ライフサイエンスコーパス: immunoreactivity

1 res of the central complex exhibit orcokinin immunoreactivity.

2 lectin B4 or calcitonin-gene-related peptide immunoreactivity.

3 nd both neuropeptide Y (NPY) and orexin (OX) immunoreactivity.

4 of cell-bound virions, thus explaining their immunoreactivity.

5 ajor impact on their transduction ability or immunoreactivity.

6 ecreased phosphorylated ribosomal protein S6 immunoreactivity.

7 itive interneurons, which show strong Kv3.1b immunoreactivity.

8 n (5-HT) concentrations, and lowered 5-HT GC immunoreactivity.

9 t colocalized GABA and MIP but not AT or ORC immunoreactivity.

10 perisomatic terminals supplying it show GABA immunoreactivity.

11 o understanding the tempo and specificity of immunoreactivity.

12 a strong phylogenetic association of the PAV immunoreactivity.

13 lanoma with different grades of nuclear BAP1 immunoreactivity.

14 (DA), revealed by tyrosine hydroxylase (TH) immunoreactivity.

15 d -9 activity nor decreased sirtuin1 (Sirt1) immunoreactivity.

16 ry levels did not always correlate with high immunoreactivity.

17 stologically normal with no evidence of EBOV immunoreactivity.

18 tic branch points in combination with SMI-32 immunoreactivity.

19 ons of ubiquitin and p62; type2 NI showed no immunoreactivity.

20 thelioma) showed uniform strong nuclear PAX8 immunoreactivity.

21 ti-NETs and citrullinated histones (cit-H2B) immunoreactivity.

22 l cells by calretinin and phospholipase C140 immunoreactivity.

23 scent cells in the INL and GCL contained VIP-immunoreactivity.

24 tation carriers showed widespread glial CYLD immunoreactivity.

25 ation was noted between NPY and TH or DbetaH immunoreactivities.

26 nsporter and GABA(A)-receptor gamma2 subunit immunoreactivities.

27 nerve density as detected with beta-tubulin immunoreactivity 2 hr after stimulation.

28 FosB immunoreactivity, 2-deoxyglucose uptake, and firing acti

29 Presence and levels of systemic immunoreactivity against A. actinomycetemcomitans Ltx ar

30 In this study, we show the distribution of immunoreactivity against CART peptides (CARTp-ir) in the

31 Presence of immunoreactivity against Ltx was associated with impaire

32 use in mice that correlated with a decreased immunoreactivity against oligomer-specific forms of aSyn

33 Leptin increased nuclear immunoreactivity against phosphorylated STAT3 (pSTAT3) w

34 nd cell membrane (especially type IIa fibre) immunoreactivity also decreased in atrophic Sol.

35 Statistically significant variation in immunoreactivity among the regions was seen in SNP-conta

36 pses in the lateral complex show AmTAR1-like immunoreactivity (AmTAR1-IR), suggesting a role of this

37 ousand [25th-75th IQR, 0.7-1.3 per thousand] immunoreactivity and 0.3 per thousand [25th-75th IQR, 0.

38 This study aimed to identify the immunoreactivity and allergenicity of stable bovine milk

39 correlation between the PAV content and the immunoreactivity and allowed to rank the relative specie

40 fically correlated to the dynamic changes of immunoreactivity and as such could serve as biomarkers f

41 e groups of ascending motor neurons based on immunoreactivity and association with calbindin baskets,

42 therapy, including oncogenic transformation, immunoreactivity and cost.

43 growth plate, with decreased phospho-Erk1/2 immunoreactivity and impaired hypertrophic chondrocyte a

44 eurons was sufficient to rescue loss of TPH2 immunoreactivity and largely preserve serotonin innervat

45 M2 immunoreactivity and M3 mRNA levels of muscarinic recept

46 Immunoreactivity and mRNA levels of IGF-1, TGF-beta1, an

47 1 receptors, in anesthetized preparation; 2) immunoreactivity and mRNA of TRPV1 receptors of laryngea

48 erotonin-neurons markedly decrease serotonin-immunoreactivity and offspring production, strongly supp

49 the delta-frequency range decreases the APP-immunoreactivity and preserves cognitive abilities after

50 COX1 immunoreactivity and prostacyclin production were primar

51 ations judging from the colocalization of TH immunoreactivity and PSST6 expression but not with PSST1

52 effects of low-dose guanfacine on BNST cFOS immunoreactivity and stress-induced reinstatement.

