ライフサイエンスコーパス: rosette

1 ed hydrogen-bonded supramolecular complexes (rosettes).

2 neurons first assemble into a multicellular rosette.

3 -driven randomization of the monomers in the rosette.

4 ngement of its immediate neighbors to form a rosette.

5 axis extension, especially at the centres of rosettes.

6 e required for the formation and dynamics of rosettes.

7 lat sheets that sometimes interleave to form rosettes.

8 lso to induce and maintain stable epithelial rosettes.

9 namics and degradative functions of podosome rosettes.

10 multicellular structures called tetrads and rosettes.

11 marrow adipocytes and mesenchymal stem cell rosettes.

12 as blotches, strands, short white lines, and rosettes.

13 hydrogen-bonded sheets built from hexameric rosettes.

14 area predominantly assembled into multilobed rosettes.

15 ramework to characterize INM dynamics within rosettes.

16 and connects the basal poles of each cell in rosettes.

17 ium and the apicolateral cell membrane in NP rosettes.

18 within cell etxracts of Arabidopsis thaliana rosettes.

19 sitive cells in blood, forming RBC-leukocyte rosettes.

20 percentage of infected erythrocytes forming rosettes.

21 cells and leukocytes, forming characteristic rosettes.

22 nd contributed to the biogenesis of podosome rosettes.

23 omers induces an integrative self-sorting of rosettes.

24 coaggregates comprising a diverse mixture of rosettes.

25 ents in the ability to self-form into neural rosettes.

26 arge matrix-degrading superstructures called rosettes.

27 are delayed in sdk mutants, in particular in rosettes.

28 parasitemia were not correlated with P vivax rosetting.

29 Here, we have identified a new type of rosetting.

30 dwarfism, characterized by reduced growth in rosettes (6.5-fold), roots (4.3-fold), bolts (4.5-fold),

31 rther investigated how different leaves on a rosette acclimate to high light and show that younger le

32 orthorhombic tablets, acicular needles, and rosette aggregates which were identified as cerium oxala

33 mutations, the plants show upward curling of rosette and cauline leaves, in addition to early floweri

34 tion rate changed in different leaves of the rosette and correlated with leaf growth rate.

35 Mutants in SPEN3 and KHD1 had reduced rosette and leaf areas.

36 lopment of these methods, focusing on neural rosette and organoid approaches, and compare their relat

37 d erythrocytes at the schizont stage to form rosettes and in promoting merozoite invasion.

38 s, apatite blades intergrown among carbonate rosettes and magnetite-haematite granules, and is associ

39 Both rosetting and cytoadherence are mediated by the parasite

40 Rosetting and cytoadherence have been widely studied as

41 iates synchronicity of division and parasite rosetting and reveals that establishment and maintenance

42 on, neural precursor cells (NPCs), assembled rosettes, and differentiated neuronal cells.

43 increased adherens junction abundance, more rosettes, and glomerular expansion.

44 s mutated exhibited serrated leaves, compact rosettes, and, most significantly, short nondehiscent an

45 Here we demonstrate that within the rosette, angiotensin II evokes periodic Ca(v)3-dependent

46 graphitic inclusions in diagenetic carbonate rosettes, apatite blades intergrown among carbonate rose

47 We review recent data to understand rosette architecture and apply maxims derived from compu

48 We measured the extent of rosette architecture at 22 degrees C and 28 degrees C in

49 us C5a increasing the retention of polarized rosette architecture in human neural progenitors after p

50 Third, later derived rosettes are characterized by temporal instability in IN

51 These rosettes are polarized, transient epithelial structures

52 Multicellular rosettes are transient epithelial structures that serve

53 Rosettes are widely used in epithelial morphogenesis dur

54 molecules involved in this so-called T-cell rosetting are important components of the immunological

55 To do this, the projected rosette area of 710 worldwide distributed natural access

56 nation of fresh weight, sequential images of rosette area, and labeling of glucose in the cell wall.

57 orphophysiological traits, such as projected rosette area, transpiration rate, and rosette water cont

58 ed predominantly toward nonmalignant T cells rosetting around Reed-Sternberg cells provided meaningfu

59 ernberg cells and by most polyclonal T cells rosetting around Reed-Sternberg cells.

