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1 that found specifically in the fission yeast Schizosaccharomyces pombe.
2 l histone modifications in the fission yeast Schizosaccharomyces pombe.
3 east, including Saccharomyces cerevisiae and Schizosaccharomyces pombe.
4 ccharomyces cerevisiae and the fission yeast Schizosaccharomyces pombe.
5 ent of Set1C and H3K4me in the fission yeast Schizosaccharomyces pombe.
6 e played by ncRNAs in the stress response of Schizosaccharomyces pombe.
7 of synchronous meiosis in the fission yeast Schizosaccharomyces pombe.
8 niscent of the distantly related ascomycete, Schizosaccharomyces pombe.
9 Rhp26, which is the homolog of CSB/ERCC6 in Schizosaccharomyces pombe.
10 odel organism database for the fission yeast Schizosaccharomyces pombe.
11 wth characteristics of the unicellular yeast Schizosaccharomyces pombe.
12 ne Na(+)/H(+) exchanger of the fission yeast Schizosaccharomyces pombe.
13 t branch of homologous recombination (HR) in Schizosaccharomyces pombe.
14 one example being Cpc2p in the fission yeast Schizosaccharomyces pombe.
15 sure successful completion of cytokinesis in Schizosaccharomyces pombe.
16 ntrinsic reproductive isolation in the yeast Schizosaccharomyces pombe.
17 f nucleosome positions in the fission yeast, Schizosaccharomyces pombe.
18 eplication origin sites in the fission yeast Schizosaccharomyces pombe.
19 ion between transcription and replication in Schizosaccharomyces pombe.
20 re required for heterochromatic silencing in Schizosaccharomyces pombe.
21 chromosome condensation in the fission yeast Schizosaccharomyces pombe.
22 which is an intact homodimeric ATM/Tel1 from Schizosaccharomyces pombe.
23 ocess for proper actomyosin ring assembly in Schizosaccharomyces pombe.
24 ct repeat recombination in the fission yeast Schizosaccharomyces pombe.
25 myces cerevisiae and the homologue, Eso1, in Schizosaccharomyces pombe.
26 scription factor, Sak1, in the fission yeast Schizosaccharomyces pombe.
27 rmentation with Saccharomyces cerevisiae and Schizosaccharomyces pombe.
28 n, genome-wide map of nucleosome turnover in Schizosaccharomyces pombe.
29 ncluding osmotic stress in the fission yeast Schizosaccharomyces pombe.
30 or telomere maintenance in the fission yeast Schizosaccharomyces pombe.
37 , little is known about replicative aging in Schizosaccharomyces pombe, a rod-shaped yeast that divid
40 e and mouse, a tra1Delta mutant is viable in Schizosaccharomyces pombe, allowing us to test these iss
41 is, Lachancea kluyveri, Lachancea waltii and Schizosaccharomyces pombe-also conform to these predicti
42 comprehensive profile of splicing events in Schizosaccharomyces pombe, amongst the simplest organism
43 d its application to the unicellular fungus, Schizosaccharomyces pombe, an organism that shares many
44 omplex Set1C purified from the fission yeast Schizosaccharomyces pombe and chromatin substrates that
45 from Homo sapiens, Drosophila melanogaster, Schizosaccharomyces pombe and Dictyostelium discoideum f
46 activities of two Dnmt2 homologs, Pmt1 from Schizosaccharomyces pombe and DnmA from Dictyostelium di
47 RPS23 hydroxylases in S. cerevisiae (Tpa1p), Schizosaccharomyces pombe and green algae catalyze an un
49 tance, and similar observations were made in Schizosaccharomyces pombe and in a mammalian cell line.
50 ents of a suppressor tRNA system specific to Schizosaccharomyces pombe and its adaptations for use to
53 ions of retrotransposon Tf1 in the genome of Schizosaccharomyces pombe and obtained the first profile
54 two recently diverged fission yeast species Schizosaccharomyces pombe and S. kambucha, which mate to
55 the TATA element, transcription in the yeast Schizosaccharomyces pombe and Saccharomyces cerevisiae t
56 y modulating proteins from Escherichia coli, Schizosaccharomyces pombe and Saccharomyces cerevisiae,
57 f RNA polymerase active sites genome-wide in Schizosaccharomyces pombe and Saccharomyces cerevisiae.
