1 rom 6.9 nM (no preincubation) to 0.4 nM (4-h
preincubation).
2 XCL16 induction was not restored by IFN-beta
preincubation.
3 ist phenylephrine with or without antagonist
preincubation.
4 otentiation of SMIT activity by myo-inositol
preincubation.
5 r at 30 degrees C and requires Mg(2+) during
preincubation.
6 in the absence of NADPH or during anaerobic
preincubation.
7 lar dTTP levels were reduced during the 5-FC
preincubation.
8 de from the dopamine D1 receptor without ATP
preincubation.
9 , which was more visible following high-dose
preincubation.
10 either concatemerization nor low temperature
preincubation.
11 cetic acid simulant, no salt addition, 5 min
preincubation,
55 min extraction at 70 degrees C, and 8
12 However, when calmodulin was omitted during
preincubation,
activity was not affected, suggesting tha
13 Additionally, the duration of
preincubation affected interactions, indicating that the
14 reduced on some days after infection in the
preincubation and prophylaxis groups.
15 Inhibition was increased by GC
preincubation,
and reductions in mRNA were prevented by
16 ble C in the soil, through 1-day and 6-month
preincubations,
and in PyOM made from maple wood at 350
17 n-4 or the claudin-4 ECL-2 peptide in both a
preincubation assay and a coincubation assay.
18 emerization for efficient responses and cell
preincubation at 28 degrees C to be functional.
19 wed that neutralization titers of MAbs after
preincubation at 37 degrees C correlated with activity i
20 However, increasing the time of
preincubation at 37 degrees C or raising the temperature
21 the genetic diversity of the serotype after
preincubation at 37 degrees C.
22 Ultrastructural studies revealed that after
preincubation at 4 degrees C mutant chloroplasts contain
23 higher than in controls and was inhibited by
preincubation by either inhibitor.
24 tion itself, inactivation resulting from ATP
preincubation can be reversed by a remodeling process me
25 phospholamban on SERCA depends on substrate
preincubation conditions.
26 TNF tolerance induced by the low
preincubation dose is mediated by glycogen synthesis kin
27 In agreement with this finding,
preincubation experiments indicate that stable protein/D
28 nocytochemical resolution, we also performed
preincubation experiments with 5-hydroxy-L-tryptophan an
29 the polymerase and a double-stranded RNA by
preincubation experiments.
30 MLA
preincubation inhibits JN403-induced Ca(2+) influx in GH
31 Results showed that the length of the
preincubation interval significantly affects the inhibit
32 Slow DNA binding in the absence of ATP
preincubation is the result of a rate-limiting ATP-induc
33 ycogen synthesis kinase-3, whereas high-dose
preincubation-
mediated tolerance is regulated by A20/gly
34 substrates or removal of Na(+) from the MTS
preincubation medium.
35 Preincubation of (67)Zn(7)-MT-2 with an excess of oxidiz
36 Notably, a 48 h
preincubation of 1g-i significantly enhanced the antipro
37 oligomer-mediated cytotoxicity observed upon
preincubation of A beta oligomers with the anti-A beta(1
38 Furthermore,
preincubation of a recombinant Sca1 peptide with host ce
39 Preincubation of accessory cells with the respective sti
40 Preincubation of Ad5 with excess heparin or pretreatment
41 This conclusion was supported by prolonged
preincubation of antagonist that failed to improve the o
42 Preincubation of apoE3 or apoE4 with Abeta42 increased t
43 es and was significantly inhibited following
preincubation of apoptotic cardiocytes with chicken and
44 Preincubation of asthmatic airway macrophages with Haemo
45 Interestingly,
preincubation of bacteria with antibodies against the ma
46 We found that
preincubation of bacteria with recombinant soluble BAI1
47 Consistent with prior observations,
preincubation of bacteria with unfractionated properdin,
48 first blocked selectively these receptors by
preincubation of BM-MSCs with specific neutralizing anti
49 n with a dominant-negative Akt adenovirus or
preincubation of cardiomyocytes with the phosphatidylino
50 However,
preincubation of CcrB-DNA complexes with increasing conc
