ライフサイエンスコーパス: immunoreactive

1 e out of five responsive neurons were sst2a -immunoreactive.

2 d in the stomach, and most of them were CGRP immunoreactive.

3 ost areas of the nervous system are SIFamide-immunoreactive.

4 cells were choline acetyltransferase (ChAT)-immunoreactive.

5 nderneath the inner hair cells were also MOR immunoreactive.

6 eurons were immunoreactive; a subset was non-immunoreactive.

7 ative if < 1% or 0% of tumor cell nuclei are immunoreactive.

8 y of spinal afferent nerve endings were CGRP-immunoreactive.

9 relative to the exosomal marker Alix, a Nogo-immunoreactive, 24-kDa protein is enriched in exosomes 2

10 f APP/PSEN1 mice, a model of AD amyloidosis, immunoreactive 7B2 co-localized with aggregation-prone p

11 ked, reactive microglia (CR3/43- and/or CD68-immunoreactive), a pathology not seen in control subject

12 In the human most of the (SG) neurons were immunoreactive; a subset was non-immunoreactive.

13 nfocal microscopy were used to determine NPY-immunoreactive afferents to the VTA.

14 e CC lining and were only rarely found to be immunoreactive against oligodendrocyte progenitor marker

15 Unexpectedly, we also find prominent p62-immunoreactive, alphaS-, NFL-, and peripherin-negative i

16 s and in PMN extracellular traps; 2) minimal immunoreactive and active Mmp-8 or Mmp-9 are detected on

17 key for orchestrating T cell infiltration in immunoreactive and immunoresponsive tumors.

18 se HGSCs most closely resemble the so-called immunoreactive and mesenchymal subsets of human HGSCs.

19 We found that the previously described immunoreactive and mesenchymal subtypes of HGSOC, which

20 key aspects of tumor-immune dynamics in the immunoreactive and mesenchymal subtypes of human HGSC, w

21 Most spinal afferent endings were CGRP-immunoreactive and morphologically classified as "simple

22 ely 14.0 MBq nmol(-1) Both radiotracers were immunoreactive and stable in human serum.

23 immobilized salivary agglutinin but remained immunoreactive and were readily aggregated by fluid-phas

24 sposon-mutant library, here we identified an immunoreactive antigen that was lost in a putative glyco

25 The immunoreactive antigens from both HN13 and JGS4143 were

26 Immunoreactive APOBEC2 was localized to the cell nucleus

27 ion in tissue homogenates and the percent TH-immunoreactive area in the NPPa.

28 ated and human fluids, consisted of the most immunoreactive areas of the protein.

29 as were telencephalic aromatase activity and immunoreactive aromatase (24 hour time point only).

30 pal sclerosis of ageing, smooth muscle actin-immunoreactive arterioles had thicker walls (P < 0.05),

31 ereologic methods were used to quantify GFAP-immunoreactive astrocyte density and soma volume in laye

32 ateral ventricle FG injection, and (2) GLP-1-immunoreactive axon terminals were observed adjacent to

33 antified the density of tyrosine hydroxylase-immunoreactive axons as a measure of dopaminergic innerv

34 mmunoreactive neurons were surrounded by TRH-immunoreactive axons that were seen in close proximity t

35 ropathological abnormality, and somatostatin-immunoreactive axons were exuberant in the dentate gyrus

36 Immunoreactive B cell lymphoma 2 (Bcl-2) and induced mye

37 rons included four distinct types of tubulin-immunoreactive bipolar cells (one likely also tyrosine h

38 here is no vesicular glutamate transporter 3-immunoreactive bouton, specific to C-LTMRs, on PKCgamma-

39 Numerous met-enkephalin (mENK) and dynorphin-immunoreactive boutons appeared to contact ARC TH neuron

40 strong, and that a large number of dynorphin-immunoreactive boutons terminate on or near anorexigenic

41 ocampi displayed proportional losses of syt2-immunoreactive boutons, PV boutons, and granule cells.

42 d, monocyte-derived AMs are initially highly immunoreactive but more plastic, able to change their fu

43 Here, we used stimulated immunoreactive Calcitonin Gene-Related Peptide (iCGRP) r

44 ein is absorbed systemically and retains its immunoreactive capacity in human serum.

