ライフサイエンスコーパス: positive cell

1 DNA double-strand breaks (>/=5% gamma-H2A.X-positive cells).

2 c markers (p53, cleaved caspase-7, and TUNEL-positive cells).

3 repression of rat macrophages by human CD47-positive cells.

4 nitor cells, and decreased the count of Sox1 positive cells.

5 xpress FLPo recombinase specifically in GFAP-positive cells.

6 g ADC could selectively target and kill HER2-positive cells.

7 an increased number of glucose transporter-1-positive cells.

8 groups exhibited less than 5% of basal layer positive cells.

9 g this multisubunit repressor complex in EBV-positive cells.

10 as positively correlated with TCTP in HpslyD-positive cells.

11 aminotransferase levels and numbers of TUNEL-positive cells.

12 rkedly reduced cyclobutane pyrimidine dimers-positive cells.

13 cient differentiation of CD4(+)CD8(+) double positive cells.

14 et-like structures containing MAFA/C-peptide-positive cells.

15 with camptothecin while sparing isogenic p53-positive cells.

16 ained a large number of CD11c, CD68, and CD3 positive cells.

17 minimal changes were seen in IL-4- and IL-5-positive cells.

18 ts accompanied by an expansion of Krt5/Krt14-positive cells.

19 N knockdown promotes PTK6 activation in PTEN positive cells.

20 groups according to the percentage of PD-L1-positive cells.

21 creased number of BrdU- and beta-III tubulin-positive cells.

22 , which colocalized with megalin, in podocin-positive cells.

23 origenic than the freshly isolated Aldefluor-positive cells.

24 genome amplification in differentiating HPV-positive cells.

25 tive (HBsA-positive) and HBV DNA- and cccDNA-positive cells.

26 stain intensity and the percentage of immune-positive cells.

27 a-SMA positive cells but showed very few NG2 positive cells.

28 and identifies a related population of NREP-positive cells.

29 ssing red fluorescent protein in retinal Cre-positive cells.

30 r alpha-SMA while they completely lacked NG2 positive cells.

31 ation of tartrate-resistant acid phosphatase-positive cells.

32 er with high expression of alpha-SMA and NG2 positive cells.

33 atory infiltrate has a larger amount of CD20 positive cells.

34 ximity to nuclear Cajal bodies in telomerase-positive cells.

35 ells and premitotic arrest of CD4/CD8 double-positive cells.

36 s with multiple islets with numerous insulin-positive cells.

37 significant specific phototoxicity in GLP-1R-positive cells (2.3% +/- 0.8% and 2.7% +/- 0.3% remainin

38 latelet-derived growth factor receptor-alpha-positive cells, 4) alpha-smooth muscle actin-positive bl

39 the A gate produced significantly more Vasa-positive cells (45.0% +/- 15.2%) than the "B" gate (0.0%

40 alists showed that all had scattered insulin-positive cells; 59 additionally had few insulin-positive

41 ed growth factor receptor alpha (PDGFRalpha) positive ( + ) cells accumulate in CTS SSCT and that the

42 During skin wound healing, CD26-positive cells accumulated over time and persisted in fo

43 ucleated tartrate-resistant acid phosphatase-positive cells along the alveolar bone surface was signi

44 Submucosal and epithelial IL-17A-positive cells and BAL IL-17A and IL-22 levels were simi

45 4 deficiency also significantly reduced Ki67-positive cells and beta-catenin expression compared with

46 ha smooth muscle actin (alphaSMA) and desmin-positive cells and collagen deposition, independent of i

47 governing entry of measles virus into SLAMF1-positive cells and identified endocytic uptake of viral

48 eta-cell mass, decreased the number of TUNEL positive cells and improved glucose tolerance after gluc

49 MG before differentiation reduced hemoglobin-positive cells and increased stem/progenitor cell surfac

50 ilar distributions in genomic regions of EBV-positive cells and is associated with oncogenic super-en

51 antly, the levels of p73 are elevated in HPV-positive cells and its knockdown impairs HPV genome ampl

