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1 three S. cerevisiae strains and the two non-Saccharomyces.
3 hether the synthetic pathway of Melatonin in Saccharomyces and non-Saccharomyces strains involves the
4 es synXII strain that would be identified as Saccharomyces bayanus by standard DNA barcoding procedur
5 pressure homogenization-induced autolysis of Saccharomyces bayanus wine yeasts, treated at 150MPa.
6 l yeasts including Saccharomyces cerevisiae, Saccharomyces bayanus, and Torulaspora delbrueckii strai
7 model, built from existing gene networks in Saccharomyces, captures most known autophagy components
9 his end, seven commercial strains comprising Saccharomyces cerevisiae (Red Fruit, ES488, Lalvin QA23,
10 expressed and purified the luminal domain of Saccharomyces cerevisiae (S. cerevisiae) Gpi8 using diff
11 amenable for structural studies, while their Saccharomyces cerevisiae (yeast) homologs are stable com
12 quence motif in irregular telomeric DNA from Saccharomyces cerevisiae (yeast), is demonstrated to ado
13 fruits using two different native isolates (Saccharomyces cerevisiae - KF551990 and Pichia gummigutt
14 tion products created specialized strains of Saccharomyces cerevisiae [3, 4] that were transported al
15 l memory confers a strong fitness benefit in Saccharomyces cerevisiae adapting to growth in galactose
16 ilus V/A-ATPase and eukaryotic V-ATPase from Saccharomyces cerevisiae allowed identification of the a
17 ondrial peroxiredoxin Prx3 when expressed in Saccharomyces cerevisiae Altogether, the processing of p
18 ion of nine genes was stably integrated into Saccharomyces cerevisiae and afforded forskolin titers o
19 found that the effects on prion formation in Saccharomyces cerevisiae and aggregation in vitro could
21 stal structures of the Mep2 orthologues from Saccharomyces cerevisiae and Candida albicans and show t
23 tion complexes (ECs) in Escherichia coli and Saccharomyces cerevisiae and found that 1-3% of all ECs
24 sive genetic epistasis analysis in the yeast Saccharomyces cerevisiae and found that simultaneous del
25 a sanitizers deactivated greater than 99% of Saccharomyces cerevisiae and greater than 99.9% of Esche
26 ulations of the partially domesticated yeast Saccharomyces cerevisiae and its wild relative Saccharom
27 e, we purified recombinant human SPCA1a from Saccharomyces cerevisiae and measured Ca(2+)-dependent A
28 n humans (or its yeast orthologues, Rad26 in Saccharomyces cerevisiae and Rhp26 in Schizosaccharomyce
29 A, a protein required for SPB duplication in Saccharomyces cerevisiae and S. pombe and PcpA, the anch
30 ations are largely restricted to two yeasts, Saccharomyces cerevisiae and Schizosaccharomyces pombe,
31 delbrueckii in sequential fermentation with Saccharomyces cerevisiae and Schizosaccharomyces pombe.
32 ved; orthologs from Arabidopsis thaliana and Saccharomyces cerevisiae are predominantly Ins(1,4,5)P3
33 ts of potassium uptake in the model organism Saccharomyces cerevisiae are the Trk1 high affinity pota
34 we used the mating differentiation in yeast Saccharomyces cerevisiae as a model and developed integr
37 of salidroside can be achieved in the yeast Saccharomyces cerevisiae as well as the plant Nicotiana
38 a multiplex genome engineering technology in Saccharomyces cerevisiae based on annealing synthetic ol
40 ne and secretion of a recombinant protein in Saccharomyces cerevisiae by up to 28- and 3-fold, respec
41 Here, we show that sexual agglutination of Saccharomyces cerevisiae can be reprogrammed to link int
42 and RNase H activity in Escherichia coli or Saccharomyces cerevisiae caused R-loop accumulation alon
43 apply it to study the growth of independent Saccharomyces cerevisiae cells in two different growth m
45 quantify transcript heterogeneity in single Saccharomyces cerevisiae cells treated with and without
48 single-molecule imaging to demonstrate that Saccharomyces cerevisiae condensin is a molecular motor
51 First, fed-batch glucose fermentations by Saccharomyces cerevisiae D5A revealed that this strain,
56 ranslation of mitochondrial gene products in Saccharomyces cerevisiae depends on mRNA-specific activa
58 to reveal aspects of the contribution of the Saccharomyces cerevisiae DNA damage-responsive kinase Te
