1 rom 6.9 nM (no preincubation) to 0.4 nM (4-h
preincubation).
2 otentiation of SMIT activity by myo-inositol
preincubation.
3 XCL16 induction was not restored by IFN-beta
preincubation.
4 ist phenylephrine with or without antagonist
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 However, when calmodulin was omitted during
preincubation,
activity was not affected, suggesting tha
11 Additionally, the duration of
preincubation affected interactions, indicating that the
12 reduced on some days after infection in the
preincubation and prophylaxis groups.
13 ble C in the soil, through 1-day and 6-month
preincubations,
and in PyOM made from maple wood at 350
14 n-4 or the claudin-4 ECL-2 peptide in both a
preincubation assay and a coincubation assay.
15 wed that neutralization titers of MAbs after
preincubation at 37 degrees C correlated with activity i
16 However, increasing the time of
preincubation at 37 degrees C or raising the temperature
17 the genetic diversity of the serotype after
preincubation at 37 degrees C.
18 Ultrastructural studies revealed that after
preincubation at 4 degrees C mutant chloroplasts contain
19 higher than in controls and was inhibited by
preincubation by either inhibitor.
20 tion itself, inactivation resulting from ATP
preincubation can be reversed by a remodeling process me
21 phospholamban on SERCA depends on substrate
preincubation conditions.
22 TNF tolerance induced by the low
preincubation dose is mediated by glycogen synthesis kin
23 In agreement with this finding,
preincubation experiments indicate that stable protein/D
24 nocytochemical resolution, we also performed
preincubation experiments with 5-hydroxy-L-tryptophan an
25 the polymerase and a double-stranded RNA by
preincubation experiments.
26 MLA
preincubation inhibits JN403-induced Ca(2+) influx in GH
27 Results showed that the length of the
preincubation interval significantly affects the inhibit
28 Slow DNA binding in the absence of ATP
preincubation is the result of a rate-limiting ATP-induc
29 ycogen synthesis kinase-3, whereas high-dose
preincubation-
mediated tolerance is regulated by A20/gly
30 substrates or removal of Na(+) from the MTS
preincubation medium.
31 Preincubation of (67)Zn(7)-MT-2 with an excess of oxidiz
32 Notably, a 48 h
preincubation of 1g-i significantly enhanced the antipro
33 oligomer-mediated cytotoxicity observed upon
preincubation of A beta oligomers with the anti-A beta(1
34 Preincubation of a multireactive serum with BGAL(266-280
35 Furthermore,
preincubation of a recombinant Sca1 peptide with host ce
36 Preincubation of accessory cells with the respective sti
37 Preincubation of Ad5 with excess heparin or pretreatment
38 This conclusion was supported by prolonged
preincubation of antagonist that failed to improve the o
39 Preincubation of apoE3 or apoE4 with Abeta42 increased t
40 es and was significantly inhibited following
preincubation of apoptotic cardiocytes with chicken and
41 Preincubation of asthmatic airway macrophages with Haemo
42 Interestingly,
preincubation of bacteria with antibodies against the ma
43 We found that
preincubation of bacteria with recombinant soluble BAI1
44 Consistent with prior observations,
preincubation of bacteria with unfractionated properdin,
45 first blocked selectively these receptors by
preincubation of BM-MSCs with specific neutralizing anti
46 n with a dominant-negative Akt adenovirus or
preincubation of cardiomyocytes with the phosphatidylino
47 However,
preincubation of CcrB-DNA complexes with increasing conc
48 Preincubation of cell cultures with BF from both oils si
49 Preincubation of cells with a peptide that contains a ph
50 xis and peroxidase release were inhibited by
preincubation of cells with anti-CCR3.
51 Preincubation of cells with glycoproteins (thyroglobulin
52 Similarly,
preincubation of cells with GW9662 inhibited inducing ef
53 Preincubation of cells with NPY up-regulated the Y5 rece
54 R1-BR)) adhered to A549 cells, and moreover,
preincubation of cells with rPsrP(SRR1-BR) inhibited TIG
55 Here, we report that
preincubation of cells with the GRGDNP peptide strongly
56 Preincubation of cells with the inhibitors of the DDR ki
57 onse was also partially caspase dependent as
preincubation of cells with the pan-caspase inhibitor zV
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 effect on adherence to HUVEC; specifically,
preincubation of D39 with both FH and sIgA led to a 21-f
61 ignificantly in the absence of Ca(2+) and by
preincubation of DC-SIGN with mannan, suggesting that C1
62 Preincubation of double positive thymocytes with exogeno
63 perature dependence of methylation of EF-Tu,
preincubation of EftM at 37 degrees C abolished methyltr
64 Preincubation of either trypomastigotes or myoblasts wit
65 Preincubation of eNOS with BH(4) decreased dimer destabi
66 Preincubation of ESAT-6 with CFP10 under conditions that
67 It is noteworthy that
preincubation of eukaryotic cells with AdpF increased P.
