ライフサイエンスコーパス: stem cell-derived

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

2 r cells, and primary and induced pluripotent stem cell-derived(6) hematopoietic stem progenitor cells

3 Stem cell-derived adipocytes exposed to caffeine (1 mM)

4 Here, using human adipose stem cell-derived adipocytes, we demonstrate that SNPs w

5 g AP morphology of human induced pluripotent stem cell derived and primary rodent cardiomyocytes.

6 nd single-cell RNA-seq using human embryonic stem cell-derived and embryonic/fetal heart-derived card

7 phB1-ephrin-B1 pathway is disrupted in human stem cell derived astrocyte and mouse models of amyotrop

8 ly showed that maturation of human and mouse stem cell-derived astrocytes - including functional glut

9 t means for expansion of functionally mature stem cell-derived astrocytes for preclinical investigati

10 differentiation factors, on mouse embryonic stem cell-derived astrocytes.

11 ns induced AHN deficits but increased neural stem cell-derived astrogliosis, associating with a downr

12 osphoproteomic survey of induced pluripotent stem cell-derived AT2s (iAT2s) infected with SARS-CoV-2

13 with SARS-CoV-2 by using induced pluripotent stem cell-derived AT2s that have been adapted to air-liq

14 mbrane fraction from MYL4-/- human embryonic stem cell derived atrial cells demonstrated increased ph

15 eplacement therapies (such as human islet or stem cell-derived beta cell transplantation) without imm

16 by inactivating key immunogenic epitopes of stem cell-derived beta cells intended for transplantatio

17 recovered from transplanted human embryonic stem cell-derived beta cells.

18 eta cell lines and human induced pluripotent stem cell-derived beta-like cells.

19 on protocol for generating human pluripotent stem-cell-derived beta (SC-beta) cells with improved in

20 ne cell clustering permits the generation of stem-cell-derived beta cells that resemble their endogen

21 migration, and in human induced pluripotent stem cell-derived bipolar mature neurons rotatin localiz

22 engagement across human induced pluripotent stem cell-derived brain endothelial-like cells.

23 Over the past decade, human stem cell-derived brain organoids have emerged as a biol

24 Here, we use human-pluripotent-stem-cell-derived brain organoids to examine SARS-CoV-2

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

26 ation conducted in human induced pluripotent stem cell-derived cardiac myocytes (hiPSC-CM) demonstrat

27 Expression) and in human-induced pluripotent stem cell-derived cardiac myocytes deficient in SCN5A.

28 unveil strategies for driving maturation of stem cell-derived cardiac myocytes.

29 or functional screening in human pluripotent stem cell-derived cardiac organoids (hCOs).

30 rthermore, canonical Wnt activation in human stem cell-derived cardiac progenitors produces functiona

31 tient-derived and isogenic human-pluripotent-stem-cell-derived cardio-myocytes that were genome-edite

32 extracellular potential of human pluripotent stem cell derived cardiomyocyte cells (hPSCs-CMs) for se

33 a patient-derived human induced pluripotent stem cell-derived cardiomyocyte (hiPSC-CM) CACNA1C-p.R51

34 recent advances in human induced pluripotent stem cell-derived cardiomyocyte (hiPSC-CM) technology an

35 and lead to better maturation of pluripotent stem cell-derived cardiomyocyte and novel therapeutic st

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

37 phenotype in human CPVT induced pluripotent stem cell-derived cardiomyocyte models with different pa

38 due to the maturation defects in pluripotent stem cell-derived cardiomyocyte, its antagonistic effect

39 ature phenotype of human induced pluripotent stem cell derived cardiomyocytes (hiPSC-CMs) is a major

40 Human induced pluripotent stem cell derived cardiomyocytes (hiPSC-CMs) offer a nov

41 7C(+/-) mutants in human induced pluripotent stem cell derived cardiomyocytes (hiPSC-CMs) using CRISP

42 Human pluripotent stem cell derived cardiomyocytes are a promising cell so

43 itro experiments showed that human embryonic stem cell-derived cardiomyocytes (hESC-CMs) contain noda

44 We identify human induced pluripotent stem cell-derived cardiomyocytes (hiCMs) as a model syst

45 trol subjects, and human induced pluripotent stem cell-derived cardiomyocytes (hiPS-CMs), and to char

46 RATIONALE: Human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CM) are increasi

47 Application of human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) as tissue t

48 Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) have been d

49 ling modulators to human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) in vitro ca

50 Human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) provide an

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

52 mation analyses in human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) with a hapl

53 K293) cells and in human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs), and we des

54 beat amplitude in human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs), but D-ala,

55 cardiomyocytes and human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs), but potent

56 In human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs), Tbx20 enha

57 uman cardiomyocytes, using human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) as the targe

58 ng cardioprotective drugs, human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) have been pr

59 Induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) allow for di

60 Induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) capture pati

61 previously reported that induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) from patient

62 re presentation of human induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) is currently

63 The development of induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) signifies an

64 cardiac disease utilizes induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs).