52 matrix metalloproteinase (MMP) 9-, and MMP13-positive cells and more proliferating cell nuclear antig

53 idine triphosphate nick end-labeling (TUNEL)-positive cells and mortality compared with vehicle-injec

54 This uptake pathway is specific to SLAMF1-positive cells and occurs within 60 min of viral attachm

55 We focused on AEC-IIs as viral antigen-positive cells and on monocytes/macrophages (Ms/M s) and

56 ed by the reduced number of propidium iodide-positive cells and the cleavage of caspase-3 and poly (A

57 By analyzing telomerase-positive cells and their human TERC knockout-derived ALT

58 enables the selective imaging of alphavbeta8-positive cells and tissues.

59 1, P-selectin, cluster of differentiation 45-positive cells); and oxidative stress (increased malondi

60 latelet-derived growth factor receptor-alpha-positive cells, and alpha-smooth muscle actin-positive b

61 amma antibody led to a decrease in IFN-gamma-positive cells, and an increase in IL-5-positive cells,

62 cultured with supernatants from Tr1 or FOXP3-positive cells, and analyzed by immunofluorescence and f

63 were associated with increased HA, vimentin-positive cells, and fibrosis in Hyal2(-/-) compared with

64 brain atrophy, neuron loss, loss of poly(PR)-positive cells, and gliosis, culminating in motor and me

65 ion of interleukin-1beta by CD11b- and Iba-1-positive cells, and loss of olfactory sensory neurons (O

66 c increase in valvular cell activation, CD45-positive cells, and matrix turnover.

67 local muscle cell compartments, such as PAX7 positive cells, and recruited macrophages during skeleta

68 rted liver morphology, accumulation of TUNEL-positive cells, and transcriptional upregulation of apop

69 ncubated with supernatants from Tr1 or FOXP3-positive cells, and transepithelial electrical resistanc

70 In juveniles only, BrdU-positive cells appeared in contact with vimentin-labeled

71 Furthermore, we show that Ntsr1-Cre-positive cells are immuno-positive for the nuclear trans

72 Importantly, CTLA-4-positive cells are present, and focally contact HRS cell

73 ndicates that Cytokeratin-Synaptophysin dual positive cells arise from the exocrine compartment.

74 Using Tomato-positive cells as a reference population, we demonstrate

75 d intestinal epithelial cells (IEC) and Hopx-positive cells as predominant fecal miRNA sources.

76 cantly higher number of TRAP and Osteocalcin positive cells at 4 weeks in the cell-seeded group compa

77 ch were replaced by a notable number of IL-6-positive cells at day 14.

78 Immunohistochemistry showed increased KRT80-positive cells at relapse and, using several clinical en

79 vor somatostatin- and pancreatic polypeptide-positive cells at the expense of insulin- and glucagon-p

80 in expression and accumulation of podoplanin-positive cells at the wound edge.

81 mpared with primary tumors (17% nanoparticle-positive cells) because they reside close to blood vesse

82 When cocultured on exosomes from Nischarin-positive cells, breast cancer cells exhibited reduced su

83 ycle arrest and eliminated Ki-67 mRNA in RB1-positive cells but had no effect in RB1-negative cells,

84 DPSC had alpha-SMA positive cells but showed very few NG2 positive cells.

85 amma-positive cells, and an increase in IL-5-positive cells, but did not impact clearance of Pneumocy

86 RT promoter in both telomerase-negative and -positive cells, but it activated the repressed hTERT pro

87 The mouse RSDL houses Sox2-positive cells, but no Wnt/beta-catenin signalling.

88 ctivated for infection of CD4-negative, CCR5-positive cells, but the infection of CD4-positive, CCR5-

89 on reduced the percentage of nucleoprotein 1-positive cells by 85, 56, and 66%, respectively (P < 0.0

90 transcriptional target that sustains ERG+85-positive cells by controlling ERG ubiquitination.