53 l populations, ectopic CSF-cNs retain PKD2L1-immunoreactivity and synaptic contacts with other neuron

54 etween P3 and P14, many hair cells lost Sox2 immunoreactivity and the density of calyceal afferent ne

55 that venlafaxine exposure reduces serotonin immunoreactivity and tyrosine hydroxylase-positive cell

56 mostly colocalized PDF, FMRFamide, and 5-HT immunoreactivities, and with terminals of ipsi- and cont

57 pyramidal and stellate, based on morphology, immunoreactivity, and functional properties.

58 Expression of AQP4 protein, AQP4 immunoreactivity, and perivascular AQP4 localization in

59 nd Il1beta, increased intracellular TNFalpha immunoreactivity, and reduced expression levels of macro

60 Cellular studies determined the affinity, immunoreactivity, and specificity of [(89)Zr]Zr-DFO-dara

61 on of the RPE, as identified by cytochrome C immunoreactivity, and that the hyporeflective band betwe

62 terns of calbindin-like and substance P-like immunoreactivity, and the organization of afferents from

63 isomatic inhibition indicated by parvalbumin immunoreactivity appears to be largely resilient to the

64 other patients whose sera also showed strong immunoreactivity around 70kDa on Western blotting were a

65 e steatosis and correlated with hepatic CD34 immunoreactivity as a marker of hepatic angiogenesis.

66 of hydrolysis (DH) and percent reduction in immunoreactivity as response variables.

67 performing spatial distribution of serotonin immunoreactivity, as well as characterizing target genes

68 l epithelial cells did not show ZIKV antigen immunoreactivity at 14, 35 or 70 DPI.

69 vely and quantitatively c-Fos and Arc/Arg3.1 immunoreactivity at 15 and 90 days after cochlea removal

70 ayer culture, showed markedly increased Cx43 immunoreactivity at areas of invasion in orthotopic xeno

71 Fluoxetine increases serotonin-immunoreactivity at low food conditions to similar maxim

72 osa patients display an increase in Brevican immunoreactivity at sites of MG aggregation, linking the

73 and P2 was found to have reduced collagen IV immunoreactivity at the muscle basement membrane.

74 e presence of phosphorylated alpha-synuclein immunoreactivity at the synapse and their relationship w

75 NPY-saporin decreased spinal Y1R immunoreactivity but did not change the primary afferent

76 m increased proliferation, as judged by Ki67-immunoreactivity, but did not alter the number of double

77 on and their morphological features and CGRP immunoreactivity characterized.

78 omas, respectively, exhibited intense LINE-1 immunoreactivity compared with adjacent, normal-appearin

79 Non-human-derived PAbs can have serious immunoreactivity complications, and when "humanized," th

80 bumin (PAV) contents and their corresponding immunoreactivity (detectability) in southern hemisphere

81 altered by reproductive status, with RFRP-3 immunoreactivity enhanced in the paraventricular nucleus

82 tons was attributable to loss versus reduced immunoreactivity, expression of synaptotagmin-2 (syt2) w

83 Thus, insulin immunoreactivity extends beyond the pancreatic lymph nod

84 central nucleus of the amygdala [CeA]) PACAP immunoreactivity, extracellular signal-regulated kinase

85 Instead, we found only FMRFamide- and HA immunoreactivity (FMRFamide: 4 optic ganglion cells, 4-5

86 ctivity for doublecortin (DCX) and increased immunoreactivity for activated caspase-3 and death recep

