ライフサイエンスコーパス: S. cerevisiae

1 S. cerevisiae declined in fitness along the evolution ex

2 S. cerevisiae GAL genes thus encode a regulatory program

3 S. cerevisiae Hop1 and Red1 are essential structural com

4 S. cerevisiae is found in multiple environments-one of w

5 S. cerevisiae Sir1, enriched at the silencers of HMLalph

6 S. cerevisiae was grown in YNB media, containing randomi

7 checkpoint with checkpoint initiators 9-1-1 (S. cerevisiae Ddc1-Mec3-Rad17 and human Rad9-Rad1-Hus1)

8 acterising 1,068 and 970 polymorphisms in 34 S. cerevisiae and 26 S. paradoxus strains respectively.

9 ually edited and annotated the genomes of 93 S. cerevisiae strains from multiple geographic and envir

10 These 93 S. cerevisiae strains, the genomes of which are near-ref

11 n unexpected resistance to cytotoxicity by a S. cerevisiae mutant with ablated post-transfer editing

12 ertebrate cofilin rescues the viability of a S. cerevisiae cofilin deletion mutant only when the stif

13 Here we identified the mRNA targets of a S. cerevisiae PUF protein, Puf5p, by ultraviolet-crossli

14 to analyze pheno-metabolomic diversity of a S. cerevisiae strain collection with different origins.

15 e wealth of mutations identified that affect S. cerevisiae MMR.

16 cluding Kluyveromyces lactis and alternative S. cerevisiae strains.

17 Surprisingly, although S. cerevisiae Hop1, a component of synaptonemal complex

18 SID showed clear differences among S. cerevisiae populations in grape fermentation samples,

19 Untargeted metabolomics analysis of an S. cerevisiae deletion mutant of YDR109C revealed ribulo

20 atabolism genes, conferred the ability of an S. cerevisiae strain to efficiently metabolize DEHU and

21 to TORC1 may differ between C. albicans and S. cerevisiae The converse direction of signaling from T

22 ll cycle in HeLa (human cervical cancer) and S. cerevisiae cells.

23 prokaryotes and eukaryotes (i.e. E. coli and S. cerevisiae).

24 monitor antimicrobial effects on E. coli and S. cerevisiae.

25 n of Arabidopsis, mammalian, C. elegans, and S. cerevisiae RBPs reveals a common set of proteins with

26 vity relationships in both P. falciparum and S. cerevisiae.

27 he luminal domains of S. cerevisiae Gpi8 and S. cerevisiae Gpi16 do not interact directly, nor do the

28 an and mouse, as well in D. melanogaster and S. cerevisiae.

29 organisms--H. sapiens, D. melanogaster, and S. cerevisiae--and show that, as compared to other annot

30 indicate that APA mechanisms in S. pombe and S. cerevisiae are largely different: S. pombe has many o

31 on some key differences between S. pombe and S. cerevisiae is included for readers with some familiar

32 consistent differences between in vitro and S. cerevisiae (in vivo) Cas9 cleavage specificity profil

33 also associated with a higher level of anti-S. cerevisiae antibodies.

34 activity, MBL2 and NOD2 polymorphisms, anti-S. cerevisiae antibody levels and clinical Crohn's disea

35 However, the anti-S. cerevisiae Ab levels showed a significant inverse cor

36 that the Pcasf1 cDNA expressed in asf1Delta S. cerevisiae cells can restore growth to wild-type leve

37 proteins in the same individual asynchronous S. cerevisiae cells, with and without DNA damage by meth

38 SEC23B encodes Sec23 homolog B (S. cerevisiae), a component of coat protein complex II (

39 n has undergone significant rewiring between S. cerevisiae and C. lusitaniae, and that a concerted se

40 th corresponding experimental data from both S. cerevisiae and human cells and provides a quantitativ

41 ates supporting significant activity of both S. cerevisiae and E. coli HADs includes 28 common metabo

42 imination against non-protein amino acids by S. cerevisiae PheRS and support a non-canonical role for

43 phagy is the cell survival mechanism used by S. cerevisiae in response to glucose starvation.

