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 percentage of programmed cell death 1 (PD-1)-expressing cells among CD4(+) T cells.

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

4 d to significantly elevated numbers of Iba-1-expressing cells in the brain, indicative of microglia a

5 ecifically internalized by all tested ICAM-1-expressing cells, including epithelial, fibroblast and n

6 escribed luminal castration-resistant Nkx3.1-expressing cells (CARNs).

7 stem cells named castration-resistant Nkx3.1-expressing cells (CARNs).

8 rs binding to recombinant NRP-1 and to NPR-1-expressing cells.

9 of an inhibitor of TGFbeta signaling to PD-1-expressing cells extends the survival of tumor-bearing m

10 plemented signal to the background of FP1-10-expressing cells compared to the commonly used split GFP

11 IL-10-expressing cells were detected among both CD4(+) and CD8

12 reduced frequencies of IFN-gamma- and IL-17-expressing cells, indicating that ROS play a role in reg

13 Neutrophils, IL-17A, and IL-17RA-expressing cells and levels of IL-17A and IL-22 were qua

14 immunoprecipitation experiments from GLP-1R-expressing cells incubated with [(3)H]BETP.

15 nd energy homeostasis and promotes, in OX-1R-expressing cells, the biosynthesis of the endogenous cou

16 with TG2-specific B-cell receptor, epitope 2-expressing cells had poorer uptake of TG2-gluten complex

17 MOR161-2-expressing cells exhibited significantly greater respons

18 Gene expression profiling analysis of miR-22-expressing cells suggested TACC1 and RAB5B as possible d

19 The major IL-33-expressing cells in skeletal muscle displayed a constell

20 ments showed eosinophils were the major IL-4-expressing cell type in the heart during EAM, IL-4(-/-)

21 x, also known as Sp7 transcription factor 7)-expressing cells in mice promotes HSC regeneration and h

22 ated by the internalization of 5B1 by CA19.9-expressing cells.

23 enitors that express lhx2/9 soxc- and lhx2/9-expressing cells can undergo both asymmetric divisions,

24 ecapillary or arteriolar smooth muscle actin-expressing cells.

25 ted a mouse line lacking Osmr in adiponectin-expressing cells (OSMR(FKO) mice).

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

27 sulted in a strong selective pressure for AE-expressing cells.

28 s recapitulated in mice lacking AT1A in AgRP-expressing cells.

29 ansgenic zebrafish in which agrp1- and agrp2-expressing cells can be visualized and manipulated.

30 OP2 religation activity by etoposide in AIRE-expressing cells had a synergistic effect on genes with

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

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

33 lesions predominantly consisting of alphaSMA-expressing cells.

34 io induces apoptosis of integrin alphavbeta3-expressing cells by recruiting and activating caspase 8

35 anchorage-independent growth of alphavbeta6-expressing cells.

36 the main ER network in Z-alpha1-antitrypsin-expressing cells.

37 The reduced ability of AnxA6-expressing cells to migrate was associated with decrease

38 ATR inhibition in APOBEC3A-expressing cells resulted in a surge of abasic sites at

39 other types of replication stress, APOBEC3A-expressing cells were selectively sensitive to ATR inhib

40 rved only when virus was produced in aptamer-expressing cells, indicating that encapsidation is requi

41 pulations comprising as few as 10% aquaporin-expressing cells are sufficient to produce MRI contrast.

42 of EphB2, was sufficient to repel both Ascl1-expressing cells in vitro and tangentially migrating cor

43 eletion of the type II BMP receptor in Ascl1-expressing cells promoted neurogenesis and reduced anxie

44 After ablation of Ascl3-expressing cells, the OE can regenerate, but lacks the n

45 ed ASOs and their parents in endogenous ASGR-expressing cells and were able to recapitulate hepatocyt

46 In addition, the Axin2-expressing cells produce a source of Wnt that acts in an

47 esponse to tooth damage and that these Axin2-expressing cells differentiate into new odontoblast-like

48 says, inhibit Gas6-inducible motility in Axl-expressing cell lines, and suppress H1299 lung cancer tu

49 work (CAR-BCMA) specifically recognized BCMA-expressing cells.