51 Preincubation of cell cultures with BF from both oils si
52 Preincubation of cells with a peptide that contains a ph
53 Similarly,
preincubation of cells with GW9662 inhibited inducing ef
54 Preincubation of cells with NPY up-regulated the Y5 rece
55 R1-BR)) adhered to A549 cells, and moreover,
preincubation of cells with rPsrP(SRR1-BR) inhibited TIG
56 Here, we report that
preincubation of cells with the GRGDNP peptide strongly
57 Preincubation of cells with the inhibitors of the DDR ki
58 omain blocked infection with HKU1 virus, but
preincubation of cells with truncated S protein containi
59 Preincubation of concentrated nNOS with H2S under turnov
60 Preincubation of cortical neurons with PolyP significant
61 effect on adherence to HUVEC; specifically,
preincubation of D39 with both FH and sIgA led to a 21-f
62 ignificantly in the absence of Ca(2+) and by
preincubation of DC-SIGN with mannan, suggesting that C1
63 Preincubation of double positive thymocytes with exogeno
64 perature dependence of methylation of EF-Tu,
preincubation of EftM at 37 degrees C abolished methyltr
65 Preincubation of either trypomastigotes or myoblasts wit
66 Preincubation of eNOS with BH(4) decreased dimer destabi
67 Preincubation of ESAT-6 with CFP10 under conditions that
68 It is noteworthy that
preincubation of eukaryotic cells with AdpF increased P.
69 Preincubation of exosomes with anti-galectin 1 antibody
70 Preincubation of experimentally aged erythrocytes with h
71 Preincubation of factor H with exogenous heparin and pre
72 We found that
preincubation of FCV with the ectodomain or D1 was suffi
73 However
preincubation of FIX with a saturating concentration of
74 Preincubation of FN with mAbIII-10 or heparin modestly i
75 Preincubation of fresh rat hepatocyte suspensions with G
76 Preincubation of FVIII with VK34 did not influence FVIII
77 Preincubation of gpK8.1A with heparin or anti-gpK8.1A an
78 Additionally,
preincubation of H441 cells with A77-1726 (20 microM), a
79 Preincubation of HCV particles with anti-HSC70 antibodie
80 Preincubation of HDL3 with human plasma-derived active P
81 CoQ(10)
preincubation of healthy monocytes before IgG-antiphosph
82 , TRAF6-dominant-negative overexpression, or
preincubation of HMVEC-Ls with a cell-permeable TRAF6 de
83 activated Tyr(P)(416)-SFK to GST-TRAF6, and
preincubation of HMVEC-Ls with SFK-selective tyrosine ki
84 Preincubation of HTBE cells with a truncated HKU1 S prot
85 Binding to SR-BI was required since
preincubation of human and murine platelets with anti-SR
86 In vitro:
Preincubation of human coronary artery endothelial cells
87 Preincubation of human monocytes with CCL2/MCP-1, the ch
88 Further, we found that
preincubation of human serum with F. alocis resulted in
89 Preincubation of HUVECs with an IL-3R-blocking Ab (CD123
90 Whereas
preincubation of HVSMCs with epinephrine before the addi
91 Preincubation of IgGs from multigravida women with recom
92 This increase was blocked by
preincubation of intact cells with apocynin (NADPH oxida
93 Preincubation of islets with subsaturating concentration
94 Preincubation of Jurkat cells with a CD4 receptor-neutra
95 Preincubation of KSHV with soluble heparin and alpha3bet
96 Preincubation of L-tyrosine with Orf13 prior to the addi
97 Preincubation of lenses with either ouabain or low-[Na(+
98 Preincubation of lymphoma cells with Ad35K(++) sensitize
99 Preincubation of MAV-1 with heparin, a heparan sulfate g
100 Preincubation of microtubules with 2 or 4 microM vinblas
101 y increased reactive oxygen species, whereas
preincubation of mito-TEMPOL, a superoxide dismutase mim
102 Infection could be enhanced by
preincubation of Moloney MLV with cathepsin B, consisten
103 L-13-stimulated 15-LO upregulation; however,
preincubation of monocytes with the antibody MEM48, whic
104 Preincubation of muscle cells with ROS scavengers (e.g.
105 Preincubation of NCMs, with 10 nm extracellular concentr
106 Preincubation of neurones with SP (10 nM, 5 min) desensi
107 ession of Balb/c Teffs; this was reversed by
preincubation of NOD Teffs with GM1.
