ライフサイエンスコーパス: -expressing cell

1 n intercellular adhesion molecule 1 (ICAM-1)-expressing cells.

2 hysical separation of the cuticle from DBL-1-expressing cells in the ventral nerve cord.

3 fic immunity and increase clearance of HIV-1-expressing cells.

4 main of SIRPalpha supports adhesion of Mac-1-expressing cells; (b) Mac-1-SIRPalpha interaction is med

5 Consistently, MTCBP-1-expressing cells show decreased ability to invade in vit

6 was taken up selectively in vitro in PARP-1-expressing cells.

7 The targeted depletion of PD-1-expressing cells contingent to the preservation of adapt

8 the immunotoxin reduced the numbers of PD-1-expressing cells, of total T cells and of cells of an au

9 main and Pseudomonas exotoxin targeting PD-1-expressing cells, selectively recognizes and induces the

10 he expression of IL-4 and TGF-1, while IL-10-expressing cells were lower in NCSRWS patients than in c

11 lation of murine colonic Foxp3- and/or IL-10-expressing cells.

12 Despite the abundance of IL-15-expressing cells, the relative levels of sIL-15 complexe

13 essing cells; however, the reduction in 16E6-expressing cells was lower than that in 6E6-expressing c

14 nd that antibody-mediated depletion of 4-1BB-expressing cells (4-1BB is also known as TNFRSF9 or CD13

15 GLP-1R-expressing cells were enriched in several key brain regi

16 However, wild-type BRCA1/2-expressing cells with defects in other DNA damage repair

17 The discovery that IL-23R-expressing cells were ensconced in healthy murine enthes

18 failed to prune and grew towards the lin-44-expressing cells.

19 cleosome acidic patch region, which in 53BP1-expressing cells is bound by 53BP1's ubiquitin-directed

20 Conditioned medium prepared from YAP 5SA-expressing cells induced GFAP(+) cell production in vitr

21 ound that the GFAP(+) cells were not YAP 5SA-expressing cells themselves but cells in the vicinity in

22 Furthermore, the YAP 5SA-expressing cells were identified as FN1(+) mesenchymal c

23 apoptosis in both of 16E6-expressing and 6E6-expressing cells; however, the reduction in 16E6-express

24 -expressing cells was lower than that in 6E6-expressing cells.

25 id cell profiling identified Gr-1- and F4/80-expressing cells as the most abundant producers of IL-27

26 high-affinity CpE receptor and that hCLDN-9-expressing cells undergo cell death when treated with Cp

27 Here, we show that A3B-expressing cells can be selectively killed by inhibiting

28 ation and migration capacity of mutant ABCB5-expressing cells, suggesting that ABCB5 plays a role in

29 infected cells are apolipoprotein- and ACE2-expressing cells of the choroid plexus epithelial barrie

30 re pseudoviruses carrying S(G614) enter ACE2-expressing cells more efficiently than those with S(D614

31 8 showed predominant localization with ACTA2-expressing cells in extensively remodeled IPAH-PAs.

32 analysis of fibronectin digested by ADAMTS9-expressing cells identified a semitryptic peptide arisin

33 by S phase arrest and DNA damage only in ADK-expressing cells.

34 Single-cell sequencing of pineal agrp2-expressing cells revealed molecular resemblance to retin

35 monstrate that M2 primarily functions in AID-expressing cells to facilitate MHV68 dissemination to di

36 T cell tolerance depends upon Aire-expressing cells to purge the T cell repertoire of autor

37 As a result, Akt3-expressing cells activate the DNA damage response pathwa

38 diator of HIV-1 interaction with alpha4beta7-expressing cells.

39 sence of tenogenic cells, extrinsic alphaSMA-expressing cells persist to form a permanent scar.

