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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
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
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
41 stal structures of the Mep2 orthologues from Saccharomyces cerevisiae and Candida albicans and show t
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.
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
60 we used the mating differentiation in yeast Saccharomyces cerevisiae as a model and developed integr
63 of salidroside can be achieved in the yeast Saccharomyces cerevisiae as well as the plant Nicotiana
66 a multiplex genome engineering technology in Saccharomyces cerevisiae based on annealing synthetic ol
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
77 quantify transcript heterogeneity in single Saccharomyces cerevisiae cells treated with and without
80 single-molecule imaging to demonstrate that Saccharomyces cerevisiae condensin is a molecular motor
84 First, fed-batch glucose fermentations by Saccharomyces cerevisiae D5A revealed that this strain,
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
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
101 nesis, and X-ray structural data analysis of Saccharomyces cerevisiae eEF1A, we identified a posttran
104 bidopsis thaliana, Dictyostelium discoideum, Saccharomyces cerevisiae, Escherichia coli and Methanoca
106 step for the synthesis of triacylglycerol in Saccharomyces cerevisiae, exerts a negative regulatory e
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
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
115 the curvature-stabilizing protein Yop1p from Saccharomyces cerevisiae form a tubular network upon add
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
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
125 d from renewable sources including wild-type Saccharomyces cerevisiae glycoproteins and lipid-linked
130 the function of synaptonemal complex (SC) in Saccharomyces cerevisiae has mainly focused on in vivo a
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
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
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
143 ia innocua, Mycobacterium parafortuitum, and Saccharomyces cerevisiae inoculated onto the surface of
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
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
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
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
172 mosan, which is the cell wall preparation of Saccharomyces cerevisiae, or poly (I:C) was coated on a
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
179 , filopodia supported the uptake of zymosan (Saccharomyces cerevisiae) particles by (i) providing fix
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
186 redox activity of the [4Fe4S](2+) cluster in Saccharomyces cerevisiae polymerase (Pol) delta, the lag
188 o-electron microscopy structure of the yeast Saccharomyces cerevisiae pre-catalytic B complex spliceo
190 of endogenous hydrogen peroxide in the yeast Saccharomyces cerevisiae promote site-specific endonucle
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
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
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
210 iption coupled DNA repair (TCR) in the yeast Saccharomyces cerevisiae Sen1, a DNA/RNA helicase that i
212 A polymerase II (RNAPII) and is catalyzed by Saccharomyces cerevisiae Set1 and Set2, respectively.
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
220 the cryo-electron microscopy structure of a Saccharomyces cerevisiae spliceosome stalled after Prp16
223 strain also affected flavour synthesis with Saccharomyces cerevisiae strain A01 producing considerab
225 tes that yeast involved in wine making, i.e. Saccharomyces cerevisiae strains and the non-Saccharomyc
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
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
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
261 crotubule (MT) dynamics in the budding yeast Saccharomyces cerevisiae This activity requires interact
264 e reconstitute the noscapine gene cluster in Saccharomyces cerevisiae to achieve the microbial produc
271 ously proposed general base residue (D210 in Saccharomyces cerevisiae Trm10) is not likely to play th
273 e used single molecule fluorescence to study Saccharomyces cerevisiae U1 and BBP interactions with RN
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
284 entification of CTPD substrates in the yeast Saccharomyces cerevisiae via a quantitative proteomic an
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
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
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
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
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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