44 luminal domain of Saccharomyces cerevisiae (S. cerevisiae) Gpi8 using different expression systems,

45 (MDSet) in interaction networks of E. coli, S. cerevisiae and H. sapiens, defined as subsets of prot

46 When combined, S. cerevisiae GAL coding regions gave rise to profound g

47 size differences among APA isoforms than did S. cerevisiae PASs in different locations of gene are su

48 h quality genome sequences from 11 different S. cerevisiae strains and stored in the SGD.

49 ces cerevisiae First, analysis of 36 diverse S. cerevisiae isolates revealed evidence of numerous pas

50 cursor into two modules, expressed in either S. cerevisiae or E. coli, neither of which can produce t

51 Here we use an engineered S. cerevisiae BY4742 strain, containing an established h

52 e design and synthesis of synIII establishes S. cerevisiae as the basis for designer eukaryotic genom

53 f gene regulation in a single-cell eukaryote S. cerevisiae is affected by interactions between transc

54 Like other eukaryotes, S. cerevisiae undergoes a dramatic reprogramming of gene

55 action of DspA/E, we screened the Euroscarf S. cerevisiae library for mutants resistant to DspA/E-in

56 For nearly every S. cerevisiae gene, the Regulation page displays a table

57 enced 28 genomes from experimentally evolved S. cerevisiae lines and found more mutations in duplicat

58 the direct binding of recombinant expressed S. cerevisiae ScUpc2 and pathogenic Candida albicans CaU

59 oped a rapid and efficient xylose-fermenting S. cerevisiae through rational and inverse metabolic eng

60 ofmeister series, as observed previously for S. cerevisiae.

61 Additionally, we argue that for S. cerevisiae the "volume increment" is not added from b

62 pigenetic states in fungi that diverged from S. cerevisiae ~200 million years ago, and in which gluco

63 ochemical studies of RNA bound exosomes from S. cerevisiae revealed that the Exo9 central channel gui

64 f seven galactose (GAL) metabolic genes from S. cerevisiae, when introduced together into S. bayanus,

65 known now 26) is a putative ENT homolog from S. cerevisiae that is expressed in vacuole membranes.

66 f the UBL domain of the WDR12 homologue from S. cerevisiae at 1.7 A resolution and demonstrate that h

67 s-end transport using purified proteins from S. cerevisiae and dissect the mechanism using single-mol

68 the ubiquitin-bound structure of Rpn11 from S. cerevisiae and the mechanisms for mechanochemical cou

69 the mediators inhibit electron transfer from S. cerevisiae.

70 - and six-gene pathways by VEGAS to generate S. cerevisiae cells synthesizing beta-carotene and viola

71 ic forms in the heterologous expression host S. cerevisiae where we were able to apply yeast genetic

72 However, S. cerevisiae uses a chemically inefficient pathway for

73 ol can be successfully exploited to identify S. cerevisiae strains in any kind of complex samples.

74 In S. cerevisiae strains, D. hansenii genes adopt the S. ce

75 In S. cerevisiae, less Pho2-dependent Pho4 orthologs induce

76 In S. cerevisiae, phosphorylation of the exocyst component

77 In S. cerevisiae, the phosphate starvation (PHO) responsive

78 In S. cerevisiae, there was no evidence for a dominant-nega

79 mammalian cells, and functional analysis in S. cerevisiae.

80 redate the sub-functionalization apparent in S. cerevisiae after the genome duplication.

81 technique for visualization of the areas in S. cerevisiae cells which contain higher amount of calci

82 egregated even within single mother cells in S. cerevisiae.

83 or producing fatty acid-derived chemicals in S. cerevisiae.

84 sembly, producing a functional chromosome in S. cerevisiae.

85 -7 subunits, and MSSB mutant combinations in S. cerevisiae Mcm2-7 are not viable.

86 Our data suggest that eccDNAs are common in S. cerevisiae, where they might contribute substantially

87 ce lifespan extension under CR conditions in S. cerevisiae.

