ライフサイエンスコーパス: bud

1 pole body (SPB, the yeast centrosome) by the bud.

2 ong which cells move to shape the early limb bud.

3 ich depends on axial progenitors in the tail bud.

4 the vacuole is transported into the emerging bud.

5 c transcriptional activity in the mouse limb bud.

6 posterior addition of tissues from the tail bud.

7 stabilizes the open neck of a nascent COPII bud.

8 into nonaxisymmetric ridges and axisymmetric buds.

9 es in oxygen availability within the dormant buds.

10 puscular endings that appose laryngeal taste buds.

11 innervation of the remaining fungiform taste buds.

12 s branching through local action in axillary buds.

13 ar the bud neck and in the cortex of nascent buds.

14 and translation, as well as deficient viral budding.

15 onal selective phenotype of nuclear membrane budding.

16 on, endosomal vesicle trafficking, and viral budding.

17 cation, and two inhibit virion formation and budding.

18 r1-dependent internal polarity cues used for budding.

19 gar compounds, it was found that fructose in buds (1.56-3.23 g/100 g DW) and glucose in berries (1.96

20 he fresh (1843.71 mg/100 g DW) and fermented buds (1198.54-1539.49 mg/100 g DW) rather than the berri

21 h factor controls WNT signalling in the tail bud(3).

22 n the neuromesodermal precursors of the tail bud(4), WNT signalling promotes the mesodermal fate that

23 le barrier between the mother and developing bud [7-9].

24 forming in-depth analysis of plasma membrane budding, a cellular process that has previously been dis

25 a nucleus in the lower quarter of the taste bud and a foot process extending to the basement membran

26 ique molecular markers separated presumptive bud and duct cells.

27 Cells of the tail bud and the posterior presomitic mesoderm, which control

28 beled vesicles that contain sorted receptors bud and undergo vesicular fission from the sorting endos

29 Ps for the evaluation of mechanisms of viral budding and entry as well as assessment of drug inhibito

30 erived from mitochondrial and nuclear DNA of budding and fission yeast.

31 Cell cycle mutants in the budding and fission yeasts have played critical roles in

32 mportant biological functions, such as viral budding and lipid-protein interactions.

33 In Saccharomyces cerevisiae, budding and mating projection (MP) formation use an over

34 during late stages of Gag assembly and HIV-1 budding and templates ESCRT-III assembly for membrane sc

35 tacks likely affects dynamic control of COPI budding and vesicle fusion at the rims.

36 cetin, and kaempferol increased in fermented buds and berries compared to fresh samples.

37 lity parameters of fresh and fermented caper buds and berries.

38 as clear benefits for the survival of flower buds and flowers, such phenological advancement may disr

39 etabolism was affected differently in floral buds and leaves.

40 ield distribution around the tips of lithium buds and results in homogeneous plating and stripping of

41 uring blastema proliferation (early- to late-bud) and studied its role during tissue regeneration by

42 rs 16 months after transformation and flower buds appeared 30-40 days on juvenile immature scions gra

43 nes required for immature rotavirus particle budding are not an extension of the ER but are COPII-der

44 Mammalian taste buds are comprised of specialized neuroepithelial cells

45 In particular, we show that axisymmetric buds are favored when the induced curvature is rapidly i

46 ectodermal compartment, using the mouse limb bud as a model.

47 les at the plasma membrane and drives virion budding, assisted by the cellular endosomal complex requ

48 erized in yeast, where they regulate vesicle budding at the trans-Golgi network.

49 Past studies predict that the cell membrane buds at low resting tensions and stalls at a flat pit at

50 ilaments that are organized along the mother-bud axis associate with circumferential single septin fi

51 ially organized and aligned along the mother-bud axis to facilitate polarized vesicle traffic.

52 ctin cables and aligns them along the mother-bud axis.

53 We hypothesize that during nuclear budding, binding of UL25 situated at the pentagonal caps

54 x fetu kidney rudiments, engineered ureteric buds branched and induced nephron formation; when grafte

55 Engineered ureteric buds branched in three-dimensional culture and expressed

56 trophic factor, a crucial factor in ureteric bud branching and subsequent nephron development.

