ライフサイエンスコーパス: stem

1 ntly in the apical approximately 4 cm of the stem.

2 ctivity of inulin and FOS from S. rebaudiana stems.

3 osperm forests distributed more nutrients in stems.

4 terchangeable, and separate exchanges of the stem and loop portions were likewise well tolerated.

5 nalyses of infected human, primary, neuronal stem and monocytic cells revealed effects on neurodevelo

6 ra) in concert with stomatal conductance and stem and petiole hydraulic measurements.

7 e hierarchical relationships between various stem and progenitor cell subpopulations driving mammary

8 choice, we transplanted human hematopoietic stem and progenitor cells (HSPCs) expressing MLL-AF9 or

9 ull span of thymopoiesis, from hematopoietic stem and progenitor cells (HSPCs) through to mature T ce

10 tered differentiation of mouse hematopoietic stem and progenitor cells and also potentiated oncogenic

11 Rev1 hematopoietic stem and progenitor cells displayed compromised prolifer

12 BACKGROUND & AIMS: Neural stem and progenitor cells from the enteric nervous syste

13 findings provide insights into how skeletal stem and progenitor cells interact with other cell types

14 Autologous transplantation of hematopoietic stem and progenitor cells lentivirally labeled with uniq

15 lations, including the cKit(+) hematopoietic stem and progenitor cells.

16 of mIDH2 and normalization of hematopoietic stem and progenitor compartments with emergence of funct

17 rs also allows residence times in the roots, stems and leaves to be estimated, calculated to be 8.3 m

18 d compounds were detected in fruits, leaves, stems and roots of three L. barbarum varieties ('No.

19 .3 min (combined residence times of root and stem) and 1.9 min mm(-1) leaf, respectively.

20 revealed by atomic-resolution scanning TEM (STEM) and single-crystal diffraction using synchrotron r

21 transcriptome sequences from the root, leaf, stem, and flower tissues, and performed de novo sequence

22 appearance of embolism in the leaves and the stem by several days.

23 Given the importance of STEM careers as drivers of modern economies, this defici

24 conomies, this deficiency in preparation for STEM careers threatens the United States' continued econ

25 lial-mesenchymal transition (EMT) and cancer stem cell (CSC) acquisitions.

26 cancer tumorigenesis, metastasis, and cancer stem cell (CSC) maintenance.

27 veral human stem cell lines: human embryonic stem cell (hESC) line carrying the common T158M mutation

28 ant RTT patient-specific induced pluripotent stem cell (iPSC) line carrying the V247fs mutation (V247

29 derived a collection of induced pluripotent stem cell (iPSC) lines capturing a range of disease stag

30 d-type (WT) and three HD induced-pluripotent stem cell (iPSC) lines.

31 of specific microRNAs in controlling mammary stem cell (MaSC) activity and breast cancer formation re

32 hibit an expansion of the mammary epithelial stem cell (MaSC) enriched basal/myoepithelial population

33 RATIONALE: Virtually all mesenchymal stem cell (MSC) studies assume that therapeutic effects

34 specific enrichment of xenogenic pluripotent stem cell (PSC) derivatives.

35 ne-rich stretches attenuate the potential of stem cell active homeobox genes to acquire oncogenic pro

36 elial population and an increase in in vitro stem cell activity.

37 oxygen supply, an environmental regulator of stem cell activity.

38 Shi et al. (2017) in this issue of Cell Stem Cell and Tiyaboonchai et al. (2017) in a recent iss

39 rticularly under conditions of limited donor stem cell availability.

40 n emerged as signaling molecules to regulate stem cell behaviors such as migration.

41 enome to facilitate further understanding of stem cell biology and engineering of stem cells for ther

42 unctions of KLFs in mammalian embryogenesis, stem cell biology and regeneration, as revealed by studi

43 uring embryonic development and for applying stem cell biology to regenerative medicine and disease m

44 ng fields such as cancer, developmental, and stem cell biology.

45 a support a model in which a single neuronal stem cell can produce a large number of interneurons wit

46 the activation of oncogenic pathways in the stem cell compartment and how wild-type cells limit the

47 pecifically into the primitive hematopoietic stem cell compartment through the utilization of a modif

48 Improvements in stem cell culture methods, materials and biophysical too

49 Most methods for inducing Wnt signaling in stem cell cultures do not control the spatial presentati

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

51 We find that during embryonic stem cell differentiation loss of HMGNs leads to down re

52 tumor cells that inhibits the rate of tumor stem cell division.