87 Immunoreactivity for both InvD1L and PDF (type II acini

88 We focused on neurons with immunoreactivity for calbindin, calretinin and nitric ox

89 GAT.Nerve ligation was followed by increased immunoreactivity for D1 in synaptic compartment (P3) in

90 these ZI neurons revealed that they display immunoreactivity for dopamine but not dopamine beta-hydr

91 AIE reduced immunoreactivity for doublecortin (DCX) and increased im

92 To verify this model, H1s were identified by immunoreactivity for GABA and 95% of these cells had an

93 SNL led to increased immunoreactivity for met-enkephalin in dorsal horn homog

94 ionized calcium-binding adapter molecule 1+ immunoreactivity for microglia, suggesting chronic infla

95 elop from a Math1/Atoh1 lineage, and exhibit immunoreactivity for NeuN.

96 Patterns of immunoreactivity for TH and DARPP-32 in "limbic" areas s

97 Whereas immunoreactivity for TH was higher in the vocal control

98 nsity of axon initial segments detectable by immunoreactivity for the alpha2 subunit of the GABAA rec

99 AIE also increased immunoreactivity for the inflammatory signaling molecule

100 We identified thalamic boutons by their immunoreactivity for the vesicular glutamate transporter

101 s form unimodal distributions based on their immunoreactivity for these subunits.

102 , where a higher number of fibers containing immunoreactivity for VIP, CGRP, SP, or nNOS were found.

103 Both time points showed widespread immunoreactivity for ZIKV and cleaved caspase 3 (CC3, a

104 d subcellular localization of striatal GluD1 immunoreactivity (GluD1-IR) in mice and monkeys.

105 logic features, nuclear and cytoplasmic BAP1 immunoreactivity grade, and patient outcome, including d

106 dissociation constant, ~3.9 nM) and retained immunoreactivity (>75%) on 2-dimensional cell cultures a

107 5-HT immunoreactivity had nearly complete overlap with PNs an

108 Serotonin immunoreactivity has been investigated in numerous tetra

109 The GABA immunoreactivity in a sister group to the nudibranchs, P

110 ociated with terminal boutons expressing GAD-immunoreactivity in addition.

111 We observed loss of NDUFB8 immunoreactivity in all patients with mutations affectin

112 however, the fluorescence intensities of PV immunoreactivity in cell bodies and of WFA labeling and

113 s, HSV-1-infected 2D cultures showed Abeta42 immunoreactivity in cells expressing the HSV-1 antigen I

114 ens in our screening, 59 of which had higher immunoreactivity in convalescent compared with acute-sta

115 We found that the majority of hcrt-1 immunoreactivity in extracted CSF was derived from unaut

116 placental sections displayed stronger LIN28B immunoreactivity in extravillous (invasive) cytotrophobl

117 es revealed that there was no detectable PC2 immunoreactivity in human beta-cells and little PCSK2 mR

118 tressed PN30 conspecifics elicit greater Fos immunoreactivity in IC -> NAc neurons than interactions

119 cell bodies and of WFA labeling and aggrecan immunoreactivity in individual PNNs around PV cells were

120 We previously demonstrated long-lived immunoreactivity in individuals with past symptomatic an

121 e was corroborated by higher malondialdehyde immunoreactivity in lesions from middle-aged compared wi

122 Furthermore, nonbreeding birds had more OX immunoreactivity in multiple brain regions.

123 In all histological experiments, PC2 immunoreactivity in neighboring alpha-cells acted as a p

124 ved PrP(CWD) seeding activity and follicular immunoreactivity in oropharyngeal lymphoid tissues at 1

125 PAM immunoreactivity in primary NENs is readily assessable a

126 ssociations and survival implications of PAM immunoreactivity in primary NENs.