40 somes, isolated from Mn(2+)-treated alphaSyn-expressing cells, into the striatum initiated Parkinsoni

41 Antibody-expressing cells were profiled with single-cell RNA sequ

42 gs suggest a role for IL-5Ralpha(+) antibody-expressing cells in facilitating local antibody producti

43 increased IL5RA, IGHG4, and IGHE in antibody-expressing cells from patients with AERD compared with a

44 Our study identifies an increase in antibody-expressing cells in AERD defined by transcript enrichmen

45 and phenotypic properties of local antibody-expressing cells in nasal polyps from subjects with AERD

46 om patients with AERD compared with antibody-expressing cells from patients with CRSwNP.

47 y, allowing detection of low surface antigen-expressing cells linked to metastasis.

48 accination with tumor cells or tumor antigen-expressing cells, that lack CD47 or were pre-coated with

49 AQP2 membrane accumulation in cultured AQP2-expressing cells and in kidney collecting duct principal

50 gnaling was required for maintenance of Aqp2-expressing cells in distal nephron and collecting duct s

51 xperimental approaches of AR knockdown in AR-expressing cells and ectopic AR expression in AR-deficie

52 PHOS enzymatic activities were reduced in AR-expressing cells and restored upon AR knockdown.

53 that circulating and tumor-infiltrating ARG1-expressing cells were mainly immature and monocytic MDSC

54 in situ hybridization we localized aromatase-expressing cells to ependymal regions bordering the vent

55 usly that ATXN3-depleted or pathogenic ATXN3-expressing cells abrogate polynucleotide kinase 3'-phosp

56 nd PS bound to GAS6 and were engulfed by AXL-expressing cells much more efficiently than those contai

57 Further, infection of AXL-expressing cells by infectious Zika virus or Ebola, Chik

58 ing and T cell responsiveness to BTNL3-BTNL8-expressing cells.

59 tosis, both of which were prevented in C674S-expressing cells.

60 Calbindin-expressing cells-located in the central core-connect wit

61 ell as with dopamine receptor- and calbindin-expressing cells within the lateral septum, the brain re

62 rdiomyocytes, immune cells, and other CaMKII-expressing cells.

63 d levels of DNA repair were observed in Cas9-expressing cell lines.

64 constant uptake and internalization by CCR2-expressing cells.

65 Atg16l1 deletion in DCs (all CD11c-expressing cells) expands aortic regulatory T cells in v

66 onal deletion of IL-10 specifically in CD11c-expressing cells in vivo implicated macrophages as a cri

67 Notably, mice with Sec22b deletion in CD11c-expressing cells of the hematopoietic system survive to

68 y active NOTCH intracellular domain in CD11c-expressing cells.

69 er stress-induced structural changes in CD1d-expressing cells.

70 chemistry demonstrated an increase in CD209a-expressing cells in the PVPV-Akt1KO thyroids.

71 6E promotes HIV-1 infection in some high-CD4-expressing cells, including human peripheral blood monon

72 is in contrast to the situation of high-CD4-expressing cells, where LY6E predominantly promotes vira

73 Given that HIV-1 can target low-CD4-expressing cells during acute infection yet replicates e

74 in the HSC compartment is restricted to CD41-expressing cells that function with short-term, and prim

75 lls with higher frequencies of IgG- and CD80-expressing cells.

76 ide additional clues as to how CD8alphaalpha-expressing cells are controlled in different tissues.

77 ge analysis tested whether Cadherin-6 (Cdh6)-expressing cells are PT progenitors.

78 ely increased SLC26A9 levels in F508del-CFTR-expressing cells, suggesting that WT-CFTR competes with

79 chat-expressing cells are prominent in motor cranial nerve nu

80 There were also glucagon and insulin co-expressing cells, and beta cells that were incapable of

81 We identify ACE2 and TMPRSS2 co-expressing cells within lung type II pneumocytes, ileal

82 l mesenchymal compartments including Col22a1-expressing cells within the myotendinous junction.

