ライフサイエンスコーパス: stem cell

1 ases susceptibility in NSCs and glioblastoma stem cells.

2 rity of RNA:DNA hybrids in human pluripotent stem cells.

3 lds was assessed using human adipose-derived stem cells.

4 diac and neural development from pluripotent stem cells.

5 ergy was also observed against breast cancer stem cells.

6 ylase ALKBH5 in maintaining myeloid leukemia stem cells.

7 d phenotypical response of human mesenchymal stem cells.

8 cells with new ones generated by adult taste stem cells.

9 ally covarying gene pairs in mouse embryonic stem cells.

10 ac myocytes derived from induced pluripotent stem cells.

11 nce and genomic stability of mouse embryonic stem cells.

12 e role for PADI4 in regulating breast cancer stem cells.

13 icronf a population of Sca-1(+) reserve-like stem cells.

14 aling pathways that are known to regulate HF stem cells.

15 es the vasculogenic potential of dental pulp stem cells.

16 Kozar et al., Cell Stem Cell 13, 626-633 (2013)], how they are impacted by

17 hat macrophages are required for dental pulp stem cell activation and appropriate reparative dentine

18 n and normalizing IOP, human adipose-derived stem cells (ADSCs) were induced to differentiate to TM c

19 w that ET-1 is required for increased neural stem cell and OPC proliferation in the adult mouse SVZ f

20 ormed a single-center retrospective study of stem cell and organ transplant recipients who received l

21 motes the normal hair cycle by activating HF stem cells and by influencing the activities of multiple

22 s important for differentiation of embryonic stem cells and development of various tissues.

23 essed on the cell surface of human embryonic stem cells and many cancer types.

24 individual regulatory elements in embryonic stem cells and measure cis and trans effects between hum

25 erm encoding of ncAAs in human hematopoietic stem cells and reconstitution of this genetically engine

26 hat specifies the basic state of pluripotent stem cells and regulates the developmental transition fr

27 sion of somatic cells to induced pluripotent stem cells and rejuvenation of the germline with each ge

28 facilitated the identification of quiescent stem cells and revealed genes that contribute to breast

29 hat parenchymal astrocytes are latent neural stem cells and that targeted interventions can guide the

30 -like cells derived from induced pluripotent stem cells, and apilimod also demonstrated antiviral eff

31 Stem cells are continuously exposed to multiple stresses

32 roenvironment, where the first hematopoietic stem cells are generated during development, we performe

33 was absent in lineage-negative hematopoietic stem cells, arguing against a direct role for CSF1R in m

34 Activation of Hoxb1 in embryonic stem cells arrests cardiac differentiation, whereas Hoxb

35 f brain organoids generated from pluripotent stem cells as a model to compensate for the limited avai

36 r isolating and characterizing human-stomach stem cells as a prerequisite for harnessing the regenera

37 splatin-induced senescence-associated cancer stem cells, as well as tumor relapse after cisplatin tre

38 To establish a stem cell-based approach to restoring TM function and no

39 systems and highlight the potential of novel stem cell-based T2D disease models.

40 ttom-up method involves direct modulation of stem cell behavior without relying on the environmental

41 eceptors are coexpressed in intestinal crypt stem cells, bind to R-spondins (RSPOs) with high affinit

42 order Tricladida, are experimental models of stem cell biology and tissue regeneration.

43 Advances in developmental and stem cell biology have allowed the development of cell-r

44 orphogens, which are essential regulators of stem cell biology, yet the structural basis of Wnt signa

45 Bone mesenchymal stem cells (BMSCs) on the 3D nanofiber assemblies with s

46 was knocked out in human induced pluripotent stem cells by CRISPR/Cas9gene editing.

47 Administration of human neural stem cells by intracerebral implantation is feasible in

48 pmental transcription factors in pluripotent stem cells by methylating lysine 27 on histone H3.

49 ion substantially reduced the numbers of CML stem cells capable of initiating CML in vivo.

50 ller glia have the ability to reprogram into stem cells capable of regenerating all classes of retina

51 rm lineage-bias within the human pluripotent stem cell compartment.

