ライフサイエンスコーパス: staining pattern

1 f cell-cell contact and displayed a punctate staining pattern.

2 r fully recapitulated the endogenous neuroD2 staining pattern.

3 nd displayed a punctate speckled fluorescent staining pattern.

4 or endothelial cells only, revealed the same staining pattern.

5 2 displayed a significant non-overlapping IF staining pattern.

6 BV-infected PHH, where it exhibits a diffuse staining pattern.

7 asia and carcinomas showed an equal, diffuse staining pattern.

8 roughout the cytoplasm and yielded a diffuse staining pattern.

9 invasive SCCs exhibited a patchy or negative staining pattern.

10 is expressed in neurons in a somatodendritic staining pattern.

11 ayed a detergent-resistant, punctate nuclear staining pattern.

12 ed a discrete punctate, as well as a diffuse staining pattern.

13 unofluorescence localization shows a nuclear staining pattern.

14 noma, manifested a heterogeneous RB-positive staining pattern.

15 96% of ANA positives had a nuclear speckled staining pattern.

16 ng in a coarse granular perinuclear PrP(TSE) staining pattern.

17 the structure of the cell envelope and Gram-staining pattern.

18 olymer revealed a characteristic filamentous staining pattern.

19 g G2/M and nuclear TREX2 displays a punctate staining pattern.

20 ty of cells showed a productive, replicative staining pattern.

21 keratinocytes, with no change in the dermal staining pattern.

22 is and alpha-smooth muscle actin (alpha-SMA) staining patterns.

23 ation preference and cytochrome oxidase (CO) staining patterns.

24 of the classical anti-nuclear antibody (ANA) staining patterns.

25 of perforin mutations, had abnormal perforin-staining patterns.

26 distinct phosphorylated tau protein (p-tau) staining patterns.

27 cence of the two proteins produces different staining patterns.

28 n-containing fibrils with computer-generated staining patterns.

29 ir position within the cell cycle using Ki67 staining patterns.

30 ctivity exhibited pericellular and reticular staining patterns.

31 astase digestion did not significantly alter staining patterns.

32 tagged proteins produced distinctive nuclear staining patterns.

33 ontrast, mature muscle fibers exhibited four staining patterns.

34 the tissue did not alter the cellular SMI-32 staining patterns.

35 and caveolin have related but nonoverlapping staining patterns.

36 cell lines and showed nearly identical skin staining patterns.

37 ues showed a very striking difference in the staining patterns.

38 butions of particular cell types or neuropil staining patterns.

39 o differences in proliferation marker (Ki67) staining patterns.

40 nized by 4 anti-PDC-E2 mAbs that give apical staining patterns (3 mouse and 1 human).

41 To interpret the CO staining pattern, [(3)H]proline was injected into the ri

42 Fluorescein staining patterns according to Oxford Schema got worse p

43 ression and no change in distribution of the staining pattern after DNA damage.

44 relative length, arm ratio, and differential staining patterns after combined propidium iodide (PI) a

45 Staining patterns after monocular enucleation revealed t

46 The incorporation of the MYC staining patterns allowed the stratification of pRCC typ

47 combination with the MYC immunohistochemical staining patterns allows a more accurate prediction of p

48 lanin and vancomycin probes produce helicoid staining patterns along the cylindrical walls of B. subt

49 FLD patients with a hepatocellular (HC) iron staining pattern also had increased serum MDA (P = 0.006

50 5 and integrin-beta1 subunits gave a similar staining pattern and interacted constitutively with TM4S

51 The uniform staining pattern and strong signal for MCM7 suggest that

52 As determined by the intracellular staining pattern and the release of beta-hexosaminidase

53 ocalizes to the nucleus in a heterochromatic staining pattern and to the cytoplasm, where it co-stain

54 and Cys4, exhibited a diffuse intracellular staining pattern and were not palmitoylated.

55 al manifestations, histologic findings, ANCA staining patterns, and the presence of antibodies to mye

56 ce of antinuclear antibodies (ANAs), the ANA staining patterns, and the presence or absence of anti-R

57 inobenzidine precipitation gives a vesicular staining pattern anterior to the nucleus at the light le

58 catalase is present primarily in a punctate staining pattern anterior to the parasite nucleus.

