ライフサイエンスコーパス: microinject

1 ing is observed when antibody against xGu is microinjected.

2 responses paralleled the amount of glutamate microinjected.

3 s of inactivation of MnPN neurons by locally microinjecting 0.2 microl of 1 mM or 10 mM solutions of

4 -1) bradykinin into the lower airways and by microinjecting 0.5 nmol capsaicin into nucleus of the so

5 me of de-afferentation, but abolished CIE if microinjected 2 h later.

6 We microinjected 6-hydroxydopamine or vitamin C into nucleu

7 We then microinjected a GABAA receptor antagonist, an inhibitor

8 Here, we microinjected a GHRH antagonist or GHRHR small interferi

9 Functional downregulation of AKAP79/150 by microinjecting a cell-permeable synthetic AKAP (A-kinase

10 euronal network for clonic AGS in GEPR-3s by microinjecting a competitive NMDA receptor antagonist, D

11 Cre-expressing transgenic mouse lines or by microinjecting a Cre-expressing adeno-associated virus i

12 activation events and embryo development by microinjecting a cRNA that encodes a constitutively acti

13 The PVN was disinhibited by microinjecting a GABA(A) receptor antagonist, bicucullin

14 resent study evaluated the effect of focally microinjecting a NMDA antagonist into the amygdala of ra

15 as mimicked in the PFC of drug-naive rats by microinjecting a peptide containing the Gialpha binding

16 Furthermore, overexpressing PLCbeta1 by microinjecting a Plcb1 cRNA significantly perturbed the

17 y electrical stimulation of the PAG and then microinjecting a selective NK(1) agonist and antagonist

18 Senktide, SP, or vehicle was microinjected above SON.

19 ted, ERK phosphorylation could be induced by microinjected activated Akt, indicating important cross-

20 rons in adult mice (NTS-HIF-1alpha(-/-) ) by microinjecting adeno-associated virus that expressed Cre

21 ional expression of 12 selected receptors by microinjecting agonists into live mouse BAT and analyzin

22 , ligands specific for TLR2 or dectin-1 were microinjected, alone or in combination, into intact spin

23 hmic brainstem slices from neonatal rats, we microinjected AMPA into the pre-BotC or the XIIMN while

24 p and wakefulness were also quantified after microinjecting an adenosine A(1) receptor antagonist int

25 (MLCK) is inhibited pharmacologically or by microinjecting an inhibitory antibody to MLCK.

26 Integrin signaling was stimulated by microinjecting an MMP activator or integrin peptide liga

27 s on both the numbers of embryos that can be microinjected and the ability of transgenes to segregate

28 sed cytosolic calcium in isolated cells when microinjected and was blocked by Ned-19.

29 Using a novel system for microinjecting and electroporating plasmid expression co

30 of tissue, resulting in prolonged ability to microinject, and algorithmic improvements that compensat

31 Inhibiting protein synthesis by microinjecting anisomycin into mPFC blocked the therapeu

32 for these proteins in Chlamydia infection by microinjecting anti-Pls1 and anti-Pls2 antibodies into i

33 Here we describe the effects of microinjecting APC- or EB1- specific monoclonal antibodi

34 oked sympathetic and behavioral responses by microinjecting artificial CSF or muscimol, a neuronal in

35 To improve therapeutic outcomes, we microinjected ASO directly into the E12.5 inner ear.

36 Microinjected at the MPTA hotspot identified, exposure o

37 nine kinase inhibitor H-7 had no effect when microinjected at the time of de-afferentation, but aboli

38 development, the guidance decisions of these microinjected axons were assayed.

