ライフサイエンスコーパス: cell-derived

1 emerged as two distinct approaches for stem cell-derived 3D tissue preparation.

2 Gene expression analysis of single cell-derived, adapted tetraploid clones showed up-regula

3 s for potency prediction of mesenchymal stem cell-derived and pluripotent stem cell-derived multicell

4 ofiling during differentiation of human stem cell-derived and primary murine oligodendrocytes indicat

5 ell clones revealed specificity for distinct cell-derived antigens and alternative transcriptional st

6 ephrin-B1 pathway is disrupted in human stem cell derived astrocyte and mouse models of amyotrophic l

7 from large oncosomes (LO), which are cancer cell-derived, atypically large (1-10 mum) extracellular

8 eactive memory B cell development and plasma cell-derived autoantibody production.

9 ement therapies (such as human islet or stem cell-derived beta cell transplantation) without immunosu

10 levant for generation of transplantable stem cell-derived beta-cells.

11 ity of a novel intranasally delivered amnion cell derived biologic to suppress inflammation, prevent

12 Mechanistically, we found that cancer-cell-derived C3 activates the C3a receptor in the choroi

13 to generate a human-induced pluripotent stem cell-derived cardiac muscle patch (hCMP), which was subs

14 nctional screening in human pluripotent stem cell-derived cardiac organoids (hCOs).

15 maturing, unlabeled induced pluripotent stem cell-derived cardiomyocyte cultures.

16 Mapping of induced pluripotent stem cell-derived cardiomyocyte networks and in vivo investig

17 Human induced pluripotent stem cell derived cardiomyocytes (hiPSC-CMs) offer a novel in

18 immature phenotype of human pluripotent stem cell derived cardiomyocytes (hPSC-CMs) constrains their

19 These Pnmt(+) cell derived cardiomyocytes (PdCMs) are similar to conve

20 RATIONALE: Human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CM) are increasingly

21 Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) are a powerful p

22 reased use of human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) for drug develop

23 effects with human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) provide new poss

24 amplitude in human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs), but D-ala,RP pr

25 Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs), fibroblasts (FB

26 In human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs), Tbx20 enhanced

27 stnatal maturation in human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs), limiting their p

28 s in animal models, induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) have not been inv

29 cardiac tissues made of mouse embryonic stem cell-derived cardiomyocytes (mESC-CMs).

30 suppression of PRRX1 in human embryonic stem cell-derived cardiomyocytes and embryonic zebrafish resu

31 from embryonic and induced pluripotent stem cell-derived cardiomyocytes and fibroblasts with organot

32 lly available human induced pluripotent stem cell-derived cardiomyocytes are a powerful model for scr

33 e of isogenic human induced pluripotent stem cell-derived cardiomyocytes as a physiologically relevan

34 Additionally, in human embryonic stem cell-derived cardiomyocytes challenged with TNFalpha or

35 The patient-derived induced pluripotent stem cell-derived cardiomyocytes display (1) significantly pr

36 ional properties of induced pluripotent stem cell-derived cardiomyocytes from a patient with D130G-CA

37 date, electrophysiological analyses of stem cell-derived cardiomyocytes has largely been limited by

38 cal maturation of the human pluripotent stem cell-derived cardiomyocytes in our system recapitulates

39 omyocytes and human induced pluripotent stem cell-derived cardiomyocytes in vitro and in vivo in mice

40 fish hearts in vivo as well as in human stem cell-derived cardiomyocytes in vitro.

41 Stem cell-derived cardiomyocytes mutated to carry the effect

42 Stem cell-derived cardiomyocytes provide a promising tool for

43 As human pluripotent stem cell-derived cardiomyocytes remain functionally fetal-ty

44 structural and functional maturation of stem cell-derived cardiomyocytes remains a key challenge for

45 from embryonic and induced pluripotent stem cell-derived cardiomyocytes under defined, serum-free co

46 unctional rescue in induced pluripotent stem cell-derived cardiomyocytes with D130G-CALM2, as shown b

47 mately 50 000 human-induced pluripotent stem cell-derived cardiomyocytes, smooth muscle cells, and en

48 Using human induced pluripotent stem cell-derived cardiomyocytes, we not only confirmed these

49 mmunity using human induced pluripotent stem cell-derived cardiomyocytes.