65 o using patient-specific induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs).

66 utilizing human isogenic induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs).

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

68 primary limitation in the use of pluripotent stem cell-derived cardiomyocytes (PSC-CMs) for both pati

69 Pluripotent stem cell-derived cardiomyocytes (PSC-CMs) hold great pr

70 nimal models of MI injected with pluripotent stem cell-derived cardiomyocytes (PSC-CMs).

71 crosstalk between human induced pluripotent stem cell-derived cardiomyocytes and CFs via the atrial/

72 roposed therapy on human induced pluripotent stem cell-derived cardiomyocytes and different pathogeni

73 e EHM from embryonic and induced pluripotent stem cell-derived cardiomyocytes and fibroblasts with or

74 ies in vitro using human induced pluripotent stem cell-derived cardiomyocytes and various in vivo mod

75 Stem cell-derived cardiomyocytes and vascular cells can

76 ercially available human induced pluripotent stem cell-derived cardiomyocytes are a powerful model fo

77 tal mouse cardiomyocytes and human embryonic stem cell-derived cardiomyocytes are considerably enhanc

78 he use of isogenic human induced pluripotent stem cell-derived cardiomyocytes as a physiologically re

79 The emergence of human induced pluripotent stem cell-derived cardiomyocytes as an in vitro research

80 ing evidence suggests that human pluripotent stem cell-derived cardiomyocytes can affect "heart regen

81 Additionally, in human embryonic stem cell-derived cardiomyocytes challenged with TNFalph

82 Genome-editing in human embryonic stem cell-derived cardiomyocytes confirms the influence

83 ctional studies on human induced pluripotent stem cell-derived cardiomyocytes demonstrated that the a

84 Induced pluripotent stem cell-derived cardiomyocytes derived from 2 differen

85 The patient-derived induced pluripotent stem cell-derived cardiomyocytes display (1) significant

86 generate and highly purify human pluripotent stem cell-derived cardiomyocytes displaying physiologica

87 To reveal the disease etiology, we generated stem cell-derived cardiomyocytes from HADHA-deficient hi

88 esis in patient-specific induced pluripotent stem cell-derived cardiomyocytes from NS patients carryi

89 was upregulated in human-induced pluripotent stem cell-derived cardiomyocytes from patients with doxo

90 and epigenomic data from induced pluripotent stem cell-derived cardiomyocytes from seven related indi

91 r, to date, electrophysiological analyses of stem cell-derived cardiomyocytes has largely been limite

92 Using human induced pluripotent stem cell-derived cardiomyocytes in cardiac microtissue

93 ological maturation of the human pluripotent stem cell-derived cardiomyocytes in our system recapitul

94 cardiomyocytes and human induced pluripotent stem cell-derived cardiomyocytes in vitro and in vivo in

95 zebrafish hearts in vivo as well as in human stem cell-derived cardiomyocytes in vitro.

96 Stem cell-derived cardiomyocytes mutated to carry the ef

97 We generated induced pluripotent stem cell-derived cardiomyocytes of the affected sibling

98 Human-induced pluripotent stem cell-derived cardiomyocytes overexpressing mutant o

99 Stem cell-derived cardiomyocytes provide a promising too

100 murine hearts and human induced pluripotent stem cell-derived cardiomyocytes provided histologic and

101 Patients' induced pluripotent stem cell-derived cardiomyocytes recapitulated the hyper

102 cing structural and functional maturation of stem cell-derived cardiomyocytes remains a key challenge

103 mitations of using human induced pluripotent stem cell-derived cardiomyocytes to represent clinical f

104 sodium channels in human induced pluripotent stem cell-derived cardiomyocytes using a high throughput

105 d a functional rescue in induced pluripotent stem cell-derived cardiomyocytes with D130G-CALM2, as sh

106 isolated cardiomyocytes and human embryonic stem cell-derived cardiomyocytes, and functional consequ

107 In human induced pluripotent stem cell-derived cardiomyocytes, GS-967 and eleclazine

108 pe 2 (LQTS2) using human induced pluripotent stem cell-derived cardiomyocytes, KCNQ1 antibodies rever

109 proximately 50 000 human-induced pluripotent stem cell-derived cardiomyocytes, smooth muscle cells, a

110 ith epigenomic data from induced pluripotent stem cell-derived cardiomyocytes, we prioritized candida

111 cardiomyocytes and human induced pluripotent stem cell-derived cardiomyocytes.