59 Here we show the SUMO isopeptidase Ulp2 in Saccharomyces cerevisiae does not prevent the accumulati
60 thway is a variant of selective autophagy in Saccharomyces cerevisiae during which hydrolases such as
61 nesis, and X-ray structural data analysis of Saccharomyces cerevisiae eEF1A, we identified a posttran
64 een DNA instability and CTD repeat number in Saccharomyces cerevisiae First, analysis of 36 diverse S
66 is-specific DNA double-strand break (DSB) in Saccharomyces cerevisiae folds into G-quadruplex, and th
67 d the resulting substrate was fermented with Saccharomyces cerevisiae for 7-10days under aerobic cond
69 the curvature-stabilizing protein Yop1p from Saccharomyces cerevisiae form a tubular network upon add
71 endpoints genome-wide at high resolution in Saccharomyces cerevisiae Full-length resection requires
73 eukaryotic genome, Sc2.0, a highly modified Saccharomyces cerevisiae genome reduced in size by nearl
74 efficient method to functionally explore the Saccharomyces cerevisiae genome using saturated transpos
77 d from renewable sources including wild-type Saccharomyces cerevisiae glycoproteins and lipid-linked
79 the function of synaptonemal complex (SC) in Saccharomyces cerevisiae has mainly focused on in vivo a
81 containing the vacuolar a-subunit isoform in Saccharomyces cerevisiae Here we demonstrate that PI(4)P
82 ortant examples of regulated RNA splicing in Saccharomyces cerevisiae Here, we report a role for the
84 olgi network (TGN) to the plasma membrane in Saccharomyces cerevisiae However, exomer mutants are hig
85 ponse element in gene promoters in the yeast Saccharomyces cerevisiae However, the roles of Msn2/4 in
87 ystal structure of an N-terminal fragment of Saccharomyces cerevisiae Hsp104 with the N domain of one
88 evel microsatellite profiling approach, SID (Saccharomyces cerevisiae IDentifier), to identify the st
98 ein 90 (Hsp90) chaperone system of the yeast Saccharomyces cerevisiae is greatly impaired in naa10Del
100 roteome and metabolome in a repertoire of 16 Saccharomyces cerevisiae laboratory backgrounds, combina
102 ave combined biochemical purification of the Saccharomyces cerevisiae Mediator from chromatin with ch
103 Under aerobic conditions, the budding yeast Saccharomyces cerevisiae metabolizes glucose predominant
104 nerated in silico by computationally pooling Saccharomyces cerevisiae microsatellite profiles, and on
109 suppressed the Mn-sensitive phenotype of the Saccharomyces cerevisiae mutant Deltapmr1 Our results in
110 f nuclear and mitochondrial encoded mRNAs in Saccharomyces cerevisiae NAD-mRNA appears to be produced
111 g of three PSTVd RNA constructs in the yeast Saccharomyces cerevisiae Of these, only one form, a cons
115 s demonstrated that degradation of Mrc1, the Saccharomyces cerevisiae ortholog of human Claspin, is f
116 TbSTT3C that can functionally complement the Saccharomyces cerevisiae OST, making it an ideal experim
117 model, we found that M1 promoted survival in Saccharomyces cerevisiae overexpressing human Apaf-1 and
118 be rescued by the expression of human PEX16, Saccharomyces cerevisiae Pex34, or by overexpression of
119 on of M. polymorpha core PTB proteins in the Saccharomyces cerevisiae pho2 mutant defective in high-a
123 redox activity of the [4Fe4S](2+) cluster in Saccharomyces cerevisiae polymerase (Pol) delta, the lag
125 o-electron microscopy structure of the yeast Saccharomyces cerevisiae pre-catalytic B complex spliceo
126 of endogenous hydrogen peroxide in the yeast Saccharomyces cerevisiae promote site-specific endonucle
128 se mutations from the affected subjects into Saccharomyces cerevisiae provided functional evidence to
132 in the ATPase-active B, C, and D subunits of Saccharomyces cerevisiae replication factor C (RFC) clam
133 ication, similar to type II ALT survivors in Saccharomyces cerevisiae Replication stresses induced by
134 specific unconventional secretion of Acb1 in Saccharomyces cerevisiae requires ESCRT-I, -II, and -III
136 e-sequenced a well characterized genome, the Saccharomyces cerevisiae S288C strain using three differ
138 iption coupled DNA repair (TCR) in the yeast Saccharomyces cerevisiae Sen1, a DNA/RNA helicase that i