59 ation and the results of immunohistochemical staining patterns are distinctive.

60 Similar staining patterns are observed for the two forms of DMT1

61 Nuclear c-Jun staining pattern around lodged eggs without ambient immu

62 nostaining had identical DNA content and GD2-staining pattern as their neuroblastic counterparts.

63 nografts in nude rats that reproduce the PAS staining patterns associated with aggressive and nonaggr

64 elanoma that predictably demonstrate the PAS staining patterns associated with nonaggressive and aggr

65 sitively in both mPEC and podocytes, but the staining pattern at cell-cell contacts was intermittent

66 tibodies (mAbs) to PDC-E2 produce an intense staining pattern at the apical surface of bile duct epit

67 n vancomycin probes because they yield clear staining patterns at concentrations well below their min

68 antitative data correlated with the antibody staining patterns because cells that were not organized

69 recombination of later buds) show polarized staining patterns before branching occurs.

70 Differences in iron staining patterns between birds and mammals may also ref

71 Cytochalasin D did not affect the staining pattern, but the pattern was eliminated by chol

72 loned from 15 lines exhibiting inflorescence staining patterns by either thermal asymmetric interlace

73 PAA reveals that at least two different UL29 staining patterns can be detected in these cells.

74 The results indicate that a distinct QD staining pattern (CD15 positive, CD30 positive, CD45 neg

75 The staining patterns changed as a function of both differen

76 At the larval-to-pupal transition, this staining pattern changes; the PM2 neurons stain weakly o

77 Two women had the specific staining pattern characteristic for anti-NMDA receptor a

78 H2D1A mutations had decreased SH2D1A protein staining patterns compared with healthy controls.

79 and lambda light chains showed a polyclonal staining pattern confirming a diagnosis of plasma cell g

80 inverse expression of the two enzymes and a staining pattern consistent with a lineage that begins w

81 ositive cells showed a fine punctate nuclear staining pattern consistent with latent infection, while

82 ll cell types showing a punctate cytoplasmic staining pattern consistent with mitochondrial localizat

83 molecule also stained HEVs and cells with a staining pattern consistent with scattered stromal cells

84 ession was localized cytoplasmically, with a staining pattern consistent with the location of the Gol

85 rs were microsatellite stable; three had IHC staining patterns consistent with germline mutation stat

86 nti-Gal-T2 antibodies revealed a perinuclear staining pattern, consistent with the localization of th

87 The staining patterns correlated with the ability of IEC to

88 ng plane of section artifacts when comparing staining pattern data between animals.

89 eactivity was seen frequently in the diffuse staining pattern described previously.

90 ts with pRCC type 1 tumors and favorable MYC staining patterns died from tumor-related causes.

91 ses and in 39.6% of controls (n=53), but the staining pattern differed between cases and controls.

92 eiotic prophase I of spermatogenesis, with a staining pattern distinct from that of the recombination

93 However, the staining pattern excluded neuropil threads and dystrophi

94 The AIPL1 staining pattern extended within the rod photoreceptor c

95 d rabbit cornea but not mouse cornea and the staining pattern followed the distribution of stromal ke

96 r podocyte diseases retained a global linear staining pattern for alpha-actinin-4.

97 orescence studies showed a largely vesicular staining pattern for BACE that colocalized well with end

98 There were minimal changes in the staining pattern for collagen type I after 24-hour treat

99 nalysis of human skin revealed a distinctive staining pattern for DAX-1 and SF-1 in skin and its appe

100 Unexpectedly, clear gaps in the staining pattern for F-actin at the H-zone were detected

101 e was developed that demonstrated a granular staining pattern for Gzm M and a cellular distribution s

102 A similar staining pattern for p21Cip1 and p27Kip1 was also presen

103 The general staining pattern for PICK1-immunoreactivity was somatode

104 ession in three patients revealed a specific staining pattern for surfactant protein-B, which was the

105 atherosclerotic lesions demonstrates similar staining patterns for APLP2 and IalphaIHC2 with macropha

106 nt muscles revealed similar abnormalities in staining patterns for both desmin and SPEG.

