1 In this study, we found that
injection of ATP into a peripheral nerve can mimic the e
2 and other tissue injury, we hypothesize that
injection of ATP into a peripheral nerve might mimic the
3 After
injection of cDNA into a single nucleus, GFP-alpha1S and
4 Direct
injection of hepatocytes into a single mouse lymph node
5 We found that intracellular
injection of Neurobiotin into a specific ganglion cell t
6 e demonstrate that a single, intraperitoneal
injection of TM into a pregnant mouse at 8.5 days postco
7 In normal animals,
injections of CTB into a single barrel column resulted i
8 Injections of HSV1 into a portion of area 7a labeled man
9 Injections of N2O into a biogas-fed engine at flow rates
10 Injection of NAC into ADAMTS13-deficient mice led to the
11 Injections of carbachol into adjacent sites dorsal or ve
12 Injection of LSKL into adult Id cDKO mice led to downreg
13 (SMKO)) specifically in vascular SM cells by
injection of tamoxifen into adult transgenic mice.
14 that was verified by intracerebroventricular
injections of colchicine into adult zebrafish.
15 =12 months) were treated with intraarticular
injections of methylprednisolone into all joints with cl
16 In the absence of Ca2+, the
injection of AxV into an aqueous subphase beneath a DMPA
17 Injection of inhibitors into animals under alkaline stre
18 d on B cells and in non-immune tissues after
injection of lipopolysaccharide into animals.
19 Discrete
injections of BDA into auditory cortex labeled bands of
20 Injection of cAMP into B51 mimicked the effects of opera
21 After intraocular
injection of VEGF into both eyes, topical pazopanib (10
22 ediate postglomerular segments identified by
injection of dye into Bowman's space of accessible surfa
23 s ciliary neurotrophic factor (CNTF), direct
injection of CNTF into brain parenchyma, and ectopic exp
24 Injection of PAL into C3H/HeJ mice stimulated production
25 e term RNAi came from the discovery that the
injection of dsRNAs into Caenorhabditis elegans interfer
26 Injection of LPS into cirrhotic rats induces pre-coma an
27 Injection of dexamethasone into control rats 60 min befo
28 y, we have shown that the intravenous (i.v.)
injection of pneumococci into CR1(+) mice also results i
29 Furthermore, direct
injection of DP1 into day 7 established MCA205 tumors in
30 Thus,
injection of capsaicin into deep tissues results in a lo
31 sistent with our observations in human skin,
injection of filler into dermal equivalent cultures caus
32 E at eclosion was supported by findings that
injection of 20E into developing pupae to delay the fall
33 POM neurons were retrogradely labeled by
injections of tracer into DM-ICo, but POM projections la
34 Injections of DiI into DMP produced anterograde label ov
35 microinfarction after intracoronary arterial
injection of MSCs into dogs.
36 omotion, and rats learned to lever-press for
injections of Delta9THC into each of these regions.
