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1 pseudosubstrate inhibitor Acm1 from budding yeast (Saccharomyces cerevisiae).
2 d complementation of iron-deficient fet3fet4 yeast (Saccharomyces cerevisiae).
3 e developed a method for scRNAseq in budding yeast (Saccharomyces cerevisiae).
4 rotein-protein interactions in planta and in yeast (Saccharomyces cerevisiae).
5 of autophagic proteasome turnover in budding yeast (Saccharomyces cerevisiae).
6 etwork that regulates fat storage in budding yeast (Saccharomyces cerevisiae).
7 as reinhardtii, Escherichia coli and baker's yeast (Saccharomyces cerevisiae).
8 ) was isolated and functionally expressed in yeast (Saccharomyces cerevisiae).
9 raminearum, and Sclerotinia sclerotiorum and yeast (Saccharomyces cerevisiae).
10 mplex replication protein A (RPA) in budding yeast (Saccharomyces cerevisiae).
11 , from simple carbon and nitrogen sources in yeast (Saccharomyces cerevisiae).
12 UTP/5-FdUTP-mediated DNA toxicity in budding yeast (Saccharomyces cerevisiae).
13 scent reporters in single, live cells of the yeast Saccharomyces cerevisiae.
14 presumed protein aggregation in the budding yeast Saccharomyces cerevisiae.
15 ion (OXPHOS) enzyme in mitochondria from the yeast Saccharomyces cerevisiae.
16 nd stability of certain mRNAs in the budding yeast Saccharomyces cerevisiae.
17 sed for most genetic construct design in the yeast Saccharomyces cerevisiae.
18 cation in trans of genomic or DI RNAs in the yeast Saccharomyces cerevisiae.
19 tral role in zinc homeostasis in the budding yeast Saccharomyces cerevisiae.
20 5' untranslated region (UTR) of mRNAs in the yeast Saccharomyces cerevisiae.
21 RNA emerging from transcribing Pol II in the yeast Saccharomyces cerevisiae.
22 n that is homologous to Glo3p of the budding yeast Saccharomyces cerevisiae.
23 ary adaptation to a stressful environment in yeast Saccharomyces cerevisiae.
24 rence, and gene deletion (CRISPR-AID) in the yeast Saccharomyces cerevisiae.
25 have adapted Strand-seq to detect SCE in the yeast Saccharomyces cerevisiae.
26 single-strand annealing (SSA) assays in the yeast Saccharomyces cerevisiae.
27 tion with purified proteins from the budding yeast Saccharomyces cerevisiae.
28 r dynamics during endocytosis in the budding yeast Saccharomyces cerevisiae.
29 m has motivated domestication of the budding yeast Saccharomyces cerevisiae.
30 cies and a surprising version present in the yeast Saccharomyces cerevisiae.
31 reated by the HO endonuclease in the budding yeast Saccharomyces cerevisiae.
32 riants in the promoters of 2503 genes in the yeast Saccharomyces cerevisiae.
33 ogen-activated protein kinase pathway in the yeast Saccharomyces cerevisiae.
34 ap8 is critical for arsenic tolerance in the yeast Saccharomyces cerevisiae.
35 chemotropic fate transitions of the budding yeast Saccharomyces cerevisiae.
36 ystems in wild and laboratory strains of the yeast Saccharomyces cerevisiae.
37 lactate cytochrome c oxidoreductase from the yeast Saccharomyces cerevisiae.
38 mechanisms underlying CR, especially in the yeast Saccharomyces cerevisiae.
39 the replicative DNA polymerase-alpha in the yeast Saccharomyces cerevisiae.
40 induce recombination when transferred to the yeast Saccharomyces cerevisiae.
41 reaction cycle of condensin from the budding yeast Saccharomyces cerevisiae.
42 s on intracellular oxidation in cells of the yeast Saccharomyces cerevisiae.
43 by cloning the centromere DNA of the budding yeast Saccharomyces cerevisiae.
