ライフサイエンスコーパス: Saccharomyces

1 nomes, present in only a few genera close to Saccharomyces.

2 stantially longer and more AUG-dense than in Saccharomyces.

3 f multiple budding yeast species, generating Saccharomyces allopolyploids of at least six species.

4 s both the evolutionary history of the genus Saccharomyces and the human history of taxonomists and b

5 er, Lactobacillus, Lactococcus, Leuconostoc, Saccharomyces and Zymomonas) and 10 species (Acinetobact

6 low-certainty evidence for the risk of anti-Saccharomyces antibodies, a serologic marker of IBD, in

7 and multi-varietal) and three autochthonous Saccharomyces bayanus yeast strains.

8 us spp and 1 or more Bifidobacterium spp and Saccharomyces boulardii reduced the number of days to re

9 ted the effect of a single probiotic strain, Saccharomyces boulardii, at a standardized dose on the r

10 TSSs) has been identified in a budding yeast Saccharomyces cerevisiae ("scanning model").

11 The DNA polymerase (Pol) delta of Saccharomyces cerevisiae (S.c.) is composed of the catal

12 is study was to investigate the influence of Saccharomyces cerevisiae (Sc) and Pichia kudriavzevii (P

13 e specificity of Cdc14 from the model fungus Saccharomyces cerevisiae (ScCdc14) are well-defined and

14 er, we recently reported that the mtSSB from Saccharomyces cerevisiae (ScRim1) forms homotetramers at

15 rd direction like the canonical isolate from Saccharomyces cerevisiae (ScTOK), and distinct from othe

16 re-constituted transcriptional complexes of Saccharomyces cerevisiae (yeast) and humans, aided with

17 We find that Saccharomyces cerevisiae accumulate lipid droplets (LDs)

18 ce of 1.6 million protein pairs in the yeast Saccharomyces cerevisiae across nine growth conditions,

19 Here, we focused on Saccharomyces cerevisiae actin cables, which provide pol

20 e replaced the enzymes catalyzing the entire Saccharomyces cerevisiae adenine de novo biosynthesis pa

21 associated substrates of the other enzyme in Saccharomyces cerevisiae Although both enzymes contribut

22 composition, being Dekkera bruxellensis and Saccharomyces cerevisiae among the main contributors to

23 a nucleotide-free Smc1-Scc1 subcomplex from Saccharomyces cerevisiae and Chaetomium thermophilium.

24 0 000 atom model of SPL C complex from yeast Saccharomyces cerevisiae and community network analysis

25 WT and mutant Pol I variants from the yeast Saccharomyces cerevisiae and compare their abilities to

26 tures of the hexadecameric AHAS complexes of Saccharomyces cerevisiae and dodecameric AHAS complexes

27 yzed a series of deletions and knockdowns in Saccharomyces cerevisiae and Drosophila melanogaster, in

28 In this Letter, in Fig. 3c and f the Saccharomyces cerevisiae and Escherichia coli networks w

29 d energy metabolism for Escherichia coli and Saccharomyces cerevisiae and found that the high-yield p

30 origin obscuring in OF sequencing data from Saccharomyces cerevisiae and human cell types.

31 factors of mitochondrial RNA polymerases in Saccharomyces cerevisiae and humans, respectively.

32 sing a combination of in vivo experiments in Saccharomyces cerevisiae and in vitro assays, we show th

33 to evaluate how the use of mixed cultures of Saccharomyces cerevisiae and Lachancea thermotolerans in

34 roceed through the Thi5-dependent pathway in Saccharomyces cerevisiae and other yeast.

35 F)-alpha secretion by macrophages induced by Saccharomyces cerevisiae and Pneumocystis carinii (Pc) b

36 microscopy structure of SAGA from the yeast Saccharomyces cerevisiae and resolve the core module at

37 : (i) Homo sapiens and Mus musculus and (ii) Saccharomyces cerevisiae and Schizosaccharomyces pombe.

38 requires well-defined DNA sequence motifs in Saccharomyces cerevisiae and some other budding yeasts,

39 We further measured serum anti-Saccharomyces cerevisiae antibodies (ASCA) as a systemic

40 rphisms, disease behavior, and positive anti-Saccharomyces cerevisiae antibody status.

