ライフサイエンスコーパス: intraperitoneal

1 V(1a) receptor antagonist, SR49059 (1 mg/kg intraperitoneal).

2 re-established by acute E2 replacement (3 h, intraperitoneal).

3 ubthreshold cocaine priming dose (2.5 mg/kg, intraperitoneal).

4 n following acute injection (0.5 or 5 mg/kg, intraperitoneal).

5 cularized microtumors of various sizes after intraperitoneal (211)At-radioimmunotherapy, we used an i

6 imulations of clinically relevant amounts of intraperitoneal (90)Y-mAbs for treatment of minimal dise

7 ural injections, subcutaneous injections and intraperitoneal access.

8 Patients with septated ascites and intraperitoneal adhesions are at potential higher risk o

9 After daily intraperitoneal administration at 90 mg kg(-1), 22m sign

10 Their intraperitoneal administration enabled triggered release

11 us silica nanoparticles are advantageous for intraperitoneal administration for the treatment of peri

12 Intraperitoneal administration had minor but significant

13 Here we compared the effects of intraperitoneal administration of 1,25(OH)(2) vitamin D(

14 educed parasitemia in animals >99% following intraperitoneal administration of 25 mg/kg/day dose for

15 Intraperitoneal administration of 25(OH)D(3) and 1,25(OH

16 Intraperitoneal administration of 9ING41, after the indu

17 We inhibited endogenous PD-L1 function by intraperitoneal administration of a blocking antibody to

18 Intranasal or intraperitoneal administration of a single dose of drug

19 ith a high dose of E faecalis 12 hours after intraperitoneal administration of anti-Factor H (FH) ant

20 Wild-type mice were sacrificed 1 week after intraperitoneal administration of doxorubicin (1-25 mg/k

21 Intraperitoneal administration of EHT 1864 in mice drama

22 Intraperitoneal administration of G418 in Mecp2R294X mic

23 Intraperitoneal administration of iCRT3 to C57BL/6 mice,

24 fractory to induction of cell shedding after intraperitoneal administration of liposaccharide (LPS),

25 lycero-3-phosphocholine was linear following intraperitoneal administration of medium and high dose.

26 The use of intraperitoneal administration of nanoparticles has been

27 NOS) in the brain which was reversed through intraperitoneal administration of PPARgamma agonists (ro

28 We induced biliary atresia in BALB/c mice by intraperitoneal administration of Rhesus rotavirus type

29 Intraperitoneal administration of S17 significantly inhi

30 Importantly, intraperitoneal administration of TAT-C1aB in mice follo

31 We further found that intraperitoneal administration of the purified Stx1a B s

32 Intraperitoneal administration of Z2 inhibits vertical t

33 ected these flavonoids in the eye upon their intraperitoneal administration.

34 cal rodent models of PD motor symptoms after intraperitoneal administration: haloperidol-induced cata

35 Pressurised intraperitoneal aerosol chemotherapy (PIPAC) was introdu

36 g (211)At, we performed a phase I trial with intraperitoneal alpha-particle therapy in epithelial ova

37 ODS AND In conscious telemetered mice, acute intraperitoneal and oral administration of azithromycin

38 o highly susceptible to CWD prions following intraperitoneal and oral exposures, a characteristic tha

39 Intraperitoneal and oral gavage administration of nicoti

40 pressed zebrafish at 37 degrees C; optimized intraperitoneal and periocular muscle cell transplantati

41 nflammation in mouse models of P. aeruginosa intraperitoneal and respiratory infection.

42 Galleria mellonella, and in mouse models of intraperitoneal and respiratory Pseudomonas aeruginosa i

43 rmacokinetics after administration via oral, intraperitoneal, and intravenous routes.