53 Therefore, the effect of sulindac on stem cell dynamics was studied.

54 AP patients significantly altered colorectal stem cell dynamics, which might explain the chemoprevent

55 paired autophagy, mitochondrial dysfunction, stem cell exhaustion, epigenetic changes, abnormal micro

56 e aim of obtaining a deeper understanding of stem cell fate computation, in order to influence experi

57 the compounds' unique abilities to regulate stem cell fate provides opportunities for developing imp

58 However, the mechanisms that regulate stem cell fates under such widely varying conditions are

59 r emphasis on mechanisms relevant for cancer stem cell formation (CSC) and function.

60 Repeated cell divisions and aging impair stem cell function.

61 With increasing age, stem cell functional abilities decline, resulting in red

62 As p53 is central to hematopoietic stem cell functions, its aberrations affect AML evolutio

63 pathway that regulate cell proliferation and stem cell functions.

64 and proved even to efficiently block cancer stem cell growth.

65 Stem cell harvest for future use may be considered in fi

66 derived from a single dominant hematopoietic stem cell lineage.

67 ibit merged chromatin profiles from distinct stem cell lineages.

68 iple human embryonic and induced pluripotent stem cell lines and have potential applications for both

69 in human cells, we established several human stem cell lines: human embryonic stem cell (hESC) line c

70 monstrate that Prdm16 is required for neural stem cell maintenance and neurogenesis in the adult late

71 nized role in mammary ductal development and stem cell maintenance, but the ligands involved are ill-

72 role of beta-catenin and SNAIL in epidermal stem cell maintenance.

73 teosarcoma cells decreases the expression of stem cell markers and suppresses sarcosphere formation,

74 expression of the master EMT regulators and stem cell markers.

75 this activates tissue-specific expression of stem cell markers.

76 uggest that programmed differences in infant stem cell metabolism correspond with differences in body

77 The role of metabolites produced from stem cell metabolism has been emerged as signaling molec

78 , using murine and human induced pluripotent stem cell models, that RPGR interacts with and activates

79 hat influenced their ability to colonize the stem cell niche.

80 uniquely affects the formation of the larval stem cell niches, without altering other midgut cell typ

81 in inflammation/gliosis and increased neural stem cell numbers in areas of tissue injury.

82 y (including embryology) is proposed as "the stem cell of biological disciplines." Genetics, cell bio

83 e integrity, but also closely correlate with stem cell pluripotency, cancer drug resistance, GSL stor

84 morsphere formation and ALDH-positive cancer stem cell population, in vitro.

85 r controlling the make-up of the pluripotent stem cell population.

86 sly to facilitate cell-cycle progression and stem cell proliferation.

87 ision is the best characterized mechanism of stem cell replacement, but other mechanisms could also b

88 Understanding the stem cell response to immune therapies in ongoing human

89 s provide a biophysical understanding of how stem cell scaling is maintained during organ growth and

90 evelopment of exogenous molecules to control stem cell self-renewal or differentiation has arrived at

91 RNAs include Wnt/beta-catenin, TGF-beta, and stem cell signaling.

92 Thus, Blimp1 expression defines a mammary stem cell subpopulation with unique functional character

93 The disease is a potential target for stem cell therapy but success is likely to be limited by

94 Application of miR-146b combined with stem cell therapy could enhance regeneration of cartilag

95 RATIONALE: Autologous stem cell therapy using human c-Kit(+) cardiac progenito

96 ating oligodendrocyte properties and discuss stem cell tools to identify microenvironmental factors o

97 Sal-like protein 4 (SALL4), an embryonic stem cell transcriptional regulator, is re-expressed by

98 e (p < 0.0001) and not undergoing allogeneic stem cell transplant (SCT, p = 0.0005) predicted poor ov

99 -melphalan with low-dose TBI after haplocord stem cell transplant assures good engraftment and leads

100 eauville score </=2) proceeded to autologous stem cell transplantation (ASCT) whereas PET-positive pa

101 of stem cells to use in early haematopoietic stem cell transplantation (HSCT) approaches for several

102 ing complication of allogeneic hematopoietic stem cell transplantation (HSCT), posing as a significan

103 ion is a major complication after allogeneic stem cell transplantation (SCT).