37 Birthdates were established by a single
injection of bromodeoxyuridine into embryos of closely s
38 Injection of dsRNA into embryos resulted in potent and s
39 Injection of replicons into established xenograft flank
40 ough intrabacterial YopD is required for the
injection of toxins into eukaryotic cells, secreted YopB
41 iesterases, but inhibition of a Ca2+ rise by
injection of EGTA into follicle-enclosed mouse oocytes d
42 Injection of TSLP into gamma(c) KO mice induced the expa
43 In contrast,
injection of Neurobiotin into ganglion cells almost alwa
44 Intravenous
injection of MPRs into glioblastoma-bearing mice led to
45 The intradermal (i.d.)
injection of LPS into gp49B1-null (gp49B-/-) but not gp4
46 We demonstrate that
injection of mycolactone into guinea pig skin results in
47 Injections of biocytin into head and limb areas of secon
48 To our surprise, an intravascular
injection of VEGF into healthy animals, but not those de
49 gle-nucleotide mutation reduces the type III
injection of YopE into HeLa cells, even though the predi
50 A single intratumoral
injection of hrR3 into HT29 flank tumors significantly r
51 very bypassed endocytosis by electrophoretic
injection of nanoparticles into human bronchial epitheli
52 p. (100 micro g/animal, every alternate day)
injection of sBG into human breast carcinoma MDA-MB-231
53 Injection of TRAIL into human skin xenografts promotes f
54 Anterior chamber
injection of OVA into IL-10 knockout mice elicited norma
55 tumors formed after either s.c. injection or
injection of cells into implanted mouse bone demonstrati
56 Injection of SHN into inguinal adipose tissue 2 weeks af
57 gh type III secretion system (T3SS)-mediated
injection of effectors into intestinal epithelial cells
58 Injection of APL into irradiated congenic (Ly-5.1) mice,
59 Injection of dsTcDDC into larvae produced a lethal pupal
60 Injection of p50 into late prophase cells removed dynein
61 Intracerebral
injections of MN into LC increased rCMRglc in morphine-d
62 TNF-alpha and TGF-beta after an intravenous
injection of PPD into LP guinea pigs.
63 rgan histology were normal after intravenous
injection of Ad35K(++) into mice that express human CD46
64 injection of lipopolysaccharide (LPS) or by
injection of antigen into mice bearing antigen-primed T
65 CP) recapitulating human disease is repeated
injection of cerulein into mice.
66 Injection of dsRNA into mice induced a rapid, dramatic,
67 cific IL-6 is produced within 24 h after the
injection of eggs into mice.
68 Injection of Flt3L into mice resulted in an increased nu
69 We found that
injection of GCsMs into mice with severe colitis abolish
70 The intraperitoneal
injection of ghrelin into mice 15 min before the adminis
71 Remarkably, intravenous
injection of IL4I1 into mice with experimental autoimmun
72 Chronic intraperitoneal
injection of JWH133 into mice also increased excitatory
73 pear resistant to induced shedding in vitro,
injection of lipopolysaccharide into mice results in los
74 n of the fact that on consecutive days after
injection of thioglycolate into mice, increased numbers
75 Injection of TNFalpha into mice caused a rapid up-regula
76 Interestingly,
injection of tx3a into mice elicits an excitatory respon
77 responses to AAV capsids after intramuscular
injection of vectors into mice and nonhuman primates.
78 Finally, intraperitoneal
injections of sulforaphane into mice during active HSV i
79 Injection of AdCA5 into mouse eyes induced neovasculariz
80 Injection of CRAMP into mouse air pouches resulted in th
81 In vivo
injection of mycolactone into mouse ears consistently al
82 Nevertheless we propose that natural
injections of sand into muddy strata at continental marg
83 After intraperitoneal
injection of XMRV into Mus pahari mice, XMRV proviral DN
84 The
injection of doxorubicin into muscle 2 days after a prev
85 After direct
injection of MDX1 into muscles of mdx mice, immunohistoc
86 Subcutaneous
injection of jacalin into neonatal mice drastically redu
87 Injection of scFvs into neonatal mice identified 2 patho
88 Injection of TSLP into neonatal mice induced the expansi
89 to stress can be restored by intra-amygdala
injection of neuropsin into neuropsin-deficient mice and
90 ssessed through adoptive transfer of MDSC or
injection of arginase into noninjured mice.
91 Injection of AdCA5 into nonischemic limb was sufficient
92 With respect to TrkB mRNA levels,
injection of BDNF into normal eyes and optic nerve crush
93 ated dishes has enabled rapid and consistent
injection of macromolecules into nuclei of CD34(+), CD34
94 Direct
injection of G207 into nude rat flank tumors suppressed
95 condary hyperalgesia induced by subcutaneous
injection of formalin into one hindpaw.