44 AlloTbet mice received weekly intraperitoneal anti-IL-17A or IgG (200 mug/mouse) start

45 transplacental transport of glucose, and 4) intraperitoneal apelin administration in neonates increa

46 Systemic varenicline (0, 0.5 or 2.5 mg/kg; intraperitoneal) blocked context-induced relapse to alco

47 Intraperitoneal bolus dantrolene before HAL prolongs tim

48 omentum, as opposed to free-floating in the intraperitoneal cavity (IP) in mice.

49 the metastatic tumor microenvironment in the intraperitoneal cavity.

50 In the end, half of the animals received an intraperitoneal CCl(4) injection of 3.0 mL/kg; the other

51 sensitivity to low light was not seen after intraperitoneal CGRP injection, but was seen after intra

52 After intraperitoneal CGRP, motility was decreased in the dark

53 ety as measured in an open-field assay after intraperitoneal CGRP.

54 ter strains and zinc-sensitive mutants in an intraperitoneal challenge model in mice revealed that EC

55 on with this pentavalent vaccine followed by intraperitoneal challenge of BALB/c mice with S. aureus

56 Anaphylactogenic potency was tested by using intraperitoneal challenge of mice sensitized intragastri

57 Mouse intraperitoneal challenge showed that soluble M1 was suf

58 um IgG against the vaccine antigens prior to intraperitoneal challenge with S. aureus prevented morta

59 Cytoreductive surgery and heated intraperitoneal chemotherapy (CRS & HIPEC) is the curren

60 Foam-based intraperitoneal chemotherapy (FBIC) was produced with ta

61 cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) across time and acc

62 ytoreductive surgery (CRS) with hyperthermic intraperitoneal chemotherapy (HIPEC) for peritoneal canc

63 sing results, but the impact of hyperthermic intraperitoneal chemotherapy (HIPEC) remains controversi

64 OVHIPEC trial, the addition of hyperthermic intraperitoneal chemotherapy (HIPEC) to interval cytored

65 oing cytoreductive surgery with hyperthermic intraperitoneal chemotherapy (HIPEC).

66 For decades, intraperitoneal chemotherapy (IPC) was delivered into th

67 Cytoreductive surgery with hyperthermic intraperitoneal chemotherapy.

68 acheal lipopolysaccharide model, 1,500 IU of intraperitoneal cholecalciferol treatment 6 hours postin

69 er's disease, hippocampal Mmp13 knockdown or intraperitoneal CL82198 administration reduced BACE1 pro

70 Strikingly, intraperitoneal delivery of Ad-TD-nsIL-12 significantly

71 of pulmonary fibrosis, as did treatment with intraperitoneal delivery of VEGF-A165b to wild-type mice

72 particle-based product has been approved for intraperitoneal delivery.

73 wild-type and P2y(2)r (-/-) knockout mice by intraperitoneal diethylnitrosamine (DEN) injection.

74 in vitro, and inhibits both tumor growth and intraperitoneal dissemination of tumor cells in vivo.

75 for at least 4 h following a single oral or intraperitoneal dose at 10 mg/kg.

76 A single intraperitoneal dose of compounds I and II exhibited a p

77 The 50% lethal intraperitoneal dose of vaccinia virus (VACV) was 3 PFU

78 d the same level for 72 h following a single intraperitoneal dose.

79 ith metalloinsertor treatment (1 mg/kg; nine intraperitoneal doses over 20 d).

80 Intraperitoneal dosing of the clinically used prodrug ir

81 esis that distal pancreatectomy (DP) without intraperitoneal drainage does not affect the frequency o

82 no prospective trial focusing on DP without intraperitoneal drainage has been reported.

83 DP without routine intraperitoneal drainage was associated with a higher in

84 utcomes are comparable in DP with or without intraperitoneal drainage.

85 h (N = 174) and without (N = 170) the use of intraperitoneal drainage.

86 The use of routine intraperitoneal drains during DP is controversial.

87 cluding 40 (80%; 95% CI, 66% to 90%) who had intraperitoneal fluid found on an abdominal CT scan, and

88 cells confirmed complete tumor ablation with intraperitoneal ganciclovir administration.

