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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.
28                                     One hour after administration, 5.2% (1.7%-9.9%) of labeled cell a
29           Caffeine enhanced performance 24 h after administration according to an inverted U-shaped d
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
33 stered quickly, and are effective, both soon after administration and for a long duration.
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
38 opic label abundance in erythrocytes 14 days after administration, and serum hepcidin.
39 nterleukin-6 and Ngal mRNA observed 24 hours after administration but did not affect renal ferroporti
40 nohistochemistry is evident for both at 16 h after administration but not at 15 min or 2 h.
41 onist impaired glucose tolerance immediately after administration but not in the long term.
42 rsistent sirolimus levels in the vessel wall after administration by a coated balloon.
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 (
45                                   At 1 month after administration for subjects who received 1 treatme
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
49                                              After administration in mice, DNA from the vaccine could
50  in liver, spleen, brain, and blood 24 hours after administration in mice.
51 ulated tissue HO-1 and delivered CO in blood after administration in vivo, supporting their potential
52 ets were significantly enriched in the brain after administration in vivo.
53                      Between 180 and 360 min after administration, INI significantly suppressed EGP b
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
57                                              After administration of (11)C-MeNER, 15 nondemented pati
58 ed for 10 min on an integrated PET/MR system after administration of (18)F-FDG or (68)Ga-DOTANOC.
59                                              After administration of (18)F-FEAnGA, the area under the
60     The retention of radioactivity in tumors after administration of (64)Cu-ATSM in vivo is substanti
61       The trafficking of (64)Cu in the brain after administration of (64)Cu-GTSM is significantly alt
62  underwent MR imaging 10, 20, and 30 minutes after administration of 0.2 mmol/kg gadobutrol with a st
63 mapping was performed before and >20 minutes after administration of 0.2 mmol/kg of gadobutrol.
64 on and 4 iterative techniques) acquired 30 h after administration of 1 MBq of (124)I.
65 s in ex vivo and in vivo preclinical studies after administration of 1 to rodents, dogs, and monkeys.
66                                              After administration of 1,2-dimethylhydrazine and DSS, i
67 )I and subsequently underwent imaging 5-10 d after administration of 1-10 GBq of (131)I.
68 ncentrations in the kidney, urine osmolality after administration of 1-deamino-8-D-arginine-vasopress
69                                              After administration of 10 muM S1P, the diameter of affe
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
74                                 Importantly, after administration of 2-MPA-TG, the concentrations of
75 T-PBV images were acquired before and 1 hour after administration of 20 mg oral sildenafil.
76 y, patients underwent serial PET/CT scanning after administration of 20-40 MBq of (124)I.
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
79                                     Directly after administration of 3 MBq/kg of FCH, PET imaging was
80                 Cardiac PET/CT was performed after administration of 370 MBq of (18)F-FDG.
81                                              After administration of 3F-NeuAc, liver enzymes in the b
82  a range of 84.6% +/- 3.0% to 90.0% +/- 3.8% after administration of 4-80 mg YLLIP2 (P < .05).
83 in response to SNP was significantly blunted after administration of 400 nm ET-1 (P < 0.05).
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
87 ent, a 20-minute dynamic study was performed after administration of 7.4 MBq/kg.
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.
90                       Biodistribution at 7 d after administration of [(89)Zr]Zr-DFO-daratumumab showe
91 d and detected by in vivo magnetic resonance after administration of [2-(13) C]-glycine.
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
94 with the reversibility of airway contraction after administration of a bronchodilator.
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
98                                              After administration of a low dose of leptin, the durati
99 he modification of airway sensory processing after administration of a placebo.
100                                              After administration of a questionnaire, general and ora
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
106 rapy and restore normal lipoprotein profiles after administration of a single dose.
107                                              After administration of a single intravenous dose, each
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
113 acc-4x (or placebo) were given intradermally after administration of adjuvant.
114  reduced deposition of IgM in the glomerulus after administration of adriamycin and attenuated the de
115 sues from guinea pigs and CFTR knockout mice after administration of alcohol.