108 Preincubation of normal human lung fibroblasts with the
109 gonist responses were robustly reduced after
preincubation of oligodendrocytes with patients' CSF or
110 Preincubation of oocytes with ibuprofen did not signific
111 Preincubation of oocytes with serine proteases prevented
112 Preincubation of P. aeruginosa with these same ex vivo f
113 the reciprocal experiment demonstrated that
preincubation of PAI-1 with PAI-039 blocked the binding
114 Preincubation of PAI-1 with vitronectin, but not bovine
115 Furthermore,
preincubation of PEDF with P1 and E5b peptides blocked t
116 onger than that previously reported and that
preincubation of photoreceptor outer segment homogenates
117 aggregation, and secretion were inhibited by
preincubation of platelets with a selective SFK inhibito
118 Notably,
preincubation of platelets with aspirin, but not with a
119 ent on direct contact with cancer cells, and
preincubation of platelets with blocking antibodies agai
120 Preincubation of platelets with human colon cancer (Caco
121 Preincubation of platelets with MPs led to CD36-dependen
122 The
preincubation of platelets with purified lysin(102-198)
123 Preincubation of PLTs with type IV collagen specifically
124 Preincubation of polyclonal IgG with CD64-IgE Fc establi
125 Binding was inhibited by
preincubation of porcine Kupffer cells with purified hum
126 of the current study previously showed that
preincubation of primary microglial-enriched cells with
127 We found that
preincubation of primary neurons with PolyP reduced glut
128 Preincubation of rat aortic rings with OxLDL resulted in
129 levels of beta-spectrin that is inhibited by
preincubation of RBCs with DMAT, a specific casein kinas
130 Furthermore, in vitro studies showed that
preincubation of recombinant alpha-syn with 1H7 and 5C1
131 We find that
preincubation of RER with KLC1B inhibits RER motility, w
132 Preincubation of sera from cockroach-allergic subjects w
133 Preincubation of SF100 with ganglioside GD3, a glycolipi
134 The effect of SE-1 on invasion required
preincubation of Shigella with SE-1, in agreement with t
135 Preincubation of strain 181/25, but not SL15649, with so
136 Adherence assays demonstrated that
preincubation of Streptococcus pneumoniae D39 with FH in
137 Preincubation of target membranes with MREG resulted in
138 Order-of-addition experiments indicate that
preincubation of tetrameric SsoSSB and SsoRadA prior to
139 Preincubation of thawed M. tuberculosis complex cells in
140 Preincubation of the cells for 16 h with either Shh or E
141 After
preincubation of the cells with anti-14-3-3 antibody and
142 cent microscopy, which were prevented by the
preincubation of the cells with either CB1 antagonist, b
143 In vitro
preincubation of the cells with the compounds resulted i
144 mg(-1) and was also effectively inhibited by
preincubation of the cells with the inhibitors pervanada
145 Preincubation of the chemokines with OPN strongly inhibi
146 Preincubation of the enzyme with iodoacetamide (17 mM) c
147 n catalyzed by CSE in vitro, is sensitive to
preincubation of the enzyme with PPG.
148 extension from an exogenous primer following
preincubation of the enzyme with template and primer cou
149 In corroboration,
preincubation of the ETEC inoculum with antiadhesin and
150 osteogenic differentiation before and after
preincubation of the fractions with the bone morphogenet
151 s was concentration-dependently inhibited by
preincubation of the human umbilical arterial endothelia
152 Preincubation of the LLC-PK1 cells with the caspase 9 in
153 Preincubation of the neurons with the PKC inhibitor bisi
154 Furthermore,
preincubation of the p13(II)-expressing cells with a far
155 geting specificity in vitro was confirmed by
preincubation of the pancreatic cancer cells with C225 a
156 Each activation event was inhibited by
preincubation of the platelets with Fab fragments of the
157 Notably,
preincubation of the preterm, but not near-term, amnioti
158 Preincubation of the purified toxin and antitoxin togeth
159 Preincubation of the slice with the selective KOR antago
160 Preincubation of the T67I mutant with PLP restored activ
161 resembling physiological conditions and the
preincubation of the two proteins.
