ライフサイエンスコーパス: yeast cell

1 level of methionine in bacterial as well as yeast cell.

2 enotypes, inactivates mismatch repair in the yeast cell.

3 ion is closely guided by experiments in live yeast cells.

4 nodes and contractile rings in live fission yeast cells.

5 isappearance of mitochondria from the mutant yeast cells.

6 f NAD into peroxisomes against AMP in intact yeast cells.

7 ies of formaldehyde-cross-linking in budding yeast cells.

8 reams and lysis of Rhodosporidium toruloides yeast cells.

9 ges in senescing and post-senescent survivor yeast cells.

10 s cytoplasmic hydrogen ion concentrations in yeast cells.

11 near invaginations at the plasma membrane of yeast cells.

12 l2-L-13 induces mitophagy in Atg32-deficient yeast cells.

13 critical role in metabolic energy control in yeast cells.

14 he toxicity of human alpha-synuclein in live yeast cells.

15 m can be visualized on the surface of living yeast cells.

16 72 is able to inhibit S6K phosphorylation in yeast cells.

17 rion fusions to encode synthetic memories in yeast cells.

18 eisosomes in both fission yeast and budding yeast cells.

19 r redox regulation of calcium homeostasis in yeast cells.

20 al data, and tracking of low-signal mRNAs in yeast cells.

21 ibute to the softening of dough through dead yeast cells.

22 replication defect when expressed in budding yeast cells.

23 anslational modification found in animal and yeast cells.

24 olesterol pathway intermediates in human and yeast cells.

25 he GG-NER E3 ligase, promotes UV survival in yeast cells.

26 r lipid droplet (LD) biogenesis in human and yeast cells.

27 nations into detached vesicles in BAR mutant yeast cells.

28 ophil phagocytosis and subsequent killing of yeast cells.

29 e expression of a protein in a population of yeast cells.

30 fined into the mother compartment of budding yeast cells.

31 g the fidelity of start codon recognition in yeast cells.

32 porters are involved in sugar transport into yeast cells.

33 terologous expression in Xenopus oocytes and yeast cells.

34 on the function of the protein and effect on yeast cells.

35 to characterize Snf1-Mig1 dynamics in single yeast cells.

36 le of nontranslating ribosomes purified from yeast cells.

37 rfering with the cadmium accumulation by the yeast cells.

38 redominant form of mtDNA replication in rho+ yeast cells.

39 that mitophagy is perturbed in CL-deficient yeast cells.

40 accumulation, unlike the OsPCS2b transformed yeast cells.

41 in vitro, and blocked autophagy induction in yeast cells.

42 ggregate activity observed in living budding yeast cells.

43 f m(6)A-modified FAA1 transcripts in haploid yeast cells.

44 to monitor glutathione import into the ER of yeast cells.

45 e joint distributions of mRNA populations in yeast cells.

46 bacteria use lactic acid to communicate with yeast cells.

47 izations as well as phenotypes of expressing yeast cells.

48 artments and cell membrane when expressed in yeast cells.

49 In fission yeast cells, a microtubule-dependent network has been id

50 found that when challenged with glucose, the yeast cells accumulate glycolytic intermediates and ATP,

51 In response to pheromones, yeast cells activate a MAPK pathway to direct processes

52 val in response to sudden glucose depletion, yeast cells activate lipid-droplet (LD) consumption thro

53 Yeast cells activate RNR in response to genotoxic stress

54 When yeast cells adapt to respiration the Snf1/4 glucose-sens

55 These multifunctional yeast cells adhere to the gold sensor surface while simu

56 isolated UPEC was subsequently determined by yeast cell agglutination and immunofluorescence microsco

57 ere, we show that in asymmetrically dividing yeast cells, aggregation of cytosolic misfolded proteins

58 d communities consisting of a basal layer of yeast cells and an upper layer of filamentous cells, tog

59 V2A in hexose transport-deficient EBY.VW4000 yeast cells and demonstrated that these cells are able t

60 , we measure gene network activity in single yeast cells and find that the activity of the compensate

61 Yeast cells and hyphae recovered from the kidney of anti

62 n plant-infecting tombusvirus replication in yeast cells and in vitro using purified components.

