ライフサイエンスコーパス: injection into

1 were delivered by transendocardial stem cell injection into 10 LV sites.

2 ble Schottky-barrier-free hole (or electron) injection into 2D semiconductors through van der Waals j

3 From AAV injections into 42 neocortical and allocortical areas, w

4 iviral vector by a single lumbar intrathecal injection into 6-month-old Gjb1-null mice, we confirmed

5 al solution for pressure build-up during CO2 injection into a cylindrical saline formation, accountin

6 on (ESI) coupled to a 25 K ion trap prior to injection into a double-focusing, tandem time-of-flight

7 The orthogonal ion injection into a funnel shaped separation region can gre

8 ns driven by spatially extended spin current injection into a microscopic magnetic disk.

9 e fault slip and seismicity induced by fluid injection into a natural fault.

10 Occasional (e.g., annual) EVO injection into a permeable Ca and bicarbonate-containing

11 mildly acidic solutions but precipitate upon injection into a pH 7 environment, i.e., the skin.

12 Following bidirectional tracer injections into a distal target of the cerebellar nuclei

13 but not the rate of escalation, while local injection into accumbens shell selectively suppressed in

14 After injection into adult Anopheles gambiae, some strains of

15 describe an original method of intrahepatic injection into adult NOD.Cg-Prkdc(scid)Il2rg(tm1Wjl)/SzJ

16 lutions that undergo a phase transition upon injection into an aqueous environment to form a solid dr

17 Our detection method is based on direct injection into an atmospheric pressure chemical ionizati

18 analytical method applied was direct liquid injection into an atmospheric pressure chemical ionizati

19 Water was added by injection into an isolated tissue volume (a 20 mm diamet

20 ond time scale and then were flash-frozen by injection into an isopentane solution surrounded by liqu

21 e fate of NIR-labeled cells from the time of injection into animals to ex vivo cellular analysis afte

22 Following injection into apoA-I-deficient mice, 5-OHTrp(72) apoA-I

23 iciently reducing excited state for electron injection into appropriate semiconductors.

24 script and activity within 30 min of sulfite injection into Arabidopsis and tomato leaves.

25 nnected with the visual dorsal thalamus, the injection into area 20a resulted in more anterograde lab

26 bserved in the visual thalamus following the injection into area 20b.

27 After injections into area 19, many more neurons were labeled

28 In contrast, injections into area 24 yielded dense, widespread connec

29 ties to bacteriophage tail, which drives DNA injection into bacteria.

30 ic CD8(+) IFN-gamma-positive cells following injection into BALB/c mice.

31 Upon injection into blastocyst, BCL2-expressing EpiSCs contri

32 ctivated hypothalamus receptors after direct injection into brain.

33 Subjects received cAMP injections into brainstem reticular motor neurons to sti

34 Injection into C57BL/6N wild-type embryos resulted in on

35 ogels prove to be promising biomaterials for injection into cavitary brain lesions to recruit endogen

36 solution within 10s facilitated their direct injection into CE.

37 -extracted into a basic aqueous solution for injection into CE.

38 Muscimol+baclofen injections into CeA but not BLA decreased cue-induced me

39 e mimicked in wild-type PNs by exogenous tPA injection into cerebellum or prevented by endogenous tPA

40 ted Carbon (AC) or other carbon sorbent (CS) injection into coal combustion flue gases can remove ele

41 f chemotherapy-induced SNS injury, while NPY injection into conditional knockout mice lacking the Y1

42 The Gd-DOTA injection into CSF was performed on the bench after whic

43 posomes, we conclude that the 1-mus electron injection into Cu(A), close to the positive membrane sid

44 Following LV.Mpz-GJB1 injection into Cx32 KO nerves, we detected Cx32 expressi

45 After injection into damaged mouse lung in vivo, human lung st

46 further evaluated for germline competence by injection into Dark Agouti (DA) X Sprague Dawley (SD) bl

47 CO(2) injection into deep geologic formations for long-term st

48 despread hazards, are often related to fluid injection into deep permeable formations that are hydrau

49 the reversible tuning of interfacial charge injection into diarylethene molecular orbitals, as a con

50 ns of retrograde labeling result from tracer injections into different NTS subdivisions, with dual re

51 ame using a straightforward, targeted route (injections into disabled forelimb muscles).

