1 mexiletine restored their sodium current and
administration of mexiletine to 1 carrier of this mutati
2 ogic changes were observed after intravenous
administration of up to 1.3 mug of (18)F-FEOBV.
3 ed doses to normal organs allow for the safe
administration of up to 550 MBq, which is sufficient for
4 Concurrent
administration of rifampicin led to 68%, 23%, and 10% de
5 A 14-day intracerebroventricular
administration of CYCLO to 8-month-old TgCRND8 mice that
6 Subcutaneous
administration of NRTN to 8-week-old male ZDF rats preve
7 Accordingly, systemic
administration of Cxcl9 led to a strong attenuation of n
8 In mice, intravenous or sublingual
administration of ICM led to a reduction in radiotracer
9 Chronic
administration of platensimycin led to a net reduction i
10 Sustained oral
administration of the compound to a variety of animal mo
11 Administration of trehalose to a mouse model of Batten d
12 Finally, central
administration of alphaCGRP to adult hybrid mice increas
13 Administration of R848 to adult SAMP mice increased migr
14 scabies control: standard care involving the
administration of permethrin to affected persons and the
15 The
administration of JAK inhibitor to aged mice for 10 wk a
16 ed strong motivation to acquire operant self-
administration of opportunities to aggress and relapse v
17 Administration of 1-azidoanthracene to albino stage 40-4
18 aryngoscopic equipment, has allowed the safe
administration of anaesthesia to almost all children wit
19 time-dependent manner in response to in vivo
administration of drugs known to alter dopamine release.
20 After i.m.
administration of Ag adsorbed to alum, we showed that al
21 In rats,
administration of T3 led to an increased cytoplasmic sta
22 In vivo experiments showed that a single
administration of WAY200070 leads to an increase in plas
23 Administration of PGE2 to Apc(Min/+) mice increased tumo
24 Administration of bifunctionalized liposomes to APP/pres
25 Administration of 2-PMAP to APPSW /PS1dE9 mice reduced b
26 med before and approximately 24 h after oral
administration of SEP-225289, to assess occupancy at tro
27 Additionally,
administration of IGF-1 to Atg5(f/f);Aqp5-Cre mice did n
28 Furthermore,
administration of Slit2 to atherosclerosis-prone LDL rec
29 Oral
administration of compound 28 to athymic nude mice impla
30 dings of this study also indicate that acute
administration of ketamine fails to attenuate CSDS-induc
31 The study focuses the dose
administration of dabigatran to avoid the deaths due to
32 Blockade of type I IFN receptor or
administration of IL-1beta to Axl(-/-) mice restored the
33 Administration of ATRA to B6 mice in which EAU was induc
34 The
administration of DT to B6.Foxp3(DTR) recipients with ac
35 Intranasal
administration of CLH001 to BALB/c and NOD SCID gamma (N
36 In this preliminary trial,
administration of MPCs appeared to be safe, and there wa
37 Exocrine regeneration was impaired following
administration of cerulein to Bmi1(-/-) mice.
38 ons including 35 original reports describing
administration of thyroid hormone to brain-dead potentia
39 Additionally,
administration of fucosylated oligosaccharides to C. rod
40 rtheless, the challenges associated with the
administration of native proteins to C. elegans have lim
41 Exogenous
administration of recombinant CCL5 to C3aR-deficient mic
42 egnancy failure was largely inhibited by the
administration of neutralizing Ab to C5.
43 Intraperitoneal
administration of iCRT3 to C57BL/6 mice, subjected to ce
44 but that this response is prevented by prior
administration of DT to CD11b-DTR mice.
45 hs through depletion of CD11c(high) cells by
administration of diphtheria toxin to CD11c.DOG mice.
46 acid feeding, and this is abrogated by oral
administration of EGCG prior to challenge.
47 many impediments to acceptable and accurate
administration of medicines to children.
48 Administration of TIV to children who previously receive
49 In immunotherapy experiments,
administration of bNAbs to chronically infected animals
50 Administration of doxycycline to Clara cell secretory pr
51 Administration of B-I09 to CLL tumor-bearing mice suppre
52 Acute
administration of exenatide to comatose patients in the
53 d increased immune cell activation following
administration of PapMV to complement-depleted mice.
54 Administration of ACTs to contacts of patients with Ebol
55 This effect could partly be reversed by
administration of PGE2 to COX-2 mice.