104 ditional studies and referral for allogeneic stem cell transplantation are also discussed.

105 lleagues asked whether the results of neural stem cell transplantation might be improved by accommoda

106 rophy treated with allogeneic haematopoietic stem cell transplantation on a compassionate basis in fo

107 atently infected cells before haematopoietic stem cell transplantation.

108 curative option for CMML remains allogeneic stem cell transplantation.

109 who are potential candidates for autologous stem cell transplantation.

110 ed into intensive strategies with autologous stem cell transplantation.

111 be achievable with allogeneic hematopoietic stem cell transplantation.

112 iduals, particularly those who have received stem cell transplants.

113 evidence unveiled the existence of different stem cell types in various tissues with efficient capabi

114 been implicated in the biology of different stem cell types, yet they have not been studied in HFSCs

115 ing tumor cell motility and invasion, cancer stem cell viability and differentiation, resistance to a

116 mation, proliferation and differentiation of stem cell, cell survival/death, and cellular metabolism

117 In this issue of Cell Stem Cell, Chen et al. (2017) delineate an elegant hista

118 In this issue of Cell Stem Cell, Kee et al. (2017) and Kirkeby et al. (2017) i

119 inuously growing mouse incisor as a model of stem cell-based tissue renewal, we found that the transc

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

121 Stem cell-derived cardiomyocytes provide a promising too

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

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

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

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

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

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

128 Importantly, AZD4547 impaired stem cell-like characteristics in primary MECs and spont

129 uffered cytotoxic stress and thereby enter a stem cell-like state, the seeds for recurrence.

130 mbination of proteins mucin-5AC and prostate stem-cell antigen could identify high-grade dysplasia/ca

131 lenalidomide versus placebo after autologous stem-cell transplantation (ASCT) was investigated for pa

132 neity associated with retinal diseases makes stem-cell-based therapies an attractive strategy for per

133 chemotherapy-induced senescence could change stem-cell-related properties of malignant cells.

134 steogenic differentiation of adipose-derived stem cells (ASCs) was significantly enhanced as indicate

135 interest from primary CD34(+) hematopoietic stem cells (cRBCs).

136 rated that DACH1 inversely related to cancer stem cells (CSCs) markers, epithelial-mesenchymal transi

137 ating and metastatic capacity, termed cancer stem cells (CSCs).

138 glioma cell lines and patient-derived glioma stem cells (GSCs), EGFR signaling promotes H3K23 acetyla

139 of self-renewing, highly tumorigenic glioma stem cells (GSCs), which contributes to tumor initiation

140 le glioblastoma (grade IV glioma) and glioma stem cells (GSCs).

141 ds (COs) from differentiated human embryonic stem cells (hESCs) or induced pluripotent stem cells (iP

142 Human induced pluripotent stem cells (hiPSCs) are invaluable to study developmenta

143 Genome editing of human induced pluripotent stem cells (hiPSCs) offers unprecedented opportunities f

144 LE: Myocardial delivery of human mesenchymal stem cells (hMSCs) is an emerging therapy for treating t

145 Cartilage grown from human mesenchymal stem cells (hMSCs) is poorly organized and unstable in v

146 f adipose tissue - derived human mesenchymal stem cells (hMSCs) was evaluated in vitro.

147 Cardiomyocyte creation by human pluripotent stem cells (hPSCs) has generated opportunities for heart

148 Human pluripotent stem cells (hPSCs) provide a valuable model for the stud

149 Single hematopoietic stem cells (HSCs) have been functionally shown to genera

150 longed exit from quiescence by hematopoietic stem cells (HSCs) progressively impairs their homeostasi

151 Hematopoietic stem cells (HSCs) reside at the top of the hematopoietic

152 rough the engraftment of human hematopoietic stem cells (HSCs) that can lead to human hematopoiesis w

153 Upon aging, hematopoietic stem cells (HSCs) undergo changes in function and struct

154 ears, rapid emergence of induced pluripotent stem cells (iPSC) and iPSC-derived cardiomyocytes presen