50 aluate the maturation state of cultured stem cell-derived cardiomyocytes.

51 as isolated adult and human pluripotent stem cell-derived cardiomyocytes; (2) 2-dimensional in vitro

52 or small clusters of human pluripotent stem cell-derived cardiomyocytes; (3) 3-dimensional multicell

53 so overexpressed in induced pluripotent stem cells derived cardiomyocytes (iPSCs-CM).

54 totoxicity in human induced pluripotent stem cells-derived cardiomyocytes (iPS-CMs).

55 activated T cells, it remains unclear how T cell-derived CD70 affects T cell function.

56 This study suggests that T cell-derived CD70 performs a critical negative feedback

57 for the first time, to our knowledge, that T cell-derived CD70 plays a novel immune checkpoint role i

58 Therefore, we have assessed the role of T cell-derived CD70 using adoptive-transfer models, includ

59 f proinflammatory/profibrotic cytokines by T cell-derived CD73.

60 ng the chemoattractant effect of endothelial cell-derived CD95L in induction of neutrophil recruitmen

61 ne cells and their descendants (i.e. Pnmt(+) cell derived cells) within the heart.

62 steer directional differentiation because ES cell-derived cells are typically immature with impaired

63 en as one of the first applications for stem cell-derived cells because of the loss of only a single

64 Integration of stem cell-derived cells into native cellular environment rema

65 ts like glutamine synthetase (GS), leukocyte cell-derived chemotaxin 2, Regucalcin, and Cyclin-D1 and

66 ntiation and followed the maturation of stem cell-derived clones using sparse lineage tracing in the

67 Human and mouse pluripotent stem cell-derived CMs (PSC-CMs) were transduced with the neur

68 myocytes, and human induced pluripotent stem cell-derived CMs, decreasing expression of hypertrophic

69 Together, our data position immune cell-derived complement production and autocrine/paracri

70 f antigens and danger signals from apoptotic cell-derived constituents that can result in immune acti

71 -of-function approaches in an embryonic stem cell-derived cortical differentiation model, we report t

72 chemical screen using human pluripotent stem cell-derived cortical neural progenitor cells (hNPCs) an

73 rotease MCPT1, as well as splenic T-helper-2 cell-derived cytokine production.

74 oclonal antibody specific for the epithelial-cell-derived cytokine thymic stromal lymphopoietin (TSLP

75 IL-21, a Tfh cell-derived cytokine, provides instructional cues for G

76 n expression of proinflammatory innate and T-cell-derived cytokines during ustekinumab therapy.

77 role of skin barrier defects and epithelial cell-derived cytokines in the initiation and maintenance

78 Emerging data now suggest that epithelial cell-derived cytokines such as thymic stromal lymphopoie

79 to HDMs is partially mediated by epithelial cell-derived cytokines that activate group 2 innate lymp

80 ) expression of proinflammatory innate and T-cell-derived cytokines were measured and compared with s

81 ncephalic and human induced pluripotent stem cells-derived DA neurons.

82 ncephalic and human induced pluripotent stem cells-derived DA neurons.

83 ent with this notion, we found that mouse ES cell-derived DCs (ES-DCs) represented less mature cells

84 In the case of cancerous tissue, stromal cell-derived differentiation signals in particular may p

85 Transplantation of human pluripotent stem cell-derived dopaminergic neurons is a promising approac

86 ed fibroblasts, and induced pluripotent stem cell-derived dopaminergic neurons.