52 dom models for a discoidal or an ellipsoidal stem cell confinement respectively.

53 In seed plants, branching is achieved by stem-cell-containing axillary meristems, which are initi

54 ge tracing revealed that airway and alveolar stem cells converge on a unique Krt8 + transitional stem

55 on generating neurons from human pluripotent stem cells could effectively treat in the future.

56 Cancer stem cells (CSCs) are a small subpopulation of quiescent

57 Cancer stem cells (CSCs) are cells within tumors that maintain

58 Cancer stem cells (CSCs) have features such as the ability to s

59 Cancer stem cells (CSCs) or CSC-like cells play crucial roles i

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

75 ompartments for orchestrating stepwise adult stem cell development and has also provided useful resou

76 reveal a mechanism regulating intestinal stem cell differentiation and epithelial repair followin

77 (CLE) peptide CLE40, a peptide regulator of stem cell differentiation in the Arabidopsis (Arabidopsi

78 both in vitro and in vivo, thereby inducing stem cell differentiation.

79 rosome asymmetries featured in self-renewing stem cell divisions.

80 dinated pathway originating from pluripotent stem cells during embryogenesis and continuing even as m

81 hogen subverts repair processes by targeting stem cells during infection and preventing epithelial re

82 Here we show that in mouse embryonic stem cells, EloA localizes to both thousands of Pol II t

83 Rosette-like stem cells erase constitutive heterochromatin marks and

84 al reprogramming at fertilization, embryonic stem cell (ESC) differentiation, and the continuous main

85 n elongation-associated factors in embryonic stem cells (ESCs) compared to somatic cells.

86 We used Chd7 null embryonic stem cells (ESCs) derived from Chd7 mutant mouse blastoc

87 nctive CpG methylation dynamics in embryonic stem cells (ESCs).

88 ced by mixed retinal cells or by mesenchymal stem cells exerted a paracrine neuroprotection on RGCs.

89 eventually lead to aberrant gene regulation, stem cell exhaustion, senescence, and deregulated cell/t

90 FGF2 induces leukemia stem cell expansion in MLL1-rearranged AML.

91 We report that in mouse embryonic stem cells, expression of a transgene comprising the fir

92 telomeres, often resulting in hematopoietic stem cell failure in the most severe cases.

93 netic regulation has a profound influence on stem cell fate during normal development in maintenance

94 meristem acts as an organizer that promotes stem cell fate in adjacent cells and patterns the surrou

95 ong investigates the mechanisms that control stem cell fate in development and disease.

96 a network of mRNAs to control embryogenesis, stem cell fate, fertility and neurological functions in

97 The derivation of tissue-specific stem cells from human induced pluripotent stem cells (iP

98 to establish a method for isolation of human stem cells from the PDL and gingiva, multilineage differ

99 ing the biological underpinnings of leukemia stem cell function, and highlight the Sdc1-Itgbeta7 sign

100 roughout life is critical for proper somatic stem cell function, but the complexities of the stem cel

101 microenvironment, the fibrotic response, and stem cell function.

102 root meristem is essential for understanding stem cell function.

103 oot apex yield insight into the processes of stem-cell function and cell-fate acquisition in the maiz

104 ion as a means of expanding MSCs to maintain stem cell functionality.

105 nal and mechanistic understanding of NONO in stem cell functions, lineage commitment and specificatio

106 tem cells (PDLMSCs) and gingival mesenchymal stem cells (GMSCs).

107 (GBM) contains a subpopulation of cells, GBM stem cells (GSCs), that maintain the bulk tumor and repr

108 Organoids derived from mouse and human stem cells have recently emerged as a powerful tool to s

109 s that reduce ACE2 levels in human embryonic stem cell (hESC)-derived cardiac cells and lung organoid

110 uman cerebral organoids from human embryonic stem cells (hESC) to investigate the effect of PCE on ea

111 When and how human embryonic stem cells (hESCs) irreversibly commit to differentiatio

112 during cell fate decisions, inflammation and stem cell heterogeneity.

113 al-component niche to modulate hair follicle stem cell (HFSC) activity.

