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1 sessment were obtained at 10, 60, and 90 min after administration.
2 draining lymph nodes (LNs) both 3 and 10days after administration.
3 d radiatum of CA3 in ovariectomized mice 6 h after administration.
4 he prodrug must hydrolyze to its parent drug after administration.
5 nal patient measurements between 5 and 10 wk after administration.
6 sistent antihyperalgesic effect up to 60 min after administration.
7 orage and potentially during its application after administration.
8 th a near-infrared fluorophore at least 36 h after administration.
9 2 h and 7.3x and 4.1x, respectively, at 24 h after administration.
10 rs for vector delivery during the first week after administration.
11 er administration; activity was greatest 7 h after administration.
12 emiquantitative uptake of (123)I-MIBG at 4 h after administration.
13 , where peak plasma glucose occurs 7 to 8 hr after administration.
14 utamate receptor plasticity for at least 6 d after administration.
15 an have adverse effects on cognition shortly after administration.
16 1 h (n = 14), 3 h (n = 12), and 24 h (n = 5) after administration.
17 ry were visible by MRI at 6 h, 24 h and 48 h after administration.
18 r-IR fluorescence signal at ca. 700 nm, 24 h after administration.
19 followed for 10 patients using PET up to 4 h after administration.
20 Serial PET was performed until 2 h after administration.
21 PET/CT demonstrated optimal imaging 5-8 d after administration.
22 hox), and protein kinase C, starting 2 hours after administration.
23 lability of 49% was obtained in the first 2h after administration.
24 followed by a test of spatial memory 30 min after administration.
25 d a profound thrombocytopenia within minutes after administration.
26 e incorporation of stable iron isotopes 14 d after administration.
27 olgus monkeys over a time period of 12 weeks after administration.
30 istered BoNT/A1 complex (1 mug) in blood 5 h after administration; activity was greatest 7 h after ad
31 sed on patient imaging during the first week after administration and determination of the activity r
32 0% of the modified T cells within 30 minutes after administration and ended the GVHD without recurren
34 in older healthy participants within minutes after administration and for the duration of infusion, w
35 ocytes persisting in the circulation 1 month after administration and the product that was infused.
36 at 20 to 30 minutes and 60 minutes or longer after administration, and neither BP nor HR changed at e
37 study product administration through 7 days after administration, and secondary safety outcomes are
39 nterleukin-6 and Ngal mRNA observed 24 hours after administration but did not affect renal ferroporti
43 es presenting different surface chemistries, after administration by convection-enhanced delivery.
44 inhibited RVP in Brown Norway rats one month after administration compared to neat quininib control (
46 e and associated alum depot, as early as 2 h after administration, had no appreciable effect on antig
47 r cell targeting and controlled drug release after administration, here we investigated the intratumo
48 ved CNIR800 reaches maximal levels 4-6 hours after administration in live animals, allowing accurate
51 ulated tissue HO-1 and delivered CO in blood after administration in vivo, supporting their potential
54 on of innate and adaptive immune cells early after administration into mice as compared with control
55 stered into the NAc shell, but had no effect after administration into the anterior cingulate cortex.
56 120 min, 9 time frames) on a PET/CT scanner after administration of (11)C-CURB ( approximately 350 M
58 ed for 10 min on an integrated PET/MR system after administration of (18)F-FDG or (68)Ga-DOTANOC.
60 The retention of radioactivity in tumors after administration of (64)Cu-ATSM in vivo is substanti
62 underwent MR imaging 10, 20, and 30 minutes after administration of 0.2 mmol/kg gadobutrol with a st
65 s in ex vivo and in vivo preclinical studies after administration of 1 to rodents, dogs, and monkeys.