87 Here, a live stem cell derived embryoid body (EB) based cardiac cell syncy

88 used comparison of induced pluripotent stem cell-derived endothelial cells (iPSC-ECs) from three fam

89 tudy indicates that induced pluripotent stem cell-derived endothelial cells are useful surrogates to

90 CRISPR-edited stem cell-derived endothelial cells demonstrate rs9349379 reg

91 monary arterial and induced pluripotent stem cell-derived endothelial cells from patients with idiopa

92 ethod for introducing human pluripotent stem cell-derived enteric neural crest cells into developing

93 Human intestinal stem cell-derived enteroid monolayers co-cultured with human

94 crophages, dendritic cells, B cells and stem-cell-derived enteroids can all support infection of cert

95 Here, we used stem cell-derived enteroids from human small intestines to st

96 Primary human airway basal stem cell-derived epithelial cultures and micro-optical coher

97 l matrix with human induced pluripotent stem cell-derived epithelium and human endothelium, and show

98 in artificial EVs, cancer cells, and cancer cell-derived EVs.

99 ential role for B cells in the response to B cell-derived exosomal proteins, B cell depletion did not

100 Plasma endothelial cell-derived exosomes (EDEs) and platelet-derived exosom

101 d cargo proteins of human plasma endothelial cell-derived exosomes in atherosclerotic cerebrovascular

102 In addition, epithelial cell-derived exosomes induced endothelial cell prolifera

103 cer, we hypothesized that corneal epithelial cell-derived exosomes may gain access to the underlying

104 Our results indicate that epithelial cell-derived exosomes mediate communication between corn

105 oblasts, demonstrating a direct role of stem cell-derived exosomes on mouse endothelium at the cellul

106 rculating Ab in mediating CTL responses to B cell-derived exosomes was ruled out using DHLMP2A mice,

107 to CSC-exposed HIV-1-infected and uninfected cell-derived exosomes, on HIV-1 replication of recipient

108 e help for CD8 T cell-mediated response to B cell-derived exosomes.

109 Herein, we demonstrate that mouse GBM cell-derived extracellular nanovesicles resembling exoso

110 mokine receptor CXCR7 and its ligand stromal cell-derived factor (SDF)-1 are known to be involved in

111 In addition, the angiogenic factors stromal cell-derived factor 1 (SDF-1alpha), vascular endothelial

112 Cepsilon1) as a crucial regulator of stromal cell-derived factor 1 alpha (SDF-1alpha)-induced Rap1 ac

113 L12</em>, which encodes a chemokine, stromal cell-derived factor 1, that is expressed in cardiomyocyt

114 Stromal cell-derived factor 1/CXCR4 inhibition impaired cell spr

115 on molecule 1; interleukin 6 [IL-6]; stromal cell-derived factor 1; tissue inhibitor of metalloprotei

116 In addition, median stromal cell-derived factor-1 (SDF-1) levels were 43% higher in

117 y may participate, together with the stromal cell-derived factor-1 (SDF-1)/C-X-C chemokine receptor 4

118 hibited CXCR4 binding to its ligand, stromal cell-derived factor-1alpha, and reduced hypoxia- and str

119 tor-1alpha, and reduced hypoxia- and stromal cell-derived factor-1alpha-mediated migration dose-depen

120 responses is regulated by airway epithelial cell-derived factors, including TRAIL and MID1, which pr

121 programmed to process internalized apoptotic cell-derived fatty acids, cholesterol and nucleotides, a

122 cation of certain prion strains upon stromal cell-derived follicular dendritic cells (FDC) in the Pey

123 g in vitro cultured induced pluripotent stem cell-derived forebrain neurons and in vivo neurons in mo

124 ownregulated in the induced pluripotent stem cell-derived forebrain neurons from the subjects carryin

125 ocrine-active human-induced pluripotent stem cell-derived foregut epithelial cells and hypothalamic n

126 the first time in human neuronal progenitor cells (derived from embryonic stem cells) and fetal musc