114 of the epigenome plays a key role in shaping stem cell hierarchies, differential expression of transc

115 Coupling human induced pluripotent stem cell (hiPSC)-based technology with CRISPR-based gen

116 Human induced pluripotent stem cells (hiPSCs) have revolutionized research on huma

117 tissue.We employed human induced pluripotent stem cells (hiPSCs) to compare patterns of Abeta42 accum

118 n vitro differentiation of human mesenchymal stem cells (hMSCs) into chondrocytes.

119 Printed human neural stem cells (hNSCs) show high viability, neural different

120 i-specific loss of 5-hmC in genes regulating stem cell homeostasis, including MBD1, RTN1, STRN4, PRKD

121 es generated from multiple human pluripotent stem cell (hPSC) myogenic differentiation protocols and

122 re, we present a multiplex human pluripotent stem cell (hPSC) platform, in which 30 isogenic disease

123 cs between differentiating human pluripotent stem cells (hPSCs) and developing mouse neurons offers a

124 In this report, human pluripotent stem cells (hPSCs) are subject to directed differentiati

125 Parallel studies using human pluripotent stem cells (hPSCs) revealed that HOXA(neg/low) CD34(+) p

126 organoid derivatives from human pluripotent stem cells (hPSCs).

127 ic defects that accumulate in haematopoietic stem cells (HSCs) are thought to be responsible for age-

128 How transplanted haematopoietic stem cells (HSCs) behave soon after they reside in a pre

129 nd self-renewing capabilities, hematopoietic stem cells (HSCs) can maintain hematopoiesis throughout

130 Hematopoietic stem cells (HSCs) develop from the hemogenic endothelium

131 alpha (IL-27Ra) expression on hematopoietic stem cells (HSCs) mediates changes in HSCs that occur in

132 As humans age, hematopoietic stem cells (HSCs) occasionally acquire mutations in gene

133 Hematopoietic stem cells (HSCs) remain quiescent to preserve long-term

134 s and interactions of residual hematopoietic stem cells (HSCs) within the leukemic niche are poorly u

135 rradiation cause DNA damage to hematopoietic stem cells (HSCs), leading to HSC depletion and dysfunct

136 l for the maintenance of adult hematopoietic stem cells (HSCs).

137 tin (TPO) levels and perturbed hematopoietic stem cells (HSCs).

138 Distinctive from other tissue stem cells, HSCs transition through multiple hematopoiet

139 ulators of proteome complexity that regulate stem cell identity and function.

140 Human neural stem cell implantation may offer improved recovery from

141 cal stimulation of human induced pluripotent stem cells in 6-well plates.

142 where they differentiate from hematopoietic stem cells in a process called granulopoiesis.

143 es regulate the function of a broad range of stem cells in culture and in tissue.

144 Proliferation of intestinal stem cells in MCL1-deficient mice required WNT signaling

145 sk in part by reducing the number of Lgr5(+) stem cells in mouse colonic organoids.

146 their counterparts derived from mesenchymal stem cells in some measures.

147 umbers of LGR5(+) and actively proliferating stem cells in the HFs.

148 the nuclear reader Ythdc1 in mouse embryonic stem cells increases chromatin accessibility and activat

149 el long noncoding RNA (lncRNA) that we named Stem Cell Inhibitory RNA Transcript (SCIRT), which was m

150 differentiated from patient-derived neuronal stem cells (iNSCs) were verified by GFAP.

151 protocols differentiating human pluripotent stem cells into beta-like cells has opened up new opport

152 his by injecting labeled wild-type embryonic stem cells into blastocysts derived from lipodystrophic

153 been published to differentiate pluripotent stem cells into RPE cells suitable for disease modelling

154 ifferentiated from human-induced pluripotent stem cells into the mouse cortex.