91 Identification of variant-positive cells by green fluorescent protein (GFP) staini

92 r- and progesterone receptor-negative (< 10% positive cells by immunohistochemistry) early breast can

93 active Rho1 and a decrease in phosphomyosin-positive cells by immunostaining, while expression of co

94 ies of reports document induction of the CK5-positive cells by progestins, it is unknown if other 3-k

95 activated the infection of CD4-negative CCR5-positive cells by several HIV-1 strains resistant to the

96 inhibited the infection of CD4-positive CCR5-positive cells by some HIV-1 strains.

97 In this study, we demonstrate that insulin-positive cells can be generated in vitro from human indu

98 ased pAKT signal suggesting that the variant-positive cells can induce lesion formation in a non-cell

99 Here, we investigate the role of CDH2 positive cell clusters in preserving healthy, biosynthet

100 heres containing HBMSCs and HUVECs, and CD31-positive cell clusters were prominent within HUVEC-impla

101 gy is preserved only when NP cells form CDH2 positive cell clusters.

102 These PDGF receptor alpha-positive cells co-localized with PDGF receptor beta, pro

103 nitor marker mesothelin, and many mesothelin-positive cells coexpressed albumin.

104 ment reduced (P < 0.001) the number of TUNEL-positive cells compared to vehicle at 24 h and day 7 pos

105 f cells in micrometastases (50% nanoparticle-positive cells) compared with primary tumors (17% nanopa

106 diminished the procoagulant activity of EMT-positive cells, confirming a functional role for TF in t

107 elanocytes, immunotargeting of the chemokine-positive cells, continuous loss of the pigment-producing

108 GFP-positive cells could be detected in the cochlea for at l

109 specificity to HER2 and integrin alphavbeta6 positive, cell culture-derived, breast and pancreatic ca

110 a filamentous pattern along regions of inner positive-cell curvature by its coiled-coil motifs, and i

111 Cdkn1a, Nr4a1, Gata2, Junb and Btg2, and the positive cell cycle regulators were correspondingly down

112 in cell-death-deficient mutants lacking the positive cell death regulator ORESARA1/ANAC092 (ORE1).

113 The mean percentage of vimentin-positive cells decreased by 0.94%, 2.75%, and 4.24% in t

114 The CD20-positive cells did not display the typical B cell morpho

115 GFP-positive cells differentiated into neurons, astrocytes a

116 opes were defined, with peptide-MHC pentamer-positive cells displaying the central and effector memor

117 Small subpopulations of CXCR4-positive cells drive the local invasion and disseminatio

118 d; (b) Layer A1 exhibits increases in SMI-32-positive cells earlier than layer A; (c) The general tra

119 rminant of functional properties of the Gram-positive cell envelope.

120 Accordingly, EMT-positive cells exhibited a higher persistance/survival i

121 elomeric lagging strands, whereas telomerase positive cells exhibited similar elongation between lead

122 We found that pdgfrb-positive cells express notch2 in addition to notch3, and

123 Hox-positive cells express PDGFRalpha and CD51, are marked b

124 Less than 10% of the BDNF-positive cells expressed BrdU, but this percentage was g

125 an average efficiency of 55% into C-peptide-positive cells, expressing markers of mature beta-cells,

126 psies revealed that SARS-CoV-2 infected NRP1-positive cells facing the nasal cavity.

127 numbers of antigen-specific CD8(+) IFN-gamma-positive cells following injection into BALB/c mice.

128 , and presence of binucleate hepatocytes and positive cells for AlkP in periodontitis versus control

129 n-3 PUFAs increased GFAP expression and GFAP positive cell formation.

130 by capturing green fluorescent protein (GFP)-positive cells from blood.

131 Finally, isolation of fluorescence-positive cells from nonresponders increased dynamic rang

132 ly GD2-expressing osteosarcomas (32%-69% GD2-positive cells) from high GD2 expressors (>99%, P < 0.05

133 Hoxa11 lineage-positive cells give rise to previously described progeni

134 d insulin independence, all examined insulin-positive cells had lost expression of the end-differenti

135 Additionally, the IL-33-positive cells had low expression of PCNA.

136 d large populations of EMT-derived, vimentin-positive cells having spindle-like morphology.

