ライフサイエンスコーパス: Saccharomyces

1 three S. cerevisiae strains and the two non-Saccharomyces.

2 Drosophila prefers a Saccharomyces-Acetobacter co-culture to the same microor

3 hether the synthetic pathway of Melatonin in Saccharomyces and non-Saccharomyces strains involves the

4 es synXII strain that would be identified as Saccharomyces bayanus by standard DNA barcoding procedur

5 pressure homogenization-induced autolysis of Saccharomyces bayanus wine yeasts, treated at 150MPa.

6 l yeasts including Saccharomyces cerevisiae, Saccharomyces bayanus, and Torulaspora delbrueckii strai

7 model, built from existing gene networks in Saccharomyces, captures most known autophagy components

8 In this investigation, Saccharomyces cerevisiae (baker's yeast) was engineered

9 his end, seven commercial strains comprising Saccharomyces cerevisiae (Red Fruit, ES488, Lalvin QA23,

10 expressed and purified the luminal domain of Saccharomyces cerevisiae (S. cerevisiae) Gpi8 using diff

11 amenable for structural studies, while their Saccharomyces cerevisiae (yeast) homologs are stable com

12 quence motif in irregular telomeric DNA from Saccharomyces cerevisiae (yeast), is demonstrated to ado

13 fruits using two different native isolates (Saccharomyces cerevisiae - KF551990 and Pichia gummigutt

14 tion products created specialized strains of Saccharomyces cerevisiae [3, 4] that were transported al

15 l memory confers a strong fitness benefit in Saccharomyces cerevisiae adapting to growth in galactose

16 ilus V/A-ATPase and eukaryotic V-ATPase from Saccharomyces cerevisiae allowed identification of the a

17 ondrial peroxiredoxin Prx3 when expressed in Saccharomyces cerevisiae Altogether, the processing of p

18 ion of nine genes was stably integrated into Saccharomyces cerevisiae and afforded forskolin titers o

19 found that the effects on prion formation in Saccharomyces cerevisiae and aggregation in vitro could

20 Saccharomyces cerevisiae and C. albicans have transporte

21 stal structures of the Mep2 orthologues from Saccharomyces cerevisiae and Candida albicans and show t

22 Using Saccharomyces cerevisiae and focusing on a matrix of DNA

23 tion complexes (ECs) in Escherichia coli and Saccharomyces cerevisiae and found that 1-3% of all ECs

24 sive genetic epistasis analysis in the yeast Saccharomyces cerevisiae and found that simultaneous del

25 a sanitizers deactivated greater than 99% of Saccharomyces cerevisiae and greater than 99.9% of Esche

26 ulations of the partially domesticated yeast Saccharomyces cerevisiae and its wild relative Saccharom

27 e, we purified recombinant human SPCA1a from Saccharomyces cerevisiae and measured Ca(2+)-dependent A

28 n humans (or its yeast orthologues, Rad26 in Saccharomyces cerevisiae and Rhp26 in Schizosaccharomyce

29 A, a protein required for SPB duplication in Saccharomyces cerevisiae and S. pombe and PcpA, the anch

30 ations are largely restricted to two yeasts, Saccharomyces cerevisiae and Schizosaccharomyces pombe,

31 delbrueckii in sequential fermentation with Saccharomyces cerevisiae and Schizosaccharomyces pombe.

32 ved; orthologs from Arabidopsis thaliana and Saccharomyces cerevisiae are predominantly Ins(1,4,5)P3

33 ts of potassium uptake in the model organism Saccharomyces cerevisiae are the Trk1 high affinity pota

34 we used the mating differentiation in yeast Saccharomyces cerevisiae as a model and developed integr

35 Using Saccharomyces cerevisiae as a model, we conducted cell-f

36 Despite the extensive use of Saccharomyces cerevisiae as a platform for synthetic bio

37 of salidroside can be achieved in the yeast Saccharomyces cerevisiae as well as the plant Nicotiana

38 a multiplex genome engineering technology in Saccharomyces cerevisiae based on annealing synthetic ol

39 The Ty1 retrotransposon of Saccharomyces cerevisiae belongs to the Ty1/Copia superf

40 ne and secretion of a recombinant protein in Saccharomyces cerevisiae by up to 28- and 3-fold, respec

41 Here, we show that sexual agglutination of Saccharomyces cerevisiae can be reprogrammed to link int

42 and RNase H activity in Escherichia coli or Saccharomyces cerevisiae caused R-loop accumulation alon

43 apply it to study the growth of independent Saccharomyces cerevisiae cells in two different growth m

44 Saccharomyces cerevisiae cells transformed with OsPCS2a

45 quantify transcript heterogeneity in single Saccharomyces cerevisiae cells treated with and without

46 ed in real time in live Escherichia coli and Saccharomyces cerevisiae cells.

