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1 rived from human neural progenitor cells and human induced pluripotent stem cells.
2 gene loci in HEK293T cells, HeLa cells, and human induced pluripotent stem cells.
3 ng human sensory neurons differentiated from human induced pluripotent stem cells.
4 ns associated with human disease in isogenic human induced pluripotent stem cells.
5 gnature that is similar but not identical to human induced pluripotent stem cells.
6 blished during intestinal differentiation of human induced pluripotent stem cells.
7 lopment, from mouse embryonic stem cells and human induced pluripotent stem cells.
8 rrent density in cardiomyocytes derived from human-induced pluripotent stem cells.
9 E cells in cerebral organoids generated from human-induced pluripotent stem cells.
10 (MI with 4x10(6) vascular cells derived from human induced pluripotent stem cells administered via a
11 alyse a total of 17 point mutations found in human induced pluripotent stem cells and demonstrate tha
13 th cardiomyocytes derived from nontransgenic human induced pluripotent stem cells and generated tissu
14 Using neuronal progenitor cells derived from human induced pluripotent stem cells and human tissues,
15 e formation of hepatic progenitor cells from human induced pluripotent stem cells and that this pheno
16 iciently with human embryonic stem cells and human induced pluripotent stem cells and was recently us
18 e studies have focused on fibroblast-derived human induced pluripotent stem cells, and it is currentl
21 rity was demonstrated in an ex vivo model of human induced pluripotent stem cell-based engineered hea
24 we found that AD model neurons derived from human induced pluripotent stem cells carrying a mutant P
27 cyte-like cells could also be generated from human induced pluripotent stem cells, demonstrating the
28 In turn, the recent derivation of mouse and human induced pluripotent stem cells depended on the pri
31 nd Participants: Neurons differentiated from human-induced pluripotent stem cells derived from 4 indi
32 n rs1421085 on expression of nearby genes in human induced pluripotent stem cell-derived (iPSC-derive
33 re to support the seeding and engraftment of human induced pluripotent stem cell-derived cardiomyocyt
34 Here we demonstrate that patient-specific human induced pluripotent stem cell-derived cardiomyocyt
35 ellularized human whole-heart scaffolds with human induced pluripotent stem cell-derived cardiomyocyt
36 the combination of human cardiac matrix and human induced pluripotent stem cell-derived cardiomyocyt
39 beating rate and decreased beat amplitude in human induced pluripotent stem cell-derived cardiomyocyt
40 we demonstrated that commercially available human induced pluripotent stem cell-derived cardiomyocyt
43 n ventricular systolic HF tissue samples and human induced pluripotent stem cell-derived cardiomyocyt
46 y downregulated in rodent cardiomyocytes and human induced pluripotent stem cell-derived cardiomyocyt
47 ndrome and also supports the use of isogenic human induced pluripotent stem cell-derived cardiomyocyt
48 e tested the role of TLR3-IFN immunity using human induced pluripotent stem cell-derived cardiomyocyt
50 Nonclinical studies of drug effects with human induced pluripotent stem cell-derived cardiomyocyt
54 Small molecule high throughput screening in human induced pluripotent stem cell-derived cells with t
55 c cells, adult rat ventricular myocytes, and human induced pluripotent stem cell-derived CMs, decreas
57 ecellularizing native intestinal matrix with human induced pluripotent stem cell-derived epithelium a
58 erefore examined the BM homing properties of human induced pluripotent stem cell-derived HSPCs (hiPS-
59 ng decellularized rat intestinal matrix with human induced pluripotent stem cell-derived intestinal e
60 ion in human SH-SY5Y neuroblastoma cells and human induced pluripotent stem cell-derived motor neuron
61 epopulating decellularized mouse hearts with human induced pluripotent stem cell-derived multipotenti
62 vitro neuronal stretch injury model employs human induced pluripotent stem cell-derived neurons (hiP
63 dopaminergic neurons in vivo and in cultured human induced pluripotent stem cell-derived neurons prot
64 ion and mitophagy, which is also apparent in human induced pluripotent stem cell-derived neurons, a d
65 ed that possess greater protective effect in human induced pluripotent stem cell-derived neurons, pro
66 fected mouse primary neurons and in isogenic human induced pluripotent stem cell-derived neurons.