45 Unlike the arterioles, CD34-immunoreactive capillaries had dimensions that were unch

46 c plaque demonstrated that RO5444101 reduced immunoreactive cathepsin S (P < 0.05), elastin degradati

47 munoreactive (PV-IR) interneurons, calbindin-immunoreactive (CB-IR) interneurons, and calretinin-immu

48 ody to the alpha(2)delta(3) subunit revealed immunoreactive cell bodies in the ganglion cell layer an

49 hrenia-1 (DISC1), although no differences in immunoreactive cell numbers were observed.

50 Normal liver contained rare COL15A1-immunoreactive cells adjacent to the bile ducts and cana

51 more, estrogen-withdrawn females had more OT-immunoreactive cells and OT messenger RNA in the paraven

52 RBPMS-immunoreactive cells and RGCs identified by other techni

53 f the caudal preoptic area, whereas LPXRFa-R-immunoreactive cells are distributed widely.

54 The presence of 5HT- and VAChT-immunoreactive cells in segments of the common carotid a

55 o analyze the distribution of chromogranin A immunoreactive cells in serial sections of human fetal p

56 The presence of 5HT- and TH-immunoreactive cells in the aorta, pulmocutaneous artery

57 e primary somatosensory cortex and increased immunoreactive cells in the basolateral amygdala compare

58 d RBPMS is not expressed in syntaxin (HPC-1)-immunoreactive cells in the inner nuclear layer (INL) an

59 with the number of choline acetyltransferase-immunoreactive cells in the NBM.

60 In addition to four large immunoreactive cells in the pars intercerebralis (group

61 The large majority (over 80%) of calretinin-immunoreactive cells is located in the inner nuclear lay

62 Notably, almost all ERalpha-immunoreactive cells of the OV/MEPO also expressed nNOS.

63 n into glial fibrillar acidic protein (GFAP)-immunoreactive cells over neurons, while overexpression

64 The staining intensity and the percentage of immunoreactive cells varied among the studied cases.

65 but not P0 or P4, mice, in which ERbeta-EGFP-immunoreactive cells were densely clustered near the thi

66 Distinct groups of NOS-immunoreactive cells were observed in pallial and subpal

67 Conspicuous CART-immunoreactive cells were observed in the bed nucleus of

68 The immunoreactive cells were quantified by computerized ima

69 tral nerve cord, we identified several other immunoreactive cells, which seem to have no corresponden

70 in regions and immunofluorescence showed TRH-immunoreactive cells/fibers in the olfactory bulb, telen

71 In POA, distinct TRH-immunoreactive cells/fibers were seen in nucleus preopti

72 Immunoreactive-cells and expression-levels of spinal PAR

73 o showed a reduction in major myelin protein immunoreactive clusters 7 and 14 days postinjury, as com

74 ompare CM formulas regarding the presence of immunoreactive CM components, IgE reactivity, allergenic

75 eactive (CB-IR) interneurons, and calretinin-immunoreactive (CR-IR) interneurons.

76 TAMs were the predominant cells expressing immunoreactive CXCR4 in chemotherapy-treated mouse tumor

77 Strong to moderate immunoreactive D1R expression was found in 30% of 751 pr

78 Distinct groups of DA immunoreactive (DA-ir) cells were observed in the olfact

79 Both round and fusiform DCX-immunoreactive (DCX-ir) cells were found in area X and H

80 The M5R-immunoreactive dendrites received a balanced input from

81 e-label experiments showed that the SIFamide-immunoreactive descending neurons are identical to previ

82 of the contralaterally projecting serotonin-immunoreactive deuterocerebral interneurons (CSDns): the

83 , the "contralaterally projecting, serotonin-immunoreactive deutocerebral neurons" (CSDns), within th

84 ser to the core amyloid plaque, whereas RTN3 immunoreactive DNs were mostly located in the outer laye

85 esize TH in the dorsomedial ARC also contain immunoreactive dopamine, and show either bursting or non

86 medial ARC where 94% of TH neurons contained immunoreactive dopamine: bursting and nonbursting neuron

87 Half (50%) of the CGRP-immunoreactive DRG neurons lacked detectable SP and had

88 njury markedly increased the number of Panx1-immunoreactive DRG neurons.