41 ntation, small bowel disease, serology (anti-Saccharomyces cerevisiae antibody, antiflagellin, and Om

42 ngly or as binary cultures with the selected Saccharomyces cerevisiae AYI7.

43 at cargo triggers local CME site assembly in Saccharomyces cerevisiae based on the discovery that cor

44 structural changes in the plasma membrane of Saccharomyces cerevisiae brought about by nutrient stres

45 e Sec complex (Sec61-Sec63-Sec71-Sec72) from Saccharomyces cerevisiae by cryo-electron microscopy (cr

46 increased the abundance of genomic rNMPs in Saccharomyces cerevisiae by depleting Rnr1, the major su

47 we demonstrate that rereplication induced in Saccharomyces cerevisiae by deregulated origin licensing

48 cts for gene expression in the budding yeast Saccharomyces cerevisiae by measuring the effects of tho

49 We tested this possibility in Saccharomyces cerevisiae by systematically altering the

50 e quantify the mutation rate and spectrum in Saccharomyces cerevisiae by whole-genome sequencing foll

51 if, CDKB emerged as a likely candidate for a Saccharomyces cerevisiae Cdc28/Pho85-like homolog in Sym

52 and toxicity of TDP-43 and FUS expressed in Saccharomyces cerevisiae Cdc48 physically interacts and

53 es, diversifying the genotype of millions of Saccharomyces cerevisiae cells in hours.

54 ck (PF) gene circuit integrated into haploid Saccharomyces cerevisiae cells to test if the population

55 lism and division of thousands of individual Saccharomyces cerevisiae cells using a droplet microflui

56 by oxidative stress promoted by H(2)O(2) in Saccharomyces cerevisiae cells.

57 We performed SisterC on mitotic Saccharomyces cerevisiae cells.

58 s that enhance or decrease UV sensitivity of Saccharomyces cerevisiae cells.

59 , we determined the crystal structure of the Saccharomyces cerevisiae Cenp-HIKHead-TW sub-module, rev

60 270,806 50-base-pair DNA fragments that span Saccharomyces cerevisiae chromosome V, other genomic reg

61 normal distribution of MCM complexes across Saccharomyces cerevisiae chromosomes.

62 Previously, we found that in glucose-limited Saccharomyces cerevisiae colonies, metabolic constraints

63 Saccharomyces cerevisiae constitutes a popular eukaryal

64 Saccharomyces cerevisiae contains two SMYD proteins, Set

65 Structural studies of Saccharomyces cerevisiae CRM1 ((Sc)CRM1) complexes with

66 Introducing this variation into E. coli and Saccharomyces cerevisiae CysRS increased resistance to t

67 The budding yeast Saccharomyces cerevisiae divides asymmetrically, like ma

68 cs of the nucleoprotein filament assembly of Saccharomyces cerevisiae Dmc1 using single-molecule teth

69 ibe the topological architecture of genes in Saccharomyces cerevisiae during the G1 and S phases of t

70 The results suggested that Saccharomyces cerevisiae EC-1118 was suitable for fermen

71 We found that the Saccharomyces cerevisiae EMC contains eight subunits (Em

72 entakisphosphate (PP-InsP(5)) phosphatase in Saccharomyces cerevisiae encoded by SIW14 Yeast strains

73 acid transporters in Xenopus oocytes and in Saccharomyces cerevisiae engineered for dicarboxylic aci

74 Saccharomyces cerevisiae flor yeast is used for the firs

75 abs were asked to evolve Escherichia coli or Saccharomyces cerevisiae for an abiotic stress-low tempe

76 Here, we use a reporter gene-based screen in Saccharomyces cerevisiae for the discovery of antifungal

77 ber distribution data for ribosomal genes in Saccharomyces cerevisiae from three previously published

78 ics with single-cell live imaging to monitor Saccharomyces cerevisiae galactokinase 1 (GAL1) expressi

79 Here, we used a Saccharomyces cerevisiae genetic system that generates g

80 number of synthetic lethal interactions with Saccharomyces cerevisiae genome instability genes, is a

81 We found that Glk1, a Saccharomyces cerevisiae glucokinase, forms two-stranded

82 In Saccharomyces cerevisiae growing in glucose-depleted med

83 erimental growth curves of the baker's yeast Saccharomyces cerevisiae growing in the presence of two

84 Genetic screening in the budding yeast Saccharomyces cerevisiae has isolated several dubious OR

85 he variety of ecological niches inhabited by Saccharomyces cerevisiae has led to research in areas as

86 The mating pathway in yeast Saccharomyces cerevisiae has long been used to reveal ne

87 of eukaryotic RNA polymerase I (Pol I) from Saccharomyces cerevisiae has not been defined.