57 ecification, low temperature-mediated floral bud break, early blooming in winter, and strong cold tol

58 tion of the growth-inhibited meristem during bud-break.

59 ought to play a supportive role in the taste bud, but little research has been done to explore their

60 MAT2) does not sort directly onto SGs during budding, but rather exit the TGN into nonregulated vesic

61 r C:N ratios and the presence of belowground buds, but was unrelated to photosynthetic pathway.

62 mic vs. viral nucleocapsids demonstrate that budding causes discrete changes in Cp-gRNA interactions.

63 can substitute for neuronal input for taste bud cell replenishment and taste bud maintenance.

64 regions of interest, micro tumor structure, budding, cell proliferation and tumor lymph vessels were

65 Type II and III taste bud cells (TBCs) detect molecules described by humans as

66 igation on the role of type I GAD65(+) taste bud cells (TBCs) in taste-mediated physiology and behavi

67 bsence of R-spondin in culture medium, taste bud cells are not generated ex vivo.

68 Taste bud cells regenerate throughout life.

69 em cells can be differentiated into ureteric bud cells.

70 For example, small budding cells use very different strategies to dissemina

71 s in patients with hepatic vein obstruction (Budd-Chiari Syndrome) and in those with portal vein thro

72 Taste buds comprise four types of taste cells: three mature, e

73 c master regulator), the absence of membrane budding correlates with failure of in vivo platelet prod

74 Ubiquitylation of the Vac17 adaptor at the bud cortex provides spatial regulation of vacuole releas

75 Once the vacuole is brought to the bud cortex via the Myo2-Vac17-Vac8 complex, Vac17 is deg

76 e than a century ago it was shown that taste buds degenerate after their innervating nerves are trans

77 They also retain H3K27ac enrichment in limb buds devoid of GLI activator and repressor, indicating t

78 In the emerging limb buds, different subgroups of Hoxd genes respond first to

79 e characterized isolated engineered ureteric buds differentiated from embryonic stem cells in three-d

80 ilitate ILV formation: Upstream ESCRT-driven budding does not require ATP consumption as only a small

81 rest by repressing genes related to axillary bud dormancy in the SAM and negative regulators of cytok

82 thylene signaling appears critical for grape bud dormancy release.

83 ng conifers, leading to cessation of growth, bud dormancy, freezing tolerance and changes in energy m

84 ry aspect of plant development from seed and bud dormancy, liberation of meristematic cells from the

85 Movement of half of the nucleus into the bud during anaphase causes the active form of the MEN GT

86 ge-scale viral processes including assembly, budding, egress, entry, and fusion.

87 ulla are derived from Pax2-positive ureteric bud epithelia that continue to express Pax2 and Pax8 in

88 ry mesenchyme that immediately surrounds the budding epithelium.

89 We proceeded to catalog the response of all bud-expressed ERFs, and identified additional ERFs that

90 Offspring also exhibited increased taste bud expression of mRNA for sweet receptor subunits T1R (

91 P/F 100/6 two inhalations b.i.d. (n = 31) or BUD/F 200/6 two inhalations b.i.d. (n = 29).

92 on low-dose ICS/LABA budesonide/formoterol (BUD/F) 200/6 one inhalation b.i.d.

93 In this primer, we review the budding field of motion capture with deep learning.

94 We then discuss the budding field of precision fMRI and findings garnered fr

95 Filoviruses such as Ebola and Marburg virus bud from the host membrane as enveloped virions.

96 only viral component required for retroviral budding from infected cells.

97 m producer cell plasma membranes, suggesting budding from specialized membrane microdomains.

98 ly acting endosomal factor involved in HIV-1 budding from the cells.

99 localization of SG cargoes immediately after budding from the TGN revealed that, surprisingly, the bu

100 Previous work reported Gag budding from yeast spheroplasts, but Gag release was ESC

101 e show that loss of GPR31 impairs pancreatic bud fusion and pancreatic duct morphogenesis.

102 ned by varying the relative rates of vesicle budding, fusion and biochemical conversion.