60 tensin II and highlight a novel role for the rosette as a facilitator of cell communication.

61 KV utilizes a rosette as a prerequisite before forming a lumen surroun

62 d immunosorbent assay, flow cytometry, and a rosetting assay.

63 Rosetting assays using CD236R knockdown normocytes deriv

64 lectrostatic interaction that can also guide rosette association allows helicoidal growth of supramol

65 Our results establish rosette-based CE as an evolutionarily conserved mechanis

66 the olfactory epithelium in adult mice, and rosette-bearing cells often have free centrioles in addi

67 atypical of the complex multi-element spine rosettes borne by most chancelloriids and N. pugio may s

68 ant architecture by increasing the number of rosette branches and reducing inflorescence height.

69 h rate, flowering time, main stem branching, rosette branching, and final plant height and observed s

70 ivator knockout did not affect the extent of rosetting, but almost completely abrogated T-cell activa

71 into dynamic extracellular matrix-degrading rosettes by distinct G protein-coupled receptor agonists

72 Formation and resolution of multicellular rosettes can drive convergent extension (CE) type cell r

73 degradation, due to a disruption of podosome rosettes caused by myosin-IIA overassembly, and a myosin

74 ports the "hexamer of trimers" model for the rosette cellulose synthesis complex that synthesizes an

75 cally place their cytokinetic bridges at the rosette center, where Rab11-associated vesicles transpor

76 Comparison of multiple reconstructed rosette colonies highlighted the variable nature of cell

77 al processes underlying the morphogenesis of rosette colonies in the choanoflagellate Salpingoeca ros

78 ered the presence of elongated cells in some rosette colonies that likely represent a distinct and di

79 ls in S. rosetta with that of multicellular 'rosette' colonies and collar cells in sponges, we recons

80 tory cycle of HPR1-T335D-complemented hpr1-1 rosettes compared to all other HPR1-containing lines.

81 of approximately up to 60 adult Arabidopsis rosettes concurrently.

82 Neural rosettes contain NSCs with strong epithelial polarity an

83 l energy per monomer and was consistent with rosette CSC morphology.

84 In summary, the multifaceted data support a rosette CSC with 18 CESAs that mediates the synthesis of

85 e space below an average FF-TEM image of the rosette CSC.

86 but its common ancestor with seed plants had rosette CSCs and a single CESA gene.

87 The moss Physcomitrella patens has rosette CSCs and seven CESAs, but its common ancestor wi

88 We find that the rosette defect of one mutant, named Rosetteless, maps to

89 isruption of multiple CRFs results in larger rosettes, delayed leaf senescence, a smaller root apical

90 ric embryonal brain tumors with multilayered rosettes demonstrate a unique oncogenic amplification of

91 Rosetteless protein is essential for rosette development and forms an extracellular layer tha

92 Overall, our biophysical perspective on rosette development complements previous genetic perspec

93 at, together, activate, enhance, and inhibit rosette development in the choanoflagellate Salpingoeca

94 with extensive wall ingrowths varied across rosette development in three ecotypes displaying differi

95 t living relatives of animals, multicellular rosette development is regulated by environmental bacter

96 Unexpectedly, the initiation of rosette development requires bacterially produced small

97 To investigate rosette development, we established forward genetics in

98 set of structural requirements for inducing rosette development.

99 demonstrate its necessity for multicellular rosette development.

100 (ros)) of Arabidopsis (Arabidopsis thaliana) rosettes displays a genuine circadian rhythmicity with a

101 ploids, but not octaploids, generated larger rosettes due to delayed flowering.