44 tions in a eukaryote chassis, namely baker's yeast Saccharomyces cerevisiae.
45 ein-protein interactions in the well-studied yeast Saccharomyces cerevisiae.
46 /S transcriptional regulation in the budding yeast Saccharomyces cerevisiae.
47 istinct replication complexes in the budding yeast Saccharomyces cerevisiae.
48 e variabilities in cell cycle of the budding yeast Saccharomyces cerevisiae.
49 of 30 general RNA degradation factors in the yeast Saccharomyces cerevisiae.
50 we report 112 putative novel lncRNAs in the yeast Saccharomyces cerevisiae, 41 of which are only exp
52 ds is carried out by fatty acid synthase: in yeast Saccharomyces cerevisiae, a 2.6-MDa molecular mass
53 bundance of 1.6 million protein pairs in the yeast Saccharomyces cerevisiae across nine growth condit
55 d VO regions of the V-ATPase by starving the yeast Saccharomyces cerevisiae, allowing us to obtain a
56 an 800 000 atom model of SPL C complex from yeast Saccharomyces cerevisiae and community network ana
57 rified WT and mutant Pol I variants from the yeast Saccharomyces cerevisiae and compare their abiliti
58 prehensive genetic epistasis analysis in the yeast Saccharomyces cerevisiae and found that simultaneo
59 ery (TIM23 complex) is conserved between the yeast Saccharomyces cerevisiae and humans; however, func
60 duced by interspecies hybrids of the brewing yeast Saccharomyces cerevisiae and its wild relative S.
61 subpopulations of the partially domesticated yeast Saccharomyces cerevisiae and its wild relative Sac
62 ectron microscopy structure of SAGA from the yeast Saccharomyces cerevisiae and resolve the core modu
64 we compare homologous genes from the budding yeast Saccharomyces cerevisiae and the fission yeast Sch
65 d yet contrasting yeast species, the baker's yeast Saccharomyces cerevisiae and the wild yeast Saccha
66 s stimulated gene targeting up to 32-fold in yeast Saccharomyces cerevisiae and up to 16-fold in huma
69 modifications are largely restricted to two yeasts, Saccharomyces cerevisiae and Schizosaccharomyces
70 a factor acting in cell cycle progression in yeast (Saccharomyces cerevisiae) and an important compon
73 onal structure of pericentromeres in budding yeast (Saccharomyces cerevisiae) and establish the relat
79 e used synthetic auxin degradation assays in yeast (Saccharomyces cerevisiae) and in plants to charac
80 5 by heterologously expressing it in budding yeast (Saccharomyces cerevisiae) and in the bacterium La
81 -PM contact site components and functions in yeast (Saccharomyces cerevisiae) and mammals, relatively
84 ression analysis, heterologous expression in yeast (Saccharomyces cerevisiae), and in vitro transport
86 n mammals, Sucrose Non-Fermenting1 (SNF1) in yeast (Saccharomyces cerevisiae), and SNF1-related kinas
87 instability in diploid cells of the budding yeast Saccharomyces cerevisiae, and have isolated clones
88 hila melanogaster, the cell cycle of budding yeast Saccharomyces cerevisiae, and the floral organ arr
89 rformed a systematic visual screen using the yeast Saccharomyces cerevisiae, and uncovered three unch
90 an integral membrane class found in plants, yeast (Saccharomyces cerevisiae), animals, and bacteria.