83 However, CX(3)CR1-expressing cells generated TRAP(+) OC on bone within 5 d

84 -CR1-expressing cells compared with high-CR1-expressing cells, and with the addition of soluble CR1,

85 eavage, in the presence of naturally low-CR1-expressing cells compared with high-CR1-expressing cells

86 Mice lacking SHP2 in Col2alpha1-Cre-expressing cells die at mid-gestation.

87 M2 was efficiently deleted in Cre-expressing cells, and the presence of loxP sites flankin

88 onally profiled the transcriptome of CeA Crh-expressing cells (Crh neurons) after fear conditioning o

89 The quantity of CSF1R-expressing cells correlated with GW-2580 sensitivity.

90 Comparison of CSF1R-expressing cells in AML vs healthy donors by mass cytome

91 Our results suggest that CSF1R-expressing cells support the bulk leukemia population th

92 y we conditionally deleted Hdac3 within Ctsk-expressing cells and examined the effects on bone modeli

93 sed RhoA abundance and t (1/2) in Cul3Delta9-expressing cells, caused by decreased ubiquitination.

94 Inducible ablation of IL-1R1 in CX3CR1-expressing cells eliminated cognitive impairment in mice

95 Here we used genetic targeting of Cxcl13-expressing cells to define the molecular identity of the

96 ce more CXCR3 protein than monoallelic CXCR3-expressing cells, and biallelic CXCR3-expressing T cells

97 Immunofluorescence microscopy in CXCR4-expressing cells revealed localized production of PI4P o

98 studies demonstrate specific uptake in CXCR4-expressing cells that can be blocked by more than 90% us

99 or kinase B (TrkB) receptor deletion from D1-expressing cells (D1-Cre-flTrkB) in which a subset of an

100 Ca(2+) channels in dopamine 1 receptor (D1R)-expressing cells in extinction of cocaine conditioned pl

101 -out of Cav1.2 in dopamine D1 receptor (D1R)-expressing cells resulted in attenuation of cocaine CPP

102 ion in mice lacking Ca(v)1.2 channels in D1R-expressing cells (D1(cre), Ca(v)1.2(fl/fl)) can be rescu

103 scued through chemogenetic activation of D1R-expressing cells within the dorsal dentate gyrus (dDG),

104 ling can be mediated by cytonemes from Delta-expressing cells.

105 rting capability and remains stable in DNase-expressing cells.

106 ane, were preferentially endocytosed by DOPr-expressing cells, and were delivered to DOPr-positive ea

107 -up of aberrant RNAs that characterizes DUX4-expressing cells.

108 easurement of RNA and protein levels in DUX4-expressing cells via RNA-seq and quantitative mass spect

109 Our results demonstrate that E6-expressing cells exhibit previously unappreciated mitoti

110 nes, such as adenovirus E1A or MYC, HPV16 E7-expressing cells are sensitized to cell death under cond

111 Sensitivity of HPV16 E7-expressing cells to metabolic stress is rescued by DINO

112 role in the cell death response of HPV16 E7-expressing cells to metabolic stress or DNA damage.

113 DINO stabilizes TP53 in HPV16 E7-expressing cells, and as it is a TP53 transcriptional ta

114 DINO levels are increased in HPV16 E7-expressing cells.

115 P53 stabilization and activation in HPV16 E7-expressing cells.IMPORTANCE Viral oncoproteins, includin

116 potent lytic and functional responses to Env-expressing cell lines and HIV-infected CD4(+) T cells bu

117 lytic response of CD4-MBL CAR-T cells to Env-expressing cell lines and HIV-infected CD4(+) T cells, s

118 , induced cytokine production and killed Env-expressing cells.

119 However, the relevant EP2-expressing cell types remain unclear.

120 junctions formed between EphA2- and ephrinA1-expressing cells, and adhesions formed by cadherin and i

121 caspase-mediated ablation of spinal ERalpha-expressing cells, we observed a significant decrease in

122 e we identify estrogen receptor alpha (Esr1)-expressing cells in the posterior amygdala (PA) as a mai

123 pairs survival and proliferation of AML1-ETO-expressing cells in vitro and in vivo.

