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1 ignificantly lower mortality than short-term infusion.
2 owing a 7-day noradrenaline (norepinephrine) infusion.
3 hese effects were reversed by corticosterone infusion.
4 ood glucose 146 +/- 2 mg/dL) with portal GLC infusion.
5 ot affected by cold exposure or phentolamine infusion.
6 to 29 months, and 8 progressed after T-cell infusion.
7 ted in bones treated with a CXCR4 antagonist infusion.
8 ernight SAL infusion followed by SAL/OCT/INS infusion.
9 g the effectiveness of prolonged beta-lactam infusion.
10 and predominantly occurred during the first infusion.
11 nous glucose production (EGP) during insulin infusion.
12 th the use of a [1-(13)C]leucine intravenous infusion.
13 cell responses from baseline to day 28 after infusion.
14 undergoing islet transplants within hours of infusion.
15 EAs after the 20-25 min intravenous insulin infusion.
16 lex mismatched BMT with or without Treg cell infusion.
17 ticipation of monetary reward and an alcohol infusion.
18 rall used 91% less factor than before vector infusion.
19 verse events occurred during or after vector infusion.
20 eral blood chimerism was assessed after each infusion.
21 occurred a median of 6 days after CAR-T-cell infusion.
22 ad and mercury in the dry product and in the infusion.
23 d in 28-day cycles by continuous intravenous infusion.
24 erfusion, or who are receiving a vasopressor infusion.
25 vasopressin (0.03 U/min.) or norepinephrine infusions.
26 m order with a 28-day washout period between infusions.
27 kines were seen after the first BV plus Nivo infusions.
28 ulation, with the use of sedative and opioid infusions.
29 7%) of 30 patients remained on once per week infusions.
32 hloremia during treatment with continuous IV infusion 3% hypertonic saline, with moderate hyperchlore
33 utput syndrome with need for a catecholamine infusion 48 hours after study drug initiation, need for
34 in healthy lean males: A) 10-h overnight GCG infusion (6 ng/[kg x min]) followed by 3-h infusion of G
36 hindered GVT effects by the combined T-cell infusion, a single injection of picogram amounts of NGR-
38 e showed that a 30-min intraduodenal glucose infusion activated half of all duodenal L cells in human
39 s with septic shock who received vasopressin infusion added to at least one concomitant vasopressor a
40 (N=19, 26.8%)) received mood ratings before infusion, after infusion, and for the subsequent 14 days
41 by 1.27-8.82-times compared with accelerated infusion alteplase plus parenteral anticoagulants (RR 1.
42 % CI, 4.1-27.2 months) from the first T-cell infusion and 24.5 months (95% CI, 17.2-34.6 months) from
43 of safety and usability by combining insulin infusion and continuous glucose measurement in a single-
44 s into the polyphenol content of jujube leaf infusion and their antioxidant activities, a 2,2-dipheny
45 d in the lungs immediately after intravenous infusion and their survival time in the host is inconsis
46 mprove depressive symptoms within 24 h after infusion and this antidepressant effect was attributed t
47 either subcutaneously or by intravenous (IV) infusion and to assess the pharmacokinetics and in vitro
48 ated the intraportal versus systemic insulin infusion and transendothelial transport of insulin, we p
49 ncentrations of elamipretide occurred at end-infusion and were undetectable by 24 hours postinfusion.
50 proteins to an expanded LD pool during lipid infusion and, via this adaptation, may support the stora
51 gical insight, e.g. the need for intravenous infusions and restriction to short-term studies (hours)
52 OP (-/-) rats were tested for heroin (20 mug/infusion) and ethanol (10% v/v) self-administration, the
53 inemic euglycemia (bolus insulin and glucose infusion), and 3) saline control with skeletal muscle bi
55 appeared more effective than intra-arterial infusion, and mobilized peripheral blood mononuclear cel
56 ein (hsCRP), FMDBA after acute ascorbic acid infusion, and vascular endothelial cell protein expressi
57 y, the total contents, leachability into tea infusions, and bioaccessibility of lithium from black, E
58 7% respondents administer sedative/analgesic infusions, and the sedation target was "sedated" or "ver
59 aline (SAL) infusion followed by GCG/OCT/INS infusion; and C) overnight SAL infusion followed by SAL/
60 infected persons, single low-dose BMS-936559 infusions appeared to enhance HIV-1-specific immunity in
62 rther promote the consumption of jujube leaf infusion as a healthy antioxidant bedtime beverage, and
64 everity was the only factor after CAR-T-cell infusion associated with infection in a multivariable an
65 ommon isatuximab-related adverse events were infusion-associated reactions (IARs) (56%), which were g
66 ent of cells for 24h with lyophilized coffee infusions at the highest dose without cytotoxic effects
68 agonist) during ATP or control vasodilatator infusion, before and after KIR channel inhibition alone
69 inhibitory mold agar (IMA), and brain heart infusion (BHI) agar with chloramphenicol and gentamicin.