88 By contrast, in S. cerevisiae, the linkage of the heteromer to Rap1 occu

89 of submitochondrial protein distribution in S. cerevisiae.

90 ns, TSSs are located 40-120 bp downstream in S. cerevisiae.

91 le for loss of transcription around a DSB in S. cerevisiae.

92 sential for the normal functions of eEF1A in S. cerevisiae However, eEF1A glutaminylation slightly re

93 The results suggest that ES7 in S. cerevisiae could play a role analogous to the multi-s

94 Complementation experiments in S. cerevisiae provide evidence for the ability of SiPHT1

95 hrome P450 enzyme DesC was also expressed in S. cerevisiae and was found to regio- and stereoselectiv

96 Pah1 expressed in S. cerevisiae or Escherichia coli was not degraded by th

97 reduces the levels of gfp mRNA expression in S. cerevisiae cells, with a concomitant decrease in gree

98 expression cassettes to enable expression in S. cerevisiae.

99 ogue of IME2, a 'diploid-specific' factor in S. cerevisiae, and STE12, the master regulator of S. cer

100 ne regulation for 5 transcription factors in S. cerevisiae.

101 HEM15 encoding the enzyme ferrochelatase in S. cerevisiae and performed a genetic suppressor screen.

102 Consistent with findings in S. cerevisiae, MoGlo3 is localized to the Golgi, and tha

103 capitulate wild-type function and fitness in S. cerevisiae We also find that the electrostatic charge

104 for the Paf1C in snoRNA 3'-end formation in S. cerevisiae, implicates the participation of transcrip

105 and compared them to those already found in S. cerevisiae We observed common features between the tw

106 Vps4 proteins and blocked Vps4p function in S. cerevisiae.

107 SynIII is functional in S. cerevisiae.

108 II transcription, with about 10% of genes in S. cerevisiae dependent on SAGA.

109 The RPS23 hydroxylases in S. cerevisiae (Tpa1p), Schizosaccharomyces pombe and gre

110 due to its large molecular mass (252 kDa in S. cerevisiae).

111 s nonacetylatable Smc3 mutants are lethal in S. cerevisiae, they are not in S. pombe We show that the

112 that involves nascent transcript mapping in S. cerevisiae strains containing foreign yeast DNA.

113 between Sch9 and sphingolipid metabolism in S. cerevisiae in vivo based on the observation that the

114 tions to rewire central carbon metabolism in S. cerevisiae, enabling biosynthesis of cytosolic acetyl

115 exts consistent with cytosine methylation in S. cerevisiae.

116 Using fast DNA tracking microscopy in S. cerevisiae cells and improved analysis of mean square

117 tes the deposition of these modifications in S. cerevisiae under conditions of replicative stress.

118 ASC1 mutants in S. cerevisiae display compromised translation of specifi

119 The 390Q mutation in S. cerevisiae TUB2 did not affect growth under basal con

120 able by A/T frequency in S. pombe but not in S. cerevisiae, suggesting that the genomes and DNA bindi

121 C1 to the PHO regulon previously observed in S. cerevisiae was genetically shown in C. albicans using

122 at the HML and HMR loci than was observed in S. cerevisiae.

123 titative measures of nucleosome occupancy in S. cerevisiae, Schizosaccharomyces pombe, and human cell

124 an short ones, a feature that is opposite in S. cerevisiae Differences in PAS placement between conve

125 ltaneously deleting a duplicate gene pair in S. cerevisiae reduces fitness significantly more than de

126 terpenes via the mevalonate (MEV) pathway in S. cerevisiae, we detail procedures for extraction and d

127 ase(s) responsible for activating the PDC in S. cerevisiae has not been conclusively defined.

128 Functional genomic analysis was performed in S. cerevisiae and zebrafish.

129 Functional studies performed in S. cerevisiae showed that the loss of HRP1 (yeast orthol

130 Our data show that pH in S. cerevisiae changes over several time scales, and that

131 fast-sedimenting, multicellular phenotype in S. cerevisiae.