52 ical mapping to guide neuroanatomical tracer injections into distal digit tip representations of Brod

53 Muscimol+baclofen injections into dmPFC, vmPFC, or OFC during late withdra

54 Tbl3 MO injection into either wild-type or p53-/- mutant embryos

55 Botulinum toxin injection into epicardial fat pads during coronary arter

56 % normal saline, 1 mL at each fat pad; n=30) injection into epicardial fat pads during surgery.

57 e the efficacy and safety of botulinum toxin injection into epicardial fat pads for preventing atrial

58 ion was induced in rats by hypertonic saline injections into episcleral veins.

59 ific neural cell types following intravenous injection into fetal and neonatal mice, using control un

60 ron trifluoride in methanol methylation, and injection into GC-FID system.

61 rstanding of the risks associated with CO(2) injection into geologic formations and the subsequent in

62 Very high strains are predicted for hole injection into GO, with reversible and irreversible valu

63 Successful spin injection into graphene makes it a competitive contender

64 Intravenous Ad3-GFP injection into hDSG2-transgenic mice resulted in hDSG2-d

65 ed in the CA1 region of hippocampus, and NPY injection into hippocampus alleviates anxiety symptoms i

66 NO2-Tyr(166)-apoA-I, after subcutaneous injection into hLCAT(Tg/Tg), apoA-I(-/-) mice, showed im

67 Upon injection into host cells, ExoU localizes to the plasma

68 pecific intracellular compartments following injection into host cells.

69 and determination of the order of substrate injection into host cells.

70 x vivo organ analysis following intratumoral injection into HT-1080 xenograft tumors.

71 roglutamate levels increased over time after injection into humans, with the rate of formation differ

72 een and the axial orientation of dual tracer injections into HVC) to reveal a massively parallel and

73 ma clearance of PEG-rHDL was estimated after injection into hypercholesterolemic Apoe-/- mice; the ha

74 sCD89 injection into IgA1-expressing mouse recipients induced

75 Dual retrograde tracer injections into IL and lateral entorhinal cortex (LEnt)

76 ective anticancer immune response upon their injection into immunocompetent mice.

77 Following injection into immunodeficient mice, signals from gold-l

78 structure by intracellular recording and dye injection into impaled cells in muscles of rabbit small

79 n transfer reactions indicates the slow hole injection into IrO2 and the fast dye excited-state quenc

80 A'), and each of them was tested for protein injection into J774 macrophages.

81 rm several pathways previously identified by injections into known auditory or vocal areas and provid

82 Interestingly, upon intracranial injection into lateral ventricles of the neonatal mouse

83 (90:10, v/v) in unsupervised mode for direct injection into LC-MS.

84 Consistent with this, NPY injection into lean mice decreased the quantity of M1-li

85 , renewal was blocked by muscimol + baclofen injections into LH.

86 When using high gavage fluid volumes or injection into ligated intestinal loops, common methods

87 localization of NPs after intravenous (i.v.) injection into live mice bearing human lung tumors that

88 eter (MSNPs500) upon single-dose intravenous injection into male and female immune-competent inbred B

89 carbon dioxide storage is likely to focus on injection into mature oil reservoirs, most of which occu

90 Here we demonstrate spin-polarized carrier injection into methylammonium lead bromide films from me

91 onstrated that carbon tetrachloride (CCl(4)) injection into mice activated ILC1s, but not natural kil

92 es sensors in solution, enabling intravenous injection into mice and the selective detection of local

93 Indeed, TGF-beta1 injection into mice in which MKs had been ablated restor

94 ding Cas9, we show that a single intravenous injection into mice induces >80% editing of Pcsk9 in the

95 ell lines with anti-CD73 AD2 mAb before i.v. injection into mice inhibited extravasation/colonization

96 Single injection into mice of furin-cleaved PCSK9 resulted in s

97 CXCL4 injection into mice resulted in a reduced number of HSCs

98 ched to virus-size particles for intravenous injection into mice that express a CD172a variant compat

99 ding omega1-mutated eggs following tail-vein injection into mice was vastly reduced.