70 ng (CGM) and continuous subcutaneous insulin infusion can be used to improve the treatment of patient
72 epigenetic changes induced by continuous GH infusion (cGH) in male mice, which rapidly feminizes the
76 tions (MDI), continuous subcutaneous insulin infusion (CSII) and islet transplantation to reduce hypo
77 ump therapy (continuous subcutaneous insulin infusion; CSII) in patients with type 1 diabetes using c
78 82; 95% CI, 0.68-0.98), and fewer vasoactive infusion days (3.0 vs 3.3 d; p < 0.001) when compared wi
80 matory cardiovascular dysfunction, apelin-13 infusion delivers distinct and optimized hemodynamic sup
83 nges in cardiac troponin T levels during the infusion did not differ between the two groups in the 55
84 G-CSF with or without haemopoietic stem-cell infusion did not improve liver dysfunction or fibrosis a
85 rong burst of thrombin and plasmin, FXa/PCPS infusion did not produce measurable levels of complement
86 To determine whether fibrinogen concentrate infusion dosed to achieve a plasma fibrinogen level of 2
88 or 1000 mg meropenem (by 30-min intravenous infusion every 8 h) for 7-14 days; regimens were adjuste
89 ime and 500 mg avibactam (by 2 h intravenous infusion every 8 h) or 1000 mg meropenem (by 30-min intr
90 received avelumab (10 mg/kg, 1 h intravenous infusion) every 2 weeks until confirmed disease progress
91 he activity enhancement in the two-component infusion evidently results from a cooperative effect in
92 ments, including imaging experiments, direct infusion experiments, and experiments employing liquid c
93 basal replacement; B) overnight saline (SAL) infusion followed by GCG/OCT/INS infusion; and C) overni
95 C/EC) coculture system as well as in vivo EC infusions following myelosuppressive injury in mice to d
96 atment period, subjects underwent a ketamine infusion for 75 min during which the effects of PF-04958
98 treatment with serelaxin intravenous (i.v.) infusion (for 60 min at 80 mug/kg/d and then 60 min at 3
99 o enhance the standard of care by decreasing infusion frequency to increase compliance, promoting pro
101 ere more frequent the in G-CSF and stem-cell infusion group (12 [43%] patients) than in the G-CSF (th
105 ials used as ingredients of herbal and fruit infusions (HFI) were analysed by means of ICP-MS for the
107 sal hippocampal, ventral hippocampal, or ACC infusions immediately 'before' testing (retrieval) did n
108 cells by pancreatic intra-ductal AAV8-shAtg7 infusion in C57BL/6 mice, resulted in decreased beta cel
111 during US presentations or in the ITI) after infusion in mPFC, whereas LMA was increased (after infus
112 autologous CD34+ cell (CLBS10) intracoronary infusion in patients with left ventricular dysfunction p
114 dex, received either a 6 h lipid or glycerol infusion in the setting of a concurrent hyperinsulinaemi
120 responses is provided by evidence that HMGB1 infusion into the hippocampus was sufficient to cause an
121 al(+/-) mice were replicated by oxotremorine infusion into the striatum, but not into the cerebellum,
123 as well as weekly maternal IV immunoglobulin infusion (IVIG), with or without additional corticostero
124 h different timing, both FXa/PCPS and E coli infusion led to robust thrombin and plasmin generation.