132 induces three times as many genes as Pho4 in S. cerevisiae does.

133 fine Ptc6p as the primary PDC phosphatase in S. cerevisiae Our analyses further suggest additional su

134 etion mutants of kinases and phosphatases in S. cerevisiae we show that epistatic NEMs can point to m

135 an, i.e., the major carbohydrates present in S. cerevisiae, and principal components analysis reveale

136 ering high-level sesquiterpene production in S. cerevisiae often requires iterations of strain modifi

137 fer a revised view of mitotic progression in S. cerevisiae that augments the relevance of mechanistic

138 cription from the synthetic tetO promoter in S. cerevisiae is dominated by its dependence on the cell

139 , cytoplasmic, and mitochondrial proteins in S. cerevisiae and S. pombe.

140 We addressed this question in S. cerevisiae, where tropomyosins (Tpm1 and Tpm2), profi

141 ome-wide searches for lifespan regulators in S. cerevisiae have never identified Pho85p.

142 sium and zinc accumulation, respectively, in S. cerevisiae.

143 erase and H3K4 demethylase, respectively, in S. cerevisiae.

144 ty with the glucose sensors Snf3 and Rgt2 in S. cerevisiae.

145 of deleting a histone deacetylase (rpd3) in S. cerevisiae.

146 r genes (25S rDNA, ARX1, CTT1, and RPL30) in S. cerevisiae under normal and stressed conditions.

147 Here we used a novel genetic screen in S. cerevisiae to identify mutants with defects in lipid

148 h of negative autoregulation to that seen in S. cerevisiae.

149 uses methyl methane sulfonate sensitivity in S. cerevisiae.

150 iction tools to screen intronic sequences in S. cerevisiae and 36 other fungi.

151 likely to contribute to glucose signaling in S. cerevisiae on the level of ScHxk2-S15 phosphorylation

152 We observed phenotypic similarity in S. cerevisiae genetic interaction data between mitochond

153 it is a key regulator of meiotic splicing in S. cerevisiae.

154 systematically identified its substrates in S. cerevisiae using phosphoproteomics and bioinformatics

155 E. coli and triacetic acid lactone (TAL) in S. cerevisiae revealed that the identified interventions

156 Expression of TbPT0 in S. cerevisiae reveals that TbPT0 is a high affinity pyru

157 omosomal reshuffling, with a higher tempo in S. cerevisiae.

158 nificantly better conserved in human than in S. cerevisiae.

159 ssue, Deng et al. (2015) demonstrate that in S. cerevisiae RPA and Mre11-Sae2 cooperate to prevent th

160 s, a biochemical basis of copper-toxicity in S. cerevisiae is analogous to other organisms.

161 hway and direct alkylation repair by Tpa1 in S. cerevisiae.

162 dinately suppress pervasive transcription in S. cerevisiae and murine embryonic stem cells (mESCs).

163 unidirectional nature of lysine transport in S. cerevisiae by the extraordinary kinetics of Lyp1 and

164 compared with the APOL1 nonrisk variants in S. cerevisiae, including impairment of vacuole acidifica

165 Prior to pathway assembly by VEGAS in S. cerevisiae, each gene is assigned an appropriate pair

166 do they form a disulfide bond in the intact S. cerevisiae GPIT.

167 we have transferred human fragile zones into S. cerevisiae in the context of a genetic assay to under

168 ification and characterization of the 89-kDa S. cerevisiae Sen1 helicase domain (Sen1-HD) produced in

169 e evaluated the ssDNA binding of full-length S. cerevisiae Cdc13 to its minimal substrate, Tel11.

170 These observations directly link S. cerevisiae Kelch proteins to the control of formin ac

171 is a powerful tool for mRNA imaging in live S. cerevisiae with high spatial-temporal resolution and

172 In this study, we surface engineered living S. cerevisiae cells by decorating quantum dots (QDs) and

173 set of the random 5' UTRs as well as native S. cerevisiae 5' UTRs.