155 cells] from primed-state induced pluripotent stem cells (iPSCs) after a 72-hour transient incubation

156 their tissue to generate induced pluripotent stem cells (iPSCs) and hepatocyte-like cells (HLCs) for

157 Human induced pluripotent stem cells (iPSCs) are ideal cell sources for personaliz

158 uman retinoblastomas and induced pluripotent stem cells (iPSCs) derived from murine rod photoreceptor

159 ming of somatic cells to induced pluripotent stem cells (iPSCs) holds enormous promise for regenerati

160 ic stem cells (hESCs) or induced pluripotent stem cells (iPSCs).

161 quiescent Bmi1(+) cells behave as intestinal stem cells (ISCs) in vivo.

162 in realizing the goal of targeting leukemic stem cells (LSCs).

163 vestigated the potential role of mesenchymal stem cells (MSCs) derived from human MT in the pathogene

164 and efficacy of allogeneic human mesenchymal stem cells (MSCs) in reducing the time to recovery from

165 ulticolor lineage tracing of skeletal muscle stem cells (MuSCs) to address these questions.

166 Neural stem cells (NSCs) are a heterogeneous population of cell

167 the normal cycling and maintenance of neural stem cells (NSCs) in the brain subependymal zone of adul

168 Periodontal ligament mesenchymal stem cells (PDLMSCs) are responsible for regeneration of

169 ifferentiated NKX2-1GFP reporter pluripotent stem cells (PSCs) in vitro to generate and isolate human

170 Using umbilical cord-derived mesenchymal stem cells (uMSC) from offspring born to normal-weight a

171 tant ovarian cancer cells and ovarian cancer stem cells and (ii) downregulation of beta-catenin is pa

172 re, we analyzed gene expression in mammalian stem cells and cells at various stages of differentiatio

173 at ablation of PRC2 genes in human embryonic stem cells and in mice results in changes in pluripotenc

174 Replicating Lgr5(+) stem cells and quiescent Bmi1(+) cells behave as intesti

175 ment was unable to improve the myogenesis of stem cells and reduce fibrosis in dKO muscle.

176 Liver-derived stem cells are in clinical development for inborn and ac

177 hed synchronized cultures of mouse embryonic stem cells as they exit the ground state of pluripotency

178 Induced pluripotent stem cells could potentially help to elucidate the compl

179 d/or proliferation of adult intestinal adult stem cells during postembryonic development in vertebrat

180 ding of stem cell biology and engineering of stem cells for therapeutic applications.

181 Neural stem cells have been envisioned as a source of donor cel

182 VIII (FVIII) synthesis site, and mesenchymal stem cells have been shown to control joint bleeding in

183 and transplanted RGC-like cells derived from stem cells have the potential to replace neurons that ha

184 hens the protective effect of amniotic fluid stem cells in a renal ischemia-reperfusion injury model.

185 To determine the role of HF keratinocyte stem cells in beta-HPV-induced skin carcinogenesis, we u

186 e therapeutic effect of human amniotic fluid stem cells in rats with renal ischemia-reperfusion injur

187 ine and biointerfacing activities of natural stem cells in therapeutic cardiac regeneration.

188 ids have been derived from human pluripotent stem cells in vitro, but generating a human ovarian foll

189 a GFP reporter gene into adult hematopoietic stem cells in vivo, which are predominantly quiescent, b

190 ) signaling and therefore differentiation of stem cells into megakaryocytes.

191 direct differentiation of human pluripotent stem cells into organoids - aggregates with multiple tis

192 etion of these shadow enhancers in embryonic stem cells leads to impaired activation of HoxA genes up

193 differentiation at which they are harvested, stem cells may exhibit different properties.

194 e effective, but reduced numbers of residual stem cells may limit their efficacy.

195 d with chimeric-competent human pluriopotent stem cells may serve as a suitable platform for the xeno

196 Typically, stem cells of independent lineages work coordinately wit

197 This review focuses on the epithelial stem cells of skin, where they come from, where they res

198 A-binding proteins (RBPs) that govern cancer stem cells remains poorly characterized.

199 ts of blastomeres, the most primitive cancer stem cells reported to date.