155 rentially spliced during induced pluripotent stem cell (iPSC) differentiation and in tumors versus no

156 esponse to this need, an induced pluripotent stem cell (iPSC) disease model has been used to test pat

157 dysregulated in a human induced pluripotent stem cell (iPSC) disease model of a common form of heart

158 ed highly enriched human induced pluripotent stem cell (iPSC)-derived motor neurons and astrocytes to

159 Using human induced pluripotent stem cell (iPSC)-derived neurons that model developing b

160 In this study, induced pluripotent stem cells (iPSC)-derived neuronal stem cell lines were

161 ic stem cells from human induced pluripotent stem cells (iPSCs) would have broad reaching implication

162 HGPS-SMCs generated from induced pluripotent stem cells (iPSCs), to study their vulnerability to flow

163 fferentiation from human induced pluripotent stem cells (iPSCs).

164 2.2 subcomplex in human induced pluripotent stem cells (iPSCs).

165 c polymorphisms arising in naive pluripotent stem cells is close to zero.

166 (2) and NIR stimulation of MoS(2) with human stem cells is investigated using whole-transcriptome seq

167 Naturally occurring stem cells isolated from humans have been used therapeut

168 appear to affect the number of quiescent HF stem cells, it leads to reduced numbers of LGR5(+) and a

169 f mammalian germ lines, acts to commit adult stem cells, known as i-cells, to the germ cell fate in t

170 t pigs and goats, SSCT with allogeneic donor stem cells led to sustained donor-derived spermatogenesi

171 emergence of cancer cell subpopulations with stem cell-like properties.

172 sis proceeds through Wnt-differential cancer stem cell-like subpopulations before differentiating int

173 oblasts on micropatterned substrates induces stem-cell-like spheroids.

174 p between H3K27me3 and telomere integrity in stem cell lineage commitment that may have implications

175 1beta-driven mechanism, both hyperplasia and stem cell lineage defects.

176 llymount's capabilities, we track intestinal stem cell lineages and gut microbial colonization in sin

177 uripotent stem cells (iPSC)-derived neuronal stem cell lines were generated from individuals with MDD

178 ALKBH5 is required for maintaining leukemia stem cell (LSC) function but is dispensable for normal h

179 However, the role of K3 in leukemic stem cell (LSC) retention and growth in the remodeled tu

180 In this issue of Cell Stem Cell, Luo et al.

181 mplications for understanding mechanisms for stem cell maintenance, niche interactions and fate deter

182 pen reading frame downstream of the melanoma stem cell marker gene ABCB5.

183 r cells in vivo, lack of crypt base columnar stem cell markers, and a failure of in vitro crypt organ

184 EGF or neuropilin-1 (NRP-1) attenuate cancer stem cell markers, inhibit the tumor-initiating cell's n

185 and fuel-switching signals in nonneoplastic stem cells may also give important insights into the cor

186 Mouse embryonic stem cells (mESCs) cultured with MEK/ERK and GSK3beta (2

187 a retinoic acid (RA)-induced mouse embryonic stem cells (mESCs) differentiation experiment.

188 Mouse embryonic stem cells (mESCs) display unique mechanical properties,

189 The introduction of induced pluripotent stem cell methodology enabled better modeling of this di

190 eated a toolkit of human induced pluripotent stem cell models and functional assays using CRISPR/Cas9

191 ive and antibacterial effects of mesenchymal stem cell (MSCs), we evaluated the safety and efficacy o

192 sfunction of bone marrow mesenchymal stromal/stem cells (MSCs) during aging.

193 y effects of bone marrow derived mesenchymal stem cells (MSCs) has been widely studied and the recent

194 iple specialized cell types, including basal stem cells, mucus-secreting goblet cells, motile ciliate

195 Transplantation of mesenchymal stem cells/multipotent stromal cells (MSCs) has been pro

196 Murine muscle stem cells (MuSCs) experience a transition from quiescen

197 is a unique brain region maintaining neural stem cells (NCSs) and neurogenesis into adulthood.

198 different specialized cell types in the root stem cell niche.

199 adjacent cells and patterns the surrounding stem cell niche.

200 ace topography, enable the control of neural stem cell (NSC) differentiation and neurite outgrowth.

201 Neural stem cells (NSCs) are multipotent progenitors that are r

202 e considered an integral component of neural stem cells (NSCs) niches.