124 ETV2-expressing cells in hCOs contributed to forming a comple

125 pact the growth kinetics of virulence factor-expressing cells.

126 on of FNDC3A increased the fitness of FAM46C-expressing cells and expression of FNDC3A in cells that

127 the spatial and temporal distribution of Fap-expressing cells in a murine model of atherosclerosis an

128 9 showed specific binding to recombinant FAP-expressing cells with high affinity.

129 ular, COPBI, was downregulated in mutant FUS-expressing cells under stress.

130 teraction inhibits the growth of YAP1 fusion-expressing cell lines in vitro.

131 Compared with G0-expressing cells, however, G1-expressing cells showed mo

132 mpared with G0-expressing cells, however, G1-expressing cells showed more dramatic phenotypes, resemb

133 In G601S-expressing cells, long-term treatment (24-48 hour) with

134 GABAAR-expressing cells equilibrated with FMP-Red-Dye exhibited

135 ualization and genetic modification of Gdf15-expressing cells.

136 The percentage of GFP-expressing cells was evaluated by using flow cytometry,

137 ction in CFU while microscopic counts of GFP-expressing cells were identical to the expected initial

138 Indeed, CNPYb addition in gp93-expressing cells improved TLR expression.

139 Accordingly, GPR124-expressing cells also displayed increased activation of

140 hosphate (cAMP) levels in mice and in GPR151-expressing cell lines that are amenable to ligand screen

141 nflammatory apoptosis to pyroptosis in GSDME-expressing cells(3-5).

142 are not significantly different from non-HbF-expressing cells and that the primary differences likely

143 NA-based screening of Rab proteins using HBV-expressing cells showed that Rab5B, one of the Rab5 isof

144 In addition, HBx-expressing cells proliferated faster than control and mu

145 significantly higher than that of mutant HBx-expressing cells.

146 liferated faster than control and mutant HBx-expressing cells.

147 We also showed that the ability of WT HBx-expressing cells to form tumors in nude mice was signifi

148 Posterior transplantation of Hedgehog-expressing cells induced mirror-image limb duplications.

149 CD47 is upregulated preferentially in HER2-expressing cells, and blocking CD47 or HER2 reduces both

150 which causes preferential killing of the HIV-expressing cells.

151 uorine, to block (99m)TcO4(-) uptake in hNIS-expressing cells was measured.

152 In both mOTR- and hOTR-expressing cells, Leu(8)-OT was more potent and modestly

153 Our studies establish that Hox-expressing cells are skeletal stem cells that arise from

154 Mitochondria isolated from IB5-expressing cells were relatively resistant to MOMP in vi

155 e is understudied in endogenous MHC class II-expressing cells, largely because the popular cell cultu

156 obe was capable of labeling immunoproteasome-expressing cells while maintaining its selectivity over

157 characterization of individual p16 (INK4a) -expressing cells (tdTom(+)).

158 Senolytic treatment reduces p16(INK4a)-expressing cell numbers, and inhibits Wnt activation and

159 ursor of squamous cell carcinoma, p16(INK4a)-expressing cells are found adjacent to dividing cells, c

160 ostatin-producing delta-cells become insulin-expressing cells after the ablation of insulin-secreting

161 Generating insulin-expressing cells in vitro is no exception, with the guid

162 ocytes, monocytes/macrophages, and CD1a(int)-expressing cell recruitment.

163 Genetic lineage analysis of Isl1-expressing cells by the lineage tracer mouse model showe

164 y the lineage tracer mouse model showed Isl1-expressing cells in the urinary tract of mouse embryos a

165 Surface Ig (sIg)kappa-expressing cells, isolated with mAb LK14 that recognizes

166 Loss of ERalpha in kisspeptin (Kiss1)-expressing cells is sufficient to recapitulate the bone

167 ibited the cell proliferation of mutant KRAS-expressing cells.