96 Thus,
injection of histones into one-cell embryos faithfully r
97 y mutations in multiple genes through direct
injection of RNAs into one-cell embryos, demonstrating t
98 Results obtained with direct
injections of drugs into one brain region at a time supp
99 However,
injection of Cdc6 into oocytes undergoing GVBD is suffic
100 Our data demonstrate both that
injection of OPN into OPN-deficient mice enhances the CR
101 Injections of muscimol into other areas known to project
102 Direct
injection of Asc into ovaries phenocopied DHAR-induced t
103 Consistently,
injection of alphaGalCer into PD-1-deficient mice failed
104 Injection of corazonin into pharate larvae elicits relea
105 proteins are required in the translocation (
injection) of effectors into plant cells.
106 Injection of ecdysone into pre-amplification stage larva
107 mbryonic neural tube, we found that a single
injection of tamoxifen into pregnant mice induced Cre-me
108 Injection of Mobilan into primary tumors of the prostate
109 Injection of NV1066 into primary breast tumors resulted
110 those projecting to PVN (identified by prior
injection of DiI into PVN), in rat hypothalamic slices.
111 However, 5 days after the intracisternal
injection of blood into rabbits to mimic SAH, cerebral a
112 Injection of M40403 into rat models of inflammation and
113 Furthermore, intravenous
injection of FS50 into rats and monkeys elicited recover
114 d secretion was stimulated after intravenous
injection of PACAP into rats treated with somatostatin a
115 Injections of PRV into rectus abdominis labeled large pr
116 In vivo, unilateral
injection of serotonin into RTN stimulated inspiratory m
117 Following
injection of AAV2 into RVLM of TH-Cre rats, phenylethano
118 As expected,
injection of Kyn into RVLM or muscimol into commNTS virt
119 expected to vary periodically, affecting the
injection of material into Saturn's E ring and its forma
120 Moreover,
injection of R4A into SCID mice in vivo significantly up
121 Intracellular
injection of DiI into secretagogin cells revealed an ave
122 D3 in vivo was also greatly increased by the
injection of CT into sham-TPTX rats and normocalcemic TP
123 Injection of Ae1a into sheep blowflies (Lucilia cuprina)
124 ied DA neuron subpopulations in slices after
injection of "Retrobeads" into single target areas of ad
125 Injection of dye into single motoneurons resulted in spa
126 f lesion studies and of studies using direct
injections of drugs into single brain areas.
127 ear than implied by studies using lesions or
injections of drugs into single brain areas.
128 allodynia and heat hypoalgesia compared with
injection of capsaicin into skin.
129 Injection of S1P into Sphk1-/- mice increased histamine
130 Intratumoral
injection of Mobilan into subcutaneously growing syngene
131 a quantitative transplantation assay, using
injection of keratinocytes into subcutis combined with l
132 nt malignant brain tumors, treated by direct
injections of MAb into surgically created resection cavi
133 Direct
injection of ethanol into symptomatic vertebral hemangio
134 ulate the expression of trkA receptors after
injection of NGF into targets.
135 Injection of acid into the gastrocnemius muscle results
136 Intramuscular
injection of AdCA5 into the ischemic limb of db/db mice
137 ctive stimulation of the carotid body by the
injection of adenosine into the carotid artery causes a
138 Local
injection of adiponectin into the POA induced prolonged
139 e cardiovascular responses to intra-arterial
injection of AEA into the hindlimb of normal, cardiomyop
140 hamber-associated immune deviation following
injection of Ag into the eye.
141 Injection of Ag into the thymus of adult animals induces
142 atory pressure by a brief, irregularly timed
injection of air into the cranial thoracic air sac durin
143 n followed 1 hour and 15 minutes later by an
injection of air into the stroma.
144 Injection of amoebae into the AC induced a robust neutro
145 ds save time and cost by allowing for direct
injection of analytes into the column; this is in stark
146 Injection of anandamide into the RF dose-dependently exc
147 Injection of AngII into the lateral ventricle (LV) incre
148 The peripheral tolerance that arises after
injection of antigen into the anterior chamber (anterior
149 ) Tr thymocytes (THYr) can be induced by the
injection of antigen into the eye, an immunologically pr
150 (ACAID), an eye-derived tolerance evoked by
injection of antigen into the ocular anterior chamber (A
151 Injection of apelin into the ischemic myocardium resulte
152 chondrial calcium uptake and was mimicked by
injection of ATP into the terminal.