89 analyzed pro-TRH-mRNA expression, mapped TRH-immunoreactive elements in the brain and pituitary, and

90 of numerous choline acetyl transferase-like immunoreactive en plaque motor endplates and substance P

91 inous peritrophic matrix (PM) that separates immunoreactive epithelial cells from microbes present wi

92 tributed to a significant reduction of their immunoreactive epitopes.

93 We report that TNX was present in calretinin-immunoreactive extrinsic nerve endings in mouse and huma

94 d cells per side with normalized striatal TH-immunoreactive fiber innervation and bidirectional synap

95 mmunoreactive neurons were contacted by CART-immunoreactive fibers and 96 +/- 2.8% NPY-immunoreactive

96 CART-immunoreactive fibers in IN showed a significant reducti

97 mmunofluorescence showed that neither LPXRFa-immunoreactive fibers nor LPXRFa-R is closely associated

98 he position of vasoactive intestinal peptide-immunoreactive fibers was more superficial compared to t

99 Portal tracts (PTs) with immunoreactive fibers were counted in each section and c

100 CART-immunoreactive fibers were found in the subpallium, hypo

101 In the pituitary, TRH-immunoreactive fibers were seen in the neurohypophysis,

102 e spinal cords of this new model showed SOD1 immunoreactive fibrillar inclusions.

103 ow that nearly half of all human cancers are immunoreactive for a LINE-1-encoded protein.

104 -sensitive dorsal root ganglion neurons were immunoreactive for an antibody to TRPV4, as assessed by

105 reported specialized basket-like structures, immunoreactive for calbindin, that likely underlie synap

106 ntial innervation by trigeminal nerve fibers immunoreactive for calcitonin gene-related peptide (CGRP

107 were the most commonly observed, while those immunoreactive for calretinin and parvalbumin were spars

108 sent study quantified axons and interneurons immunoreactive for choline acetyltransferase (ChAT) in r

109 tress to activate hindbrain neurons that are immunoreactive for either prolactin-releasing peptide or

110 the lateral accessory lobe cluster were also immunoreactive for GABA and the GABA-synthesizing enzyme

111 identified fewer bulbospinal non-C1 neurons immunoreactive for GABA(Aalpha1) but a higher percentage

112 higher percentage of bulbospinal C1 neurons immunoreactive for GABA(Aalpha1) in sedentary animals.

113 e number of bulbospinal C1 or non-C1 neurons immunoreactive for GABA(Aalpha2) .

114 ly approximately 25% of the PV population is immunoreactive for m1AChRs.

115 Cortical interneurons, immunoreactive for neuronal nitric oxide synthase (nNOS)

116 Similarly, rat beta-cells were not immunoreactive for PC2.

117 of the striatum and ubiquitinated inclusions immunoreactive for polyglutamine (polyQ) antibodies.

118 ease groups, marked decreases of PV neurons (immunoreactive for PV) and WFA/PNNs were observed in the

119 ls in a superficial sub-layer (L2a) that are immunoreactive for reelin and project to the dentate gyr

120 s of PV neurons and PNNs labeled with WFA or immunoreactive for the major PNN protein, aggrecan, in t

121 e quantified the densities of ChC cartridges immunoreactive for vesicular GABA transporter (vGAT+), w

122 In addition, the number of Fos-immunoreactive (Fos-ir) neurons in the nucleus accumbens

123 (177)Lu-octapa-trastuzumab constructs, with immunoreactive fractions of 0.99 for each compared to 0.

124 Substance P-like immunoreactive free nerve endings were also present in t

125 the distribution of gamma-aminobutyric-acid;-immunoreactive (GABA-ir) neurons in four species of sea

126 describes the gamma-aminobutyric acid (GABA)-immunoreactive (GABA-ir) neurons in the buccal ganglia o

127 n the moderately variable group, we detected immunoreactive IL-27 (953 +/- 504 pg/mg lysate), a media

128 photoreceptor-associated proteins, and Iba1-immunoreactive immune cells.

129 ons in the Botzinger Complex (BotC) and NK1R-immunoreactive/inspiratory neurons in the preBotC.