67 ble to induce presynaptic differentiation in human induced pluripotent stem cell-derived neurons.
68 ed and fails to enhance synapse formation in human induced pluripotent stem cell-derived neurons.
69 human neural crest differentiation systems; human induced pluripotent stem cell-derived nociceptors
72 loride channel expressed in either rodent or human induced pluripotent stem cell-derived sensory neur
73 stigated doxorubicin-induced cytotoxicity in human induced pluripotent stem cells-derived cardiomyocy
74 NF signaling in both mouse mesencephalic and human induced pluripotent stem cells-derived DA neurons.
75 rategy that involved mouse mesencephalic and human induced pluripotent stem cells-derived DA neurons.
76 induced pluripotent stem cells to generate a human-induced pluripotent stem cell-derived cardiac musc
77 ing and electric pacing on the maturation of human-induced pluripotent stem cell-derived cardiac tiss
78 chanical, and force generation properties of human-induced pluripotent stem cell-derived cardiac tiss
80 sphate, with hours of dofetilide exposure in human-induced pluripotent stem cell-derived cardiomyocyt
82 caffold was seeded with approximately 50 000 human-induced pluripotent stem cell-derived cardiomyocyt
83 and butylhydroxytoluene, in endocrine-active human-induced pluripotent stem cell-derived foregut epit
84 L cells, an effect that was also observed in human-induced pluripotent stem cell-derived JNCL neural
85 humans and specific ones are deregulated in human-induced pluripotent stem cell-derived MNs carrying
86 roach can also be used with patient-specific human-induced pluripotent stem cell-derived neural model
87 erent in schizophrenia-associated vs control human-induced pluripotent stem cell-derived neurons and
88 hip approach was developed through combining human induced pluripotent stem cells, Electric Cell-subs
90 ncy in standards of access to and quality of human induced pluripotent stem cells has lagged behind t
91 ncluding both human embryonic stem cells and human-induced pluripotent stem cells, has opened up nove
93 s), including human embryonic stem cells and human induced pluripotent stem cells, have emerged as a
95 base resolution in individual gene-corrected human induced pluripotent stem cell (hiPSC) clones in th
96 ontaneous neural differentiation of hESC and human induced pluripotent stem cell (hiPSC) colonies.
97 cells lines have been produced from cord and human induced pluripotent stem cell (hiPSC) haematopoiet
98 ber variation (CNV) in neurons obtained from human induced pluripotent stem cell (hiPSC) lines and po
100 conventional hESC and transgene-independent human induced pluripotent stem cell (hiPSC) lines could
102 uman Embryonic Stem Cell (hESC) and multiple human induced Pluripotent Stem Cell (hiPSC) lines over t
103 sites in a discovery cohort of 25 phenotyped human induced pluripotent stem cell (hiPSC) lines reveal
106 med to establish a patient-/disease-specific human induced pluripotent stem cell (hiPSC) model of ARV
107 We aimed to establish a patient-specific human induced pluripotent stem cell (hiPSC) model of CPV
108 t cells and genetic engineering, to generate human induced pluripotent stem cell (hiPSC) models of JL
111 CR screen complemented by a novel orthogonal human induced pluripotent stem cell (hiPSC)-based RPE re
113 fic ErbB2/4 mouse model of SZ, as well as in human induced pluripotent stem cell (hiPSC)-derived fore
116 expression of sialyl-lactotetra on hESC and human induced pluripotent stem cells (hiPSC) was demonst
118 l differentiation method, based on confluent human induced pluripotent stem cells (hiPSC), bypassing
120 a population of cardiomyocytes derived from human induced pluripotent stem cells (hiPSC-CMs), 41 wer
121 age in hESC-CMs and in myocytes derived from human induced pluripotent stems cells (hiPSC-CMs) falls
122 o survival, engraftment, and distribution of human-induced pluripotent stem cell (hiPSC) derivatives
123 f these compounds, gentamicin and PTC124, in human-induced pluripotent stem cell (hiPSC)-derived card