91 that were recently discovered in the budding yeast Saccharomyces cerevisiae are interesting because t
92 he major cytoplasmic Hsp70 chaperones in the yeast Saccharomyces cerevisiae are the Ssa proteins, and
93 d some unpublished, tetrad data from budding yeast (Saccharomyces cerevisiae) are analyzed for dispar
95 Here we used the mating differentiation in yeast Saccharomyces cerevisiae as a model and developed
98 onsider a recent evolution experiment on the yeast Saccharomyces cerevisiae as a unique platform to a
99 uction of salidroside can be achieved in the yeast Saccharomyces cerevisiae as well as the plant Nico
101 reviously inaccessible proteins from baker's yeast Saccharomyces cerevisiae, as well as two clinicall
102 of extracellular glucose is crucial for the yeast Saccharomyces cerevisiae because of its fermentati
103 eIF4E1c-type proteins support translation in yeast (Saccharomyces cerevisiae) but promote translation
104 been extensively studied in prokaryotes and yeast (Saccharomyces cerevisiae), but little is known fo
105 r Control of ATP Synthase2 (NCA2) protein in yeast (Saccharomyces cerevisiae), but lost in Metazoa.
106 cence imaging of individual cisternae in the yeast Saccharomyces cerevisiae, but those experiments di
107 l effects for gene expression in the budding yeast Saccharomyces cerevisiae by measuring the effects
108 translational efficiencies (TEs) in budding yeast Saccharomyces cerevisiae by ribosome footprint pro
109 aneously arising mutation that activates the yeast (Saccharomyces cerevisiae) CDC25 family phosphatas
112 re recently, a synthetic designer version of yeast Saccharomyces cerevisiae chromosome III has been g
113 cell imaging of the MAT-locus located on the yeast Saccharomyces cerevisiae chromosome III, we recove
117 bons, and heterologous expression of CER2 in yeast (Saccharomyces cerevisiae) demonstrated that it ca
122 global proteomic alterations in the budding yeast Saccharomyces cerevisiae due to differences in car
125 , we show that DDR activation in the budding yeast Saccharomyces cerevisiae, either by genetic manipu
128 port on experimental results for the budding yeast Saccharomyces cerevisiae, finding, surprisingly, t
130 factors, such as TFB2M in humans and Mtf1 in yeast Saccharomyces cerevisiae, for promoter-specific tr
131 ic genetic array (SGA) analyses in the model yeast, Saccharomyces cerevisiae, functional genomics is
132 is direction arose via the completion of the yeast Saccharomyces cerevisiae gene-knockout collection
133 nisms in model organisms such as the budding yeast Saccharomyces cerevisiae Gpa2 is a yeast Galpha pr
134 acids and glycerophosphocholine (GPC) in the yeast Saccharomyces cerevisiae GPC can be reacylated by
136 ng experimental growth curves of the baker's yeast Saccharomyces cerevisiae growing in the presence o
143 de gene network (DPH1-DPH7) from the budding yeast Saccharomyces cerevisiae has significantly advance
145 es of this regulatory circuit in the budding yeast Saccharomyces cerevisiae have been recently define
146 ositive feedback, and studies in the budding yeast Saccharomyces cerevisiae have suggested distinct p
147 The Mag1 and Tpa1 proteins from budding yeast (Saccharomyces cerevisiae) have both been reported
148 ss-response element in gene promoters in the yeast Saccharomyces cerevisiae However, the roles of Msn
149 , we evolved 20 replicate populations of the yeast Saccharomyces cerevisiae in 11 laboratory environm