174 s fermentation was completed by three native S. cerevisiae strains.

175 ide of cell wall protein alpha-agglutinin of S. cerevisiae, the serine-threonine-rich region of epith

176 is consistent with a genome-wide analysis of S. cerevisiae, which reveals that under favourable growt

177 in laboratory and industrial applications of S. cerevisiae.

178 bly system), exploits the native capacity of S. cerevisiae to perform homologous recombination and ef

179 In the case of S. cerevisiae, the OD600 method failed to distinguish be

180 cation concentrations in the yeast cells of S. cerevisiae.

181 light into the holistic characterization of S. cerevisiae pheno-metabolome in must fermentative cond

182 by the construction and characterization of S. cerevisiae strains whose growth depended on two nonna

183 yl region of the cell wall protein (Cwp2) of S. cerevisiae, respectively.

184 mainly formed and degraded in the cytosol of S. cerevisiae cells in a process that couples D-2HG meta

185 ined the role of TFIID by rapid depletion of S. cerevisiae TFIID subunits and measurement of changes

186 with insect cell expressed luminal domain of S. cerevisiae Gpi16.

187 We determined that the tandem SH2 domain of S. cerevisiae Spt6 binds the linker region of the RNA po

188 T, our data show that the luminal domains of S. cerevisiae Gpi8 and S. cerevisiae Gpi16 do not intera

189 g that deletion of the activation domains of S. cerevisiae Med2 and Med3, as well as C. dubliniensis

190 BiP within the nuclear and peripheral ER of S. cerevisiae (commonly referred to as 'clusters').

191 ed in-line during fed-batch fermentations of S. cerevisiae.

192 of-principle, we explore the interactions of S. cerevisiae Proliferating Cell Nuclear Antigen (yPCNA)

193 effects on mRNA recruitment of a library of S. cerevisiae eIF3 functional variants spanning its 5 es

194 a previously unappreciated wild lifestyle of S. cerevisiae outside the restrictions of human environm

195 ion is supported by lower-resolution maps of S. cerevisiae nucleosome lengths based on micrococcal nu

196 s dominula social wasps favors the mating of S. cerevisiae strains among themselves and with S. parad

197 The preparation of S. cerevisiae cells for superresolution imaging takes 2-

198 revisiae, and STE12, the master regulator of S. cerevisiae mating, were each required for progression

199 ff-line 2D LC-MS/MS analysis (HILIC-RPLC) of S. cerevisiae whole cell lysate has been used to acquire

200 Off-line 2D LC-MS/MS analysis (SCX-RPLC) of S. cerevisiae whole cell lysate was used to generate a r

201 ession phenotypes in a filamentous strain of S. cerevisiae.

202 idy is well tolerated in the wild strains of S. cerevisiae that we studied and that the group of gene

203 n natural variants and laboratory strains of S. cerevisiae, we evaluated the karyotype and gene expre

204 y was frequently observed in wild strains of S. cerevisiae.

205 Here, from the crystal structure of S. cerevisiae Cdh1 in complex with its specific inhibito

206 sent a cryo-electron microscopy structure of S. cerevisiae Hrd1 in complex with its endoplasmic retic

207 the transcriptome and chromatin structure of S. cerevisiae upon quiescence entry.

208 ultipurpose resource to advance the study of S. cerevisiae population genetics, quantitative genetics

209 derivatives, but the endogenous substrate of S. cerevisiae Ydr109c and human FGGY has remained unknow

210 In the suspensions of S. cerevisiae cells subjected to varying extracellular p

211 The three-locus system of S. cerevisiae, which uses a nonconservative mechanism to

212 ustrated by the finding that YMR291W/TDA1 of S. cerevisiae and the homologous KLLA0A09713 gene of Klu

213 isiae; inoculum size and inoculation time of S. cerevisiae; fermentation time and temperature) result

214 t viability highlights inherent tolerance of S. cerevisiae to changes in gene order and overall chrom

215 tage relative to S. bayanus; transgenesis of S. cerevisiae GAL promoter alleles or GAL coding regions

216 aboratory strains nor in natural variants of S. cerevisiae.