140 A polymerase II (RNAPII) and is catalyzed by Saccharomyces cerevisiae Set1 and Set2, respectively.
141 stal structure of the interacting domains of Saccharomyces cerevisiae Sgt1 and Skp1 at 2.8 A resoluti
142 se II-catalyzed transcription in the rDNA of Saccharomyces cerevisiae Sir2 is recruited to nontranscr
145 the cryo-electron microscopy structure of a Saccharomyces cerevisiae spliceosome stalled after Prp16
147 strain also affected flavour synthesis with Saccharomyces cerevisiae strain A01 producing considerab
149 tes that yeast involved in wine making, i.e. Saccharomyces cerevisiae strains and the non-Saccharomyc
152 d rescued the growth of Escherichia coli and Saccharomyces cerevisiae strains with inactivations of t
153 We present the crystal structure of the Saccharomyces cerevisiae Stu2 C-terminal domain, reveali
154 y during anaphase to promote mitotic exit in Saccharomyces cerevisiae Surprisingly, human CDC14A is n
155 e, synXII, based on native chromosome XII in Saccharomyces cerevisiae SynXII was assembled using a tw
156 nit of the ubiquitin ligase GID in the yeast Saccharomyces cerevisiae targeted the gluconeogenic enzy
157 ts of 235 single-nucleotide mutations in the Saccharomyces cerevisiae TDH3 promoter (PTDH3 ) on the a
158 acuole protein sorting) complex in the yeast Saccharomyces cerevisiae tethers membranes through its a
160 e, we designed dCas9-Mxi1-based NOR gates in Saccharomyces cerevisiae that allow arbitrary connectivi
161 c mitogen-activated protein kinase (MAPK) in Saccharomyces cerevisiae that couples spore morphogenesi
162 , we engineered strains of the budding yeast Saccharomyces cerevisiae that differ only in the presenc
163 tion, we focused on a highly diverged IDR in Saccharomyces cerevisiae that is involved in regulating
164 assembly factor, Pet117, and demonstrate in Saccharomyces cerevisiae that this evolutionarily conser
165 s and Candida albicans but is cytoplasmic in Saccharomyces cerevisiae The P. pastoris strain carrying
166 genome-wide gene perturbation experiments in Saccharomyces cerevisiae The results suggest that predic
167 es the repair of DNA double-strand breaks in Saccharomyces cerevisiae The role of Sae2 is linked to t
169 occurring DSBs at (GAA)n microsatellites in Saccharomyces cerevisiae These data gave us important in
170 ital cellular functions in the budding yeast Saccharomyces cerevisiae These include regulation of tel
171 crotubule (MT) dynamics in the budding yeast Saccharomyces cerevisiae This activity requires interact
177 ously proposed general base residue (D210 in Saccharomyces cerevisiae Trm10) is not likely to play th
179 e used single molecule fluorescence to study Saccharomyces cerevisiae U1 and BBP interactions with RN
181 as constructed, which is fully functional in Saccharomyces cerevisiae under all conditions tested and
182 In response to starvation, diploid cells of Saccharomyces cerevisiae undergo meiosis and form haploi
183 rget the ACT1 promoter of the model organism Saccharomyces cerevisiae using a dCas9-based transcripti
184 ISH protocol termed sFISH for budding yeast, Saccharomyces cerevisiae using a single DNA probe labele
185 motypic vacuolar lysosome membrane fusion in Saccharomyces cerevisiae Using cell-free fusion assays a
186 cation, we conducted a genome-wide screen in Saccharomyces cerevisiae using DNA polymerase active-sit
187 apping hybrid-prone regions in budding yeast Saccharomyces cerevisiae Using this methodology, we iden
188 entification of CTPD substrates in the yeast Saccharomyces cerevisiae via a quantitative proteomic an
190 dentifying Mms1 binding sites genome-wide in Saccharomyces cerevisiae we connected Mms1 function to g
191 of the genetically tractable model organism Saccharomyces cerevisiae We used this system to determin
193 we aimed at identifying the function of the Saccharomyces cerevisiae Ydr109c protein and its human h
196 y arising mutation that activates the yeast (Saccharomyces cerevisiae) CDC25 family phosphatase, Mih1