127 CCK immunoreactivity in the BNC was observed in somata and p

128 investigate possible differences in galanin immunoreactivity in the brain of both male morphs and fe

129 were to examine the distribution of polySia immunoreactivity in the brainstem and thoracolumbar spin

130 We found a decline in Map2 immunoreactivity in the CA1 area that reached minimal le

131 itory postsynaptic current and reduced c-Fos immunoreactivity in the CeA of IP3K-A KO mice suggest th

132 RF-amide, and gamma-aminobutyric acid (GABA) immunoreactivity in the central nervous system (CNS), ey

133 The alpha3-immunoreactivity in the cerebellar cortex was relatively

134 We also noted minor differences in GABA immunoreactivity in the CNS compared to previous work on

135 We found a significant increase of TREM2 immunoreactivity in the cortex in response to HFD, most

136 egulated with a concurrent reduction of 5-HT-immunoreactivity in the DRN and its two major projection

137 served time-of-day oscillation in microglial immunoreactivity in the hippocampus, which was disrupted

138 was associated with decreased phospho-ERK1/2 immunoreactivity in the hypertrophic chondrocyte layer a

139 However, VEGF (Vegfa) immunoreactivity in the hypertrophic chondrocytes of c-R

140 Fasting dramatically increased cFos- and NPY-immunoreactivity in the IN, followed by rapid reduction

141 d a significant reduction (P < 0.001) in NPY-immunoreactivity in the IN.

142 ce, increased early growth response factor 1 immunoreactivity in the nucleus accumbens core and anter

143 Immunoreactivity in the nucleus and cytoplasm were grade

144 ed microglia cell numbers and decreased 5-HT immunoreactivity in the nucleus of the solitary tract (n

145 Immunofluorescence against DA revealed immunoreactivity in the OB that was denser in the medial

146 revealed high levels of microvascular nestin immunoreactivity in the same region.

147 were selected based on the immunoglobulin G immunoreactivity in the serum of patients with periodont

148 ving IN + FUS had significantly increased TH immunoreactivity in the treated hemisphere compared to t

149 h microglia/macrophage infiltration and CD68 immunoreactivity in the tumor mass; (3) decreases astrog

150 und maximal Fos (a neuronal activity marker) immunoreactivity in the ventral medial prefrontal cortex

151 Due to the lack of TH immunoreactivity in this region, the hypothalamic CSF-c

152 thetic neurons and vesicular ACh transporter immunoreactivity in tyrosine hydroxylase-positive cardia

153 We demonstrated extensive positive RD3 immunoreactivity in various normal tissues and particula

154 At later stages, more neurons showed ZIKV immunoreactivity, in part potentially due to ZIKV releas

155 occurred in parallel with reduced microglia immunoreactivity, increased circulating chemokine expres

156 The resulting immunoreactivity index (IR) if greater than 1 implies in

157 Furthermore, DCX immunoreactivity indicated participation of the cortical

158 rescent cells expressed syntaxin 1A and GABA-immunoreactivity indicating they were amacrine cells.

159 hthalmia transcription factor and tyrosinase immunoreactivity inversely related to SMPD3 and ceramide

160 and their spinal cords were examined for the immunoreactivities (ir) of the IGF-I, IGF binding protei

161 nts of vagal pulmonary C-neurons, and 4) the immunoreactivity (IR) and mRNA expression of 5-HT(3A) an

162 First, the impact of DID on NPY immunoreactivity (IR) was assessed in the mPFC.

163 ohistochemistry, we found that 90% of ERbeta-immunoreactivity (-ir) colocalized with EGFP.

164 Strong evidence shows that in AD, p62 immunoreactivity is associated with neurofibrillary tang

165 ine granular proteinase K digestion (PrPres) immunoreactivity is found in the entorhinal cortex but n

166 In human TB, pulmonary TNF-alpha immunoreactivity is increased and circulating PD-1 expre

167 nobutyric acid (GABA) membrane transporter 1 immunoreactivity is lower, whereas the density of axon i

168 We now demonstrate that enteric CDNF immunoreactivity is restricted to neurons (submucosal >

169 n, the regional distribution of Pcdh-gammaC4 immunoreactivity is similar to that of Pcdh-gammaC4 mRNA

170 ctivity was increased, but M2/M3 mRNA and M3 immunoreactivity levels were decreased at day 28.

