ライフサイエンスコーパス: bud

1 espread cell death within the embryonic limb bud.

2 a smooth transition from an open to a closed bud.

3 cles with the plasma membrane of the growing bud.

4 a successful delivery of the vacuole to the bud.

5 in ecodormant buds than that of endodormant buds.

6 terning and morphogenesis of tooth and taste buds.

7 Tomato-positive innervation within all taste buds.

8 ian curvature neck of the nanoscale membrane buds.

9 Grasses possess basal and aerial axillary buds.

10 r for the formation of both aerial and basal buds.

11 ion, which may slow down or prevent membrane budding.

12 a process referred to nuclear envelope (NE) budding.

13 trafficked to the plasma membrane for virus budding.

14 ights, reported in the past, to asexual nest budding.

15 ruption of Vps4 recruitment stalled membrane budding.

16 ment formation with minimal effects on virus budding.

17 roposed role of M2 in scission at the end of budding.

18 migration signatures characteristic of organ budding.

19 e main driving force for virion assembly and budding.

20 simultaneously and relatively rapidly after budding.

21 ving limited effects on total virus particle budding.

22 oylated and plays an important role in virus budding.

23 be palmitoylated and to positively regulate budding.

24 asm to the plasma membrane leading to virion budding.

25 ethod for making a branch-competent ureteric bud, a tissue fundamental to kidney development, from mo

26 lactone treatment reduces the probability of bud activation by parallel effects on BRC1 transcription

27 n these data, we propose that BRC1 regulates bud activation potential in concert with an auxin transp

28 auxin transport-based mechanism underpinning bud activity.

29 ch PpeS6PDH gene is down-regulated in flower buds after dormancy release, concomitantly with changes

30 We benchmark three-dimensional liver buds against fetal and adult human liver single-cell RNA

31 m channel was conditionally deleted in taste buds (alphaENaC knockout).

32 pondence between the three-dimensional liver bud and fetal liver cells.

33 e in RA FLS, we recently identified the limb bud and heart development (LBH) gene as a key dysregulat

34 therto unknown function for Fgf20 in mammary budding and branching morphogenesis.

35 cation of the mRNAs bound to PUF proteins in budding and filamentous fungi and by computational analy

36 Therefore, knowledge from the budding and fission yeast systems illuminates highly con

37 lopments in studies of Cdc42 polarization in budding and fission yeasts and demonstrate that models d

38 The data suggest that influenza A virus budding and genome incorporation can occur independently

39 s a stable site of polarization that induces budding and inhibits formation of competing sites.

40 ast, which undergoes polarized growth during budding and mating, has been a useful model system to st

41 cholesterol-dependent manner to cause virus budding and release.

42 ijacked by many enveloped viruses to mediate budding and release.

43 ings and a potential relationship between NE budding and the NPC.

44 i membrane dispersal process that drives the budding and transport of secretory vesicles.

45 ession is up-regulated by low temperature in buds and leaves, whereas desiccation treatment induces P

46 rmation of Eda-induced supernumerary mammary buds and normalizes the embryonic and postnatal hyperbra

47 articularly relevant for cell types in taste buds and other tissues that can be identified only by ph

48 as desiccation treatment induces PpeS6PDH in buds and represses the gene in leaves.

49 y impacted by frost through damage to flower buds and reproductive structures.

50 , to a process that is both endogenous (nest budding) and exogenous (loss of preferred habitat), resu

51 ), early epithelial NP derivatives, ureteric bud, and cortical stroma; p-Creb was present in differen

52 -specific RNA-seq data from seedling, floral bud, and root of 19 Arabidopsis thaliana accessions to e

53 vitro basal crypt organoid proliferation and budding, and in vivo significantly reduced the number of

54 ocytosis, membranes transition among planar, budding, and vesicular topographies through nanoscale re

55 ids and sweeping of the fornices with cotton buds, and maintaining clinical suspicion of contact lens

56 tor assay to interrogate signalling in liver buds, and show that vascular endothelial growth factor (

57 pression of TRU1 and TB1 overlap in axillary buds, and TB1 binds to two locations in the tru1 gene as

58 trigger physiological stress in endodormant buds, and that these stress-associated signals induced t

59 entrilobular nodules, large nodules, tree-in-bud appearance and the main lesion being located in S1,

60 Taste buds are innervated by neurons whose cell bodies reside

61 was inhibited by LdSar1:T34N in an in vitro budding assay, indicating that GTP-bound LdSar1 is requi

62 re selected because of the pronounced mother-bud asymmetry for these proteins distributions, Trx2p as

63 t few cell cycles regardless of their mother-bud asymmetry.