137 ion for why this microRNA is targeted in HPV-positive cells.IMPORTANCE We describe here for the first

138 F1, a TopBP1-binding partner, and p73 in HPV-positive cells in contrast to its effects in other cell

139 a decrease in infectious virus and fewer RSV-positive cells in cultures after neutrophil exposure tha

140 ced the number of CD31(+) vessels and VEGF-A-positive cells in fibrotic peritoneum.

141 ammation, BOT-64 reduced the number of SETD1-positive cells in inflamed periodontal tissues, restored

142 ot alter the numerical density of surfactant positive cells in lung tissue.

143 The percentage of CXCR3 expression in CD3-positive cells in PBMCs was inversely correlated with se

144 n the hippocampus and in GABA- and glutamate-positive cells in the basolateral amygdala.

145 developmental emergence of parvalbumin (PV)-positive cells in the BLA and increased anatomical conne

146 scued through optogenetic inactivation of PV-positive cells in the BLA.

147 increased numbers of CD25-, FoxP3-, and CD4-positive cells in the CNS.

148 further detected a significant loss of OLIG2-positive cells in the corpus callosum of Tmem106b-/- mic

149 ric metaplasia to include Gkn3 mRNA and GKN3-positive cells in the corpus, allowing a more accurate a

150 t the large majority (80%) of the calretinin positive cells in the ganglion cell layer are ganglion c

151 sion and stimulates accumulation of alphaSMA-positive cells in the gel, while knockdown of endothelia

152 last activation protein was evidenced in YFP-positive cells in the heart after MI.

153 cleotidyl transferase dUTP nick-end labeling positive cells in the hippocampus, and improved spatial

154 iments yielded no glycinergic or cholinergic positive cells in the IC, and descending projections to

155 PAE cells stimulate accumulation of alphaSMA-positive cells in the implanted gel, while Twist1 knockd

156 n addition, a small proportion of calretinin-positive cells in the inner nuclear layer and in the gan

157 is active in a distinct population of Notch-positive cells in the intestinal epithelium.

158 e ionized calcium-binding adapter molecule 1-positive cells in the ischemic cortex of GPR37 KO mice,

159 the DDC-stimulated number of cytokeratin-19-positive cells in the liver of wild-type animals was sli

160 ially confined holographic patterns to opsin-positive cells in the living mouse cortex.

161 on, there were fewer 5-bromo-2'-deoxyuridine-positive cells in the LK population in Chd7(f/f)Mx1-CreC

162 e in proliferative alpha-smooth muscle actin-positive cells in the lungs of ITSN-deficient mice, tran

163 timal hyperplasia (alpha-smooth muscle actin positive cells in the neointima) and endothelial activat

164 ium-induced pathology and displayed less GFP-positive cells in the skin.

165 wever, there were significantly more IL-17RA-positive cells in the submucosa and epithelium in childr

166 cells (P < .01) and with the presence of CD8-positive cells in the surrounding stroma (P = .04).

167 onfirmed the presence of alphaFAP- and FSP-1-positive cells in the tumor stroma, and their presence c

168 We found fewer beta-catenin and more pSMAD5 positive cells in the uninjured AC of MRL/MpJ mice than

169 as performed to identify and quantify CHI3L1-positive cells in tissue sections from ALS, DCs and non-

170 in tissue lysates and the number of SIV RNA-positive cells in tissue sections.

171 erial and assessed the frequency of BCR-ABL1-positive cells in various hematopoietic subpopulations;

172 oxin-based fusion protein that depletes CD25-positive cells including regulatory T cells and has been

173 nct subtypes of somatostatin+/Reelin+ double-positive cells, including Hpse+ layer IV cells targeting

174 d to a more potent nanomedicine against HER2-positive cells; incorporation of the chemotherapeutic pa

175 CD163-positive, CD206-positive, and arginase-positive cells, indicating a M2 macrophage phenotype.

176 ased number of activated microglia and COX-2-positive cells induced by Al exposure.