103 Tree-in-bud, ground-glass-opacity, bronchiectasis, cicatricial e

104 Suppression of bud growth may be attained by direct binding of NtBRCs t

105 ding, a routine procedure that prevents horn bud growth through cauterization, is painful for calves.

106 In cuttlefish limb buds, Hedgehog is expressed anteriorly.

107 n cellular protein that is incorporated into budding HIV-1 particles and reduces HIV-1 infectivity by

108 that upon ectopic expression in distal limb buds, HOXA11 binds sites normally HOX13-specific.

109 a consequence of an energy crisis within the bud; (ii) VvERF-VIIs function as part of an energy-regen

110 ntivirus-host interactions involved in virus budding.IMPORTANCE FIV is a nonprimate lentivirus that i

111 With the discovery of lateral budding in 'Kolteria novifilia' and the capability of th

112 imulates proliferation in crypts and induces budding in organoids, in part through elevated and susta

113 the chorda tympani nerve to innervate taste buds in fungiform papillae.

114 dest but significant loss of fungiform taste buds in Phox2b-Cre; p75(fx/fx) mice, although there was

115 vation pattern and the discovery of terminal buds in the external surface of the filaments, we demons

116 Here, we deepen our understanding of prazole budding inhibition by studying a range of viruses in the

117 t define specific cellular landmarks for the bud initiation stage, when the neural crest-derived ecto

118 aracterize their molecular identities during bud initiation.

119 There is strong evidence for gut-taste bud interactions that influence taste function, behavior

120 Elongation of such a bud into a transport intermediate commensurate with bulk

121 iver organoids from iPSCs, namely iPSC-liver buds (iPSC-LBs), by mimicking the organogenic interactio

122 colysis regulates WNT signalling in the tail bud is currently unknown.

123 Here we show that the mammalian tail bud is generated through an independent functional devel

124 and how curved coats are generated to enable budding is yet unclear.

125 of the mammary placode or descending mammary bud, it is essential for both the prenatal hormone-indep

126 (neuro-)endocrine cells, we now quantify TGN budding kinetics of constitutive and regulated secretory

127 evelopment starts with the formation of limb buds (LBs), which consist of tissues from two different

128 Here we used chicken embryos and human tail bud-like cells differentiated in vitro from induced plur

129 ic membrane-derived cholesterol, we observed budding lipid membranes elongating into the cytosol and/

130 Taste bud maintenance depends on continuous replacement of sen

131 t for taste bud cell replenishment and taste bud maintenance.

132 tion of differentiated taste cells and taste bud maintenance.

133 velopmental regulatory system and a ureteric bud marker.

134 provide compelling support for the proposed budding mechanism, where each nascent betaOMP forms a hy

135 cle coat and progress on understanding COPII budding mechanisms are considered.

136 reduce the virus's ability to accumulate at budding microdomains and the VS.

137 ings imply that IRX3/5 coordinate early limb bud morphogenesis with skeletal pattern formation.

138 c10, Cdc11, Cdc12, and Shs1) localize to the bud neck and form an hourglass before cytokinesis that a

139 a membrane, concentrated in patches near the bud neck and in the cortex of nascent buds.

140 w that Hof1 and septins are patterned at the bud neck into evenly spaced axial pillars (~200 nm apart

141 est that Hof1, while bound to septins at the bud neck, not only regulates Bnr1 activity, but also bin

142 Here, we show that the bud neck-associated F-BAR protein Hof1, independent of i

143 cellular machinery that coats the inside of budding necks to perform membrane-modeling events necess

144 lying NtBRC2A-mediated outgrowth of axillary buds needs to be further addressed.

145 ridisation for RFX6 in the dorsal pancreatic bud of a Carnegie stage 14 human embryo.

146 P egress and that Amot co-expression rescues budding of eVP40 VLPs in a dose-dependent and PPxY-depen

147 When expressed alone, VP40 induces budding of filamentous virus-like particles, suggesting

148 lar protein Alix is sufficient to rescue the budding of FIV mutants devoid of canonical L-domains.