68 Preincubation of experimentally aged erythrocytes with h
69 Preincubation of factor H with exogenous heparin and pre
70 We found that
preincubation of FCV with the ectodomain or D1 was suffi
71 However
preincubation of FIX with a saturating concentration of
72 Preincubation of FN with mAbIII-10 or heparin modestly i
73 Preincubation of fresh rat hepatocyte suspensions with G
74 Preincubation of FVIII with VK34 did not influence FVIII
75 Preincubation of gpK8.1A with heparin or anti-gpK8.1A an
76 Additionally,
preincubation of H441 cells with A77-1726 (20 microM), a
77 Preincubation of HCV particles with anti-HSC70 antibodie
78 Preincubation of HDL3 with human plasma-derived active P
79 CoQ(10)
preincubation of healthy monocytes before IgG-antiphosph
80 , TRAF6-dominant-negative overexpression, or
preincubation of HMVEC-Ls with a cell-permeable TRAF6 de
81 activated Tyr(P)(416)-SFK to GST-TRAF6, and
preincubation of HMVEC-Ls with SFK-selective tyrosine ki
82 Preincubation of host cells with sG resulted in dose-dep
83 Preincubation of HTBE cells with a truncated HKU1 S prot
84 Binding to SR-BI was required since
preincubation of human and murine platelets with anti-SR
85 In vitro:
Preincubation of human coronary artery endothelial cells
86 Preincubation of human monocytes with CCL2/MCP-1, the ch
87 Further, we found that
preincubation of human serum with F. alocis resulted in
88 Preincubation of HUVECs with an IL-3R-blocking Ab (CD123
89 Whereas
preincubation of HVSMCs with epinephrine before the addi
90 Preincubation of IgGs from multigravida women with recom
91 This increase was blocked by
preincubation of intact cells with apocynin (NADPH oxida
92 Preincubation of islets with subsaturating concentration
93 Preincubation of KSHV with soluble heparin and alpha3bet
94 Preincubation of L-tyrosine with Orf13 prior to the addi
95 Preincubation of lenses with either ouabain or low-[Na(+
96 Preincubation of lymphoma cells with Ad35K(++) sensitize
97 Preincubation of MAV-1 with heparin, a heparan sulfate g
98 Preincubation of microtubules with 2 or 4 microM vinblas
99 y increased reactive oxygen species, whereas
preincubation of mito-TEMPOL, a superoxide dismutase mim
100 Infection could be enhanced by
preincubation of Moloney MLV with cathepsin B, consisten
101 L-13-stimulated 15-LO upregulation; however,
preincubation of monocytes with the antibody MEM48, whic
102 Preincubation of muscle cells with ROS scavengers (e.g.
103 Preincubation of NCMs, with 10 nm extracellular concentr
104 Preincubation of neurones with SP (10 nM, 5 min) desensi
105 ession of Balb/c Teffs; this was reversed by
preincubation of NOD Teffs with GM1.