89 ral gas, portomesenteric vein gas, extensive intraperitoneal gas and intraabdominal free fluid.

90 (pSTAT5) in adult male mice that received an intraperitoneal GH injection.

91 exhibited mild glucose intolerance after an intraperitoneal glucose administration and showed increa

92 ight gain and better glucose handling during intraperitoneal glucose challenge than the B6 allele con

93 lood sugar in mice following an oral but not intraperitoneal glucose load.

94 Unexpectedly, oral and intraperitoneal glucose tolerance and the insulin respon

95 es in the open field test, ABA paradigm, and intraperitoneal glucose tolerance test (IGTT).

96 iography for cardiac structure and function, intraperitoneal glucose tolerance test (IPGTT) for gluco

97 glucose and insulin concentrations during an intraperitoneal glucose tolerance test (ipGTT).

98 and glucose tolerance was measured using an intraperitoneal glucose tolerance test (IPGTT).

99 ovement in glucose metabolism observed in an intraperitoneal glucose tolerance test on male C57BL/6J

100 nd adipokines; glucose and insulin during an intraperitoneal glucose tolerance test; and Glut4 and Ap

101 rough nonfasting blood glucose measurements, intraperitoneal glucose tolerance testing (IPGTT), and h

102 ulin, and proinsulin stainings and performed intraperitoneal glucose tolerance testing in transgenic

103 comparable with those of controls following intraperitoneal glucose, or insulin tolerance tests, or

104 expression in this second model accelerates intraperitoneal growth.

105 aluated in ICRscid mice with subcutaneous or intraperitoneal human OVCAR-3 OvCa xenografts by dynamic

106 BALB/c mice and established a mouse model of intraperitoneal (i.p.) A. baumannii infection.

107 Here, we demonstrate that intraperitoneal (i.p.) administration of MDP triggered r

108 Upon a single intraperitoneal (i.p.) administration, the optimized for

109 Intravenous (i.v.) anti-VCAM-1 or intraperitoneal (i.p.) beta7 blocking antibody administr

110 Furthermore, intraperitoneal (i.p.) delivery of SSO Ex5 in MMTV-PyMT

111 g alcohol (6% w/v) or water before receiving intraperitoneal (i.p.) doses of ketamine or memantine, o

112 Systemic intraperitoneal (i.p.) injection for 2 weeks significant

113 sting and by 76 +/- 22% (n = 5) at 1 h after intraperitoneal (i.p.) injection of glucagon, which is k

114 Intraperitoneal (i.p.) injections of alphaS fibrils in h

115 n which BALB/c mice were sensitized by three intraperitoneal (i.p.) injections of OVA/alum.

116 In this study, using the mouse model of intraperitoneal (i.p.) mucin-enhanced A. baumannii infec

117 In lean mice, intraperitoneal (i.p.) or intracerebroventricular (i.c.v

118 y and tolerability of intravenous (i.v.) and intraperitoneal (i.p.) paclitaxel combined with S-1, "an

119 tigate the efficiency of intravenous (i.v.), intraperitoneal (i.p.), and intramuscular (i.m.) routes

120 lly elicited an IL-22 response compared with intraperitoneal immunization.

121 Intraperitoneal implantation of pancreatic islets seeded

122 d during culture when functional, and in all intraperitoneal implants that corrected diabetes in mice

123 Murine gammaherpesvirus-68 (MHV-68) intraperitoneal infection is a gammaherpesvirus model fo

124 b+) mice rapidly cleared S. aureus following intraperitoneal infection with elimination of ~99% of an

125 auses of readmission were dehydration (42%), intraperitoneal infections (33%), and extraperitoneal in

126 Dams received a daily intraperitoneal injection (i.p.) of vehicle control or D

127 ehicle (DMSO) (n = 30) was delivered through intraperitoneal injection (IP) 24 hours after the fungal

128 enged with peanut by means of oral gavage or intraperitoneal injection and assessed for anaphylaxis.