171 Piezo2 immunoreactivity localized specifically within EC cells

172 M2R immunoreactivity (M2R-ir) was absent from the perikarya

173 fically, 2D neuronal cultures showed Abeta42-immunoreactivity mainly in HSV-1-infected cells and only

174 trated that microtubule-associated-protein-2 immunoreactivity (MAP2-IR) in A1 deep layer 3 is lower,

175 Using the AlphaScreen-based immunoreactivity measurements, antibody reactivity again

176 ath was shorter in patients with reduced PAM immunoreactivity: median times to death were 11.3 (PAM-n

177 In marked contrast to Fos immunoreactivity, neuroanatomical mapping of Neurobiotin

178 ts, colocalization of SIFamide and histamine immunoreactivity occurred not in group 1, but in group 4

179 tivated, as in cases with dysplasia, but the immunoreactivities of nucleoporin p62, DEP-domain contai

180 In human and mouse AAA tissues, increased immunoreactivity of activated Notch signaling correlated

181 the shape, distribution, and synapse-related immunoreactivity of adult rat TH cells.

182 In NB tissues from TH-MYCN mice, high immunoreactivity of both NPY and Y5R marked angioinvasiv

183 J mice, analysing mRNA expression levels and immunoreactivity of GlyR subunits, as well as ethanol se

184 findings on the phylogeny, infectivity, and immunoreactivity of HBoV1 capsid variants improve our un

185 there is a marked species difference in the immunoreactivity of Kv3.1b in pyramidal neurons, and thi

186 ion of W50R into residues 44-65 restored the immunoreactivity of mAbs whose epitope being within resi

187 aptic proteins, (3) soluble Abeta levels and immunoreactivity of mutant APP and Abeta levels and (4)

188 Consistent with this finding, immunoreactivity of NEP was increased in the hippocampus

189 re examined in pre-BotC neurons localized by immunoreactivity of neurokinin 1 receptors.

190 We assessed the immunoreactivity of onchocerciasis patient sera (n = 152

191 genase-2 pathway in astrocytes and decreased immunoreactivity of parvalbumin-positive presynaptic inh

192 say (ELISA) was formatted to assess relative immunoreactivity of PAV.

193 tractability from and immunoglobulin E (IgE) immunoreactivity of peanut, almond, hazelnut, and pistac

194 pines with ChR2-EYFP virus, showed increased immunoreactivity of phosphorylation of FAK (p-FAK) and p

195 Glucagon-like peptide 1 (GLP-1) immunoreactivity of plasma collected immediately before

196 to analyze the correlation between the BAP1 immunoreactivity of primary uveal melanoma and other cli

197 The effect of heat on extractability and immunoreactivity of proteins from roasted peanut flours

198 Anti-NET/cit-H2B immunoreactivity of selected RA-rmAbs was abrogated in t

199 The immunoreactivity of the anti-PSMA antibody was preserved

200 Preservation of the immunoreactivity of the antibody on site-specific conjug

201 s also reflected in differential patterns of immunoreactivity of the immediate early gene c-Fos, with

202 We examined the number, distribution, and immunoreactivity of the infracortical white matter neuro

203 Histological processing revealed increased immunoreactivity of the pro-inflammatory cytokine Interl

204 Immunoreactivity of the rVP2 was confirmed by using a pa

205 tantly, after successful HP eradication, the immunoreactivity of the studied parameters was similar t

206 MSP and DBLMSP2 to IgM inhibited the overall immunoreactivity of these proteins to IgG from patients

207 , and calcitonin gene-related peptide (CGRP)-immunoreactivity of uterine spinal afferent endings supp

208 C for 5, 10, or 20min) on the solubility and immunoreactivity of walnut proteins.

209 sex differences in either the pattern of AR immunoreactivity or of the afferent projections to the A

210 ousand [25th-75th IQR, 0.1-0.5 per thousand] immunoreactivity, P < .001), ASM-associated nerves (452.

211 a pruritogen-like but not algogen-like c-Fos immunoreactivity pattern in the cervical spinal cord.

212 , with little changes in the overall humoral immunoreactivity pattern measured after immunization.