106 Preincubation of normal human lung fibroblasts with the
107 Preincubation of oocytes with ibuprofen did not signific
108 Preincubation of oocytes with serine proteases prevented
109 Preincubation of P. aeruginosa with these same ex vivo f
110 uld be inhibited or significantly delayed by
preincubation of P. gingivalis W83 gingipain-active extr
111 the reciprocal experiment demonstrated that
preincubation of PAI-1 with PAI-039 blocked the binding
112 Preincubation of PAI-1 with vitronectin, but not bovine
113 Furthermore,
preincubation of PEDF with P1 and E5b peptides blocked t
114 onger than that previously reported and that
preincubation of photoreceptor outer segment homogenates
115 aggregation, and secretion were inhibited by
preincubation of platelets with a selective SFK inhibito
116 Notably,
preincubation of platelets with aspirin, but not with a
117 ent on direct contact with cancer cells, and
preincubation of platelets with blocking antibodies agai
118 Preincubation of platelets with human colon cancer (Caco
119 Preincubation of platelets with MPs led to CD36-dependen
120 The
preincubation of platelets with purified lysin(102-198)
121 Preincubation of PLTs with type IV collagen specifically
122 Preincubation of polyclonal IgG with CD64-IgE Fc establi
123 Binding was inhibited by
preincubation of porcine Kupffer cells with purified hum
124 of the current study previously showed that
preincubation of primary microglial-enriched cells with
125 At low concentrations of Rad53,
preincubation of Rad53 with immune complexes containing
126 Preincubation of rat aortic rings with OxLDL resulted in
127 levels of beta-spectrin that is inhibited by
preincubation of RBCs with DMAT, a specific casein kinas
128 Furthermore, in vitro studies showed that
preincubation of recombinant alpha-syn with 1H7 and 5C1
129 We find that
preincubation of RER with KLC1B inhibits RER motility, w
130 Preincubation of sera from cockroach-allergic subjects w
131 Preincubation of SF100 with ganglioside GD3, a glycolipi
132 The effect of SE-1 on invasion required
preincubation of Shigella with SE-1, in agreement with t
133 Preincubation of strain 181/25, but not SL15649, with so
134 Adherence assays demonstrated that
preincubation of Streptococcus pneumoniae D39 with FH in
135 Preincubation of target membranes with MREG resulted in
136 Order-of-addition experiments indicate that
preincubation of tetrameric SsoSSB and SsoRadA prior to
137 Preincubation of thawed M. tuberculosis complex cells in
138 Preincubation of the cells for 16 h with either Shh or E
139 After
preincubation of the cells with anti-14-3-3 antibody and
140 cent microscopy, which were prevented by the
preincubation of the cells with either CB1 antagonist, b
141 In vitro
preincubation of the cells with the compounds resulted i
142 mg(-1) and was also effectively inhibited by
preincubation of the cells with the inhibitors pervanada
143 Preincubation of the chemokines with OPN strongly inhibi
144 Preincubation of the enzyme with iodoacetamide (17 mM) c
145 extension from an exogenous primer following
preincubation of the enzyme with template and primer cou
146 In corroboration,
preincubation of the ETEC inoculum with antiadhesin and
147 osteogenic differentiation before and after
preincubation of the fractions with the bone morphogenet
148 s was concentration-dependently inhibited by
preincubation of the human umbilical arterial endothelia
149 Preincubation of the LLC-PK1 cells with the caspase 9 in
150 Preincubation of the neurons with the PKC inhibitor bisi
151 Furthermore,
preincubation of the p13(II)-expressing cells with a far
152 geting specificity in vitro was confirmed by
preincubation of the pancreatic cancer cells with C225 a
153 g-dependent reduction in I(A) was blocked by
preincubation of the photoreceptors with Csp antisense o
154 Each activation event was inhibited by
preincubation of the platelets with Fab fragments of the
155 Notably,
preincubation of the preterm, but not near-term, amnioti
156 which the binding sites were blocked through
preincubation of the proteins with the corresponding lig
157 Preincubation of the purified toxin and antitoxin togeth
158 Preincubation of the slice with the selective KOR antago
159 Preincubation of the T67I mutant with PLP restored activ
160 resembling physiological conditions and the
preincubation of the two proteins.
161 n of caspase-3 activity to detect apoptosis,
preincubation of these cells with isoproterenol was foun
162 Preincubation of these oocytes with phosphocholine, howe
163 Preincubation of trypomastigotes with a concentration of
164 Preincubation of trypomastigotes with defensin alpha-1 f
165 Preincubation of trypomastigotes with either TcGP63 anti
166 Preincubation of tubulin with tau resulted in decreased
167 Preincubation of tumor cells with bortezomib had no effe
168 hibited diminished neutralizing activity but
preincubation of virions with soluble CD4 restored it, s
169 Preincubation of virus with soluble EphA2, knockdown of
170 Preincubation of vitreous samples with anti-PEDF partial
171 Preincubation of vitronectin with plasminogen activator
172 Preincubation of WKO nTreg cells with exogenous interleu
173 Preincubation of WT-TTR with small molecules that occupy
174 culture through a two-step process requiring
preincubation on an auxin-rich callus induction medium.
175 , as measured by differences in potency upon
preincubation or by progress curve analysis.
176 using a rabbit small intestinal loop assay,
preincubation or coincubation of CPE with the claudin-4
177 Preincubation or coincubation with AGN 211334 significan
178 hat was entirely prevented by d-tubocurarine
preincubation or nAChRalpha1 silencing.