162 iratory epithelial cells were increased upon
preincubation of these cells with eBD1, -2, and -3.
163 n of caspase-3 activity to detect apoptosis,
preincubation of these cells with isoproterenol was foun
164 Preincubation of these oocytes with phosphocholine, howe
165 Preincubation of trypomastigotes with a concentration of
166 Preincubation of trypomastigotes with defensin alpha-1 f
167 Preincubation of trypomastigotes with either TcGP63 anti
168 Preincubation of tubulin with tau resulted in decreased
169 Preincubation of tumor cells with bortezomib had no effe
170 hibited diminished neutralizing activity but
preincubation of virions with soluble CD4 restored it, s
171 Preincubation of virus with soluble EphA2, knockdown of
172 Furthermore,
preincubation of virus with soluble Nrp-1 dramatically i
173 Preincubation of virus with subneutralizing concentratio
174 Preincubation of vitronectin with plasminogen activator
175 Preincubation of WKO nTreg cells with exogenous interleu
176 Preincubation of WT-TTR with small molecules that occupy
177 culture through a two-step process requiring
preincubation on an auxin-rich callus induction medium.
178 , as measured by differences in potency upon
preincubation or by progress curve analysis.
179 using a rabbit small intestinal loop assay,
preincubation or coincubation of CPE with the claudin-4
180 Preincubation or coincubation with AGN 211334 significan
181 hat was entirely prevented by d-tubocurarine
preincubation or nAChRalpha1 silencing.
182 ons near their respective IC(50) values, the
preincubation period associated with 2-AEMP's onset of i
183 ere performed using either a 5-min or a 24-h
preincubation period.
184 ssibility assays showed that sigma1R agonist
preincubation potentiated cocaine-induced changes in DAT
185 te and induction tolerance, whereas low-dose
preincubation predominantly mediates absolute tolerance.
186 es matched the IC(50) values measured with a
preincubation:
S-1360 (0.17 microM), L-731,988 (34 nM),
187 In addition, fullerene
preincubation significantly inhibited IgE-induced elevat
188 of delaying initiation, mimicking a physical
preincubation step required for evaluating time-dependen
189 By performing a variety of
preincubation studies and examining the ability of these
190 Time-dependent
preincubation study of compound 3 was consistent with it
191 mage to endothelial cells (EA.hy926) without
preincubation suggest the high potential of this cationi
192 ons, indicating that there may be no optimal
preincubation time for SOC mineralization studies.
193 ndent 17-fold drop in IC(50) from 6.9 nM (no
preincubation)
to 0.4 nM (4-h preincubation).
194 structurally distinct INIs decreased when a
preincubation was included: S-1360 (1.3 microM vs 0.12 m
195 NAC eliminated 1,4-BzQ caused toxicity, but
preincubation was required for the same NAC detoxificati
196 agonism of GABArho1 was strongly enhanced by
preincubation,
was slightly voltage-dependent, and its w
197 Preincubation with (+)-pentazocine or PRE-084 increased
198 ession of phospholipase Cgamma (PLCgamma) or
preincubation with 10 microm wortmannin markedly reduced
199 CbAST-B1-LI was blocked by
preincubation with 10(-6) M CbAST-B1 and was partially b
200 Preincubation with 100 microm m-iodobenzylguanidine or 5
201 PGE(2) release was suppressed by means of
preincubation with 8-bromo-cyclic AMP and forskolin.
202 tration of the HIF-1 inhibitor digoxin or by
preincubation with a beta(2) integrin-blocking antibody.
203 ase at synaptic sites, and were prevented by
preincubation with a beta1-integrin blocking antibody.