112 ction potential in human-induced pluripotent stem cell-derived cardiomyocytes.

113 ockout and control human induced pluripotent stem cell-derived cardiomyocytes.

114 ssue from knockout human induced pluripotent stem cell-derived cardiomyocytes.

115 highly abundant GSLs on the cell surface of stem cell-derived cardiomyocytes.

116 dynamics in both mammalian neurons and human stem cell-derived cardiomyocytes.

117 IFN immunity using human induced pluripotent stem cell-derived cardiomyocytes.

118 aP)) recorded from human induced pluripotent stem cell-derived cardiomyocytes.

119 such as isolated adult and human pluripotent stem cell-derived cardiomyocytes; (2) 2-dimensional in v

120 ayers or small clusters of human pluripotent stem cell-derived cardiomyocytes; (3) 3-dimensional mult

121 Human-induced pluripotent stem cells derived cardiomyocytes (hiPSC-CMs) are a virt

122 nd also overexpressed in induced pluripotent stem cells derived cardiomyocytes (iPSCs-CM).

123 TNNT2:p.R286H iPSC-CMs (induced pluripotent stem cells derived cardiomyocytes) show hypercontractili

124 Using human induced-pluripotent-stem-cell-derived cardiomyocytes (hiPSC-CMs) and MAP4K4

125 Here, we use primate pluripotent stem-cell-derived cardiomyocytes that mimic fetal cardio

126 CF-7, MDA-231, and human-induced pluripotent stem-cell-derived cardiomyocytes; hiPSC-CMs) at ~kHz wit

127 mentary studies in human induced pluripotent stem cell derived-cardiomyocytes reveal Cx43 gap junctio

128 in many tissues, as well as both primary and stem cell-derived cell lines.

129 en seen as one of the first applications for stem cell-derived cells because of the loss of only a si

130 Integration of stem cell-derived cells into native cellular environment

131 g and future therapies using bone-marrow- or stem-cell-derived cells for the treatment of neurologica

132 IUS reveals unrecognized complexity in human stem cell-derived cellular populations.

133 novations that permit generating pluripotent stem cell-derived cerebral organoids from chimpanzee.

134 fferentiation and followed the maturation of stem cell-derived clones using sparse lineage tracing in

135 hen knocked out in human induced pluripotent stem cell derived CMs, these cells exhibit reduced contr

136 comere function in human induced pluripotent stem cell derived CMs.

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

138 ular myocytes, and human induced pluripotent stem cell-derived CMs, decreasing expression of hypertro

139 transcriptome atlas to benchmark pluripotent stem cell-derived cone photoreceptors and an adult Mulle

140 cell lines, primary astrocytes and embryonic stem cell-derived cortical interneurons.

141 fically, using human neurons (male embryonic stem cell-derived) cultured in the absence of glia to ex

142 mesencephalic and human induced pluripotent stem cells-derived DA neurons.

143 een mouse embryonic stem cells and embryonic stem cell-derived definitive endoderm cells, screening 7

144 for the first time that induced pluripotent stem cell-derived dendritic cells (iPS-DCs) with biallel

145 Induced pluripotent stem cell-derived dopaminergic cultures reveal a signatu

146 regation and toxicity in induced pluripotent stem cell-derived dopaminergic cultures treated with PD

147 al program in dopamine neurons both in human stem cell-derived dopaminergic neurons and in mice.

148 l of DNA methylation, in induced pluripotent stem cell-derived dopaminergic neurons from patients wit

149 Transplantation of human pluripotent stem cell-derived dopaminergic neurons is a promising ap

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

151 ived skin fibroblasts or induced pluripotent stem cell-derived dopaminergic neurons.

152 ensitive detection of dopamine released from stem cell-derived dopaminergic-neurons.