130 , associated with increased plasma levels of immunoreactive insulin and proinsulin.

131 Individuals with more galanin-immunoreactive intermediate nucleus neurons had less fra

132 stereology to quantify the number of galanin-immunoreactive intermediate nucleus neurons in each indi

133 , they demonstrate that a paucity of galanin-immunoreactive intermediate nucleus neurons is accompani

134 ivation of parvalbumin- (PV) or somatostatin-immunoreactive interneurons aborted spontaneously occurr

135 PKCgamma-immunoreactive interneurons appear to receive exclusivel

136 The majority of synapses on PKCgamma-immunoreactive interneurons are asymmetric (likely excit

137 PKCgamma-immunoreactive interneurons contain GABAA ergic and glyc

138 ary afferents were found to contact PKCgamma-immunoreactive interneurons suggests that myelinated, bu

139 ive bouton, specific to C-LTMRs, on PKCgamma-immunoreactive interneurons.

140 ion imbalances involving loss of parvalbumin immunoreactive interneurons.

141 coverage of blood vessels by endfeet of AQP4-immunoreactive (IR) astrocytes was significantly reduced

142 lretinin- and gamma-aminobutyric acid (GABA)-immunoreactive (IR) cells were highly vulnerable to glau

143 r, a thorough characterization of AVP and OT-immunoreactive (ir) fibers and cell bodies across age an

144 We also compared ChAT-immunoreactive (ir) interneuron morphological types amon

145 a subset of calcitonin gene-related peptide-immunoreactive (IR) myenteric plexus neurons thought to

146 We tested the hypothesis that SST-immunoreactive (IR) neurons are decreased in the amygdal

147 ach neuron, we determined if hypothalamic TH-immunoreactive (ir) neurons express vesicular glutamate

148 m against sbLPXRFa2, which revealed sbLPXRFa-immunoreactive (ir) perikarya in the olfactory bulbs-ter

149 In contrast, individual gephyrin-immunoreactive (IR) puncta, a postsynaptic scaffolding p

150 Most calbindin-immunoreactive (IR) Renshaw cells survive to end stage b

151 other markers, to characterize the Galphat-S-immunoreactive (ir) system in the CNS of the sea lamprey

152 present in 24 +/- 0.7% of somatostatin (SOM)-immunoreactive (IR) varicosities; 20 +/- 4.3% of substan

153 aim was to map the distribution of GFRalpha3-immunoreactive (-IR) axons in the female rat bladder, us

154 ndicated by a greater number of somatostatin-immunoreactive (-ir) cells in the CA1 pyramidal layer an

155 ition, we comprehensively characterized 5-HT-immunoreactive (-ir) innervation throughout the brain, i

156 ChAT-immunoreactive (-ir) perikarya were seen in the olfactor

157 croscopy and 3D reconstruction of melanopsin immunoreactive (-ir) RGCs, we applied the criteria used

158 Corazonin-immunoreactive (-ir) terminals overlapped with projectio

159 y non-calcitonin gene-related peptide (CGRP)-immunoreactive (-IR), medium- to large-sized neurons tha

160 SGCs, which were identified by expression of immunoreactive Kir4.1 and glutamine synthetase, were clo

161 dicate cultured APCs release high amounts of immunoreactive LEP following exposure to hypoxia, contin

162 t amino acid position 100 (p.D100Y) and high immunoreactive levels of leptin.

163 About 50% of the GABA-like immunoreactive (-lir) spiking type I local interneurons

164 c shafts and 60% of dendritic spines were M2 immunoreactive (M2R(+) ).

165 nd decreased peritoneal proinflammatory CD86 immunoreactive macrophage number.

166 Immunoreactive materials were localized in neuronal peri

167 and CLOVAR subtypes (CLOVAR differentiated, immunoreactive, mesenchymal, and proliferative).

168 plant, we found host-derived synapses on GFP-immunoreactive MGE cells bodies and dendrites.