204 Preincubation with a cell-permeable derivative of C3 tra
205 Furthermore,
preincubation with a cysteine protease inhibitor prevent
206 Preincubation with a DNA substrate known to promote tetr
207 Preincubation with a high TNF dose induces both absolute
208 Of note,
preincubation with a low concentration of bupropion that
209 Preincubation with a non-selective JAK inhibitor restore
210 723R) in the cytoplasmic domain of beta3, or
preincubation with a peptide ligand.
211 Preincubation with a plasmin inhibitor, a PAR-1 antagoni
212 Palmitoyl transfer is abolished by
preincubation with a specific LRAT antagonist both in me
213 ceptor - mRNA and - protein expression after
preincubation with Abeta .
214 Preincubation with amifostine reversed the high-glucose
215 Preincubation with an anti-fusion protein (anti-F) monoc
216 This effect was inhibited by
preincubation with an anti-GR Ab, indicating that GR its
217 Preincubation with an antibody specific for aggregation
218 , was inhibited by TIMP-3, was blocked after
preincubation with an antibody to a sequence in the cata
219 activity of APF is effectively inhibited by
preincubation with anti-CKAP4/p63-specific antibodies, a
220 fic MB (P < .001), which was abrogated after
preincubation with anti-MAdCAM-1 antibodies (P < .001).
221 e activity in HCE cells, which is blocked by
preincubation with anti-MIP-133 antibody.
222 ls were reduced by 67% (P = 0.009) following
preincubation with anti-P5 antisera.
223 iral uptake were significantly diminished by
preincubation with antibody for Dynamin 2 but not for Co
224 Preincubation with antioxidants and peroxynitrite (ONOO(
225 In the in vitro experiments, 15-minute
preincubation with antioxidants significantly reduced me
226 treated with sucrose after 6, 20, or 48 h of
preincubation with arginine exhibited a recovery to high
227 Preincubation with As(3+), Cd(2+), Co(2+), Ni(2+), Ag(+)
228 rate can be dramatically increased either by
preincubation with ATP or by inclusion of mutations that
229 Preincubation with Au-ACRAMTU-PEt3 suppresses the prolif
230 0 mug/mL) for 4 to 48 hours, with or without
preincubation with azithromycin (1-50 mug/mL), TLR2 anti
231 Preincubation with azumolene, an analog of dantrolene us
232 Preincubation with bilberry extract ameliorated the intr
233 Moreover,
preincubation with butylmalonate but not phenylsuccinate
234 Preincubation with caspofungin (32 microg/mL for R. oryz
235 After a 4-h
preincubation with cathepsin L, this compound became eve
236 ull) grown in cell culture demonstrated that
preincubation with cisplatin increased expression of p53
237 Finally, we found that
preincubation with clusterin antagonizes the toxic effec
238 Preincubation with competitor DNA and DNase treatment bo
239 reactive IgE was only partially inhibited by
preincubation with Cor a 1.
240 cells, and the AA effects were inhibited by
preincubation with CYP epoxygenase inhibitors.
241 ation conferred by EC conditioned media, and
preincubation with CypA augmented Ang II-induced vascula
242 liver failure plasma, which was abrogated by
preincubation with deoxyribonuclease-I.
243 -induced activation of AMPK was abolished by
preincubation with dipyridamole or 5-iodotubercidin.
244 these structures because it is prevented by
preincubation with DNase, which has been shown to disman
245 (>70%, 3 microM) that could be prevented by
preincubation with E-4031.
246 Sequential HCV
preincubation with ECL2 and acidic buffer in the absence
247 ivity was enhanced approximately 2.5-fold by
preincubation with either an anti-CUB mAb (20E9) or VWF
248 ivation was also blunted in heart muscles by
preincubation with either anti-sauvagine-30, a neutraliz
249 Preincubation with excess human vascular endothelial gro
250 Preincubation with Fab 4E10 inhibited both specific and
251 y TBHP decreased markedly in the L6 cells on
preincubation with flavonoids in a dose-dependent manner
252 g is inhibited in a dose-dependent manner by
preincubation with free MadA.