124 Srxn1 protects dopaminergic neural cells and human-induced pluripotent stem cell (hiPSC)-derived neur
125 l patch-clamp recordings in RPE derived from human-induced pluripotent stem cells (hiPSC) exhibit an
126 , both human embryonic stem cells (hESC) and human-induced pluripotent stem cells (hiPSC), can give r
127 that human embryonic stem cells (hESCs) and human induced pluripotent stem cells (hiPSCs) also exhib
128 R636S missense mutation were reprogrammed to human induced pluripotent stem cells (hiPSCs) and differ
130 To address this, we generated panels of human induced pluripotent stem cells (hiPSCs) and hiPSC-
131 our ability to generate cardiomyocytes from human induced pluripotent stem cells (hiPSCs) and human
134 we show using a stage-matching approach that human induced pluripotent stem cells (hiPSCs) and human
135 ogrammed fibroblasts from SCZD patients into human induced pluripotent stem cells (hiPSCs) and subseq
138 d preservation of hepatic cells derived from human induced pluripotent stem cells (hiPSCs) are essent
143 crape loading/dye transfer assay showed that human induced pluripotent stem cells (hiPSCs) contained
145 ositive cells can be generated in vitro from human induced pluripotent stem cells (hiPSCs) derived fr
146 gineered cardiac tissue (LF-ECT) composed of human induced pluripotent stem cells (hiPSCs) derived mu
148 R-302a activity that can specifically detect human induced pluripotent stem cells (hiPSCs) down to a
150 eat expansions using engineered nucleases in human induced pluripotent stem cells (hiPSCs) from a hea
151 eport, for the first time, the derivation of human induced pluripotent stem cells (hiPSCs) from patie
152 eneration of vascular progenitors (VPs) from human induced pluripotent stem cells (hiPSCs) has great
156 ion of human embryonic stem cells (hESCs) or human induced pluripotent stem cells (hiPSCs) into neuro
157 veloped a strategy by which to differentiate human induced pluripotent stem cells (hiPSCs) into OPCs.
161 he immaturity of neurons differentiated from human induced pluripotent stem cells (hiPSCs) presents d
162 bility to reprogram adult somatic cells into human induced pluripotent stem cells (hiPSCs) provides a
163 ent protocols for hepatic differentiation of human induced pluripotent stem cells (hiPSCs) result in
165 intestinal "organoids" (iHOs) generated from human induced pluripotent stem cells (hIPSCs) to explore
166 dies (EBs) of defined sizes from dissociated human induced pluripotent stem cells (hiPSCs) was develo
167 ient; an abundant autologous source, such as human induced pluripotent stem cells (hiPSCs), is theref
175 ng that neurons differentiated in vitro from human-induced pluripotent stem cells (hiPSCs) are immatu
177 of our study was to evaluate the utility of human-induced pluripotent stem cells (hiPSCs) for bone t
180 is study was to establish a patient-specific human-induced pluripotent stem cells (hiPSCs) model of c
181 using human embryonic stem cells (hESCs) or human-induced pluripotent stem cells (hiPSCs), may provi
182 as well as the application of differentiated human induced pluripotent stem cells in hepatology, incl
185 ree protocol for directed differentiation of human induced pluripotent stem cells into cholangiocyte-
186 in vivo, and is sufficient to differentiate human induced pluripotent stem cells into electrophysiol
187 rentiation of human embryonic stem cells and human induced pluripotent stem cells into forebrain neur
191 unlabelled colony image libraries of various human induced pluripotent stem cell (iPSC) lines for sup
192 uencing and gene expression profiling of 215 human induced pluripotent stem cell (iPSC) lines from di
195 realization of personalized medicine through human induced pluripotent stem cell (iPSC) technology ca
199 We investigated the therapeutic potential of human induced pluripotent stem cell (iPSC)-derived cells
201 t, we demonstrated successful engraftment of human induced pluripotent stem cell (iPSC)-derived hepat
203 with multifocal motor neuropathy (MMN) using human induced pluripotent stem cell (iPSC)-derived motor
