ライフサイエンスコーパス: Saccharomyces cerevisiae

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

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

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

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

5 by fermentation using a distilling strain of Saccharomyces cerevisiae.

6 roorganisms, including Bacillus subtilis and Saccharomyces cerevisiae.

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

8 regulates meiosis and pseudohyphal growth in Saccharomyces cerevisiae.

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

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

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

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

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

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

15 ted by the Zap1 transcriptional activator of Saccharomyces cerevisiae.

16 ntracellular oxidation in cells of the yeast Saccharomyces cerevisiae.

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

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

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

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

21 were performed against Escherichia coli and Saccharomyces cerevisiae.

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

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

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

25 nscriptional regulation in the budding yeast Saccharomyces cerevisiae.

26 mbrane protein quality control mechanisms in Saccharomyces cerevisiae.

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

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

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

30 di1, another conserved predicted protease in Saccharomyces cerevisiae.

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

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

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

34 In Saccharomyces cerevisiae, a prion form of a deacetylase

35 In Saccharomyces cerevisiae, a vestigial FA pathway is pres

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

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

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

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

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

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

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

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

44 0 000 atom model of SPL C complex from yeast Saccharomyces cerevisiae and community network analysis

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

46 s tested in milk as well as in living cells (Saccharomyces cerevisiae and Debaryomyces spp.) by TC or

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

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

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

50 mily of ATPases, ABCF family members eEF3 in Saccharomyces cerevisiae and EttA in Escherichia coli ha

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

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

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

54 IM23 complex) is conserved between the yeast Saccharomyces cerevisiae and humans; however, functional

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

56 by interspecies hybrids of the brewing yeast Saccharomyces cerevisiae and its wild relative S. eubaya

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

72 Here, we propose yeast Saccharomyces cerevisiae as a model system that can be u

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

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

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

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

77 In Saccharomyces cerevisiae, budding and mating projection

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

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

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

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

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

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

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

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

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

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

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

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

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

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

92 We performed SisterC on mitotic Saccharomyces cerevisiae cells.

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

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

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

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

97 270,806 50-base-pair DNA fragments that span Saccharomyces cerevisiae chromosome V, other genomic reg

98 normal distribution of MCM complexes across Saccharomyces cerevisiae chromosomes.

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

100 duce functional NifB in aerobically cultured Saccharomyces cerevisiae Combinatorial pathway design wa

101 Saccharomyces cerevisiae constitutes a popular eukaryal

102 Saccharomyces cerevisiae contains two SMYD proteins, Set

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

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

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

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

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

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

109 The budding yeast Saccharomyces cerevisiae divides asymmetrically, like ma

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

111 In Saccharomyces cerevisiae, dna2Delta inviability is rever

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

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

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

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

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

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

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

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

120 In Saccharomyces cerevisiae, five septins comprise two spec

121 Saccharomyces cerevisiae flor yeast is used for the firs

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

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

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

125 In Saccharomyces cerevisiae, formin-polymerized actin cable

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

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

128 In Saccharomyces cerevisiae, galactose-inducible rare-cutti

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

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

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

132 w that CaGpi15 is functionally homologous to Saccharomyces cerevisiae Gpi15.

133 In Saccharomyces cerevisiae growing in glucose-depleted med

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

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

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

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

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

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

140 Saccharomyces cerevisiae has the most comprehensively ch

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

142 ubunit protein uS9 (formerly called rpS16 in Saccharomyces cerevisiae), has a long protruding C-termi

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

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

145 The Saccharomyces cerevisiae HO gene is a model regulatory s

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

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

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

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

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

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

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

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

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

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

156 Here we demonstrate how Saccharomyces cerevisiae integrates multiple temporally

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

158 The yeast Saccharomyces cerevisiae is a powerful model system for

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

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

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

162 Saccharomyces cerevisiae is amenable to studying membran

163 A first draft of the complete complexome of Saccharomyces cerevisiae is now available to browse and

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

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

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

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

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

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

170 s (MCF-7, MDA-435 and CD34(+)), yeast cells (saccharomyces cerevisiae, listeria innocua and E. coli)

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

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

173 guarding their asymmetric inheritance during Saccharomyces cerevisiae mitosis.

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

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

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

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

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

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

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

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

182 Crystal structures of Saccharomyces cerevisiae Pan2 in complex with RNA show t

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

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

185 Saccharomyces cerevisiae Pif1 (ScPif1) is known as an AT

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

187 t PCNA also stimulates the catalytic rate of Saccharomyces cerevisiae Pol delta by >10-fold.

188 Saccharomyces cerevisiae Poldelta consists of catalytic

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

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

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

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

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

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

195 Investigating the Saccharomyces cerevisiae proteasome, we found that perip

196 The Saccharomyces cerevisiae protein Ddi1 and its homologs i

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

198 Reconstitution in yeast (Saccharomyces cerevisiae) proteoliposomes revealed that

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

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

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

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

203 The Saccharomyces cerevisiae RecQ helicase Sgs1 is orthologo

204 Saccharomyces cerevisiae regulates mating, osmoregulatio

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

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

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

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

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

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

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

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

213 Specifically, Saccharomyces cerevisiae Rnq1 amyloid reduces chaperone-

214 The Saccharomyces cerevisiae RSC (Remodeling the Structure o

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

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

217 969 genes that comprise the ito977 model of Saccharomyces cerevisiae's metabolic network.

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

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

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

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

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

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

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

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

226 elbrueckii, Kluyveromyces thermotolerans and Saccharomyces cerevisiae simultaneously.

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

228 The Saccharomyces cerevisiae spindle pole body (SPB) serves

229 During exon ligation, the Saccharomyces cerevisiae spliceosome recognizes the 3'-s

230 The Saccharomyces cerevisiae Ssy5 signaling protease is a co

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

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

233 Saccharomyces cerevisiae strains in which MutLgamma cann

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

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

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

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

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

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

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

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

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

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

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

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

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

247 In Saccharomyces cerevisiae, the classic metabolic intermed

248 In Saccharomyces cerevisiae, the complex life cycle and mat

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

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

251 In Saccharomyces cerevisiae, the Pif1 helicase functions in

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

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

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

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

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

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

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

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

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

261 t 5-bromodeoxyuridine (BrdU) incorporated by Saccharomyces cerevisiae to reveal, at a genomic scale a

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

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

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

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

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

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

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

269 In the yeast Saccharomyces cerevisiae, translation elongation require

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

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

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

273 by SUMO proteases, of which there are two in Saccharomyces cerevisiae, Ulp1 and Ulp2.

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

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

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

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

278 nsequences when these genes are expressed in Saccharomyces cerevisiae Using this approach, we demonst

279 In Saccharomyces cerevisiae, variations in external osmolar

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

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

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

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

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

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

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

287 In Saccharomyces cerevisiae, we demonstrate that centromeri

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

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

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

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

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

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

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

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

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

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

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

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

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