ライフサイエンスコーパス: microinject

1 responses paralleled the amount of glutamate microinjected.

2 ing is observed when antibody against xGu is 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 ional expression of 12 selected receptors by microinjecting agonists into live mouse BAT and analyzin

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

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

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

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

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

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

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

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

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

30 lar inhibition of Tf recycling was caused by microinjecting anti-kinesin antibody.

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

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

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

34 Microinjected at the MPTA hotspot identified, exposure o

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

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

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

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

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

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

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

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

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

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

45 ridyl]carbamoyl]-in doline), or vehicle were microinjected bilaterally through a chronically implante

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

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

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

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

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

51 The daughters of microinjected cells displayed inequalities in microtubul

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

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

54 We stereotaxically microinjected collagenase, which causes localized bleedi

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

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

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

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

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

60 LPS microinjected directly into the LC increased the activit

61 omammillary nucleus (TMN): when gabazine was microinjected directly into the TMN, it attenuated the s

62 When microinjected directly into the VLPO of a mouse lightly

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

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

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

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

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

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

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

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

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

72 Here, we microinjected epitope-tagged (Myc and Flag) cDNAs for mZ

73 In contrast, microinjected Fab fragments against Listeria monocytogen

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

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

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

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

78 monitoring the Brownian motion of individual microinjected fluorescent particles.

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

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

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

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

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

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

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

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

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

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

89 .34 +/- 0.30), while those in NMDA/8-OH-DPAT-microinjected hamsters (0.67 +/- 0.17) were smaller (P<0

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

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

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

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

94 We microinjected helper virus-free herpes simplex virus vec

95 metabolite exhibits biological effects when microinjected in living cells.

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

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

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

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

100 Whereas microinjected intact immunoglobulin G molecules against

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

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

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

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

105 5166017 (1.5 or 5.0 mug/side) or vehicle was microinjected into each brain region immediately before

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

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

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

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

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

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

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

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

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

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

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

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

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

119 0-kb genomic D(k) fragment was subcloned and microinjected into MCMV-susceptible (Cmv(s)) (MA/My.L-H2

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

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

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

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

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

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

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

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

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

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

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

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

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

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

134 The retrograde tracer Fluoro-Gold (FG) was microinjected into the anterior or posterior VTA in rats

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

177 When purified HDHB protein was microinjected into the nucleus of cells in early G(1), t

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

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

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

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

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

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

184 Microinjected into the preoptic anterior hypothalamus (P

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

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

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

188 antagonist aminophosphonopentanoic acid were microinjected into the rostral ACC.

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

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

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

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

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

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

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

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

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

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

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

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

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

202 (100 or 1000 ng/side), or vehicle (aCSF) was microinjected into the VTA 20 min before social defeat s

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

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

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

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

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

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

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

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

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

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

213 To study Aurora B kinase in vertebrates, we microinjected mitotic XTC cells with inhibitory antibody

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

215 %) would alter the antinociceptive effect of microinjecting morphine into the vlPAG.

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

217 By microinjecting multiple molecular beacons with different

218 Microinjecting muscimol into the DMH prior to MDMA preve

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

220 By microinjecting mutant MSY2-EGFP chimeric mRNAs into mous

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

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

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

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

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

226 modified polystyrene microspheres, which are microinjected or endocytosed, often show directed motion

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

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

229 Microinjecting purified anti-Glu tubulin antibody into B

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

231 We microinjected seven keratin monoclonal antibodies into h

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

252 ltures of rabbit corneal epithelial cells by microinjecting them with C3 resulted in an inhibition of

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

254 Microinjecting this antibody or the C-terminal fragment

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

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

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

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

259 By microinjecting wild-type and mutant proteins into the cy

260 When microinjected with a constitutively active AMPK, about 2

261 ith Bcl-XL and completely inhibited in cells microinjected with a dominant-negative caspase 9 express

262 ock is rapidly overridden when the cells are microinjected with a dominant-negative construct of Mad2

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

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

265 Here, we show that HeLa cells microinjected with a polyclonal antibody to survivin exh

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

267 tic spindles of Drosophila embryos that were microinjected with anti-EB1 antibodies.

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

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

270 tor-mediated cell death was blocked in cells microinjected with Bcl-XL and completely inhibited in ce

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

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

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

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

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

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

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

278 act muscle fibers were isolated from FDB and microinjected with indo-1 to measure changes in sarcopla

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

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

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

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

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

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

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

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

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

293 Somata of Mauthner neurons were microinjected with various RNAs.

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).