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

1 etwork that regulates fat storage in budding yeast (Saccharomyces cerevisiae).

2 as reinhardtii, Escherichia coli and baker's yeast (Saccharomyces cerevisiae).

3 ) was isolated and functionally expressed in yeast (Saccharomyces cerevisiae).

4 raminearum, and Sclerotinia sclerotiorum and yeast (Saccharomyces cerevisiae).

5 mo sapiens), rice (Oryza sativa) and budding yeast (Saccharomyces cerevisiae).

6 rotein-protein interactions in planta and in yeast (Saccharomyces cerevisiae).

7 of autophagic proteasome turnover in budding yeast (Saccharomyces cerevisiae).

8 ogen-activated protein kinase pathway in the yeast Saccharomyces cerevisiae.

9 ap8 is critical for arsenic tolerance in the yeast Saccharomyces cerevisiae.

10 chemotropic fate transitions of the budding yeast Saccharomyces cerevisiae.

11 ystems in wild and laboratory strains of the yeast Saccharomyces cerevisiae.

12 lactate cytochrome c oxidoreductase from the yeast Saccharomyces cerevisiae.

13 tral role in zinc homeostasis in the budding yeast Saccharomyces cerevisiae.

14 mechanisms underlying CR, especially in the yeast Saccharomyces cerevisiae.

15 5' untranslated region (UTR) of mRNAs in the yeast Saccharomyces cerevisiae.

16 the replicative DNA polymerase-alpha in the yeast Saccharomyces cerevisiae.

17 induce recombination when transferred to the yeast Saccharomyces cerevisiae.

18 ied and characterized in vivo in the budding yeast Saccharomyces cerevisiae.

19 logous recombination with chromosomal DNA in yeast Saccharomyces cerevisiae.

20 ed cell cycle reentry from quiescence in the yeast Saccharomyces cerevisiae.

21 enzymatic activity is present in the budding yeast Saccharomyces cerevisiae.

22 nstitutively active promoters in the budding yeast Saccharomyces cerevisiae.

23 broadly across eukaryotes but absent in the yeast Saccharomyces cerevisiae.

24 ipophilic and hydrophilic mediators with the yeast Saccharomyces cerevisiae.

25 d to automate microdissection of the budding yeast Saccharomyces cerevisiae.

26 of yeast tolerance against HMF in industrial yeast Saccharomyces cerevisiae.

27 l wall of yeasts, especially that of baker's yeast Saccharomyces cerevisiae.

28 oci that influence protein expression in the yeast Saccharomyces cerevisiae.

29 on protein isolated from wild strains of the yeast Saccharomyces cerevisiae.

30 RNA emerging from transcribing Pol II in the yeast Saccharomyces cerevisiae.

31 tions in 145 diploid MA lines of the budding yeast Saccharomyces cerevisiae.

32 n that is homologous to Glo3p of the budding yeast Saccharomyces cerevisiae.

33 of MMR in vivo has been most advanced in the yeast Saccharomyces cerevisiae.

34 facultative multicellularity in the budding yeast Saccharomyces cerevisiae.

35 s mating-pheromone-mediated signaling in the yeast Saccharomyces cerevisiae.

36 (heat shock protein) gene regulation in the yeast Saccharomyces cerevisiae.

37 metaphase-anaphase transition in the budding yeast Saccharomyces cerevisiae.

38 ein and inserted in the same genomic site of yeast Saccharomyces cerevisiae.

39 st transit peptide and expressed them in the yeast Saccharomyces cerevisiae.

40 and human cultured cells, as well as in the yeast Saccharomyces cerevisiae.

41 body (P body) and the stress granule, in the yeast Saccharomyces cerevisiae.

42 s a master regulator of cell behavior in the yeast Saccharomyces cerevisiae.

43 of epsin Ent1 and the HIP1R homolog Sla2 in yeast Saccharomyces cerevisiae.

44 ary adaptation to a stressful environment in yeast Saccharomyces cerevisiae.

45 rence, and gene deletion (CRISPR-AID) in the yeast Saccharomyces cerevisiae.

46 have adapted Strand-seq to detect SCE in the yeast Saccharomyces cerevisiae.