200 viously showed that MCPH1 deletion in neural stem cells results in early mitotic entry that distracts

201 Stem cells self-renew and produce progenitors with limit

202 used fibroblast-derived induced pluripotent stem cells to generate retinal pigment epithelium (RPE)

203 attempts to differentiate human pluripotent stem cells to lung epithelium rely on passing through pr

204 paB-mediated signaling that activates neural stem cells to reconstitute the olfactory epithelium.

205 al cord blood (UCB) is a promising source of stem cells to use in early haematopoietic stem cell tran

206 48 hours later, immune-matched or mismatched stem cells were implanted into osteochondral defects of

207 Muscle satellite cells are myogenic stem cells whose quiescence, activation, self-renewal, a

208 d autosome loss in aneuploid mouse embryonic stem cells with an extra human chromosome and human indu

209 Moreover, human embryonic stem cells with deletion of EZH1 or EZH2 fail to differe

210 man chromosome and human induced pluripotent stem cells with trisomy 21, as well as cancer cells.

211 In conclusion, CMMPs act as 'synthetic stem cells' which mimic the paracrine and biointerfacing

212 e mechanism is not active in mouse embryonic stem cells, and in vitro differentiation promotes only p

213 specific effects of high iron on the brain, stem cells, and the process of erythropoiesis and identi

214 e milieu for the recruitment of the CXCR2(+) stem cells, as validated by in vitro and in-matrix migra

215 eneration of more robust induced pluripotent stem cells, characterized by enhanced pluripotency-assoc

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

217 ompared with bone marrow-derived mesenchymal stem cells, displayed a 55-fold increase in the expressi

218 triple antibiotic paste, ferret dental pulp stem cells, encapsulated in a hydrogel scaffold, were in

219 Activity of satellite cells, skeletal muscle stem cells, is altered following a burn injury and likel

220 ults from somatic mutations in hematopoietic stem cells, which give an advantage to mutant cells, dri

221 NPCs are largely preexisting in pluripotent stem cells.

222 disease to be generated-e.g., in pluripotent stem cells.

223 nes in Naa10p-knockout embryos and embryonic stem cells.

224 of Runx1 in the generation of hematopoietic stem cells.

225 induce osteogenesis of human adipose-derived stem cells.

226 monly occurs among aging human hematopoietic stem cells.

227 panding a therapeutically relevant number of stem cells.

228 ntly replenished by differentiation of taste stem cells.

229 select subsets of ribosomes within embryonic stem cells.

230 pulation during differentiation of embryonic stem cells.

231 protein normally expressed only in embryonic stem cells.

232 ukemic ETV6-RUNX1 expression in hematopoetic stem cells/precursor cells (HSC/PC) and postnatal infect

233 evealed diurnal patterns in the rate of tree-stem CH4 emissions.

234 in mucosal damage occurs through decline in stem/clonogenic epithelial cell loss mediated by microva

235 a global database of 108753 trees for which stem diameter, height and crown diameter have all been m

236 For stem diameter, IPaS-Di generated the most accurate estim

237 ays a critical role in controlling embryonic stem (ES) cell self-renewal and pluripotency.

238 ells are malignant counterparts of embryonic stem (ES) cells and serve as useful models for investiga

239 g, BRD1, at bivalent loci in human embryonic stem (ES) cells.

240 nal signature 24, previously hypothesized to stem from aflatoxin exposure, indeed likely represents A

241 enotypic commonalities have been proposed to stem from disruption of conserved regulatory mechanisms

242 The remarkable properties of graphene stem from its two-dimensional (2D) structure, with a lin

243 The conformational differences stem from the orientations of the apical domain.

244 Chronic IFN production stemmed from the accumulation of DNA in the cytoplasm of

245 ress highly pathogenic and lethal infections stemming from bacterial, fungal, and viral origins.

246 Recent findings stemming from the Cap Analysis of Gene Expression (CAGE)

247 The catalytic power of Au(I) in BC stems from a combination of two sources: stereoelectroni

248 This gap in knowledge stems from a lack of understanding of the physics of sur

249 at the increased toxicity upon mutating UbS2 stems from disrupting the autoprotective role that patho

250 The opposed defined-pathway model stems from experimental results that show that proteins

251 The association that stems from our results reinforces the benefits of 2 key

252 Despite this, stem growth rates were similar to today.

253 Plants with photosynthetic stems have extra carbon gain that can help cope with the

254 hat Psi56 dampens conformational dynamics of stem II and stabilizes stem IIc.