126 An Angiotensin II (AngII)-aldosterone (Ald) infusion mouse model of hypertension was utilised in thi
127 secutive cohorts, 0.3-100 mg/kg) or 4 weekly infusions (n = 16; 2 consecutive cohorts, 30 and 60 mg/k
128 d showed that in the presence of the alcohol infusion, nalmefene significantly reduced the BOLD respo
129 entional dosing of 16 g/2 g/24 hr continuous infusion, obese patients were more likely than nonobese
130 lmonary embolism was induced by jugular vein infusion of (125)I-fibrin or fluorescein isothiocyanate-
131 hanced nitrogen flux into the urea cycle and infusion of (15)N-arginine shows that Arg2 loss causes s
135 racranial multiphoton imaging, we found that infusion of 100 ng of HIV-1 Tat into the lateral ventric
139 ier and the value calculated from the simple infusion of a solution of polymer into the commercial at
143 targets in these neurons and show that local infusion of agonists for specific receptors on these neu
144 cal treatment were randomized to intravenous infusion of allogenic UC-MSCs (Cellistem, Cells for Cell
145 d therapy, streptokinase and non-accelerated infusion of alteplase were significantly associated with
150 purate), BP, and hemodynamic responses to an infusion of angiotensin II (assessment of intrarenal ren
152 ous or >/=3 h) versus short-term (</=60 min) infusion of antipseudomonal beta-lactams for the treatme
153 effectiveness of prolonged versus short-term infusion of antipseudomonal beta-lactams in patients wit
157 However, the responses after intracoronary infusion of autologous bone marrow-derived mononuclear c
158 be also delivered intratumorally, including infusion of autologous dendritic cells and even tumor-re
159 for 5 days, followed by a single intravenous infusion of autologous TILs and high-dose interleukin-2
161 trieval of non-social and social memory, icv infusion of BIBO3304 trifluoroacetate and BIIE0246 block
162 dministration of caspase-1 inhibitors or the infusion of bone marrow-derived macrophages genetically
163 In women with severe post-partum depression, infusion of brexanolone resulted in a significant and cl
165 Lymphodepletion chemotherapy followed by infusion of CD19-specific chimeric antigen receptor-modi
167 oproteins was studied using a stable isotope infusion of D3-leucine, gas chromatography/mass spectrom
169 Collectively, these findings suggest that infusion of donor ILC2s to restore gastrointestinal trac
170 failure to receive a continuous intravenous infusion of either ularitide at a dose of 15 ng per kilo
171 tion fraction and demonstrates that a single infusion of elamipretide is safe and well tolerated.
172 ize the vascular effects of a mixed meal and infusion of exogenous glucose-dependent insulinotropic p
175 G infusion (6 ng/[kg x min]) followed by 3-h infusion of GCG, octreotide (OCT), and insulin (INS) for
176 ats was also attenuated (n = 7; P < 0.01) by infusion of gp91ds-tat, a peptide that blocks the activi
180 ugh a central osmoreceptor; however, central infusion of hypertonic NaCl produces a greater sympathoe
184 intervention group (n=14) received a single infusion of MSC (1.0 x 10(5) or 2.5 x 10(5) cells/kg; n=
186 hemoablation with ethanol lavage followed by infusion of paclitaxel is effective for the treatment of
187 vascular conductance (FVC) to intra-arterial infusion of phenylephrine (PE; alpha1 -agonist) during A
194 platelet IgG Fc receptor IIA (FcgammaRIIA), infusion of the HIT-like monoclonal antibody KKO increas
198 sed ultrasound (pFUS) combined with systemic infusion of ultrasound contrast agent microbubbles (MB)
199 oppler) were measured before and after rapid infusion of warmed saline (15 mL kg(-1) , approximately
203 individuals with schizophrenia to 3 monthly infusions of 8 mg/kg tocilizumab or placebo (normal sali
205 ually to receive 15 double-blind intravenous infusions of adjunctive lanicemine 50 mg, lanicemine 100
206 edly higher locomotor responses to intra-VTA infusions of AMPA, suggesting a paradoxical increase in
211 ways was achieved using unilateral intra-PFC infusions of DA antagonists combined with contralateral
212 In the present work, the edible petals and infusions of dahlia, rose, calendula and centaurea, were
214 arm blood flow in response to intra-arterial infusions of endothelial-dependent and -independent vaso
216 al (i.p.) doses of ketamine or memantine, or infusions of memantine directly into the prelimbic (PLmP