100 d bioimaging performance after intravenously injection into mice, but not the rod-like aggregates of

101 ities, and formation of metastases following injection into mice.

102 rs of significantly reduced volume following injection into mice.

103 heating to deactivate proteins and for safe injections into mice.

104 development of semi-cloned (SC) embryos upon injection into MII oocytes and thus have potential appli

105 ells become metastatic to the lung following injection into mouse fat pads while ectopically expresse

106 Furthermore, CNP injection into mouse hindpaw led to the development of t

107 Furthermore, in vitro transcribed Wwp2 mRNA injection into mouse joints reduces the severity of expe

108 This peptide was active in vivo by injection into mouse lateral ventricle, thereby suppress

109 ion in vivo when administered by stereotaxic injection into mouse spinal cords.

110 In concert, toxin injections into mouse brain result in reduced basal acti

111 timally, even after large bilateral muscimol injections into MSTd.

112 and positive-mean noise, also accounting for injections into multiple regions.

113 (vS1), we illustrate that retrograde tracer injections into multiple subcortical structures allow id

114 ification in the aortic ring assay and after injection into murine vascular lesions.

115 Glycerol injection into muscle is known to induce myopathy, and g

116 nd in vivo after murine erythrocyte membrane injection into neointimal lesions of hypercholesterolemi

117 Dye injections into neurons connecting the central complex w

118 While hole injection into neutral quantum dots is generally conside

119 When acutely administered by injection into NOD mice via the tail vein, this FSI form

120 ived xenografts was assessed by subcutaneous injection into nonobese diabeteic.Cg-Prkdc(scid)Il2rg(tm

121 cells from human PBMCs prior to intrasplenic injection into NSG mice completely abrogated IL-15 super

122 y for each cellular population was tested by injection into nude mice.

123 ugh hole carrier conduction followed by hole injection into (or electron extraction from) Si.

124 progress on efficient spin-polarized carrier injection into organic semiconductors from ferromagnetic

125 Tracer injection into ovarian ligaments has been shown to detec

126 om DPPIV+ rats were transplanted via splenic injection into partial hepatectomized DPPIV- rats that h

127 onds to several nanoseconds, due to electron injection into PCBM and electron-hole recombination at t

128 Following injection into pre-blastoderm embryos, 20-40% of fertile

129 pressed the mRNA over 72 h after intradermal injections into primary, human, skin explants.

130 of active layers, and balance electron/hole injection into QDs, which prevents nonradiative recombin

131 a series of retrograde neuronal tract tracer injections into rat cortical areas along the cortical pr

132 ris), cMRF neurons labeled retrogradely from injections into RIP had numerous anterogradely labeled t

133 Following intrathecal injection into rodents, the nanoparticles, containing th

134 and Mentha piperita were analysed by direct injection into RPLC.

135 ed change in rate of dissolution of AgNPs on injection into seawater thereby facilitating improved pr

136 This suggests that CO(2) injection into sediments may store more CO(2) and cause

137 ith potential application as dyes for charge injection into semiconductor solar cells and in sensitiz

138 y increased in plasma in response to notexin injection into several muscles, namely miR-1-3p, -133a-3

139 Moreover, systemic ASO injection into severely affected mice leads to reversal

140 h an in vitro melanization reaction prior to injection into shrimp significantly increased the shrimp

141 al day 18 through 75 using retrograde tracer injections into specific spinal cord segments associated

142 Injections into subareas of the arcopallium and posterio

143 ate or coumarin 343 adsorbates, exhibit hole injection into surface states when photoexcited with vis

144 side effects due to leakage from the site of injection into systemic circulation.

145 ggregation of soluble tau upon intracerebral injection into tau transgenic (Tg) and wild-type mice, t

146 food intake and body weight when wortmannin injection (into the third ventricle) occurred prior to E

147 but a similar response is not observed after injection into the 4V.

148 ed for reproducible sample handling and bead injection into the acoustic trap.

