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1 per kilogram of maternal weight, in a single intravenous administration).
2 ility to specifically reach tumors following intravenous administration.
3 s models and aqueous solubility suitable for intravenous administration.
4  transport of plasmid DNA to the brain after intravenous administration.
5 ownregulation in GFP-expressing tumors after intravenous administration.
6 ulting in a failure to reach the brain after intravenous administration.
7 se of their short half-life and the need for intravenous administration.
8 r compared with levels typically found after intravenous administration.
9 ntegrins was detected in the lungs 1 h after intravenous administration.
10 ially longer-circulating particles following intravenous administration.
11 assembled into 120 nm particles suitable for intravenous administration.
12  to lactate and alanine within seconds after intravenous administration.
13 n with mPEG reduced toxicity associated with intravenous administration.
14 relbine plasma exposure, both after oral and intravenous administration.
15 7) at a relatively high level after 2 h upon intravenous administration.
16 n tumour tissues versus normal tissues after intravenous administration.
17 in in experimental PD are observed following intravenous administration.
18 idly enter the mouse brain in vivo following intravenous administration.
19  refrigeration requirements and the need for intravenous administration.
20 ry of siRNA to proximal tubule cells follows intravenous administration.
21 n while achieving a similar concentration to intravenous administration.
22 o-blood ratio double what was observed after intravenous administration.
23 de, except in the United States, for oral or intravenous administration.
24 ld-type antibody in cynomolgus monkeys after intravenous administration.
25 od that can be achieved safely and simply by intravenous administration.
26 early all conditions, but particularly under intravenous administration.
27 itor for treatment of influenza infection by intravenous administration.
28  transport of plasmid DNA to the brain after intravenous administration.
29 cal barriers that a particle encounters upon intravenous administration.
30 rrier and deliver DNA to the brain following intravenous administration.
31 ity can occur in up to 60% of patients after intravenous administration.
32 ungs for treating acute lung injury (ALI) by intravenous administration.
33 trant" drugs were dosed to rats via oral and intravenous administration.
34 th the observed plasma clearance values upon intravenous administration.
35 ation of individual bacteria in tumors after intravenous administration.
36                                        After intravenous administration (5 mg/kg), systemic exposure
37 lic substrates in vitro and their subsequent intravenous administration allow both the location of th
38  biexponential pharmacokinetic profile after intravenous administration and a terminal half-life of a
39  efficiently transduce skeletal muscle after intravenous administration and have shown efficacy in th
40 ced miR-221 levels in liver within a week of intravenous administration and in situ hybridization stu
41    Unfavorable liposome biodistribution upon intravenous administration and membrane destabilization
42 nocrystals were determined immediately after intravenous administration and up to 48 h by scintillati
43 table, with effective doses of 9.5 muSv/MBq (intravenous administration) and 18.1 muSv/MBq (oral admi
44  the dose eliminated within 15 minutes after intravenous administration, and also not significantly a
45 ystemic therapeutic brain delivery following intravenous administration are also reviewed.
46                            Several routes of intravenous administration are discussed along with pati
47 asma concentrations than wild-type mice upon intravenous administration but higher concentrations upo
48 hosphonic acid 4a was observed in rats after intravenous administration, but partial conversion of 4c
49                                 Upon oral or intravenous administration, E. coli encoding shRNA again
50 nificantly greater with intracoronary versus intravenous administration: first bolus, 94+/-9% versus
51 dependent antinociceptive activity following intravenous administration in a chronic constriction inj
52  growth inhibition following intratumoral or intravenous administration in a mouse tumor model.
53 he IgG-GDNF fusion protein following delayed intravenous administration in acute stroke.
54 gold nanorods (GNRs) in various tissues upon intravenous administration in mice.
55 ic capsids displaying systemic tropism after intravenous administration in mice.
56 nctional delivery of mRNA to the lungs after intravenous administration in mice.
57 enetration of the brain parenchyma following intravenous administration in mice.