47 tion with purified proteins from the budding yeast Saccharomyces cerevisiae.

48 r dynamics during endocytosis in the budding yeast Saccharomyces cerevisiae.

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

50 m has motivated domestication of the budding yeast Saccharomyces cerevisiae.

51 cies and a surprising version present in the yeast Saccharomyces cerevisiae.

52 reated by the HO endonuclease in the budding yeast Saccharomyces cerevisiae.

53 ividing cells during aging using the budding yeast, Saccharomyces cerevisiae.

54 ting for diurnal oscillations in the budding yeast, Saccharomyces cerevisiae.

55 we report 112 putative novel lncRNAs in the yeast Saccharomyces cerevisiae, 41 of which are only exp

56 The alpha pheromone from the budding yeast Saccharomyces cerevisiae, a 13-residue peptide tha

57 ds is carried out by fatty acid synthase: in yeast Saccharomyces cerevisiae, a 2.6-MDa molecular mass

58 tes and have been studied extensively in the yeast Saccharomyces cerevisiae, a model eukaryote previo

59 rnalization of labeled proteins and DNA into yeast Saccharomyces cerevisiae, a model eukaryotic syste

60 arginine and its metabolic precursors, and a yeast (Saccharomyces cerevisiae) ACOAT mutant was comple

61 In response to Fe deficiency, the yeast Saccharomyces cerevisiae activates transcription o

62 In the budding yeast Saccharomyces cerevisiae, Adr1-Cat8 and Adr1-Oaf1/

63 d VO regions of the V-ATPase by starving the yeast Saccharomyces cerevisiae, allowing us to obtain a

64 e heat stress response of this system in the yeast Saccharomyces cerevisiae and demonstrate how the c

65 prehensive genetic epistasis analysis in the yeast Saccharomyces cerevisiae and found that simultaneo

66 subpopulations of the partially domesticated yeast Saccharomyces cerevisiae and its wild relative Sac

67 is a multidomain protein called Mpe1 in the yeast Saccharomyces cerevisiae and RBBP6 in metazoans.

68 show that an obligate mutualism between the yeast Saccharomyces cerevisiae and the alga Chlamydomona

69 Here, we establish budding yeast Saccharomyces cerevisiae and the avian DT40 cell l

70 we compare homologous genes from the budding yeast Saccharomyces cerevisiae and the fission yeast Sch

71 d yet contrasting yeast species, the baker's yeast Saccharomyces cerevisiae and the wild yeast Saccha

72 as empirical measurements of GAL network in yeast Saccharomyces cerevisiae and TyrR-LiuR network in

73 s stimulated gene targeting up to 32-fold in yeast Saccharomyces cerevisiae and up to 16-fold in huma

74 The budding yeast, Saccharomyces cerevisiae and the nematode, Caenor

75 We used the budding yeasts Saccharomyces cerevisiae and Torulaspora delbruec

76 We additionally engineered the yeasts Saccharomyces cerevisiae and Yarrowia lipolytica

77 modifications are largely restricted to two yeasts, Saccharomyces cerevisiae and Schizosaccharomyces

78 a factor acting in cell cycle progression in yeast (Saccharomyces cerevisiae) and an important compon

79 Complementation studies in yeast (Saccharomyces cerevisiae) and Arabidopsis demonst

80 Since biochemical analysis of SAD6 in yeast (Saccharomyces cerevisiae) and Escherichia coli fa

81 In yeast (Saccharomyces cerevisiae) and human (Homo sapiens

82 We apply RPL in both baker's yeast (Saccharomyces cerevisiae) and human cells and gen

83 trols ribosome biogenesis and cell growth in yeast (Saccharomyces cerevisiae) and human.