149 BMSCs and BCs in vitro and in vivo following injection into the amputation site.

150 Following SC injection into the animal thigh, the LC-MEs had more pro

151 and B6 mice (42 eyes) using polystyrene bead injection into the anterior chamber with 126 control CD1

152 Climate simulations that consider injection into the atmosphere of 15,000 Tg of soot, the

153 Following injection into the atmosphere, the soot is heated by sun

154 esis that autologous dermal fibroblast (ADF) injection into the AV nodal area would reduce ventricula

155 ata pertaining to the efficiency of electron injection into the benzannelated enediynes.

156 require debriding of the urothelial lining, injection into the bladder wall, specialized imaging equ

157 inhibited the CBF increase caused by glycine injection into the brain.

158 and test the embryonic potency of iCPCs via injection into the cardiac crescent of mouse embryos.

159 Similarly, their injection into the carotid adventitia of ApoE(-/-) mice

160 ination in the absorber, facilitated carrier injection into the carrier transport layers, and maintai

161 modified ASOs were also well tolerated after injection into the central nervous system of wild-type a

162 ice and nonhuman primates following a single injection into the cerebrospinal fluid.

163 ng that the 1T/2H interface controls carrier injection into the channel.

164 Local DT injection into the colon wall results in focal, specific

165 t (111)In-diethylenetriaminepentaacetic acid injection into the CSF intraventricular space followed b

166 Abeta1-42 injection into the dentate gyrus (DG) of mice caused los

167 After Cath LL-37 injection into the dermis, MC-deficient B6.Cg-Kit(W-sh)/

168 Upon injection into the diaphragm muscle of rats, we show tha

169 l cord and brainstem following intramuscular injection into the diaphragm of rats.

170 r glutamate transporter 1 (VGLUT1) following injection into the dorsal hippocampus of adult mice, as

171 selective reexpression of SERT by lentiviral injection into the dorsal raphe restored the prodepressi

172 GCs do not contribute to chimaeras following injection into the early mouse embryo.

173 latter case, the time difference between ion injection into the ELIT and ion detection after release

174 Following tracer injection into the EOM nuclei, we observed tracer-positi

175 xudative AMD (wet AMD) is treated by monthly injection into the eye of anti-VEGF proteins.

176 cing of the Duox and catalase genes, or H2O2 injection into the female hemocoel.

177 The kinetic energy injection into the flow takes place over the whole casca

178 On injection into the fly, MitoB is rapidly taken up by mit

179 a gaseous injection unit allowing the direct injection into the GC-MS of the VOC previously transferr

180 Controlled dye injection into the GF interneuron results in a dramatic

181 d a bilateral visual field defect after CaHA injection into the glabella region.

182 backbone cleavage that inhibits viral genome injection into the host cell.

183 d by the phage particle's low-efficiency DNA injection into the host.

184 Tracer injection into the IAF resulted in retrogradely labeled

185 ne marrow MSCs, mononuclear cells, or saline injection into the infarct, with and without early (4 h

186 S100A8/A9 heterodimer injection into the intact nerve stimulated macrophage in

187 In all species, current injection into the interneuron drives artificial song pa

188 Excited-state injection into the ITO by RuP* generated ITO(e(-))|Ru(II

189 M LiClO4 MeCN results in efficient electron injection into the ITO NPs on the picosecond time scale

190 utable to the more negative AP threshold and injection into the LBB.

191 mbination of PTEN deletion and salmon fibrin injection into the lesion can significantly improve volu

192 h that Mn(2+) accumulates intracellularly on injection into the living Aplysia and that its concentra

193 Botulinum toxin injection into the lower esophageal sphincter is an esta

194 ayer tunnel barrier for both charge and spin injection into the lower graphene channel.

195 iquid extraction into ethyl acetate and flow injection into the mass spectrometer.

196 CTb injection into the medullary RF labels cells and axonal

197 arrested in the lungs 2-3 s after tail-vein injection into the mice, which is consistent with the bl

198 ration of Tat-Sab(KIM1) via an intracerebral injection into the mid-forebrain bundle increased the nu

199 stem extraordinarily sensitive to convective injection into the mid-latitude lower stratosphere in su

200 strate LRiMM with simulations of 30 years of injection into the Mt.