129 8852 was administered to mice and ferrets by intraperitoneal injection at varying doses, 24 hours pri

130 oATP or sterile saline was administered via intraperitoneal injection for 2 weeks postoperatively.

131 space at Embryonic Day 20 or after birth by intraperitoneal injection for 2 weeks.

132 After intraperitoneal injection in a patient, retrieved single

133 showed more potent anti-tumor efficacy than intraperitoneal injection in B16F10 melanoma models.

134 of the chimeric recombinant VHSV (rVHSV) by intraperitoneal injection in juvenile rainbow trout show

135 Intraperitoneal injection in mice showed that exendin-4

136 protein) function after in vivo delivery by intraperitoneal injection in neonatal and adult RyR2(R44

137 alf-life of OS47720 in mouse brain, a single intraperitoneal injection induces rapid and long-lasting

138 oietic response, acute alcohol intoxication (intraperitoneal injection of 5 g alcohol/kg body weight)

139 as induced in male Wistar rats with a single intraperitoneal injection of 60 mg/kg of monocrotaline,

140 od to label CNS demyelinating lesions by the intraperitoneal injection of a vital dye, neutral red (N

141 Intraperitoneal injection of A. baumannii-mucin or mucin

142 Intraperitoneal injection of alphaS fibrils also induced

143 In vivo, intraperitoneal injection of an antimiR to miR-370-3p in

144 Intraperitoneal injection of an engineered angiopoietin-

145 Intraperitoneal injection of anti-SQSTM1-neutralizing mo

146 Systemic subcutaneous or intraperitoneal injection of butyrate did not have any s

147 CFTR was inhibited in C57BL/6 mice via 8-day intraperitoneal injection of CFTRinh172.

148 characterized, many of these experiments use intraperitoneal injection of coxsackievirus to infect mi

149 Intraperitoneal injection of E18 exosomes into E15 mice

150 Adult male CD-1 mice received an intraperitoneal injection of either LPS (0.83 mg/kg) or

151 The results showed that intraperitoneal injection of ethanol (3.0 g/kg) at 21:00

152 Sepsis was induced by intraperitoneal injection of fecal slurry.

153 Here, using MS, we found that a single intraperitoneal injection of fluoxetine disrupts the int

154 In rats, intraperitoneal injection of GC7 substantially reduced r

155 HUHEP and HIS-HUHEP mice were given an intraperitoneal injection of HBV.

156 Here, we show that intraperitoneal injection of human amniotic mesenchymal

157 itis was induced in 8-wk-old C57Bl/6 mice by intraperitoneal injection of K/BxN serum.

158 duct ligation with caerulein stimulation or intraperitoneal injection of l-arginine in mice with del

159 he administration of metformin per os and an intraperitoneal injection of lactic acid.

160 Furthermore, intraperitoneal injection of levodopa could significantl

161 tration of a malaise-inducing agent, such as intraperitoneal injection of LiCl.

162 psis: cecal ligation and puncture as well as intraperitoneal injection of LPS.

163 Intraperitoneal injection of luseogliflozin (0.9 mg kg(-

164 Intraperitoneal injection of pLL induced IL-1beta, sugge

165 y) for one week before anesthesia induced by intraperitoneal injection of propofol and maintained by

166 Intraperitoneal injection of RGFP966 (a selective inhibi

167 A single, intraperitoneal injection of streptozotocin (STZ) (35 mg

168 ometry based metabolomics, we show here that intraperitoneal injection of THC in C57BL/6 mice modulat

169 Intraperitoneal injection of the antioxidant N-acetylcys

170 Intraperitoneal injection of the HuR small-molecule inhi

171 inent dendritic spine density reduction, yet intraperitoneal injection of these amyloids did not affe

172 +) increases in tissues when administered by intraperitoneal injection to C57BL/6J mice.