68 ncentrations in the kidney, urine osmolality after administration of 1-deamino-8-D-arginine-vasopress
70 pound lowered the parasitemia level by 99.4% after administration of 100 mg/kg single oral dose and p
71 2, 3, 3.5, 4, 5, 6, 8, 10, 12, and 14 hours after administration of 1000 mg acetaminophen on Days 0
72 1% +/- 9.3% before surgery to 90.5% +/- 3.2% after administration of 1200 mg pancreatin (P < .05); CF
73 in turn, correlated with radiation response after administration of 2-deoxyglucose, which significan
77 from baseline to either 60 minutes or nadir after administration of 23.4% saline was 55.6% (se 5.90;
78 ging and biodistribution were performed 24 h after administration of 25 mug of (89)Zr-MSB0010853 to m
84 ment, using a 90-min dynamic PET acquisition after administration of 42.1 +/- 3.9 MBq of (18)F-FMISO
85 e index were recorded at baseline and 3 days after administration of 500 mg clarithromycin, twice dai
86 pneumococcal carriage and on IPD before and after administration of 7-valent PCV (PCV7) were availab
88 icant therapeutic reduction of thrombus size after administration of 75 U/g body weight scFvSCE5-scuP
89 dure was repeated for the (99m)Tc-DTPA group after administration of 96 MBq (2.6 mCi) of the tracer.
92 Compared with standard CT images acquired after administration of a 35% iodinated contrast agent,
93 vels decreases whole-body energy expenditure after administration of a beta3-agonist and reduces beig
95 igated coronary MR angiography was performed after administration of a contrast agent in 78 patients
96 e in a time window between 45 and 70 minutes after administration of a dose of 24 international units
97 Fly camera system to detect fluorescent SLNs after administration of a dual-labeled molecular imaging
101 ge in forced expiratory volume in 1 s (FEV1) after administration of a short-acting bronchodilator ha
102 1)) or forced vital capacity (FVC), or both, after administration of a shortacting beta(2) agonist (1
103 study performed on male Sprague-Dawley rats after administration of a single dose of 5 and 10 mg/kg
104 ma and declining mental status that improved after administration of a single dose of factor eight in
105 erious adverse events (SAEs)--up to 3 months after administration of a single dose of the PsA-TT vacc
108 n egg yolk and white was measured during and after administration of a SMM/TMP combination in laying
109 9 +/- 0.8 MBq of (89)Zr-cetuximab within 2 h after administration of a therapeutic dose of 500 mg.m(-
110 87 have a 9% risk of developing pancreatitis after administration of a thiopurine, whereas homozygote
111 nalysis were significantly decreased 4 hours after administration of a vascular disrupting agent (VDA
112 hly predictive for the time to relapse, also after administration of adjuvant androgen deprivation th
114 reduced deposition of IgM in the glomerulus after administration of adriamycin and attenuated the de
116 n emission tomography and [(11)C]raclopride, after administration of an injection of placebo or 0.5 m
117 ace in millimeters squared before and 1 hour after administration of an IV fluid bolus in the emergen
119 emoving the anterior chamber fibrous complex after administration of antibody to vascular endothelial
123 n each treatment group, the risk of vomiting after administration of any dose of the study agents was
127 atients who underwent PET /: CT 24 and 120 h after administration of approximately 25 MBq of (124)I a
128 by (124)I PET/CT at 2, 24, 48, 72, and 96 h after administration of approximately 30-63 MBq of (124)
129 wer, smaller tumors than VP16 (control) mice after administration of azoxymethane and dextran sodium
130 d more inflammation and formed larger tumors after administration of azoxymethane and dextran sulfate
132 -Apc (Apc(HET)) mice, which develop adenomas after administration of beta-naphthoflavone, were crosse
135 epots of mice during fasting, refeeding, and after administration of catecholamines and insulin.
139 It also reduces intestinal tumor formation after administration of chemical carcinogens, and in Apc
141 nausea and vomiting in patients with cancer after administration of cisplatin-based highly emetogeni
142 matched expanded cord blood progenitor cells after administration of clofarabine, cytarabine, and gra
145 nostic CT at 24 h using a triple-phase delay after administration of contrast; and diagnostic SPECT/C
148 ee different stimulus intensities before and after administration of CRF (0.1, 0.3, 1.0, 3.0 or 10.0
150 d proliferation in the neoplastic epithelium after administration of dextran sodium sulfate and azoxy
151 These mice developed less-severe colitis after administration of dextran sodium sulfate or trinit
152 ith LF82 chiA, developed more severe colitis after administration of dextran sodium sulfate than mice
154 oped more severe colitis than wild-type mice after administration of dextran sulfate sodium or 2,4 di
155 t1IEC-KO mice, developed more severe colitis after administration of dextran sulfate sodium than cont
158 ia length in human chondrocytes in vitro and after administration of dietary lithium to Wistar rats i
159 ainst Anln mRNA developed fewer liver tumors after administration of diethylnitrosamine and carbon te
160 essenger RNA and studied liver tumorigenesis after administration of diethylnitrosamine and carbon te
161 ablation of immature DCX-expressing neurons after administration of diphtheria toxin while leaving t
162 bumin-challenged asthmatic mice up to 27days after administration of DNA nanoparticles carrying thymu
163 nt BM volumes and to predict the average ADs after administration of dosimetry-guided (131)I activity
165 l EPAS1 attenuated the inflammatory response after administration of DSS or C rodentium, and intestin
166 erferon-gamma, and T-helper (Th)17 cytokines after administration of DSS, compared with wild-type mic
167 rs (FaDu) and human colorectal tumors (HT29) after administration of either (64)Cu-ATSM or (64)CuCl2.