213 In this study, we compare the immunoreactivity patterns of 14 neuropeptides in three c

214 cerevisiae, Lactobacillus helveticus) on the immunoreactivity, physicochemical and sensory properties

215 tential cation channel subfamily V member 1) immunoreactivity (polymodal nociceptor) revealed that th

216 In lung nodules, cathepsin K immunoreactivity predominantly co-localized with LAM-ass

217 pite this nucleus having remarkably low KCC2 immunoreactivity relative to other regions of the adult

218 PSMA-IHC (using an anti-PSMA-antibody and an immunoreactivity score system [IRS]) and ARG using (177)

219 Analysis of SynI immunoreactivity showed that exposure to microglial MVs

220 and comprehensive analysis of peptide-MHC II immunoreactivity showed the population possessed lower a

221 Similarly, p53 immunoreactivity significantly decreased in the corpus (

222 nic stress decreases glucocorticoid receptor immunoreactivity specifically in a subset of inhibitory

223 Nonbreeding birds had more NPY immunoreactivity, specifically in three brain regions: l

224 type 2 diabetes, beta-cells had elevated PC2 immunoreactivity, suggesting that aberrant PC2 expressio

225 re associated with a significant decrease in immunoreactivity, suggesting that pulsed light could be

226 There was a significant increase in immunoreactivity surrounding atrophied myofibers.

227 limus exhibit a predominant decrease in AMD1 immunoreactivity that is associated with a decrease in p

228 non EAE spinal cords did not show the IGF-I immunoreactivity, they were numerously positive for the

229 atecholaminergic neurons which express c-Fos immunoreactivity throughout the rostrocaudal extent of t

230 ent study is to examine presence of systemic immunoreactivity to A. actionmycetemcomitans Ltx with re

231 er removed, then fresh-fixed and stained for immunoreactivity to calcitonin-gene-related-peptide (CGR

232 ant counterpart resulted in 90% reduction in immunoreactivity to cit-H2B.

233 particular, the paraventricular organ showed immunoreactivity to dopamine but not to TH.

234 ExPANs in live mice and then quantified Fos immunoreactivity to identify activated spinal neurons.

235 lammatory biomarkers, ex vivo blood tests on immunoreactivity to lipopolysaccharide (LPS) stimulation

236 Immunoreactivity to Ltx is a marker for presence of leuk

237 of RA synovial B cells is necessary for the immunoreactivity to NET-Ags.

238 Our data show that differences in immunoreactivity to variant antigenic peptides may be us

239 Approximately 50% of serum immunoreactivities toward ZnT8 were mapped to its transm

240 le in mouse and human sera and preserved the immunoreactivity toward CD30.

241 n the SON and the translocation of alphaENaC immunoreactivity towards the plasma membrane.

242 afaxine in embryos recovered brain serotonin immunoreactivity, tyrosine hydroxylase-positive cell pop

243 estern blots and ELISA were used to evaluate immunoreactivity using human sera.

244 alnuts maintained substantial amounts of IgG immunoreactivity (using anti-raw and anti-roasted walnut

245 metastasis, and relapse, whereas strong Y5R immunoreactivity was a marker of angioinvasive tumor cel

246 nt inflammation exists, the pattern of ANXA1 immunoreactivity was abnormal because the typical periva

247 Moreover, tyramine-like immunoreactivity was also found in brain regions without

248 This immunoreactivity was also significantly associated with

249 Thus, ERalpha, GPER1, and aromatase cellular immunoreactivity was assessed in perinatal, prepubertal,

250 led that the highest intensity of fibrinogen immunoreactivity was at 14 days.

251 ack of Api m 10, whereas Api m 1 and Api m 3 immunoreactivity was comparable to that of crude HBV.

252 -neurotrophic factor mRNA was increased, but immunoreactivity was decreased at day 7.

