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 old mice and transplanted by intraperitoneal injection into 8- to 12-week-old fumarylacetoacetate hyd

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

9 AV9-mediated motor neuron transduction after injection into a newborn cynomolgus macaque.

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 nses to tones and to guide retrograde tracer injections into A1 and VAF.

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

15 After injection into adult Anopheles gambiae, some strains of

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

17 - 1.7 and 3.9 +/- 0.8, respectively), but GH injections into Ames dwarf mice restored the normal leve

18 05 for dwarf vs. nonmutant control mice.) T4 injections into Ames dwarf mice, in contrast, did not re

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

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

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

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

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

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

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

26 Upon intravenous injection into arthritic mice, tolerogenic DCs migrated

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

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

29 Injection into basalt formations provides unique and sig

30 Upon injection into blastocyst, BCL2-expressing EpiSCs contri

31 ctivated hypothalamus receptors after direct injection into brain.

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

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

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

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

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

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

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

39 th a neutralizing anti-CXCR6 antibody before injection into chimeras.

40 which reproduced all aspects of the tumor on injection into closely related chickens.

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

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

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

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

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

51 Tracer injections into distinct zones of the BF map in AI retro

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

53 r of cells retrogradely labeled after tracer injection into either hindbrain region.

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

55 Bilateral muscimol (MUS) injections into either the hippocampus or PR equally pro

56 Injection into embryos of a non-coding RNA bearing multi

57 Botulinum toxin injection into epicardial fat pads during coronary arter

58 % normal saline, 1 mL at each fat pad; n=30) injection into epicardial fat pads during surgery.

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

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

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

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

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

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

65 Successful spin injection into graphene makes it a competitive contender

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

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

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

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

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

71 pecific intracellular compartments following injection into host cells.

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

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

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

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

76 sCD89 injection into IgA1-expressing mouse recipients induced

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

78 Notably, rmIL-23 injections into IL-17A(-/-) mice produced little ear swe

79 As expected, rmIL-23 injections into IL-22(-/-) mice resulted in relatively l

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

81 Ras(G12D) cells was observed on intrafemoral injection into immunodeficient mice, presumably because

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

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

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

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

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

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

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

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

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

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

92 ing helps objectively distinguish between an injection into low versus high compliance tissue (e.g. i

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

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

95 us arterial blood (30 mul) or thrombin (5 U) injection into mice brains.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

114 Dye injections into neurons connecting the central complex w

115 We observed a modest preference for injection into neutrophils over injection into other cel

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

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

118 uces skin inflammation following intradermal injection into normal mice.

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

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

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

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

123 eference for injection into neutrophils over injection into other cell types, but in general the repe

124 Tracer injection into ovarian ligaments has been shown to detec

125 dINs, which normally fire singly to current injection, into pacemakers firing within the normal swim

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

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

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

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

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

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

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

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

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

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

139 als studied direct antisense oligonucleotide injections into single peripheral lower limb muscles, wh

140 lasia following recombinant murine (rm)IL-23 injections into skin.

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

142 Following retrograde tracer injection into SSN (biotinylated dextran amine 3K or Flu

143 Injections into subareas of the arcopallium and posterio

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

145 of these cells in vivo following their s.c. injection into syngeneic immunocompetent (but not immuno

146 In order to increase the accuracy of tracer injections into target sites, we first conducted a syste

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

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

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

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

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

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

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

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

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

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

157 aged vasculature after expansion ex vivo and injection into the bloodstream.

158 In nonimmunized mice, direct VSV-G/GFP injection into the brain invariably resulted in lethal e

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

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

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

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

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

164 olecular desorption is maximized by electron injection into the chemisorbed molecular ring at low vol

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

166 Stereotaxic retroviral injection into the dentate gyrus of wild-type and alpha7

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

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

189 Balanced saline solution was injection into the left eye of each rabbit as a control.

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

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

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

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

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

195 CTb injection into the medullary RF labels cells and axonal

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

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

198 a neutralizing anti-CXCR6 antibody prior to injection into the mouse chimeras.

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

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

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

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

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

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

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

206 ZIP injection into the nucleus accumbens reduced expression

207 -arterial chemotherapy involves single-agent injection into the ophthalmic artery under careful neuro

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 CE2-eGFP) or the control virus (Ad-eGFP) via injection into the pancreas.

211 CTb injection into the PBN retrogradely labels cells in the

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

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

214 e chemisorbed molecular ring at low voltage, injection into the physisorbed molecular ring above a th

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

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

217 IGF-1 injection into the POA caused dose-dependent hyperthermi

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

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

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

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

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

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

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

225 Two days after direct injection into the rat infarcted myocardium, Sfrp2 inhib

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

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

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

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

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

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

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

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

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

235 l nervous system demyelination, lysolecithin injection into the spinal cord white matter, we performe

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

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

238 Tracer injection into the sulcal cortex demonstrated that at le

239 Injection into the suprachoroidal space using a micronee

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

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

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

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

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

245 Remarkably, injection into the vitreous of OIR mice of hematopoietic

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

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

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

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

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

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

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

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

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

255 bsequent VSV-G/GFP, VSV-CT1, and VSV-CT9-M51 injections into the brain.

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

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

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

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

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

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

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

263 en the hippocampus and PR, contralateral MUS injections into the hippocampus and PR resulted in sever

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

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

266 Most corticosteroid injections into the joint are guided by the clinical exa

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

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

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

270 Fluorogold injections into the NI resulted in retrograde labeling i

271 aortic afferents (at 3 and 6 months), or DiI injections into the nucleus ambiguus to label vagal card

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

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

274 1 systematically acquired anterograde-tracer injections into the right cortical and subcortical regio

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

276 ss biocytin/biotinylated dextran amine (BDA) injections into the SG or extrastriate cortex labeled in

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

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

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

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

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

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

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

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

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

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

290 ucleus (Uva), which was substantiated by BDA injections into Uva that labeled terminals in Av.

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

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

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

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

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

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

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

298 After injection into Xenopus oocyte nuclei, representative GAN

299 1 RNA translates very poorly if at all after injection into Xenopus oocytes.

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