217 effects of amphotericin-B and miconazole on S. cerevisiae through the device's time-dependent freque

218 hologs identified in mammals, C. elegans, or S. cerevisiae in addition to 595 novel candidate RBPs.

219 tein interaction networks of five organisms, S. cerevisiae, H. sapiens, D. melanogaster, A. thaliana,

220 testine of social wasps hosts highly outbred S. cerevisiae strains as well as a rare S. cerevisiaexS.

221 By tuning the MAPK pathway, S. cerevisiae therefore programs the number of offspring

222 C. elegans dauer larvae and stationary phase S. cerevisiae require elevated amounts of the disacchari

223 constituted retrotranslocation with purified S. cerevisiae proteins, using proteoliposomes containing

224 In this work, we show that recombinant S. cerevisiae Grx5 purified aerobically, after prolonged

225 d the expression of gtf-1 in the recombinant S. cerevisiae.

226 e previously reported to bind to recombinant S. cerevisiae cells, expressing members of the C. albica

227 of the molecular-cellular network regulating S. cerevisiae.

228 er suggest additional substrates for related S. cerevisiae phosphatases and describe the overall phos

229 verge quantitatively from its highly similar S. cerevisiae ortholog Ded1p.

230 ntified Ptc6p as the primary-and likely sole-S. cerevisiae PDC phosphatase, closing a key knowledge g

231 n integrated database covering four species (S. cerevisiae, C. elegans, D. melanogaster and H. sapien

232 ciency in two closely related yeast species (S. cerevisiae and S. paradoxus).

233 enylation sites (PASs) in two yeast species, S. cerevisiae and S. pombe Although >80% of the mRNA gen

234 to produce bioactive yields that allow spent S. cerevisiae growth media to have antibacterial action

235 o higher eukaryotes, the extensively studied S. cerevisiae dynein behaves distinctly from mammalian d

236 be appears to have evolved less rapidly than S. cerevisiae so that it retains more characteristics of

237 Our results demonstrate that S. cerevisiae Replication Factor C (yRFC) can load yPCNA

238 This work demonstrates that S. cerevisiae can be engineered to perform the complex b

239 We show here that S. cerevisiae also acquires mutations in a gene encoding

240 Here, we report that S. cerevisiae Kelch proteins, Kel1 and Kel2, associate w

241 Here, we show that S. cerevisiae actively forms the D enantiomer of 2HG.

242 Here we show that S. cerevisiae eIF4A and Ded1p directly interact with eac

243 We further show that S. cerevisiae experiences homologous metabolic constrain

244 inase remains unclear, but we speculate that S. cerevisiae Ydr109c and human FGGY could act as metabo

245 Combined, these data suggest that S. cerevisiae could serve as an effective model system f

246 The S. cerevisiae Wee1 homolog Swe1 prevents the formation o

247 Accordingly, the S. cerevisiae genome encodes two homologs of the human D

248 G1 varies greatly around origins across the S. cerevisiae genome, and nucleosome occupancy around or

249 evisiae strains, D. hansenii genes adopt the S. cerevisiae polyadenylation profile, indicating that t

250 /- 20.1 nmol*min(-1)*mg(-1)) that allows the S. cerevisiae strain to show significant growth with xyl

251 Although the S. cerevisiae and Escherichia coli HADs share low sequen

252 alization of leading-strand synthesis by the S. cerevisiae replisome at the single-molecule level.

253 In one, we disrupted the S. cerevisiae INO80 protein interaction network by isola

254 ometry (GC/TOF-MS), here used to examine the S. cerevisiae metabolome.

255 nal properties of an 81-residue IDR from the S. cerevisiae transcription factor Ash1.