102 Rosette dynamics are regulated by both planar cell polar

103 xhibits a 6-fold symmetry and is known as a "rosette." Each CSC is believed to contain between 18 and

104 Embryonal tumours with multilayered rosettes (ETMRs) are aggressive paediatric embryonal bra

105 Embryonal tumors with multilayered rosettes (ETMRs) are highly lethal infant brain cancers

106 Embryonal tumors with multilayered rosettes (ETMRs) are primitive neuroectodermal tumors ar

107 ototropin-deficient mutants display impaired rosette evapotranspiration and leaf cooling at high temp

108 Rosette expansion and leaf movement exhibited a circadia

109 light signaling to the diurnal regulation of rosette expansion growth and leaf movement in Arabidopsi

110 stomatal development in cotyledons, promotes rosette expansion, and modulates guard cell mechanics in

111 eoretical model of the supramolecular barrel-rosette, favored by a network of intermolecular hydrogen

112 SAX-3 are localized to contracting edges and rosette foci and act to specify edge contraction during

113 oth the expulsion of apoptotic cells and the rosette formation among their neighbor cells.

114 ding defects in the outer limiting membrane, rosette formation and a reduction in functional acuity.

115 ignificant cellular rearrangement, including rosette formation and apical displacement of inner retin

116 We discuss and compare specific models for rosette formation and highlight outstanding questions in

117 eficient cells demonstrating abnormal neural rosette formation and neural progenitor cell proliferati

118 d CD58 knockout or CD2 blockade reduced both rosette formation and T-cell activation.

119 i and act to specify edge contraction during rosette formation and to mediate timely rosette resoluti

120 bind mouse RBCs suggesting a role for CIR in rosette formation and/or invasion.

121 cytoskeletal rearrangements responsible for rosette formation appear to be conserved.

122 genes, we show Fgfr2 is required for adrenal rosette formation by regulating adherens junction abunda

123 two factors interact with IGFBP7 to mediate rosette formation by the IRBC.

124 ere oxidative stress plays a key role in the rosette formation during the degenerative loss of CE.

125 Rosette formation has been studied in various developmen

126 that centrioles are amplified via centriole rosette formation in both embryonic development and turn

127 vestigate the function and factors affecting rosette formation in Plasmodium vivax.

128 We have identified a unique contributor to rosette formation in zebrafish Kupffer's vesicle (KV) th

129 Agonist-induced rosette formation is blocked by pertussis toxin, depende

130 ens junction-mediated constriction, and that rosette formation underlies the maturation of adrenal gl

131 Similarly, modeling of rosette formation with menadione (MN), led to phospho-Pa

132 binding of infected RBCs to uninfected RBCs (rosette formation), while antibodies targeting STEVOR in

133 D58 expression correlated with the extent of rosette formation, and CD58 knockout or CD2 blockade red

134 stored structural features, including neural rosette formation, and dampened the impact of infection

135 ional tension, a disruption of multicellular rosette formation, and defective convergent extension.

136 re frequently demonstrated lobular disarray, rosette formation, and hemorrhage than those with choles

137 blation of integrin beta1 abolishes the semi-rosette formation, preventing zippering and causing spin

138 Cdc42 activity is essential for rosette formation, whereas G12/13-mediated RhoA-ROCK sig

139 ulation and cellular transitions involved in rosette formation.

140 le of glycophorin C as a receptor in P vivax rosette formation.

141 C 4 region of CD236R significantly inhibited rosette formation.

142 the LD2,3 motifs of Hic-5, is necessary for rosette formation.

143 vadopodia and rosettes, which may facilitate rosette formation.

144 neage and embryonal tumors with multilayered rosettes fully recapitulate a neuronal lineage, while gr

145 computational network modeling to understand rosette function.

146 or family has been implicated in restricting rosette growth in response to stress.

147 loem companion cells caused strongly reduced rosette growth in the absence of wounding.

148 Here, we analyzed the leaf and rosette growth response of six Arabidopsis (Arabidopsis

149 nstructing a multiscale model of Arabidopsis rosette growth.

150 Lipid profiling revealed ala4/5 rosettes had perturbations in glycerolipid and sphingoli

151 Importantly, the IGFBP7-induced type II rosetting hampers phagocytosis of IRBC by host phagocyte

152 In some studies, rosetting has been associated with malaria pathogenesis.

153 Multicellular rosettes have recently been appreciated as important cel

154 Here, we study NSC dynamics within Neural Rosettes--highly organized multicellular structures deri

155 ential for the formation and organization of rosettes in active Src-transfected NIH3T3 fibroblasts an

156 sis and a framework for studying the role of rosettes in adult zona glomerulosa tissue maintenance an

157 e of individual invadopodia and invadopodial rosettes in CAFs.