84 Prior studies in both budding yeast (Saccharomyces cerevisiae) and in human cells have

85 In yeast (Saccharomyces cerevisiae) and in planta, we furth

86 e used synthetic auxin degradation assays in yeast (Saccharomyces cerevisiae) and in plants to charac

87 ired for isotropic bud growth1 protein) from yeast (Saccharomyces cerevisiae) and its paralog Reh1p (

88 In many eukaryotic organisms, including yeast (Saccharomyces cerevisiae) and mammals, copper and

89 -PM contact site components and functions in yeast (Saccharomyces cerevisiae) and mammals, relatively

90 SsMT2-transgenic yeast (Saccharomyces cerevisiae) and plants (Arabidopsis

91 In bacteria, yeast (Saccharomyces cerevisiae), and mammals, these hyd

92 hila melanogaster, the cell cycle of budding yeast Saccharomyces cerevisiae, and the floral organ arr

93 rformed a systematic visual screen using the yeast Saccharomyces cerevisiae, and uncovered three unch

94 an integral membrane class found in plants, yeast (Saccharomyces cerevisiae), animals, and bacteria.

95 fusion between the C-terminal domain of the yeast (Saccharomyces cerevisiae) AP-1-like (YAP1) transc

96 that were recently discovered in the budding yeast Saccharomyces cerevisiae are interesting because t

97 Ypt31/32 in the yeast Saccharomyces cerevisiae are involved in regulatin

98 rs of histone gene expression in the budding yeast Saccharomyces cerevisiae are known, yet the key os

99 he major cytoplasmic Hsp70 chaperones in the yeast Saccharomyces cerevisiae are the Ssa proteins, and

100 d some unpublished, tetrad data from budding yeast (Saccharomyces cerevisiae) are analyzed for dispar

101 Most genomes, including yeast Saccharomyces cerevisiae, are pervasively transcri

102 Here we used the mating differentiation in yeast Saccharomyces cerevisiae as a model and developed

103 onsider a recent evolution experiment on the yeast Saccharomyces cerevisiae as a unique platform to a

104 n aggregates was addressed using the bakers' yeast Saccharomyces cerevisiae as the model.

105 uction of salidroside can be achieved in the yeast Saccharomyces cerevisiae as well as the plant Nico

106 Yeasts (Saccharomyces cerevisiae), as used in brewing an

107 of extracellular glucose is crucial for the yeast Saccharomyces cerevisiae because of its fermentati

108 eIF4E1c-type proteins support translation in yeast (Saccharomyces cerevisiae) but promote translation

109 been extensively studied in prokaryotes and yeast (Saccharomyces cerevisiae), but little is known fo

110 translational efficiencies (TEs) in budding yeast Saccharomyces cerevisiae by ribosome footprint pro

111 The budding yeast Saccharomyces cerevisiae can respond to nutritiona

112 aneously arising mutation that activates the yeast (Saccharomyces cerevisiae) CDC25 family phosphatas

113 In the budding yeast Saccharomyces cerevisiae, Cdh1 associates with the

114 lly identify candidate substrates of budding yeast Saccharomyces cerevisiae Cdk1 and show dependency

115 otein activity was also observed in vivo, in yeast (Saccharomyces cerevisiae) cells expressing TCP pr

116 s EF can orient cell polarization in budding yeast (Saccharomyces cerevisiae) cells, directing the gr

117 re recently, a synthetic designer version of yeast Saccharomyces cerevisiae chromosome III has been g

118 cell imaging of the MAT-locus located on the yeast Saccharomyces cerevisiae chromosome III, we recove

119 During the entire meiotic prophase of the yeast Saccharomyces cerevisiae, chromosomes perform rapi

120 In animals and yeast (Saccharomyces cerevisiae), CL depletion affects t

121 For the model yeast Saccharomyces cerevisiae, claims that trehalose is

122 ne and protein information about the budding yeast Saccharomyces cerevisiae, containing a variety of

123 ne and protein information about the budding yeast Saccharomyces cerevisiae, containing a variety of

124 ing these methods to 46 traits measured in a yeast (Saccharomyces cerevisiae) cross, we estimate that

125 In the budding yeast Saccharomyces cerevisiae, cytosolic Hsp70 interact

126 Here, we show that the yeast Saccharomyces cerevisiae DEAD box protein Mss116p,

127 bons, and heterologous expression of CER2 in yeast (Saccharomyces cerevisiae) demonstrated that it ca

128 In the yeast Saccharomyces cerevisiae, Dgk1 diacylglycerol (DAG

129 In the yeast Saccharomyces cerevisiae, different types of stres

130 Remarkably, we show that the baker's yeast Saccharomyces cerevisiae does not reject mates eng

131 global proteomic alterations in the budding yeast Saccharomyces cerevisiae due to differences in car