63 Moreover, Becn1(+/-) mice as well as yeast cells and nematodes lacking the ortholog of human

64 s rapid screening of ADAR variants in single yeast cells and provides quantitative evaluation for enz

65 Uptake assays with yeast cells and radiolabeled (32)P revealed that PvPht1;

66 ies to track the replicative aging of single yeast cells and reveal that the temporal patterns of het

67 sensitive marker of increased ROS levels in yeast cells and suggest that changes in ribosomes may be

68 significant decrease in both phagocytosis of yeast cells and the frequency of nonlytic exocytosis.

69 e heat-stress response within populations of yeast cells and the presence of subpopulations that are

70 s approach, employing proteomics analysis in yeast cells and transcriptional analysis in human cells.

71 y in cultured mammalian cells, as well as in yeast cells and zebrafish embryos We disrupted murine bd

72 Actin is critical for endocytosis in yeast cells, and also in mammalian cells under tension.

73 mplate for DNA double-strand break repair in yeast cells, and Rad52, a member of the homologous recom

74 When yeast cells are challenged by a fluctuating environment,

75 Fast growing yeast cells are predicted to perform significant amount

76 LM), we probed this question in live fission yeast cells at unprecedented resolution.

77 previously observed that upon expression in yeast cells, bacterial beta-barrel proteins including th

78 As confer a competitive fitness advantage to yeast cells because expression of these non-coding molec

79 f molecular noise that is inevitable in tiny yeast cells, because mistakes in sequencing cell cycle e

80 scriptionally formed G4 DNA in vivo and that yeast cells become highly sensitivity to G4-stabilizing

81 urrent study we found that when expressed in yeast cells both the monomeric and trimeric forms of ful

82 gnificant regulatory variation in individual yeast cells, both before and after stress.

83 (CPDs), increases survival of UV irradiated yeast cells but attenuates TCR.

84 Cdc42 activator, was essential for growth in yeast cells but not in established hyphae.

85 nd is toxic to wheat, tobacco, bacterial and yeast cells, but not to Z. tritici itself.

86 MG inhibits the growth of glucose-fermenting yeast cells by inducing endocytosis and degradation of t

87 ed for oxidative stress responses in fission yeast cells by promoting transcription initiation.

88 platform, we measure noise dynamics in aging yeast cells by tracking the generation-specific activity

89 ully folded bioactive cyclotides inside live yeast cells by using intracellular protein trans-splicin

90 mediate cell signaling events, ensuring that yeast cells can adapt and remain viable.

91 Metabolism in yeast cells can be manipulated by supplying different ca

92 stributes homogeneously in wild-type fission yeast cells, can be made to concentrate at cell ends by

93 Here, we show that fission yeast cells carrying a mutation in the DNA-binding prote

94 Exposure of haploid yeast cells, carrying mating type "a," to "alpha pheromo

95 The major chitin synthase activity in yeast cells, Chs3, has become a paradigm in the study of

96 of alpha-synuclein was also demonstrated in yeast cells coexpressing TG2.

97 Au level was increased in COPT2, expressing yeast cells compared to vector transformed control.

98 duce rejuvenated daughters, dividing budding yeast cells confine aging factors, including protein agg

99 e presence of a proteasome inhibitor or when yeast cells contained mutations in the CDC48 or SSA1 gen

100 Yeast cells containing the intracellular beta-glucosidas

101 nal microscopic diagnosis, as characteristic yeast cells could be observed only in 14 pus samples.

102 two complex biological samples obtained from yeast cell cultures at the proteome level.

103 Using fission yeast cell cycle as an example, we uncovered that the no

104 Empirically, on synthetic yeast cell cycle data, CPchi(2) achieved much higher sta

105 ability, speed and robustness of the fission yeast cell cycle oscillations.

106 In data from the Yeast cell cycle SW1PerS identifies genes not preferred

107 we provide a stochastic model of the budding yeast cell cycle that accurately accounts for the variab

108 rom peripheral leukocytes, brain tissue, and yeast cell cycle, revealed novel marker genes that were

109 expand a previous mathematical model of the yeast cell cycle.