253 Furthermore, parvalbumin (PV) immunoreactivity was decreased in the OFC of ketamine-tr

254 CB1 immunoreactivity was detected in axon terminals that wer

255 Galanin immunoreactivity was detected in cholangiocytes, hepatic

256 lumbar cord showed that oxytocin-neurophysin-immunoreactivity was detected in large numbers of neuros

257 Neuropeptide immunoreactivity was detected in the brain, the ventral

258 Within most plaques, strong gephyrin immunoreactivity was detected, partially colocalizing wi

259 al stability was studied in human serum, and immunoreactivity was determined by cellular binding assa

260 In the absence of serum, FGF2 immunoreactivity was distributed diffusely in cytoplasmi

261 PV immunoreactivity was found in the labeled somata, dendri

262 f polySia, both in vitro and in vivo polySia immunoreactivity was found throughout the adult rat NTS.

263 CSF-2 immunoreactivity was higher in abruption-complicated or

264 Immunoreactivity was identified against 2239 functionall

265 GC dopamine immunoreactivity was increased in BPA- and BPS-exposed p

266 M2 immunoreactivity was increased, but M2/M3 mRNA and M3 im

267 ed the enhanced excitability, and (v) Cav1.2-immunoreactivity was increased.

268 Intense Slick channel immunoreactivity was observed in processes, varicosities

269 Galphat-S immunoreactivity was observed in some neuronal populatio

270 Significantly lower (P = 0.025) nuclear BAP1 immunoreactivity was observed in the metastatic melanoma

271 No pathological immunoreactivity was observed outside the FCD-II or in c

272 Increased immunoreactivity was observed with 150 mW excitation pow

273 Nav 1.1 and Nav 1.2 immunoreactivity was preferentially localized to CH axon

274 (excitatory amino acid transport protein 2) immunoreactivity was reduced next to corticostriatal ter

275 ormal because the typical perivascular ANXA1 immunoreactivity was reduced.

276 higher order integration centers, whereas AT immunoreactivity was restricted to the central complex,

277 ral hilus (CH) of the dentate gyrus, Nav 1.1 immunoreactivity was selectively expressed in presynapti

278 /11.88 and RA056/11.23.2, NET and/or cit-H2B immunoreactivity was solely dependent on SHM in the IgVH

279 Glutamine synthetase immunoreactivity was sparse like in the area postrema an

280 in-dependent protein kinase II (CAMKIIalpha) immunoreactivity was used as a selective marker of princ

281 ctions, protein electrophoretic mobility and immunoreactivity) was investigated.

282 For HA immunoreactivity, we documented both consistently and va

283 ential link between dysfunctional repair and immunoreactivity, we investigate the immunological conse

284 We present a comprehensive atlas of polySia immunoreactivity: we report that polySia labeling is par

285 In comparison, VGLUT1 and NPY immunoreactivities were not altered.

286 e-mediated dUTP nick-end labeling, and Ki-67 immunoreactivity were evaluated.

287 No differences in Nav 1.6 immunoreactivity were found between axon terminals of CH

288 l insulin content and insulin:chromogranin A immunoreactivity were reduced by approximately 60%, and

289 t demonstrated a significant increase in TRH-immunoreactivity when collected during preparatory and p

290 large pallidal neurons labeled by calretinin immunoreactivity, which could be co-localized to the sam

291 Since these contact sites have immunoreactivity with a glutamate receptor antibody, and

292 Partial co-localization of JN immunoreactivity with F-actin (labeled with phalloidin)

293 er antibodies by ELISA assays, and selective immunoreactivity with MUC4(+) cells by western blot and

294 of two neoantigens that demonstrated strong immunoreactivity with patient T cells in vitro, suggesti

295 revealed tissue vacuolation and loss of AQP4 immunoreactivity with preserved axons.

296 Immunoreactivity with unauthentic hcrt-1 metabolites may

297 copic analysis of (1) the distribution of PV immunoreactivity within the neuropil, (2) the properties

298 Finally, suvorexant did not alter Fos-immunoreactivity within tyrosine hydroxylase-immunolabel

299 s exhibit a cell-autonomous increase in GFAP immunoreactivity without affecting astrocyte or microgli

300 d their content of GM2 ganglioside and Abeta-immunoreactivity without detectably altering amyloid pre