132 In the yeast Saccharomyces cerevisiae, each strategy is able to

133 In the budding yeast Saccharomyces cerevisiae, ECM remodeling refers to

134 The yeast Saccharomyces cerevisiae employs multiple pathways

135 The budding yeast Saccharomyces cerevisiae expresses different isofo

136 port on experimental results for the budding yeast Saccharomyces cerevisiae, finding, surprisingly, t

137 e investigated this question by evolving the yeast Saccharomyces cerevisiae for 2200 generations unde

138 Some strains of the budding yeast Saccharomyces cerevisiae form colony biofilms, and

139 As one of four FKBPs within the yeast Saccharomyces cerevisiae, Fpr4 has been described

140 We show that origin positions in the yeast Saccharomyces cerevisiae genome conform to all thr

141 In the yeast Saccharomyces cerevisiae, glucose starvation cause

142 In the budding yeast Saccharomyces cerevisiae, GPCRs detect and respond

143 The budding yeast, Saccharomyces cerevisiae, harbors several prions

144 The budding yeast Saccharomyces cerevisiae has been used in laborato

145 A mutagenesis screen in the yeast Saccharomyces cerevisiae has identified several ga

146 de gene network (DPH1-DPH7) from the budding yeast Saccharomyces cerevisiae has significantly advance

147 ed to investigate unicellular processes, the yeast Saccharomyces cerevisiae has the ability to form c

148 The budding yeast, Saccharomyces cerevisiae, has one PFN1 ortholog.

149 s of homotypic vacuole-vacuole fusion in the yeast Saccharomyces cerevisiae have been instrumental in

150 ies of copper-dependent transcription in the yeast Saccharomyces cerevisiae have focused on the respo

151 ositive feedback, and studies in the budding yeast Saccharomyces cerevisiae have suggested distinct p

152 ss-response element in gene promoters in the yeast Saccharomyces cerevisiae However, the roles of Msn

153 both phosphorylated and ubiquitylated in the yeast Saccharomyces cerevisiae, identifying 466 proteins

154 Laboratory evolution of the yeast Saccharomyces cerevisiae in bioreactor batch cultu

155 ome sequences for 85 diverse isolates of the yeast Saccharomyces cerevisiae-including wild, domestica

156 Starvation of diploid cells of the budding yeast Saccharomyces cerevisiae induces them to enter mei

157 The Ty1 retrotransposon of the yeast Saccharomyces cerevisiae integrates upstream of RN

158 The budding yeast Saccharomyces cerevisiae is a long-standing model

159 The industrial yeast Saccharomyces cerevisiae is a traditional ethanolo

160 The yeast Saccharomyces cerevisiae is able to use para-amino

161 Yeast Saccharomyces cerevisiae is among preferred cell f

162 The yeast Saccharomyces cerevisiae is an advanced model orga

163 The yeast Saccharomyces cerevisiae is consequently thought t

164 k protein 90 (Hsp90) chaperone system of the yeast Saccharomyces cerevisiae is greatly impaired in na

165 l3p, the major triacylglycerol lipase of the yeast Saccharomyces cerevisiae, is a component of lipid

166 The [PSI(+)] prion, endogenous to the yeast Saccharomyces cerevisiae, is a dominantly inherite

167 expression of the sole PP1, Glc7, in budding yeast, Saccharomyces cerevisiae, is lethal.

168 nted by a second co-repressor that the model yeast Saccharomyces cerevisiae lacks.

169 Here we show that in the yeast Saccharomyces cerevisiae, LDs can also be turned o

170 ier family, however, have been identified in yeast (Saccharomyces cerevisiae; Leu-5p) and mammals (SL

171 Ethanol toxicity in the yeast Saccharomyces cerevisiae limits titer and producti

172 Under aerobic conditions, the budding yeast Saccharomyces cerevisiae metabolizes glucose predo

173 Activity assays with yeast (Saccharomyces cerevisiae) microsomes showed a hig

174 on and Thr-446 autophosphorylation using the yeast Saccharomyces cerevisiae model system.