110 ture are linked to ER inheritance during the yeast cell cycle.

111 In budding yeast, cell cycle progression and ribosome biogenesis ar

112 lity, as observed in the budding and fission yeast cell- cycle.

113 Using a well-known yeast cell-cycle data set with 6,178 genes, we identifie

114 We consider yeast cell-cycle gene expression data, and show that the

115 er investigations of the budding and fission yeast cell-cycle, we identify two generic dynamical rule

116 In fission and budding yeast, cell-cycle progression depends on cell size, alth

117 rus, F1L does not prevent caspase-9-mediated yeast cell death.

118 We show that fission yeast cells deficient in ER-PM contacts exhibit aberrant

119 ast homologues are "not essential" proteins, yeast cells deficient in the homologue of PAF53 grow at

120 Yeast cells deficient in the Rieske iron-sulfur subunit

121 Cytokinesis in fission yeast cells depends on conventional myosin-II (Myo2) to

122 In the absence of LDs, yeast cells display alterations in their phospholipid co

123 However, yeast cells display polarized receptors.

124 We show that RNase H2-deficient yeast cells displayed elevated frequency of Rad52 foci,

125 Finally, Yjr129c-deficient yeast cells displayed phenotypes related to eEF2 functio

126 r9 positions mitotic spindles during budding yeast cell division.

127 ined the range of proteins that aggregate in yeast cells during normal growth and after exposure to s

128 w that both vegetative and pheromone-treated yeast cells exhibit discrete and asynchronous Ca(2+) bur

129 Budding yeast cells exist in two mating types, a and alpha, whic

130 the sizes of many mRNAs change when budding yeast cells exit mitosis and enter the meiotic different

131 We study cell polarization when fission yeast cells exit starvation.

132 Compared with yeast cells expressing Arabidopsis thaliana Pht1;5, cell

133 wth of hexose transport-deficient EBY.VW4000 yeast cells expressing human SV2A.

134 Infection of yeast cells expressing the reference SUP35 gene sequence

135 probe the effects of polyethylene glycol and yeast cell extract as crowding agents.

136 alogs to thiophosphorylate its substrates in yeast cell extracts as well as when produced as recombin

137 re-RCs support replication of plasmid DNA in yeast cell extracts in a reaction that exhibits hallmark

138 Yeast cell factories encounter physical and chemical str

139 molecules, have been proposed to explain how yeast cells filter fluctuations and detect shallow gradi

140 In mitotically growing yeast cells, five septin subunits are expressed (Cdc3, C

141 terized by emergence of a germ tube from the yeast cell followed by mold-like growth of branching hyp

142 Purification of Ty1-IN from yeast cells followed by mass spectrometry (MS) analysis

143 eplication of hundreds of individual fission yeast cells for over seventy-five generations.

144 cation of Tomato bushy stunt virus (TBSV) in yeast cell-free extracts and in plant extracts.

145 ngation-can be recapitulated in vitro with a yeast cell-free system.

146 Yeast cells from colonies or liquid cultures are lysed b

147 biased proof that trehalose does not protect yeast cells from dying and that the stress-protecting ro

148 for the SWI/SNF complex in the transition of yeast cells from fermentative to respiratory modes of me

149 Here we find DnaJB6-protected yeast cells from polyglutamine toxicity and cured yeast

150 Rod-shaped fission yeast cells grow in a highly polarized manner, and genet

151 sterol biosynthesis in single living fission yeast cells grown in mixtures of normal and (13)C-labele

152 For yeast cells grown in synthetic defined (SD) medium, the

153 rformed a genome-wide expression analysis in yeast cells grown in the presence or absence of the drug

154 port vigorous and sustainable restoration of yeast cell growth by replacing missing protein ion trans

155 nment and that either K113E or E195K induces yeast cell growth defects rescued by E/K.