149 that is activated during, or shortly after, budding of viral particles from the surface of infected

150 ix protein (eVP40) orchestrates assembly and budding of virions in part by hijacking select WW-domain

151 Buds of horse-chestnut trees are covered with a viscous

152 Dried flower buds of Japanese sophora (Sophora japonica) comprising r

153 which transmits taste information from taste buds on the anterior tongue to the brain, previously rev

154 Geophytes, plants with buds on underground structures, are found throughout the

155 e winter/spring transition may damage flower buds or open flowers, limiting fruit and seed production

156 ells, the developmental ontology of the limb bud, or definitive endoderm.

157 Axillary bud outgrowth in general is negatively regulated by the

158 on the Wolffian duct that regulates ureteric bud outgrowth in the development of a functional renal s

159 gnals involved in the regulation of axillary bud outgrowth.

160 ive PTB were centrilobular nodules, 'tree-in-bud' pattern densities, macro-nodules, consolidations, c

161 nce of the geophytic habit (i.e. belowground bud placement).

162 ecification of the paraxial mesoderm in tail bud precursors.

163 ern formation, IRX3/5 help to shape the limb bud primordium by promoting the separation and intercala

164 -1 release, but how ESCRTs contribute to the budding process and how their activity is coordinated wi

165 stically divergent ESCRT-mediated lentivirus budding process in general, and to the role of Alix in p

166 Accordingly, we propose that membrane budding, rather than proplatelet formation, supplies the

167 uired to reduce the amount of protein in the budded region by one half, and find a quadratic relation

168 Our studies demonstrate that membrane budding results in the sustained release of platelets di

169 with fatty acyl-coenzyme A ligase Faa1 at LD bud sites.

170 (CG) simulations of ESCRT assembly at HIV-1 budding sites suggest that formation of a 12-membered ri

171 membrane and recruiting nucleocapsids to the budding sites.

172 (Shh) signalling in the embryonic chick wing bud specifies positional information required for the fo

173 ispensable for Alix-mediated rescue of virus budding, suggesting the involvement of other regions of

174 Active growth of tiller bud (TB) requires high amount of mineral nutrients; howe

175 lands, lung, and kidney, arise as epithelial buds that are morphologically very similar.

176 ning of the limbs, the formation of the limb bud, the establishment of the principal limb axes, the s

177 I vesicles likely become tethered while they bud, thereby promoting efficient retrograde transport.

178 anodes, particularly on the tips of lithium buds, through spatial conformation and secondary structu

179 g; however, the mechanisms controlling human bud tip differentiation into specific lineages are uncle

180 Here, we used homogeneous human bud tip organoid cultures and identified SMAD signaling

181 Bud tip progenitor cells give rise to all murine lung ep

182 elopmental biology, human lung organoids and bud tip progenitor organoids may be implemented in regen

183 ied SMAD signaling as a key regulator of the bud tip-to-airway transition.

184 This engineered ureteric bud tissue also organized the mesenchyme into smooth mus

185 ic stem cells to differentiate into ureteric bud tissue.

186 the characteristic shapes from branched and budded to invaginated structures.

187 as well as their ability to undergo amitotic budding to escape dormancy.

188 the root was highly correlated with root-to-bud transport of theanine, in seven tea plant cultivars.

189 d body plan, primarily multiplying through a budding type of asexual reproduction.

190 In murine circumvallate taste buds, Type I cells represent just over 50% of the popula

191 Ectopic or supernumerary ureteric bud (UB) branches can result in urinary tract obstructio

192 gametophore initial cells are produced, and buds undergo premature developmental arrest.

193 First, a hemogenic progenitor buds up from the endothelium and undergoes division form

194 containing filopodial protrusions possessing budding viral particles.

195 ses HIV-1 infectivity when incorporated into budding virions.