253 mulate the potentiation induced in islets by
preincubation with glucose and the reduction in second-p
254 nd primary mucociliary-differentiated cells,
preincubation with H. influenzae enhanced RV serotype 39
255 Preincubation with H2O2 strongly inhibited this activity
256 Conversely,
preincubation with hBD2:Ig or hBD3:Ig inhibited MCP-1 in
257 FGF binding is abolished by
preincubation with HS, but BMP4 association is partially
258 Preincubation with ILT7 cross-linking Ab inhibited IFN-I
259 Furthermore,
preincubation with KN93 prevented the AMPH-induced decre
260 ro studies, macrophage morphine priming (MP;
preincubation with low-dose morphine) attenuated the eff
261 activity of RegIIIbeta could be inhibited by
preincubation with LPS, lipid A, or gentiobiose.
262 tance P (SP) or IgE/anti-IgE with or without
preincubation with luteolin, methlut, or cromolyn (1-100
263 p)-OH, a derivative of bradykinin, following
preincubation with metal chelate-lisinopril compounds.
264 Preincubation with micafungin or anidulafungin had simil
265 e of phosphatidylserine was also revealed by
preincubation with mitochondrial uncouplers prior to ATP
266 urmountable mechanism that only occurs after
preincubation with MLA.
267 nositol phosphate formation was decreased by
preincubation with NAC (1 h) or alpha-lipoic acid (24 h)
268 The effect is blocked by
preincubation with neurokinin 1 (NK1; L-732138, 10 mum)
269 e and impedance changes were prevented after
preincubation with NK1R antagonists aprepitant and L-730
270 hich are electrically silent, is extended by
preincubation with NMDA, mimicking axonal activity, and
271 ble PAI-1(-/-) neutrophils was diminished by
preincubation with PAI-1.
272 ription and translation were inhibited after
preincubation with Par37.
273 actin-binding MARCKS protein--was blocked by
preincubation with PEG-catalase, which degrades H2O2.
274 Preincubation with peptides prevented viral fusion to ta
275 CAM-1 in vitro, an effect that is blocked by
preincubation with pertussis toxin.
276 ma by PmPPAE2 was significantly decreased by
preincubation with recombinant WSSV453.
277 Preincubation with S-allyl-l-cysteine and isoliquiritige
278 appaB-signaling pathway and demonstrate that
preincubation with select rPAP2 mutant proteins affect t
279 Preincubation with Stx offered full protection against S
280 o trachea and kidney could not be blocked by
preincubation with synthetic alpha-2,3-linked sialic aci
281 Preincubation with the anti-CD81 monoclonal antibody blo
282 ated SMs, and this binding can be blocked by
preincubation with the C-terminal peptide of nod26.
283 tor BAPTA in the pipette-filling solution or
preincubation with the calcineurin inhibitors, cyclospor
284 0.68) and was completely abolished by serum
preincubation with the CCD inhibitor (n = 15).
285 tor of Icmt whose potency was increased upon
preincubation with the enzyme.
286 Cl(-) channel inhibitor niflumic acid and by
preincubation with the G-protein inhibitor GDP-beta-S.
287 oth RER and vesicle movement is inhibited by
preincubation with the GST-tagged C-terminal domain of u
288 We were surprised to find that
preincubation with the H(4)-selective antagonist JNJ7777
289 tivation of enteric neurons was prevented by
preincubation with the HuD antigen.
290 The overexpression of RKIP or
preincubation with the p38 inhibitor reduced MMP-13 mRNA
291 cell apoptosis; this effect was reverted by
preincubation with the peptide mimicking CD163 or with a
292 Mean 53BP1 foci were also reduced by
preincubation with the radioprotectant.
293 Preincubation with the reducing agent dithiothreitol (DT
294 Furthermore,
preincubation with the reverse-mode Na+-Ca2+ exchange bl
295 this property to select mutants resistant to
preincubation with the soluble receptor.
296 8 x 10(-12) M, respectively, after 20 min of
preincubation with these irreversible inhibitors of BChE
297 cruitment, which again could be inhibited by
preincubation with thioperamide.
298 a-arrestin recruitment could be inhibited by
preincubation with thioperamide.
299 tion in culture medium that was abolished by
preincubation with TRP channel antagonists.
300 -1 cells was also significantly inhibited by
preincubation with U0126.