156 selected differently in haploid and diploid yeast cells: haploid cells bud in an axial manner, while

157 We demonstrate here that fission yeast cells harbouring a hyperactive Cdc2CDK1 mutation (

158 Budding yeast cells have a finite replicative life span; that is

159 Yeast cells have a single CL-specific phospholipase, Cld

160 n early after telomerase inactivation (ETI), yeast cells have accelerated mother cell aging and mildl

161 ental conditions, employing basic catalysts, yeast cells have become the nucleation centers for a sil

162 Within a single generation time a growing yeast cell imports approximately 14 million ribosomal pr

163 activity of cytochromes b and c in freezing yeast cells in a contactless, label-free manner.

164 d to improve the enrichment of low-abundance yeast cells in an iDEP channel.

165 ies revealed that PfPAT mediated survival of yeast cells in low pantothenate concentrations and resto

166 of Mediator subunits in wild-type and mutant yeast cells in which RNA polymerase II promoter escape i

167 function is required for sterol secretion in yeast cells, indicating that members of this superfamily

168 ch as triterpene sapogenins, from engineered yeast cells into the growth medium, thereby greatly enha

169 Mating of budding yeast cells is a model system for studying cell-cell int

170 mice, secretion of the Cfp4 glycoprotein by yeast cells is consistent across clinical and laboratory

171 Amino acid uptake in yeast cells is mediated by about 16 plasma membrane perm

172 er-recombination phenotype of Top3-deficient yeast cells is partially a result of unprocessed D loops

173 yeast expression system and discovered that yeast cells lacking endogenous potassium channels could

174 function of Dna2 in end resection in budding yeast cells lacking exonuclease 1.

175 itive phenotype that has long been noted for yeast cells lacking functional Get3.

176 Yeast cells lacking LDs are severely defective in PSM gr

177 Yeast cells lacking Msn2 and Msn4 exhibit prevalent repr

178 e concentrations and restored sensitivity of yeast cells lacking pantothenate uptake to fenpropimorph

179 ed, genome-wide synthetic lethal screen with yeast cells lacking profilin (pfy1Delta).

180 to cellular toxicity and cell cycle delay in yeast cells lacking PSH1, but not in cells lacking UBR1,

181 rnover as Cse4 degradation is compromised in yeast cells lacking RCY1 Excessive Cse4 accumulation in

182 of chromosomal rearrangements recovered from yeast cells lacking Sae2 or the Mre11 nuclease.

183 Yeast cells lacking Snf1 (AMP-activated protein kinase)

184 In human somatic cells or yeast cells lacking telomerase, telomeres are shortened

185 Using fission yeast cells lacking the debranching enzyme Dbr1, LaSSO n

186 Yeast cells lacking the ORF YCL047C/POF1 release conside

187 Expression of ORAOV1 restores viability to yeast cells lacking YNL260c.

188 Inhibition of Hsp104 function in yeast cells leads to a failure to generate new propagons

189 Yeast cell lines were genetically engineered to display

190 of millions of individual RNAs isolated from yeasts, cell lines, Arabidopsis thaliana leaves, mouse l

191 and formation of a shmoo-like morphology in yeast cells, lower pheromone doses elicit elongated cell

192 purified a high quantity of mRNA from crude yeast cell lysate compared to a phenol/chloroform extrac

193 closporine A with cyclophilin A protein in a yeast cell lysate is successfully detected and quantifie

194 for cross-linked protein-DNA complexes from yeast cell lysate.

195 Over the course of 17 d, immobilized yeast cells maintained >95% viability, whereas the viabi

196 [GAR(+)] is advantageous to bacteria because yeast cells make less ethanol and is advantageous to yea

197 mimetic FUS reduces aggregation in human and yeast cell models, and can ameliorate FUS-associated cyt

198 XR2), deletion of mitochondrial MXR2 renders yeast cells more sensitive to oxidative stress than the

199 During mating, yeast cells must perforate their rigid cell walls at the

200 homeostasis of cation concentrations in the yeast cells of S. cerevisiae.

201 mely, the geometrical effect of the dividing yeast cell on the diffusion of protein aggregates, and t

202 at constitutive membrane anchoring of GIV in yeast cells or rapid membrane translocation in mammalian

203 ulation of stress tolerance and longevity of yeast cells, our data provide a model in which Sch9 regu

204 rvative replication in extracts from budding yeast cells overexpressing firing factors.