201 ed in vivo gene transfer of cMyBPC by direct injection into the myocardium of cMyBPC-deficient (cMyBP

202 Virus injection into the NAc core enhanced cue-induced cocaine

203 TP were markedly depressed following Abeta42 injection into the neuron through the patch pipette.

204 In vivo, ATP injection into the NTS increased cardiorespiratory activ

205 ver, reduction of food intake following MTII injection into the NTS ipsilateral to nodose ganglion re

206 Accordingly, amiloride injection into the NTS reduced phrenic nerve activity of

207 ZIP injection into the nucleus accumbens reduced expression

208 anic spin valves is incompatible with charge injection into the organic's lowest unoccupied molecular

209 e SN procedure in ovarian cancer with tracer injection into the ovarian ligaments and to establish wh

210 CTb injection into the PBN retrogradely labels cells in the

211 ve efficacy of applying hormone solutions by injection into the peduncle compared to direct applicati

212 infiltration within a few hours of IL-1beta injection into the peritoneal cavity.

213 Plasmin injection into the pleural cavity of BALB/c mice induced

214 Plg/Pla injection into the pleural cavity of BALB/c mice induced

215 ter hair cells in an adult cochlea via virus injection into the posterior semicircular canal.

216 se in respiratory burst frequency after AMPA injection into the pre-BotC.

217 The protocol is based on co-injection into the pronuclei of fertilized oocytes of sy

218 A scenario of late supernova injection into the protoplanetary disk is consistent wit

219 xcitation of the MOF frameworks and electron injection into the Pt nanoparticles.

220 ety and efficacy of ProSavin after bilateral injection into the putamen of patients with Parkinson's

221 the cerebral hemispheres following bilateral injection into the rat cortex and higher levels of N434A

222 m to the logic high level due to self-charge injection into the redox active polymeric system.

223 ight hemisphere of the brain was seen during injection into the right carotid artery.

224 Furthermore, with injection into the rodent eye, human ND4 DNA levels in m

225 with substance P-saporin prior to lentivirus injection into the rostral ventrolateral medulla, increa

226 ect use samples in the DPPH assay as well as injection into the RP-HPLC system containing a PFP (pent

227 As a positive control we confirmed that ATP injection into the RTN increased breathing and blood pre

228 a subsequent noxious challenge from formalin injection into the same TMJ.

229 Upon Ca(2+) injection into the sample chamber, our system therefore

230 maximal distribution of microbubble contrast injection into the SCS were assessed by 2D and 3D ultras

231 se pericyte coverage substantially upon PGE2 injection into the skin.

232 A big bubble was created by air injection into the stroma of organ-cultured corneas befo

233 GA and examined alterations to the drug upon injection into the subcutaneous space.

234 e in the activation of persulfate during its injection into the subsurface for ISCO.

235 Tracer injection into the sulcal cortex demonstrated that at le

236 Injection into the suprachoroidal space using a micronee

237 No adverse effects of injection into the suprachoroidal space were observed.

238 into the choroid/retina, in order to target injection into the supraciliary space.

239 s the T1 decay of the hyperpolarization upon injection into the system under study.

240 rge carrier mobility, and decreased electron injection into the TiO2.

241 ion to enhance tumor immunogenicity with the injection into the tumor of a TLR9 agonist.

242 alamic ventromedial nucleus (VMH), and Ucn 3 injection into the VMH suppresses feeding.

243 At In Salah, injection into the water leg of a gas reservoir has incr

244 Doxycycline was administered by local injection into the wound base following injury.

245 l of vascular invasion of cancer cells after injection into the yolk sac and extravasation of cancer

246 In contrast, rats that received LV-PKCtheta injections into the 3rd Ventricle did not show any chang

247 Cells retrogradely labeled by injections into the AAF were primarily found in the medi

248 DGCs were also labeled after injections into the anterior dorsolateral thalamus.

249 ns with the ATL by placing retrograde tracer injections into the ATL: the temporal polar (n = 3), per

250 Botulinum toxin injections into the bladder have become established in t

251 These therapies have relied on direct injections into the brain, whereas a clinically desirabl

252 Neurons labeled from tracer injections into the caudal oculomotor complex were distr

253 involving inactivation of the BG by muscimol injections into the caudate nucleus of monkeys and asses

254 he loss of the anorectic response to insulin injections into the central nucleus of the amygdala (CeA

255 We found that muscimol injections into the central PVT dose-dependently increas

256 ing these observations, bidirectional tracer injections into the cerebellar cortex retrogradely label

257 Our data show that chondroitinase injections into the contralesional gray matter of the ce

258 By performing iontophoretic dye injections into the CX, we traced 16 subtypes of neuron

259 ections to MOC neurons by labeling them with injections into the dorsal cochlear nucleus.