168 P domain did not bind to Nup62, and in L126A-expressing cells, host mRNA nuclear export occurred norm

169 In conclusion, deletion of AhR in langerin-expressing cells diminishes the number and activation of

170 Although fetal LGR5-expressing cells can give rise to adult intestinal stem

171 ithelial precursor cells; distinct from LGR5-expressing cells.

172 mpaired T cell expansion toward CD137 ligand-expressing cells.

173 amer binding and reactivity against EBV-LMP2-expressing cell-lines.

174 d cytotoxicity when stimulated with EBV-LMP2-expressing cell-lines.

175 ver cells expressing Lose isoforms, but Lose-expressing cells are not eliminated if their neighbours

176 ntical, implicating distinct roles for Lpar1-expressing cell types.

177 activation, was deleted in lysozyme M (Lysm)-expressing cells, which were found to be Cd11b(+)Ly6c(+)

178 ere that MNT localizes to the nucleus of MAX-expressing cells and that MNT-MAX dimers bind and repres

179 Melanopsin-expressing cells occur at an average peak density of bet

180 Melanopsin-expressing cells occur at an average peak density of bet

181 The dendritic field diameter of melanopsin-expressing cells ranges from 250 (near the fovea) to 1,0

182 The dendritic field diameter of melanopsin-expressing cells ranges from 250 (near the fovea) to 1,0

183 About half of the melanopsin-expressing cells (or 80% of the outer stratifying cells)

184 lls make up on average 60% of the melanopsin-expressing cells.

185 While melanopsin-expressing cells are usually associated with behaviors l

186 d through the TIM23 complex is lower in mHTT-expressing cell lines and brain tissues of HD patients c

187 In mHTT-expressing cell lines, membrane-bound TIM23-imported pro

188 ty to TIM23, and that mitochondria from mHTT-expressing cells and brain tissues of HD patients have r

189 tent with this, we uncovered MCL- and MINCLE-expressing cells in brain lesions of MS patients and we

190 Depletion of Miwi2-expressing cells results in a transient impact on testic

191 icate that in this regenerative state, mpeg1-expressing cells are located in regions containing regen

192 ncreased CDA expression and activity in MUC1-expressing cells as compared with MUC1 knockdown cells.

193 Inoculation of these mutant-expressing cells in athymic nude mice induced rapid tumo

194 tumor cell motility and invasion, kills Myc-expressing cells in a TRAP1-dependent manner, and suppre

195 etabolomics to examine the metabolome of MYC-expressing cells upon AHR knockdown.

196 ression of diverse allotypes of MHC-I in Nef-expressing cells and inhibited Nef alleles from divergen

197 cated that ER binding is reduced in neoGATA3-expressing cells, especially at distal regions, suggesti

198 -ires-Cre amacrine cells form a neuropeptide-expressing cell population with multiple cell types, whi

199 However, two NG2-expressing cell populations, pericytes and glia, may als

200 beta-cells did not derive from Sox9- or Ngn3-expressing cells.

201 Conditioned medium from NICD3-expressing cells enhanced osteoblast differentiation and

202 rmulations, in vitro uptake of iodide by NIS-expressing cells was not significantly affected by ICM.

203 bitory neuronal nitric oxide synthase (nNOS)-expressing cells.

204 liver/bone/kidney (ALPL)-expressing and non-expressing cell types.

205 Exposure of Notch-expressing cells to JAG1(Ndr), compared with JAG1, led t

206 tion and through direct conversion of Notch1-expressing cells to ameloblasts.

207 No NPY- or Npy-expressing cell bodies were observed in the VTA.

208 ial cells (RWPE1), but the identity of OLFM4-expressing cells within these populations and OLFM4's ph

209 udy, we investigated the distribution of OPN-expressing cells in the airway epithelium of normal lung

210 and c-opsin and reveal a novel type of opsin-expressing cell that, like jawed vertebrate rods, enclos

211 Variant 2.2 infected both alpha-DG-null or -expressing cells.

212 Lastly, in vivo LRP5-deficiency in osterix-expressing cells inactivated Wnt signaling in the nucleu

213 ted inactivation of Wnt signaling in osterix-expressing cells may limit regeneration by depleting the

214 anscriptome profiling of fetal osterix (Osx)-expressing cells, followed by lineage mapping, cell trac

215 ucible deletion of one allele of Dkk1 in Osx-expressing cells in adult mice inhibited the recovery of

216 xytocinergic and destinate GABAergic and OTR-expressing cells inside RAIC.