177 s tartrate-resistant acid phosphatase (TRAP)-positive cell induction than M0 or M2 macrophage transfe

178 and cystic index and markedly reducing CD45-positive cell infiltration.

179 t endoscopy if the procedure identified TFF3-positive cells (intervention group).

180 our samples revealed that the number of ODZ1-positive cells inversely correlated with overall and pro

181 The sensitivity of AR-positive cells is due to a distal K79 methylation-marked

182 A heterogeneous population of CNA-positive cells is present in the bone marrow of non-meta

183 Deletion of IFT80 in type I collagen-positive cells led to a disorganized outer AF (OAF) with

184 Median peak blood CAR-positive cell levels were higher among patients with a D

185 ormed with C4-2 cells, a subline of the PSMA-positive cell line LNCaP (human lymph node carcinoma of

186 ted HLA-B*51:08 subtype expressed in a Hap10-positive cell line was isolated, characterized by mass s

187 gen receptor (ER)/progesterone receptor (PR)-positive cell line) with negligible cytotoxicity against

188 ibiting cell proliferation in T47D, a triple positive cell line, it had limited activity in TNBC.

189 ased HIV-1 infection of a CD4-negative, CCR5-positive cell line.

190 and cytotoxicity studies in the alphavbeta6 positive cells line A375Pbeta6.

191 SR1 (Y537S) mutations in MCF7 and SUM44 ESR1-positive cell lines after acquisition of resistance to l

192 In this study, we determined which EBV-positive cell lines are reactivated by classes of HIF-1a

193 distal estrogen-responsive region in ERalpha-positive cell lines by upregulation of ERalpha.

194 telomerase RNA) gene knockouts in telomerase positive cell lines that resulted in long-term surviving

195 Trop-2 positive cell lines were highly sensitive to sacituzumab

196 ell cycle arrest and apoptosis of human EVI1-positive cell lines, and prolonged survival in both orth

197 ter analyzing human lymphoma tissues and EBV-positive cell lines, we now document a strong correlatio

198 l carcinomas, consistent with studies in HPV-positive cell lines.

199 During this process, agonist-selected double-positive cells lose CD4/8 coreceptor expression and masq

200 significant proportion of hepatocyte marker-positive cells maintaining a less well-differentiated ph

201 Here we confirm that relative to ER-positive cells (MCF7), TNBC cells (MBA-MD-231) rely more

202 ther groups were confirmed by a greater TRAP-positive cell number and reabsorption surface on both th

203 BMP-2-induced 5-bromo-2'-deoxyuridine (BrdU)-positive cell numbers at the injected site on day 7 and

204 ls, neutrophils), pathological score and PAS positive cells observed between both genotypes.

205 The expression in YFP-positive cells of fibroblast markers was determined in m

206 f15 is normally expressed within aquaporin 1-positive cells of the S3 segment of the proximal tubule,

207 eotidyl transferase dUTP nick end labeling])-positive cells) of NPIs compared with AIs.

208 assays revealed a strong dependence of HER2-positive cells on MUCL1 for cell proliferation.

209 RASGRP1-overexpressing, GFP-positive cells outcompeted wild type cells and dominated

210 h was suppressed with S3I-201 (percentage of positive cells per field: 31.7% +/- 3.4 vs 3.8% +/- 1.7;

211 esistance in mice with Mig-6 ablation in Pgr-positive cells (Pgr(cre/+)Mig-6(f/f)).

212 hage and decreased alpha-smooth muscle actin-positive cell population, fibrous cap thinning, and decr

213 Lfng also resulted in accumulation of Aldh1-positive cell population.

214 ineralocorticoids effectively expand the CK5-positive cell population.