39 To this end, we microinjected BDNF or the highly selective TrkB receptor

40 mpus of otherwise normal (wild-type) mice by microinjecting before training a single herpes simplex v

41 the CaMKII activation inhibitor, KN-93, were microinjected bilaterally (100 nl/site) into the PPT of

42 (PACAP(6-38), 15 pmol; minocycline 10 mg/ml) microinjected bilaterally into RVLM had no effect on sei

43 against dopamine beta hydroxylase (DSAP) was microinjected bilaterally into the BNST to remove its NA

44 in conjugated to an antibody against DbH was microinjected bilaterally into the caudal NST in adult r

45 g expression of a truncated form of eNOS was microinjected bilaterally into the NTS to inhibit endoge

46 ve ionotropic glutamate receptor antagonist) microinjected bilaterally into the paraventricular nucle

47 theterized Sprague-Dawley rats that had been microinjected bilaterally to the VMH with an adeno-assoc

48 We have microinjected Box C/D RNAs from Pyrococcus furiosus, a h

49 t increase in proliferative ability in FGF-4 microinjected cardiac cushion mesenchyme as compared wit

50 rs can be modeled in immunocompetent mice by microinjecting CCR9-expressing cancer cell lines into ea

51 a-actinin in non-muscle cells: alpha-actinin-microinjected cells are stiffer and yet mechanically mor

52 The daughters of microinjected cells displayed inequalities in microtubul

53 s and associated with actin stress fibers in microinjected cells.

54 [FFA(i)] was measured by microinjecting cells with ADIFAB, a fluorescently labele

55 We stereotaxically microinjected collagenase, which causes localized bleedi

56 diac cushion mesenchyme as compared with BSA-microinjected controls.

57 e activates NTS GLP-1-expressing neurons, we microinjected corticosterone (0.5 mug) directly into the

58 eggshell; dipping the eggs into CR leachate; microinjecting CR leachate into the air cell or yolk.

59 We microinjected CRISPR-Cas9 and a homology-directed repair

60 alirin in fiber initiation and outgrowth, we microinjected cultured sympathetic neurons with vectors

61 then manipulate nuclear volume in embryos by microinjecting different nuclear scaling factors, includ

62 LPS microinjected directly into the LC increased the activit

63 When microinjected directly into the VLPO of a mouse lightly

64 bens elicits antinociception, we bilaterally microinjected dopamine D1- and D2-receptor subtype selec

65 dy, we found that inactive Drf3 variants and microinjected Drf3 antibodies interfered with Cdc42-indu

66 manipulated rostral ILn activity in rats by microinjecting drugs or applying electrical current and

67 n running-wheel rhythms induced by 8-OH-DPAT microinjected during the midsubjective day.

68 but its use has been limited by the need to microinject dye-labeled nonfunction-blocking antibodies.

69 In addition to calcium fluxes, microinjected dye tracers can be transferred through the

70 We microinjected either FGF2 (200 ng, i.c.v.) or the FG loo

71 antidiabetic effect elicited by icv FGF1, we microinjected either saline vehicle or a low dose of FGF

72 We microinjected embryos with azidosugars at the one-cell s

73 elopmental events in control and CRISPR-Cas9 microinjected embryos.

74 This was tested by microinjecting embryos with venlafaxine immediately afte

75 We provide evidence that microinjected endothelin-1 produces a dose-dependent ele

76 In contrast, microinjected Fab fragments against Listeria monocytogen

77 omal antigen 1 readily stained this antigen, microinjected Fab fragments against M. tuberculosis did

78 orescent protein-expressing M. tuberculosis, microinjected Fab fragments directed against a major sur

79 To test this, we microinjected ferritin into intact adult rat spinal cord

80 luorescence recovery after photobleaching of microinjected FITC-dextran, was 4.9 +/- 0.2- vs. 2.2 +/-

81 monitoring the Brownian motion of individual microinjected fluorescent particles.

82 To investigate this idea, we microinjected fluorescent tracers into live antral folli

83 We microinject fluorescently-labeled tRNA into living cells

84 showed that calpains were active in vivo by microinjecting fluorogenic calpain substrates into corti

85 Next we microinjected forty-five embryos each with five sgRNAs t

86 efined by pressor and depressor responses to microinjected GABA (500 pmol, 50 nl).