58 l activity, and in vivo efficacy by oral and intravenous administration in two rodent infection model
59  in vivo infectivity of the Ad vectors after intravenous administration into integrin alpha(v)beta(3)
60                                              Intravenous administration into LDL receptor null mice o
61           The drug-carrier association after intravenous administration is essential for efficient dr
62 n of radioactivity in different organs after intravenous administration is measured by whole body PET
63                                              Intravenous administration led to systemic efficacy agai
64                                      However intravenous administration more closely mimics human coc
65 nd were scanned using small-animal PET after intravenous administration of (11)C-(R)-PK11195 and by M
66 stational term, 172 d) were imaged after the intravenous administration of (11)C-verapamil (30-72 MBq
67                                        After intravenous administration of (125)I-labeled mouse album
68 age IV renal cell cancer was performed after intravenous administration of (15)O-water (10-min dynami
69 retherapy (18)F-FDG PET for which, after the intravenous administration of (18)F-FDG, both early (app
70 s (5 men, 4 women) for 190-440 min after the intravenous administration of (18)F-FPEB.
71 ion in the heart was studied over time after intravenous administration of (18)F-LMI1195 in healthy m
72                                        After intravenous administration of (18)F-RO6958948, (11)C-RO6
73  studies were performed in B6.SJL mice after intravenous administration of (63)Zn-zinc citrate.
74 n 24 h and were imaged as early as 3 h after intravenous administration of (99m)Tc-anti-CD56.
75 but only one of the tumors was ablated after intravenous administration of (99m)Tc-liposomal doxorubi
76 ography, all mice were scanned 2 hours after intravenous administration of 0.2 mmol/kg body weight of
77 5 was performed at baseline and 40 min after intravenous administration of 1 mg of BMS-207940 per kil
78                          In the adult mouse, intravenous administration of 1 x 10(11) vector genomes
79                                              Intravenous administration of 1.5 mg/kg anti-miR-155 loa
80                                              Intravenous administration of 1.5 mg/kg of ubiquitin (n
81  In a rhesus monkey model of EVD, once-daily intravenous administration of 10 mg kg(-1) GS-5734 for 1
82                  The data also show that the intravenous administration of 10(5) WBCs is sufficient t
83                           However, while the intravenous administration of 10(6) CD45(+) or CD4(+)/8(
84 phy of the lower limb (0.625-mm collimation, intravenous administration of 100 mL of iomeprol [400 mg
85 (CT) of the chest, abdomen, and pelvis after intravenous administration of 120 mL of iohexol (Omnipaq
86 derwent dynamic PET scans of the heart after intravenous administration of 126-240 MBq 18F-FBnTP.
87                                    Following intravenous administration of 15-A(2t)-IsoP containing s
88  scans per subject) for up to 48 h after the intravenous administration of 185 MBq (5 mCi) of (123)I-
89                                              Intravenous administration of 2 mg kg(-1) chemically mod
90 everal antiglaucoma drugs and improved after intravenous administration of 20% hyperosmotic glucose s
91 0-min dynamic PET/CT scan of the chest after intravenous administration of 200 MBq of (18)F-fluoromet
92 analyzed ex vivo at 3, 6, 24, and 96 h after intravenous administration of 25 mug of (89)Zr-MSB001085
93 sessed at 6 time points, up to 110 min after intravenous administration of 302 +/- 11 MBq of BAY 8643
94 nt 45-min dynamic PET/CT of the thorax after intravenous administration of 366.3 +/- 14.8 (337.44-394
95                                        After intravenous administration of 37 MBq (5 mg) of (89)Zr-fr
96 f the breasts and axillary regions 4 d after intravenous administration of 37 MBq of (89)Zr-bevacizum
97 nce of metastatic PCa were studied after the intravenous administration of 370 MBq (10 mCi) of (18)F-
98  (n = 8) underwent PET/CT of the chest after intravenous administration of 370 MBq of (18)F-fluciclov
99                                              Intravenous administration of 3A in naive rats decreased
100                                              Intravenous administration of 4.4 to Zucker diabetic fat
101                                              Intravenous administration of 4F-PCC 50, 25, or 10 IU/kg
102                   We compared the effects of intravenous administration of 6% hydroxyethyl starch (ma
103 fed Sprague-Dawley rats, respectively, using intravenous administration of [2-(13) C]-glycine and obs
104  spectroscopic acquisition immediately after intravenous administration of a 0.1 mmol/kg dose of hype