169 TNBCs with an immunoreactive microenvironment exhibited tumoral infilt

170 y) loss of choline acetyl-transferase (ChAT)-immunoreactive motoneurons which remained virtually unch

171 e compared methods for the quantification of immunoreactive NAT1 and NAT2 with seven different antibo

172 Most FFA3-immunoreactive nerve fibres and nerve endings were choli

173 in response to mucosal stroking, reduces MET-immunoreactive neurites, and increases susceptibility to

174 r's disease are amyloid-beta plaques and tau-immunoreactive neurofibrillary tangles.

175 -NC was generated based on density of TDP-43 immunoreactive neuronal cytoplasmic inclusions in the ne

176 ASP-immunoreactive neuronal populations were rather similar

177 More tyrosine hydroxylase-immunoreactive neurons and significant behavioral improv

178 n of E2 BSA alone increases the number of PR-immunoreactive neurons and the expression level of PR pr

179 RT-immunoreactive fibers and 96 +/- 2.8% NPY-immunoreactive neurons expressed cFos during fasting.

180 antibody, enhanced migration of doublecortin-immunoreactive neurons in 1 d differentiated FMRP-defici

181 n NPPa are hypophysiotropic, none of the TRH-immunoreactive neurons in NPPa accumulated neuronal trac

182 Although tyrosine hydroxylase (TH)-immunoreactive neurons in NPPa are hypophysiotropic, non

183 The density of c-Fos immunoreactive neurons in other brain regions that recei

184 tensive, global loss of c-Fos and Arc/Arg3.1 immunoreactive neurons in the auditory cortex 15 days af

185 aptic inputs to specific types of calretinin-immunoreactive neurons in the guinea-pig colon.

186 Moreover, MHFD offspring had fewer oxytocin immunoreactive neurons in the hypothalamus.

187 these data, we have identified all orcokinin-immunoreactive neurons in the locust central complex and

188 A great proportion of nNOS-immunoreactive neurons in the OV/MEPO and ARH were seen

189 ter ipl injection of CFA, the number of NK1R-immunoreactive neurons in the RVM was increased by 30%,

190 creased preservation of tyrosine hydroxylase immunoreactive neurons in the substantia nigra (p<0.05).

191 melanin-containing and tyrosine hydroxylase-immunoreactive neurons in the substantia nigra pars comp

192 ology of individually identifiable serotonin-immunoreactive neurons in the ventral nerve cord of Zyge

193 were used to estimate the total number of PR-immunoreactive neurons in the VMN and the PR protein con

194 , the distribution of quinine-stimulated Fos-immunoreactive neurons in two taste-associated forebrain

195 Tilapia LPXRFa-immunoreactive neurons lie in the posterior ventricular

196 he data suggest that the descending SIFamide-immunoreactive neurons play a developmental role in orga

197 Furthermore, we show that not all immunoreactive neurons produce serotonin, but have the c

198 labeling intensity of c-Fos- and Arc/Arg3.1-immunoreactive neurons progressively increase in neighbo

199 In the preBotC 54% of sst2a -immunoreactive neurons were also positive for NK1R.

200 luorescence revealed that 94 +/- 2.1% of NPY-immunoreactive neurons were contacted by CART-immunoreac

201 The majority of TH-like immunoreactive neurons were detected in the peripheral n

202 onversely, the total numbers of NPY- and VIP-immunoreactive neurons were reduced by 55% and 30%, resp

203 No differences in ZNF804A-immunoreactive neurons were seen in schizophrenia or rel

204 However, 87 +/- 1.6% NPPa TH-immunoreactive neurons were surrounded by TRH-immunoreac

205 The first tubulin-immunoreactive neurons, a small group of four to six cel

206 ontains a comparably low number of serotonin-immunoreactive neurons, facilitating individual identifi

207 pathways of uptake and release of ASP by ASP-immunoreactive neurons.

208 ve fibers and a trend toward decreased c-Fos immunoreactive neurons.