88 onmental stimuli in a classic model organism Saccharomyces cerevisiae has not been systematically inv

89 Saccharomyces cerevisiae has the most comprehensively ch

90 terminal end of the Aga2p mating adhesion of Saccharomyces cerevisiae have been used in many studies

91 The Saccharomyces cerevisiae HO gene is a model regulatory s

92 Here, we report that the Saccharomyces cerevisiae homolog Yta7(ATAD2) is a deposi

93 Herein, we characterize Saccharomyces cerevisiae homologs Put6 and Put7 of MCUR1

94 levels of antibodies against microbes (anti-Saccharomyces cerevisiae IgA or IgG, anti-Escherichiacol

95 volved 20 replicate populations of the yeast Saccharomyces cerevisiae in 11 laboratory environments a

96 o experimentally address this, we cultivated Saccharomyces cerevisiae in bioreactors with or without

97 o-EM structures of the core TOM complex from Saccharomyces cerevisiae in dimeric and tetrameric forms

98 Here, we examined global RBP dynamics in Saccharomyces cerevisiae in response to glucose starvati

99 Here we demonstrate how Saccharomyces cerevisiae integrates multiple temporally

100 Encapsulation process by Saccharomyces cerevisiae is a popular technique to prese

101 The yeast Saccharomyces cerevisiae is a powerful model system for

102 The Nem1-Spo7 complex in the yeast Saccharomyces cerevisiae is a protein phosphatase requir

103 The Nem1-Spo7 complex in the yeast Saccharomyces cerevisiae is a protein phosphatase that c

104 Implementation of this design in Saccharomyces cerevisiae is also demonstrated.

105 Saccharomyces cerevisiae is amenable to studying membran

106 motor proteins (Drosophila melanogaster Ncd, Saccharomyces cerevisiae Kar3, Saccharomyces pombe Pkl1,

107 Here we report reconstitution of functional Saccharomyces cerevisiae kinetochore assemblies from rec

108 copper homeostatic systems between human and Saccharomyces cerevisiae made this organism a suitable m

109 mitochondrial matrix protein called Mam33 in Saccharomyces cerevisiae mitoribosome biogenesis.

110 guarding their asymmetric inheritance during Saccharomyces cerevisiae mitosis.

111 e strain-specific metabolic models for 1,143 Saccharomyces cerevisiae mutants and we test 27 machine-

112 tiating meiotic recombination is elevated in Saccharomyces cerevisiae mutants that are globally defec

113 se adaptive laboratory evolution to generate Saccharomyces cerevisiae mutants tolerant to two aromati

114 haracterize de novo mutations in 274 diploid Saccharomyces cerevisiae mutation accumulation lines.

115 ound the universally conserved tyrosine 837 (Saccharomyces cerevisiae numbering), that contacts the c

116 Similar results were obtained with the Saccharomyces cerevisiae PCNA sliding clamp, suggesting

117 termine the structure of a class D GPCR, the Saccharomyces cerevisiae pheromone receptor Ste2, in an

118 Here we report cryo-EM structures of the Saccharomyces cerevisiae Pmt1-Pmt2 complex bound to a do

119 Saccharomyces cerevisiae Poldelta consists of catalytic

120 re and reveal functional differences between Saccharomyces cerevisiae Pols I and II using a series of

121 We present cryo-EM structures of the Saccharomyces cerevisiae Polzeta holoenzyme in the act o

122 Using a highly recombined Saccharomyces cerevisiae population, we found 30 distinc

123 We profiled circular DNA in Saccharomyces cerevisiae populations sampled when young

124 over time in experimental sexual and asexual Saccharomyces cerevisiae populations, we provide direct