173 osomes, and is rapidly absorbed following an intraperitoneal injection to rats and readily crosses th

174 inistered Edn2 were randomized to receive by intraperitoneal injection treatments that inhibited the

175 Rats were acutely pretreated by intraperitoneal injection with a single dose of ketamine

176 ation in the Col11a1 gene, were subjected to intraperitoneal injection with Adv-RFP-LOXL2 every 2 wee

177 Our findings showed that thirty days of intraperitoneal injection with amylin or pramlintide inc

178 al fibrillary acidic protein administered by intraperitoneal injection) in surviving mice (n >/= 5).

179 king antiprogrammed cell death 1 antibodies (intraperitoneal injection).

180 m systemic ethanol administration (either by intraperitoneal injection, 2 g/kg, twice/day, for 7 days

181 rican Type Culture Collection 17978 using an intraperitoneal injection, and blood was extracted at 8

182 .2 mg/kg/day) and Nec-1s (1.6 mg/kg/day) via intraperitoneal injection.

183 x 108 B. microti-infected red blood cells by intraperitoneal injection.

184 Peripheral (intraperitoneal) injection of CGRP resulted in light-ave

185 o the cimetidine group (CimG: received daily intraperitoneal injections of 100 mg/kg of body weight o

186 Intraperitoneal injections of 3-HAA into Apoe(-/-) and A

187 chase periods without BrdU, or combined with intraperitoneal injections of 5-ethynyl-2'-deoxyuridine.

188 Mice were given intraperitoneal injections of 5-fluorouracil, which bloc

189 Some mice were given intraperitoneal injections of a plasmid encoding LNA-ant

190 maintained on a high-fat diet received five intraperitoneal injections of adropin(34-76) (450 nmol/k

191 Some mice were given intraperitoneal injections of anti-IL11 (X203), anti-IL1

192 livers of C57BL/6 mice; some mice were given intraperitoneal injections of antibodies against PD1, T-

193 ted without distinction of gender with daily intraperitoneal injections of betaOHB during 5 d.

194 RAG(-/-) mice were given intraperitoneal injections of CD4(+)CD62L(-)CD44(hi) T c

195 Intraperitoneal injections of CD4-CCR5-VLP produced only

196 PF was induced by repetitive intraperitoneal injections of chlorhexidine gluconate (C

197 y divided in to 2 groups that received daily intraperitoneal injections of either (1) an oil-based ve

198 ollowing 3 weeks diet adapting, a multi-dose intraperitoneal injections of ethyl carbamate (urethane,

199 e Sprague-Dawley rats (4 weeks old) received intraperitoneal injections of gadoterate meglumine (0.6

200 C57BL/6 mice were given intraperitoneal injections of high-dose tamoxifen to ind

201 Male C57BL/6 mice were given intraperitoneal injections of IL1B and intestinal recycl

202 lsants, we examined acute seizures evoked by intraperitoneal injections of kainic acid (KA) and piloc

203 However, intraperitoneal injections of LIF can initiate embryo im

204 Nr1d1(-/-) mice and control mice were given intraperitoneal injections of LPS to induce peritoneal i

205 Daily intraperitoneal injections of rapamycin reduced AVF wall

206 Some mice were fed or given intraperitoneal injections of S100A8 or subcutaneous inj

207 t tumors (grown from OE-33 cells) were given intraperitoneal injections of simvastatin; tumor growth

208 and Makona) and in vivo 3 or 5 daily F(ab')2 intraperitoneal injections provided 100% protection to B

209 Using intraperitoneal injections, we administered SS31 to an A

210 ibody cocktail (C-Ab) and lipopolysaccharide intraperitoneal injections.

211 gonists for mutant INSR, were then tested by intraperitoneal injections.

212 intracerebroventricular, intratracheal, and intraperitoneal injections.

213 these studies, we demonstrate that a single intraperitoneal inoculation of a cDNA clone encoding an

214 However, intraperitoneal inoculation of mice with gammaHV68 was a

215 Importantly, intraperitoneal inoculation of pancreatic homogenates co

216 y, infectious rZIKV was also recovered after intraperitoneal inoculation of the rZIKV cDNA in the abs

217 Intraperitoneal inoculation of the thermally injured mic

218 equired for tissue colonization upon oral or intraperitoneal inoculation.