209 d by highly similar morphologies of SIFamide-immunoreactive neurons: immunolabeling in various insect

210 nally, we distinguished three subtypes of PV-immunoreactive neurons: multipolar, bipolar and spherica

211 bipolar neuron type (tubulin- and FMRFamide-immunoreactive) occurred deeper in the tissue, associate

212 H), but JH tumors were significantly more ER-immunoreactive (P = 0.0001) than AH tumors.

213 d directly contact pigment-dispersing factor-immunoreactive (PDF-ir) circadian pacemaker neurons with

214 and to determine the absorption kinetics of immunoreactive peanut protein in relation to the allergi

215 thods were successful in demonstrating that: immunoreactive peanut protein was absorbed shortly after

216 To identify the specific immunoreactive peptides in apoA-I, we have developed a s

217 The immunoreactive peptides were further sequenced by mass s

218 r approach successfully identified two novel immunoreactive peptides, recognized by autoantibodies fr

219 e major complexes contained or could contain immunoreactive peptides.

220 ed consistent results and showed that ssGnih-immunoreactive perikarya were present in the olfactory b

221 neurofibrillary tangles interacted with PHF1-immunoreactive phosphorylated tau.

222 aused a 50-70% reduction in Golgi-associated immunoreactive PI-4P that correlated with Golgi localiza

223 d nerves (452.6 [25th-75th IQR, 196.0-811.2] immunoreactive pixels per mm(2) and 62.7 [25th-75th IQR,

224 er mm(2) and 62.7 [25th-75th IQR, 0.0-230.3] immunoreactive pixels per mm(2), P = .02), and epithelia

225 outcomes are not completely understood, this immunoreactive platform is crucial for precipitating isl

226 , leading ultimately to a two-part FMRFamide-immunoreactive plexus and an apparently separate tyrosin

227 issue, associated with part of the FMRFamide-immunoreactive plexus.

228 an apparently separate tyrosine hydroxylase-immunoreactive plexus.

229 Phenylethanolamine N-methyl transferase-immunoreactive (PNMT-ir) axons were detected among orexi

230 Therefore, the immunoreactive potential of old and modern wheat cultiva

231 breeding may have inadvertently changed the immunoreactive potential of wheat.

232 Immunoreactive preparations of the radiolabeled antibodi

233 Der p 1 in milk is immunoreactive, present in similar amounts as dietary eg

234 and there was a concomitant increase in NK1R-immunoreactive processes in CFA-treated rats.

235 glion cell layer and inner nuclear layer and immunoreactive processes in the inner plexiform layer an

236 terns of both 5-HT- and tyrosine hydroxylase-immunoreactive processes relative to each other, to olfa

237 was filled with a beaded network of SIFamide-immunoreactive processes that especially strongly invade

238 In conclusion, PACAP-immunoreactive projections with colocalized CtB represen

239 , we have expanded the subset of C. burnetii immunoreactive proteins validated by enzyme-linked immun

240 reduction in the density of alpha-synuclein immunoreactive puncta in dendritic processes of cultured

241 ndrites express postsynaptic density (PSD95) immunoreactive puncta suggesting that they receive synap

242 In the mouse retina, Cx50-immunoreactive puncta were predominantly localized on la

243 y on PC dendrites, as indicated by VGLUT2(+) immunoreactive puncta, and computational modeling demons

244 Previously, it was reported that parvalbumin immunoreactive (PV(+) ) interneurons receive strong exci

245 Normally parvalbumin-immunoreactive (PV) interneurons strongly inhibit granul

246 icular that the vast majority of parvalbumin-immunoreactive (PV) neurons in macaque V1 express the m1

247 ions of inhibitory interneurons: parvalbumin-immunoreactive (PV-IR) interneurons, calbindin-immunorea

248 SAXS) to determine the structure of the main immunoreactive region from a major antigen from Leptospi

249 To evaluate whether PACAP-immunoreactive retinal projections are useful as a marke

250 eks, and all Brn3a-, SMI-32-, and melanopsin-immunoreactive RGCs also express RBPMS immunoreactivity.

251 gested that the raised P dimers might expose immunoreactive S/P1-1 subdomain epitopes.

252 chnologies, we previously identified several immunoreactive Salmonella Typhi antigens that seem promi

253 stained cells was 20% +/- 14.24%, and median immunoreactive score (IRS) was 1.

254 Applying an immunoreactive score (IRS), we found Piwi-like 1 positiv

255 Immunoreactive secretin and its mRNA were predominantly

256 Calcitonin gene-related peptide-immunoreactive sensory innervation is distributed primar

257 Immunoreactive signals for the desmosomal protein plakog

258 ns of both viruses, indicating that a common immunoreactive site exists in this region.