215 in immunoreactivity and tyrosine hydroxylase-positive cell populations in specific larval brain regio

216 confirmed the proliferative advantage of MB-positive cell populations relative to MB-negative and G2

217 We found HDC-positive cell populations throughout the CNS, including

218 tonin immunoreactivity, tyrosine hydroxylase-positive cell populations, and rescued venlafaxine-media

219 f FITC-labeled Ki-67 antibody TuBB-9 in EGFR-positive cells pre-loaded with the photoactive dye BPD.

220 o-infected with rAAV-CFP-Neo, 27% of the CFP-positive cells present rHSV48Y replication compartments.

221 PDGFB signaling plays a key role in alphaSMA-positive cell proliferation and migration in PH.

222 uated MPTP-induced CSF1R activation and Iba1-positive cell proliferation, without a reduction of the

223 repair, CHK1 and Wee1, are suppressed in HPV-positive cells, providing an explanation for why this mi

224 Analysis of 16S rRNA sequences from BONCAT-positive cells recovered by fluorescence-activated cell

225 tic drop in the number of Pax7- and myogenin-positive cells relative to WT muscles, suggesting that d

226 Although the number of SIV-DNA-positive cells remained unchanged after CD8 depletion an

227 kat lymphoma cells (CD20-positive and TAG-72-positive cells, respectively).

228 Deletion of IFT80 in type II collagen-positive cells resulted in cilia loss in GP and EP, and

229 th conditional activation of KRAS in the PGR positive cells reveal an increase of SIRT1 expression in

230 We also showed that Aldefluor-positive cells revealed significantly higher expression

231 Pitx2-positive cells significantly decreased in treated and co

232 aling, expression of AP-1B (and ARH in AP-1B-positive cells) slowed epithelial-cell migration.

233 NA sequencing comparison of VEC-null and VEC-positive cells suggested a more general role of VEC in a

234 o facilitate EBV latency, though whether HPV-positive cells support a latent EBV infection has not be

235 ed proliferation did not affect basal, Krt14-positive cells, supporting the fact that Foxa1-regulated

236 Although the density of CD3 positive cells (T cells) did not differ between the two

237 genome levels in their TG but many fewer LAT-positive cells than wild-type mice from day 7 to day 30

238 destly GD2-expressing osteosarcomas (32% GD2-positive cells) than in a GD2-negative tumor (9.8% vs. 1

239 ut also to maintain higher cell uptake (>90% positive cells) than the most densely PEGylated particle

240 from an ER/PR-negative cell or from an ER/PR-positive cell that later lost ER/PR.

241 that experimental mice had a decrease in tk-positive cells that arose from proliferation.

242 oplastic growth of smooth muscle-alpha-actin-positive cells that destroy lung parenchyma and by the f

243 t cardiac fibroblasts into Periostin (Postn)-positive cells that express high levels of extracellular

244 entify a population of glutamatergic Adcyap1-positive cells, the activity of which accurately determi

245 The mean numbers of CD31-, KI67-, and MYOD1-positive cells, the optical density of TGF-beta, and the

246 filtration of Ly-6G-, CD11b-, Iba-1- and CD3-positive cells, the production of interleukin-1beta by C

247 crine progenitors into insulin- and glucagon-positive cells through non-cell-autonomous regulation of

248 in mortality and in brain cell death (TUNEL positive cells) throughout the whole brain, and in the i

249 eurons, the parvalbumin and the somatostatin positive cells, tightly control both up-to-down and down

250 s9 to delete PML and APB components from ALT-positive cells to cleanly define the function of APBs in

251 lass of inhibitory interneurons-somatostatin-positive cells-to the generation of slow waves during NR

252 mouse, we recently discovered that an Hnf1b positive cell type in the lung is sensitive to adenoma f

253 e to loss of Atoh1 function than other Atoh1-positive cell types and that heterozygous mice actually

254 get for molecular imaging of different CXCR4-positive cell types in cardiovascular diseases such as a

255 lammatory cytokine secretion from other ROCK-positive cell types, corroborating the selective in vivo

256 However, not all Ngn1-positive cells undergo delamination, nor has the mechani

257 easured by the percentage of nucleoprotein 1-positive cells using flow cytometry.