50 We show that within the cerebellum, BDNF-expressing cells are restricted to the internal granular

51 Lineage tracing experiments show that Bglap-expressing cells in adult sheath tissues possess clonoge

52 ression in polarized Th17 cells, and Bhlhe40-expressing cells exhibited an encephalitogenic transcrip

53 to show that these castration-resistant Bmi1-expressing cells (or CARBs) are capable of tissue regene

54 ovo AML patients at diagnosis based on JAM-C-expressing cells frequencies in the blood served as an i

55 somatostatin-expressing cells and calretinin-expressing cells account for modest proportions of BNST

56 we observed tumors from differentiated Car1-expressing cells with Apc/Kras mutations, suggesting tha

57 ating mice lacking betacatenin in CathepsinK-expressing cells (Ctnnb1(f/f);CtsKCre mice).

58 Mixed BM chimeras further revealed that CB2-expressing cells contributed to ECM development.

59 uced tumor growth in vivo compared with CCL2-expressing cells.

60 uptake was diminished by elimination of CCR2-expressing cells.

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

62 in which p38alpha was deleted only in CD11c-expressing cells, we surprisingly found that CD8 T cell-

63 igen receptor to identify and eliminate CD19-expressing cells.

64 ytoplasmic PLA2 activity to neighboring CD1a-expressing cells.

65 However, the relevant CD1d-expressing cells that influence the effects of NKT cells

66 In humans, the mechanism by which CD23-expressing cells take up IgE-ICs and process them is not

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

68 However, deletion of Pten in CD45-expressing cells induces development of T-cell acute lym

69 ic (prolonged) co-incubation of F508del-CFTR-expressing cells with lumacaftor and ivacaftor deactivat

70 uscle, but only in type I myosin heavy chain-expressing cells.

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

72 ntain a subpopulation of cytokeratin 5 (CK5)-expressing cells that are therapy resistant and exhibit

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

74 observed endoglin expression on the HCV core-expressing cell surface of human hepatocyte origin and a

75 that more efficiently transduce defined Cre-expressing cell populations in vivo.

76 -Cre- and collagen 10alpha1(Col10alpha1)-Cre-expressing cells, predominantly proliferating and hypert

77 hich SHP2 was ablated in the Col10alpha1-Cre-expressing cells appeared normal but were osteopenic.

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

79 harboring a Notch2(DeltaPEST) allele in Cre-expressing cells and control littermates expressing a wi

80 Knocking down ILK in Olig1-Cre-expressing cells reduces the pool of oligodendrocyte pro

81 s for binding and for full toxicity on CSPG4-expressing cells.

82 CXCL14 did not activate CXCR4-expressing cells (i.e., failed to trigger chemotaxis and

83 omal cells and modulates the homing of CXCR5-expressing cells toward the FDC-containing B cell follic

84 g area and areas of abnormal foci of CYP11B2-expressing cells, called aldosterone-producing cell clus

85 icylate was observed in the medium of CYP1a2-expressing cells.

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

87 a supporting contribution of hippocampal D1R-expressing cells in this process.

88 phosphoprotein (DARPP-32) exclusively in D2R-expressing cells exhibited preferential D2R changes in t

89 cifically in dopamine beta-hydroxylase (DBH)-expressing cells is both necessary and sufficient for st

90 sheep cortex and in large populations of DCX-expressing cells within the external capsule and the sur

91 Here, we analyzed the DCX-expressing cells in the whole sheep brain of both sexes

92 Conversely, the low DDX3-expressing cell line, PC3, exhibited few changes followi

93 f Cdc25, ECs in lateral contact with a Delta-expressing cell experience higher levels of Notch signal

94 by more distant neighbours, and lastly Delta-expressing cells.

95 ndependent mechanism by which DeltaNp63alpha-expressing cells within a TGFbeta-rich microenvironment

96 scriptomic analysis revealed that these dual-expressing cells represent a population of less well-dif

97 ated by Dux were similarly increased in DUX4-expressing cells.

98 a loss of kinetochore-associated Mad2 in E6-expressing cells.

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

100 informatics analysis, pathways altered in E7-expressing cells were identified.

101 We found that in E7-expressing cells, the steady-state level of WDHD1 protei

102 , one of the genes that is upregulated in E7-expressing cells, was found to play an important role in

103 one of the genes that was upregulated in E7-expressing cells.

104 ple transcription factors were altered in E7-expressing cells.

105 ly expressed genes, most of them novel to E7-expressing cells, was further confirmed by real-time PCR

106 C) toxins, for their ability to kill HIV Env-expressing cells.

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

108 However, coculture of normal PBMCs with Env-expressing cells resulted in selective CD4 loss that was

109 tin differential between ephrin-B1- and EphB-expressing cells.

110 s well as invasiveness of wild-type ephrinB1-expressing cells.

111 nase CKMT1 as necessary for survival of EVI1-expressing cells in subjects with EVI1-positive AML.