127 ysing PTEN in malignant glioblastoma primary cells derived from 16 of our patients, we report mutatio

128 l state underlies the behaviour of persister cells derived from a wide range of cancers and drug trea

129 shown histone deacetylases are modulated in cells derived from alcohol users and after in vitro acut

130 ays revealed lower proliferation rates of MG cells derived from betaENaC MG KO than control mice, sug

131 or activator of NF-kappaB ligand bone marrow cells derived from BLT1(+/+) and/or BLT1(-/-) mice and u

132 The protocol can be used with cells derived from both fresh and cryopreserved tissue s

133 ux, which was conserved in kidney epithelial cells derived from both Pkd1-null mice and ADPKD patient

134 ayers is a hybrid zone, which is composed of cells derived from both the Nppa(+) and Hey2(+) populati

135 a hybrid myocardial zone that is composed of cells derived from both trabecular and compact layers.

136 limiting factor in the tumor specificity of cells derived from bulk CD8 TILs.

137 In vitro cultured neural stem cells derived from Cic conditional knockout mice bypasse

138 Interestingly, in mouse embryonic fibroblast cells derived from CIZ1-null embryos, Xist RNA localizat

139 ically and developmentally specified sets of cells derived from common progenitors.

140 Human dental pulp cells (DPCs), adherent cells derived from dental pulp tissues, are potential to

141 lear how RICD sensitivity is calibrated in T cells derived from different individuals or subsets.

142 Cells derived from drug-resistant tumors were sensitive

143 E+P treatment of patient-derived epithelial cells derived from ductal carcinoma in situ (DCIS) incre

144 HIV-specific B cells derived from elite controllers displayed greater a

145 Epithelial cells derived from ERG transgenic mouse prostates have i

146 Further, gene expression analysis of CD34(+) cells derived from fetal SMGs showed significant upregul

147 Cells derived from genomically unstable tumors exhibit e

148 n the regulation of PDH activity in striatal cells derived from HD knock-in mice and YAC128 mice.

149 nucleoli also expand as aging progresses in cells derived from healthy individuals.

150 and enhanced p53/p21 activation relative to cells derived from healthy patients.

151 Primary hippocampal cells derived from heterozygous mice showed an attenuate

152 uman bone marrow stem cells (BMSC) with stem cells derived from human dental pulp (DPSC), apical papi

153 In primary cells derived from human patient-derived xenograft (PDX)

154 Endothelial cells derived from human pluripotent stem cells are a pr

155 itro differentiation of pancreatic endocrine cells derived from human pluripotent stem cells mimics k

156 CD34(+)CD38(-)) and differentiated (CD34(-)) cells derived from individuals with CML, and we compared

157 Exposure of cells derived from individuals with PPM1D truncating mut

158 1 deficiencies observed in neural progenitor cells derived from induced pluripotent stem cells from s

159 We found that differentiated cells derived from isogenic iPSCs and nt-ESCs showed com

160 nd realistic picture of ChHV5 replication in cells derived from its natural host and may be crucial n

161 ted TLR7- and TLR9-dependent responses using cells derived from lupus patients, suggesting that inhib

162 of beta-agonist stimulation in SBMA myotube cells derived from mice and patients, and in knock-in mi

163 Moreover, isolated cells derived from Muc4(ko)/NDL tumors interact with few

164 e combined treatment is further confirmed in cells derived from OPMD patients.

165 Since cells derived from other normal human cell types are ful

166 Previously, we found that in cancer cells derived from pancreatic ductal adenocarcinoma (PDA

167 GPCs) produced from induced pluripotent stem cells derived from patients with childhood-onset SCZ.

168 its ability to read-through PTC mutations in cells derived from patients with RDEB.