87 cious, unrestrained animals before and after microinjecting glutamate receptor agonists and antagonis

88 These hypotheses were tested by microinjecting glutamate receptor antagonists and morphi

89 The lack of effect of microinjecting glutamate receptor antagonists into the v

90 Microinjected golgin-84 or CASP also inhibited Golgi-enz

91 By microinjecting gRNA, hCas9 mRNA and single-stranded dono

92 cted group and one of the two control saline microinjected groups were selectively deprived of REM sl

93 .34 +/- 0.30), while those in NMDA/8-OH-DPAT-microinjected hamsters (0.67 +/- 0.17) were smaller (P<0

94 ler (P<0.05) than those in vehicle/8-OH-DPAT-microinjected hamsters (0.97 +/- 0.10).

95 s (mean +/- S.E.M., h) in muscimol/8-OH-DPAT-microinjected hamsters (1.02 +/- 0.30) were not differen

96 ent (P=0.11) from those in vehicle/8-OH-DPAT-microinjected hamsters (1.34 +/- 0.30), while those in N

97 is a dynamic shuttling transport factor, we microinjected HeLa cells with recombinant hGle1 and cond

98 We microinjected helper virus-free herpes simplex virus vec

99 In subsequent experiments, we microinjected IL-1beta in the nTS bilaterally in anaesth

100 skinesias more potently and effectively when microinjected in striatum than substantia nigra (SN) ret

101 In vivo, gabapentin microinjected in the nucleus accumbens core attenuated c

102 Interleukin (IL)-1beta microinjected in the nucleus tractus solitarii increases

103 receptor antagonist L-703,606 (5 microg) was microinjected in the RVM following LH stimulation with c

104 Cobalt chloride (100 nM) was then microinjected in the RVM to block synaptic activation of

105 Whereas microinjected intact immunoglobulin G molecules against

106 n order that serotonergic compounds could be microinjected into behaviorally identifiable regions of

107 se hnRNP K morpholino oligonucleotides (MOs) microinjected into blastomeres suppressed hnRNP K expres

108 paration (LLPS) in physiologic salt and when microinjected into cell nuclei, producing dense and dyna

109 When oligonucleotide probes are microinjected into cells to image the distribution of RN

110 When these cells were microinjected into E12 to E13 metanephroi and then place

111 5166017 (1.5 or 5.0 mug/side) or vehicle was microinjected into each brain region immediately before

112 he selective 5-HT(2C)R agonist CP-809101 was microinjected into either the BLA or the DS of adult Fis

113 pluripotent mouse, rat, and human cells and microinjected into embryonic-day-8.5 embryos.

114 The transgene cassette was microinjected into fertilized eggs from B6C3 (C3H x C57B

115 g its recognition sites, and is subsequently microinjected into fertilized eggs.

116 use a model system where DNA constructs are microinjected into HeLa cell nuclei, to follow the fates

117 when applied at the basolateral membrane or microinjected into IBDU lumen.

118 nd prevented apoptosis when cytochrome c was microinjected into intact cells.

119 intestinal fatty acid-binding protein), was microinjected into isolated cardiomyocytes from wild typ

120 When IL1beta was microinjected into layer VI, increases in Fos-immunoreac

121 ot actin-depolymerizing factor (ADF)/cofilin microinjected into Listeria-infected cells.

122 s fully targeted to the plasma membrane when microinjected into live Chinese hamster ovary and Madin-

123 ing the response of the QD-based FRET sensor microinjected into live HeLa cells upon extracellular ex

124 e cytosol and nucleus when incubated with or microinjected into macrophages.

125 0-kb genomic D(k) fragment was subcloned and microinjected into MCMV-susceptible (Cmv(s)) (MA/My.L-H2

126 the FnCas9-ribonucleoprotein complex can be microinjected into mouse zygotes to edit endogenous site

127 scribed by endogenous RNA polymerase II when microinjected into nuclei of Xenopus laevis oocytes.

128 ce correlation spectroscopy analysis of CAII microinjected into OLs reveals freely diffusing protein

129 ction of TRE-driven transgenes from plasmids microinjected into one-cell embryos.