105                                        After intravenous administration of a diuretic, dual-phase CT
106 agnetic resonance (MR) images obtained after intravenous administration of a gadolinium-based contras
107                                              Intravenous administration of a green fluorescent protei
108  Ad5 liver transgene expression at 48 h post-intravenous administration of a high viral dose (1x10(1)
109       Each animal underwent MR imaging after intravenous administration of a high-molecular-weight co
110                         Adverse reactions to intravenous administration of a nonionic contrast materi
111                                              Intravenous administration of a novel recombinant rhesus
112 ation transfer) images on a 3T scanner after intravenous administration of a pH-responsive contrast a
113     PDT was performed 48 hours following the intravenous administration of a photosensitizer using li
114  changes in CNS activity within 15 min after intravenous administration of a physiological dose of 4
115 atients underwent cTACE with doxorubicin and intravenous administration of a placebo (cTACE-C) or bev
116 ncrease of Kir4.1 expression was obtained by intravenous administration of AAV9-gfaABC1D-Kir4.1-EGFP.
117 mages, to reveal colonic neoplasms after the intravenous administration of activatable "smart" probes
118  tissue and serum samples were confirmed via intravenous administration of Ad-tPA-Her.
119                     Hyperemia was induced by intravenous administration of adenosine triphosphate.
120  Translation of these findings revealed that intravenous administration of alpha2MG-microcapsules (bu
121                                          The intravenous administration of an adenoviral encoding Fst
122  in which neointima formation was induced by intravenous administration of an adenovirus that encoded
123                                We found that intravenous administration of an indole thiazole or a ga
124                        Furthermore, systemic intravenous administration of an miR-26a inhibitor, lock
125 a discrete cue (a light) associated with the intravenous administration of an opioid drug (the short-
126 ers, and radiotelemetric transducers for the intravenous administration of ANG II and the measurement
127 ers, and radiotelemetric transducers for the intravenous administration of ANG II and the measurement
128                                              Intravenous administration of antagomirs against miR-16,
129 ent consisted of removal of all hardware and intravenous administration of antibiotics.
130 f hematopoietic cells via intrabronchial and intravenous administration of antibodies within the same
131                                              Intravenous administration of AnxA1(2-50) markedly reduc
132 nsection (to remove sympathetic influences), intravenous administration of atropine increases LV cont
133                                              Intravenous administration of BB-FCF (1-100 mug kg(-1) )
134 Early termination of prolonged seizures with intravenous administration of benzodiazepines improves o
135 onstitutively active form of HIF-1alpha, and intravenous administration of BMDACs that were cultured
136                                              Intravenous administration of both probes resulted in hi
137                                              Intravenous administration of CAR peptide resulted in in
138 th stress cardiomyopathy precipitated by the intravenous administration of catecholamines and beta-re
139  2 W/cm(2), 50% duty cycle, 5 minutes) after intravenous administration of CBLuc with cationic, neutr
140 amuscular administration was not inferior to intravenous administration of ceftriaxone for bacterial
141                                        After intravenous administration of cholate to Oatp1b2-null mi
142                                              Intravenous administration of cLDL in mice accelerated a
143                                              Intravenous administration of CNH molecules in mice (C57
144 behavior in freely moving rats following the intravenous administration of cocaine.
145 ormal organs and tumor at 48h and 144h after intravenous administration of conjugates.
146  (corticomedullary and nephrographic phases) intravenous administration of contrast agent.
147 ted contrast-enhanced US was performed after intravenous administration of contrast material before t
148                     CT was performed without intravenous administration of contrast material in 155 p
149 wel occurs on average about 50 seconds after intravenous administration of contrast material or 14 se
150 T2-weighted sequences, was performed without intravenous administration of contrast material to evalu
151                     Thirty seconds after the intravenous administration of contrast material, a seria
152  at 60 seconds (UP) and 5 minutes (EP) after intravenous administration of contrast material.