205 l tubes had increased adhesion compared with yeast cells ( P < 0.05).

206 Interestingly, in contrast with animal or yeast cells, plants contain a second nucleolin gene.

207 During yeast cell polarization localization of the small GTPase

208 Yeast cell populations harboring the same defined aneupl

209 In dividing yeast cells, protein aggregates that form under stress o

210 1R) ) in the FRB domain of Tor2 that renders yeast cells rapamycin resistant and temperature sensitiv

211 show that upon growth at higher temperature, yeast cells relax the retention of DNA circles, which ac

212 r fit, our model quantitatively predicts the yeast cell response to pheromone gradient providing an i

213 Nitrogen replenishment of nitrogen-starved yeast cells resulted in substantial transcriptome change

214 gnaling guided neutrophils to migrate to the yeast cells, resulting in optimal phagocytosis and subse

215 enically cooled biological sample--a budding yeast cell (Saccharomyces cerevisiae)--using hard (7.9 k

216 Yeast cells (Saccharomyces cerevisiae and Schizosaccharo

217 Haploid yeast cells secrete mating pheromones that are sensed by

218 Prior work in HeLa and yeast cells showed that a decrease in ATAD5 protein leve

219 report comprehensive ribosome profiling of a yeast cell size series from the time of cell birth, to i

220 In budding yeast, cell size is thought to be controlled almost enti

221 In budding yeast, cell size primarily modulates the duration of the

222 In budding yeast cells, Slx5 resides in the nucleus, forms distinct

223 d abundantly and specifically by Histoplasma yeast cells, suggesting its role in pathogenesis.

224 nked to the end of DNA in RNase H2-deficient yeast cells, supporting this model.

225 We use yeast cell surface display to engineer E6AP to exclusive

226 osition of both murine and human C3 onto the yeast cell surface, with M1g4 showing delayed activation

227 g1 in removing exposed beta-glucans from the yeast cell surface.

228 The yeast cell-surface glucose sensors Rgt2 and Snf3 functio

229 Similarly, in yeast cells that are defective for transcription termina

230 To answer this question, we monitor yeast cells that are genetically engineered to display e

231 In yeast cells that do not readily take up pyruvate, the ad

232 (GET) pathway was described in mammalian and yeast cells that serve as a blueprint of TA protein inse

233 In fission yeast cells, the formin Fus1, which nucleates linear act

234 H did not allow the complete inactivation of yeast cells; the treatment shall be optimized before win

235 of the replicative lifespan, and tracking of yeast cells throughout their entire lifespan.

236 The ability of a yeast cell to propagate [PSI(+) ], the prion form of the

237 Diverse bacteria can elicit yeast cells to acquire [GAR(+)], although the molecular

238 pression assays in Nicotiana benthamiana and yeast cells to examine its functionality.

239 We tested the platform to force yeast cells to express a desired fixed, or time-varying,

240 used time-resolved reporter assays in living yeast cells to gain insights into the coordination of po

241 Transient exposure to lactic acid caused yeast cells to heritably circumvent glucose repression.

242 nthetic genetic array screen using taz1Delta yeast cells to identify genes whose deletion aggravated

243 tion localization microscopy of live fission yeast cells to improve the spatial resolution to approxi

244 tical ER to the plasma membrane in human and yeast cells to maintain ER morphology and stabilize ER-p

245 sensors by glucose concentration may enable yeast cells to maintain glucose sensing activity at the

246 activator of TORC1, is somehow required for yeast cells to recover efficiently from a period of trea

247 llular traffic of the Chs3 protein, allowing yeast cells to regulate morphogenesis, depending on envi

248 Here we characterized mechanisms that allow yeast cells to survive under conditions of thiol peroxid

249 trehalose and/or the Tps1 protein, may serve yeast cells to withstand exposure to stress.

250 highly conserved from simple systems, e.g., yeast cells, to the much more complex human system.