130 However, fluorescently labeled calmodulin microinjected into oocytes is shown to have crossed thro

131 ag in onset of transcriptional activity when microinjected into oocytes.

132 e reporter, bacterial beta-galactosidase was microinjected into stage 18 chick cardiac cushion mesenc

133 n expansion in vivo (ovo), FGF-4 protein was microinjected into stage 18 chick inner curvature.

134 KCl was microinjected into such cortical areas to test the effec

135 microg/0.5 microl) or saline was bilaterally microinjected into the ACC, OFC, and DMS of food-deprive

136 ular matrix protein binding to integrins was microinjected into the accumbens core during self-admini

137 The antinociceptive action of morphine microinjected into the amygdala on VAD thresholds was co

138 specific antagonist dihydrokainate (DHK) was microinjected into the anaesthetized rat nTS or applied

139 A receptor agonists (baclofen/muscimol) were microinjected into the anterior cingulate, and prelimbic

140 Baclofen or saline was microinjected into the anterior or posterior VTA of male

141 lofen reduced binge-like ethanol intake when microinjected into the anterior VTA, whereas posterior V

142 ult rats using a standard anterograde tracer microinjected into the caudal visceral sensory region of

143 neuronal tracer pseudorabies virus (PRV) was microinjected into the CEAm or MEAad.

144 ockout mice we show that (125)I-amyloid-beta microinjected into the central nervous system cleared at

145 temporarily inactivates neurons and tracts, microinjected into the central nucleus of the amygdala (

146 ee days after stroke, chondroitinase ABC was microinjected into the cervical spinal cord to induce lo

147 mice, we show that [I]Abeta40 and [I]Abeta42 microinjected into the CNS clear at half the rate that t

148 fer, DNA nanoparticles of various sizes were microinjected into the cytoplasm.

149 The cells were then harvested and microinjected into the developing eyes of day 5 to day 7

150 culline methiodide (BMI) was stereotaxically microinjected into the DMH/PeF region of isoflurane-anes

151 ating hormone (alpha-MSH), were unilaterally microinjected into the DMV of rats, and their effects we

152 mol failed to change reflex micturition when microinjected into the dorsal caudal PAG, microinjection

153 droxy-2-(di-n-propylamino)tetralin (10 muM), microinjected into the dorsal raphe 6 h before lights of

154 Retrograde and anterograde tracers were microinjected into the folia of crus I of the cat cerebe

155 entified chemoattractant sensed by TlpB) was microinjected into the gastroid lumen, it prevented the

156 e, mecamylamine precipitated withdrawal when microinjected into the habenula or the interpeduncular n

157 We have demonstrated that NMU microinjected into the hypothalamic paraventricular nucl

158 he selective Hcrt-1/Ox-A antagonist SB334867 microinjected into the hypothalamic paraventricular nucl

159 in 2-positive medullary collecting duct when microinjected into the kidneys of neonatal mice.

160 insight into the synaptic role of talin, we microinjected into the large lamprey axons reagents that

161 (AMPA), and kainate (KA) elicit feeding when microinjected into the lateral hypothalamus (LH) of sati

162 sts, NMDA, AMPA, and KA, elicit feeding when microinjected into the lateral hypothalamus (LH) of sati

163 ntral antagonism of AT1 receptors (losartan) microinjected into the lateral ventricle reduced BP leve

164 ned that rhodamine-labeled MCH (R-MCH), when microinjected into the lateral ventricle, is internalize

165 cholinergic agonist carbachol (125 nmol) was microinjected into the LH of female Sprague-Dawley rats

166 Vegetative C. difficile, microinjected into the lumen of HIOs, persisted in a via

167 S. Typhimurium microinjected into the lumen of iHOs was able to invade

168 ligand and pretreated with Ni(2+) were then microinjected into the mCherry-expressing COS-1 cells.