217 Instead, almost 50% of OTR-expressing cells in the VTA were glutamate (GLU) neurons

218 ted down-regulation of ADAM15 in ADAM15 over-expressing cells reduced Claudin-1 levels.

219 rigenic potential was observed when P152Lp53-expressing cells were xenografted into nude mice.

220 role of androgen signaling in prostatic p63-expressing cell initiated oncogenic transformation and t

221 lized beta-catenin expression, prostatic p63-expressing cells possess the ability to initiate oncogen

222 ating stabilized beta-catenin sensitizes p63-expressing cells and increases their sensitivity to andr

223 uptake was confined to proliferating, PARP1-expressing cells.

224 the cell densities of GAD65- and parvalbumin-expressing cells across major nodes of the song network,

225 st how the density of GAD65- and parvalbumin-expressing cells may inform on a CP for complex behavior

226 dominantly in stratum oriens and parvalbumin-expressing cells mostly in stratum pyramidale.

227 Lower numbers of parvalbumin-expressing cells and a reduction in the inhibitory VGAT/

228 essed in distinct populations of Parvalbumin-expressing cells and functionally classified RGCs.

229 s mostly composed by prospective parvalbumin-expressing cells.

230 When Ldb1 is deleted in Pax3-expressing cells in vivo, specification of migratory myo

231 ns through differentiation of Sox2- and PLP1-expressing cells, which represent enteric glia and/or ne

232 Expression of DTA in PLP1-expressing cells selectively eliminated enteric glia fro

233 bes influence the thymic homeostasis of PLZF-expressing cells in early life.

234 presence of a transient population of Pou3f4-expressing cells around and within the spiral ganglion.

235 Using calcium imaging, we found that ppk301-expressing cells show ppk301-dependent responses to wate

236 identified a population of prepronociceptin-expressing cells in the central amygdala (Pnoc(CeA)) tha

237 y ARC neurons, including proopiomelanocortin-expressing cells.

238 ine array with a range of controlled protein-expressing cell lines using 6 monoclonal antibodies (SP1

239 ne expression was terminated in late protein-expressing cells.

240 abled a reliable expression of EGFP in Prox1-expressing cells of the transgenic rats and allowed a co

241 nating 2,8/9-linkages and screening with PSA-expressing cells.

242 ar affinity and high internalization by PSMA-expressing cells when compared with the reference radiop

243 d under metabolic stress in contrast to PTEN-expressing cells.

244 cells and the fast-spiking, parvalbumin (PV)-expressing cells.

245 rneuron population, which contains the Pvalb-expressing cells, correlate with differences in morpholo

246 The authors characterized cardiac PW1-expressing cells and their cell fate potentials in norma

247 poptotic activity, promotes survival of PyST-expressing cells.

248 rofile, and the selective uptake into hY(1)R-expressing cells was demonstrated by internalization stu

249 hatidic acid receptors was augmented in R7BP-expressing cells.

250 ohesion and delay genome replication in Rec8-expressing cells.

251 rity, suggesting that nonimmune EP2 receptor-expressing cell types contribute to cerebral injury.

252 nd MOR23 odorant (Lyral-responsive) receptor-expressing cell populations in F1 offspring, and DNA met

253 nd mediates viral entry into IgG Fc receptor-expressing cells through canonical viral-receptor-depend

254 with allergic asthma involving RGMb and RGMb-expressing cells, such as interstitial macrophages and b

255 ntibody, has potent cytotoxicity toward ROR2-expressing cells.