175 Among them, yeast Saccharomyces cerevisiae Mss116 participates in mi

176 t TaVIT1, was able to rescue the growth of a yeast (Saccharomyces cerevisiae) mutant defective in vac

177 reover, heterologous expression of SynAas in yeast (Saccharomyces cerevisiae) mutants lacking the maj

178 Such a set was produced for the yeast, Saccharomyces cerevisiae near the end of the 20th

179 manifestations and applied this approach to yeast (Saccharomyces cerevisiae), nematode worm (Caenorh

180 hCNT1, -2, and -3) produced individually in yeast Saccharomyces cerevisiae Nilotinib inhibited hENT1

181 tography analysis, split ubiquitin assays in yeast (Saccharomyces cerevisiae NMY51), and bimolecular

182 e mapping, which revealed that 5% of budding yeast (Saccharomyces cerevisiae) nucleosome positions ha

183 cessing of three PSTVd RNA constructs in the yeast Saccharomyces cerevisiae Of these, only one form,

184 we grew cross-feeding strains of the budding yeast Saccharomyces cerevisiae on agar surfaces as a mod

185 est protein and DHFR are coexpressed, in the yeast Saccharomyces cerevisiae, on a low-copy plasmid fr

186 l3p, the major triacylglycerol lipase of the yeast Saccharomyces cerevisiae, on lipid droplets.

187 A yeast (Saccharomyces cerevisiae) one-hybrid screen with

188 In the yeast Saccharomyces cerevisiae, organelles and macromole

189 (AHK1) can complement the osmosensitivity of yeast (Saccharomyces cerevisiae) osmosensor mutants lack

190 hetic auxin response circuits in the budding yeast Saccharomyces cerevisiae Our analysis revealed tha

191 In yeast (Saccharomyces cerevisiae), PEX2, PEX10, and a thi

192 In polarizing cells of the model yeast Saccharomyces cerevisiae, positive feedback can tr

193 he cryo-electron microscopy structure of the yeast Saccharomyces cerevisiae pre-catalytic B complex s

194 synthetic amyloid fibrils assembled from the yeast (Saccharomyces cerevisiae) prion protein Sup35NM.

195 evels of endogenous hydrogen peroxide in the yeast Saccharomyces cerevisiae promote site-specific end

196 a benthamiana) plants that overexpress three yeast (Saccharomyces cerevisiae) protein subunits of DNA

197 ally defined point centromere in the budding yeast Saccharomyces cerevisiae provides a unique opportu

198 The yeast Saccharomyces cerevisiae provides a valuable model

199 In the yeast Saccharomyces cerevisiae, Q is synthesized by the

200 are the major triacylglycerol lipases of the yeast Saccharomyces cerevisiae Recently we demonstrated

201 ionally repressed chromosomal domains in the yeast Saccharomyces cerevisiae represent specialized sit

202 In the yeast Saccharomyces cerevisiae, respiratory chain superc

203 es or a defect in nucleosome assembly in the yeast Saccharomyces cerevisiae results in increased mito

204 Here we show that the loss of Set2 in yeast, Saccharomyces cerevisiae, results in transcriptio

205 equencing of these fragments in DNA from the yeast Saccharomyces cerevisiae revealed widespread ribon

206 In the yeast Saccharomyces cerevisiae, ribosome biogenesis is h

207 e more recently evolved circuit in the model yeast Saccharomyces cerevisiae (Sc), the generalist repr

208 rmined for Homo sapiens (Hs) and the budding yeasts Saccharomyces cerevisiae (Sc) and Kluyveromyces l

209 Here, a yeast (Saccharomyces cerevisiae) SEIPIN deletion mutant

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

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

212 In the budding yeast Saccharomyces cerevisiae, septins form an 'hourgla

213 Phospholipid signaling in the budding yeast Saccharomyces cerevisiae shares similarities with

214 s examining sugar utilization in the budding yeast Saccharomyces cerevisiae, show that considerable h

215 ana as well as functional complementation in yeast (Saccharomyces cerevisiae) showed that both AtCNGC

216 oform Delta0-ELO1 Heterologous expression in yeast (Saccharomyces cerevisiae) showed that NgDelta0-EL

217 In the budding yeast Saccharomyces cerevisiae, size control occurs in G

218 ) and LCB2 and the small subunit of SPT in a yeast (Saccharomyces cerevisiae) SPT-deficient mutant.