158 ution, but not the formation, of tetrads and rosettes in Fgfr2 mutant limb-bud ectoderm.

159 the formation and resolution of tetrads and rosettes in the mouse embryo, possibly in part by spatia

160 primitive patterns such as neural tube-like rosettes in vitro.

161 In conclusion, T-cell rosetting in HL is established by formation of the IS, a

162 at induces S. rosetta to form multicellular "rosettes." In this study, we report the identification o

163 reported the planar structure and femtomolar rosette-inducing activity of one rosette-inducing small

164 emical ecology between choanoflagellates and rosette-inducing bacteria, and provide a synthetic probe

165 We find that the rosette-inducing bacterium Algoriphagus machipongonensis

166 one rosette-inducing small molecule, dubbed rosette-inducing factor 1 (RIF-1), produced by the Gram-

167 but synergizes with activating sulfonolipid rosette-inducing factors (RIFs) to recapitulate the full

168 femtomolar rosette-inducing activity of one rosette-inducing small molecule, dubbed rosette-inducing

169 Rosette-induction assays using synthetic RIF-1 stereoiso

170 -week-old plants enabled them to produce new rosette inflorescence stems.

171 sures, in agreement with progressive loss in rosette integrity at later developmental stages.

172 AX-3/Robo pathway cooperate to regulate, via rosette intermediaries, the intercalation of post-mitoti

173 ene core, as pivotal moieties for the barrel-rosette ion channel formation, and the activity of such

174 olecule that self-organizes to form a barrel rosette ion channel in the lipid membrane environment.

175 ation of a bacterially produced inhibitor of rosettes (IOR-1) as well as the total synthesis of this

176 The rosette is therefore a reversible pluripotent intermedia

177 he mechanism by which AHLs repress growth in rosettes is unknown.

178 In malaria, rosetting is described as a phenomenon where an infected

179 Rosetting is more common in vivax than falciparum malari

180 e hexagonal nature of the cellulose synthase rosette, it is assumed that the number of chains must be

181 or five 14-3-3 protein isoforms expressed in rosettes lacked circadian activation of K (ros) Two of t

182 ased numbers of inflorescences, reduction in rosette leaf photosynthesis and earlier fruit ripening.

183 1 displayed an increased number of secondary rosette-leaf branches.

184 novel cross talk existing between seeds and rosette leaves along with mutual effects between the Asp

185 es were obtained for mechanically inoculated rosette leaves and systemically infected cauline leaves

186 s antagonistic effect was blocked in younger rosette leaves by PBS3, a signaling component of the def

187 six Arabidopsis importin-alphas expressed in rosette leaves have an almost identical NLS-binding site

188 igns of early senescence in 6- or 7-week-old rosette leaves in the absence of any pathogen challenge,

189 s to reveal that SMM that was synthesized in rosette leaves of RNAi plants significantly contributed

190 rly, abcb19 mutants develop irregularly wavy rosette leaves that are less sensitive to blue light-med

191 d drought, blunted immune responses in older rosette leaves through the phytohormone abscisic acid si

192 a (i.e., the shoot apical zone versus mature rosette leaves) revealed that the antagonistic interplay

193 This ask1 mutant produces twisted rosette leaves, a reduced number of petals, fewer viable

194 AT) plants have longer hypocotyls and larger rosette leaves, but they also uniquely display early flo

195 ction of genes operating in the SMM cycle of rosette leaves, leading to elevated transport of SMM tow

196 o other common plant traits (e.g., number of rosette leaves, total volume occupied).

197 trolled by gibberellins (GAs) in Arabidopsis rosette leaves.

198 ession of Arabidopsis (Arabidopsis thaliana) rosette leaves.