64 igidity of the coat, allowing for successful budding at higher membrane tensions.

65 l for maintaining the correct polarity of LD budding at the nuclear envelope, restricting it to the o

66 Influenza virus assembles and buds at the plasma membrane of virus-infected cells.

67 An exception to this rule are budding bacteria, in which new offspring emerges de novo

68 spruce seedling height (0.64), and for beech bud break and leaf senescence (0.52 and 0.46).

69 species required 84% more spring warming for bud break, EU ones 49% and EA ones only 1%.

70 a developmental time course of white spruce bud burst and shoot growth revealed two UGTs, PgUGT5 and

71 ystem must overcome at the stage of membrane budding by an assembling protein coat.

72 nt signaling are mural cells of periureteric bud capillaries in the nascent renal medulla of embryoni

73 MTs and directs spindle movements toward the bud cell.

74 tion, and degradation in MDCK and peripheral bud cells for regulating cell dynamics.

75 populations of cap mesenchymal and ureteric bud cells in a cyclical, predictable manner.

76 on profiles between proximal and distal limb bud cells isolated from mutant stocks where various part

77 tions associated with cleft formation; inner bud cells remain unaffected.

78 e, we show that differentiation of new taste bud cells, but not progenitor proliferation, is interrup

79 nockout results in more tightly packed outer bud cells, which display stronger E-cadherin localizatio

80 nes, primarily localizes to the cytoplasm in budding cells.

81 an altered migration pattern from glandular buds (cellular aggregates) to epithelial cell sheets.

82 ic shunt (TIPS) in a series of patients with Budd-Chiari syndrome (BCS), and to determine the predict

83 ic and portal veins, resulting in functional Budd-Chiari syndrome and portal hypertension.

84 atidylinositol-4-phosphate immediately after budding coincides with a burst of phosphatidylinositol-3

85 hat separate the ER membrane into mother and bud compartments caused premature formation of deposits

86 Taste buds contain multiple cell types with each type expressi

87 equent to internalization, arguing that they bud continuously from stable subdomains.

88 In this study, we report that the bud cortex is a landmark that signals a successful deliv

89 We demonstrate that upon arrival at the bud cortex, Vac17 is phosphorylated by Cla4.

90 ce lacking talins in the developing ureteric bud developed kidney agenesis and collecting duct cells

91 ly flower development and showed that floral buds developed more slowly at 15 degrees C versus 20 deg

92 AGE: RNA-seq of Vitis during early stages of bud development, in male, female and hermaphrodite flowe

93 nnotated genomic loci during early stages of bud development.

94 e essential for retention in the mother when bud-directed transport is enforced.

95 ontact.ARMMs are extracellular vesicles that bud directly at the plasma membrane; their function is p

96 with the plasma membrane, whereas ectosomes bud directly from the plasma membrane.

97 Mouse mammary buds dissected at E14 and cultured for 5 days showed tha

98 nstrated that hierarchical copper- and zinc- buds dressing gamma-AlOOH mesostrands, which are oriente

99 We hypothesize that decellularized tooth buds (dTBs) created from unerupted porcine tooth buds (T

100 resulted in monotonic inhibition of mammary buds ductal growth.

101 enhancer responsible for patterning the limb bud during development.

102 ombined with other features of chicken taste buds, e.g., uniquely patterned array and short turnover

103 last frost-free day of the year, plants that bud earlier might be directly impacted by frost through

104 of tetrads and rosettes in Fgfr2 mutant limb-bud ectoderm.