196 Similarly, antioxidant capacity of buds was found to be markedly higher than berries.

197 clade to divide by binary fission as well as budding, we identified previously unknown modes of bacte

198 l phenolic components in fresh and fermented buds while quercetin-3-O-rutinoside in fresh and ferment

199 in, premalignant basal cell carcinomas form 'buds', while invasive squamous cell carcinomas initiate

200 ling of the basement membrane promote tumour budding, while stiffening of the basement membrane promo

201 mproved detection technique for end users in bud-wood certification and quarantine programs and a pro

202 -dimensional structure of pericentromeres in budding yeast (Saccharomyces cerevisiae) and establish t

203 n TMEM165 by heterologously expressing it in budding yeast (Saccharomyces cerevisiae) and in the bact

204 The lysosomal vacuole of budding yeast (Saccharomyces cerevisiae) has served as a

205 active subunit Rrp44/Dis3 of the exosome in budding yeast (Saccharomyces cerevisiae) is considered a

206 The yeast vacuolar H(+)-ATPase (V-ATPase) of budding yeast (Saccharomyces cerevisiae) is regulated by

207 Budding yeast (Saccharomyces cerevisiae) responds to low

208 Here, we used budding yeast (Saccharomyces cerevisiae) to explore how

209 In budding yeast (Saccharomyces cerevisiae), EVs function a

210 K-PPn was originally discovered in budding yeast (Saccharomyces cerevisiae), in which polyP

211 tages, we developed a method for scRNAseq in budding yeast (Saccharomyces cerevisiae).

212 e modeled pathogenic EXOSC5 variants in both budding yeast and mammalian cells.

213 Using the budding yeast Ase1, we identify unique contributions for

214 Budding yeast can produce ATP from carbon sources by mec

215 We conclude that aneuploid budding yeast cells mount the ESR, rather than the CAGE

216 The gene that allows budding yeast cells to switch their mating type evolved

217 The localization of Ipl1 to kinetochores in budding yeast depends upon multiple pathways, including

218 ior requires the microtubule regulator Stu2 (budding yeast Dis1/XMAP215 ortholog), which we demonstra

219 Budding yeast divide asymmetrically and HO is expressed

220 Using the reconstituted budding yeast DNA replication system, we find that the f

221 Our findings indicate that size control in budding yeast does not fundamentally originate from the

222 Here, we find that involvement of the budding yeast Hsp70 chaperones Ssa1 and Ssa2 in nuclear

223 our assay robustly detects small changes in budding yeast initiation kinetics, which could not be re

224 nto the first gap phase of the cell cycle in budding yeast is controlled by the Mitotic Exit Network

225 Here, we show that key functions of budding yeast Kinesin-14 Cik1-Kar3 are accomplished in a

226 ored the potential for autophagy to regulate budding yeast meiosis.

227 examine the DDC, induced by DNA DSBs, in the budding yeast model system and in mammals.

228 Here, we uncover a mechanism by which budding yeast modulate viscosity in response to temperat

229 Fission yeast Mso1 shares homology with budding yeast Mso1 and human Mint1, proteins that intera

230 ears ago, the first isolation of conditional budding yeast mutants that were defective in cell divisi

231 tly image and quantitate these dynamics in a budding yeast nuclear extract that reconstitutes activat

232 Here, we show that Mph1, the budding yeast ortholog of Fanconi anemia helicase FANCM,

233 reconstituting these processes with purified budding yeast proteins, we show that ubiquitylation is t

234 The Mitotic Exit Network (MEN), a budding yeast Ras-like signal transduction cascade, tran

235 cative DNA helicase, CMG, demonstrating that budding yeast replisomes lack intrinsic mechanisms that

236 Using reconstituted budding yeast replisomes, we show that mutational inacti

237 Modeling the dysregulation in budding yeast resulted in disrupted structural integrity

238 start sites (TSSs) has been identified in a budding yeast Saccharomyces cerevisiae ("scanning model"

239 The budding yeast Saccharomyces cerevisiae divides asymmetri

240 Genetic screening in the budding yeast Saccharomyces cerevisiae has isolated seve

241 c view of the eukaryal cell cycle, using the budding yeast Saccharomyces cerevisiae Protein synthesis

242 In the budding yeast Saccharomyces cerevisiae, nearly all H2A i

243 In the budding yeast Saccharomyces cerevisiae, the five mitotic

244 In the budding yeast Saccharomyces cerevisiae, we demonstrate t

245 Here, using the budding yeast Saccharomyces cerevisiae, we report the di

246 -driven reaction cycle of condensin from the budding yeast Saccharomyces cerevisiae.

