ライフサイエンスコーパス: immunoreactive

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

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

3 cells were choline acetyltransferase (ChAT)-immunoreactive.

4 nderneath the inner hair cells were also MOR immunoreactive.

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

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

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

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

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

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

11 dicated GABAergic feedback onto RBCs via NOS-immunoreactive ACs.

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

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

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

15 We found that immunoreactive APC is transiently induced in the oligode

16 Immunoreactive APOBEC2 was localized to the cell nucleus

17 oc analysis showed a difference in the GLAST immunoreactive area of patients with Meniere's disease w

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

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

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

21 and NAAG elicited the expression of a novel immunoreactive ASPA species in select GSC nuclei, sugges

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

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

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

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

26 Four immunoreactive bands at 120, 70, 50, and <30 kDa were de

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

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

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

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

31 also Abeta40-, Abeta42-, and Abeta oligomer-immunoreactive, but only weakly thioflavine S- or 6-CN-P

32 n human samples, polo-like kinase (PLK)1/2/3-immunoreactive cancer cells were present in the preponde

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

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

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

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

37 RFRP-3-immunoreactive cell bodies were found scattered within t

38 present study, only a small number of GLP-1-immunoreactive cell bodies were observed in the nucleus

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

40 showed a significant reduction in calbindin-immunoreactive cells (range: 36-67% lower), whereas fema

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

42 RBPMS-immunoreactive cells and RGCs identified by other techni

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

44 t there was a notable reduction in calbindin-immunoreactive cells in midline/intralaminar/posterior d

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

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

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

48 he spatial distribution pattern of calbindin-immunoreactive cells in the dorsal thalamus was similar

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

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

51 The majority of GLP-1-immunoreactive cells in the NTS were not FOS-positive.

52 hormone, and corticotropin-releasing factor immunoreactive cells in the paraventricular nucleus.

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

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

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

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

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

58 The number of calretinin-immunoreactive cells was similar for all experimental gr

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

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

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

62 The immunoreactive cells were quantified by computerized ima

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

64 Immunoreactive cholinergic boutons were found to be colo

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

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

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

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

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

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

71 The M5R-immunoreactive dendrites received a balanced input from

72 to the extrasynaptic membrane of parvalbumin-immunoreactive dendrites.

73 n due to tau, and TAR DNA-binding protein 43 immunoreactive deposits, alpha-synucleinopathies, hippoc

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

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

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

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

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

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

80 alpha-Syn immunoreactive dystrophic neurites contained numerous el

81 ing and memory showed the occurrence of RTN3-immunoreactive dystrophic neurites in the cortex.

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

83 ally, we observed persistent levels of Abeta-immunoreactive entities that were of a size consistent w

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

85 increased extractability of pectin and xylan immunoreactive epitopes in apap1 mutant aerial biomass s

86 reactive projections; we also quantified AVP-immunoreactive fiber density in gonadectomized and sham-

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

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

89 CART-immunoreactive fibers in IN showed a significant reducti

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

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

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

93 -melanocortin stimulating hormone (alphaMSH)-immunoreactive fibers were significantly reduced in neur

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

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

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

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

98 they, like extraocular motoneurons, are also immunoreactive for calcitonin gene-related peptide.

99 The proportion of GABAergic neurons immunoreactive for CB or CR varied depending on the subd

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

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

102 pecimens, and showed that reversal cells are immunoreactive for factors typically expressed by osteob

103 Syt2-labeled cells were immunoreactive for glycine but lacked immunoreactivity f

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

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

106 ation is little understood, cortical neurons immunoreactive for neuronal nitric oxide synthase (nNOS)

107 CCA cells were strongly immunoreactive for PDGF-A and -D, whereas CAFs expressed

108 Most ChR2-expressing VLM neurons (75%) were immunoreactive for phenylethanolamine N-methyl transfere

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

110 se multicentric amyloid plaques, selectively immunoreactive for prion protein, within the cerebral an

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

112 we identified a novel variant of INR that is immunoreactive for the 40 kDa huntingtin associated prot

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

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

115 f the ChR2-positive axonal varicosities were immunoreactive for vesicular glutamate transporter-2 (78

116 neurons are innervated by primary afferents immunoreactive for vesicular glutamate transporters 1 an

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

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

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

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

121 Numerous glycine-immunoreactive (Gly-ir) neurons were observed in differe

122 Because the total number of NeuN-immunoreactive hilar neurons was unaffected, the decline

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

124 TAR DNA-binding protein 43 immunoreactive inclusions and neurites were also found i

125 Large FUS-immunoreactive inclusions fill the perikaryon of survivi

126 rontotemporal lobar degeneration with TDP-43 immunoreactive inclusions have been described (types A-D

127 rons as well as a significant increase in SP-immunoreactive innervation onto these neurons.

128 ous regions in which males have a denser AVP-immunoreactive innervation than females.

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 er spiking in pyramidal cells or parvalbumin immunoreactive interneurons (PV) in the hippocampus and

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

136 PKCgamma-immunoreactive interneurons appear to receive exclusivel

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

138 PKCgamma-immunoreactive interneurons contain GABAA ergic and glyc

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

140 ion imbalances involving loss of parvalbumin immunoreactive interneurons.