56 Therefore, after sequential
administration of magnetic attraction to CPT-loaded FA-C
57 The
administration of ESAs to critically ill trauma patients
58 Administration of LPS to CTRP9-KO mice also resulted in
59 Administration of CBD to cultured human sebocytes and hu
60 Intrascrotal
administration of Gal-3 to CX3CR1(gfp/+) mice confirmed
61 Administration of an inhibitor to cyclooxygenase-2, the
62 A single
administration of 27C3 to cynomolgus monkeys led to a ra
63 Administration of bardoxolone methyl to cynomolgus monke
64 Administration of LR17938 to dam-fed rats significantly
65 Administration of Sulf2 ASO to db/db mice suppressed hep
66 Administration of these compounds to Delta7 mice, a mode
67 In addition, the
administration of purified PT to DeltaPT(high)-infected
68 Furthermore, we demonstrate that
administration of tamoxifen to demyelinated rats in vivo
69 tion, and reinstatement of intragastric self-
administration of lipid emulsions to determine the exten
70 Further,
administration of EGCG to dextran sodium sulfate-induced
71 Subcutaneous
administration of CD to diabetic BTBR (black and tan, br
72 Daily
administration of quercetin to diabetic pregnant mice du
73 In addition,
administration of ketamine led to differential regulatio
74 We conclude that
administration of CD47mAb400 to donor grafts may reduce
75 Administration of CD47mAb400 to donor livers increased r
76 Administration of actin to Drosophila melanogaster trigg
77 Finally, therapeutic
administration of fingolimod to EAE mice hampered astroc
78 Oral
administration of ABT263 to either sublethally irradiate
79 Systemic
administration of neutralizing Abs to either TNF-alpha o
80 Moreover, chronic
administration of penfluridol failed to elicit significa
81 npregnant women for telephone follow-up, and
administration of informed consent to eligible women.
82 WHO's provisional strategy of biannual mass
administration of albendazole to eliminate lymphatic fil
83 Administration of cyclosporine-A to enhance graft surviv
84 sequences, was performed without intravenous
administration of contrast material to evaluate the brai
85 This substudy of the Intravenous and Oral
Administration of Elinogrel to Evaluate Tolerability and
86 Moreover, repeated
administration of senktide to female rats with pubertal
87 Administration of IFN-alpha to females induced anti-card
88 Administration of antibiotics to food animals may select
89 Administration of specific IgG to food allergy-prone IL4
90 Administration of IFN-gamma to G2A(-/-) mice during dext
91 Moreover, in vivo
administration of NOD1 ligand to germ-free mice restored
92 In contrast,
administration of ganciclovir to Gfap(HSV-TK) mice elimi
93 Administration of glucosamine to GFP-LC3-transgenic mice
94 Chronic in vivo
administration of isoproterenol to guinea pigs reduced I
95 Conversely,
administration of rosuvastatin (RSV) to hamsters increas
96 the basis of the current study results, the
administration of antibiotics appears to have no clinica
97 Administration of 1F5 to hCD27-Tg mice enhanced Ag-speci
98 Intradermal
administration of BoNT-A to healthy volunteers produced
99 The
administration of endotoxin to healthy humans reduces ce
100 Exogenous
administration of IL-37 to healthy mice, not subjected t
101 Administration of LSD to healthy subjects produced prono
102 Strikingly, 3 days or more of oral
administration of Maraviroc to healthy volunteers confer
103 ory FVIII antibodies, allowing for effective
administration of FVIII to hemophilia mice to prevent bl
104 Additionally, timely
administration of hepcidin agonists to hepcidin-deficien
105 validation of NLRP3 priming in vivo involved
administration of lipopolysaccharide (LPS) to HIV transg
106 Recently, we demonstrated that
administration of chemotherapy to human bladder cancer x
107 Administration of chymase to human bronchial rings abrog
108 Given that intravenous
administration of L-arginine to human patients is well t
109 The
administration of nitrite to human primary myotubes acut
110 Oral
administration of RG7112 to human xenograft-bearing mice
111 cially for benralizumab, although reports of
administration of these antibodies to humans suggest tha
112 Subcutaneous
administration of 34 to hyperglycemic Kuo Kondo rats car
113 Administration of BBR to hyperlipidemic mice and hamster
114 Administration of fungicide to hypersensitive rats reduc
115 rmed before and after i.v. or intrapulmonary
administration of the nanoparticles to identify and segm
116 Furthermore,
administration of HBD peptide to Igfbp2(-/-) mice increa
117 The
administration of ILY to ihCD59+ mice crossed with vario
118 Subconjunctival
administration of neutralizing Ab to IL-6 blocked lympha
119 Administration of CoPP to Il10(-/-) mice before transiti
120 dies herein investigated alternatives to CIV
administration of pinometostat to improve patient conven
121 udies in the mdx mouse demonstrate that oral
administration of SMT022357 leads to increased utrophin
122 Administration of HBIG to infants born to HBeAg-negative
123 Administration of rAAV:Fst to innervated or denervated m
124 In vivo
administration of these compounds to insulin resistant C
125 ting HSCs and progenitor cells, and systemic
administration of Dkk1 to irradiated mice increased hema
126 In vitro
administration of DT to isolated islets significantly re
127 Administration of FTY720 to JHMV-infected mice resulted
128 Administration of acetaminophen to Jnk(Deltahepa) mice p
129 Administration of LM-Kras to KPC mice 4-6 weeks old (wit
130 Administration of 27HC to Ldlr(-/-) mice, following the
131 Weekly
administration of PF-06747143 to leukemic mice significa
132 hical and economic perspectives on mass drug
administration of primaquine to limit transmission of P.