47 We performed high-resolution HRF for Saccharomyces cerevisiae centromeric nucleosome of unkno

48 single-molecule imaging to demonstrate that Saccharomyces cerevisiae condensin is a molecular motor

49 Saccharomyces cerevisiae contains several prion elements

50 T. denticola Cpt complemented a Saccharomyces cerevisiae CPT1 mutant, and expression of

51 First, fed-batch glucose fermentations by Saccharomyces cerevisiae D5A revealed that this strain,

52 Our results on Saccharomyces cerevisiae data show that the marginal rib

53 The proposed method SCP is evaluated on Saccharomyces cerevisiae datasets and compared with five

54 We applied the methods to five Saccharomyces cerevisiae datasets related to environment

55 and ASH1) endogenously tagged with MBSV6 in Saccharomyces cerevisiae degrade normally.

56 ranslation of mitochondrial gene products in Saccharomyces cerevisiae depends on mRNA-specific activa

57 The Saccharomyces cerevisiae deubiquitinase Ubp7 has been ch

58 to reveal aspects of the contribution of the Saccharomyces cerevisiae DNA damage-responsive kinase Te

59 Here we show the SUMO isopeptidase Ulp2 in Saccharomyces cerevisiae does not prevent the accumulati

60 thway is a variant of selective autophagy in Saccharomyces cerevisiae during which hydrolases such as

61 nesis, and X-ray structural data analysis of Saccharomyces cerevisiae eEF1A, we identified a posttran

62 The yeast Saccharomyces cerevisiae employs multiple pathways to co

63 Saccharomyces cerevisiae encodes two Pif1 family DNA hel

64 een DNA instability and CTD repeat number in Saccharomyces cerevisiae First, analysis of 36 diverse S

65 The Saccharomyces cerevisiae FLO1 gene encodes a cell wall p

66 is-specific DNA double-strand break (DSB) in Saccharomyces cerevisiae folds into G-quadruplex, and th

67 d the resulting substrate was fermented with Saccharomyces cerevisiae for 7-10days under aerobic cond

68 We recently identified Saccharomyces cerevisiae Forkhead 1 (Fkh1) and Forkhead

69 the curvature-stabilizing protein Yop1p from Saccharomyces cerevisiae form a tubular network upon add

70 Saccharomyces cerevisiae Fpr4 is one such protein.

71 endpoints genome-wide at high resolution in Saccharomyces cerevisiae Full-length resection requires

72 In Saccharomyces cerevisiae generation of export-competent

73 eukaryotic genome, Sc2.0, a highly modified Saccharomyces cerevisiae genome reduced in size by nearl

74 efficient method to functionally explore the Saccharomyces cerevisiae genome using saturated transpos

75 typical RBP Vts1 for every transcript in the Saccharomyces cerevisiae genome.

76 thogen related in yeast), are encoded in the Saccharomyces cerevisiae genome.

77 d from renewable sources including wild-type Saccharomyces cerevisiae glycoproteins and lipid-linked

78 MoGsk1 is functionally homologues to the Saccharomyces cerevisiae GSK3 homolog MCK1.

79 the function of synaptonemal complex (SC) in Saccharomyces cerevisiae has mainly focused on in vivo a

80 Studies in Saccharomyces cerevisiae have led the way in our underst

81 containing the vacuolar a-subunit isoform in Saccharomyces cerevisiae Here we demonstrate that PI(4)P

82 ortant examples of regulated RNA splicing in Saccharomyces cerevisiae Here, we report a role for the

83 The Saccharomyces cerevisiae high-mobility group protein Hmo

84 olgi network (TGN) to the plasma membrane in Saccharomyces cerevisiae However, exomer mutants are hig

