ライフサイエンスコーパス: stem

1 ccharides covalently cross-linked by peptide stems.

2 recently implicated in regulating embryonic stem and hematopoietic progenitor cells.

3 causally related to its function in mammary stem and precursor cells, this is not the case for its f

4 Hematopoietic stem and progenitor cell (HSPC) formation and lineage di

5 Haematopoietic stem and progenitor cell (HSPC) gene therapy has emerged

6 Definitive hematopoietic stem and progenitor cells (HSPCs) arise from the transdi

7 Hematopoietic stem and progenitor cells (HSPCs) develop in distinct wa

8 nts results from dysfunctional hematopoietic stem and progenitor cells (HSPCs).

9 ermed RDCs, in cultured primary mouse neural stem and progenitor cells (NSPCs).

10 er an advantage by enhancing self-renewal of stem and progenitor cells and inhibiting their different

11 abel-retaining (LR) and non-LR hematopoietic stem and progenitor cells both had indistinguishable loc

12 ffectively clears SCs and rejuvenates tissue stem and progenitor cells in naturally aged mice without

13 on factors in the majority of haematopoietic stem and progenitor cells.

14 more uniform population compared with adult stem and progenitor cells.

15 lant mass, diaspore mass, mass allocation to stem and reproductive organs and total number and propor

16 the characterization of PCs of wines, bunch stems and grape canes.

17 agro-morphological traits related to leaves, stems and roots with high heritability.

18 s invested proportionally similar biomass to stems as trees and not less, as expected; (2) lianas wer

19 Here we describe a crow-sized stem bird, Falcatakely forsterae gen. et sp. nov., from

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

56 root meristem is essential for understanding stem cell function.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

71 adjacent cells and patterns the surrounding stem cell niche.

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

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

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

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

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

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

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

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

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

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

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

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

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

85 endothelial cell apoptosis boosts intestinal stem cell radiosensitivity.

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

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

88 cells often wrap membrane extensions around stem cell surfaces.

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

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

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

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

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

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

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

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

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

98 Bone marrow stem cell transplantation had not been accessible during

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

100 Stem cell treatments are thought to functionally regener

101 Now in Cell Stem Cell, Sommerkamp et al.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

164 Stem cells are continuously exposed to multiple stresses

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

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

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

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

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

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

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

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

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

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

175 Rosette-like stem cells erase constitutive heterochromatin marks and

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

207 Stem cells undergo dynamic changes in response to injury

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

223 es the vasculogenic potential of dental pulp stem cells.

224 ases susceptibility in NSCs and glioblastoma stem cells.

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

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

227 diac and neural development from pluripotent stem cells.

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

229 nce and genomic stability of mouse embryonic stem cells.

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

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

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

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

234 Keywords: Adults and Pediatrics, Brain/Brain Stem, CNS, Computer Aided Diagnosis (CAD), Computer Appl

235 ive response to weight stimulus resulting in stem collapse after just 3 months.

236 strong binding of OLE RNA by OapB requires a stem containing a precisely located single-nucleotide bu

237 ring drought, inner Selaginella lepidophylla stems curl into a spiral shape to prevent photoirradiati

238 iding insight into the regulation of monocot stem development.

239 d, active-learning course designs across the STEM disciplines and suggest that innovations in instruc

240 and their evolution into overt psychosis may stem from an aberrant functional reorganization of the b

241 The high complication rates stem from difficulty with laryngoscopy and tube placemen

242 Most of their concerns stem from disagreement on data inclusion criteria and an

243 -reasoning skills and enhanced social skills stemmed from the onset of a more basic cognitive ability

244 The current data surplus stemming from all types of devices together with the rel

245 ity of a unified mechanical gating mechanism stemming from membrane deformation induced by a non-plan

246 alyzing glycoproteomes with uncommon glycans stemming from the green alga Chlamydomonas reinhardtii a

247 mparing the diastereomeric transition states stemming from the two half-chair conformations of their

248 ron type-specific pathology and the deficits stemming from them in male heterozygous Q175 mice, compa

249 r the ALT mechanism, and that this necessity stems from APBs' role in localizing the BLM-TOP3A-RMI (B

250 Lack of overlap likely stems from biological rather than technical limitations

251 erstanding of organismal responses to change stems from studies over relatively short timescales.