204 for detecting analytes secreted from single human induced pluripotent stem cell (iPSC)-derived neura
207 on ZIKV entry or ZIKV-mediated cell death in human induced pluripotent stem cell (iPSC)-derived NPCs
208 t and accelerates maturation of neurons from human induced pluripotent stem cell (iPSC)-derived NPCs,
209 ocols to generate oligodendrocytes (OL) from human induced pluripotent stem cells (iPSC) are currentl
214 investigated the innate immune properties of human induced-pluripotent stem cell (iPSC)-derived RPE c
216 ing amyotrophic lateral sclerosis (ALS) with human induced pluripotent stem cells (iPSCs) aims to ree
217 nt and tolerance towards murine ESCs, hESCs, human induced pluripotent stem cells (iPSCs) and hESC-de
218 rentiating dopaminergic neurons derived from human induced pluripotent stem cells (iPSCs) and in deve
219 The emergence of novel technologies such as human induced pluripotent stem cells (iPSCs) and nucleas
220 O induced skeletal muscle differentiation in human induced pluripotent stem cells (iPSCs) and produce
221 w how two such experiments-the generation of human induced pluripotent stem cells (iPSCs) and the dev
229 issues, we derived MSCs from transgene-free human induced pluripotent stem cells (iPSCs) efficiently
233 ing neurodevelopment, the present study used human induced pluripotent stem cells (iPSCs) from RTT an
234 Here we use in vitro differentiation of human induced pluripotent stem cells (iPSCs) generated f
239 iciency of reprogramming methods to generate human induced pluripotent stem cells (iPSCs) impose majo
245 paper, we show that astrocytes derived from human induced pluripotent stem cells (iPSCs) support the
247 a novel strategy of teratoma formation from human induced pluripotent stem cells (iPSCs) to isolate
248 In this study, we compared the potential of human induced pluripotent stem cells (iPSCs), derived fr
249 we first established a liver organoid using human induced pluripotent stem cells (iPSCs), mesenchyma
250 g the mechanisms of somatic reprogramming to human induced pluripotent stem cells (iPSCs), we have es
265 e an approach using macrophages derived from human induced pluripotent stem cells (iPSdMs) to study m
266 cells (NPCs), lymphoblastoid cells, and two human induced pluripotent stem cell lines (hiPSCs), and
267 characterize the genomic integrity of eight human induced pluripotent stem cell lines derived from f
268 studies analyzing large-scale collections of human induced pluripotent stem cell lines provide valuab
272 ansplantation of vascular cells derived from human induced pluripotent stem cells mobilized endogenou
274 Here we demonstrate the generation from human induced pluripotent stem cells of a self-formed ec
275 derived from human neural progenitor cells, human induced pluripotent stem cells, or in primary rat
277 sleading and that human neurons derived from human induced pluripotent stem cells provide a unique si
281 oding mutations are a general feature of the human induced pluripotent stem cell state and are indepe
282 ansplantation of vascular cells derived from human induced pluripotent stem cells stimulated c-kit(+)
283 s have been derived from cord blood and from human induced pluripotent stem cells, suggesting that la
285 rdiomyocytes that are derived from mouse and human induced pluripotent stem cells through a mechanism
286 on of human embryonic stem cells (hESCs) and human-induced pluripotent stem cells to defined and func
287 lial cells that had been differentiated from human-induced pluripotent stem cells to generate a human
288 mbryonic skin, and also in the commitment of human induced pluripotent stem cells toward an epithelia
289 On a pulsed-SILAC experiment performed on human induced pluripotent stem cells, TRIC was able to a
291 reprogramming of patient skin fibroblasts to human induced pluripotent stem cells, which can be diffe
293 tem cells with an extra human chromosome and human induced pluripotent stem cells with trisomy 21, as
294 nock out the Tafazzin gene by CRISPR/Cas9 in human-induced pluripotent stem cells with 54% efficiency
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