105 vel role of Wnt7b signaling and the ureteric bud epithelium in renal medullary capillary development.

106 rofound defect in lung development with lung buds failing to undergo branching morphogenesis and prog

107 In the early limb bud, for instance, Sonic hedgehog (Shh) is expressed in

108 Down-regulation of SPL4 promoted aerial bud formation and increased basal buds, while overexpres

109 overexpression of SPL4 seriously suppressed bud formation and tillering.

110 Overexpression of miR156 induced aerial bud formation in switchgrass.

111 sion, and force from actin polymerization on bud formation.

112 ng the efficiency with which virus particles bud from infected cells and restoring filament formation

113 of mitosis, HPV-harboring transport vesicles bud from the TGN, followed by association with mitotic c

114 onfirmed for C. lytica that the vesicles are budded from cell surfaces in a manner consistent with th

115 y acquire their primary envelope not through budding from cellular membranes but by forming and exten

116 Moreover, Ldgp63-containing COPII vesicle budding from the ER was inhibited by LdSar1:T34N in an i

117 plasma membrane inner leaflet to facilitate budding from the host cell.

118 SH3 domain of Boi2, which is dispensable for bud growth and targets Boi2 to the site of abscission, i

119 o the plasma membrane, rescued secretion and bud growth defects in boi mutant cells, and abrogated No

120 eral correlation between BRC1 expression and bud growth inhibition.

121 ary gland induction, but compromises mammary bud growth, as well as TEB formation, ductal outgrowth a

122 late secretory vesicles and are defective in bud growth.

123 One-dimensional coordinates recovered by BUDS help researchers discover sample attributes or cova

124 We find that liver bud hepatoblasts diverge from the two-dimensional lineag

125 eristems within specialized structures named buds in order to survive low temperatures and water depr

126 t of the periodic pattern of hair or feather buds in the developing skin.

127 icrovilli of the chemosensory cells of taste buds including the epithelium of lips and olfactory epit

128 recent findings regarding sexual dimorphism, bud induction, branching morphogenesis and cellular diff

129 reported genes acting as activators of basal bud initiation, SPL4 acts as a suppressor for the format

130 pocket has a chaperone function involved in bud initiation.

131 treatments, disrupts taste papilla and taste bud integrity and can eliminate responses from taste ner

132 Together with its role in HIV-1 entry and budding into host cells, the data herein indicate that H

133 t interactions that promote or inhibit viral budding is warranted.

134 summary, the growth and maturation of floral buds is associated with variable petal number in C. hirs

135 Buds lacking BRC1 expression can remain inhibited and se

136 and neural supply of Shh are removed, taste buds largely disappear.

137 m of oleosin targeting ER-LDs and extracting budding LDs to the cytosol as well as reveal potential a

138 ed oleosin to enter the ER lumen and extract budding LDs to the ER lumen.

139 retical modeling of cell migration in a tail-bud-like geometry with experimental data analysis to ass

140 y innervation, neurotrophic support of taste buds likely involves a complex set of factors.

141 borated with grapes from a vine with a lower bud load (20 per plant; sample M1) stood out among the o

142 CTxB diffusion was observed at the nanoscale bud locations, suggesting a local increase in the effect

143 -type specific biological processes, such as budding, mating, mating type switch, consumption of nutr

144 disruption of Tsc2 in craniofacial and limb bud mesenchymal progenitors.

145 g that the developing mandibular molar tooth bud mesenchyme expresses significantly higher levels of

146 ntly upregulated and expanded into the tooth bud mesenchyme in Inhba(-/-) embryos in comparison with

147 Recent studies indicate that NE budding might be an endogenous cellular process for the

148 Two models have been put forward: the budding model, based largely on structural data, and the

149 C. albicans budding mother cells were found to be nonadherent, which

150 After arrival in the bud, Myo2 releases the vacuole, and Vac17 is degraded.

151 ding hair follicles, sebaceous glands, taste buds, nails and sweat ducts.