247 tructed by cloning the centromere DNA of the budding yeast Saccharomyces cerevisiae.

248 The budding yeast SCF(Met30) complex is an essential cullin-

249 Budding yeast SER3 is repressed under serine-replete con

250 Here we purified the budding yeast Smc5/6 holocomplex and characterized its c

251 n (iHyPr) to combine the genomes of multiple budding yeast species, generating Saccharomyces allopoly

252 A strain of budding yeast that contains one large chromosome reveals

253 Using budding yeast to gain temporal and genetic traction on c

254 We show that budding yeast Ty3/Gypsy co-opts binding sites of the ess

255 The budding yeast v-SNARE, Snc1, mediates fusion of exocytic

256 rom IMR90 (human lung fibroblast), and (iii) budding yeast whole-genome Hi-C data at a single restric

257 nced toolbox of cell cycle tag constructs in budding yeast with defined and compatible peak expressio

258 In budding yeast, a conserved signaling network surrounding

259 We investigated these questions in budding yeast, an organism found in diverse environments

260 to show that autoinhibition is conserved in budding yeast, and plays a key role in coordinating in v

261 h defined positions throughout the genome of budding yeast, as seen in mammalian cells.

262 In budding yeast, CDK substrates with Leu/Pro-rich (LP) doc

263 In budding yeast, cortical and cytoplasmic ER-phagy require

264 In budding yeast, histone H3 threonine 11 phosphorylation (

265 In budding yeast, meiotic kinetochore remodeling is mediate

266 In budding yeast, Saccharomyces cerevisiae, CR is commonly

267 We used the budding yeast, Saccharomyces cerevisiae, to investigate

268 We forced the budding yeast, Saccharomyces cerevisiae, to use the meio

269 g the hourglass-to-double-ring transition in budding yeast, septins acquire a "zonal architecture" in

270 he environment drive cell fate decisions. In budding yeast, the decision to enter meiosis is controll

271 In budding yeast, the myosin-V Myo2 is aided by the kinesin

272 In budding yeast, the retention of kinetochores on dynamic

273 Prior to anaphase of budding yeast, the ribosomal DNA (RDN) condenses to a th

274 In budding yeast, the transcription factors SBF and MBF act

275 In aneuploid budding yeast, two opposing gene-expression patterns hav

276 ion of two plant AMTs (AtAMT1;2 and AMT2) in budding yeast, we found that systematic replacements in

277 To overcome these hurdles for budding yeast, we recently optimized an artificial fluor

278 tion systems by using extracts prepared from budding yeast, wheat germ, and rabbit reticulocyte lysat

279 focus on recent systematic studies, many in budding yeast, which have revealed that large numbers of

280 ding intermediates prior to DNA insertion in budding yeast.

281 or the asymmetric cell shape and division of budding yeast.

282 s the centromeric base of the kinetochore in budding yeast.

283 at centromeric (CEN) chromatin in wild-type budding yeast.

284 biquitin chain required for damage bypass in budding yeast.

285 litates MutLgamma-dependent crossing over in budding yeast.

286 e first cell division cycle (CDC) mutants in budding yeast.

287 unction for MRX in limiting transcription in budding yeast.

288 p40, an essential RNA-splicing factor in the budding yeast.

289 nfluences both of these replication steps in budding yeast.

290 is orchestrated by the Atg1-Atg13 complex in budding yeast.

291 ents suggest that bet hedging has evolved in budding yeast.

292 emerging coding sequences impact fitness in budding yeast.

293 3' exoribonuclease, as a cofactor of RNAi in budding yeast.

294 To identify other factors that act in the budding-yeast pathway, we performed an unbiased genetic

295 romyces cerevisiae, RNAi is present in other budding-yeast species, including Naumovozyma castellii,

296 variation to uncover a novel means by which budding yeasts can overcome highly successful genetic pa

297 Compared to other budding yeasts in the subphylum Saccharomycotina, we not

298 s in Saccharomyces cerevisiae and some other budding yeasts, but most eukaryotes lack sequence-specif

299 e split of Yarrowia lipolytica and the other budding yeasts.

300 nuclear parasites that have co-evolved with budding yeasts.