153                    The results indicate that intravenous administration of curcumin before the onset
154          Recently, we have demonstrated that intravenous administration of curcumin limits burn injur
155                                              Intravenous administration of cyclic Arg-Gly-Asp-d-Phe-C
156  highly expressed in mouse erythrocytes, and intravenous administration of D-e-MAPP decreased both SP
157                                              Intravenous administration of DMI-4983 reduced infarct s
158                                        After intravenous administration of either (64)Cu-TP3939 or (6
159 nding expressed as SUVrs were compared after intravenous administration of either 111 MBq (3 mCi) or
160 ntervention (control, CONT) as well as after intravenous administration of either propranolol (PROP),
161 .0 T) 11 d postimplantation before and after intravenous administration of either Robo4- or alpha(V)b
162  with manganese intoxication associated with intravenous administration of ephedrone.
163 rdiomyopathy precipitated immediately by the intravenous administration of epinephrine (n = 6) or dob
164                                   Continuous intravenous administration of epoprostenol remains the t
165                                              Intravenous administration of etelcalcetide (n = 503) or
166                                              Intravenous administration of EV loaded in LPH-PEG-AA le
167 e were the first to test the hypothesis that intravenous administration of exogenous ghrelin acutely
168                                              Intravenous administration of exogenous ghrelin increase
169                                              Intravenous administration of Fab'-CCE conjugate, follow
170 furosemide stress test (FST), which involves intravenous administration of furosemide (1.0 or 1.5 mg/
171 ived from LNPs was detected seven days after intravenous administration of FXN LNPs, suggesting that
172 upt the BBB in rat somatosensory cortex, and intravenous administration of GABA then produced a dose-
173 ood flow (RBF) by using a technique based on intravenous administration of gadolinium chelate and eva
174 marrow contrast enhancement (NMCE) following intravenous administration of gadopentate dimeglumine.
175 liver parenchyma before and 20 minutes after intravenous administration of gadoxetic acid).
176 liver parenchyma before and 20 minutes after intravenous administration of gadoxetic acid.
177 ighted (DW) images acquired before and after intravenous administration of Gd-EOB-DTPA.
178                                              Intravenous administration of GE-137 leads to its accumu
179                                              Intravenous administration of ghrelin completely restore
180                                              Intravenous administration of GLP-1 elicited transient r
181                                              Intravenous administration of glucosamine causes insulin
182                                              Intravenous administration of GS-5734 to nonhuman primat
183        He was gradually relieved by repeated intravenous administration of high-dose corticosteroid,
184                                              Intravenous administration of HN3-PE38 alone, or in comb
185 lity barriers is modulated by intrathymic vs intravenous administration of HSCs.
186 mediated plasmonic photothermal therapy, and intravenous administration of HSP targeted HPMA copolyme
187 of this study was to determine the effect of intravenous administration of hUCB cells into a mouse mo
188                                              Intravenous administration of hybrid 13a (H-Dmt-d-Arg-Ab
189 d signals from fumarate and malate following intravenous administration of hyperpolarized fumarate wi
190 and the adaptive immune system, mitigated by intravenous administration of immunoglobulin-G, and link
191                                 Furthermore, intravenous administration of in vivo-jetPEI formulated
192  addition, a second rabbit was studied after intravenous administration of iodinated and tungsten clu
193 ad trauma who had undergone intraarterial or intravenous administration of iodinated contrast materia
194  highest perceived risk of postcontrast AKI, intravenous administration of iodixanol for contrast mat
195            All adverse events related to the intravenous administration of iopamidol during CT examin
196 ted the efficacy of twice- and thrice-weekly intravenous administration of ketamine in sustaining ini
197                                              Intravenous administration of KLe increases the level of
198      Systemic L-arginine depletion following intravenous administration of l-arginine hydrolyzing enz
199                                   Given that intravenous administration of L-arginine to human patien
200                                 In vivo, the intravenous administration of lactoferrin-bearing DAB de
201 is of the fusion protein in rabbit following intravenous administration of lipidated TN-ApoA1.
