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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

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