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
118                                              After administration of anti-CD3 or antigen, with or wit
119 emoving the anterior chamber fibrous complex after administration of antibody to vascular endothelial
120 ntriguingly, miR135a levels were upregulated after administration of antidepressants.
121 ks for (re)infection and symptomatic malaria after administration of antimalarial drugs.
122 sitive for FV at immunofluorescence staining after administration of antisense MO or U7snRNA.
123 n each treatment group, the risk of vomiting after administration of any dose of the study agents was
124 Min/+) mice and in Spdef(dox-intestine) mice after administration of AOM + DSS.
125 -fold more colon tumors than Spdef(+/+) mice after administration of AOM and DSS.
126 trols in an Apc(Min/+) background as well as after administration of AOM and DSS.
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
131 orolac did not impact total RH FBF before or after administration of BaCl2 plus ouabain.
132 -Apc (Apc(HET)) mice, which develop adenomas after administration of beta-naphthoflavone, were crosse
133 PV) 3 and one case linked to mOPV1 presented after administration of bivalent OPV 1 + 3 (bOPV).
134  rats, FGF23 increased significantly 6 hours after administration of calcium gluconate.
135 epots of mice during fasting, refeeding, and after administration of catecholamines and insulin.
136  AP induction and trypsin activation in mice after administration of cerulein or L-arginine.
137      Bcl3(-/-) mice developed more severe AP after administration of cerulein or sodium taurocholate
138 -induced metaplasia was investigated in mice after administration of cerulein.
139   It also reduces intestinal tumor formation after administration of chemical carcinogens, and in Apc
140             Audiologic testing was completed after administration of cisplatin alone (< 400 mg/m(2);
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
143  and at least one time after imaging (>1 day after administration of contrast material).
144 rate their navigation in the vascular system after administration of contrast material.
145 nostic CT at 24 h using a triple-phase delay after administration of contrast; and diagnostic SPECT/C
146 A), and docosahexanoic acid (22:6, DHA) soon after administration of CPB in all cases.
147 hort unmethylated CpG dinucleotide sequences after administration of CpG 7909.
148 ee different stimulus intensities before and after administration of CRF (0.1, 0.3, 1.0, 3.0 or 10.0
149 ateral thalamus were noninvasively sonicated after administration of Definity microbubbles.
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
153        LL-IL-27 also reduced colitis in mice after administration of dextran sodium sulfate.
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
156                                              After administration of dextran sulfate sodium, Tnfsf14(
157               Analysis of uterine mRNAs 24 h after administration of DHT identified significant chang
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
164 tates were measured several times before and after administration of drugs.
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,
169 ain uptake of (11)C-erlotinib was not higher after administration of elacridar.
170 gh activity (303.4 MBq +/- 48.1) acquisition after administration of enalaprilat.
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
173 developed a less-severe form of pancreatitis after administration of ethanol and CCK.
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.
176                     Aqueous FAc was measured after administration of FAc implants or 0.2 mug/day (low
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
180                            No adverse events after administration of ferumoxytol were recorded.
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
185  were not significantly different before and after administration of Gd-EOB-DTPA.
186 er the anorexigenic effects of GLP-1 release after administration of glutamine.
187 littin (Api m 4) were detected in the tissue after administration of HBV immunotherapy preparations.
188 subsets, which reached their nadir 4-8 hours after administration of HC.
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
194                               In responders, after administration of IFN-alpha, intrahepatic ISG expr
195 les were collected before and up to 48 hours after administration of IFN-alpha-2a to measure HCV RNA
196        Protective effects were also observed after administration of IL-17F but not IL-17C or IL-17E.
197 nophils that persist in the blood and airway after administration of IL-5 neutralizing antibodies has
198 ines by these cells, which increased further after administration of IL6.
199 tcomes of stillbirth or spontaneous abortion after administration of influenza vaccine during pregnan
200                                              After administration of insecticide and fungus, activiti
201 c stent in angiographic vasomotor reactivity after administration of intracoronary nitrate.