255 rmational dynamics of stem II and stabilizes stem IIc.

256 We show that stem-like activity in serial passage culture and in vivo

257 There is mounting evidence that cancer stem-like cells (CSC) are selectively enriched in residu

258 air and to block tumorigenesis by modulating stem-like cells and beta-Cat signaling.

259 ling promotes the survival of ALDH1-positive stem-like cells and cooperates with TGFbeta to drive gem

260 exit from dormancy of therapy-induced cancer stem-like cells and leading to endocrine therapy resista

261 Differentiation of glioblastoma stem-like cells drives the nuclear translocation of an i

262 cer fail to address therapy-resistant cancer stem-like cells that have been characterized by changes

263 implanted with gliosarcoma tumors or glioma stem-like cells, respectively.

264 cancers, and promotes self-renewal of cancer stem-like cells.

265 in markedly attenuates glycolysis and cancer stem-like characteristics by suppressing both H19 and PD

266 MT, in addition to suppressing migratory and stem-like properties of tumor cells, also inhibit endoth

267 ture with PC3 cells, which might boost tumor stem-like properties.

268 opulation with a proliferative advantage and stem-like transcriptional features.

269 as a telomere-binding protein in the common stem lineage of marsupial and placental mammals.

270 d otoccipital division of the braincase in a stem lobe-finned fish.

271 tify two bulge-depleted regions on the miRNA stem, located approximately 16-21 nt and approximately 2

272 rmined that the xRRM of LARP7 binds to the 3 stem loop of 7SK and inhibits the methyltransferase acti

273 Stem-loop A (SLA), a part of the viral 5' untranslated r

274 In bulge-stem-loop constructs of HIV-1 transactivation response e

275 llustrates the recognition of unbranched RNA stem loops.

276 phase ERA promotes the establishment of the stem niche at the bract axis but, after the reproductive

277 The complexity of the HRMS data stems partly from the presence of isotopes that give ris

278 d that intrathecal transplantation of neural stem/precursor cells (NPCs) in mice with experimental au

279 Our data show that Troy marks a renal stem/progenitor cell population in the developing kidney

280 erlying taste cell differentiation and taste stem/progenitor cell proliferation.

281 Stem/progenitor cell-based interventions represent a nov

282 hough the presence of resident hematopoietic stem/progenitor cells (Lin-/Sca+/c-Kit+; LSK phenotype)

283 mortalization of primary mouse hematopoietic stem/progenitor cells compared to analogous gammaretrovi

284 previously unknown population of multipotent stem/progenitor cells that are capable of not only contr

285 vanced much faster than our understanding of stem/progenitor cells.

286 ing model where the kinked GGA motifs in the stem region of TGGAA repeat DNA act as hot spots to faci

287 olution of the receptor-binding site and the stem region on HA is severely constrained by their funct

288 xecutive regions, with its peak in the brain stem reticular activating system.

289 picule homology, and supports the primitive, stem-silicean interpretation of simpler-structured fossi

290 caused the sudden emergence of Verticillium stem striping in the UK, whereas in continental Europe V

291 , whereas in continental Europe Verticillium stem striping is predominantly caused by the more geneti

292 we report the application of adipose-derived stem/stromal cells (ASCs) for engineering the pulmonary

293 d xeno-free human umbilical cord-mesenchymal stem/stromal cells reduce the severity of rodent E. coli

294 on and the number of bone marrow mesenchymal stem/stromal cells, likely due to decreased expression o

295 r of the ribosomal RNA transcript and has a 'stem' structure-containing precursor.

296 approximately 28-32 nt from the base of the stem, that are less tolerant of unpaired bases.

297 olated fibres and other portions of the flax stem, together with fibre metabolism characterization, h

298 opsis thaliana) flowering, the inflorescence stem undergoes rapid growth, with elongation occurring p

299 Stem villus arteries in human IUGR placentas displaying

300 hed PRETEXT groups I, II, III, and IV as our stems, we created risk stratification trees based on 5 y