202 umor-bearing mice were imaged with FMT after intravenous administration of long-circulating near-infr
203 f contrast material in 155 patients and with intravenous administration of low-osmolality contrast ma
204                                              Intravenous administration of low-osmolality contrast ma
205 id not significantly differ before and after intravenous administration of low-osmolar CT contrast.
206 ansient increase in blood pressure following intravenous administration of LPA to mice.
207                                              Intravenous administration of M8-B was more effective in
208                                              Intravenous administration of MAA both induced tolerance
209 rom co-culture experiments demonstrated that intravenous administration of MAA led to the generation
210 LDK procurement, we changed the protocol for intravenous administration of mannitol (i.e., 12.5 or 25
211                                    Following intravenous administration of model and biodegradable BP
212                 If this hypothesis is valid, intravenous administration of MSCs should improve outcom
213  systemic hypertension induced by subsequent intravenous administration of murine tetrameric hemoglob
214                                     Notably, intravenous administration of mutant CXCL12 also inhibit
215                                              Intravenous administration of Na(125)I-filled glyco-sing
216                        Finally, we show that intravenous administration of NAADP-AM into anesthetized
217 tractive option for cancer gene therapy, the intravenous administration of naked Ad still encounters
218                    However, the conventional intravenous administration of nanoparticles for detoxifi
219                                              Intravenous administration of NEP to wild-type and APP23
220 ute baseline emission scans were followed by intravenous administration of nicotine (1.5 mg/70 kg bod
221                                 Importantly, intravenous administration of nitrated CCL2 also inhibit
222                                              Intravenous administration of OPN-305 before reperfusion
223                                   Once-daily intravenous administration of oritavancin was effective
224                        Some mice received an intravenous administration of OX40-activating antibody o
225                                              Intravenous administration of OxoM (0.01-5 microg/kg) di
226                             We conclude that intravenous administration of PEG-asparaginase is tolera
227                 Thirty minutes after oral or intravenous administration of PhIP (1 mg/kg), the PhIP l
228      Photodynamic therapy (PDT) involves the intravenous administration of photosensitizers followed
229 en patients with NSCLC underwent CT prior to intravenous administration of pimonidazole (0.5 g/m(2)),
230                                          The intravenous administration of PN2KPI into WT mice dramat
231                                              Intravenous administration of PN2KPI prolonged the clott
232                                              Intravenous administration of polyclonal and monoclonal
233                                              Intravenous administration of prophylactic IL-22 signifi
234                                              Intravenous administration of recombinant sialidase incr
235                                              Intravenous administration of recombinant tissue plasmin
236                                              Intravenous administration of recombinant TRX in wild-ty
237                We previously determined that intravenous administration of rituximab results in limit
238 ncy did not influence bacterial growth after intravenous administration of S. pneumoniae.
239 d, double-blinded, crossover study, with 2-h intravenous administration of saline, GIP, or GLP-1.
240 (11)C-Cimbi717 to 5-HT7R was investigated by intravenous administration of SB-269970 before a second
241 neurotoxic effects of scorpion envenomation, intravenous administration of scorpion-specific F(ab')(2
242 ematoma, underwent a CE-US examination after intravenous administration of sculpture hexafluoride (do
243                                              Intravenous administration of sodium nitrite (48 nmol) 5
244                                     Systemic intravenous administration of sodium nitrite (8.7 mumol/
245 n-specific CD8(+) T cells in the liver after intravenous administration of soluble protein antigen.
246 missing EDA was compensated for by postnatal intravenous administration of soluble recombinant EDA.
247 cell population and toxicity associated with intravenous administration of synthetic RNAs and carrier
248 ic resonance imaging (MRI) and enhance after intravenous administration of the contrast medium.
249 ey radiotracer activity to fall by 50% after intravenous administration of the diuretic (T1/2).