112 monstrating that the other major FcgammaRIIB-expressing cell type, liver sinusoidal endothelial cells

113 is a substantial involvement of FcgammaRIIIa-expressing cells, such as NK cells.

114 in increased physical attraction of ferritin-expressing cells to magnets and increased contrast for c

115 -type hosts revealed that circulating Fgfbp1-expressing cells migrate into healing wounds.

116 that tissue-resident and circulating Fgfbp1-expressing cells modulate skin carcinogenesis and inflam

117 nodules expressed YFP, indicating that Foxl1-expressing cells are not the origin for hepatotoxin-indu

118 tion of Prdm1 in either Keratin 14- or Foxn1-expressing cells in mice resulted in multisymptom autoim

119 To facilitate visualization of Fpr3-expressing cells, we generated and validated two new ant

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

121 ell swelling and cell death compared with G0-expressing cells.

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

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

124 Here we show that in Gag-expressing cells, secretion of biologically active p17 t

125 and induces generation of submucosal gastrin-expressing cell hyperplasia.

126 -size PB transposon resulting in 50+/-5% GFP-expressing cells after stable transposition.

127 form filaments in blebs in 41% of NM-IIB-GFP-expressing cells, whereas filaments form in only 12 and

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

129 lacking the beta1AR specifically in ghrelin-expressing cells, ghrelin secretion was markedly blunted

130 ting glutamate aspartate transporter (GLAST)-expressing cells, replicates such alterations.

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

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

133 -, and (177)Lu-NeoBOMB1 radioligands in GRPR-expressing cells and mouse models.

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

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

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

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

138 Here, we clarified the roles of HDC-expressing cells and histamine in heart failure post-MI

139 in mouse embryonic stem cells and hemoglobin-expressing cells in the mouse cortex and hippocampus.

140 (125)I-Z2395-TCO bound specifically to HER2-expressing cells in vitro with an affinity of 45 +/- 16

141 The HERVH-expressing cells have a similar, but nonidentical, expre

142 and is inappropriately sequestered in the hh-expressing cells.

143 as key cytokines to generate langerin(high)-expressing cells but only in serum-free conditions.

144 HIV-expressing cells were associated with tissue macrophages

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

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

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

148 covered that corticotropin-releasing hormone-expressing cells contain GABAergic and glutamatergic sub

149 Introduction of miR-200c into hPMR1-expressing cells reduced motility and miR-200 target gen

150 ation or inhibition, or blocked in D226A HuR-expressing cells.

151 rived xenograft tumors enriched for ST6Gal-I-expressing cells relative to pair-matched untreated tumo

152 rain, a dramatically lower percentage of IE2-expressing cells was detected in the ventricular zone (V

153 r, promotes the robust generation of insulin-expressing cells from multiple hPSC lines.

154 neither antibodies/ECM-proteins nor integrin-expressing cells are required for detection, and (iii) i

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

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

157 JAG1-expressing cells, but not JAG1(Ndr)-expressing cells, bo

158 lator, E7017, selectively kills SF3B1(K700E)-expressing cells.

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

160 ion method to specifically silence NF-kappaB-expressing cells during place preference conditioning.

161 leus, and found that disruption of NF-kappaB-expressing cells using Daun02 attenuated the development

162 These PD-L1-expressing cells were immunosuppressive and were capable

163 cking the AT1A receptor specifically in LEPR-expressing cells failed to show an increase in RMR in re

164 otch activation initiated by adjacent ligand-expressing cells, TCR stimulation is sufficient to induc

165 KIR2DL3 responses toward some KIR2DS2 ligand-expressing cells were also undiminished after beta2-micr

166 ing that the inability to clear NKG2D ligand-expressing cells was important in tumor suppression and

167 h bacterial infections and stimulated LILRA2-expressing cells.

168 ecifically targeting TbetaRI kinase in LOXL2-expressing cells.

169 +)); however, only CD11b(+) Ly6G(+) Ly6C(++)-expressing cells exerted a significant suppressive effec

170 to a high-fat diet required TLR9 on lysozyme-expressing cells, and a clinically applicable TLR9 antag

171 specific deletion of Nod2 in villin and Lyz2-expressing cells.

172 Notch2(COIN) inversion in Lyz2-expressing cells had no skeletal consequences and did no

173 in mice carrying a deletion of Nod2 in Lyz2-expressing cells.

