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

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

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

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

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

5 otic ribosome assembly in the model organism Saccharomyces cerevisiae.

6 colonization with either Candida albicans or Saccharomyces cerevisiae.

7 specific RNA extension activity of Poleta of Saccharomyces cerevisiae.

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

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

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

11 aptation to a stressful environment in yeast Saccharomyces cerevisiae.

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

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

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

15 se protein-fragment complementation assay in Saccharomyces cerevisiae.

16 ith purified proteins from the budding yeast Saccharomyces cerevisiae.

17 etails underlying ribosome binding of Ssb in Saccharomyces cerevisiae.

18 ectiveness for transcriptional repression in Saccharomyces cerevisiae.

19 mics during endocytosis in the budding yeast Saccharomyces cerevisiae.

20 o cell cycle regulatory network analysis for Saccharomyces cerevisiae.

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

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

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

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

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

26 oding metabolic activities in the eukaryote, Saccharomyces cerevisiae.

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

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

29 thod (PRIM) to ChIP-seq data superposed on a Saccharomyces cerevisiae 3D genome reconstruction can di

30 of purified hepatitis B capsid particles and Saccharomyces cerevisiae 80S ribosomes.

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

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

33 In mitochondria of Saccharomyces cerevisiae, a single aminoacyl-tRNA synthe

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

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

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

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

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

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

40 Saccharomyces cerevisiae and C. albicans have transporte

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

42 , Aspergillus ochraceus, Fusarium oxysporum, Saccharomyces cerevisiae and Candida albicans.

43 Using Saccharomyces cerevisiae and focusing on a matrix of DNA

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

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

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

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

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

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

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

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

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

53 We used the budding yeasts Saccharomyces cerevisiae and Torulaspora delbrueckii to

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

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

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

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

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

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

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

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

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

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

64 The essential Saccharomyces cerevisiae ATPase Mot1 globally regulates

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

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

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

68 In Saccharomyces cerevisiae, beta5 (Doa3/Pre2) has a 75-res

69 In Saccharomyces cerevisiae, both pathways require the ubiq

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

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

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

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

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

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

76 Saccharomyces cerevisiae cells transformed with OsPCS2a

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

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

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

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

81 In Saccharomyces cerevisiae, conditions that trigger Acb1 s

82 Saccharomyces cerevisiae contains several prion elements

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

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

85 During cytokinesis in Saccharomyces cerevisiae, damaged proteins are distribut

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

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

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

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

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

91 ific Expression (ASE) in six F1 hybrids from Saccharomyces cerevisiae derived from crosses between re

92 The Saccharomyces cerevisiae deubiquitinase Ubp7 has been ch

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

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

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

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

97 ajority of noncoding transcription events in Saccharomyces cerevisiae does not rely on RNA cleavage f

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

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

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

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

102 The yeast Saccharomyces cerevisiae employs multiple pathways to co

103 Saccharomyces cerevisiae encodes two Pif1 family DNA hel

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

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

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

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

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

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

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

111 The Saccharomyces cerevisiae FLO1 gene encodes a cell wall p

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

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

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

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

116 Saccharomyces cerevisiae Fpr4 is one such protein.

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

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

119 In Saccharomyces cerevisiae generation of export-competent

120 The Saccharomyces cerevisiae genome has undergone extensive

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

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

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

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

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

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

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

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

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

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

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

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

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

134 The Saccharomyces cerevisiae high-mobility group protein Hmo

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

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

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

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

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

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

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

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

143 ia innocua, Mycobacterium parafortuitum, and Saccharomyces cerevisiae inoculated onto the surface of

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

145 Activation of Saccharomyces cerevisiae Ire1 coincides with autophospho

146 Saccharomyces cerevisiae is a common yeast with several

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

148 Although Saccharomyces cerevisiae is a pervasive model organism f

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

150 The yeast Saccharomyces cerevisiae is consequently thought to be i

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

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

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

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

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

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

157 ntation (Bacillus subtilis, Rhizopus oryzae, Saccharomyces cerevisiae, Lactobacillus helveticus) on t

158 Saccharomyces cerevisiae mating-type switching is initia

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

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

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

162 Recently, the Saccharomyces cerevisiae minimal replication reaction ha

163 Mammalian and Saccharomyces cerevisiae mismatch repair (MMR) proteins

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

165 Among them, yeast Saccharomyces cerevisiae Mss116 participates in mitochon

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

167 1, was able to rescue the growth of a yeast (Saccharomyces cerevisiae) mutant defective in vacuolar i

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

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

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

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

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

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

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

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

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

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

178 In Saccharomyces cerevisiae, oxidative stress triggers Med1

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

180 In Saccharomyces cerevisiae, peroxisomes are the sole site

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

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

183 In Saccharomyces cerevisiae pho84 mutants, constitutively a

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

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

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

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

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

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

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

191 The Saccharomyces cerevisiae protein kinase Rad53 is a key r

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

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

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

195 port signal consensus sequence identified in Saccharomyces cerevisiae Prp40.

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

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

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

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

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

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

202 Saccharomyces cerevisiae RNA polymerase (Pol) II locates

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

204 In Saccharomyces cerevisiae, Rrp6 is exclusively nuclear an

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

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

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

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

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

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

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

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

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

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

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

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

217 Saccharomyces cerevisiae sir2Delta or top1Delta mutants

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

219 Like other eukaryotes, Saccharomyces cerevisiae spatially organizes its chromos

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

221 CB2 and the small subunit of SPT in a yeast (Saccharomyces cerevisiae) SPT-deficient mutant.

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

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

224 The Saccharomyces cerevisiae strain QA23 was the most effici

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

241 r its attachment to tRNA(Phe) We now show in Saccharomyces cerevisiae that PheRS misacylation of tRNA

242 Ras1 is a small GTPase in the budding yeast Saccharomyces cerevisiae that regulates nutrient signali

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

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

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

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

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

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

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

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

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

252 In Saccharomyces cerevisiae, the myosin V motor Myo2 binds

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

254 In Saccharomyces cerevisiae, the Pif1 helicase, a telomeras

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

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

257 In the yeast Saccharomyces cerevisiae, the Zap1 transcriptional activ

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

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

260 In contrast, Saccharomyces cerevisiae thiazole synthase (THI4p) uses

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

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

263 In Saccharomyces cerevisiae, three conserved Arf-GEFs funct

264 e reconstitute the noscapine gene cluster in Saccharomyces cerevisiae to achieve the microbial produc

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

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

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

268 Here, we use the GAL locus in Saccharomyces cerevisiae to investigate the influence of

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

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

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

272 We show that in Saccharomyces cerevisiae TRmD represents approximately 2

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

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

275 In Saccharomyces cerevisiae, UBI4 encodes five tandem ubiqu

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

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

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

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

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

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

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

283 ls is not observed in recently isolated wild Saccharomyces cerevisiae variants.

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

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

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

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

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

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

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

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

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

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

294 The cultures of Saccharomyces cerevisiae were treated with pulsed electr

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

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

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

298 Three commercial Saccharomyces cerevisiae yeast strains: Viniferm Revelac

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

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