107 The staining patterns for both probes exhibit a strong depen

108 Staining patterns for cone arrestin in transduced and wi

109 The staining patterns for Cx45 rather were typified by granu

110 Immunostaining showed similar staining patterns for cytokeratins in large cell acantho

111 ystem (CNS) by examining immunohistochemical staining patterns for F95 in the normal adult rat brain.

112 Indistinguishable immunohistochemical staining patterns for GLT-1 were obtained with antibodie

113 The staining patterns for mouse semaphorin D/III and chick c

114 t immunofluorescence produced highly similar staining patterns for striatin, SG2NA, and mMOB1, with t

115 The homologous coincidence in staining patterns for the D4 DA receptor transcripts and

116 ensory afferents that project into them show staining patterns for the enzyme nitric oxide synthase,

117 nd in the annectant gyrus, with differential staining patterns found for areas V3d, DM, V3A, DI, PO,

118 monstrate a remarkable loss of expression of staining patterns from late gestational ages to P20.

119 taining for HSP70 demonstrates a cytoplasmic staining pattern; heat shock greatly increased the HSP70

120 bodies, ICP8 could be observed in a diffuse staining pattern; however, using more sensitive staining

121 lymerase III demonstrated a robust nucleolar staining pattern in 4 of 5 available tumors from patient

122 Furthermore, reexamination of the UL29 staining pattern in cells infected with wild-type virus

123 stripe5-lacZ transgene exhibits an abnormal staining pattern in dCtBP mutants that is consistent wit

124 the remaining 13 patients with PV, the c-mpl staining pattern in each case was heterogeneous and was

125 The staining pattern in glomeruli of rats injected with LBD

126 ddition, the antibody showed a mitochondrial staining pattern in HEp2 cells and apically stained the

127 reast, colon, lung, and ovary, with a weaker staining pattern in normal tissues of the same patient.

128 rrelation between changes in SC and PTC CD55 staining pattern in patients with no PTC C4d staining.

129 eb antibody showed a punctate, intracellular staining pattern in platelets, megakaryocytes, and HEK-2

130 three enzymes, also show a uniquely intense staining pattern in the apical region of BEC in patients

131 o PDC-E2 have demonstrated an intense linear staining pattern in the apical region of biliary epithel

132 revealed a segmental and irregular granular staining pattern in the capillary walls of preserved glo

133 y disappear, and HSF-1 appears in a diffused staining pattern in the cytoplasm and nucleus.

134 fected cells, with a characteristic punctate staining pattern in the cytoplasm.

135 Overall 31% of the lines generated exhibit a staining pattern in the inflorescence.

136 r, TUB and TULP1 show a distinctly different staining pattern in the nucleus of these neurons, perhap

137 The other was a diffuse cytoplasmic staining pattern in the transient hair follicle epitheli

138 stage, both PI3K and Akt exhibited an apical staining pattern in the trophectoderm cells.

139 orated by myelin basic protein intensity and staining pattern in these areas.

140 This reciprocal staining pattern in vivo is similar to the in vitro obse

141 body was selected for each MMP, based on its staining pattern in Western blot.

142 After careful annotation, LacZ staining patterns in a high percentage of mutants reveal

143 gnificantly higher levels than the other ANA staining patterns in both RA and healthy population (p <

144 Pre-ablation biopsies showed the normal staining patterns in columnar epithelium, ie, normal Ki-

145 Pimonidazole staining patterns in FSA and 9L tumors supported these r

146 uble immunofluorescence reveals two distinct staining patterns in GABA-labeled hair cells.

147 CB(1) cannabinoid receptor, we have studied staining patterns in groups of males at 25, 50, 75, and

148 GUS staining patterns in most vegetative tissues corresponde

149 zation of Muc1/TLR5 and Muc1/phosphotyrosine staining patterns in mouse airway epithelium and increas

150 Notably, the lineage staining patterns in mutant and control kidneys were ide

151 Similarities to staining patterns in other mammals included a higher den

152 choring protein had distinct but overlapping staining patterns in rat hippocampal neurons.