259 ses in the diameters of tyrosine hydroxylase immunoreactive soma in cave Astyanax in the olfactory bu

260 The lack of PDF-like-immunoreactive somata associated with the onychophoran o

261 We visualize PV- and mAChR-immunoreactive somata by dual-immunofluorescence confoca

262 neral rule, at least four prominent SIFamide-immunoreactive somata occur in the pars intercerebralis.

263 intercerebralis (group 1), smaller SIFamide-immunoreactive somata were detected in the pars intercer

264 Immunoblotting revealed rab17 immunoreactive species at 25 kDa (the predicted rab17 mo

265 On the other hand, a approximately 70-kDa immunoreactive species of Panx3, likely glycosylated, si

266 The GABA-like immunoreactive, spiking type I local interneurons had no

267 In total, 88 proteins in 40 2DE immunoreactive spots were identified via mass spectromet

268 Surprisingly, immunoreactive SQSTM1 also accumulated in the olfactory

269 Although counts of p-ERK1/2 immunoreactive synapses did not correlate with OLM perfo

270 (C) correlating with the formation of UCH-L1-immunoreactive tau tangles, whereas UCH-L1(M) has been i

271 CB1-immunoreactive terminals frequently contacted dendrites

272 hich completely eliminated spinal cord TRPV1-immunoreactive terminals, altered dorsal horn GRP immuno

273 rom symmetric gamma-aminobutyric acid (GABA)-immunoreactive terminals, whereas 3.6% received two syna

274 ass, we detected an extensive filigree of TH-immunoreactive (TH-ir) arborizations in the appendage ne

275 inal field measures correlate with nigral TH immunoreactive (TH-ir) cell counts only when nigral TH-i

276 ty, also enabled us to relate activity in TH-immunoreactive (TH-ir) neurons to appetitive and consumm

277 cells (one likely also tyrosine hydroxylase immunoreactive) that bore ciliated dendrites penetrating

278 plaque motor endplates and substance P-like immunoreactive, thin and varicose free nerve endings.

279 significant sparing of tyrosine hydroxylase-immunoreactive (THir) neurons in the substantia nigra pa

280 TH-like immunoreactive (THli) neurons were distributed throughou

281 glial tau pathology in CTE is composed of 4R-immunoreactive thorn-shaped astrocytes, echoing the morp

282 The gliomas were immunoreactive to BRAF V600E antibody.

283 at differed was the high proportion of WMICs immunoreactive to calbindin, whereas in primates (macaqu

284 to visualize single axons and nerve endings immunoreactive to calcitonin gene-related peptide (CGRP)

285 to visualize traced nerve axons and endings immunoreactive to CGRP.

286 (NTS) of brainstem including the NTS neurons immunoreactive to dopamine beta-hydroxylase (DBH).

287 aled perivascular, neuronal, and glial cells immunoreactive to IL-9, and quantitative analysis in ind

288 A subpopulation of SGCs expressed immunoreactive TRP vanilloid 4 (TRPV4) and responded to

289 Circulating immunoreactive trypsinogen (IRT), a biomarker of exocrin

290 nce the late 1970s when the potential of the immunoreactive trypsinogen assay for early identificatio

291 lastase-1 concentrations increased and serum immunoreactive trypsinogen concentrations decreased), an

292 the composition of the epitope, we isolated immunoreactive tryptic fragments by Western blotting and

293 CCL5 and CXCL9 coexpression revealed immunoreactive tumors with prolonged survival and respon

294 ot exposed on free particles, rapidly become immunoreactive upon virus-cell binding.

295 Overall, we identified 608 immunoreactive V. cholerae antigens in our screening, 59

296 effective method for generating safe, highly immunoreactive vaccines.

297 Nearly 72% of immunoreactive VEGF was similarly released over 42 days,

298 burnetii proteins, previously identified as immunoreactive, were screened for reactivity to naturall

299 ns were composed only of mouse tau, and were immunoreactive with antibodies to 4R tau, phosphotau, mi

300 0-60 min), but some proteins were stable and immunoreactive with simulated intestinal digestive condi