalence rate of invasive candidiasis (IC) was 11.4% (95% CI 9.2-13.6%), and the rate of non-Ca
79 the posterior limb of the internal capsule (IC), comprised primarily of corticofugal fibers, showed
80 curs either spontaneous in inactive carrier (IC) patients or therapy-induced by nucleos(t)ide analogu
83 extended to protein labeling in live cells (IC-FPOP), allowing the study of protein conformations in
84 eater potency in drug-resistant NSCLC cells (IC(50) = 17 nM) and in mice with H1975 xenograft tumor.
87 IRI) model, we show that intercalated cells (ICs) rapidly adopted a proinflammatory phenotype after I
88 cells expressing multiple immune checkpoint (IC) molecules, including programmed death (PD)-1, T cell
91 No difference in ischemic cholangiopathy (IC), vascular thrombosis/stenosis or graft, and patient
92 n rice is reported using ion chromatography (IC) and dynamic reaction cell inductively coupled plasma
93 tion density of silicon integrated circuits (ICs) have progressed at an unprecedented pace in the pas
95 ed in the midbrain, the inferior colliculus (IC) integrates information from numerous auditory nuclei
97 n auditory nucleus, the inferior colliculus (IC), but have not examined the cellular patterns of expr
100 s significantly higher following combination IC blockade compared with other latency-reversing agents
105 ency (half-maximal inhibitory concentration (IC(50)) <1 muM) and selectivity (>=12-fold) for skeletal
106 ifted-half-maximal inhibitory concentration (IC(50)) for CYP4Z1 compared to ABT, efficient mechanism-
107 howed half-maximal inhibitory concentration (IC(50)) values 1 order of magnitude better than diflunis
108 cells with median inhibitory concentration (IC(50)) values between 24 picomolar and 35 nanomolar.
109 I-04 (half maximal inhibitory concentration [IC(50)] = 32 nM), the glycoconjugate, FGlc-FAPI (IC(50)
111 a to lower IgG antibodies and IgG containing ICs may also reduce the risk of venous thromboembolism.
113 induced FXa activity, whereas IgG-containing ICs with an Fc engineered to be unable to engage FcRn di
115 demonstrated that, instead of a conventional IC pathway, an unexpected intramolecular singlet fission
117 epth (ACD), lens vault (LV), iris curvature (IC), anterior chamber width, lens thickness, vitreous ca
118 Apart from its remarkably high cytotoxicity (IC(50) = 0.07-0.7 muM in different cancerous cell lines)
119 ucted include, Ag-Phen induced cytotoxicity (IC(50) 4.5 muM at 72 h) and 2-fold ROS generation, and a
122 argeting of antibiotic administration during IC could decrease subsequent infectious complications in
123 than MG (log P = - 0.14) in donating H/e(-) (IC(50) = 36.4 vs. 39.9 muM and FRAP value = 598 vs. 514
124 processing (HHP) on the inhibitory effects (IC(50)) of kiwiberries (cv. 'Weiki'), on the formation o
125 so evaluated the anti-proliferative effects (IC(50)) of these samples on triple-negative breast cance
129 0)] = 32 nM), the glycoconjugate, FGlc-FAPI (IC(50) = 167 nM), showed slightly lower affinity for FAP
130 contrast to our previous study in the ferret IC, task engagement had little effect on sound-evoked ac
131 ropy (FA) in callosal and projection fibers (IC and corona radiata) relative to controls, but lower F
132 a holding potential of -90 mV, the following IC(50) values were found (in micromolars): >1000 (Ca(V)2
135 s advocate SET before invasive treatment for IC, but early revascularization remains widespread, espe
136 increasing aroma intensity in SC while, for IC, all loads of microparticles improved aroma intensity
140 NUC-treated patients differed markedly from IC patients, especially in DC, monocytes and CD8+ T cell
141 xpression of purified leukocyte subsets from IC versus NUC-treated patients, and evaluated the putati
144 omycin as the inhibitor of cyst germination (IC(50) = 19.8 mug/L); beta-rubromycin did not inhibit gr
152 ted UDD to be a significant predictor of HGD/IC in those remote lesions (odds ratio: 4.41, P = 0.039)
154 elling scavenging efficiencies against HOCl (IC(50) = 0.79 ug/mL) and O(2)(-) (IC(50) = 12.92 ug/mL)
156 e of recent antifungal prophylaxis; however, IC and non-Candida breakthrough IFIs were observed, most
158 ilonRI on allergic effector cells, while IgE-ICs were noninflammatory because of reduced FcepsilonRI
159 netic depletion of HIF1alpha, attenuated IgG IC-induced activation of macrophages in vitro, including
162 Conversely, FcRn induced responses to IgG IC independently of classical FcgammaR, but optimal resp
163 go a switch to glycolysis in response to IgG IC stimulation, mirroring macrophage metabolic changes i
164 ant, CD32aH more avidly bound human (h) IgG1 IC and formed a ternary complex with the neonatal Fc rec