153 Staining patterns in tangential sections were related to

154 Analysis of staining patterns in the C laminae and monocular zone of

155 post-ablation biopsies demonstrated abnormal staining patterns in the glandular area at the new squam

156 antibodies characterized by region-specific staining patterns in the inner ear epithelia.

157 anti-CD31 antibodies show largely identical staining patterns in the vasculature of different tissue

158 Antibody staining patterns in the zebra finch show that the prote

159 ckout mice showed similar actin stress fiber staining patterns in unstimulated conditions.

160 2a subunit exhibited a diffuse intracellular staining pattern, in contrast to the plasma membrane dis

161 wild-type KOS (6 and 8 h postinfection), 5C staining patterns indicate that capsids are present in n

162 ght field by phase imaging, and fluorescence-staining patterns indicate they contain membrane lipids

163 In vitro, the staining pattern indicated a cytoplasmic localization fo

164 Analysis of the staining pattern indicates that EVI1 and CBP or EVI1 and

165 ion mutations had no effect on histochemical staining patterns indicating that strict spacing require

166 All of these MAbs produced similar staining patterns indicative of reactivity with prehairp

167 By 10weeks, the mature laminar and cellular staining pattern is established and the major subsequent

168 Although PLD1 had a diffuse staining pattern, it was enriched significantly in the G

169 tal sites inactivates the notochord-specific staining pattern mediated by an otherwise normal Ci-trop

170 Staining patterns morphologically similar to antirabies

171 g showed no signal overlap, identical to the staining pattern observed for dual-labeling with anti-GF

172 to the back of motile bacteria (an identical staining pattern observed with the anti-ActA FS-1 antibo

173 Here, we compare the staining patterns observed in Bacillus subtilis using fl

174 tumor, ignoring the complex tissue-specific staining patterns observed on tissue arrays.

175 500 fluorescent micrographs depicting actual staining patterns observed upon indirect immunofluoresce

176 n calyx cup, accounting for the disparity in staining patterns observed with membrane and cytosolic d

177 The staining pattern obtained closely resembled the intracel

178 The temporal staining patterns obtained allow classification of the a

179 However, the staining pattern of acetylation and the mof gene product

180 d hippocampus there was no difference in the staining pattern of AMPA receptor subunits in the dentat

181 s with brefeldin A disrupted the perinuclear staining pattern of both PI3K-C2alpha and the AP-1 compl

182 d and cross-correlated with the experimental staining pattern of both reconstituted type II collagen

183 The staining pattern of C4d mirrored the staining patterns o

184 ype of glycosylation influences the negative-staining pattern of collagen fibrils.

185 P14 homozygous clp mice showed an atypical staining pattern of immature myelin, which resolved into

186 ttern of PDE7A also showed similarity to the staining pattern of MTG, supporting the immunoprecipitat

187 The staining pattern of mutant receptors is similar across s

188 mmunofluorescence, we observed a cytoplasmic staining pattern of neogenin and UNC5A/B that also incre

189 Generally, the staining pattern of nNOS and NADPH-diaphorase in the NTS

190 ing pattern similar to each other and to the staining pattern of NR1.

191 The minor differences in staining pattern of particular subdivisions apparently d

192 The staining pattern of PDE7A also showed similarity to the

193 The immunohistochemical staining pattern of podocan protein in normal kidney glo

194 the nucleus, as revealed by a unique nuclear staining pattern of receptors possessing a point mutatio

195 Although the immunofluorescent staining pattern of several Golgi proteins was indisting

196 calization of ICP0, its ability to alter the staining pattern of the nuclear domain 10 (ND10)-associa

197 In vivo, the staining pattern of the relaxed form was identical with

198 This characteristic staining pattern of the TPR network was considerably enh

199 mutant-expressing cells revealed a vacuolar-staining pattern of the V2R instead of the normal plasma

200 The normal punctate immunohistochemical staining pattern of these complexes is disrupted by vira

201 The theoretical staining pattern of type II collagen was compared and cr

202 expression resulted in loss of the striated staining pattern of type II PKA (RII), indicating loss o