169 in VS, archived tumor specimens, fresh tumor cells derived from patients with sporadic VS, and an est

170 In tumor cells derived from patients, ATRis also overcome the byp

171 nize autologous tumor cells, suggesting that cells derived from PD-1(+) TILs can be used in adoptive

172 UN-KC-6141 cells (pancreatic cancer cells derived from Pdx1-Cre;LSL-Kras(G12D) mice) were in

173 Daughter cells derived from PGCCs showed attenuated capacity for

174 proliferation of uterine artery endothelial cells derived from pregnant (P-UAECs), but not non-pregn

175 Indeed, AML cells derived from relapsed cases exhibited higher CBFB

176 hether electrophysiologically-active somatic cells derived from separate germ layers can be interconv

177 and HAP1), as well as haploid embryonic stem cells derived from several organisms.

178 In this proof-of-concept study, using stem cells derived from skeletal muscle of a DMD patient (mdc

179 fferentiation compared with that observed in cells derived from solid tumors.

180 Differentiated and transplanted RGC-like cells derived from stem cells have the potential to repl

181 beta-Cells derived from stem cells hold great promise for cel

182 In hepatic tumor cells derived from Tet-O-MYC mice, the expression of mRN

183 ded alphabetaTCR pairs expressed on CD4(+) T cells derived from the BAL of DR3(+) LS patients.

184 Mouse embryonic stem cells derived from the epiblast contribute to the somati

185 ised by inflammation and the accumulation of cells derived from the monocyte and macrophage lineages,

186 nectivity, based on induced pluripotent stem cells derived from the respective individuals.

187 Induced pluripotent stem cells (iPSCs), and cells derived from them, have become key tools for model

188 opportunistic infections and the capacity of cells derived from these animals to execute inflammatory

189 his, the in vitro proliferation of satellite cells derived from these muscles was reduced by CR.

190 sion in cultured human LAD2 and primary mast cells derived from umbilical cord blood.

191 This enabled us to discover that neural stem cells, derived from the murine spinal cord and organized

192 In contrast, for cell-derived giant plasma membrane vesicles (GPMVs), bre

193 sma membrane and in actin cytoskeleton-free, cell-derived giant plasma membrane vesicles (GPMVs).

194 he opposite direction from that reported for cell-derived GPMVs.

195 discuss the importance of benchmarking stem cell-derived hepatocyte-like cells to their terminally d

196 efficient differentiation protocols for stem-cell-derived hepatocytes and broaden our understanding o

197 ut using cell lines, primary cells, and stem cell-derived hepatocytes.

198 nfected fibroblasts and human embryonic stem cell-derived (hESC) neurons.

199 ases PDE11A mRNA in induced pluripotent stem cell-derived hippocampal neurons originating from lithiu

200 properties of human induced pluripotent stem cell-derived HSPCs (hiPS-HSPCs).

201 ed from in vitro modeling of primary or stem cell-derived human CNS cells and cell lines.

202 hat the epithelium of human pluripotent stem-cell-derived human intestinal organoids is globally simi

203 Moreover, ZIKV productively infects stem-cell-derived human neural crest cells and peripheral neu

204 Using ES-cell-derived human neurons, we show that ApoE secreted b

205 Pluripotent stem cell-derived human primordial germ cell-like cells (hPGC

206 CD8(+) cell-derived IFN-gamma suppresses osteoclast function an

207 deficient in IL-18 production, and lacked NK cell-derived IFN-gamma.

208 B-cell-derived IGF-1 is critical for resistance of melanom

209 ug resistance mediated by tumor-associated B cells-derived IGF-1.

210 ompetent mice, indicating a major role for T cell-derived IL-10 in TB susceptibility.

211 Notably, mice deficient in T cell-derived IL-10, but not mice deficient in monocyte-d

212 rs have previously demonstrated a role for T cell-derived IL-13 in mediating the induction of collage

213 malignant Lin(-)IELs is driven by epithelial cell-derived IL-15.