258 The Gram-positive cell wall consists of peptidoglycan functionali

259 ting for the physical properties of the Gram-positive cell wall, was developed.

260 P biosynthesis into the multi-component Gram-positive cell wall.

261 bears striking resemblance to a related Gram-positive cell-wall remodeling strategy that also promote

262 An increased level of STAT3 in IL22R-positive cells was associated with shorter survival time

263 Numerical density of surfactant protein positive cells was determined by immunohistochemistry.

264 In general, the density of UPR protein-positive cells was found to decrease significantly when

265 lls, but the infection of CD4-positive, CCR5-positive cells was inhibited.

266 Increased number of TRAP-positive cells was observed in DBG/LV and DBG/HV (P <=0.

267 The percentage of MYL4 positive cells was significantly higher in male subjects

268 cytosed myelin within Iba1-positive or P2Y12-positive cells was significantly lower after DHA treatme

269 ing these ALT cells with parental telomerase positive cells, we observed that ALT cells possess exces

270 by using a model of in vivo ablation of PAX7 positive cells, we show that this radiosensitive skeleta

271 tral fovea and found evidence that rod opsin positive cells were absent and violet-sensitive cone and

272 Following IUCT, the antihuman mitochondria-positive cells were detected in the liver of recipient r

273 Moesin-positive cells were embedded within the fibrotic areas b

274 Moreover, ID1-positive cells were enriched by chemotherapy and drove t

275 Although Pcdh19-positive cells were evenly distributed in layer V of wil

276 oliferating cell nuclear antigen- and pSMAD5-positive cells were found in the DMM-injured AC in MRL/M

277 ctive within glial fibrillary acidic protein-positive cells were generated and this allowed for selec

278 with NC/02 or MN/99 plus TX/96, H1/H3 double-positive cells were identified.

279 ged with angiotensin II, PDGF receptor alpha-positive cells were increased in the skin and heart.

280 MS lesions, and changes in the percentage of positive cells were more relevant in MS than in other wh

281 atic increase in alpha-SMA(+), EP4(+) double-positive cells were observed in EP4cKO(S100a4) suggestin

282 Reduced overall TUNEL positive cells were observed in HT+M (47.1 cells/mm(2))

283 Increased numbers of CHI3L1-positive cells were observed in postmortem ALS motor cor

284 ng hypertrophic-like scars, whereas few CD26-positive cells were present in the regenerated gingival

285 Also, US28-positive cells were present within arterial neointima.

286 ensitive cone and green-sensitive cone opsin positive cells were present.

287 ition, alpha-SMA (alpha-smooth muscle actin)-positive cells were reduced in the infarcted myocardium

288 expression/activity and the number of TUNEL-positive cells were significantly low.

289 Leptin receptor-positive cells were synaptically connected to respirator

290 egative, stem cell antigen-1-positive, c-Kit-positive) cells were quantified and proliferation assess

291 or killing epithelial cell adhesion molecule-positive cells when used as a targeting domain on chimer

292 MSPCs are observed as leptin receptor (LepR)-positive cells, whereas osteoblasts can be classified as

293 panded epithelia are Sox9-, Pitx2-, and Tbx1-positive cells, which are markers of the dental epitheli

294 nding protein 1 foci, after incubating SSTR2-positive cells with (177)Lu-diethylene triamine pentaace

295 CD4-positive cells with TRIM33 knock down show increased HIV

296 itive cells; 59 additionally had few insulin-positive cells within a few islets; and 14 additionally

297 eriostin and transforming growth factor beta-positive cells within Asm bundles, in addition to lower

298 cing, that sNCCs are the source of the PROX1-positive cells within the NoR.

299 on therapy (ADT), destroy the bulk of the AR-positive cells within the tumor, eradicating this popula

300 tive immunohistochemical scoring (percentage positive cells x intensity) were calculated.