225 , and biomechanics under acute or continuous infusions of the apelinergic agonists ELA or Apelin-13 (
227 ur cycles of 175 mg/m(2) paclitaxel as a 3 h infusion on day 1 every 3 weeks) or epirubicin, cyclopho
229 Conversely, we found no effect of tiron infusion on the pressor reflex in rats with patent femor
230 f these pregnancies with prophylactic plasma infusions (one pregnancy resulted in p-aHUS, one intraut
232 ents of composite processing including resin infusion, onset of crosslinking, gel time, degree and ra
233 , we discovered that intracerebroventricular infusion or local OVLT injection of hypertonic NaCl incr
236 L-leucovorin 175 mg or D,L-leucovorin 350 mg infusion over 2 h, and 400 mg/m(2) bolus fluorouracil fo
237 Gramont chemotherapy; 85 mg/m(2) oxaliplatin infusion over 2 h, L-leucovorin 175 mg or D,L-leucovorin
239 nezumab (15 mg/kg) or placebo as intravenous infusions over 1 h every 2 weeks for 46 weeks, followed
242 tive lever press resulted in an i.v. cocaine infusion paired with one of two cues that alternated wit
244 iotracer was administered using a bolus-plus-infusion protocol, the arterial input function was measu
245 ans using rubidium-82 with various adenosine infusion protocols identified (1) the protocol with maxi
246 ppearance (glucose RA) during three separate infusion protocols in healthy lean males: A) 10-h overni
247 igate whether perioperative hepatic arterial infusion pump chemotherapy (HAI) was associated with ove
251 al by immune cells and may contribute toward infusion-related adverse effects such as allergic respon
252 of any grade were fatigue/asthenia (31.8%), infusion-related reaction (20.5%), and nausea (11.4%).
253 ade were fatigue (46 [25%] of 184 patients), infusion-related reaction (38 [21%]), and nausea (23 [13
254 n (occurring in more than two patients) were infusion-related reaction (four [2%] patients) and incre
256 effect of NPS seen after i.c.v. or intra-PVN infusion requires responsive OXT neurons of the PVN and
258 b(-/-)) mice and intravenous myeloperoxidase infusion revealed that neutrophil infiltration is a prer
260 ignificantly increased the number of alcohol infusions self-administered (percent change: 24.97+/-10.
261 356, 494) were achieved 1 hour after the IV infusion series of 30 mg/kg and 10 mg/kg doses, respecti
264 1) and in two patients in the placebo group (infusion site pain, n=1; tension headache, n=1); one pat
267 who participated in an intravenous nicotine infusion study that followed overnight smoking abstinenc
269 nfirmed or excluded by an intravenous saline infusion test or captopril challenge test and subtype di
270 showed a higher urinary pH at the end of the infusion than patients randomized to the saline group (n
272 lative to baseline at greater than 24 h post-infusion, the most robust reduction observed to date in
273 ltrasound (cerebral blood flow) and constant infusion thermodilution (femoral blood flow) with net ex
276 ancreatic clamping with a [U-(13)C]palmitate infusion to determine the insulin concentration needed t
278 mposite end point of prolonged catecholamine infusion, use of left ventricular mechanical assist devi
281 rate by IWCLL imaging criteria 4 weeks after infusion was 74% (CR, 4/19, 21%; PR, 10/19, 53%), and 15
283 in the pgACC caused by ketamine at 24 h post infusion was reproduced in an enlarged sample (placebo,
285 itabine 1000 mg/m(2) as a 30-min intravenous infusion, weekly, for 7 weeks followed by a 1-week break
288 Th, and U) in green coffee samples and their infusions were determined by using inductively coupled p
289 f catechins and other phenolics in green tea infusions were monitored using fast HPLC/MS separation.
290 eparation, the antioxidant properties of the infusions were monitored using two spectrophotometric me
293 y injury, and shorter duration of vasoactive infusions when compared with exclusive use of unbalanced
294 ct intramyocardial injection and intravenous infusion, whereas intracoronary infusion demonstrated no
295 al bone-marrow recovery within 5 days of HSC infusion, which was up to 20 days before engraftment bec
296 ase in LV end-diastolic pressure with saline infusion, while enhancing the saline-mediated increase i
297 tients (23%) within 28 days after CAR-T-cell infusion with an infection density of 1.19 infections fo
299 tly 15.7% higher than the 4-minute adenosine infusion with rubidium-82 injection at 2 minutes and sig
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