214 Cord blood mononuclear cell-derived IL-1beta levels were measured by means of E

215 ion, and autoantibodies, indicating that Tfh cell-derived IL-21 is critical for pathological B cell c

216 We demonstrate that donor T cell-derived IL-22 significantly exacerbates cutaneous c

217 icroMT) mice, we reveal a central role for B cell-derived IL-4 and IL-4Ralpha in the optimal inductio

218 Additionally, Tfh cell-derived IL-4 was required to maintain the Th2 respo

219 on and transcription in bronchial epithelial cell-derived immortal cells was performed.

220 Donor T-cell-derived interleukin-17A (IL-17A) can mediate late i

221 Thus, we posit that stem cell-derived interneuron transplants may be an effective

222 These data suggest that the stem cell-derived interneuron transplants may represent a nov

223 l matrix with human induced pluripotent stem cell-derived intestinal epithelium and human endothelium

224 Using human embryonic stem cell-derived intestinal organoids, we demonstrate that t

225 uced in PWS patient induced pluripotent stem cell-derived (iPSC-derived) neurons.

226 as the contractile development of human stem cell-derived laminar cardiac tissues over four weeks.

227 kout mouse line, we report that PDGFRbeta(+) cell-derived laminin inhibits their proliferation and ad

228 -3 (omega-3) fatty acid epoxides as new mast cell-derived lipid mediators and show that they are prod

229 examined the structure and function of CD4 T cell-derived LMCs, and we established a role for ASMC-de

230 clinical and clinical studies for not only B-cell-derived lymphoblastic leukemia and lymphoma but als

231 sical Hodgkin lymphoma (cHL) is an unusual B-cell-derived malignancy in which rare malignant Hodgkin

232 lar matrix protein fibronectin by peritoneal cell-derived mast cell lysates diminished GBS adherence.

233 ur studies showed that BMCMCs and peritoneal cell-derived mast cells produced substantially different

234 cultured mast cells (BMCMCs) and peritoneal cell-derived mast cells were used as "surrogates" for mu

235 mc3(-/-) retina or when tested in vitro with cell-derived matrix.

236 Measurements on cell-derived membrane vesicles, in the plasma membrane o

237 es in vivo and permits generating single-EPS-cell-derived mice by tetraploid complementation.

238 regression model confirmed that endothelial cell-derived microparticles were associated with dissemi

239 These results support a scenario by which T cell-derived microvesicles act as intercellular carriers

240 Here we demonstrate that pCRP by binding to cell-derived microvesicles undergoes a structural change

241 eregulated in human-induced pluripotent stem cell-derived MNs carrying the FUS(P525L) mutation associ

242 ved fibroblasts and induced pluripotent stem cell-derived motor neurons.

243 oma cells and human induced pluripotent stem cell-derived motor neurons.

244 hymal stem cell-derived and pluripotent stem cell-derived multicellular organoids.

245 ngs reveal a novel mechanism by which cancer cell-derived MVs influence the tumour microenvironment a

246 have used human primary CD56(Pos) satellite cell-derived myogenic progenitors obtained from healthy

247 These cell-derived nanovesicles allowed us to separate single

248 ting in human induced pluripotent stem (iPS) cell-derived neural progenitor cells (NPCs) to repair th

249 or cells in vivo and on human embryonic stem cell-derived neural progenitors.

250 Induced pluripotent stem cell-derived neural stem cells (iNSCs) have significant

251 studies using induced pluripotent stem (iPS) cell-derived neuronal cells are needed to validate our p

252 following infection of human embryonic stem cell-derived neurons and that this activation of JNK is

253 Similarly, induced pluripotent stem cell-derived neurons from a patient carrying a null muta

254 ocampal neurons and induced pluripotent stem cell-derived neurons from a patient carrying a null muta

255 thophysiology using induced pluripotent stem cell-derived neurons from AS patients and unaffected con

256 r SLP-2, as well as induced pluripotent stem cell-derived neurons from Parkin mutation carriers, show

257 landscape of open chromatin regions in stem cell-derived neurons helps functional interpretation of

258 sing embryonic stem cells and embryonic stem cell-derived neurons indicated that Nf1 RasGAP activity

259 o apparent in human induced pluripotent stem cell-derived neurons, a disease-relevant cell type.