203 eurogenic potential, radial glia-like neural stem cells (NSCs) proliferation and differentiation, mig

204 he proper size and structure requires neural stem cells (NSCs) to divide with tight temporal and spat

205 was due to inhibited proliferation of neural stem cells (NSCs).

206 optic lobe neuroepithelium to produce neural stem cells (NSCs).

207 a function of position, and thus functional stem cell number in each organ.

208 cells ("iBCs"), a population resembling the stem cell of the airway epithelium.

209 The delivery of stem cells on an extracellular matrix (ECM)-based platfo

210 a common complication after peripheral blood stem cell or bone marrow transplantation, rarely occurs

211 man immunodefiency virus (HIV)/AIDS, cancer, stem cell or organ transplantation, nonsteroid immunosup

212 ectable in non-neoplastic astrocytes, neural stem cells or normal brain.

213 RNA-sequencing and stem cell pathway real-time RT-PCR analysis revealed pro

214 mparison of periodontal ligament mesenchymal stem cells (PDLMSCs) and gingival mesenchymal stem cells

215 Furthermore, the ability to induce stem cell persistence after radiation provides a paradig

216 etic regulation are critical for maintaining stem cell phenotype and cancer progression.

217 emic and local microenvironments that impact stem cell plasticity and impair regenerative capacity.

218 Taken together, our studies identified a stem cell population in the JE and have potential clinic

219 eat interest in understanding how the cancer stem cell population may be maintained in solid tumors.

220 ter the metabolic requirements of the cancer stem cell population.

221 sist stochastically throughout the epidermal stem cell population.

222 l and adult stages exclusively in a skeletal stem cell population.

223 Cancer stem cells possess the capacity for self-renewal and res

224 Stem cells produced daughter cells with an extraordinari

225 ablation of the Cdkn2a locus restored muscle stem cell properties in lamin A/C-null dystrophic mice.

226 endothelial cell apoptosis boosts intestinal stem cell radiosensitivity.

227 Upon removal of 5-Fu, slow-cycling stem cells regenerated both the structure and barrier fu

228 ntified processes of tissue regeneration and stem cell regulation.

229 ontrolled self-renewal through inhibition of stem cell-related signaling pathways has proven challeng

230 uman neuronal cell model of HD, using neural stem cells (ReNcell VM NSCs) stably transduced to expres

231 uate the ability of such scaffold to support stem cell repopulation.

232 (RNA-seq) data from human naive pluripotent stem cells reported multiple point "mutations" in cancer

233 However, how stem cells respond to dynamic variations in differentiat

234 m cell function, but the complexities of the stem cell response to increases in damaged or aggregated

235 r shape changes of human-induced pluripotent stem cells resulting from drug treatments.

236 Global gene expression profile of stem cells reveals significant influence of MoS(2) and N

237 aintenance of transcriptional plasticity and stem cell robustness.

238 athic RPL patient-specific human trophoblast stem cells (RPL-TSCs), we show that loss of TEAD4 is ass

239 We show that a +4 stem cell (SC) in the gastric antrum, marked by expressi

240 ighly specialized microenvironments, such as stem cell (SC) niches.

241 ns of the canonical asymmetric vs. symmetric stem cell self-renewal strategies and are distinguished

242 Now in Cell Stem Cell, Sommerkamp et al.

243 l transition driver transcription factors in stem cell-specific accessible regions that become repres

244 investigate the ability of resident skeletal stem-cell (SSC) populations to regenerate cartilage in r

245 Spermatogonial stem cells (SSCs) are generally characterized by excelle

246 lls converge on a unique Krt8 + transitional stem cell state during alveolar regeneration.

247 is and the transition between progenitor and stem cell states are unclear.

248 e periodontal ligament (PDL), which contains stem cells supporting tissue turnover.

249 cells often wrap membrane extensions around stem cell surfaces.

250 Planarians have an abundant population of stem cells that are rapidly eliminated after radiation e

251 from sympathetic nerves, which depletes the stem cells that give hair their color.

252 s a novel connection between dying cells and stem cells that remain.

253 tions where patients' own cells are used for stem cell therapies and immunotherapies.