150 K-PPn was originally discovered in budding yeast (Saccharomyces cerevisiae), in which polyP anaboli
151 ome sequences for 85 diverse isolates of the yeast Saccharomyces cerevisiae-including wild, domestica
152 Starvation of diploid cells of the budding yeast Saccharomyces cerevisiae induces them to enter mei
163 k protein 90 (Hsp90) chaperone system of the yeast Saccharomyces cerevisiae is greatly impaired in na
164 is of plasma membrane proteins, which in the yeast Saccharomyces cerevisiae is mediated by the HECT E
165 subunit Rrp44/Dis3 of the exosome in budding yeast (Saccharomyces cerevisiae) is considered a protein
166 t vacuolar H(+)-ATPase (V-ATPase) of budding yeast (Saccharomyces cerevisiae) is regulated by reversi
167 enic amino acid originally isolated from the yeast Saccharomyces cerevisiae, is an intermediate in ly
168 a subunit of the GID ubiquitin ligase in the yeast Saccharomyces cerevisiae, is the recognition compo
173 trongly impaired interactions with LCB1 in a yeast (Saccharomyces cerevisiae) model, providing struct
175 e selectivity and sensitivity of the budding yeast (Saccharomyces cerevisiae) multidrug response to b
176 t TaVIT1, was able to rescue the growth of a yeast (Saccharomyces cerevisiae) mutant defective in vac
178 hCNT1, -2, and -3) produced individually in yeast Saccharomyces cerevisiae Nilotinib inhibited hENT1
179 pressor candidate region gene2 (GLTSCR2) and yeast (Saccharomyces cerevisiae) Nucleolar protein53 (No
180 e mapping, which revealed that 5% of budding yeast (Saccharomyces cerevisiae) nucleosome positions ha
181 cessing of three PSTVd RNA constructs in the yeast Saccharomyces cerevisiae Of these, only one form,
182 est protein and DHFR are coexpressed, in the yeast Saccharomyces cerevisiae, on a low-copy plasmid fr
183 hetic auxin response circuits in the budding yeast Saccharomyces cerevisiae Our analysis revealed tha
185 he cryo-electron microscopy structure of the yeast Saccharomyces cerevisiae pre-catalytic B complex s
186 synthetic amyloid fibrils assembled from the yeast (Saccharomyces cerevisiae) prion protein Sup35NM.
187 evels of endogenous hydrogen peroxide in the yeast Saccharomyces cerevisiae promote site-specific end
188 f the eukaryal cell cycle, using the budding yeast Saccharomyces cerevisiae Protein synthesis and cen
189 a benthamiana) plants that overexpress three yeast (Saccharomyces cerevisiae) protein subunits of DNA
192 are the major triacylglycerol lipases of the yeast Saccharomyces cerevisiae Recently we demonstrated
195 ionally repressed chromosomal domains in the yeast Saccharomyces cerevisiae represent specialized sit
198 es or a defect in nucleosome assembly in the yeast Saccharomyces cerevisiae results in increased mito
200 equencing of these fragments in DNA from the yeast Saccharomyces cerevisiae revealed widespread ribon
204 ranscription coupled DNA repair (TCR) in the yeast Saccharomyces cerevisiae Sen1, a DNA/RNA helicase
205 structures at up to 2.6 A resolution of the yeast Saccharomyces cerevisiae separase-securin complex.
206 s examining sugar utilization in the budding yeast Saccharomyces cerevisiae, show that considerable h
207 oform Delta0-ELO1 Heterologous expression in yeast (Saccharomyces cerevisiae) showed that NgDelta0-EL
208 othenic acid for CoA biosynthesis in budding yeast (Saccharomyces cerevisiae), significantly regulate
210 ) and LCB2 and the small subunit of SPT in a yeast (Saccharomyces cerevisiae) SPT-deficient mutant.