125 Investigating the Saccharomyces cerevisiae proteasome, we found that perip

126 The Saccharomyces cerevisiae protein Ddi1 and its homologs i

127 eukaryal cell cycle, using the budding yeast Saccharomyces cerevisiae Protein synthesis and central c

128 coverage in vivo mRNA display library of the Saccharomyces cerevisiae proteome and demonstrated its p

129 GalOA or the full GalA catabolic pathway in Saccharomyces cerevisiae proved challenging, presumably

130 ctional analyses of PunPgp-2 and PunPgp-9 in Saccharomyces cerevisiae provide evidence for an interac

131 Saccharomyces cerevisiae regulates mating, osmoregulatio

132 We use an in vitro reconstituted Saccharomyces cerevisiae replisome to demonstrate that P

133 amics simulations, and DNA enzymology on the Saccharomyces cerevisiae Rev1 protein.

134 Expression of selected proteins in Saccharomyces cerevisiae revealed specific targeting to

135 Heterologous expression in Saccharomyces cerevisiae revealed that QsOSC1-3 respecti

136 Specifically, Saccharomyces cerevisiae Rnq1 amyloid reduces chaperone-

137 The Saccharomyces cerevisiae RSC (Remodeling the Structure o

138 in family, we focused on a subcomplex of the Saccharomyces cerevisiae RSC comprising its ATPase (Sth1

139 elbrueckii, Kluyveromyces thermotolerans and Saccharomyces cerevisiae simultaneously.

140 Cryo-electron microscopy structures of Saccharomyces cerevisiae Spf1 revealed a large, membrane

141 The Saccharomyces cerevisiae spindle pole body (SPB) serves

142 The Saccharomyces cerevisiae Ssy5 signaling protease is a co

143 o11A domains from different yeast species or Saccharomyces cerevisiae strains confer weak adhesive fo

144 Berry extracts were tested on different Saccharomyces cerevisiae strains expressing disease prot

145 Saccharomyces cerevisiae strains in which MutLgamma cann

146 Specifically, the community consists of two Saccharomyces cerevisiae strains, each engineered to rel

147 ive elongating transcript sequencing data in Saccharomyces cerevisiae suggests that these downstream

148 ER, and additional experimental evidence in Saccharomyces cerevisiae supports the possibility that t

149 rt the cryo-electron microscopy structure of Saccharomyces cerevisiae SWI/SNF bound to a nucleosome,

150 gh the majority of the 1,157-nucleotide (nt) Saccharomyces cerevisiae telomerase RNA, TLC1, is rapidl

151 e mutational load in a population of haploid Saccharomyces cerevisiae that are deficient for mismatch

152 is a multifunctional transcription factor in Saccharomyces cerevisiae that plays dual roles in activa

153 Here we describe 34 excised introns in Saccharomyces cerevisiae that-despite being rapidly degr

154 l respiration and Sod1 function in the yeast Saccharomyces cerevisiae The histone H3-H4 tetramer, the

155 he Not5 subunit with the ribosomal E-site in Saccharomyces cerevisiae This interaction occurred when

156 dated a 3.4 angstrom resolution structure of Saccharomyces cerevisiae THO-Sub2 by cryo-electron micro

157 Here we demonstrate that the roles of the Saccharomyces cerevisiae Timeless protein Tof1 in DRC si

158 ence microscopy studies in the budding yeast Saccharomyces cerevisiae to identify a protein, Laa2, th

159 We performed a genetic screen in Saccharomyces cerevisiae to identify histone mutants tha

160 Therefore, we developed an assay in Saccharomyces cerevisiae to identify proteins mediating

161 o mitochondrial DNA mutagenesis of the yeast Saccharomyces cerevisiae to introduce single point mutat

162 We have improved the ability of Saccharomyces cerevisiae to produce HT by heterologously

163 Here, we use the model eukaryote Saccharomyces cerevisiae to show that exposure to sublet

164 chromatin-associated HMGB protein Nhp6A from Saccharomyces cerevisiae to travel along DNA in the pres

165 We previously showed that wild isolates of Saccharomyces cerevisiae tolerate chromosome amplificati

166 Substitution of s(2)C(32) for C(32) in the Saccharomyces cerevisiae tRNA(Ile)(IAU) anticodon stem a

167 code expansion technology with an engineered Saccharomyces cerevisiae tryptophanyl tRNA-synthetase (T

168 ity changes during experimental evolution of Saccharomyces cerevisiae under nitrogen and carbon limit

169 e peroxidase (PO), which were synthesized by Saccharomyces cerevisiae US-05.

