ライフサイエンスコーパス: rosette

1 des form a particle and six particles form a rosette.

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

3 ium and the apicolateral cell membrane in NP rosettes.

4 within cell etxracts of Arabidopsis thaliana rosettes.

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

6 percentage of infected erythrocytes forming rosettes.

7 cells and leukocytes, forming characteristic rosettes.

8 nd contributed to the biogenesis of podosome rosettes.

9 lat sheets that sometimes interleave to form rosettes.

10 lso to induce and maintain stable epithelial rosettes.

11 formation of transient intermediates called rosettes.

12 that were arranged within retinal folds and rosettes.

13 to histologically visible photoreceptor cell rosettes.

14 iple RSV F oligomers arranged in the form of rosettes.

15 namics and degradative functions of podosome rosettes.

16 s, ensuring that they form stable epithelial rosettes.

17 ed by PAX6(+) neural cells competent to form rosettes.

18 multicellular structures called tetrads and rosettes.

19 marrow adipocytes and mesenchymal stem cell rosettes.

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

21 hydrogen-bonded sheets built from hexameric rosettes.

22 area predominantly assembled into multilobed rosettes.

23 ramework to characterize INM dynamics within rosettes.

24 parasitemia were not correlated with P vivax rosetting.

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

26 ons of the S-cells outside phloem bundles in rosette and cauline leaves and in flower stalks were vis

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

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

29 Separately, Slbo in the border cell rosette and Cut in the pole cells have antagonistic inte

30 morphology in functioning meristems of both rosette and inflorescence.

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

32 Our data further suggest that the distinct rosette and root glucosinolate profiles in Arabidopsis a

33 ic, and transport mutants show that both the rosette and roots are able to synthesize aliphatic and i

34 th the highest level at the junction between rosette and stem.

35 the reorganization of cells into epithelial rosettes and by initiating atoh1a expression.

36 , and thecate cells) and two colonial forms (rosettes and chains).

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 podosome stability and their organization as rosettes and three-dimensional podosomes, (ii) regulates

40 Both rosetting and cytoadherence are mediated by the parasite

41 Rosetting and cytoadherence have been widely studied as

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

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

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

45 light on Arabidopsis (Arabidopsis thaliana) rosette architecture is demonstrated using a narrow-band

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

47 Simulations suggest that while rosettes are not essential for AVE migration, they are c

48 These rosettes are polarized, transient epithelial structures

49 psi3-1 and particularly psi2-1 psi3-1 rosettes are small.

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

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

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

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

54 in the VE and an increase in multi-cellular rosette arrangements (five or more cells meeting at a po

55 that S100-positive cells appear in olfactory rosettes as early as at 2day postfertilization (dpf).

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

57 Rosetting assays using CD236R knockdown normocytes deriv

58 ) leaves, but formed such buds in almost all rosette axils.

59 llular fluxes in intact Arabidopsis thaliana rosettes based on time-dependent labeling patterns in th

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

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

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

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

64 lation of Arabidopsis (Arabidopsis thaliana) rosette bud outgrowth by the R:FR and the associated mec

65 Moreover, pht4;2 rosettes, but not roots, were significantly larger than

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

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

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

69 ms of hESC-derived multipotent cells (neural rosette cells) and primary differentiated cells (microva

70 Within rosettes, cells are polarized with apical ends constrict

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

72 zed with apical ends constricted towards the rosette center and nuclei basally displaced.

73 hat pin"-shaped molecules that aggregated as rosettes, characteristic of the posttriggered form.

74 flagellate Salpingoeca rosetta, we find that rosette colony development is induced by the prey bacter

75 ary and secondary CESAs forming a functional rosette complex has been investigated.

76 ther than reticulocytes, preferentially form rosetting complexes, indicating that this process is unl

77 ssed at the onset of rosette formation, when rosettes comprise no more than 3-5 cells, and that its e

78 of approximately up to 60 adult Arabidopsis rosettes concurrently.

79 While rosettes constitute the major source and storage site fo

80 Neural rosettes contain NSCs with strong epithelial polarity an

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

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

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

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

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

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

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

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

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

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

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

92 To investigate rosette development, we established forward genetics in

93 set of structural requirements for inducing rosette development.

94 uding a touch-induced delay in flowering and rosette diameter reduction.

95 However, some of the rosettes did not have any S100-positive cells until 4 dp

96 To probe the role of rosettes during AVE migration, we develop a mathematical

97 Rosette dynamics are regulated by both planar cell polar

98 Rosette dystrophies are more complex structures that rem

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

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

101 Rosette expansion and leaf movement exhibited a circadia

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

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

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

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

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

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

108 accompanied by a reduction in multicellular rosette formation and axis elongation.