169 IL-1beta (10 ng) microinjected into the medial hypothalamus induced two s

170 beta), an immune and brain-derived cytokine, microinjected into the medial hypothalamus, potentiates

171 full genetic differentiation potential when microinjected into the mosquito haemocoel and cdpk3- spo

172 In other naive rats, L-NAME or saline was microinjected into the MPOA before each of 7 daily expos

173 In addition, MK-801, microinjected into the MPOA before each of 7 noncopulato

174 report here that the NMDA antagonist MK-801, microinjected into the MPOA, impaired copulatory behavio

175 a-benzyloxyaspartate (TBOA), was bilaterally microinjected into the NAc and found to dose-dependently

176 ng elicited by the GABA-B agonist, baclofen, microinjected into the NAC shell was dose-dependently bl

177 ing elicited by the GABA-B agonist, baclofen microinjected into the NACs was dose-dependently blocked

178 When PLA2 or melittin was microinjected into the normal spinal cord, the former in

179 e receptor antagonists and the kappa agonist microinjected into the NRM attenuated mu-opioid-induced

180 Furthermore, DOR and MOR agonists microinjected into the NRM in vivo also produced a PLA(2

181 rotoxin saporin (DSAP) or saline vehicle was microinjected into the NTS to lesion catecholaminergic n

182 inhibits voluntary alcohol consumption when microinjected into the nucleus accumbens (AcbSh) of P ra

183 yethylenimine (PEI)/DNA polyplexes that were microinjected into the oocytes of Xenopus laevis, as an

184 the NR2B-receptor-antagonist Ro25-6981 were microinjected into the pACC.

185 combinase and green fluorescent protein were microinjected into the PB to permanently and selectively

186 ) or MK-801 (10 microM; 5 x 100 nl) was also microinjected into the phrenic motonucleus region in oth

187 or artificial cerebrospinal fluid (ACSF) was microinjected into the POAH of rats at the time of hemor

188 os cells were isolated from the epiblast and microinjected into the precardiac mesoderm or neural pla

189 Microinjected into the preoptic anterior hypothalamus (P

190 re incubated with cortical cell cultures and microinjected into the primary somatosensory cortex (SSc

191 also eliminated the inhibitory effect of AP5 microinjected into the PVN on sympathetic nerve activity

192 locked sympathoexcitatory responses to AngII microinjected into the PVN.

193 , N-Me-Phe4, Gly-ol5)-enkephalin (DAMGO) was microinjected into the raphe magnus, a manipulation that

194 antagonist aminophosphonopentanoic acid were microinjected into the rostral ACC.

195 rol) or muscimol (0.34 nmol; 0.5 microl) was microinjected into the rostral LH of halothane-anestheti

196 agonists; and (v) produces hypertension when microinjected into the rostroventrolateral medulla.

197 et, cholera toxin beta subunit (CT-beta) was microinjected into the RVLM to retrogradely label the PV

198 ive 5-HT(2) antagonist, LY-53,857, which was microinjected into the same medial hypothalamic site.

199 ith the NK(1) antagonist, GR82334 (16 nmol), microinjected into the same sites.

200 s end, the SST analogue octreotide (OCT) was microinjected into the striatum prior to a systemic inje

201 ehaviors were not affected by RO5166017 when microinjected into the substantia nigra, infralimbic cor

202 se transition, frequency, and amplitude when microinjected into the ventrolateral medulla (VLM) of th

203 neurons and explain how noradrenergic drugs microinjected into the vlBNST reduce aversive aspects of

204 was conducted using a red fluorescent tracer microinjected into the VLH.

205 ta or kappa opioid receptor antagonists were microinjected into the vlPAG 5 min before intraperitonea

206 DMSO had no effect on nociception when microinjected into the vlPAG alone, but 2% DMSO enhanced

207 al anesthetic lidocaine (2%; 0.5 microl) was microinjected into the vlPAG of halothane-anesthetized r

208 (100 or 1000 ng/side), or vehicle (aCSF) was microinjected into the VTA 20 min before social defeat s

209 ts of a spacer of well-known stiffness, were microinjected into Xenopus laevis oocytes, and the Gd(II

210 been found to prematurely activate CDK2 when microinjected into Xenopus oocytes and when expressed in

211 Micellar solutions of the protein were then microinjected into Xenopus oocytes expressing KCNQ1 chan

212 The TH-GFP constructs were microinjected into zebrafish embryonic cells.

213 Plasma from mice subjected to RIC was microinjected into zebrafish, and neutrophil migration w

214 ollowed by mitochondrial-encoded mCherry was microinjected into zygotes.