168 gas exchange data were obtained at baseline, after administration of either iNO or sildenafil alone,
171 uries were fully reversible after 3-6 months after administration of eribulin, vinorelbine, and ixabe
172 eptor antagonist or ovariectomy but restored after administration of estradiol in ovariectomized mice
174 -/-) mice had reduced inflammatory responses after administration of ethanol or TNBS compared with co
175 chemokines and cytokines in culture and mice after administration of ethanol, TNBS, or C rodentium.
177 uring cardiac ablation that rapidly resolved after administration of Factor Eight Inhibitor Bypassing
178 variate, intracranial hypertension increased after administration of fentanyl and/or midazolam (overa
179 as calculated in 15-minute epochs before and after administration of fentanyl and/or midazolam for th
181 who experienced renal failure developed NSF after administration of gadobenate dimeglumine after mor
182 lar level before and at 12- and 25-min delay after administration of gadolinium contrast by using a m
183 mic fibrosis (NSF), a rare disease occurring after administration of gadolinium-based contrast agents
184 -enhanced gradient-recalled echo MR sequence after administration of gadopentetate dimeglumine was ob
187 littin (Api m 4) were detected in the tissue after administration of HBV immunotherapy preparations.
189 cranial hypertension increased significantly after administration of high-dose fentanyl (p = 0.02), l
190 tional studies have shown beneficial effects after administration of high-titer CMV hyperimmunoglobul
191 d vomiting during the at-risk period (120 h) after administration of highly emetogenic cisplatin-base
192 ate and (13)CO(2) by magnetic resonance (MR) after administration of hyperpolarized [1-(13)C]pyruvate
193 The appearance of (13)C-bicarbonate signal after administration of hyperpolarized [1-(13)C]pyruvate
195 les were collected before and up to 48 hours after administration of IFN-alpha-2a to measure HCV RNA
197 nophils that persist in the blood and airway after administration of IL-5 neutralizing antibodies has
199 tcomes of stillbirth or spontaneous abortion after administration of influenza vaccine during pregnan
203 ts, we measured hemodynamics at baseline and after administration of iodixanol or iopamidol contrast.
205 ording local field potentials in two ferrets after administration of isoflurane in concentrations of
206 imum changes in all the parameters were 48 h after administration of KBrO(3) after which recovery too
207 ase of CaMKII, which lasted 10 to 20 minutes after administration of ketamine, occurred concurrently
210 lean mice to sweet compounds were increased after administration of leptin antagonist (LA) but not a
212 nstream effector of GC-C, cGMP, was released after administration of linaclotide and also inhibited n
213 fference in the relative uptake measurements after administration of low and high activities (P > .99
214 nt a dual-source, dual-energy CT examination after administration of low-concentration contrast mater
215 tasks (short-term memory) before and 1 hour after administration of low-dose methylene blue or a pla
216 nausea and vomiting in patients with cancer after administration of moderately emetogenic chemothera
217 ng during the 5-day (0-120 h) at-risk period after administration of moderately emetogenic chemothera
218 n by circulating insulin was more pronounced after administration of nasal insulin than after placebo
220 and the changes in gamma power were measured after administration of NMDA-R antagonists with differen
221 This difference in heart rate dissipated after administration of norepinephrine, and there were n
222 owed an increase of mean FLT-uptake on day 2 after administration of NVP-AUY299, but a significant re
226 sma drug levels of acyclovir can be achieved after administration of oral valacyclovir or intravenous
230 Mice given hgd40 did not develop colitis after administration of oxazolone or 2,4,6-trinitrobenze
231 e and ADAM17 activation in vivo are examined after administration of p40-containing pectin/zein hydro
232 canal were performed successfully before and after administration of pilocarpine, 1%, in 9 healthy ey
233 ng/ml, compared with 18% and 11% of subjects after administration of plain aspirin and PL2200 (p < 0.