133 Administration of dexamethasone to live mice recapitulat
134 Furthermore,
administration of JH4 to LmnaG609G/G609G-mutant mice, wh
135 Collectively, our data suggest that
administration of IL-2 to lupus-prone mice protects agai
136 Administration of recombinant IL6 to LysM-Cre; Egfr(f/f)
137 ne model, we demonstrated that endobronchial
administration of antibodies (Abs) to major histocompati
138 In contrast,
administration of disodium cromoglycate to mast cell-def
139 recovery in function observed after systemic
administration of BMSCs to MCAO rats is likely due to th
140 nce of benefit or harm with the prophylactic
administration of pantoprazole to mechanically ventilate
141 Administration of rIL18 to Mefv-/- mice reduced epitheli
142 Administration of GLP-2 to men causes the release of chy
143 We demonstrated that intrabronchial
administration of antibodies to MHC class I resulted in
144 Administration of (S)-CPP to mice leads to the full acti
145 Administration of 14g to mice produced a significant, do
146 The oral
administration of 3d to mice translated into preferentia
147 ssion assays following central or peripheral
administration of AAs to mice in vivo.
148 We previously demonstrated that
administration of Akkermansia muciniphila to mice preven
149 Oral
administration of anti-CD3 to mice induces changes in th
150 Administration of antibiotics to mice on the high-fiber
151 Here we show that systemic
administration of apoptotic cells to mice induced spleni
152 Intracerebroventricular
administration of BMP7 to mice led to an acute decrease
153 in vitro and to initiate tumors in vivo Oral
administration of CBL0137 to mice bearing orthotopic GBM
154 Oral
administration of CDDO-Me to mice with SMAD4-deficient T
155 After systemic
administration of diaCEST liposomes to mice bearing CT26
156 Administration of dinaciclib to mice bearing MLL-AF9-dri
157 Administration of DNase I to mice reduced neutrophil inf
158 NETs were depleted by
administration of DNase I to mice.
159 Administration of DOX to mice suppressed cardiac SIRT3 e
160 Administration of Dp44mT to mice catalyzed metHb and car
161 Administration of duvelisib to mice engrafted with a PTC
162 Furthermore, in vivo
administration of Fgf15 protein to mice led to a strong
163 Upon excision of iBAT (X-BAT) and
administration of FGF21 to mice housed at 80 degrees F o
164 Administration of Gal3 to mice causes insulin resistance
165 d GDF15 correlates with weight loss, and the
administration of GDF15 to mice with obesity reduces bod
166 Oral
administration of GSK2656157 to mice shows a dose- and t
167 Administration of IL28 to mice with induced colonic woun
168 Oral
administration of KPT-330 to mice reduced growth of subc
169 Administration of LPS to mice induced secretion of MIR12
170 Consistent with this hypothesis, in vivo
administration of LT175 to mice fed a high-fat diet decr
171 In vivo, the
administration of metformin to mice inhibited the growth
172 The
administration of oral atovaquone to mice inhibited tumo
173 Administration of PDSinh-C01 to mice at predicted therap
174 We report that
administration of prednisolone to mice increased reactiv
175 Consistent with this was our finding that
administration of recombinant MANF to mice decreased tis
176 Oral
administration of regacin to mice, commencing 15 min bef
177 eER(T2) was activated in developed tumors by
administration of tamoxifen to mice.