197 The related protein Hsp110 (Sse1/Sse2 in Saccharomyces cerevisiae) functions as a nucleotide exch
198 1, was able to rescue the growth of a yeast (Saccharomyces cerevisiae) mutant defective in vacuolar i
199 , filopodia supported the uptake of zymosan (Saccharomyces cerevisiae) particles by (i) providing fix
201 elta0-ELO1 Heterologous expression in yeast (Saccharomyces cerevisiae) showed that NgDelta0-ELO1 coul
206 The alpha pheromone from the budding yeast Saccharomyces cerevisiae, a 13-residue peptide that elic
207 duced by cyclic AMP (FIC)-1, respectively-in Saccharomyces cerevisiae, a eukaryote that lacks endogen
208 rm for multiplex genome-scale engineering in Saccharomyces cerevisiae, an important eukaryotic model
209 viable counts of Staphylococcus epidermidis, Saccharomyces cerevisiae, and MS2 Bacteriophage after li
210 date the molecular basis of TCS mutations in Saccharomyces cerevisiae, and present a new model for ho
213 t other kinesins, Cin8, a kinesin-5 motor in Saccharomyces cerevisiae, can move bidirectionally along
219 bidopsis thaliana, Dictyostelium discoideum, Saccharomyces cerevisiae, Escherichia coli and Methanoca
221 step for the synthesis of triacylglycerol in Saccharomyces cerevisiae, exerts a negative regulatory e
224 n experimental results for the budding yeast Saccharomyces cerevisiae, finding, surprisingly, that ce
228 genes encoding these enzymes in E. coli and Saccharomyces cerevisiae, I was in a position to alter p
229 gation factors (E4), represented by Ufd2p in Saccharomyces cerevisiae, is a pivotal regulator for man
230 otein and DHFR are coexpressed, in the yeast Saccharomyces cerevisiae, on a low-copy plasmid from two
231 mosan, which is the cell wall preparation of Saccharomyces cerevisiae, or poly (I:C) was coated on a
234 netic studies in various fungi, particularly Saccharomyces cerevisiae, provided the key initial break
236 nd six different commercial yeasts including Saccharomyces cerevisiae, Saccharomyces bayanus, and Tor
237 ere, leveraging population genomic data from Saccharomyces cerevisiae, Schizosaccharomyces pombe, and
239 ortant examples of regulated RNA splicing in Saccharomyces cerevisiae, such as splicing of meiotic tr
253 agenesis of the mitochondrial COX1 gene from Saccharomyces cerevisiae, we demonstrate that mutations
254 tive attributes of PKA dynamics in the yeast Saccharomyces cerevisiae, we developed an optogenetic st
256 vivo crosslinking and genetic approaches in Saccharomyces cerevisiae, we found that both domains of
257 context of an actively transcribed locus in Saccharomyces cerevisiae, we tested whether co-transcrip
259 hydroxyglutarate in tumors were generated in Saccharomyces cerevisiae, which has histone demethylases
260 quences for 85 diverse isolates of the yeast Saccharomyces cerevisiae-including wild, domesticated, a
287 chromosome conformation capture on diverged Saccharomyces hybrid diploids to obtain the first global
289 ary range of yeasts: inside the best-studied Saccharomyces species complex, and across the entire and
290 egulation is recently evolved; in a diverged Saccharomyces species, GAL genes show constitutively fas
291 athway of Melatonin in Saccharomyces and non-Saccharomyces strains involves these intermediates.
292 species identity, were swapped to generate a Saccharomyces synXII strain that would be identified as
293 Saccharomyces cerevisiae strains and the non-Saccharomyces Torulaspora delbrueckii, can synthesise HT
294 A23, Uvaferm BC, and Lalvin ICV GRE) and non-Saccharomyces (Torulaspora delbrueckii and Metschnikowia
295 either conserved sequence or position within Saccharomyces uORFs initiating with UUG are particularly
296 We mapped transcription leaders in multiple Saccharomyces yeast species and applied a novel machine
298 trengthen the fact that metabolites from non-Saccharomyces yeasts may contribute to form stable polym
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