170 Strains of Saccharomyces cerevisiae used to make beer, bread, and w

171 Here, we study Saccharomyces cerevisiae using a combination of bioinfor

172 Here we present a Saccharomyces cerevisiae version of the protocol that ca

173 n of ethanol by the widely used cell factory Saccharomyces cerevisiae was adopted as a case study to

174 Recently Opi3, a PLMT of the yeast Saccharomyces cerevisiae was proposed to perform in tran

175 and potent inducer of autophagy in the yeast Saccharomyces cerevisiae We found that potassium-depende

176 ion, and posttranscriptional consequences in Saccharomyces cerevisiae We show that TSSs of chromatin-

177 ne in vitro evolution and genome analysis in Saccharomyces cerevisiae with molecular, metabolomic, an

178 Here, we demonstrate that Saccharomyces cerevisiae yeast strains harboring a delet

179 969 genes that comprise the ito977 model of Saccharomyces cerevisiae's metabolic network.

180 xamine this issue with an in silico model of Saccharomyces cerevisiae's metabolism.

181 elative to the slow-translating pairs across Saccharomyces cerevisiae's proteome, while the slow-tran

182 ructure of pericentromeres in budding yeast (Saccharomyces cerevisiae) and establish the relationship

183 In yeast (Saccharomyces cerevisiae) and human (Homo sapiens) mitoc

184 terologously expressing it in budding yeast (Saccharomyces cerevisiae) and in the bacterium Lactococc

185 shy stunt virus (TBSV) replication in yeast (Saccharomyces cerevisiae) and plants.

186 Yeast (Saccharomyces cerevisiae) cells lacking the N-terminal (

187 The lysosomal vacuole of budding yeast (Saccharomyces cerevisiae) has served as a seminal model

188 e Mag1 and Tpa1 proteins from budding yeast (Saccharomyces cerevisiae) have both been reported to rep

189 Rrp44/Dis3 of the exosome in budding yeast (Saccharomyces cerevisiae) is considered a protein presen

190 lar H(+)-ATPase (V-ATPase) of budding yeast (Saccharomyces cerevisiae) is regulated by reversible dis

191 impaired interactions with LCB1 in a yeast (Saccharomyces cerevisiae) model, providing structural cl

192 candidate region gene2 (GLTSCR2) and yeast (Saccharomyces cerevisiae) Nucleolar protein53 (Nop53) ar

193 Reconstitution in yeast (Saccharomyces cerevisiae) proteoliposomes revealed that

194 Budding yeast (Saccharomyces cerevisiae) responds to low cytosolic iron

195 xin Response Circuit recapitulated in yeast (Saccharomyces cerevisiae) system to functionally annotat

196 this end, we have developed gates for yeast (Saccharomyces cerevisiae) that are connected using RNA p

197 , Leuconostoc gelidum, Zymomonas mobilis and Saccharomyces cerevisiae) that were present >= 1% in at

198 We engineered unicellular baker's yeast (Saccharomyces cerevisiae) to develop either clonally ("s

199 Here, we used budding yeast (Saccharomyces cerevisiae) to explore how the ESCRT machi

200 In this study, baker's yeast (Saccharomyces cerevisiae) was considered as a positive c

201 ndividual mitochondria isolated from yeasts (Saccharomyces cerevisiae) were let to sediment on the ar

202 In budding yeast (Saccharomyces cerevisiae), EVs function as carriers to t

203 was originally discovered in budding yeast (Saccharomyces cerevisiae), in which polyP anabolism and

204 acid for CoA biosynthesis in budding yeast (Saccharomyces cerevisiae), significantly regulates the l

205 it fly (Drosophila melanogaster), and yeast (Saccharomyces cerevisiae), this core NatA complex intera

206 Using a yeast system (Saccharomyces cerevisiae), we experimentally show that c

207 eplication protein A (RPA) in budding yeast (Saccharomyces cerevisiae).