219 The budding yeast Saccharomyces cerevisiae stores iron in the vacuol

220 eins (at a 1% false discovery rate (FDR)) in yeast (Saccharomyces cerevisiae strain BY4741) over 70 m

221 ility to complement the defects of a Baker's yeast (Saccharomyces cerevisiae) strain lacking the mito

222 ul1 and Sul2 are sulfate transporters in the yeast Saccharomyces cerevisiae, strongly induced upon su

223 ficial odorant sensing system in the budding yeast Saccharomyces cerevisiae suffered from low sensiti

224 8, is capable of excising and reinserting in yeast (Saccharomyces cerevisiae), suggesting that yeast

225 4 subunit of the ubiquitin ligase GID in the yeast Saccharomyces cerevisiae targeted the gluconeogeni

226 and vacuole protein sorting) complex in the yeast Saccharomyces cerevisiae tethers membranes through

227 t of strong, synthetic promoters for budding yeast Saccharomyces cerevisiae that are inducible under

228 stacle, we engineered strains of the budding yeast Saccharomyces cerevisiae that differ only in the p

229 Pah1 is the phosphatidate phosphatase in the yeast Saccharomyces cerevisiae that produces diacylglyce

230 Ras1 is a small GTPase in the budding yeast Saccharomyces cerevisiae that regulates nutrient s

231 y, we established a BTHS-mutant panel in the yeast Saccharomyces cerevisiae that successfully models

232 vide an overview of protein synthesis in the yeast Saccharomyces cerevisiae The mechanism of protein

233 In the yeast Saccharomyces cerevisiae the TOR complex 1 (TORC1)

234 In budding yeast (Saccharomyces cerevisiae) the multilayered spindl

235 Here we show that, in the budding yeast Saccharomyces cerevisiae, the catalytic activity o

236 In the yeast Saccharomyces cerevisiae, the complex binds discre

237 In the yeast Saccharomyces cerevisiae, the DGK1-encoded diacylg

238 In the yeast Saccharomyces cerevisiae, the essential nuclear he

239 In the yeast Saccharomyces cerevisiae, the exposure to mating p

240 In the budding yeast Saccharomyces cerevisiae, the F-BAR protein Hof1 l

241 In the yeast Saccharomyces cerevisiae, the genes encoding the m

242 In the yeast Saccharomyces cerevisiae, the large ribosomal subu

243 We found that in the yeast Saccharomyces cerevisiae, the MMR system and the f

244 In the yeast Saccharomyces cerevisiae, the nuclear-encoded prot

245 In the yeast Saccharomyces cerevisiae, the oleate-induced PTS2-

246 In the yeast Saccharomyces cerevisiae, the Opi1p repressor cont

247 In the yeast Saccharomyces cerevisiae, the regulation of cell t

248 AMPK's homolog in the yeast Saccharomyces cerevisiae, the SNF1 protein kinase,

249 In the yeast Saccharomyces cerevisiae, the switch from respirat

250 In the yeast Saccharomyces cerevisiae, the synthesis of phospho

251 In budding yeast Saccharomyces cerevisiae, the ten-subunit Dam1/DAS

252 In the yeast Saccharomyces cerevisiae, the transcription factor

253 In the yeast Saccharomyces cerevisiae, the UPR activation invol

254 In the yeast Saccharomyces cerevisiae, the Zap1 transcriptional

255 iple vital cellular functions in the budding yeast Saccharomyces cerevisiae These include regulation

256 In the budding yeast Saccharomyces cerevisiae, these domains are struct

257 ear microtubule (MT) dynamics in the budding yeast Saccharomyces cerevisiae This activity requires in

258 In the yeast Saccharomyces cerevisiae, this inner membrane comp

259 Yeast (Saccharomyces cerevisiae) three-hybrid and bimole

260 AGG2, or AGG3) with differing specificity in yeast (Saccharomyces cerevisiae) three-hybrid assays.

261 en S. pombe and the highly divergent budding yeast Saccharomyces cerevisiae Thus, transcriptional int