85 ponse element in gene promoters in the yeast Saccharomyces cerevisiae However, the roles of Msn2/4 in

86 Overexpression of Saccharomyces cerevisiae Hsp104 (Sc-Hsp104) trimmed the

87 ystal structure of an N-terminal fragment of Saccharomyces cerevisiae Hsp104 with the N domain of one

88 evel microsatellite profiling approach, SID (Saccharomyces cerevisiae IDentifier), to identify the st

89 Addition of glucose to starved Saccharomyces cerevisiae initiates collective NADH dynam

90 Ribosome biogenesis in Saccharomyces cerevisiae involves a regulon of >200 gene

91 Activation of Saccharomyces cerevisiae Ire1 coincides with autophospho

92 Saccharomyces cerevisiae is a common yeast with several

93 The budding yeast Saccharomyces cerevisiae is a long-standing model for th

94 Although Saccharomyces cerevisiae is a pervasive model organism f

95 The yeast cell wall of Saccharomyces cerevisiae is an important source of beta-

96 The yeast Saccharomyces cerevisiae is consequently thought to be i

97 of mitochondrial DNA (mtDNA) replication in Saccharomyces cerevisiae is controversial.

98 ein 90 (Hsp90) chaperone system of the yeast Saccharomyces cerevisiae is greatly impaired in naa10Del

99 e main microtubule binding components of the Saccharomyces cerevisiae kinetochore.

100 roteome and metabolome in a repertoire of 16 Saccharomyces cerevisiae laboratory backgrounds, combina

101 Saccharomyces cerevisiae mating-type switching is initia

102 ave combined biochemical purification of the Saccharomyces cerevisiae Mediator from chromatin with ch

103 Under aerobic conditions, the budding yeast Saccharomyces cerevisiae metabolizes glucose predominant

104 nerated in silico by computationally pooling Saccharomyces cerevisiae microsatellite profiles, and on

105 Recently, the Saccharomyces cerevisiae minimal replication reaction ha

106 Mammalian and Saccharomyces cerevisiae mismatch repair (MMR) proteins

107 Through multi-omic profiling of diverse Saccharomyces cerevisiae mitoprotease deletion strains,

108 Among them, yeast Saccharomyces cerevisiae Mss116 participates in mitochon

109 suppressed the Mn-sensitive phenotype of the Saccharomyces cerevisiae mutant Deltapmr1 Our results in

110 f nuclear and mitochondrial encoded mRNAs in Saccharomyces cerevisiae NAD-mRNA appears to be produced

111 g of three PSTVd RNA constructs in the yeast Saccharomyces cerevisiae Of these, only one form, a cons

112 Thus, mammalian cells, unlike Saccharomyces cerevisiae or Escherichia coli cells, requ

113 ent to the essential ORC-binding site within Saccharomyces cerevisiae origin DNA.

114 X3X and compare these to its closely related Saccharomyces cerevisiae ortholog Ded1p.

115 s demonstrated that degradation of Mrc1, the Saccharomyces cerevisiae ortholog of human Claspin, is f

116 TbSTT3C that can functionally complement the Saccharomyces cerevisiae OST, making it an ideal experim

117 model, we found that M1 promoted survival in Saccharomyces cerevisiae overexpressing human Apaf-1 and

118 be rescued by the expression of human PEX16, Saccharomyces cerevisiae Pex34, or by overexpression of

119 on of M. polymorpha core PTB proteins in the Saccharomyces cerevisiae pho2 mutant defective in high-a

120 In Saccharomyces cerevisiae pho84 mutants, constitutively a

121 However, Saccharomyces cerevisiae Pol delta-PCNA is a rapid and p

122 Here, we solve a structure of Saccharomyces cerevisiae Pol I-CF-DNA to 3.8 A resolutio

123 redox activity of the [4Fe4S](2+) cluster in Saccharomyces cerevisiae polymerase (Pol) delta, the lag

124 n vitro with a high-fidelity DNA polymerase, Saccharomyces cerevisiae polymerase (pol) delta.

125 o-electron microscopy structure of the yeast Saccharomyces cerevisiae pre-catalytic B complex spliceo

126 of endogenous hydrogen peroxide in the yeast Saccharomyces cerevisiae promote site-specific endonucle

127 Using biochemistry with Saccharomyces cerevisiae proteins, we show that Rrp47 an

128 se mutations from the affected subjects into Saccharomyces cerevisiae provided functional evidence to

129 port signal consensus sequence identified in Saccharomyces cerevisiae Prp40.