240 amic (11)C-GSK1482160 PET/CT of mice at 72 h after administration of saline, lipopolysaccharide, or l
241 ivo PET/CT was performed on the mice at 72 h after administration of saline, lipopolysaccharide, or l
243 line rate, which is similar to that observed after administration of seasonal influenza vaccines over
244 s muscle force and grip strength immediately after administration of single doses of CK-2017357 in a
247 red liver cells; levels of Hamp were reduced after administration of small interfering RNAs against P
248 s conducted on 24 000 infants in 2 countries after administration of SP-IPTi during routine immunizat
250 (wt) control mice of the same age before and after administration of superparamagnetic iron oxide nan
251 R signal enhancement was observed 48 to 72 h after administration of targeted Mn micelles, with coloc
253 group of obese and T2DM subjects before and after administration of the antilipolytic drug acipimox
254 afV600E/Pten-driven murine model of melanoma after administration of the B-Raf(V600E) small molecule
255 mall-animal PET of (18)F-fluciclatide uptake after administration of the clinically relevant antiangi
256 to the effects seen after tacrine treatment, after administration of the codrug no hepatotoxicity and
258 f the upper airway were performed before and after administration of the DREADD ligand clozapine-N-ox
259 thylene blue vs placebo) and time (before vs after administration of the drug) as factors to assess d
262 (AUC) for the viral load, which was assessed after administration of the first dose through the 12th
263 lcSph levels in the brains of wild-type mice after administration of the GCase inhibitor conduritol b
264 session to measure plasma CBD concentrations after administration of the highest CBD dose (800 mg).
266 red to larger children and adults (>/=25 kg) after administration of the manufacturers' currently rec
267 Adverse events identified within 1 week after administration of the medication occurred in appro
268 ncreased contrast-to-noise ratio for the CBD after administration of the mixture, compared with image
270 of SCCs and BCCs was observed in 2 patients after administration of the quadrivalent HPV vaccine.
272 th cocaine at various times (15 min to 48 h) after administration of the selective KOR agonist salvin
273 mes and to predict the therapy-delivered ADs after administration of the therapeutic (131)I activity.
275 Vs delivered systemically to mice before and after administration of the vasopressin V2 receptor anta
278 fic PET radiotracer, was measured before and after administration of tiagabine (0.2 mg/kg of body wei
279 TIMP-3-KO mice developed severe colitis after administration of TNBS, whereas TIMP-3-Tg mice wer
280 as delivered intraperitoneally less than 4 h after administration of trastuzumab (4 mg/kg intravenous
281 +/-8.4 to 67.0+/-9.5 s(-1); P>0.05) 24 hours after administration of ultrasmall superparamagnetic par
282 veloping unexplained ARF without hypovolemia after administration of vancomycin without coadministrat
283 , we elucidate the human antibody repertoire after administration of vesicular stomatitis virus (VSV)
286 tion vs. 0.4 events per year [range, 0 to 4] after administration; P=0.02), as was factor use (mean d
290 c release of the agents at the selected time after administration so that they can reach their intrac
292 I-prolactin were very low, even up to 90 min after administration, the data suggest that CSF is not t
293 a Abeta40 levels in a dose-dependent fashion after administration to a mouse model that overexpress h
294 pharmacokinetic evaluation of empagliflozin after administration to Egyptian volunteers, and the res
296 elocity in first-order arterioles, 5 minutes after administration was zero for these three groups) co
298 enabled clear tumor visualization on PET 4 h after administration, with a resultant peak tumor-to-liv
299 f hind paw mechanical allodynia for up to 1h after administration, with no noticeable behavioral or m
300 f these cationic vesicles to promote a depot after administration, with the liposomal adjuvant and th
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