153 Moreover, in vivo
injection of ATPgammaS into the sciatic nerve increased
154 Dermal fibrosis was induced by subcutaneous
injection of bleomycin into the dorsal skin of MCP-1-/-
155 The
injection of blood into the subdural space or into the b
156 In sham-operated rats,
injection of BMI into the PVN increased MAP by 13 +/- 3
157 the ISLN was anaesthetised by transcutaneous
injection of bupivacaine into the paraglottic compartmen
158 Injection of cAMP into the extracellular spaces in the r
159 Stimulation of the TRPv1 receptor by
injection of capsaicin into the arterial supply of the h
160 r 100 mg/kg, i.p.) was administered prior to
injection of capsaicin into the hindpaw of rats, which p
161 plasma extravasation induced by intradermal
injection of capsaicin into the paw.
162 Injection of capsaicin into the plantar or palmar surfac
163 ult cats in which atonia was produced by the
injection of carbachol into the pontine tegmentum (AS-ca
164 ase of extinction was coincident with a slow
injection of carbon into the atmosphere, and ocean pH re
165 y week for 4 weeks) or vehicle 4 hours after
injection of carrageenan into the air pouch using previo
166 and the thermal hyperalgesia induced by the
injection of carrageenan into the paw are suppressed by
167 The
injection of carrageenin into the rat hind paw induced a
168 and titanium oxide, possibly mediated by the
injection of carriers into the semiconducting titanium o
169 In vivo,
injection of CDCs into the infarcted mouse hearts result
170 Compared to PO CFA injection, the
injection of CFA into the TMJ produced a significantly s
171 Large-scale
injection of CO2 into the Earth's crust requires an unde
172 This effect was specific to
injection of CRH into the caudal DRN and was not produce
173 Injection of CTB into the GG muscle resulted in retrogra
174 Following
injection of CTB into the lateral DRN, retrogradely labe
175 Injection of DiI into the node, and electroporation of a
176 oxicity of doxorubicin could be amplified by
injection of doxorubicin into the eyelid of rabbits 2 da
177 spatial navigational learning and memory and
injection of drugs into the hippocampus can affect both
178 Injection of electrons into the particles causes pronoun
179 The
injection of electrons into the quantum-confined states
180 We show for the first time that
injection of EMU into the infarcted myocardium increases
181 One week after unilateral
injection of FG into the cAMY, cells containing FG+TH mR
182 Furthermore, stereotactic
injection of fibrinogen into the mouse cortex is suffici
183 The intramyocardial
injection of FL into the infarct border zone decreased i
184 Injection of formalin into the hind paw induces a biphas
185 ats using microdialysis techniques following
injection of formalin into the hindpaw.
186 e first study that reports that subcutaneous
injection of formalin into the rat's hind paw induces mi
187 chment procedure involving transconjunctival
injection of gas into the vitreous cavity, combined with
188 ined hyperglycemia was induced with a single
injection of glucose into the yolk on day 0.
189 firing rate of LC neurons in vivo, and local
injection of hcrt1 into the LC induced the expression of
190 In addition, direct
injection of histones into the renal arteries of mice de
191 Injection of insulin into the preoptic area of the hypot
192 oth as an accumulation device for the pulsed
injection of ions into the ELIT and as a collision cell
193 view includes the following observations: 1)
Injection of IP3 into the animal hemisphere produced lar
194 Consistent with this explanation direct
injection of IP3 into the soma promoted wave propagation
195 Injection of KA into the vitreous humor led to an up-reg
196 Injection of lidocaine into the nucleus basalis magnocel
197 Since acute
injection of lidocaine into the RVM also affected baseli
198 Finally, stereotactic intracerebral
injection of lipopolysaccharide into the developing peri
199 Injection of LPS into the lacrimal gland inhibited neura
200 Injection of LPS into the portal vein resulted in increa
201 Injection of LPS into the skin provides a model for stud
202 optimized the timing and dosing regimen for
injection of mAb into the cortex.