130 Using the Saccharomyces cerevisiae Rab GTPase Sec4p as a model, we

131 The madC gene complements the Saccharomyces cerevisiae Ras-GAP ira1 mutant and the enc

132 in the ATPase-active B, C, and D subunits of Saccharomyces cerevisiae replication factor C (RFC) clam

133 ication, similar to type II ALT survivors in Saccharomyces cerevisiae Replication stresses induced by

134 specific unconventional secretion of Acb1 in Saccharomyces cerevisiae requires ESCRT-I, -II, and -III

135 Termination of Saccharomyces cerevisiae RNA polymerase II (Pol II) tran

136 e-sequenced a well characterized genome, the Saccharomyces cerevisiae S288C strain using three differ

137 A screening of 400 Saccharomyces cerevisiae selected strains deleted in nuc

138 iption coupled DNA repair (TCR) in the yeast Saccharomyces cerevisiae Sen1, a DNA/RNA helicase that i

139 tures at up to 2.6 A resolution of the yeast Saccharomyces cerevisiae separase-securin complex.

140 A polymerase II (RNAPII) and is catalyzed by Saccharomyces cerevisiae Set1 and Set2, respectively.

141 stal structure of the interacting domains of Saccharomyces cerevisiae Sgt1 and Skp1 at 2.8 A resoluti

142 se II-catalyzed transcription in the rDNA of Saccharomyces cerevisiae Sir2 is recruited to nontranscr

143 The Hsp104 disaggregase from Saccharomyces cerevisiae solubilizes stress-induced amor

144 Like other eukaryotes, Saccharomyces cerevisiae spatially organizes its chromos

145 the cryo-electron microscopy structure of a Saccharomyces cerevisiae spliceosome stalled after Prp16

146 The budding yeast Saccharomyces cerevisiae stores iron in the vacuole, whi

147 strain also affected flavour synthesis with Saccharomyces cerevisiae strain A01 producing considerab

148 The Saccharomyces cerevisiae strain QA23 was the most effici

149 tes that yeast involved in wine making, i.e. Saccharomyces cerevisiae strains and the non-Saccharomyc

150 rforming indigenous Hanseniaspora uvarum and Saccharomyces cerevisiae strains as multistarters.

151 During must fermentation by Saccharomyces cerevisiae strains thousands of volatile a

152 d rescued the growth of Escherichia coli and Saccharomyces cerevisiae strains with inactivations of t

153 We present the crystal structure of the Saccharomyces cerevisiae Stu2 C-terminal domain, reveali

154 y during anaphase to promote mitotic exit in Saccharomyces cerevisiae Surprisingly, human CDC14A is n

155 e, synXII, based on native chromosome XII in Saccharomyces cerevisiae SynXII was assembled using a tw

156 nit of the ubiquitin ligase GID in the yeast Saccharomyces cerevisiae targeted the gluconeogenic enzy

157 ts of 235 single-nucleotide mutations in the Saccharomyces cerevisiae TDH3 promoter (PTDH3 ) on the a

158 acuole protein sorting) complex in the yeast Saccharomyces cerevisiae tethers membranes through its a

159 ty to rescue the cold-growth inhibition of a Saccharomyces cerevisiae tgs1Delta mutant in vivo.

160 e, we designed dCas9-Mxi1-based NOR gates in Saccharomyces cerevisiae that allow arbitrary connectivi

161 c mitogen-activated protein kinase (MAPK) in Saccharomyces cerevisiae that couples spore morphogenesi

162 , we engineered strains of the budding yeast Saccharomyces cerevisiae that differ only in the presenc

163 tion, we focused on a highly diverged IDR in Saccharomyces cerevisiae that is involved in regulating

164 assembly factor, Pet117, and demonstrate in Saccharomyces cerevisiae that this evolutionarily conser

165 s and Candida albicans but is cytoplasmic in Saccharomyces cerevisiae The P. pastoris strain carrying

166 genome-wide gene perturbation experiments in Saccharomyces cerevisiae The results suggest that predic