152 ing, followed by constriction of the nascent bud neck and ultimately ILV generation by vesicle fissio

153 Here we analyze how Gps1 is recruited to the bud neck during the cell cycle.

154 Gin4 are involved in maintaining Gps1 at the bud neck from late G1 phase until midanaphase.

155 cal for inheritance and transport across the bud neck in myo2 mutants.

156 geting function of Gin4 is taken over by the bud neck-associated protein Nba1.

157 asm in anaphase, where it accumulates at the bud neck.

158 ociated with activation of senescence, while budding of daughter cells was associated with senescence

159 mechanism of eHAV egress involving endosomal budding of HAV capsids into multivesicular bodies.

160 of M2-mediated membrane scission during the budding of influenza viruses.

161 RT-III executes membrane scission during the budding of intralumenal vesicles (ILVs) at endosomes.

162 cating that GTP-bound LdSar1 is required for budding of Ldgp63-containing COPII vesicles.

163 transport (ESCRT) machinery is necessary for budding of many enveloped viruses.

164 ena such as perturbation growth, necking and budding of offspring droplets from a bulk body are obser

165 oscopy and super-resolution imaging show the budding of syntaphilin cargos, which then share a ride o

166 The secretory duct begins as buds of chitin at the apical surface of individual secre

167 ated to mediate sorbitol synthesis in flower buds of peach concomitantly with specific chromatin modi

168 olerance to environmental stresses in flower buds of peach.

169 developmental biology continues to roll on, budding off more disciplines, while retaining its own id

170 How an LD buds off from the endoplasmic reticulum bilayer is still

171 We demonstrated usefulness and accuracy of BUDS on a set of published microbiome 16S and RNA-seq an

172 collect phenological data (number of flower buds, open flowers and fruits) from specimens of two com

173 ffectively prevents TF from participating in budding or being incorporated into virus particles.

174 anching morphogenesis, new branches form by "budding" or "clefting." Cell migration, proliferation, r

175 ing branch development: whether the axillary bud, or branch primordium, grows out to give a lateral s

176 Sonic hedgehog (Shh) expression in the limb bud organizing centre called the zone of polarizing acti

177 cation, virion assembly, or virus egress via budding out of infected cells.

178 lines overexpressing SVP2 showing suppressed bud outgrowth.

179 hment, not much is known about how different budding patterns give rise to different functions at the

180 to correlate the plant morphogen auxin with bud positioning in Sargassum, nor could we predict cell

181 To complete the budding process, eVP40 utilizes its PPXY L-domain motif

182 ed branching in brc1 mutants, the effects of bud-regulating hormones on BRC1 expression, and a genera

183 In the context of strigolactone-mediated bud regulation, our data suggest a coherent feed-forward

184 e a source of sonic hedgehog (Shh) for taste bud renewal.

185 of exomer, polarized delivery of Ena1 to the bud requires functional exomer.

186 We showed that these lateral buds resulted from mislocalization of DivIVA, a major de

187 Population means of timing of bud set were highly correlated with latitude.

188 od we studied the genetic basis of timing of bud set, a surrogate trait for timing of yearly growth c

189 been focused on the molecular details of the bud site selection and polarity establishment, not much

190 yeast paralogs regulate actin organization, bud site selection, and mRNA localization, although how

191 ng division site and, consequently, abnormal bud-site selection in daughter cells.

192 could we predict cell wall softening at new bud sites.

193 eassemble before arriving at plasma membrane budding sites.IMPORTANCE Hendra virus and Nipah virus ar

194 In particular, passive diffusion and a bud-specific dilution remain as possible explanations.

195 restricted to the distal epithelium from the bud stage and throughout branching morphogenesis.

196 tion of Bmp4 ( Bmp4(ncko/ncko)) both exhibit bud-stage developmental arrest of the mandibular molar t

197 nidegib treatment led to rapid loss of taste buds (TB) in both fungiform and circumvallate papillae,

198 (dTBs) created from unerupted porcine tooth buds (TBs) can be used to guide reseeded dental cell dif

199 ghly invasive structures called terminal end buds (TEBs) that form at ductal tips at the onset of pub

200 introduce a Bayesian Unidimensional Scaling (BUDS) technique which extracts dominant sources of varia

201 were also significantly lower in ecodormant buds than that of endodormant buds.