153 vascular constructs, wherein human embryonic stem cell-derived endothelial cells (hESC-ECs) are seede

154 Human-induced pluripotent stem cell-derived endothelial cells (iPSC-ECs) and a hig

155 e, we used comparison of induced pluripotent stem cell-derived endothelial cells (iPSC-ECs) from thre

156 a of stem cell research, induced pluripotent stem cell-derived endothelial cells (iPSC-ECs) have emer

157 our study indicates that induced pluripotent stem cell-derived endothelial cells are useful surrogate

158 CRISPR-edited stem cell-derived endothelial cells demonstrate rs934937

159 e pulmonary arterial and induced pluripotent stem cell-derived endothelial cells from patients with i

160 scular meshes from human induced pluripotent stem cell-derived endothelial cells, opening a way to en

161 Human intestinal stem cell-derived enteroid monolayers co-cultured with h

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

163 fibroblasts, demonstrating a direct role of stem cell-derived exosomes on mouse endothelium at the c

164 e tested the hypothesis that human perinatal stem cell derived extracellular matrix (ECM) promotes hi

165 Mesenchymal stem cell-derived extracellular vesicles (MSC-EVs) have

166 Bone marrow mesenchymal stem cell-derived extracellular vesicles (MSC-EVs), whic

167 onstrate that endogenous expression of E4 by stem-cell-derived forebrain excitatory neurons predispos

168 n endocrine-active human-induced pluripotent stem cell-derived foregut epithelial cells and hypothala

169 interneurons (cINs) from induced pluripotent stem cells derived from 14 healthy controls and 14 subje

170 In this study, both induced pluripotent stem cells derived from a MFS-patient and the line with

171 ells differentiated from induced pluripotent stem cells derived from an affected individual showed re

172 Therefore, here we tested the ability of the stem cells derived from bone marrow (BMSC), dental pulp

173 oresistance to sorafenib or cisplatin in HCC stem cells derived from four HCC cell lines.

174 cent in situ hybridization (smFISH) on mouse stem cells derived from haematopoietic tissue to measure

175 arly and functionally similar to trophoblast stem cells derived from human blastocysts or first-trime

176 ll characterized and compared in mesenchymal stem cells derived from human dental pulp (DP-MSCs) and

177 of human bone marrow stem cells (BMSC) with stem cells derived from human dental pulp (DPSC), apical

178 AIP was also tested on induced pluripotent stem cells derived from patients with CPVT with differen

179 KBM7 and HAP1), as well as haploid embryonic stem cells derived from several organisms.

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

181 r results demonstrate that human pluripotent stem cell-derived glomeruli can develop an appropriate b

182 tation medicine, even when using pluripotent stem cell-derived grafts.

183 we characterize human and mouse pluripotent stem cell-derived gray and white matter astrocyte subtyp

184 Human stem cell-derived hepatocyte-like cells (HLCs) offer an

185 rimary human hepatocytes (PHHs), pluripotent stem cell-derived hepatocyte-like cells (HLCs), and hepa

186 larly discuss the importance of benchmarking stem cell-derived hepatocyte-like cells to their termina

187 ampus of AD patients, in induced pluripotent stem cell-derived human AD neurons, and in animal AD mod

188 -chip BBB model lined by induced pluripotent stem cell-derived human brain microvascular endothelium

189 ul ante hoc deliberations on the prospect of stem cell-derived human gametes with an eye toward minim

190 Stem cell-derived human gametes, a disruptive technology

191 ved either endobronchial induced pluripotent stem cell-derived human MSCs (hMSCs) (n = 7) or cell-fre

192 Here we report on the generation of stem cell-derived human pancreatic alpha (SC-alpha) cell

193 In-vivo studies using stem-cell derived human astrocytes are allowing explorat

194 ate that the epithelium of human pluripotent stem-cell-derived human intestinal organoids is globally

195 Moreover, ZIKV productively infects stem-cell-derived human neural crest cells and periphera

196 Stem cell-derived insulin-producing beta cells (SC-beta)

197 Thus, we posit that stem cell-derived interneuron transplants may be an effe

198 These data suggest that the stem cell-derived interneuron transplants may represent

199 In mouse xenograft studies, human stem cell-derived-interneuron precursors could different

200 Transplantation of human stem cell-derived interneurons is a promising cell-based

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

202 Loss of YIPF5 function in stem cell-derived islet cells resulted in proinsulin ret

203 Replacing beta cells using stem cell-derived islets while fostering immune toleranc

204 d subsequent maturation of human pluripotent stem cell-derived kidney organoids after renal subcapsul