199 osetting that involves direct interaction of rosetting ligands on IRBC and receptors on URBC, the IGF

200 scope and many more taste buds, patterned in rosette-like clusters, were found than previously report

201 Rosette-like stem cells erase constitutive heterochromat

202 ly, combined WNT and MEK inhibition supports rosette-like stem cells, a self-renewing naive-primed in

203 n shortening, establishing a transitory semi-rosette-like structure at the zippering point that promo

204 Invadosomes can reassemble into circular rosette-like superstructures, but the underlying signali

205 Together, our data provide an example of rosette-mediated postnatal tissue morphogenesis and a fr

206 ow that IE of the IT/R29 strain expressing a rosette-mediating PfEMP1 variant (IT4var09) cytoadhere i

207 We established a novel rosetting model by coculturing HLA-II-matched peripheral

208 previously noted specificity and potency of rosette-modulating molecules, expand our understanding o

209 ally secreted extracellular matrix (ECM) for rosette morphogenesis and show that the interaction of t

210 Rosette nanotubes (RNTs) are a class of materials formed

211 (15)N-labeled rosette nanotubes were synthesized and investigated usin

212 lts in disrupted adherens junctions, reduced rosette number, and dysmorphic glomeruli, whereas beta-c

213 Although rosetting occurs in all causes of human malaria, most da

214 ive cells are located lateral to the central rosette of exorhodopsin-positive cells.

215 ent transforms the amorphous epiblast into a rosette of polarized cells.

216 addition, global transcriptional changes in rosettes of amiCOX19 plants resembled those observed und

217 Quantitative proteomics of PG from senescing rosettes of PGM48 overexpression lines showed a dramatic

218 from a single cell-the zygote-multicellular rosettes of S. rosetta develop from a founding cell.

219 iomas and embryonal tumors with multilayered rosettes of the brain both display LIN28A positivity.

220 es known to regulate leaf size in developing rosettes of the hybrids, with the patterns of altered ex

221 nstrated centrilobular cholestasis and focal rosetting of hepatocytes, consistent with a cholestatic

222 ls and trailing cells, which form epithelial rosettes, or protoneuromasts.

223 hallenge going forward is to uncover how the rosette orchestrates the behavior of a functional networ

224 s separate entities; however, the ability of rosetting P. falciparum strains to cytoadhere has receiv

225 Rosetting phenomenon has been linked to malaria pathogen

226 d erythrocyte aggregation reminiscent of the rosetting phenomenon.

227 ocyst WNT signals drives the transition into rosette pluripotency by inducing OTX2.

228 We identify here a rosette pluripotent state defined by the co-expression o

229 ion) by suppressing bud outgrowth from lower rosette positions under low R:FR.

230 Grafts of wild-type floral stems to mutant rosettes produce progeny with enhanced growth and altere

231 oflagellate Salpingoeca rosetta We find that rosettes reproducibly transition from an early stage of

232 eptors on URBC, the IGFBP7-mediated, type II rosetting requires two additional serum factors, namely

233 ring rosette formation and to mediate timely rosette resolution.

234 by cytokinetic bridges that position at the rosette's center.

235 A cellulose synthesis complex with a "rosette" shape is responsible for synthesis of cellulose

236 In seed plants, cellulose is synthesized by rosette-shaped cellulose synthesis complexes (CSCs) that

237 a well-established phenotyping need: imaging rosette-shaped plants.

238 cell migration and the self-organization of rosette-shaped sensory organs in the zebrafish lateral l

239 ow the distal wound response is regulated in rosettes, showing that both axial (shoot-to-root) and ra

240 IP2;1), a major plasma membrane aquaporin in rosettes, shows circadian oscillations and is correlated

241 CDA mutants display a reduction in rosette size and have fewer leaves compared with the wil

242 s, indicating cosegregation of the genes for rosette size and the germination trait.

243 o as radial organization, is associated with rosette size, presumably via mechanical constraints of t

244 nts showed different degrees of reduction in rosette size, thus confirming the role of these genes in

245 In adult plants, PGX3 affects rosette size.

246 nteraction to a negative one, as measured by rosette size.

247 ryza sativa) and petiole elongation in Rumex rosette species.

248 tubule acetylation, which increases podosome rosette stability and is sufficient to inhibit macrophag

249 Infection of rosette stage Arabidopsis with a virulent S. sclerotioru

250 ally provided by a Wnt/Fgf signaling system, rosettes still self-organize in the presence of Notch si

251 IGFBP7-mediated rosette-stimulation was rapid yet reversible.

252 es in response to parasite stimulation, as a rosette-stimulator for Plasmodium falciparum- and P. viv

253 currence, and a multifunctional role for the rosette structure in activity-prolongation and coordinat

254 aMP3 and imaged zG cells within their native rosette structure.