251 d chromosomal loci during interphase in live yeast cells together with polymer models of chromatin ch

252 on on the nature of the encapsulation of the yeast cells, together with the architecture of the three

253 Yeast cells track gradients of pheromones to locate mati

254 de enzymes produced by SSF were utilised for yeast cell treatment leading to simultaneous release of

255 t, we systematically monitored the growth of yeast cells under various frequencies of oscillating osm

256 shown that in response to pheromone, budding yeast cells undergo a rise of cytosolic Ca(2+) that is m

257 osed to a high dose of mating pheromone, the yeast cell undergoes growth arrest and forms a shmoo-lik

258 In a yeast cell undergoing budding, cables are in constant dy

259 Fission yeast cells use Arp2/3 complex and formin to assemble di

260 Ultrastructural analysis of yeast cells using electron microscopy reveals a signific

261 in-containing protein Mps3 on the NE in live yeast cells using fluorescence cross-correlation spectro

262 mmobilizing fungal laccase on the surface of yeast cells using synthetic biology techniques.

263 was found in glycolytic oscillations in real yeast cells, verifying that chronotaxicity could be used

264 n1, a DNA/RNA helicase that is essential for yeast cell viability and homologous to human senataxin,

265 small binders readily penetrate through the yeast cell wall and thus eliminate the requirement for i

266 chemokinesis, whose activity is enhanced by yeast cell wall components and aromatic alcohols.

267 In the present study, the yeast cell wall fractionation process involving enzymati

268 esence of caffeine, a known modulator of the yeast cell wall integrity (CWI) mitogen-activated protei

269 The yeast cell wall integrity MAPK Slt2 mediates the transcr

270 The yeast cell wall of Saccharomyces cerevisiae is an import

271 bone-marrow-derived DCs stimulated with the yeast cell wall preparation zymosan.

272 Results showed that the sorption capacity by yeast cell walls for 4-EG was greater than that for 4-EP

273 tments (activated charcoal, bentonite, PVPP, yeast cell walls, potassium caseinate, zeolite and grape

274 ermodynamics of sorption of 4-EG and 4-EP by yeast cell walls, using a synthetic wine.

275 yield of 18.0% of the original ratio in the yeast cell walls.

276 ic process for the isolation of glucans from yeast cell walls.

277 the ability of adsorbing color molecules by yeasts' cell walls was assessed.

278 of an indirect diffusion of wood aromas from yeast cell-walls.

279 of polyphenols and volatile compounds to the yeast cell-walls.

280 the maximum accumulation of both ions in the yeast cells was observed.

281 er to monitor Fus3 and Kss1 activity in live yeast cells, we demonstrate that overall mating MAPK act

282 wild-type levels of mcm10-m2,3,4 in budding yeast cells, we observed a severe growth defect and a su

283 ing transcription at the GAL locus in living yeast cells, we show that antisense GAL10 ncRNA transcri

284 compaction of the chromatin fiber in living yeast cells, we show that chromosome condensation entail

285 Yeast cells were encapsulated in a matrix consisting of

286 Yeast cells were genetically modified to display both si

287 oleaginous Cryptococcus curvatus VKM Y-3288 yeast cells were immobilized in a bimodal silica-organic

288 incidence of alphaSyn cytoplasmic foci, and yeast cells were rescued from alphaSyn-generated proteot

289 one redox homeostasis were also monitored as yeast cells were subjected to oxidative stress.

290 When yeast cells were treated with hydroxyurea (HU) to block

291 The surface engineered yeast cells were unaffected by the QDs present on their

292 silica capsule was found to form around each yeast cell when using 85 vol% MTES.

293 ntial to aid the enrichment of low-abundance yeast cells when filler volume fractions approximately 1

294 reas it displays internal staining of select yeast cells which also show propidium iodide staining, i

295 This looping provides yeast cells with a transcriptional memory, enabling them

296 Third, treatment of wild-type yeast cells with E9591 or LMT generated cellular defects

297 Treatment of yeast cells with pyrodach-2 (D2) or pyrodach-4 (D4) reve

298 his issue, Dudin et al. image mating fission yeast cells with unprecedented spatiotemporal resolution

299 rowth and DNA replication defects in budding yeast cells, with diminished DDK phosphorylation of Mcm2

300 improved the ability to metabolize xylose of yeast cells without adaptive evolution, suggesting that