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

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

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

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

178 Tracing Mesp1-expressing cells and their progeny allows isolation and

179 However, upon injury, Miwi2-expressing cells are essential for the efficient regener

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

181 fficient to promote the proliferation of Mkx-expressing cells in sheath tissues, and its action is me

182 , as deletion of either Mll1 or Dot1l in MN1-expressing cells abrogated the cell of origin-derived ge

183 g centers, specialized clusters of morphogen-expressing cells.

184 directions non-cell autonomously, toward MP-expressing cells.

185 displaying diverse TCRs and reacting to MR1-expressing cells in the absence of microbial ligands.

186 nance of non-photosensitive, cone opsin mRNA-expressing cells in the retina.

187 s cytokinesis in INCENP actin-binding mutant-expressing cells.

188 sitol (3,4,5)-trisphosphate (PIP3) in mutant-expressing cells.

189 n-deficient or separase cleavage site mutant-expressing cells, and an increase in MCPH1-deficient cel

190 cogene in myogenic factor 5-expressing (Myf5-expressing) cells develop fully penetrant sarcomagenesis

191 JAG1-expressing cells, but not JAG1(Ndr)-expressing cells, bound soluble Notch1 extracellular dom

192 The mice lacking Rargamma in Nes-expressing cells also had smaller thymi, with reductions

193 In contrast, deletion of Rargamma in Nes-expressing cells resulted in reductions in peripheral bl

194 a regulator of B and T lymphopoiesis via Nes-expressing cells in the BM and thymic microenvironments,

195 T, and in human pancreatic epithelial nestin-expressing cells, activates both the AKT and MAPK pathwa

196 Cell-specific loss of Tsc1 within nestin-expressing cells in adult mice leads to the formation of

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

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

199 NG2-expressing cells are a population of periportal vascular

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

201 at these cells are normally cleared by NKG2D-expressing cells.

202 ove properties could be imparted to IRF8-non-expressing cells by ectopic expression of the protein.

203 ECM protein Decorin in the neighbouring non-expressing cells.

204 nes, primarily caused by a proportion of non-expressing cells.

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

206 Here we identify mitotic Olig2-expressing cells as tumor-propagating cells in proneural

207 pendent growth and proliferation of oncogene-expressing cells.

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

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

210 enhanced by bax silencing in pUL37 x 1 over-expressing cells, suggesting a bax-dependent mechanism o

211 ly the re-expression of CHFR in miR-26a over-expressing cells partially rescues normal mitosis and im

212 terized tdTomato reporter mice to study P2X4-expressing cells in the brain, new insights on feeding-r

213 Neutrophils were also the predominant P2X7R-expressing cells during Streptococcus pneumoniae corneal

214 Further, they resensitized mutant p53-expressing cell lines resistant to 5-fluorouracil.

215 In p53-expressing cells, citral increases phosphorylation of se

216 rentiation process led to suppression of p63-expressing cells with a decreased number of CK5(+) basal

217 hTERT-P785L-expressing cells did not show growth defects, and this v

218 nx1-null cells were less abundant than Panx1-expressing cells, suggesting that Panx1 is required for

219 in-mediated endocytosis is increased in PAPC-expressing cells, subsequently affecting CDH2 internaliz

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

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

222 Almost no parvalbumin-expressing cells were found in the BNST, while somatosta

223 Foxc1 and Foxc2 genes were targeted to Pax3-expressing cells.

224 The number of perforin-expressing cells in the lamina propria of acutely HIV-in

225 ults define the myofibroblast as a periostin-expressing cell type necessary for adaptive healing and

226 Due to increased lysosomal DOX trapping, Pgp-expressing cells became more resistant to DOX.

227 Here, we confirmed that PIN1-expressing cells exhibit higher p27 levels but have incr

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

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

230 We investigated whether elimination of PLP1-expressing cells compromises epithelial maintenance or g

231 Elimination of PLP1-expressing cells did not reduce survival of neurons in t

232 Second, unlike other known POMC-expressing cells, tanycytes rarely contained detectable

233 PR3-expressing cells produced significantly fewer MVs during

234 an neutrophils, and those generated from PR3-expressing cells hampered this inhibition.

235 Functionally, activation-evoked MVs from PR3-expressing cells induced a significantly larger respirat

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

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

238 data set indicate a similarity of the pSHP2-expressing cell population to previously characterized m

239 than 6 h and showed specific binding to PSMA-expressing cells (concentration giving 50% inhibition of

240 Conversely, RET/PTC3-expressing cells were characterized by a high IDO1 expre

241 PW1-expressing cells are detected in the heart but are not w

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

243 entify, track, isolate, and characterize PW1-expressing cells in the LV myocardium in normal and isch

244 ulmonary arterial hypertension patients, PW1-expressing cells were observed in large numbers in remod

245 e increased mutation rate in the POLD1-R689W-expressing cells.