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

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

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

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

113 otably, deficits in proliferation and neural rosette formation are rapidly reversed upon silencing on

114 Rosette formation has been studied in various developmen

115 cal regulator of cell spreading and podosome rosette formation in immature DCs.

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

117 aling was previously shown to be crucial for rosette formation in the pLLp.

118 n network to promote apical constriction and rosette formation in the pLLp.

119 hich is required for apical constriction and rosette formation in the pLLp.

120 roblast growth factor (Fgf) signals regulate rosette formation in the zebrafish posterior lateral lin

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

122 The potential for rosette formation is included, along with various juncti

123 macrophages, (iii) is required for podosome rosette formation triggered by Hck, and (iv) is necessar

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

125 s, intra-acinar lymphocytes and eosinophils, rosette formation, and canalicular cholestasis yielded a

126 s, the presence or absence of emperipolesis, rosette formation, and cholestasis in a blinded fashion

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

128 Portal and intra-acinar plasma cells, rosette formation, and emperiopolesis were features that

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

130 in, NR2F1, NR2F2, and IRX2 - in the onset of rosette formation, during spontaneous neural differentia

131 hat OTX2 is highly expressed at the onset of rosette formation, when rosettes comprise no more than 3

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

133 contrast to the conventional way of studying rosette formation, which involves induction of neuronal

134 mitive neuroectoderm, which is manifested by rosette formation, with consecutive differentiation into

135 ulation and cellular transitions involved in rosette formation.

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

137 C 4 region of CD236R significantly inhibited rosette formation.

138 During migration, the pLLp deposits rosettes from the trailing edge, while cells are polariz

139 nally, at basal endogenous ABA levels, whole-rosette gas exchange measurements revealed reduced stoma

140 bilization from leaves, and thereby increase rosette growth rate and the weight and nitrogen content

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

142 nstructing a multiscale model of Arabidopsis rosette growth.

143 Multicellular rosettes have recently been appreciated as important cel

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

145 In Arabidopsis thaliana, the rosette hydraulic conductivity (Kros) is higher in darkn

146 e of individual invadopodia and invadopodial rosettes in CAFs.

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

148 helial (NE) cells that form neural tube-like rosettes in the absence of morphogens in the first 2 wee

149 are polarized and incorporated into nascent rosettes in the leading region.

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

151 ts show that the formation of multi-cellular rosettes in the mouse VE is dependent on normal PCP sign

152 prevents effective maturation of epithelial rosettes in the pLLp.

153 l and experimental observations suggest that rosettes in the VE epithelium do not form passively in r

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

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

156 number of S100-positive cells in individual rosettes increased steadily over the next 3days before i

157 tion of glucosinolates between the roots and rosettes, indicating phloem and xylem as their transport

158 Here we show that a rosette inducing factor (RIF-1) produced by A. machipong

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

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

161 We find that the rosette-inducing bacterium Algoriphagus machipongonensis

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

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

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

165 Rosette-induction assays using synthetic RIF-1 stereoiso

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

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

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

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

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

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

172 alysis of Arabidopsis (Arabidopsis thaliana) rosettes is an important nondestructive method for study

173 Rosetting is more common in vivax than falciparum malari

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

175 g DCF loss-of-function alleles are devoid of rosette leaf cutin ferulate and exhibit a 50% reduction

176 flowering occurs, as determined from higher rosette leaf number at flowering in RILs (Recombinant In

177 were also phenotyped for flowering time and rosette leaf number in long and short days.

178 duced few rosette leaves, tfl1-14 produced a rosette leaf number similar to Col-0, suggesting that th

179 The method was applied to the first rosette leaf of Arabidopsis (Arabidopsis thaliana) and r

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

181 egrees C prior to the emergence of the first rosette leaf.

182 1 displayed an increased number of secondary rosette-leaf branches.

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

184 Z altered expression of AG, SEP3, and AP2 in rosette leaves and flowers, while ectopic expression of

185 pic meristems occurred along margins of late rosette leaves at serration sinuses in an ERECTA-depende

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

187 that the development of a minimum number of rosette leaves is necessary to initiate ARR competence u

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

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

190 higher accumulation of free phenylalanine in rosette leaves, as well as altered accumulation of sever

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

192 of intriguing phenotypes, including serrated rosette leaves, irregular flowers, floral organs inside

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

194 While svp-31, svp-32 and Ws-2 produced few rosette leaves, tfl1-14 produced a rosette leaf number s

195 ession of Arabidopsis (Arabidopsis thaliana) rosette leaves.