205 Human pluripotent stem cell-derived kidney organoids recapitulate developm

206 nction in the transplanted human pluripotent stem cell-derived kidney tissue 1, 2, and 3 weeks after

207 eliability of the model and the capacity for stem cell-derived kidney tissue to recapitulate both nor

208 well as the contractile development of human stem cell-derived laminar cardiac tissues over four week

209 primary mouse and human induced pluripotent stem cell-derived lung epithelial cells to model early-s

210 Using induced pluripotent stem cell-derived megakaryocyte clones that produce func

211 tically engineered human induced pluripotent stem cell-derived microglia-like cells to show that TREM

212 Taken together, our study illustrates how stem cell derived models can be used to uncover and resc

213 Advances in stem cell-derived models of human organogenesis, in the

214 Indeed, previous human pluripotent stem-cell-derived models of kidney tissue either contain

215 Yet, timely transfusion of haematopoietic-stem-cell-derived monocytic cells in newborn mice is suf

216 Co-cultures of induced pluripotent stem cell-derived motor neurons and myotubes from patien

217 cle progenitors mixed with human pluripotent stem cell-derived motor neurons self-organize to form fu

218 sected motor neurons, or induced pluripotent stem cell-derived motor neurons specifically from amyotr

219 complex at DSB sites in induced pluripotent stem cell-derived motor neurons.

220 -derived fibroblasts and induced pluripotent stem cell-derived motor neurons.

221 blastoma cells and human induced pluripotent stem cell-derived motor neurons.

222 ved from Megf10-/- mice, induced pluripotent stem cell-derived myoblasts from MEGF10 myopathy patient

223 old, skeletal muscle tissue, and optogenetic stem cell-derived neural cluster containing motor neuron

224 NIR-based biosensing of neurotransmitters in stem cell-derived neural interfaces present a unique too

225 Human induced pluripotent stem cell-derived neural progenitor cells (hNPCs) are a

226 citation of transplanted induced pluripotent stem cell-derived neural progenitor cells (iPS-NPCs) cou

227 Using induced pluripotent stem cell-derived neural progenitor cells (iPS-NPCs) exp

228 ophrenia, and studies of induced pluripotent stem cell-derived neural progenitor cells.

229 duced CDKL5-mutant human induced pluripotent stem cell-derived neural progenitors, which were subsequ

230 Induced pluripotent stem cell-derived neural stem cells (iNSCs) have signifi

231 rigger glial competency of human pluripotent stem cell-derived neural stem cells within 5 days and to

232 Joseph disease patients' induced pluripotent stem cells-derived neural stem cells incubated with ibup

233 is dysregulated in human induced pluripotent stem cell-derived neuron models of ASD.

234 ata, and our own mouse hippocampal and human stem cell-derived neuron PAC-seq data-strongly supports

235 frontal cortex (PFC) and induced pluripotent stem cell-derived neuronal cultures from patients with s

236 at tau overexpression in induced pluripotent stem cell-derived neurons altered chromatin structure an

237 ted the utility of human induced pluripotent stem cell-derived neurons and astrocytes as tools to sys

238 ed manipulation in human induced pluripotent stem cell-derived neurons and RNAi-based knockdown in Dr

239 vated following infection of human embryonic stem cell-derived neurons and that this activation of JN

240 enomic analyses on human induced pluripotent stem cell-derived neurons at 22, 50 and 78 days (D) post

241 ry after stroke in animal models but whether stem cell-derived neurons become functionally integrated

242 MN2 accumulated in human induced pluripotent stem cell-derived neurons depleted of TDP-43, but not in

243 ocalization was altered in primary and human stem cell-derived neurons expressing ALS-linked FUS vari

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

245 hippocampal neurons and induced pluripotent stem cell-derived neurons from a patient carrying a null

246 into excitatory neurons, induced pluripotent stem cell-derived neurons from all three patients displa

247 ng pathophysiology using induced pluripotent stem cell-derived neurons from AS patients and unaffecte

248 kin or SLP-2, as well as induced pluripotent stem cell-derived neurons from Parkin mutation carriers,

249 g the landscape of open chromatin regions in stem cell-derived neurons helps functional interpretatio

250 udy using embryonic stem cells and embryonic stem cell-derived neurons indicated that Nf1 RasGAP acti

251 we show that the use of induced pluripotent stem cell-derived neurons of monozygotic twins from pair

252 Overexpression of NLGN4 in human embryonic stem cell-derived neurons resulted in an increase in exc

253 s also apparent in human induced pluripotent stem cell-derived neurons, a disease-relevant cell type.