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

247 We report that hTERT-P721R- and hTERT-R811C-expressing cells exhibited growth defects likely due to

248 w that upon MSK1 depletion in oncogenic RAF1-expressing cells, H3S28ph presence at the INK4 locus and

249 Tbx21 was excised in IL-17-producing or Rag1-expressing cells is indistinguishable from that observed

250 ased incorporation of [(3)H]leucine in K-Ras-expressing cells, suggesting that Golgi-localized K-Ras

251 uncontrolled proliferation in oncogenic Ras-expressing cells, and arises in response to genotoxic st

252 sed the effects of EBI3 on cytokine receptor-expressing cells.

253 ls within the hippocampus and in D1 receptor-expressing cells in extinction of cocaine-associated mem

254 a role of Cav1.2 within dopamine D1 receptor-expressing cells of the hippocampus for extinction of co

255 e the infection of DENV in Fc gamma receptor-expressing cells, offsetting the concern of ZIKV vaccine

256 To identify P2X4 receptor-expressing cells, we generated BAC transgenic mice expre

257 rized tool with which to study P2X4 receptor-expressing cells.

258 ed with higher abundance of the Wnt receptor-expressing cells and greater activation of the downstrea

259 effect of these molecules on other RORgammat-expressing cells is unknown.

260 Selective ablation of S100A4-expressing cells was sufficient to block tumor growth in

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

262 me analysis of high- vs. low-Sost/sclerostin-expressing cells identified known and novel genes.

263 aused an increase in the number of serotonin-expressing cells and at higher dose converted most of th

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

265 ested the hypothesis that migration of SLFN4-expressing cells from the bone marrow to peripheral orga

266 at express Pax4 specifically in somatostatin-expressing cells.

267 Pharmacogenetic activation of somatostatin-expressing cells reduced pyramidal neuron hyperactivity

268 s were found in the BNST, while somatostatin-expressing cells and calretinin-expressing cells account

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

270 st describe steps for how to establish SoNar-expressing cells, and then discuss how to use the system

271 By inducing clones in sox10-expressing cells, we trace and quantitatively compare th

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

273 and mass spectrometric analysis of SPRIGHTLY-expressing cells revealed changes in the expression of g

274 eveloped significantly higher number of ST2L-expressing cells in spleen and liver.

275 Most of the ST2L-expressing cells in liver were F4/80(+) macrophages, ind

276 n of the non-coding RNA Malat-1, in Stabilin-expressing cell lines.

277 scent reporter gene activation only in Stra8-expressing cells, newly-formed oocytes.

278 Furthermore, MCAs formed from MT1-MMP-T567E-expressing cells adhere avidly to both intact ex vivo pe

279 Interestingly, a population of Tax-expressing cells exhibited antisense but not activated s

280 ng for the presence and distribution of Tbr2-expressing cells in the prenatal cortex of reptilian and

281 activated cell sorting (FACS)-purified Tbx18-expressing cells behaved as MSCs in vitro.

282 In a murine model, ablation of TBX4-expressing cells or disruption of TBX4 signaling attenua

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

284 Some TCF1-expressing cells in DLNs acquired an alternative, follic

285 We report the distribution of tdTomato-expressing cells throughout the brain and particularly s

286 GFP reporter lines showed that the tdTomato-expressing cells were mainly AgRP-NPY neurons and tanycy

287 lytic inactive mutant (Mut), TET2 in low-TET-expressing cells results in an increase in the level of

288 Exposure of TF-expressing cells to factors (F) VIIa and Xa triggered th

289 of cnidocytes and that many of these Nv-TLR-expressing cells also express Nv-NF-kappaB.

290 ected with Torso and when presented to Torso-expressing cells in conditioned medium.

291 In uninjured animals, tph1b-expressing cells contribute fibroblast progeny that rema

292 g protection of vector-transduced, transgene-expressing cells from microglial phagocytosis.

293 llating stimuli are presented to transporter-expressing cells, and activity is measured through imagi

294 The UL46-expressing cell lines also rescued the defects of the De

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

296 ifferential gene expression profiles of WIF1-expressing cells were performed.

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

298 ignificantly shorter tumor latencies vs Wwox-expressing cells.

299 BGJ398 treatment of YAP-expressing cells induced cell death due to Mcl-1 depleti

300 recognized rare cell types, including Zscan4-expressing cells within mouse embryonic stem cells and h