179 ons near their respective IC(50) values, the
preincubation period associated with 2-AEMP's onset of i
180 ere performed using either a 5-min or a 24-h
preincubation period.
181 ssibility assays showed that sigma1R agonist
preincubation potentiated cocaine-induced changes in DAT
182 te and induction tolerance, whereas low-dose
preincubation predominantly mediates absolute tolerance.
183 es matched the IC(50) values measured with a
preincubation:
S-1360 (0.17 microM), L-731,988 (34 nM),
184 In addition, fullerene
preincubation significantly inhibited IgE-induced elevat
185 of delaying initiation, mimicking a physical
preincubation step required for evaluating time-dependen
186 By performing a variety of
preincubation studies and examining the ability of these
187 Time-dependent
preincubation study of compound 3 was consistent with it
188 mage to endothelial cells (EA.hy926) without
preincubation suggest the high potential of this cationi
189 ons, indicating that there may be no optimal
preincubation time for SOC mineralization studies.
190 ndent 17-fold drop in IC(50) from 6.9 nM (no
preincubation)
to 0.4 nM (4-h preincubation).
191 structurally distinct INIs decreased when a
preincubation was included: S-1360 (1.3 microM vs 0.12 m
192 NAC eliminated 1,4-BzQ caused toxicity, but
preincubation was required for the same NAC detoxificati
193 agonism of GABArho1 was strongly enhanced by
preincubation,
was slightly voltage-dependent, and its w
194 Preincubation with (+)-pentazocine or PRE-084 increased
195 Preincubation with 0.1 nm okadaic acid, a PP2A >> phosph
196 ession of phospholipase Cgamma (PLCgamma) or
preincubation with 10 microm wortmannin markedly reduced
197 CbAST-B1-LI was blocked by
preincubation with 10(-6) M CbAST-B1 and was partially b
198 Preincubation with 100 microm m-iodobenzylguanidine or 5
199 PGE(2) release was suppressed by means of
preincubation with 8-bromo-cyclic AMP and forskolin.
200 tration of the HIF-1 inhibitor digoxin or by
preincubation with a beta(2) integrin-blocking antibody.
201 ase at synaptic sites, and were prevented by
preincubation with a beta1-integrin blocking antibody.
202 Preincubation with a CaM antagonist significantly slows
203 Preincubation with a cell-permeable derivative of C3 tra
204 Furthermore,
preincubation with a cysteine protease inhibitor prevent
205 Preincubation with a DNA substrate known to promote tetr
206 Preincubation with a high TNF dose induces both absolute
207 Preincubation with a non-selective JAK inhibitor restore
208 723R) in the cytoplasmic domain of beta3, or
preincubation with a peptide ligand.
209 Preincubation with a plasmin inhibitor, a PAR-1 antagoni
210 Palmitoyl transfer is abolished by
preincubation with a specific LRAT antagonist both in me
211 ceptor - mRNA and - protein expression after
preincubation with Abeta .
212 Preincubation with amifostine reversed the high-glucose
213 Preincubation with an anti-fusion protein (anti-F) monoc
214 This effect was inhibited by
preincubation with an anti-GR Ab, indicating that GR its
215 Preincubation with an antibody specific for aggregation
216 , was inhibited by TIMP-3, was blocked after
preincubation with an antibody to a sequence in the cata
217 croglial responses were totally abolished by
preincubation with an MMP-3 inhibitor, NNGH [N-isobutyl-
218 activity of APF is effectively inhibited by
preincubation with anti-CKAP4/p63-specific antibodies, a
219 fic MB (P < .001), which was abrogated after
preincubation with anti-MAdCAM-1 antibodies (P < .001).
220 e activity in HCE cells, which is blocked by
preincubation with anti-MIP-133 antibody.
221 ls were reduced by 67% (P = 0.009) following
preincubation with anti-P5 antisera.