254 xpression profiling of human neuroepithelial stem cell-derived neurons, stimulated with normal consum

255 On human induced pluripotent stem cell-derived neurons, the nanobody prevents C3 depo

256 acting proteins in human induced pluripotent stem cell-derived neurons.

257 neuroglioma cells and in induced pluripotent stem cell-derived neurons.

258 disease phenotypes in SCA7 mice and patient stem cell-derived neurons.

259 oting viability of human induced pluripotent stem cell-derived neurons.

260 utilizing isogenic human-induced pluripotent stem cells-derived neurons from PD patients with autosom

261 ei isolated from C9orf72 induced pluripotent stem-cell-derived neurons (iPSNs).

262 we show that endogenous expression of E4 in stem-cell-derived neurons predisposes them to injury and

263 newable source for human induced pluripotent stem cell-derived NK (hnCD16-iNK) cells.

264 (-/-)) NK cells using an induced pluripotent stem cell-derived NK cell (iPSC-NK cell) platform.

265 cal NK cells, umbilical cord blood NK cells, stem cell-derived NK cells, NK cell lines, adaptive NK c

266 hange in excitability in induced pluripotent stem cell derived nociceptors with the C110R mutation an

267 of chronic HIF1a accumulation in pluripotent-stem-cell-derived oligodendrocyte progenitors (OPCs), we

268 ctives, like the combination of editing with stem cell derived organoid development.

269 Stem cell-derived organoid models have emerged as a valu

270 lucloxacillin and in primary hepatocytes and stem cell-derived organoids from multiple donors treated

271 ron and astrocyte cytoplasm of TREX1 mutated stem cell-derived organoids.

272 ial (RG) cells in both primary tissue and in stem cell-derived organoids.

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

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

275 zed a protocol to generate human pluripotent stem cell-derived Purkinje cells (hPSC-PCs) that formed

276 RNA-seq of human pluripotent stem cell-derived regional astrocytes revealed distinct

277 a protein kinase inhibitor library in human stem cell-derived retinal ganglion cells (hRGCs).

278 The advent of stem cell-derived retinal organoids has brought forth un

279 This correlation is also retained in stem cell-derived retinal organoids, but is accelerated

280 ted using clinical-grade induced pluripotent stem cell-derived retinal pigment epithelial cells (iPSC

281 Here, we utilized induced pluripotent stem cell-derived retinal pigment epithelium (iPSC-RPE)

282 s' fibroblasts and their induced pluripotent stem cell-derived retinal pigment epithelium.

283 as a resource for molecular staging of human stem-cell-derived retinal organoids.

284 th, addressing a major issue in the field of stem cell-derived retinas.

285 how that the same pathway is active in human stem cell-derived RGCs.

286 egenerative medicine approaches that utilise stem cell-derived RPE cells to treat conditions such as

287 Here, human stem cell-derived RPE samples were stressed with ROS for

288 omatin using sequencing on human pluripotent stem cell-derived SAN-like pacemaker cells and ventricle

289 ell differentiated, while hair follicle (HF) stem cell-derived SCCs frequently exhibit EMT, efficient

290 Recent studies have demonstrated an array of stem cell-derived, self-organizing miniature organs, ter

291 onditions by which human induced pluripotent stem cell-derived sensory neurons can be cultured with r

292 We found that human induced pluripotent stem cell-derived sensory neurons expressed the receptor

293 n either rodent or human induced pluripotent stem cell-derived sensory neurons in vitro potently inhi

294 eled in subject-specific induced pluripotent stem cell-derived sensory neurons in vitro; second, that

295 co-cultures using human induced pluripotent stem cell-derived sensory neurons thus provide insights

296 Dmd C3333Y animals, induced-pluripotent-stem-cell-derived skeletal muscle cells from patients wi

297 n platelet alloantigens by using gene-edited stem cell-derived target cells.

298 Stem-cell-derived tissues could transform disease resear

299 te if transplantation of induced pluripotent stem cell derived TM like cells (iPSC-TM) restores TM ce

300 Well-characterized human pluripotent stem-cell-derived ventricular cardiomyocytes are strateg