215 We also found that SB microinjected intra-VP attenuated cue-induced reinstatem

216 40) RNA in stage 6 oocytes of Xenopus laevis microinjected intranuclearly with SV40 DNA.

217 ap of the early embryo was constructed using microinjected lineage tracers.

218 effects of Group II mGlu agents on sleep, we microinjected LY37 and LY34 into the basal amygdala (BA)

219 We microinjected micelles of Bodipy TMR-PIP(2) into cells,

220 Tolerance to the antinociceptive effect of microinjecting morphine into the ventrolateral periaqued

221 %) would alter the antinociceptive effect of microinjecting morphine into the vlPAG.

222 tolerance to the antinociceptive effects of microinjecting morphine into the vPAG.

223 By microinjecting multiple molecular beacons with different

224 Microinjecting muscimol into the DMH prior to MDMA preve

225 Using single cell assays, we showed that microinjecting mutant abi1-1 protein inhibited the activ

226 By microinjecting mutant MSY2-EGFP chimeric mRNAs into mous

227 he REM sleep-like state (REM(Neo)) caused by microinjecting neostigmine into the PRF.

228 tant did not allow intercellular transfer of microinjected neurobiotin; the alanine mutant allowed tr

229 In this study, we microinjected normal and mutated Tau protein into cultur

230 This was accomplished either by microinjecting NPY conjugated to saporin (NPY-SAP) bilat

231 were previously infected by feeding with DC-microinjected nymphal ticks.

232 section lesion was induced at T9, cells were microinjected on each side of the transection site.

233 y regulate microtubule behavior in cells, we microinjected physiological levels of these two isoforms

234 ours, stained for lamins and the products of microinjected plasmids, and scored blindly using previou

235 Microinjecting purified anti-Glu tubulin antibody into B

236 E and reduced nucleocytoplasmic shuttling of microinjected, recombinant hGle1.

237 We microinjected seven keratin monoclonal antibodies into h

238 In this paper, we microinjected skeletal muscle alphaTM into epithelial ce

239 equired for cortical reorganization, because microinjected sperm chromatin fails to induce cortical r

240 The presence of spindle/chromosomes or microinjected sperm chromatin in the cortical region ini

241 port that cortical reorganization induced by microinjected sperm chromatin is blocked by inhibitors o

242 apsaicin challenge on cough were mimicked by microinjecting substance P (0.5-5 nmol) into the nTS and

243 callosum) compared with WT microglia toward microinjected Tat(1)(-)(7)(2) (2 mug/mouse) in hippocamp

244 inished docked synaptic vesicles in oAbeta42-microinjected terminals, without affecting clathrin-coat

245 ue additionally requires fewer embryos to be microinjected than traditional methods to obtain transge

246 We microinjected the GLT-1 inhibitor, dihydrokainic acid (D

247 We microinjected the GLT-1 inhibitor, dihydrokainic acid (D

248 pression of the opioid peptide dynorphin, we microinjected the kappa-opioid receptor (KOR) agonist U5

249 rgic-induced antinociception was examined by microinjecting the acetylcholine (ACh) agonist carbachol

250 tress-induced elevation of plasma ACTH after microinjecting the alpha(1)-adrenoreceptor antagonist be

251 vo biocompatibility was also demonstrated by microinjecting the compact ligand coated QDs into cells

252 cell stage have been genetically modified by microinjecting the CRISPR/Cas9 components for the genera

253 red the efficiency of target mutations after microinjecting the CRISPR/Cas9 system in metaphase II (M

254 We determined the cardiovascular effects of microinjecting the GABA(A) receptor antagonist, bicucull

255 al activity in the caudal arcuate nucleus by microinjecting the local anesthetic lidocaine (2%; 0.1 o

256 at meiotic arrest can be released in mice by microinjecting the oocyte within the follicle with an an

257 ace with minute quantities of NanO2-IR or by microinjecting the probe into the lumen of small or larg

258 oteins with a FRET donor and acceptor before microinjecting them into cultured cells.