202 n epithelium that includes specialized taste buds, the basal lamina, and a lamina propria core with m

203 Here we show that, inside the buds, the TEOSINTE BRANCHED1, CYCLOIDEA, PCF (TCP) trans

204 al ridge (AER) at the distal tip of the limb bud to direct outgrowth along the proximal to distal (PD

205 rves that carry taste information from taste buds to the nucleus of the solitary tract (NST) in the m

206 y to promote tooth morphogenesis through the bud-to-cap transition and that the differential effects

207 t Osr2 and the Bmp4-Msx1 pathway control the bud-to-cap transition of tooth morphogenesis through ant

208 When crown buds transitioned from endo- to ecodormancy, the ABA met

209 In mammals, taste buds typically contain 50-100 tightly packed taste-recep

210 rough generation of underground adventitious buds (UABs) on the crown and lateral roots.

211 docytosis and on syntenin-syndecan endosomal budding, upstream of ARF6 small GTPase and its effector

212 nd ECM dynamics have varied roles in driving budding versus clefting in different organs.

213 matically inhibited production of infectious budded virions (BV).

214 ed for efficient entry and nuclear egress of budded virions of AcMNPV.IMPORTANCE Little is known rega

215 ol mediates M2 clustering to the neck of the budding virus to cause the necessary curvature for membr

216 vitro crypt organoid proliferation and crypt budding was abrogated by the Wnt inhibitor IWP2.

217 Membrane buds were first detected with <50 nm radius, grew to >20

218 Genotypes with and without aerial buds were identified in switchgrass (Panicum virgatum),

219 peripheral cells of branching epithelial end buds, where it enhances cell motility and cell-cell adhe

220 ated cargoes to trap them at the site of ILV budding while the cargoes undergo deubiquitination.

221 ted aerial bud formation and increased basal buds, while overexpression of SPL4 seriously suppressed

222 Furthermore, buds with high BRC1 transcript levels can be active.

223 a Cdc42 GTPase-activating protein, prevents budding within the division site by inhibiting Cdc42 rep

224 gene expression output, we have conducted in budding yeast a large-scale measurement of the activity

225 In contrast, herein we analyze Hi-C data for budding yeast and identify 200-kb scale TADs, whose boun

226 ily of endocytic adaptors, including Syp1 in budding yeast and its mammalian orthologue, FCHo1.

227 in and regulate force, we purified SPBs from budding yeast and used laser trapping to manipulate sing

228 e role of mitochondria in this process using budding yeast as a model.

229 The interaction pattern of budding yeast as measured from genome-wide 3C studies ar

230 r to produce rejuvenated daughters, dividing budding yeast cells confine aging factors, including pro

231 in have shown that in response to pheromone, budding yeast cells undergo a rise of cytosolic Ca(2+) t

232 properties of formaldehyde-cross-linking in budding yeast cells.

233 One such locus is the budding yeast centromere, which is a paradigm for target

234 to argue that the small, highly constrained budding yeast chromosomes could not have these structure

235 a two-dimensional agent-based model to study budding yeast colonies with cell-type specific biologica

236 Purification of budding yeast condensin reveals that it occurs not only

237 report the finding of a new function for the budding yeast Cse4/CENP-A histone-fold domain interactin

238 In particular, budding yeast daughter cells are more vulnerable to stre

239 The spindle pole body (SPB) of budding yeast duplicates once per cell cycle.

240 c cells because most prior studies have used budding yeast for RLS studies.

241 Here we study budding yeast in dynamic environments of hyperosmotic st

242 lucose-mediated repression of respiration in budding yeast is at least partly due to the low cellular

243 d here the forces that ensembles of purified budding yeast kinesin-5 Cin8 produce in microtubule glid

244 iscussion, we will use the relatively simple budding yeast kinetochore as a model, and extrapolate in

245 anisms of group formation in the unicellular budding yeast Kluyveromyces lactis.