219 ty was assessed 48 h after training using an intraperitoneal insulin tolerance test (ITT) and BP was

220 yed favorable pharmacokinetic profiles after intraperitoneal/intravenous (I.P./I.V.) injection alone

221 good pharmacokinetics properties in mice via intraperitoneal (ip) administration and provides a means

222 Intraperitoneal (IP) administration can be used to impro

223 d on this relationship, we hypothesized that intraperitoneal (IP) administration of rAAV produces uni

224 Following intraperitoneal (IP) administration of SBI-425, mass spe

225 PH is bioavailable after intramuscular (im), intraperitoneal (ip) and even transbuccal (tb) administr

226 simultaneously with DPOAE and EP while using intraperitoneal (IP) and intravenous injection of furose

227 nd neuropathic pain, respectively, following intraperitoneal (IP) doses of 30 mg/kg.

228 odes after IN infection nor the spleen after intraperitoneal (IP) infection required M2, although the

229 ed, and EX-4 or vehicle was administered via intraperitoneal (IP) injection.

230 estigated whether repeated scruff restraint, intraperitoneal (IP) injections and anaesthesia negated

231 The objective of this study was to evaluate intraperitoneal (IP) metronomic chemotherapy using susta

232 the S. flexneri lux1 strain was used with an intraperitoneal (IP) murine model of shigellosis to test

233 creatic islets that are unconstrained in the intraperitoneal (IP) space of healthy and diabetic mice.

234 administration of JZL184 [4, 8 and 16 mg/kg, intraperitoneal (IP)] 4 h before testing caused dose-dep

235 After a D-amphetamine challenge (5 mg/kg, intraperitoneal), Kmo(-/-) mice showed potentiated horiz

236 Pretreatment or single intraperitoneal lavage with YC-1 significantly reduced p

237 hypothalamic and medullary centers, whereas intraperitoneal leptin had no effect.

238 creased food intake and body weight, whereas intraperitoneal leptin had no effect.

239 Acute intranasal, but not intraperitoneal, leptin decreased the number of oxygen d

240 Oral but not intraperitoneal lipid administration strongly suppressed

241 A-Seq from newborn C57BL/6 mice treated with intraperitoneal lipopolysaccharide (LPS) to mimic system

242 tion-induced cardiac dysfunction" induced by intraperitoneal lipopolysaccharide injection (10 mg/kg),

243 his study was to investigate the efficacy of intraperitoneal local anesthetic (IPLA) on pain after ac

244 Our results demonstrated that intraperitoneal maternal DNAC administration significant

245 es, as a primary regulator of ovarian cancer intraperitoneal metastatic dissemination and identifies

246 ce CXCL6 ex vivo, but provoked a cooperative intraperitoneal neutrophil recruitment in mice when co-i

247 of the MILOS operation with the laparoscopic intraperitoneal onlay mesh operation (IPOM) and open sub

248 The administration of AAV GCG-EGFP by intraperitoneal or intraductal injection led to EGFP exp

249 tides showed no nephrotoxicity to mice after intraperitoneal or intravenous administration for 1 wk.

250 via nebulization) versus the systemic route (intraperitoneal or intravenous).

251 y suppressed, partially or completely, after intraperitoneal or oral administration of several indene

252 Intraperitoneal or topical application of the pharmacolo

253 nd treated with rhIGF-1/BP3 (0.02-20 mg/kg/d intraperitoneal) or buffer for 2 weeks.

254 erent routes of administration: intravenous, intraperitoneal, or intrathecal injections.