255 ase complex (CSC), visualized as a hexameric rosette structure.

256 Plant cellulose is synthesized by rosette-structured cellulose synthase (CESA) complexes (

257 Yet, emerging data indicate that in native rosette structures in situ, zG cells are electrically ex

258 iferation, and resulted in loss of polarized rosette structures in the aggregates.

259 ow a six-particle cellulose synthase complex rosette synthesizes microfibrils likely comprised of eit

260 ed by formation of the IS, and activation of rosetting T cells critically depends on the interaction

261 cells were CD25(-) provided that associated rosetting T cells expressed CD25.

262 s and showed IS formation with activation of rosetting T cells.

263 LH39, bHLH100, and bHLH101 developed smaller rosettes than wild-type plants in soil.

264 -signaling cells forming a single cell thick rosette that demarcates: domains of cell proliferation i

265 that CGCs could be connected to the multiple rosettes that arise from a single MF input.

266 Cs exist in the plasma membrane as six-lobed rosettes that contain at least three different cellulose

267 nal gland arrange in distinct multi-cellular rosettes that provide a structural framework for adrenal

268 Unlike type I rosetting that involves direct interaction of rosetting

269 The rosette then activates MEK signals that induce lumenogen

270 ls in the adult adrenal cortex organize into rosettes through adherens junction-mediated constriction

271 es of the Arabidopsis (Arabidopsis thaliana) rosette throughout the vegetative stage of growth.

272 abolites was confined locally to the central rosette tissue.

273 oaches to leaves of the Arabidopsis thaliana rosette to characterize their protein degradation rate a

274 Next, we used rosettes to investigate radial cell-to-cell transport of

275 Rosetting to P vivax asexual and sexual stages was evide

276 X-7, HMR-1 and DLG-1 function redundantly in rosette-to-epidermis attachment.

277 inactive regions of human chromosomes yields rosettes, topological domains and contact maps much like

278 Evaluation of root and rosette transcriptomes revealed an early transcriptional

279 fect of deer exclusion on Alliaria came from rosette transitions, whereas the largest positive effect

280 scopy (TEM) images and image averages of the rosette-type CSC, revealing the frequent triangularity a

281 epiblast of the mouse blastocyst generates a rosette, undergoes lumenogenesis and forms the primed pl

282 Rosette vernalization increased seed germination in dive

283 We first tested whether effects of rosette vernalization persisted to influence seed germin

284 sion at different life stages in response to rosette vernalization.

285 PAR-6 is localized to the rosette vertex and dendrite tips, and promotes DYF-7 loc

286 jected rosette area, transpiration rate, and rosette water content, were correlated with changes in t

287 Using a strain-rosette, we demonstrate the existence of transverse stra

288 nd redox-related genes, whereas those of the rosette were related to the regulation of development an

289 adopodia dynamics and their coalescence into rosettes were also dependent on Rac1, formin, and myosin

290 These rosettes were preferentially disassembled in response to

291 The vertex of the rosette, which becomes the dendrite tips, is attached to

292 ine and cyanuric acid units into a hexameric rosette, which brings together poly(A) triplexes with a

293 Second, early forming rosettes, which are abundant with founder NSCs and corre

294 In contrast, later derived rosettes, which are characterized by reduced NSC capacit

295 -actin fibers emanating from invadopodia and rosettes, which may facilitate rosette formation.

296 rganization of invadopodia into higher-order rosettes, which may promote the localized matrix degrada

297 cytoadherence of IT/R29 IE is distinct from rosetting, which is primarily mediated by NTS-DBL1alpha

298 , homochiral polymers comprised of hexameric rosettes with structural features that resemble nucleic

299 oadhere to microvascular endothelium or form rosettes with uninfected erythrocytes to survive in vivo

300 was induced by thrombin-activated platelets rosetting with neutrophils and was inhibited by anti-P-s