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

142 lm KO mice reduces the number of parvalbumin-immunoreactive interneurons.

143 ving hippocampal neurons contained ubiquitin-immunoreactive intranuclear inclusions.

144 y were mostly gamma-aminobutyric acid (GABA)-immunoreactive (IR) and located in the GC layer.

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

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

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

148 and sacral DRG neuronal subpopulations were immunoreactive (IR) for CGRP (30 +/- 3% and 29 +/- 3%, r

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

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

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

152 gonadal steroids and GnRH-1- and kisspeptin-immunoreactive (ir) neurons in subordinate adults and in

153 In general, CB-immunoreactive (ir) neurons were less abundant than CR-i

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

155 y to adult levels, whereas the density of PV-immunoreactive (IR) puncta (presumed PVBC boutons) incre

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

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

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

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

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

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

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

163 vious studies and the distribution of VGluT2-immunoreactive (-ir) puncta.

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

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

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

167 Within the DMV >95% mCherry-immunoreactive(ir) axonal varicosities were tyrosine hyd

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

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

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

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

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

173 nd decreased peritoneal proinflammatory CD86 immunoreactive macrophage number.

174 munoreactivity was present in some Aif1/Iba1-immunoreactive macrophages.

175 human tears or saliva surprisingly detected immunoreactive material with a higher molecular weight a

176 Immunoreactive materials were localized in neuronal peri

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

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

179 pinal-projecting groups were often glutamate-immunoreactive, mostly in the hindbrain.

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

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

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

183 related decreases in GAD67- and somatostatin-immunoreactive neuron number beyond the hilus were regio

184 ASP-immunoreactive neuronal populations were rather similar

185 t not parvalbumin (PV); almost all CB- or CR-immunoreactive neurons (98-100%) were GABAergic.

186 More tyrosine hydroxylase-immunoreactive neurons and significant behavioral improv

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

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

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

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

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

192 he locus ceruleus nor tryptophan hydroxlyase-immunoreactive neurons in the dorsal raphe nucleus were

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

194 Neither tyrosine hydroxlyase-immunoreactive neurons in the locus ceruleus nor tryptop

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

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

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

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

199 increased the number of tyrosine hydroxylase immunoreactive neurons in the substantia nigra pars comp

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

201 Lower density of tyrosine hydroxylase-immunoreactive neurons in the ventral tegmental area was

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

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

204 Tilapia LPXRFa-immunoreactive neurons lie in the posterior ventricular

205 ating hormone (MCH) and tyrosine hydroxylase immunoreactive neurons of the hypothalamus and the locus

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

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

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

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

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

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

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

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

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

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

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

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

218 ated cells differentiate into N-beta-tubulin-immunoreactive neurons.

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

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

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

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

223 The immunoreactive peptides were further sequenced by mass s

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

225 e major complexes contained or could contain immunoreactive peptides.

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

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

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

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

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

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

232 an apparently separate tyrosine hydroxylase-immunoreactive plexus.

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

234 revealed near-equivalent proportions of Met-immunoreactive pre- (axons and terminals) and postsynapt

235 Immunoreactive preparations of the radiolabeled antibodi

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

237 By P21, Met-immunoreactive presynaptic profiles predominated and ~20

238 Strikingly, Met-immunoreactive presynaptic profiles predominated over po

239 1) YAP was mainly expressed on CGRP- and IB4-immunoreactive primary afferent nerve terminals without

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

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

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

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

244 A different distribution of Met-immunoreactive profiles was observed in layer V of somat

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

246 e the SCN, effectively eliminating those AVP-immunoreactive projections; we also quantified AVP-immun

247 To identify the immunoreactive proteins, we performed Western blots of 2

248 sing Mimivirus strains, to identify specific immunoreactive proteins.

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

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

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

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

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

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

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

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

257 Immunoreactive RFRP-3 fibers were distributed throughout

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

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

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

261 Immunoreactive secretin and its mRNA were predominantly

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

263 Immunoreactive signals for the desmosomal protein plakog

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

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

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

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

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

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

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

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

272 Immunoreactive spots stained by sera collected at the ti

273 Surprisingly, immunoreactive SQSTM1 also accumulated in the olfactory

274 n of calbindin-D28k (CB) and calretinin (CR) immunoreactive structures in the brain of Xenopus laevis

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

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

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

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

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

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

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

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

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

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

285 The gliomas were immunoreactive to BRAF V600E antibody.

286 ed or those with no documented infection but immunoreactive to ebolavirus did not neutralize.

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

288 ting hormone (h(2)=0.58, P=2 x 10(-)(5)) and immunoreactive trypsinogen (h(2)=0.52, P=3 x 10(-)(9)) a

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

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

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

294 effective method for generating safe, highly immunoreactive vaccines.

295 rtion of vesicular acetylcholine transporter-immunoreactive (VAChT-IR) varicosities (80% +/- 1.7%, n

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

297 Finally, the density of FABP4-immunoreactive vessels in endobronchial biopsy specimens

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

299 In the present study we identified neurons immunoreactive with antisera against octopamine, tyramin

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