167 es the repair of DNA double-strand breaks in Saccharomyces cerevisiae The role of Sae2 is linked to t

168 In the yeast Saccharomyces cerevisiae the TOR complex 1 (TORC1) contr

169 occurring DSBs at (GAA)n microsatellites in Saccharomyces cerevisiae These data gave us important in

170 ital cellular functions in the budding yeast Saccharomyces cerevisiae These include regulation of tel

171 crotubule (MT) dynamics in the budding yeast Saccharomyces cerevisiae This activity requires interact

172 Here, we used Saccharomyces cerevisiae to address this question.

173 II) independently of its capping activity in Saccharomyces cerevisiae to control transcription.

174 We used Drosophila melanogaster and Saccharomyces cerevisiae to help clarify these mechanism

175 Here we engineer the baker's yeast Saccharomyces cerevisiae to produce and secrete the anti

176 Here, we present the structure of Saccharomyces cerevisiae TORC2 determined by electron cr

177 ously proposed general base residue (D210 in Saccharomyces cerevisiae Trm10) is not likely to play th

178 We show that in Saccharomyces cerevisiae TRmD represents approximately 2

179 e used single molecule fluorescence to study Saccharomyces cerevisiae U1 and BBP interactions with RN

180 Using the Saccharomyces cerevisiae UBI4 gene, we show that this mu

181 as constructed, which is fully functional in Saccharomyces cerevisiae under all conditions tested and

182 In response to starvation, diploid cells of Saccharomyces cerevisiae undergo meiosis and form haploi

183 rget the ACT1 promoter of the model organism Saccharomyces cerevisiae using a dCas9-based transcripti

184 ISH protocol termed sFISH for budding yeast, Saccharomyces cerevisiae using a single DNA probe labele

185 motypic vacuolar lysosome membrane fusion in Saccharomyces cerevisiae Using cell-free fusion assays a

186 cation, we conducted a genome-wide screen in Saccharomyces cerevisiae using DNA polymerase active-sit

187 apping hybrid-prone regions in budding yeast Saccharomyces cerevisiae Using this methodology, we iden

188 entification of CTPD substrates in the yeast Saccharomyces cerevisiae via a quantitative proteomic an

189 Here, the yeast Saccharomyces cerevisiae was used as model to investigat

190 dentifying Mms1 binding sites genome-wide in Saccharomyces cerevisiae we connected Mms1 function to g

191 of the genetically tractable model organism Saccharomyces cerevisiae We used this system to determin

192 The cultures of Saccharomyces cerevisiae were treated with pulsed electr

193 we aimed at identifying the function of the Saccharomyces cerevisiae Ydr109c protein and its human h

194 Three commercial Saccharomyces cerevisiae yeast strains: Viniferm Revelac

195 SsMT2-transgenic yeast (Saccharomyces cerevisiae) and plants (Arabidopsis thalia

196 y arising mutation that activates the yeast (Saccharomyces cerevisiae) CDC25 family phosphatase, Mih1

197 The related protein Hsp110 (Sse1/Sse2 in Saccharomyces cerevisiae) functions as a nucleotide exch

198 1, was able to rescue the growth of a yeast (Saccharomyces cerevisiae) mutant defective in vacuolar i

199 , filopodia supported the uptake of zymosan (Saccharomyces cerevisiae) particles by (i) providing fix

200 ic amyloid fibrils assembled from the yeast (Saccharomyces cerevisiae) prion protein Sup35NM.

201 elta0-ELO1 Heterologous expression in yeast (Saccharomyces cerevisiae) showed that NgDelta0-ELO1 coul

202 In budding yeast (Saccharomyces cerevisiae) the multilayered spindle pole

203 protein interactions in planta and in yeast (Saccharomyces cerevisiae).

204 eling at the bud sites (Candida albicans and Saccharomyces cerevisiae).

205 phagic proteasome turnover in budding yeast (Saccharomyces cerevisiae).