252 This distinctive feature stems from the mechanism of TCR activation, which is tho

253 We show that this improvement stems from the negativity of a particular quasiprobabili

254 hat this unusually high degree of catenation stems from the secondary nucleation of the precursor mol

255 demonstrate that the compelling performance stems from the SMSIR, favoring the formation of surface

256 dational issues that we claim this inability stems from.

257 Unlike ESCs or EpiSCs, formative stem (FS) cells respond directly to germ cell induction.

258 he oldest compelling evidence for an aquatic stem group for either Myriapoda or Hexapoda, previously

259 ine or freshwater fossils that belong to the stem groups of the major terrestrial arthropod radiation

260 Specifically, we found stem growth stops at soil moisture potentials of -0.47 M

261 This stems in part from the predominance of studies using stu

262 ioblastomas we tested including glioblastoma stem/initiating cells, but hardly detectable in non-neop

263 Maintaining an upright stem is expected to require vertical proprioception thro

264 accumulation of muropeptides with tripeptide stems lacking the terminal d-ala-d-ala and reduced pepti

265 a suboptimal terminal loop and a suboptimal stem length, accumulates to 40-fold higher levels when c

266 ved tumor cells enriched in CSCs, which show stem-like characteristics and induce metastases.

267 ll RNA sequencing showed that SNP-IV induced stem-like genes (Tcf7, Slamf6, Xcl1) whereas SNP-SC enri

268 presence of host factor PCBP2 that binds to stem-loop IV of the IRES.

269 ect binding between endogenous TruB1 and the stem-loop structure of pri-let-7, which also binds Lin28

270 eriments, we studied how frameshift-inducing stem-loops from E. coli dnaX mRNA and the gag-pol transc

271 30% preferred structured motifs folding into stem-loops.

272 n vitro experiments reveal that this feature stems mainly from two mechanisms: efficient recruitment

273 ng demonstrate that the base pairings in the stem of these DRs control sfRNA formation by maintaining

274 chemical composition of leaves, flowers and stems of jambu cultivated in hydroponic and conventional

275 round of human olfactory neurosphere-derived stem (ONS) cell matrix.

276 izes a small subregion of OLE RNA, including stem P13, with a dissociation constant (K(D) ) of ~700 p

277 nd cell-state-specific signaling networks in stem, Paneth, enteroendocrine, tuft and goblet cells, as

278 ume and survival after unprotected left main stem percutaneous coronary intervention (uLMS-PCI) is po

279 obese mice enhanced mammary epithelial cell stem/progenitor activity, elevated expression of estroge

280 Neural stem/progenitor cell (NSPC) grafts can integrate into si

281 1, one of the nuclear lamins in adult neural stem/progenitor cells (ANSPCs), underlies age-related al

282 Mobilization of hematopoietic stem/progenitor cells (HSPC) from the bone marrow (BM) i

283 unction and disease progression that involve stem/progenitor cells and inflammation in a tissue-speci

284 of limbal melanocytes with limbal epithelial stem/progenitor cells on fibrin hydrogels pre-incubated

285 Deleting Gata3 enhances adult prostate stem/progenitor cells self-renewal capacity in both orga

286 scranial magnetic stimulation, intracerebral stem/progenitor cells) that consider precise lesion loca

287 yer over the shaped scaffold and cultured as stem/proliferative cells to expand them and cover the sc

288 Stem rust is an important disease of wheat that can be c

289 s time point is not required for immunity to stem rust.

290 In addition, this stem-salamander shares plesiomorphic characters with tem

291 Yet the most ancient stem-salamanders, known from mid-Jurassic rocks, shed li

292 ly revealed spermatocyte anaphase A does not stem solely from kinetochore microtubule shortening.

293 hestnut starch nanoparticles (WSP) and Lotus stem starch nanoparticles (LSP) was found to be 420, 606

294 scanning/transmission electron microscopes (STEM/TEM) provide a critical tool for understanding the

295 Humeri of stem tetrapods share a unique suite of functional adapta

296 Mechanical weakness of the stem was ruled out as an explanation for the downward be

297 nsus H5 as globular head and consensus H1 as stem was shown to elicit broadly protective CD4(+) and C

298 prioception through feedback between sensing stem weight and responding with radial growth.

299 Stems were the richest tissue in woody plants, whereas r

300 ues were shown to regulate CAM expression in stems, whereas the shift from C(4) to C(4) -CAM hybrid p