212 eins (at a 1% false discovery rate (FDR)) in yeast (Saccharomyces cerevisiae strain BY4741) over 70 m
213 ility to complement the defects of a Baker's yeast (Saccharomyces cerevisiae) strain lacking the mito
214 ul1 and Sul2 are sulfate transporters in the yeast Saccharomyces cerevisiae, strongly induced upon su
215 8, is capable of excising and reinserting in yeast (Saccharomyces cerevisiae), suggesting that yeast
216 lear Auxin Response Circuit recapitulated in yeast (Saccharomyces cerevisiae) system to functionally
217 4 subunit of the ubiquitin ligase GID in the yeast Saccharomyces cerevisiae targeted the gluconeogeni
218 and vacuole protein sorting) complex in the yeast Saccharomyces cerevisiae tethers membranes through
220 eparation of function mutants in the budding yeast Saccharomyces cerevisiae that allow global origin
221 ed an in vitro transcription system from the yeast Saccharomyces cerevisiae that allows conversion of
223 t of strong, synthetic promoters for budding yeast Saccharomyces cerevisiae that are inducible under
224 stacle, we engineered strains of the budding yeast Saccharomyces cerevisiae that differ only in the p
226 To this end, we have developed gates for yeast (Saccharomyces cerevisiae) that are connected usin
227 ondrial respiration and Sod1 function in the yeast Saccharomyces cerevisiae The histone H3-H4 tetrame
228 vide an overview of protein synthesis in the yeast Saccharomyces cerevisiae The mechanism of protein
250 iple vital cellular functions in the budding yeast Saccharomyces cerevisiae These include regulation
252 ear microtubule (MT) dynamics in the budding yeast Saccharomyces cerevisiae This activity requires in
253 s), fruit fly (Drosophila melanogaster), and yeast (Saccharomyces cerevisiae), this core NatA complex
256 AGG2, or AGG3) with differing specificity in yeast (Saccharomyces cerevisiae) three-hybrid assays.
257 en S. pombe and the highly divergent budding yeast Saccharomyces cerevisiae Thus, transcriptional int
258 xpressed cause chromosome instability in the yeast Saccharomyces cerevisiae To better understand the
259 e used a chemical genomics approach with the yeast Saccharomyces cerevisiae to better understand the
260 uorescence microscopy studies in the budding yeast Saccharomyces cerevisiae to identify a protein, La
261 lity to mitochondrial DNA mutagenesis of the yeast Saccharomyces cerevisiae to introduce single point
263 ein-based element of inheritance that allows yeast (Saccharomyces cerevisiae) to circumvent a hallmar
268 rescence microscopy approaches in a purified yeast Saccharomyces cerevisiae translation system to mon
271 arrest of ribosome biogenesis in the budding yeast Saccharomyces cerevisiae triggers rapid activation
274 ns and interacted with both TIR1 and IAA7 in yeast (Saccharomyces cerevisiae) two-hybrid experiments,
276 a] Soybean Response to Cold [AtSRC2.2]) in a yeast (Saccharomyces cerevisiae) two-hybrid screen and h
277 induction of PDR genes to growth rate in the yeast Saccharomyces cerevisiae Using diverse PDR inducer
278 for mapping hybrid-prone regions in budding yeast Saccharomyces cerevisiae Using this methodology, w
279 probe FISH protocol termed sFISH for budding yeast, Saccharomyces cerevisiae using a single DNA probe
280 smid-based NHEJ DNA repair screen in budding yeast (Saccharomyces cerevisiae) using 369 putative none
281 scribe the control of growth of the brewer's yeast, Saccharomyces cerevisiae, using both transcriptio
282 the identification of CTPD substrates in the yeast Saccharomyces cerevisiae via a quantitative proteo
287 a new and potent inducer of autophagy in the yeast Saccharomyces cerevisiae We found that potassium-d
288 ants from a cross between two strains of the yeast Saccharomyces cerevisiae We identified a nonsynony
290 l genomics approach leveraged from the model yeast Saccharomyces cerevisiae, we demonstrate how such
292 antitative attributes of PKA dynamics in the yeast Saccharomyces cerevisiae, we developed an optogene
294 d single nucleotide polymorphism data in the yeast, Saccharomyces cerevisiae, we constructed gene reg
295 ons of individual mitochondria isolated from yeasts (Saccharomyces cerevisiae) were let to sediment o
296 ween Pih1 and the proteasome subunit Rpn8 in yeast Saccharomyces cerevisiae when HSP90 co-chaperone T
298 escribed in model species, especially in the yeast Saccharomyces cerevisiae, which helped to shape ge
299 this question, we fused every protein in the yeast Saccharomyces cerevisiae with a partner from each
300 ) in mammalian cells to extremely low in the yeast Saccharomyces cerevisiae Yeast strains deficient i