260 ive effect in human induced pluripotent stem cell-derived neurons, protecting up to 80% of neurons ag

261 sion profiling of human neuroepithelial stem cell-derived neurons, stimulated with normal consumption

262 ding in mouse primary neurons and human stem cell-derived neurons.

263 Here we identify glial cell-derived neurotrophic factor (GDNF) receptor alpha-l

264 Our study highlights the utility of iPS cell-derived NPCs to elucidate the role of astrocytes in

265 Stem cell-derived organoids and other 3D microtissues offer e

266 Here we present human iPS cell-derived organoids through sequential rounds of diff

267 nd astrocyte cytoplasm of TREX1 mutated stem cell-derived organoids.

268 RG) cells in both primary tissue and in stem cell-derived organoids.

269 e formation, carried out by mesenchymal stem cell-derived osteoblasts, and bone resorption, carried o

270 Here we identify epithelial-cell-derived phospholipase A2 group 1B (PLA2g1B) as a ho

271 These findings uncover epithelial-cell-derived Pla2g1b as an essential mediator of helmint

272 Stem cell-derived platelets have the potential to replace don

273 These results reveal that stem cell-derived PNS neurons are able to form functional con

274 bated cell death in induced pluripotent stem cell-derived primary human neurons under oxidative stres

275 Human resistin (hRetn) is an immune cell-derived protein that is highly elevated in helminth

276 HUVEC-filled RSs, and less cellularized host cell-derived pulp-like tissue was observed in the G2 ace

277 eby downregulates its expression in the beta-cell-derived rat INS-1 cell line and primary mouse and h

278 , respectively, result in tubular epithelial cell-derived renal cysts.

279 The advent of stem cell-derived retinal organoids has brought forth unprece

280 resource for molecular staging of human stem-cell-derived retinal organoids.

281 hat the same pathway is active in human stem cell-derived RGCs.

282 ifferentiated, while hair follicle (HF) stem cell-derived SCCs frequently exhibit EMT, efficiently fo

283 Treatment with specific bone marrow cell-derived secreted proteins may provide an alternativ

284 ions by which human induced pluripotent stem cell-derived sensory neurons can be cultured with rat Sc

285 her rodent or human induced pluripotent stem cell-derived sensory neurons in vitro potently inhibited

286 lin-1 (TIIINRG1) in induced pluripotent stem cell-derived sensory neurons strongly enhances myelinati

287 ultures using human induced pluripotent stem cell-derived sensory neurons thus provide insights into

288 In vitro CD34(+) cell derived SG-MSCs revealed multilineage differentiati

289 Furthermore, we show that MAIT cell-derived signals synergize with microbial stimuli to

290 oped novel methods to co-culture neural stem cell-derived spiral ganglion-like neurons (ScNs) and mou

291 of memory stem T cells and central memory T cell-derived T cells compared with IL-2.

292 ans, representing over 4,600 in-frame single-cell-derived TCRalphabeta sequence pairs from 110 subjec

293 The paracrine activity of regulatory T cell-derived TGF-beta1 contributes to immunosuppression

294 Thus, Kupffer cell-derived Tnf favors cholangiocellular proliferation/

295 ental cells in vitro, as well as in H157CisR cell-derived tumors than H157P cell-derived tumors.

296 s in H157CisR cell-derived tumors than H157P cell-derived tumors.

297 Well-characterized human pluripotent stem-cell-derived ventricular cardiomyocytes are strategicall

298 Extracellular vesicles (EVs) are cell-derived vesicles present in body fluids that play a

299 Analysis is demonstrated for cell membranes, cell-derived vesicles, model membranes, and microbubbles

300 ts were also observed on the growth of HepG2 cell-derived xenografts expressing SLC13A5-shRNA in nude