203 Single-cell staining patterns of 61 protein antigens by MxIF in 747

204 taining patterns of TRPC6-IR fibers with the staining patterns of a number of other neurotransmitters

205 taining patterns of CARTp-IR fibers with the staining patterns of a number of other neurotransmitters

206 We compared the immunohistochemical staining patterns of CARTp-IR fibers with the staining p

207 andscapes (MIEL), which captures the nuclear staining patterns of epigenetic marks and employs machin

208 The staining pattern of C4d mirrored the staining patterns of Ig and C3.

209 Staining patterns of membranes were observed in individu

210 eir corresponding immunohistochemical tissue staining patterns of MET receptors from the same animals

211 this idea, immunostaining revealed that the staining patterns of p-MARCKS and the active form of the

212 ariation in the dolichos biflorus agglutinin-staining patterns of the intestines of these mouse strai

213 Further experiments compared the staining patterns of the rat anti-pan Ly-6C (Ly-6.1 and

214 transepithelial resistance and disrupted the staining patterns of the tight junction proteins ZO-1 an

215 ns to this structure and comparing them with staining patterns of the vesicular glutamate transporter

216 When used in combination, the staining patterns of these antibodies enable one to opti

217 Comparisons of the GUS staining patterns of these plants with that of AtCPS-GUS

218 We compared the immunohistochemical staining patterns of TRPC6-IR fibers with the staining p

219 The staining patterns of uPAR and beta1 integrins were strik

220 ent proceeded, MAGI-1 occurred in a punctate staining pattern on stereocilia, which was maintained in

221 Additionally, H3.3 S31P forms a speckled staining pattern on the metaphase plate, whereas H3 S10

222 xhibiting aberrant bride of sevenless (Boss) staining patterns on eye imaginal disc epithelia, we hav

223 lectin MAA produced an intense fluorescence-staining pattern only at the J1/J2 interface.

224 NPM1 association with ATF5, whose staining patterns partially overlap in the nucleoli, pro

225 mmunofluorescence showed three distinct AQP2-staining patterns: plasma membrane and endosomal stainin

226 a, iota/lambda, zeta) showed distinct TE/ICM staining patterns (predominantly at the cell membrane wi

227 The immunofluorescent staining patterns produced by each antibody in the epide

228 considered as markers of pan BECs and their staining pattern proved similar to that of a control pol

229 Neuronal morphology and immunohistochemical staining patterns provided further information about VEN

230 human sera, resulting in a punctate nuclear staining pattern reminiscent of LANA in BCBL-1 cells.

231 The staining patterns resulting from a 5-d mission on the or

232 shown by its sensitivity to pronase and the staining pattern revealed by in situ amplification of HI

233 The viral-staining patterns revealed a striking columnar organizat

234 Staining patterns revealed strong expression of TRPV4 al

235 However, staining patterns revealed that in contrast to CD4(+) DC

236 The staining patterns seen in both these preparations are in

237 Comparison of the staining patterns showed that the organisation of collag

238 -yotiao antibodies display a somatodendritic staining pattern similar to each other and to the staini

239 inding experiment, EpCAM aptamer generated a staining pattern similar to that of antibody, but the bi

240 nulomas from neutrophil-depleted mice showed staining patterns similar to that for wild-type mice.

241 y did not show a significant change in their staining pattern, suggesting that the transmitter levels

242 and NPPA exhibit distinct, but overlapping, staining patterns, suggesting partial colocalization in

243 The staining pattern suggests that all types of ON bipolar c

244 expressed in most epithelial cells, and its staining pattern suggests that it might be involved in t

245 The staining pattern suggests that the tumor cells are clona

246 thologic analysis illustrated characteristic staining patterns supporting a potential mechanism of tr

247 tein 1, colocalize within a fingerprint-like staining pattern that correlates with ultrastructural mo

248 a rostrocaudal gradient, with a distinctive staining pattern that distinguishes known cytoarchitecto

249 ned staining for p63 and AMACR resulted in a staining pattern that greatly facilitated the identifica

250 hermore, a fraction of PIR1 showed a speckle-staining pattern that superimposed with that of the spli