254 ng enzyme PADI4 in suppressing breast cancer stem cells through epigenetic repression of stemness mas

255 Adult tissues and organs rely on resident stem cells to generate new cells that replenish damaged

256 d window of time surrounding radiation cause stem cells to outlast those in uninjured animals.

257 synapse-like" connections with hair follicle stem cells to promote hair regeneration in response to c

258 ture treatments based on the mobilization of stem cells to regenerate anagen hair follicles in AA and

259 n tested the capacity of transplanted neural stem cells to restore myelin in the context of PLP overe

260 accomplished in cultured human keratinocyte stem cells to show similar Ca(++)-induced differentiatio

261 eatment starts with diffusion of mesenchymal stem cells to the wounded region and their subsequent di

262 regulates the developmental transition from stem cells to various cell types.

263 Therapeutic hematopoietic stem cell transplant (HSCT) during chronic infection gen

264 d mortality in solid organ and hematopoietic stem cell transplant recipients.

265 eria included: infant ALL, relapsed ALL, and stem cell transplant recipients.

266 n age at cancer diagnosis and haematopoietic stem-cell transplant.

267 yeloid leukemia (AML) who undergo allogeneic stem cell transplantation (alloSCT), and carries a grave

268 ed and reinfused after a standard autologous stem cell transplantation (ASCT).

269 iation (TBI) before allogeneic hematopoietic stem cell transplantation (HSCT) in pediatric patients w

270 s complication post allogeneic hematopoietic stem cell transplantation (HSCT).

271 agnosis, our patient underwent hematopoietic stem cell transplantation and is well 8 years later.

272 Hematopoietic stem cell transplantation and NF-kappaB1 pathway-targete

273 atients had received high-dose melphalan and stem cell transplantation and/or treatment with a protea

274 nts undergoing chemotherapy or hematopoietic stem cell transplantation for hematological malignancy a

275 ineural deafness that requires hematopoietic stem cell transplantation for survival.

276 sis and the curative effect of hematopoietic stem cell transplantation for the hematopoietic features

277 Bone marrow stem cell transplantation had not been accessible during

278 or B-cell reconstitution after hematopoietic stem cell transplantation has been observed, we hypothes

279 s can be made on the impact of hematopoietic stem cell transplantation on allergy transfer or cure of

280 erlying malignancy, allogeneic hematopoietic stem cell transplantation, and neutropenia were not.

281 g olanzapine in the setting of hematopoietic stem cell transplantation.

282 n both models were history of haematopoietic stem-cell transplantation, cumulative alkylating drug do

283 -dose chemotherapy and subsequent autologous stem-cell transplantation, had an Eastern Cooperative On

284 Stem cell treatments are thought to functionally regener

285 objective was to develop macaque trophoblast stem cells (TSCs) as an in vitro platform for future ass

286 om radial glial progenitors (RGs), a type of stem cell typically extending from the apical to the bas

287 Stem cells undergo dynamic changes in response to injury

288 tudy the origin of individual cell types and stem cell units.

289 Moreover, induced pluripotent stem cells used to model ND diseases are discussed to ev

290 studies on in vitro RGC differentiation from stem cells utilized classical RGC signaling pathways mim

291 atic alpha (SC-alpha) cells from pluripotent stem cells via a transient pre-alpha cell intermediate.

292 L-6 enhances the self-renewal of dental pulp stem cells via STAT3 signaling and induction of Bmi-1.

293 ntial of patient-derived induced pluripotent stem cells was skewed toward the myeloid lineage.

294 ncluding patient-derived induced pluripotent stem cells, we further demonstrated that MCM10 is requir

295 e, using patient-derived induced pluripotent stem cells, we show that a mutation at the C terminus of

296 ilitate focal adhesion and mechanosensing of stem cells, which are collectively effective both in vit

297 amine neurons derived from human pluripotent stem cells, which have several advantages over fetal cel

298 ed neurons (iNeurons) derived from embryonic stem cells with quantitative proteomics to reveal the dy

299 ting protein, in the radial glia-like neural stem cells within the ventricular zone of the medial gan

300 Two recent papers in Cell Stem Cell (Zhu et al., 2020) and Cell Reports (Wang et a