203 then challenged on day 21 by intraarticular
injection of mBSA into the right knee.
204 Furthermore,
injection of mEAR2 into the air pouches of mice resulted
205 Previous research has shown that
injection of morphine into the ventral tegmental area (V
206 into the medulla, forebrain, (or both) after
injection of morphine into the vPAG.
207 In this work, we show that
injection of MPP+ into the presynaptic terminal of the s
208 and these were virtually abolished by prior
injection of muscimol into the DMH.
209 ed tachycardia was markedly suppressed after
injection of muscimol into the RP, but the response was
210 Bilateral
injection of muscimol into the ventral respiratory colum
211 dosages comparable to those used in humans,
injection of NBPs into the peritoneum caused recruitment
212 Injection of neurobiotin into the LM and CM confirmed th
213 Injection of Neurobiotin into the spinal cord revealed t
214 els of NR3A normally persist into adulthood,
injection of NMDA into the eye killed more retinal gangl
215 Injection of NMDA into the fifth lumbar (L5)-DRG induced
216 In contrast, central
injection of NMDA into the lateral ventricle increased p
217 und that the brain damage produced by direct
injection of NMDA into the somatosensory cortex is atten
218 Similarly,
injection of Noggin into the postnatal rat eye failed to
219 ystemic nicotine (0.5 mg/kg, s.c.) and local
injection of norBNI into the amygdala.
220 of embryonic DA neurons, and in vivo, direct
injection of NTN into the substantia nigra protects matu
221 t are reprogrammed up to 100% within 24 h by
injection of nuclei into the germinal vesicle (GV) of gr
222 Injection of OSM into the footpad increased CCL21 mRNA e
223 Injection of OVA into the AC of eyes of mice with EAU fa
224 e immune deviation similar to that evoked by
injection of OVA into the anterior chamber of the eye.
225 The results showed that
injection of physostigmine into the SFO induced water in
226 both drinking and cellular activation after
injection of physostigmine into the SFO.
227 Pressure
injection of picrotoxin into the antennal lobe eliminate
228 Thus, the
injection of pMCKhLPL into the peritoneum or quadriceps
229 Injection of procaine into the pericardial space effecti
230 Thirty-six to 40 hours following
injection of PRV into the contralateral PFC, numerous ca
231 Further, direct
injection of QA into the striatum produces selective deg
232 vation of mTOR was prevented by posttraining
injection of rapamycin into the amygdala, formation of t
233 Local
injection of riluzole into the LC dose-dependently reduc
234 We show that
injection of RNase into the yolk cell after the 1K cell
235 o the RP, but the response was unaffected by
injection of saline into the same region.
236 One used the direct
injection of sample into the luminol reagent stream, and
237 munolabeling of the original tumor and after
injection of SG231 into the liver of BALB/cByJ-scid mice
238 The continuous
injection of sulfur into the stratosphere has been sugge
239 nce of procedural or drug toxicity following
injection of TA into the SCS in porcine eyes.
240 hesis, we blocked axonal conduction by focal
injection of tetrodotoxin into the spinal cord.
241 We also show that
injection of tPA into the cerebrospinal fluid in the abs
242 k of tumor dissemination associated with the
injection of tracers into the ovarian cortex.
243 To our knowledge, the
injection of tracers into the ovarian ligaments has not
244 ster mice received a 20-microL intramuscular
injection of turpentine into the right thigh.