178 Oral
administration of the drug to mice reduces growth of xen
179 Intravenous
administration of the MagMBs to mice bearing orthotopic
180 Systemic
administration of this probe to mice bearing S. aureus m
181 Moreover, daily oral
administration of bardoxolone methyl to monkeys for 1 ye
182 Systemic
administration of these agonists to monkeys performing a
183 Administration of TGFBRII-Fc to monocrotaline-treated or
184 Oral
administration of I-BET726 to mouse xenograft models of
185 However,
administration of rAAV:Fst to muscles at the time of den
186 Importantly, direct
administration of recombinant FIZZ1 to naive WT mice led
187 Finally, a single
administration of estradiol to naturally cycling women s
188 ntify the optimal dose, timing, and route of
administration of EGF to NEC patients.
189 However, oral
administration of recombinant CCL20 to neonatal mice sig
190 Administration of suberoylanilide hydroxamine to neuroLS
191 Sustained
administration of epinephrine to NLB rats mimicked sound
192 Further, oral
administration of AEA to NOD mice provides protection fr
193 Intravenous
administration of GS-5734 to nonhuman primates resulted
194 Administration of CORT to nonrestricted animals was suff
195 Repeated
administration of antipsychotic drugs to normal rats has
196 Here we show that oral
administration of DHA to normal adult mice as lysophosph
197 Previously, we demonstrated that
administration of GnRH to normal rats increased intrahep
198 Recent studies demonstrate that
administration of cyclodextrin (CD) to Npc1(-/-) mice el
199 icient in the adipokine leptin) and that the
administration of leptin to ob/ob mice restored Th17 cel
200 Consistent with in vitro results, oral
administration of rosiglitazone to ob/ob mice for 2 week
201 Chronic
administration of SR1555 to obese diabetic mice resulted
202 Patients were followed from first
administration of ceftriaxone to occurrence of CDI or ad
203 Notably, a single
administration of TGFbeta prior to oHSV therapy was suff
204 Administration of epoetin alfa to older adult patients w
205 Three days after
administration of LDL-TO or sham surgery, the control ra
206 n a multivariable logistic regression model,
administration of statins prior to or during hospitaliza
207 These studies suggest that chronic
administration of CsA to organ transplant patients could
208 Furthermore,
administration of SPHK1 inhibitors to orthotopic AML pat
209 Intranasal
administration of LTC4 to OVA-sensitized C57BL/6 mice ma
210 Administration of the flavonoids to P. aeruginosa alters
211 The systematic
administration of a questionnaire to patients who have u
212 , among other critical interventions, timely
administration of antibiotics to patients with sepsis or
213 Administration of antioxidants to patients with painful
214 Upstream
administration of antithrombotic drugs to patients with
215 Administration of disulfiram to patients on antiretrovir
216 unotherapy, current approaches seek to limit
administration of immunosuppressive therapy to patients
217 In this small trial,
administration of lanadelumab to patients with hereditar
218 o estimate the cost-effectiveness of routine
administration of pasireotide to patients undergoing PD,
219 We show that intranasal but not systemic
administration of alpha-GalCer to piglets infected with
220 Administration of DL-propargylglycine to pregnant mice i
221 Administration of HbF to pregnant rabbits increased the
222 Administration of probiotics to premature newborns has b
223 Passive protection, the
administration of antibodies to prevent infection, has g
224 r autoimmune diseases will likely require co-
administration of soluble gp130 to prevent the side effe
225 comycin can cure C. difficile infection, and
administration of these agents to prevent C. difficile i
226 The
administration of NO donors to primary dorsal root gangl
227 Conversely,
administration of BMP signals to PSM or forced expressio
228 Administration of rapamycin to Pten(ptKO) mice diminishe
229 Administration of NOTCH inhibitors to RA mice prevented
230 Oral
administration of 69 to rats reduced food intake in an a
231 In addition, subchronic
administration of imatinib to rats had no effect on brai
232 Correspondingly,
administration of MSU crystals to rats during late gesta
233 The oral
administration of olives to rats and its determination i
234 nt of anemia that was further accelerated by
administration of ENU to recipients, demonstrating that
235 s published data regarding the safety of the
administration of these medications to recipients with f
236 atic filariasis are based on the annual mass
administration of antifilarial drugs to reduce the micro
237 Oral
administration of LPS led to reduced IL-6 production fro
238 nced immediate hypersensitivity, whereas the
administration of soluble OX40 to regulatory T-cell-depl
239 In vitro,
administration of TGF-beta to renal epithelial cells inc
240 x vivo and in vivo preclinical studies after
administration of 1 to rodents, dogs, and monkeys.
241 tion of salient molecular changes induced by
administration of addictive drugs to rodents.
242 ion is essential to ensure early appropriate
administration of antibiotics to save lives of patients,
243 sanitation, and health education (WSH) with
administration of praziquantel to school-aged children.