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

197 ly, the retinas of these mice show localized rosette-like arrangements in the outer nuclear layer, an

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

199 r, the node precursors form several ciliated rosette-like clusters; they then rapidly undergo a mesen

200 Round tubular, rosette-like structures located in the outer nuclear lay

201 ics, including SOX1 expression, formation of rosette-like structures, and high neurogenic capacity.

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

203 Some work on automatic rosette measurement using image analysis has been propos

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

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

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

207 crocycles, which then stack linearly to form rosette nanotubes.

208 Such embryos have significantly reduced rosette numbers, altered epithelial packing, and show ab

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

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

211 spring composed of cohesin, condensin, and a rosette of intramolecular chromatin loops.

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

213 girostrine morphology and a bulbous anterior rosette of premaxillary teeth also occurs in the spinosa

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

215 rified with several hundred transcripts from rosettes of plants cultivated at 23 degrees C or transfe

216 hosphorylated and predominantly localized to rosettes of podosomes.

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

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

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

220 Comprehensive analysis of sphingolipids in rosettes of these mutants revealed a 50% reduction in gl

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

222 There were 7.8 S100-positive cells per rosettes on average in larvae at 7 dpf.

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

224 3T enantiomers form mirror related hexameric rosette patterns.

225 Rosetting phenomenon has been linked to malaria pathogen

226 n Hawai'i, but is a highly charismatic giant rosette plant that is viewed by 1-2 million visitors ann

227 In rosette plants, root flooding (waterlogging) triggers ra

228 lant-plant signaling in horizontally growing rosette plants.

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

230 Buds from specific rosette positions, exhibiting divergent fates to increas

231 of axillary buds to runners or axillary leaf rosettes, probably through the activation of gibberellin

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

233 taining GABAA receptors in subsets of neural rosette progenitors, accompanied by increased proneural

234 lants, cellulose is synthesized by so-called rosette protein complexes with cellulose synthases (CESA

235 rimordium, which is organized into polarized rosettes (proto-NMs).

236 posterior NMs and live imaging reveals that rosette renewal fails during later stages of migration.

237 ring rosette formation and to mediate timely rosette resolution.

238 sets: aerial tissue, flowers, leaves, roots, rosettes, seedlings, seeds, shoots and whole plants.

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

240 of S. rosetta can develop into multicellular rosette-shaped colonies through a process of incomplete

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

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

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

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

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

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

247 In adult plants, PGX3 affects rosette size.

248 manipulative experiments that leaves of the rosette species Arabidopsis thaliana first need to move

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

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

251 Whole-rosette stomatal conductance (Gst) measurements revealed

252 motion was possible by using three 3-element rosette strain gauges bonded at the diaphyseal midshaft

253 ex and defining the relationship between the rosette structure and the cellulose microfibrils they sy

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

255 staining within the electron dense podosome rosette structure.

256 -Bazooka prevents formation of multicellular rosette structures and cell motility across the segment

257 potentially form the bases of the multiloop rosette structures at the Igh locus that compact during

258 The rosette sucrose content correlated with overall and with

259 s in agreement with their self-assembly into rosette supermacrocycles, which then stack linearly to f

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

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

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

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

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

265 Lastly, we show that cells derived from rosettes that emerge during spontaneous differentiation

266 lls can be induced to form similar polarized rosettes that initiate lumenogenesis.

267 vo, leading to the formation of neuroblastic rosettes that resemble primitive neuroepithelial tumors.

268 n CESA3 was replaced by CESA7 in the primary rosette, the velocity of the mixed complexes was slightl

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

270 abolites was confined locally to the central rosette tissue.

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

272 ng to a pattern transformation of OPV3T from rosettes to dimers, and a change in chiral expression as

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

274 Rosetting to P vivax asexual and sexual stages was evide

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

276 with previously described monitoring tools, Rosette Tracker allows us to simultaneously quantify pla

277 Freely available, Rosette Tracker facilitates the rapid understanding of A

278 We introduce Rosette Tracker, a new open source image analysis tool f

279 Evaluation of root and rosette transcriptomes revealed an early transcriptional

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

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

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

286 s (PIP1;2, PIP2;1, and PIP2;6) contribute to rosette water transport, and PIP2;1 can fully account fo

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

288 iation in Arabidopsis (Arabidopsis thaliana) rosettes, we have characterized the vegetative pin1 phen

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

290 These rosettes were preferentially disassembled in response to

291 d to cones with single boutons, doublets, or rosettes, whereas the rod HCs connected to rods with sin

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

296 vo isotopic labeling of Arabidopsis thaliana rosettes with (13)CO2 and estimated fluxes throughout le

297 osinolates are synthesized both in roots and rosettes with roots as the major storage site.

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

299 on of individual cells based on differential rosetting with microspheres functionalized with monoclon

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