255 Allergic asthma was induced by intraperitoneal OVA/alum sensitization followed by repea

256 rm carrying fluorescent dyes to mice bearing intraperitoneal ovarian cancer allowed visualization of

257 rtantly, we demonstrate the visualization of intraperitoneal ovarian cancer micrometastasis as small

258 is therapy, we conducted genomic analyses of intraperitoneal ovarian tumors in which adaptive resista

259 The statistical analysis of intraperitoneal OVASC-1 tumor burden and survival rates

260 Intraperitoneal oxytocin administration blocked escalate

261 During intraperitoneal P. aeruginosa infection, phosphorylated

262 mined at 3, 10, and 14 days using a model of intraperitoneal P. aeruginosa infection.

263 the 16 CC strains had allergic reactions to intraperitoneal peanut challenge, whereas only CC027/Gen

264 grown for 2 weeks, and mice were then given intraperitoneal penfluridol for 35 days.

265 epilepticus (intra-amygdala kainic acid and intraperitoneal pilocarpine).

266 At the time of CVH repair, intraperitoneal placement of the biosynthetic mesh signi

267 Intraperitoneal POL5551 injections in wild-type mice (8

268 The resulting elevation in intraperitoneal pressure (IPP), from normal values of 5

269 In addition, intrathecal as well as intraperitoneal pretreatment with l-THP reduced the mech

270 yl disaccharides at 48 and 24 hours prior to intraperitoneal Pseudomonas aeruginosa or IV Staphylococ

271 In that model, relatively high-dose intraperitoneal rapamycin extended lifespan and improved

272 ontrast, deficiency of alphaXbeta2 abrogated intraperitoneal recruitment and adhesive functions of mo

273 A 4-week intraperitoneal regimen of fluoxazolevir in humanized ch

274 ynthetic mesh (open, sublay, retrorectus, or intraperitoneal) repair with fascial closure (n = 104).

275 properties using human whole blood, and the intraperitoneal response after three weeks in Wistar rat

276 We used the intraperitoneal route and injected purified plasma IgG f

277 inst Leishmania donovani/BALB/c mice via the intraperitoneal route for 5 days and displayed >91 and >

278 yed compared with infection via the standard intraperitoneal route.

279 iency in the order of intravenous, oral, and intraperitoneal routes.

280 After 19 d, mice received an intraperitoneal saline or endotoxin challenge 4 h before

281 ne marrow of pair-fed control mice receiving intraperitoneal saline stored a large number of mature g

282 vely, our data emphasize the role of Ncad in intraperitoneal seeding of EOC and provide the rationale

283 Acute AAD was induced in C57BL/6 mice by intraperitoneal sensitization with ovalbumin (OVA) in co

284 ifying their relative abundances at multiple intraperitoneal sites.

285 d in it after implant transplantation in the intraperitoneal space of immunocompetent mice.

286 that peripheral treatment using TCMCB07 with intraperitoneal, subcutaneous, and oral administration i

287 previous abdominal surgery (P = 0.047), and intraperitoneal surgical technique (P = 0.008) were risk

288 P32-directed intraperitoneal targeting of other anticancer agents and

289 ant ascites and solid peritoneal tumors upon intraperitoneal transplantation in mice.

290 omplete response with chemotherapy, received intraperitoneal treatment with escalating (20-215 MBq/L)

291 clopramide baseline PET scans or scans after intraperitoneal treatment with the rodent pregnane X rec

292 clopramide baseline PET scans or scans after intraperitoneal treatment with the rodent pregnane X rec

293 peritoneal tumors with high specificity upon intraperitoneal tumor targeting and selective etching of

294 esigned sequence and timeline eradicated all intraperitoneal tumors and provided survival benefits.

295 After comparing two TAM delivery methods (intraperitoneal versus oral gavage) and different doses,

296 Urine excretion after an acute intraperitoneal water load was significantly increased i

297 rowning response', with a bigger size of the intraperitoneal white adipose cell and decreased a numbe

298 we show that oral WR-2721 is as effective as intraperitoneal WR-2721 in promoting survival of intesti

299 bitors effectively suppresses development of intraperitoneal xenografts and prolongs the survival of

300 strate poor growth as either subcutaneous or intraperitoneal xenografts.