208 simple carbon and nitrogen sources in yeast (Saccharomyces cerevisiae).

209 oped a method for scRNAseq in budding yeast (Saccharomyces cerevisiae).

210 RFC1, has been replaced with ATAD5 (ELG1 in Saccharomyces cerevisiae).

211 ansferase Set2, control choice of pA site in Saccharomyces cerevisiae, a powerful model for studying

212 In Saccharomyces cerevisiae, a pre-initiation complex (PIC)

213 In Saccharomyces cerevisiae, a prion form of a deacetylase

214 In Saccharomyces cerevisiae, a vestigial FA pathway is pres

215 nding the functions and transport of Dbp5 in Saccharomyces cerevisiae, alanine scanning mutagenesis w

216 ry using examples from Bacillus subtilis and Saccharomyces cerevisiae, and show that sharing informat

217 ed by DNA-binding proteins, such as Cdc13 in Saccharomyces cerevisiae, and the propensity of G-rich s

218 sly inaccessible proteins from baker's yeast Saccharomyces cerevisiae, as well as two clinically rele

219 In Saccharomyces cerevisiae, budding and mating projection

220 a central role in the natural life cycle of Saccharomyces cerevisiae, but its evolutionary origin is

221 ic lipid vesicles and the plasma membrane of Saccharomyces cerevisiae, but the permeability is much l

222 Using cross-platform analysis in Saccharomyces cerevisiae, C. elegans, and Xenopus laevis

223 In the yeast Saccharomyces cerevisiae, coq1-coq9 deletion mutants are

224 In budding yeast, Saccharomyces cerevisiae, CR is commonly defined by redu

225 In Saccharomyces cerevisiae, cytochrome c oxidase (CIV) for

226 rochromatin-like structure at HML and HMR in Saccharomyces cerevisiae, depends on progression through

227 In Saccharomyces cerevisiae, dna2Delta inviability is rever

228 In Saccharomyces cerevisiae, early in the cell cycle, a por

229 rimentally using a single microbial species, Saccharomyces cerevisiae, expanding in multiple environm

230 In Saccharomyces cerevisiae, five septins comprise two spec

231 s, such as TFB2M in humans and Mtf1 in yeast Saccharomyces cerevisiae, for promoter-specific transcri

232 In Saccharomyces cerevisiae, formin-polymerized actin cable

233 In Saccharomyces cerevisiae, galactose-inducible rare-cutti

234 ors are prevalent among identified prions in Saccharomyces cerevisiae, however, it is unclear how pri

235 f ubiquitin functions in stress responses in Saccharomyces cerevisiae, including the oxidative stress

236 Rdh54 (a.k.a. Tid1), a Rad54 paralog in Saccharomyces cerevisiae, is well-known for its role wit

237 In Saccharomyces cerevisiae, it is controlled by a system o

238 In the budding yeast Saccharomyces cerevisiae, nearly all H2A isoforms can be

239 sion data sets, one from the model eukaryote Saccharomyces cerevisiae, proliferating at different gro

240 genome-wide loss-of-heterozygosity (LOH) in Saccharomyces cerevisiae, providing support for an addit

241 The tractable model yeast, Saccharomyces cerevisiae, relocates its polarity site wh

242 om two different organisms (Homo Sapiens and Saccharomyces cerevisiae, respectively) are chosen for e

243 Although absent from Saccharomyces cerevisiae, RNAi is present in other buddi

244 In Saccharomyces cerevisiae, the 3'-end sequences of at lea

245 In Saccharomyces cerevisiae, the complex life cycle and mat

246 In the budding yeast Saccharomyces cerevisiae, the five mitotic septins (Cdc3

247 In the yeast Saccharomyces cerevisiae, the Nt-amidase, arginyltransfe

248 In Saccharomyces cerevisiae, the Pif1 helicase functions in

249 We used the budding yeast, Saccharomyces cerevisiae, to investigate the evolutionar

250 We forced the budding yeast, Saccharomyces cerevisiae, to use the meiosis-specific kl

251 In the yeast Saccharomyces cerevisiae, translation elongation require

252 the long-terminal-repeat retrotransposon of Saccharomyces cerevisiae, Ty1, which is a retrovirus mod