251 f a speckled 14-3-3zeta mitotic cell nuclear-staining pattern that usually becomes diffuse during mit

252 PIR1 exhibited a nuclear-staining pattern that was sensitive to RNase A, but not

253 -/- cells displayed a faint cyclin G nuclear staining pattern, there was no increased expression and

254 for all stain-excluding mass observed in the staining pattern; this additional mass may be accounted

255 -RyR antibodies showed a patchy network-like staining pattern throughout the cell cytoplasm, excludin

256 EBPbeta localization from a punctate nuclear staining pattern to diffuse nuclear distribution.

257 four antibodies (MBEC 1-4) that reacted in a staining pattern typical of mucin.

258 EGFR immunoreactivity staining patterns varied among the asthmatic airways: st

259 This staining pattern was also consistent in ferrets, the pri

260 The staining pattern was cytoplasmic.

261 A similar staining pattern was demonstrated for wtp53.

262 A corresponding staining pattern was found using the second method with

263 A similar staining pattern was found with the anti-CML antibody.

264 trained to stand unilaterally, this elevated staining pattern was limited to the trained side and ext

265 ellum and dentate gyrus, a distinct punctate-staining pattern was observed consistent with a synaptic

266 A characteristic canalicular-staining pattern was observed in normal hepatocytes and

267 the percentage of cells displaying a diffuse staining pattern was obtained.

268 A classic cytokeratin 7/20 staining pattern was present in 23 cases (62%), within t

269 e stratum granulosum and the plasma membrane staining pattern was seen throughout the spinous layer.

270 Qualitatively the overall NR2B subunit staining pattern was similar in +/+ and NR2A-/- neurones

271 This staining pattern was similar to that of alpha-mannosidas

272 This difference in staining patterns was essentially disrupted in Syn KO bo

273 Based on fibrillin staining patterns, we identified three distinct zones in

274 Patients with the RES iron-staining pattern were more likely to have advanced fibro

275 ound that morphology, proliferation, and p53 staining pattern were preserved during cultivation.

276 These staining patterns were almost identical to those seen wh

277 Immunofluorescent staining patterns were also consistent with the exclusio

278 Staining patterns were characterized and cell counts per

279 ional oligodendrocyte populations and myelin staining patterns were comparable in Igf1(-/-) and WT br

280 Theoretical negative-staining patterns were created based upon the "bulkiness

281 In ANA-positive individuals, cellular staining patterns were determined, and specific autoanti

282 Serial sectioning showed that staining patterns were distinctive for each nephron.

283 Both smooth and punctate staining patterns were observed over the surface of the

284 m/progenitor cells are found, and the tissue staining patterns were similar to the established stem c

285 Antigenic staining patterns were variable and heterogeneous.

286 autoantibodies revealed a new sinusoidal C4d staining pattern when compared with HLA DSA (71% vs 3%;

287 acellular protein with differing cytoplasmic staining patterns, whereas other fibroblast lines displa

288 nfected with the UL32 mutant exhibit a hexon staining pattern which is more diffusely distributed thr

289 nsor produced a copper-dependent perinuclear staining pattern, which colocalizes with the subcellular

290 use tissues identified a distinctive NMO-IgG staining pattern, which we characterised further by dual

291 tion frequency (3 Hz) produced a ring-shaped staining pattern, while at a higher frequency (10 Hz) th

292 As a conclusion, ACA displays a specific ANA staining pattern with a bimodal distribution, and ACA-po

293 Immunofluorescence data reveals a punctate staining pattern with an apical organization in late sch

294 rod shape and developed a punctate acid-fast staining pattern with carbolfuchsin.

295 s stained with anti-PDE7A showed overlapping staining patterns with the Golgi marker GM130, suggestin

296 Simulations of the fibril-derived staining patterns with theoretical patterns composed of

297 gave the same distinctive immunofluorescent staining pattern, with unstained heterochromatic regions

298 CTIP1, which exhibited a punctate staining pattern within the nucleus of transfected cells

299 Early establishment of staining patterns within rostral telencephalic song regi

300 the various clinical conditions had distinct staining patterns within the various compartments of the