169 T) are also frequently contacted by incoming IC axons, but the strength of this connection is weak.
170 ic compounds content, and anti-inflammatory (IC(50) = 72 ug/mL) and cytotoxic (GI(50) of 30-79 ug/mL)
172 ections onto either excitatory or inhibitory IC neurons, and adeno-associated viral tracings to label
173 characterization of positive hits (that is, IC(50) and K(i) ), as well as inhibition-reactivation as
174 ncy against human class I HDACs (e.g., JT86, IC(50) 0.7 nM, HDAC1), 25-fold increased cytotoxicity ag
177 Ca(2+) transients were observed in c-Kit(+) ICs, smMHC(+) PDGFRalpha cells and smMHC(-) PDGFRalpha c
179 All extracts inhibited pancreatic lipase (IC(50) between 1.15 and 0.59 mg/mL), although the hydrol
180 ability to inhibit the function of P-gp (log IC(50) of 4.20 nM for quinidine and 4.61 nM for the mPEG
181 -regulated reporters for leucocidin A (lukA, IC(50) 0.4-25 muM) and glycerol ester hydrolase or lipas
185 of alpha-glucosidase, showing low-micromolar IC(50) values, far lower than that of the antidiabetic d
190 icacy but evoked more potent UDB of I (NaP) (IC(50) = 0.07 and 0.6 uM, respectively) than ranolazine
201 followed up patients from index diagnosis of IC for 5 years, or until patients discontinued insurance
202 or patient gender, age at index diagnosis of IC, and diagnosis with diabetes mellitus) followed up pa
206 st that it is the level of disorder in H2 of IC along with its charge, rather than sequence specifici
209 alysis of TLR stimulation in the presence of IC predicted the downstream activation of AKT and the in
214 to trastuzumab and capecitabine doubled ORR-IC, reduced risk of intracranial progression or death by
215 e aimed to determine whether these and other IC molecules have a functional role in maintaining HIV l
216 her than protein binding-adjusted IC(90) (PA-IC(90)) of LPV for HIV-1 (140 ng/mL) following oral admi
219 novel series of compounds reaching picomolar IC(50) inhibition in WNT/beta-catenin signaling cellular
224 uctural replacements to improve the potency (IC(50)), pharmacokinetic properties including the free f
225 of these dual inhibitors were highly potent (IC(50) < 10 nM) and selective against PI3Kgamma, delta a
226 ectrum Collection, with the two most potent (IC(50) = ~2 mum) being symmetrically substituted dichlor
227 amination point to the need for prioritizing IC interventions to control the spread of C. auris and C
229 falciparum in vitro in the nanomolar range (IC(50) = 74 nM) with high selectivity index (SI > 1350).
232 nzothiazoline-6-sulfonic) acid assays showed IC(50) values of 7.07 and 65.67 ug/mL, and 17.96 and 201
235 rinted sensors and circuits, thinned silicon ICs, printed antennas, printed energy harvesting and sto
236 ple adrenergic receptor subtypes in a single IC cell, we measured co-expression of alpha(1) , alpha(2
238 Gynecology and Obstetrics (FIGO; 1988) stage IC-IIA high-grade serous, clear cell, or any poorly diff
239 ederation of Gynecology and Obstetrics stage IC-IV ovarian cancer and an Eastern Cooperative Oncology
241 V activities with nanomolar to submicromolar IC(50) values and high selectivity indexes (SI > 100), i
242 against thiobarbituric reactive substances (IC(50) = 23 +/- 2 ug/mL) and oxidative haemolysis (IC(50
244 the DPPH (SC(50)10.30-15.87 mug/mL), TBARS (IC(50) 18.46-20.84 mug/mL), and FRAP (RC(50) 0.203-0.309
251 We uncover a strong connection between the IC and the lateral hypothalamus (LH) with a monosynaptic
252 fied a direct line of connection between the IC and the lateral hypothalamus (LH), which engages nume
253 rtical regions was highly bidirectional, the IC connectivity with subcortical structures was often un
254 Results: Regional metabolism of both the IC and the PAC was significantly reduced contralateral t
258 We found greater proportions of cells in the IC that expressed no adrenergic receptor-encoding mRNA,
264 selectivity filter drastically increased the IC(50) value, suggesting that MDIMP binds to the extrace
267 sis of the structure and interactions of the IC from Chaetomium thermophilum demonstrates that the H2
269 r-encoding mRNA across the subregions of the IC, alpha(2A) and beta(2) receptor-encoding mRNA was exp
270 Owing to these unique advantages of the IC-WiS electrolyte, the NaTiOPO(4) anode and Prussian bl
274 he alpha (2) or beta (3) subunit reduces the IC(50) of TETS by ~700-fold in whole-cell patch-clamp ex
277 trates that the H2 region of C. thermophilum IC has a low helical propensity and establishes that H2
283 new class of the inert-cation-assisted WiS (IC-WiS) electrolytes containing the tetraethylammonium (
284 tently neutralized authentic SARS-CoV-2 with IC(100) as low as 0.04 mug/mL, showing a broad spectrum
285 fectively inhibited the Sulf-1 activity with IC(50) = 0.53 muM, K(i) = 0.36 muM, and K(D) = 12 nM.
286 ed enhanced radical scavenging activity with IC(50) value equivalent to 39.57 and 6.23 uL/mL for DPPH
287 moiety displayed the highest activity, with IC(50) and EC(50) values in the lower micromolar range i
289 a virus glycoprotein-driven cell entry (with IC(50) values down to 95 pM), but only partially block D
292 active as inhibitors of PDE1 isoforms, with IC(50) values in the high nanomolar/low micromolar conce
293 ptides, VRP, LKY, VRY, KYKA, and LKYKA, with IC(50) values of 0.034-5.77 mug/mL, respectively, and fo
294 ) transport in a non-competitive manner with IC(50) ~ 2.5 muM, a value 400-fold lower than the K(M) f
296 on diagnoses of maculopathy in patients with IC were exudative AMD (1.5%), drusen (0.8%), nonexudativ
297 ignificant cytotoxicities of porphyrins with IC(50) values between 23.3 and 44.2 muM in the dark, whe
298 found to inhibit Fyn A and BTK proteins with IC(50) values in the low micromolar range, with the most
299 MAO-A) and AChE inhibitor in the series with IC(50) values of 4.27 +/- 0.07 and 0.79 +/- 0.03 muM, re
300 tive to sacituzumab govitecan in vitro, with IC(50) values in the range of 0.18 to 0.26 nM (p = 0.02,