256 dies have suggested that hub proteins in the S. cerevisiae physical interaction network are more like

257 In this study, we investigate changes in the S. cerevisiae proteome resulting from cultures grown in

258 Insertion of Ty1 elements into the S. cerevisiae genome, which occurs upstream of genes tra

259 cterization of the dynamic modularity of the S. cerevisiae interactome that incorporated gene express

260 However, colocalization of the S. cerevisiae mispair recognition proteins with the repl

261 Here we report the structure of the S. cerevisiae Pol II-Rad26 complex solved by cryo-electr

262 To aid in the understanding of the S. cerevisiae population and quantitative genetics, as w

263 uding antibiotics and the prion state of the S. cerevisiae translation termination factor eRF3, Rps23

264 th efficient mating with cells producing the S. cerevisiae pheromone and near-perfect discrimination

265 d mating efficiency with cells producing the S. cerevisiae pheromone, resulting in low fitness.

266 expression of Cryptococcus HXS1 rendered the S. cerevisiae mutant lacking all 20 hexose transporters

267 Here we show that the S. cerevisiae Atg19, Atg34 and the human p62, Optineurin

268 plication fork directionality throughout the S. cerevisiae genome, which permits the systematic analy

269 y of SANTA in several case studies using the S. cerevisiae genetic interaction network and genome-wid

270 entation and in the must inoculated with the S. cerevisiae EC1118 strain.

271 share almost no sequence similarity with the S. cerevisiae homolog.

272 tonin during the fermentation process: three S. cerevisiae strains and the two non-Saccharomyces.

273 In contrast to S. cerevisiae SIR1's partially dispensable role in silen

274 We demonstrate that, in contrast to S. cerevisiae, C. lusitaniae exhibits a highly integrate

275 Today, S. cerevisiae strains residing in vineyards around the w

276 Then, using transcriptome data from tolerant S. cerevisiae strain NRRL Y-50049 and a wild-type intole

277 tol phosphate levels in alpha-factor-treated S. cerevisiae, which allows cells to progress synchronou

278 ucose supplemented with galactose, wild-type S. cerevisiae repressed GAL gene expression and had a ro

279 Using S. cerevisiae data, we show that NetProphet can predict

280 stitution of Pol epsilon-dependent MMR using S. cerevisiae proteins.

281 icting synthetic lethality in S. pombe using S. cerevisiae data, then identify over one million putat

282 ation of conditions (cell ratio of H. uvarum/S. cerevisiae; inoculum size and inoculation time of S.

283 translocations and transpositions), whereas S. cerevisiae accumulates unbalanced rearrangements (nov

284 ion studies performed by Hose et al. on wild S. cerevisiae strains.

285 ns (which last shared a common ancestor with S. cerevisiae some 300 million years ago), we show that

286 Here, we demonstrate with S. cerevisiae RNAP II that a cleavage-deficient elongati

287 ent was higher than in ciders fermented with S. cerevisiae.

288 glabrata cells (the calibration genome) with S. cerevisiae samples (the experimental genomes) prior t

289 Genetic studies with S. cerevisiae Poldelta (pol3-L612M) and Polepsilon (pol2

290 nce variation and allelic differences within S. cerevisiae.

291 ce that the GAL lncRNAs in the budding yeast S. cerevisiae promote transcriptional induction in trans

292 C. parapsilosis and the environmental yeast S. cerevisiae, imaged using 3D multichannel laser scanni

293 s up to 250 kb from complex genomes in yeast S. cerevisiae has been developed more than a decade ago.

294 e major triacylglycerol lipases of the yeast S. cerevisiae identified so far are Tgl3p, Tgl4p, and Tg

295 scriptional silencing" is found in the yeast S. cerevisiae mating-type switch [1, 2].

296 namely >700 export substrates from the yeast S. cerevisiae, approximately 1000 from Xenopus oocytes a

297 focus on two metabolic enzymes of the yeast S. cerevisiae, neutral trehalase (Nth1) and glycogen pho

298 exemplified for the cell cycle in the yeast S. cerevisiae.

299 ncrease upon Puf3 deletion in budding yeast (S. cerevisiae) suggests that the output of the RNA regul

300 restricted than that for two distant yeasts (S. cerevisiae and S. pombe), the only other organisms co