244 Daily
administration of these compounds to severe SMA Delta7 m
245 Chronic in vivo
administration of apocynin led to significant (p < 0.001
246 Such
administration of GeRPs to silence the inflammatory cyto
247 Intra-arterial
administration of lactic acid (to simulate exercising mu
248 he reduced lipid level was combined with the
administration of pioglitazone to simulate the clinical
249 Administration of SptP to sites of E. coli infection mar
250 insight into the time window of response to
administration of antisense oligonucleotides to SMA mice
251 ion of Spdef also was induced transiently by
administration of tetracycline to Spdef(dox-intestine) m
252 Furthermore, the
administration of VU0409551 to SR-/- mice reverses their
253 Src was investigated in vivo by
administration of PP2 to streptozotocin (STZ)-induced di
254 DHT, could be blocked by the third ventricle
administration of finasteride prior to stress applicatio
255 Administration of PBA to Taconic mice resulted in the in
256 However, in vivo intratumoral
administration of TLR7L led to TApDC activation and disp
257 Hepatocytes were depleted by
administration of metronidazole to Tg(fabp10a:CFP-NTR) a
258 ment of integrated models that link systemic
administration of a drug to the probability of survival.
259 ment, prompted us to determine the safety of
administration of AAV2-hRPE65v2 to the contralateral eye
260 also observed in animals after intravascular
administration of Ad5RGE compared to the parental Ad5 ve
261 GPR17 agonists induced food intake, whereas
administration of an antagonist to the receptor reduced
262 We also examined the times to the
administration of antibiotics and to the completion of a
263 Administration of IL-10 to the IL-10-deficient mice rest
264 trol algorithm to automatically regulate the
administration of inducer molecules to the cells by comp
265 the day, or ad libitum for 4 wk, followed by
administration of LPS prior to the onset of either the a
266 nd randomized clinical trials indicate daily
administration of nevirapine to the infant can prevent b
267 -regression analysis, we found evidence that
administration of probiotics closer to the first dose of
268 eishmania is sensitive to ROS either by oral
administration of ROS to the infected fly or by silencin
269 in a model of allergic airway inflammation,
administration of SAA to the lungs functions as an adjuv
270 Finally, the
administration of sulforaphane to the ALL xenograft mode
271 onal oncogenic mutations in Kras or Braf The
administration of tamoxifen to the resulting adult Tg(Tf
272 Conversely,
administration of IL-4 to thermoneutral mice increases b
273 r) under Cu deficiency and that subcutaneous
administration of Cu to these animals restore normal ATP
274 feration and STAT3 activation, compared with
administration of DSS alone to these mice.
275 Administration of rapamycin to these mice, which are def
276 Administration of RvD1 to these mice during plaque progr
277 men to identify those colonized with GBS and
administration of peripartum prophylaxis to those identi
278 ional anomalies were completely corrected by
administration of GDNF to Tlr2(-/-) mice.
279 Administration of PGE(2) to TLR2(-/-) mice resulted in i
280 Administration of ponezumab to transgenic mice also led
281 Chronic
administration of ponezumab to transgenic mice led to a
282 Early
administration of acetaminophen to treat fever due to pr
283 nstrated prolonged mitotic arrest after oral
administration of 12c to tumor bearing nude mice.
284 In vivo
administration of 17-DMAG to tumor-bearing mice led to s
285 Consistently,
administration of NAADP to type 2 diabetic mice improved
286 g the anterior chamber fibrous complex after
administration of antibody to vascular endothelial growt
287 Intracerebroventricular
administration of kisspeptin-10 to Vgat-Cre;Lepr(lox/lox
288 Taken together, our results reveal that the
administration of MPA prior to viral infection of mucosa
289 Intracolonic
administration of bacterial DNA to wild-type mice induce
290 Finally, the
administration of exogenous NGF to wild-type mice was fo
291 Intranasal
administration of IL-33 to wild-type mice induced airway
292 Intravenous
administration of NEP to wild-type and APP23 transgenic
293 Activation of GC-C by
administration of ST to wild type, but not Gucy2c(-/-),
294 Administration of tunicamycin to wild-type mice caused i
295 gth in human chondrocytes in vitro and after
administration of dietary lithium to Wistar rats in vivo
296 Administration of betamethasone to women at risk for lat
297 tion and lung pathology after intra-tracheal
administration of bleomycin to WT and STC1 Tg mice.
298 Administration of IL-33 to WT mice markedly increased ch
299 We tested the hypothesis that systemic
administration of porphyrin precursors to zebrafish larv
300 Administration of CQ to ZIKV-infected pregnant SJL mice