206 The alpha pheromone from the budding yeast Saccharomyces cerevisiae, a 13-residue peptide that elic

207 duced by cyclic AMP (FIC)-1, respectively-in Saccharomyces cerevisiae, a eukaryote that lacks endogen

208 rm for multiplex genome-scale engineering in Saccharomyces cerevisiae, an important eukaryotic model

209 viable counts of Staphylococcus epidermidis, Saccharomyces cerevisiae, and MS2 Bacteriophage after li

210 date the molecular basis of TCS mutations in Saccharomyces cerevisiae, and present a new model for ho

211 Verprolin proteins, such as Vrp1 in Saccharomyces cerevisiae, are conserved family proteins

212 In Saccharomyces cerevisiae, both pathways require the ubiq

213 t other kinesins, Cin8, a kinesin-5 motor in Saccharomyces cerevisiae, can move bidirectionally along

214 During cytokinesis in Saccharomyces cerevisiae, damaged proteins are distribut

215 In the yeast Saccharomyces cerevisiae, Dgk1 diacylglycerol (DAG) kina

216 In the yeast Saccharomyces cerevisiae, different types of stresses in

217 In the yeast Saccharomyces cerevisiae, each strategy is able to stimu

218 In the budding yeast Saccharomyces cerevisiae, ECM remodeling refers to seque

219 bidopsis thaliana, Dictyostelium discoideum, Saccharomyces cerevisiae, Escherichia coli and Methanoca

220 We show that in Saccharomyces cerevisiae, ESCRT-III complexes are stabil

221 step for the synthesis of triacylglycerol in Saccharomyces cerevisiae, exerts a negative regulatory e

222 During meiotic prophase in Saccharomyces cerevisiae, expression of the kinetochore

223 In Saccharomyces cerevisiae, extracellular [Pi] is "sensed"

224 n experimental results for the budding yeast Saccharomyces cerevisiae, finding, surprisingly, that ce

225 In Saccharomyces cerevisiae, H2A.Z is deposited by the SWR-

226 In Saccharomyces cerevisiae, H2A.Z is deposited into chroma

227 The budding yeast, Saccharomyces cerevisiae, harbors several prions that ar

228 genes encoding these enzymes in E. coli and Saccharomyces cerevisiae, I was in a position to alter p

229 gation factors (E4), represented by Ufd2p in Saccharomyces cerevisiae, is a pivotal regulator for man

230 otein and DHFR are coexpressed, in the yeast Saccharomyces cerevisiae, on a low-copy plasmid from two

231 mosan, which is the cell wall preparation of Saccharomyces cerevisiae, or poly (I:C) was coated on a

232 In Saccharomyces cerevisiae, oxidative stress triggers Med1

233 In Saccharomyces cerevisiae, peroxisomes are the sole site

234 netic studies in various fungi, particularly Saccharomyces cerevisiae, provided the key initial break

235 In Saccharomyces cerevisiae, Rrp6 is exclusively nuclear an

236 nd six different commercial yeasts including Saccharomyces cerevisiae, Saccharomyces bayanus, and Tor

237 ere, leveraging population genomic data from Saccharomyces cerevisiae, Schizosaccharomyces pombe, and

238 At HMS2 in Saccharomyces cerevisiae, sgRNA/dCas9 targeting to the n

239 ortant examples of regulated RNA splicing in Saccharomyces cerevisiae, such as splicing of meiotic tr

240 In the yeast Saccharomyces cerevisiae, the complex binds discrete sit

241 In the yeast Saccharomyces cerevisiae, the exposure to mating pheromo

242 In the yeast Saccharomyces cerevisiae, the genes encoding the metallo

243 In Saccharomyces cerevisiae, the myosin V motor Myo2 binds

244 In the yeast Saccharomyces cerevisiae, the Opi1p repressor controls t

245 In Saccharomyces cerevisiae, the Pif1 helicase, a telomeras

246 In Saccharomyces cerevisiae, the post-genome-duplication Di

247 In budding yeast Saccharomyces cerevisiae, the ten-subunit Dam1/DASH comp

248 In the yeast Saccharomyces cerevisiae, the Zap1 transcriptional activ

249 In the yeast Saccharomyces cerevisiae, this inner membrane complex is

250 In Saccharomyces cerevisiae, three conserved Arf-GEFs funct

251 In Saccharomyces cerevisiae, UBI4 encodes five tandem ubiqu

252 Here, in Saccharomyces cerevisiae, we analysed Rad51-dependent br

253 agenesis of the mitochondrial COX1 gene from Saccharomyces cerevisiae, we demonstrate that mutations