222 iral uptake were significantly diminished by
preincubation with antibody for Dynamin 2 but not for Co
223 Preincubation with antioxidants and peroxynitrite (ONOO(
224 In the in vitro experiments, 15-minute
preincubation with antioxidants significantly reduced me
225 treated with sucrose after 6, 20, or 48 h of
preincubation with arginine exhibited a recovery to high
226 Preincubation with As(3+), Cd(2+), Co(2+), Ni(2+), Ag(+)
227 rate can be dramatically increased either by
preincubation with ATP or by inclusion of mutations that
228 Preincubation with Au-ACRAMTU-PEt3 suppresses the prolif
229 0 mug/mL) for 4 to 48 hours, with or without
preincubation with azithromycin (1-50 mug/mL), TLR2 anti
230 Preincubation with azumolene, an analog of dantrolene us
231 Preincubation with bilberry extract ameliorated the intr
232 Moreover,
preincubation with butylmalonate but not phenylsuccinate
233 Preincubation with caspofungin (32 microg/mL for R. oryz
234 After a 4-h
preincubation with cathepsin L, this compound became eve
235 ull) grown in cell culture demonstrated that
preincubation with cisplatin increased expression of p53
236 Finally, we found that
preincubation with clusterin antagonizes the toxic effec
237 Preincubation with competitor DNA and DNase treatment bo
238 reactive IgE was only partially inhibited by
preincubation with Cor a 1.
239 cells, and the AA effects were inhibited by
preincubation with CYP epoxygenase inhibitors.
240 ation conferred by EC conditioned media, and
preincubation with CypA augmented Ang II-induced vascula
241 liver failure plasma, which was abrogated by
preincubation with deoxyribonuclease-I.
242 -induced activation of AMPK was abolished by
preincubation with dipyridamole or 5-iodotubercidin.
243 these structures because it is prevented by
preincubation with DNase, which has been shown to disman
244 (>70%, 3 microM) that could be prevented by
preincubation with E-4031.
245 Sequential HCV
preincubation with ECL2 and acidic buffer in the absence
246 ivity was enhanced approximately 2.5-fold by
preincubation with either an anti-CUB mAb (20E9) or VWF
247 ivation was also blunted in heart muscles by
preincubation with either anti-sauvagine-30, a neutraliz
248 Preincubation with excess human vascular endothelial gro
249 Preincubation with Fab 4E10 inhibited both specific and
250 y TBHP decreased markedly in the L6 cells on
preincubation with flavonoids in a dose-dependent manner
251 g is inhibited in a dose-dependent manner by
preincubation with free MadA.
252 mulate the potentiation induced in islets by
preincubation with glucose and the reduction in second-p
253 nd primary mucociliary-differentiated cells,
preincubation with H. influenzae enhanced RV serotype 39
254 Preincubation with H2O2 strongly inhibited this activity
255 Conversely,
preincubation with hBD2:Ig or hBD3:Ig inhibited MCP-1 in
256 FGF binding is abolished by
preincubation with HS, but BMP4 association is partially
257 Preincubation with ILT7 cross-linking Ab inhibited IFN-I
258 Furthermore,
preincubation with KN93 prevented the AMPH-induced decre
259 In addition,
preincubation with l-NAME and ODQ inhibited phenylephrin
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 Preincubation with the anti-CD81 monoclonal antibody blo
281 ated SMs, and this binding can be blocked by
preincubation with the C-terminal peptide of nod26.
282 tor BAPTA in the pipette-filling solution or
preincubation with the calcineurin inhibitors, cyclospor
283 0.68) and was completely abolished by serum
preincubation with the CCD inhibitor (n = 15).
284 tor of Icmt whose potency was increased upon
preincubation with the enzyme.
285 Cl(-) channel inhibitor niflumic acid and by
preincubation with the G-protein inhibitor GDP-beta-S.
286 oth RER and vesicle movement is inhibited by
preincubation with the GST-tagged C-terminal domain of u
287 We were surprised to find that
preincubation with the H(4)-selective antagonist JNJ7777
288 tivation of enteric neurons was prevented by
preincubation with the HuD antigen.
289 The overexpression of RKIP or
preincubation with the p38 inhibitor reduced MMP-13 mRNA
290 cell apoptosis; this effect was reverted by
preincubation with the peptide mimicking CD163 or with a
291 Mean 53BP1 foci were also reduced by
preincubation with the radioprotectant.
292 Preincubation with the reducing agent dithiothreitol (DT
293 Furthermore,
preincubation with the reverse-mode Na+-Ca2+ exchange bl
294 this property to select mutants resistant to
preincubation with the soluble receptor.
295 8 x 10(-12) M, respectively, after 20 min of
preincubation with these irreversible inhibitors of BChE
296 cruitment, which again could be inhibited by
preincubation with thioperamide.
297 a-arrestin recruitment could be inhibited by
preincubation with thioperamide.
298 reduction in MVO2 in nNOS-/- was restored by
preincubation with Tiron, ascorbic acid, Tempol, oxypuri
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.