259 to export these bile acids was confirmed by microinjecting them together with inulin in Xenopus laev

260 codon to green fluorescent protein (GFP) and microinjected this construct to generate stable transgen

261 Microinjecting this antibody or the C-terminal fragment

262 By microinjecting tru-RGN RNAs into zygotes, FVII KO mice w

263 Rather than crossing independent lines, we microinjected two transgenes into single-cell embryos fr

264 In a separate experiment, ghrelin microinjected unilaterally into the dorsal vagal complex

265 Blocking nuclear pore formation with microinjected wheat germ agglutinin does not inhibit the

266 When microinjected with a constitutively active AMPK, about 2

267 Grasshopper serotonergic neurons were microinjected with a fluorescent tracer dye and either a

268 mosanum or Lilium longiflorum) pollen tubes, microinjected with a low concentration of the pH-sensiti

269 Then, the BC was microinjected with a sodium channel blocker, tetrodotoxi

270 Mitotic cells microinjected with antibodies to GRASP65 fail to form pr

271 to 10 days following surgery, the rats were microinjected with artificial extracellular fluid, the G

272 In rats previously microinjected with CSF, MDMA elicited significant increa

273 Embryos (1-4 cell stage) were microinjected with either 1 or 10 ng venlafaxine, which

274 Xenopus laevis oocytes microinjected with either AQP7 or AQP9 cRNA exhibited in

275 In intact cells microinjected with fluorescent DNAs and studied by fluor

276 One fibre within a bundle was microinjected with furaptra, a low-affinity rapidly resp

277 uced GABA current rundown in Xenopus oocytes microinjected with HH membrane proteins, but not in the

278 Rats microinjected with ibotenic acid, muscimol, or a CRF ASO

279 Lewis rats (n = 30) were microinjected with LPS (1 or 10 mug) or saline (1 muL) i

280 en fluorescent protein-alpha-tropomyosin and microinjected with mAb17 revealed that the thin filament

281 Embryos microinjected with MO targeting zfAPEX1a intron-exon jun

282 Embryos microinjected with morpholino oligonucleotide (MO) targe

283 Xenopus oocytes were microinjected with mRNA encoding HA-tagged protein VII a

284 developed from MTH1 knock-out zebrafish eggs microinjected with N6-methyl-dATP compared with noninjec

285 for enhanced transfection, HuH-7 cells were microinjected with naked or compacted plasmids encoding

286 In Xenopus laevis oocytes microinjected with PCFT cRNA, uptake of 2, like that of

287 same-oil control during adolescence and then microinjected with retrograde tracer into the medial amy

288 Embryos microinjected with single sgRNA targeting FOXN1, RAG2, I

289 I cells (a rat bladder tumor cell line) were microinjected with the caged FAK peptide and locally pho

290 , normal human thyroid epithelial cells were microinjected with the papillary thyroid carcinoma oncog

291 Finally, living cells microinjected with the peptide substrate exhibit a 2-fol

292 nt on pol III transcription, HeLa cells were microinjected with the selective pol III inhibitor, Tage

293 Consistent with these observations, cells microinjected with these antibodies exhibited a marked d

294 Drugs were given systemically or microinjected within the rostral ventromedial medulla (R

295 ent is essential to mediate RNA transport in microinjected Xenopus laevis oocyte nuclei.

296 Although microinjected Xenopus oocytes and/or transfected cells i

297 te microtubules when eggs are inseminated or microinjected, yet numerous maternally-nucleated cytaste

298 To explore physiological relevance, we microinjected zebrafish embryos with the same oligonucle

299 Microinjecting zebrafish embryos with full-length mouse

300 nt loci with high efficiency (0.62%-5.13% of microinjected zygotes).