254 tive attributes of PKA dynamics in the yeast Saccharomyces cerevisiae, we developed an optogenetic st

255 By mapping the SUMO proteome in Saccharomyces cerevisiae, we discovered a specific set o

256 vivo crosslinking and genetic approaches in Saccharomyces cerevisiae, we found that both domains of

257 context of an actively transcribed locus in Saccharomyces cerevisiae, we tested whether co-transcrip

258 This cannot apply to the yeast Saccharomyces cerevisiae, where this mechanism would pro

259 hydroxyglutarate in tumors were generated in Saccharomyces cerevisiae, which has histone demethylases

260 quences for 85 diverse isolates of the yeast Saccharomyces cerevisiae-including wild, domesticated, a

261 erging from transcribing Pol II in the yeast Saccharomyces cerevisiae.

262 otic ribosome assembly in the model organism Saccharomyces cerevisiae.

263 is homologous to Glo3p of the budding yeast Saccharomyces cerevisiae.

264 colonization with either Candida albicans or Saccharomyces cerevisiae.

265 specific RNA extension activity of Poleta of Saccharomyces cerevisiae.

266 , Mig1, from a paradigm signaling pathway of Saccharomyces cerevisiae.

267 to its targeted C2 site both in vitro and in Saccharomyces cerevisiae.

268 ation with a "pioneer" phenotypic program in Saccharomyces cerevisiae.

269 aptation to a stressful environment in yeast Saccharomyces cerevisiae.

270 and gene deletion (CRISPR-AID) in the yeast Saccharomyces cerevisiae.

271 dapted Strand-seq to detect SCE in the yeast Saccharomyces cerevisiae.

272 in trans of genomic or DI RNAs in the yeast Saccharomyces cerevisiae.

273 se protein-fragment complementation assay in Saccharomyces cerevisiae.

274 ith purified proteins from the budding yeast Saccharomyces cerevisiae.

275 etails underlying ribosome binding of Ssb in Saccharomyces cerevisiae.

276 ectiveness for transcriptional repression in Saccharomyces cerevisiae.

277 mics during endocytosis in the budding yeast Saccharomyces cerevisiae.

278 o cell cycle regulatory network analysis for Saccharomyces cerevisiae.

279 lus subtilis and the single-celled eukaryote Saccharomyces cerevisiae.

280 ole in zinc homeostasis in the budding yeast Saccharomyces cerevisiae.

281 ranslated region (UTR) of mRNAs in the yeast Saccharomyces cerevisiae.

282 x states for red blood cells, platelets, and Saccharomyces cerevisiae.

283 eased Pol II catalysis on gene expression in Saccharomyces cerevisiae.

284 oding metabolic activities in the eukaryote, Saccharomyces cerevisiae.

285 We present the Cryo-EM structure of Saccharomyces cerevsisae Tra1 to 3.7 A resolution, revea

286 Acetobacter metabolism of Saccharomyces-derived ethanol was necessary, and acetate

287 chromosome conformation capture on diverged Saccharomyces hybrid diploids to obtain the first global

288 ccharomyces cerevisiae and its wild relative Saccharomyces paradoxus.

289 ary range of yeasts: inside the best-studied Saccharomyces species complex, and across the entire and

290 egulation is recently evolved; in a diverged Saccharomyces species, GAL genes show constitutively fas

291 athway of Melatonin in Saccharomyces and non-Saccharomyces strains involves these intermediates.

292 species identity, were swapped to generate a Saccharomyces synXII strain that would be identified as

293 Saccharomyces cerevisiae strains and the non-Saccharomyces Torulaspora delbrueckii, can synthesise HT

294 A23, Uvaferm BC, and Lalvin ICV GRE) and non-Saccharomyces (Torulaspora delbrueckii and Metschnikowia

295 either conserved sequence or position within Saccharomyces uORFs initiating with UUG are particularly

296 We mapped transcription leaders in multiple Saccharomyces yeast species and applied a novel machine

297 Non-Saccharomyces yeasts may contribute to enrich wine aroma

298 trengthen the fact that metabolites from non-Saccharomyces yeasts may contribute to form stable polym

299 The non-Saccharomyces yeasts used were Lachancea thermotolerans,

300 d non-AUG uORFs are both frequently found in Saccharomyces yeasts.