256 conversion of c-Kit(-) ILC2s into RORgammat-expressing cells by inducing the upregulation of IL23R,

257 ngle-lumen cyst formation in GFP-FIP2(S227E)-expressing cells in three-dimensional (3D) culture.

258 rt that loss of Abl1 specifically in SCGB1A1-expressing cells leads to a significant increase in the

259 ltiple cortical regions, and persistent SCGN-expressing cells were observed in cortex.

260 eptor (Tgfbr2) was targeted in the Scleraxis-expressing cell lineage using the ScxCre deletor.

261 tion, we show for the first time that SEMA7A-expressing cells deposit fibronectin to promote tumor ce

262 ptor (LepR)- or steroidogenic factor-1 (SF1)-expressing cells were studied.

263 analysis revealed that descendants of Sfrp5-expressing cells at E7.5 contribute not only to the SV b

264 We found that Shh-expressing cells contributed to the most posterior digit

265 actor)), when compared to wild-type dog SOD1-expressing cells.

266 By contrast, somatostatin-expressing cells-which reside along the surrounding edge

267 ibuted across cell layers, with somatostatin-expressing cells predominantly in stratum oriens and par

268 te Hedgehog co-receptor, Smoothened, in Sox9-expressing cells prior to injury results in a near-compl

269 ositive fibroblasts stem from a pool of SOX9-expressing cells, and in vivo loss of Sox9 blunted the c

270 ype is the low-threshold, somatostatin (SST)-expressing cell, which is one of the first types of inte

271 nclude the low-threshold, somatostatin (SST)-expressing cells and the fast-spiking, parvalbumin (PV)-

272 luorescence and the inability to make stably-expressing cell lines limit its use.

273 entiation of BoNT/B binding to synaptotagmin-expressing cells.

274 Scattered tac3-expressing cells are also present in telencephalic parts

275 ble-fluorescent staining, we localized tac3a-expressing cells in relation to GnRH and kisspeptin cell

276 The presence of tac3a-expressing cells throughout the brain, including in soci

277 Tai-expressing cells evade death signals by repressing the i

278 TCF1-expressing cells from later divisions in the DLN could s

279 ng signaling, adhesion, and migration in TG2-expressing cells.

280 but does not have functional effects on TG2-expressing cells.

281 it was absent from tyrosine hydroxylase (TH)-expressing cells, but tac3a cells were located in areas

282 pairment of motor functions, reduction of TH-expressing cells in SN, and TH mRNA/protein levels in mi

283 and immunohistology, we identified the TLR2-expressing cells involved in this early neutrophil recru

284 With continued ionophore application,TMEM16F-expressing cells then undergo extensive shedding of ecto

285 Using transporter-expressing cell lines, we show that mIBG is an excellent

286 mechanism to prevent overstimulation in TSHR-expressing cells.

287 mechanism to prevent overstimulation of TSHR-expressing cells.

288 eige adipocyte precursors, and expanded UCP1-expressing cell clusters in inguinal white adipose tissu

289 The UL46-expressing cell lines did not activate interferon-stimul

290 hich transcripts are synthesized in the UPRT-expressing cells.

291 UTS2B-expressing cells appear early in males, prior to project

292 d enhance mitotic rounding, so that Ras(V12)-expressing cells are softer in interphase but stiffen mo

293 and primary tissue identifies distinct venom-expressing cell types as well as proliferative cells exp

294 e of antiretroviral therapy and target virus-expressing cells for elimination.

295 ed us to determine the contribution of VPAC2-expressing cells (~35% of SCN cells) to SCN time-keeping

296 anipulate the cell-autonomous TTFLs of VPAC2-expressing cells.

297 Thus, VPAC2-expressing cells are a distinct, functionally powerful s

298 in certain contexts during development, Wnt-expressing cells can direct neighboring cells to take on

299 uces synthetic lethal cell death in high xCT-expressing cell lines susceptible to glucose deprivation

300 2+)-containing Ca(2+)-free solution to ZnT10-expressing cells triggers an influx of Mn(2+), (b) reint