245 e sites to the PVH were evident after direct
injection of virus into the PVH, suggesting that these r
246 Using stereotactic
injection of viruses into the hippocampus of adult wild-
247 Injection of viruses into the rat brain showed that a SI
248 Furthermore,
injection of viruses into the subretinal space of the ra
249 Injection of VU573 into the hemolymph of adult female mo
250 Under constant-flow conditions,
injections of AngII into the hindquarters perfusion circ
251 hout affecting nursing behavior, and control
injections of baclofen into the region dorsal to VTA wer
252 In contrast, single or double
injections of bFGF into the eyeball had no effect on RGC
253 Extracellular
injections of biocytin into the anteroventral cochlear n
254 ward auditory fibers in the ICX, labelled by
injections of biocytin into the central nucleus of the i
255 Single
injections of ChABC into the spinal cord led to long-ter
256 trogradely labeled cells in area X following
injections of CTB into the locus coeruleus.
257 We have used focal
injections of DiI into the developing mouse hindbrain in
258 Injections of DSAP into the PVH abolished 2DG-induced fe
259 "Control"
injections of FG into the neocortex, septum, and ventral
260 After
injections of Fluorogold into the tensor tympani muscle,
261 However,
injections of GSH into the antennal lobes prior to mians
262 Bilateral
injections of Kyn into the ventrolateral medulla at the
263 In turn,
injections of lidocaine into the VMT only transiently re
264 Injections of losartan into the LV blocked the dipsogeni
265 ) and three strains of mice had stereotactic
injections of LPS into the caudate.
266 disease was induced in Balb/c mice by direct
injections of LPS into the palatal gingival tissues adja
267 disease was induced in Balb/c mice by direct
injections of LPS into the palatal gingival tissues adja
268 In contrast, unilateral
injections of muscimol into the AcbSh consistently incre
269 Injections of muscimol into the median raphe nucleus (MR
270 the drug, we also observed food intake after
injections of muscimol into the overlying ventricle or l
271 The NPR was abolished following bilateral
injections of muscimol into the perihypoglossal premotor
272 e noradrenergic agent yohimbine or by direct
injections of NMDA into the DMH.
273 Direct bilateral
injections of orexin into the DVC increased intake of pa
274 Single
injections of rAAV into the substantia nigra pars compac
275 Using focal
injections of retrovirus into the ventral telencephalon
276 Site-directed
injections of T1AM into the LC elicited a significant, d
277 distribution of corticospinal neurons after
injections of tracers into the lower cervical segments o
278 s characteristic of animals receiving direct
injections of virus into the cortex.
279 Conversely,
injection of glucose into these same brain regions enhan
280 ion in the hippocampus and that stereotactic
injection of anisomycin into this region impairs memory
281 f the heart, at least in carnivores, because
injection of glutamate into this area decreases heart ra
282 Four monkeys (Cebus apella) received
injections of HSV1 into three different subregions of th
283 Injection of electrons into TiO2 resulted in a blue shif
284 Direct
injection of DNA into tissue, although safer than viral
285 Intravenous
injection of tPA into tPA-/- or wild-type mice produced
286 Importantly,
injection of Eg5 into TPX2-CT-arrested blastomeres cause
287 Injection of DT into transgenic rats but not wild-type r
288 Injection of KKO into transgenic mice expressing differe
289 , and opens possibilities towards electrical
injection of spins into transition metal dichalcogenides
290 l of fluids and gas from the subsurface, and
injection of fluids into underground formations.
291 m Pneumocystis-infected mice as well as i.p.
injection of Pneumocystis into uninfected IFrag(-/-) mic
292 Moreover, the
injection of eggs into vaccinated mice resulted in a red
293 xamined sucrose intake in response to direct
injections of ondansetron into various sites of the dors
294 Injections of RDA into VL consistently labeled dense fib
295 Acute pancreatitis was induced by
injection of cerulein into wild-type and Trpc3-/- mice.
296 d daily starting 4 days after intraarticular
injection of mBSA into wild-type (WT) mice, and inflamma
297 Injection of obELVs into wild-type C57BL/6 mice results
298 Second, we found that
injection of RA into wild-type adult males induced, inde
299 In vivo testing was performed through direct
injections of G207 into xenografts of human colorectal c
300 t in Drosophila oocytes but not embryos, and
injection of dmos into Xenopus embryos blocks mitosis an