250                                          The intravenous administration of the drug ensures complianc
251 onal MRI, we determined the acute effects of intravenous administration of the GLP-1 receptor agonist
252 te the delay in glucose uptake observed with intravenous administration of the hormone.
253 erm mortality between patients who underwent intravenous administration of the iso-osmolar contrast m
254                                     Finally, intravenous administration of the luciferase reporter Ni
255                                              Intravenous administration of the MagMBs to mice bearing
256                  We previously reported that intravenous administration of the N-methyl-D-aspartate a
257 ated to enable transport across the BBB, the intravenous administration of the neurotrophin results i
258 ol condition in response to noxious heat and intravenous administration of the opioid antagonist nalo
259                                              Intravenous administration of the PLL-dendrimer molecule
260                     Up to 48 hours after the intravenous administration of the TNF-alpha antagonist i
261                          Here we report that intravenous administration of the Toll-like receptor 7 (
262                        Radiation doses after intravenous administration of the tracer in mice and pig
263                                              Intravenous administration of the XO inhibitor allopurin
264                 Significantly, a single-dose intravenous administration of these small neutral NPs lo
265 tection can be achieved through a peripheral intravenous administration of this agent after the initi
266                     Our results suggest that intravenous administration of this vaccine will lead to
267                                              Intravenous administration of this vector resulted in ap
268                             In addition, the intravenous administration of tocotrienol entrapped in t
269                                              Intravenous administration of tPA increased circulating
270 skeletal muscle of healthy volunteers during intravenous administration of triglycerides plus heparin
271 c or physiologic changes were observed after intravenous administration of up to 1.3 mug of (18)F-FEO
272 e of Blood, Pitchford et al demonstrate that intravenous administration of VEGF-A promotes megakaryoc
273 recting blood-related diseases is the direct intravenous administration of viral vectors, so-called i
274 spite the apparent low infectious titer, the intravenous administration of white blood cells (WBC) re
275 be restored to leukotriene-deficient mice by intravenous administration of wild-type neutrophils.
276 f ziconotide in CSF following intranasal and intravenous administration of ziconotide solution was fo
277 ar: r = 0.173, P = .42.) Conclusion Multiple intravenous administrations of these macrocyclic GBCAs i
278 frame count (cTFC) with intracoronary versus intravenous administration: pre-PCI, 36 (median) (25th a
279                                 Furthermore, intravenous administration (pretreatment) of CocE-L169K/
280  complement-mediated phagocytosis, and their intravenous administration resulted in high animal morta
281  miR-21i and Dox using HGNPs under NIR after intravenous administration showed high tumor accumulatio
282 occur in the body as a result of therapeutic intravenous administration, surgery, infections or decom
283 of different size has been studied following intravenous administration, the fate of LNCs following p
284                          Additionally, after intravenous administration, the labeled reagents had the
285 cally induced and xenograft tumors following intravenous administration, thereby enabling site-specif
286 nanoparticles on their journey from point of intravenous administration to desired destinations such
287  well as its excretion profile following its intravenous administration to male Sprague-Dawley rats.
288                                          Its intravenous administration to mice and Wistar rats gener
289 compared to the protein (R(h): 3.0 nm) after intravenous administration to mice.
290 f (89)Zr-AMG 110 was studied up to 6 d after intravenous administration to nude BALB/c mice bearing h
291 ctor to mediate systemic gene delivery after intravenous administration to perinatal mice and late-ge
292                                    Following intravenous administration to rodents, 3 exhibits brain
293 xtracellular calcium in vitro or by means of intravenous administration to sensitized mice in vivo be
294 d increase in tumor accumulation, 24 h after intravenous administration to tumor-bearing mice, compar
295                      Additionally, following intravenous administration w-MWNTs-ANG showed significan
296                           In most cases, the intravenous administration was more effective.
297 Cmax and Tmax of ziconotide in CSF following intravenous administration were found to be 37.78+/-6.8n
298                                    Following intravenous administration, wild-type CXCL12 was cleared
299 ird day for experimental period after single intravenous administration with ABP/TSTA-SP-exendin-4.
300                                     Systemic intravenous administration without immunosuppression res

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