202 ny) before (baseline) and 1 week and 1 month after administration of intravitreal ranibizumab.
203 ts, we measured hemodynamics at baseline and after administration of iodixanol or iopamidol contrast.
204 e ICa,L current density was decreased by 28% after administration of ISO in TG cardiomyocytes.
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
208 ients with cirrhosis, and may further change after administration of lactulose.
209                                   Three days after administration of LDL-TO or sham surgery, the cont
210  lean mice to sweet compounds were increased after administration of leptin antagonist (LA) but not a
211 llowing overnight withdrawal of levodopa and after administration of levodopa.
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
219                                      At 24 h after administration of NeutrAvidin, labeled with either
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
223 ge injected dose per gram of tissue) 50 days after administration of one gadoteridol dose.
224                    In the absence of IRF4 or after administration of oral antibiotics, MHC II(+)CD226
225 the blood glucose level by insulin secretion after administration of oral glucose.
226 sma drug levels of acyclovir can be achieved after administration of oral valacyclovir or intravenous
227 in lesion size of 20% or more 48 to 72 hours after administration of oritavancin.
228 ration of a rescue antibiotic 48 to 72 hours after administration of oritavancin.
229  tolerated with no additional safety signals after administration of oseltamivir.
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.
234 incter (IAS) smooth muscle cells, before and after administration of pooledhIgG.
235 ety, tolerability and feasibility before and after administration of proton pump inhibitors.
236                                              After administration of raclopride and d-amphetamine, th
237 re obtained before and between 0.5 and 120 h after administration of radioiodine.
238         All patients underwent (124)I PET/CT after administration of recombinant human thyroid-stimul
239                             HI reversibility after administration of salbutamol (400 mug) was defined
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
242          At concentrations reached in plasma after administration of salsalate or of aspirin at high
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
245 declining by ~3-4 log10 in infected patients after administration of single oral doses of DCV.
246                                              After administration of siRNAs targeting Serpinc1 and Pr
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
249 ed with 2 isogenic strains of S. typhimurium after administration of streptomycin.
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
252 ver clearance time (24 hours in both groups) after administration of the 2 study treatments.
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
257        However, genotype differences emerged after administration of the COMT inhibitor tolcapone: pe
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
260                 The optimal time for imaging after administration of the dual-labeled antibody was 2-
261                             We now show that after administration of the first dose of OFA, there was
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).
265    Drug concentrations peaked about 89-106 h after administration of the highest dose.
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
269                                     At 2.5 h after administration of the Org 25935 or placebo, subjec
270  of SCCs and BCCs was observed in 2 patients after administration of the quadrivalent HPV vaccine.
271  scans followed at 30 min, 1 h, 2 h, and 4 h after administration of the radiopharmaceutical.
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.
274                                    One month after administration of the third dose of RTS,S/AS01, 99
275 Vs delivered systemically to mice before and after administration of the vasopressin V2 receptor anta
276 pression profile of TG mice, both before and after administration of the xenobiotic mitogens.
277              No obvious disease was observed after administration of this phage in mice.
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)
284 d plus maze were assessed in postpartum rats after administration of yohimbine or idazoxan.
285 n vs. 49.3 IU per kilogram [range, 0 to 376] after administration; P=0.004).
286 tion vs. 0.4 events per year [range, 0 to 4] after administration; P=0.02), as was factor use (mean d
287                                              After administration, participants studied faces and hou
288 miquantitative uptake of (123)I-MIBG at 24 h after administration (r = 0.64, P = 0.04).
289 he protection it confers in the first months after administration remain unknown.
290 c release of the agents at the selected time after administration so that they can reach their intrac
291                        At 3, 6, 12, and 24 h after administration, SPECT/CT images were acquired or m
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
295 ting the infusion with cessation of bleeding after administration was complete.
296 elocity in first-order arterioles, 5 minutes after administration was zero for these three groups) co
297 induce MAIT cell accumulation in mouse lungs after administration with a co-stimulant.
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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