262 xpressed cause chromosome instability in the yeast Saccharomyces cerevisiae To better understand the

263 Here we engineer the baker's yeast Saccharomyces cerevisiae to produce and secrete th

264 ental Prisoner's Dilemma game in the budding yeast Saccharomyces cerevisiae to show that, despite los

265 ein-based element of inheritance that allows yeast (Saccharomyces cerevisiae) to circumvent a hallmar

266 We used the budding yeast, Saccharomyces cerevisiae, to ask whether nutrient

267 In the yeast Saccharomyces cerevisiae, trehalose is essential f

268 t two Arabidopsis genes encoding homologs of yeast (Saccharomyces cerevisiae) tRNA adenosine deaminas

269 vivo protein interactions were evidenced by yeast (Saccharomyces cerevisiae) two-hybrid analysis and

270 We used yeast (Saccharomyces cerevisiae) two-hybrid analysis to

271 In yeast (Saccharomyces cerevisiae) two-hybrid and bimolecu

272 Here, we report that using a yeast (Saccharomyces cerevisiae) two-hybrid approach, we

273 ns and interacted with both TIR1 and IAA7 in yeast (Saccharomyces cerevisiae) two-hybrid experiments,

274 Using a yeast (Saccharomyces cerevisiae) two-hybrid library of S

275 a] Soybean Response to Cold [AtSRC2.2]) in a yeast (Saccharomyces cerevisiae) two-hybrid screen and h

276 protein phosphoglycerate dehydrogenase in a yeast (Saccharomyces cerevisiae) two-hybrid screen; othe

277 By means of yeast (Saccharomyces cerevisiae) two-hybrid screening, w

278 tion of RISAP, a RAC5 effector identified by yeast (Saccharomyces cerevisiae) two-hybrid screening.

279 A membrane-based yeast (Saccharomyces cerevisiae) two-hybrid system estab

280 ins, a mutant screen was performed using the yeast (Saccharomyces cerevisiae) two-hybrid system in Ar

281 oteins involved in this process, we used the yeast (Saccharomyces cerevisiae) two-hybrid system to sc

282 for mapping hybrid-prone regions in budding yeast Saccharomyces cerevisiae Using this methodology, w

283 probe FISH protocol termed sFISH for budding yeast, Saccharomyces cerevisiae using a single DNA probe

284 smid-based NHEJ DNA repair screen in budding yeast (Saccharomyces cerevisiae) using 369 putative none

285 scribe the control of growth of the brewer's yeast, Saccharomyces cerevisiae, using both transcriptio

286 the identification of CTPD substrates in the yeast Saccharomyces cerevisiae via a quantitative proteo

287 In this study, using a yeast (Saccharomyces cerevisiae) vps23Delta bro1Delta do

288 Here, the yeast Saccharomyces cerevisiae was used as model to inve

289 The extract of sugar-cane yeast (Saccharomyces cerevisiae) was enzymatically hydro

290 ants from a cross between two strains of the yeast Saccharomyces cerevisiae We identified a nonsynony

291 antitative attributes of PKA dynamics in the yeast Saccharomyces cerevisiae, we developed an optogene

292 cell cycle function of Cdc48 in the budding yeast Saccharomyces cerevisiae, we found that double mut

293 Using the yeast Saccharomyces cerevisiae, we report that SOD1 tran

294 In the budding yeast Saccharomyces cerevisiae, we show that spindle len

295 ween Pih1 and the proteasome subunit Rpn8 in yeast Saccharomyces cerevisiae when HSP90 co-chaperone T

296 This cannot apply to the yeast Saccharomyces cerevisiae, where this mechanism wou

297 ABA-GE transport activity when expressed in yeast (Saccharomyces cerevisiae), which also supports th

298 been extensively studied in the unicellular yeast Saccharomyces cerevisiae, which exhibits separate

299 escribed in model species, especially in the yeast Saccharomyces cerevisiae, which helped to shape ge

300 this question, we fused every protein in the yeast Saccharomyces cerevisiae with a partner from each