260 Finally, dual retrograde injections into the IC and amygdala plus corpus striatum

261 As revealed by anterograde tracer injections into the insular cortex, corticothalamic proj

262 (KD21) or scrambled control sequence (Scr21) injections into the left atrial myocardium.

263 We made focal neurobiotin injections into the midshipman PAG to both map its audit

264 ed cells in the DRif after retrograde tracer injections into the mPFC of stressed rats.

265 Fluorogold injections into the NI resulted in retrograde labeling i

266 Subsequent bilateral isoguvacine injections into the nucleus of the solitary tract furthe

267 phere plus unilateral muscimol plus baclofen injections into the OFC in the contralateral, but not ip

268 romedial medulla (RVM), but not following co-injections into the periaqueductal gray (PAG) or into th

269 Unilateral muscimol plus baclofen injections into the Pir in one hemisphere plus unilatera

270 ealed that alpha-synuclein preformed fibrils injections into the putamen induced intraneuronal inclus

271 1 systematically acquired anterograde-tracer injections into the right cortical and subcortical regio

272 ophysiological assessments in vivo after mAb injections into the rodent hippocampus.

273 h yielded outcomes similar to open-abdominal injections into the same region.

274 Glacial NH eruptions, volcanogenic sulphate injections into the stratosphere cooled the NH preferent

275 nd isolation of ALDHbr cells, followed by 10 injections into the thigh and calf of the index leg.

276 Neurotracer injections into the trigeminal motor nucleus revealed bi

277 is to the pattern of labeled cells following injections into the ventral striatum.

278 ion of retrograde-labeled neurons stained by injections into the ventral tegmental area (VTA), the te

279 Using anterograde injections into this region of the mcIO, we found the fo

280 xcitation of the chromophore, rapid electron injection into TiO(2) and intra-assembly electron transf

281 cm(-1) electric field is created by electron injection into TiO(2) nanocrystallites that induces ion

282 he Ru(III) centers were oxidized resulted in injection into TiO2 [TiO2/Ru(III)-NAr3 + hnu --> TiO2(e(

283 reduction is initiated by ultrafast electron injection into TiO2, followed by rapid (ps-ns) and seque

284 inner Ru(II) is followed by rapid, efficient injection into TiO2.

285 It can quickly solidify upon injection into tissue so as to increase drug retention i

286 a catheter, and exhibits rapid gelation upon injection into tissue.

287 mpatible with the encapsulation of cells and injection into tissues.

288 to the DCs in comparison with controls after injection into tumor-bearing mice, and promoted DC matur

289 s can be turned into an advantage for direct injections into tumors, which then allow the use of high

290 Dual tracer injections into two sites responding to low- and high-fr

291 Injection into Tyr heterozygous (B6CBAF1/JxFVB/NJ) zygot

292 Injections into V1 in 4- and 8-week-old monkeys labeled

293 Injections into V2 labeled neurons in V1, V3, DL/V4, and

294 rt here on experiments that use rabies virus injections into V4 to retrogradely label mono- and disyn

295 In primates, we combined neuronal tracer injections into various arms of the circuit through spec

296 l offspring following intracytoplasmic sperm injection into wild-type ova and implantation of the fer

297 aster clearance of ApoE-deficient TRLs after injection into WT Ndst1f/fAlbCre(-) versus mutant Ndst1f

298 which were analysed for enhancer activity by injection into Xenopus laevis embryos.

299 After injection into Xenopus oocyte nuclei, representative GAN

300 ut not other immune cell populations, and DT injection into zDC-DTR bone marrow chimeras results in c