246 is study, we find that Stu1 recruits Stu2 to budding yeast KTs, which promotes MT generation there.

247 In budding yeast meiosis, homologous chromosomes become lin

248 Here we show that the budding yeast mismatch repair related MutLbeta complex,

249 Fluorescent labeling of budding yeast nucleoli with CDC14-GFP revealed that a sp

250 work defines spatial organization within the budding yeast nucleus, demonstrates the conserved role o

251 Boi1 and Boi2 (Boi1/2) are budding yeast plasma membrane proteins that function in

252 The budding yeast Polo-like kinase Cdc5 is a key regulator o

253 is essential, we previously interrogated the budding yeast proteome to identify candidates that funct

254 ith our in vitro results, our experiments in budding yeast provide evidence that Rad52 inverse strand

255 Although budding yeast Rad51 has been extensively characterized i

256 Here we show that Y1F substitution in budding yeast resulted in a strong slow-growth phenotype

257 The budding yeast Saccharomyces cerevisiae is a long-standin

258 Under aerobic conditions, the budding yeast Saccharomyces cerevisiae metabolizes gluco

259 The budding yeast Saccharomyces cerevisiae stores iron in th

260 of nuclear microtubule (MT) dynamics in the budding yeast Saccharomyces cerevisiae This activity req

261 In the budding yeast Saccharomyces cerevisiae, ECM remodeling r

262 In budding yeast Saccharomyces cerevisiae, the ten-subunit

263 ys a central role in zinc homeostasis in the budding yeast Saccharomyces cerevisiae.

264 P protein that is homologous to Glo3p of the budding yeast Saccharomyces cerevisiae.

265 unctional similarities between Ppc89 and the budding yeast SPB scaffold Spc42, distribution of Sad1 t

266 dics to investigate the adaptive response of budding yeast to temporally controlled H2O2 stress patte

267 tubules assembled in vitro from mammalian or budding yeast tubulin.

268 the oscillations of the anaphase spindle in budding yeast, but in A. gossypii, this system is not re

269 In budding yeast, cell cycle progression and ribosome bioge

270 In budding yeast, cell size is thought to be controlled alm

271 In budding yeast, cell size primarily modulates the duratio

272 In budding yeast, centromere establishment begins with the

273 This mutant, when expressed in budding yeast, diminished cell growth and DNA replicatio

274 In budding yeast, dynein moves the mitotic spindle to the p

275 In budding yeast, each chromosome has a point centromere up

276 ere are two distinct TRAPP complexes, yet in budding yeast, four distinct TRAPP complexes have been r

277 series of transcriptome sequencing data from budding yeast, in high temporal resolution over ca. 2.5

278 We discovered that in budding yeast, kinetochore inactivation occurs by reduci

279 In budding yeast, polarization is associated with a focus o

280 In budding yeast, Rph1 transcriptionally represses many DNA

281 In budding yeast, the 3' end processing of mRNA and the cou

282 In budding yeast, the nuclear RNA surveillance system is ac

283 In budding yeast, the protein Gps1 plays a pivotal role in

284 , bead-spring representation of chromatin in budding yeast, we find enrichment of protein-mediated, d

285 Budding yeast, which undergoes polarized growth during b

286 and in enhancing promoter directionality in budding yeast.

287 sm for the emergence of copper resistance in budding yeast.

288 conformation and 3D nuclear organization in budding yeast.

289 e signal transduction and gene expression in budding yeast.

290 re immediate effect in the early anaphase of budding yeast.

291 at is called B55 in vertebrates and Cdc55 in budding yeast.

292 owth rate via the TORC2 signaling network in budding yeast.

293 larizes dynein-mediated spindle movements in budding yeast.

294 is play a major role in cell size control in budding yeast.

295 tial to fulfil recombinational DNA repair in budding yeast.

296 g numerous pathways that lack equivalents in budding yeast.

297 one of the two major osmosensing pathways in budding yeast.

298 two splicing isoforms of the same protein in budding yeast.

299 lance of defective nuclear pore complexes in budding yeast.

300 at links mitotic entry to membrane growth in budding yeast.