253 In Saccharomyces cerevisiae, variations in external osmolar

254 In Saccharomyces cerevisiae, we demonstrate that centromeri

255 Here, in Saccharomyces cerevisiae, we demonstrate that changes in

256 In the budding yeast Saccharomyces cerevisiae, we demonstrate that NVJ1- and

257 Using a Spn1 depletion system in Saccharomyces cerevisiae, we demonstrate that Spn1 broad

258 ugh a systematic high-throughput approach in Saccharomyces cerevisiae, we determined mtDNA-to-nuclear

259 Using purified proteins from Saccharomyces cerevisiae, we have reconstituted transles

260 Here, using the budding yeast Saccharomyces cerevisiae, we report the discovery that H

261 nstituted system with purified proteins from Saccharomyces cerevisiae, we show that the ubiquitin lig

262 ver, using sub-cellular proteomics data from Saccharomyces cerevisiae, we uncover a novel group of pr

263 in the promoters of 2503 genes in the yeast Saccharomyces cerevisiae.

264 by fermentation using a distilling strain of Saccharomyces cerevisiae.

265 roorganisms, including Bacillus subtilis and Saccharomyces cerevisiae.

266 g glucose deprivation-induced ATP decline in Saccharomyces cerevisiae.

267 regulates meiosis and pseudohyphal growth in Saccharomyces cerevisiae.

268 OM) proteins as novel model QC substrates in Saccharomyces cerevisiae.

269 pt profiles of 1484 single gene deletions of Saccharomyces cerevisiae.

270 on cycle of condensin from the budding yeast Saccharomyces cerevisiae.

271 se Ubp15 as a regulator of nuclear export in Saccharomyces cerevisiae.

272 ogenesis and in a distantly related species, Saccharomyces cerevisiae.

273 s and select for transport-active mutants in Saccharomyces cerevisiae.

274 ted by the Zap1 transcriptional activator of Saccharomyces cerevisiae.

275 ntracellular oxidation in cells of the yeast Saccharomyces cerevisiae.

276 tein that initiates mating-type switching in Saccharomyces cerevisiae.

277 are both needed for efficient CTD binding in Saccharomyces cerevisiae.

278 ning the centromere DNA of the budding yeast Saccharomyces cerevisiae.

279 in a eukaryote chassis, namely baker's yeast Saccharomyces cerevisiae.

280 were performed against Escherichia coli and Saccharomyces cerevisiae.

281 in Saccharomyces uvarum, a sister species of Saccharomyces cerevisiae.

282 lts of previous work in the simple eukaryote Saccharomyces cerevisiae.

283 otein interactions in the well-studied yeast Saccharomyces cerevisiae.

284 reporters in single, live cells of the yeast Saccharomyces cerevisiae.

285 r most genetic construct design in the yeast Saccharomyces cerevisiae.

286 e-strand annealing (SSA) assays in the yeast Saccharomyces cerevisiae.

287 di1, another conserved predicted protease in Saccharomyces cerevisiae.

288 halophilicum, and E. repens; Mrakia frigida; Saccharomyces cerevisiae; Xerochrysium xerophilum; Xerom

289 that shortening a heterochromatic domain in Saccharomyces had no impact on the strength of silencing

290 The genus Saccharomyces is an evolutionary paradox.

291 ncipient species of the undomesticated yeast Saccharomyces paradoxus.

292 nogaster Ncd, Saccharomyces cerevisiae Kar3, Saccharomyces pombe Pkl1, and Xenopus laevis XCTK2) are

293 hanisms have caused the evolution of diverse Saccharomyces species and hybrids, which occupy a variet

294 On the other hand, Saccharomyces species have a long evolutionary history o

295 e base of the CEH are nearly invariant among Saccharomyces species, our results with sequence-randomi

296 ntroduce readers to the mechanisms isolating Saccharomyces species, the circumstances in which reprod

297 or this partial reproductive isolation among Saccharomyces species.

298 perimental testing of gene dispensability in Saccharomyces uvarum, a sister species of Saccharomyces

299 S1pr-TDA1pr alleles in saturated cultures of Saccharomyces yeast is mediated by three transcription f

300 to investigate the effect of commercial non-Saccharomyces yeasts and Oenococcus oeni on the formatio