58 division site positioning in fission yeasts Schizosaccharomyces pombe and Schizosaccharomyces japoni
59 trategies between the related fission yeasts Schizosaccharomyces pombe and Schizosaccharomyces japoni
61 bstrate for thioredoxin in the fission yeast Schizosaccharomyces pombe and, as such, competitively in
62 c shift in gene expression in fission yeast (Schizosaccharomyces pombe), and this response is driven
64 ESR, in the distantly related fission yeast, Schizosaccharomyces pombe, and in humans can explain gen
65 genomic data from Saccharomyces cerevisiae, Schizosaccharomyces pombe, and Lachancea kluyveri, we ex
66 to two yeasts, Saccharomyces cerevisiae and Schizosaccharomyces pombe, and one filamentous fungus, N
77 ed pre-mRNAs in an intron-specific manner in Schizosaccharomyces pombe Both fission yeast and human S
78 jump in yeast and the Tf1 retrotransposon of Schizosaccharomyces pombe, both of which prefer nucleoso
79 posttranslational modification in eEF1A from Schizosaccharomyces pombe but not in various other eukar
80 dida albicans, Saccharomyces cerevisiae, and Schizosaccharomyces pombe, but not zymosan preparations
81 ct in a ded1 temperature-sensitive strain of Schizosaccharomyces pombe, but the cancer-associated mut
82 s activation of the DNA damage checkpoint in Schizosaccharomyces pombe by physically coupling the Rad
83 heptapeptide repeat of the CTD of RNAP II in Schizosaccharomyces pombe by substituting non-phosphoryl
84 pressure on endocytosis in the fission yeast Schizosaccharomyces pombe by time-lapse imaging of indiv
86 logue of the human RNA-binding protein La in Schizosaccharomyces pombe, causes irregularities in tRNA
89 omain of the essential cytokinetic scaffold, Schizosaccharomyces pombe Cdc15, during cytokinesis.
91 n to a set of time-course experiments on the Schizosaccharomyces pombe cell-cycle gene expression.
92 We observe the dynamic behavior of Wee1 in Schizosaccharomyces pombe cells and manipulate its local
93 We show that in the absence of telomerase, Schizosaccharomyces pombe cells can survive telomere seq
94 we show that upon quiescence establishment, Schizosaccharomyces pombe cells drastically rearrange bo
101 cent findings show that in the fission yeast Schizosaccharomyces pombe, cleavage furrow ingression is
102 ifferent stress conditions in fission yeast, Schizosaccharomyces pombe, combining dynamic genome-wide
103 r model organism; however, the fission yeast Schizosaccharomyces pombe community currently lacks prot
107 ermine the nanoscale spatial organization of Schizosaccharomyces pombe contractile ring components re
109 ta from 116 transcriptomes in fission yeast (Schizosaccharomyces pombe), covering multiple physiologi
114 y and enzyme kinetics, we show that Trp43 of Schizosaccharomyces pombe Dcp2 is a conserved gatekeeper
117 c chromosome movements in the fission yeast, Schizosaccharomyces pombe, depend on astral microtubule
118 complementation group M (FANCM)-ortholog of Schizosaccharomyces pombe, directs the formation of NCOs
119 rmline mutations in DIS3L2, a homolog of the Schizosaccharomyces pombe dis3 gene, in individuals with
122 ular fungi like Saccharomyces cerevisiae and Schizosaccharomyces pombe do not harbor genes coding for
123 epair and Tel1 (ATM) checkpoint signaling in Schizosaccharomyces pombe, double-strand break resection
124 stand the morphogenesis of the fission yeast Schizosaccharomyces pombe drove us to investigate cellul
125 Here we show that, in the fission yeast Schizosaccharomyces pombe, ectopically induced domains o
128 sponding iron-binding position, with that of Schizosaccharomyces pombe Epe1, which plays an essential
132 rs in Smc5/6 hypomorphs in the fission yeast Schizosaccharomyces pombe following genotoxic and replic
134 calization and silencing when transformed in Schizosaccharomyces pombe Furthermore, multiple copies o
136 d its loader complex, Mis4(Scc2)-Ssl3(Scc4) (Schizosaccharomyces pombe gene names appear throughout w
137 mere repeat and the promoter regions of many Schizosaccharomyces pombe genes, including all of those
138 Yeast cells (Saccharomyces cerevisiae and Schizosaccharomyces pombe) genetically depleted of La gr
140 We report a systematic reappraisal of the Schizosaccharomyces pombe genome that ignores thresholds
141 egration events within silent regions of the Schizosaccharomyces pombe genome, we focused on performi
143 lore the high-resolution organization of the Schizosaccharomyces pombe genome, which despite its smal
145 copper is essential for spore germination in Schizosaccharomyces pombe Germinating spores develop a s
148 genome editing system in the model organism Schizosaccharomyces pombe has been hampered by the lack
149 es in the 1940s and 1950s, the fission yeast Schizosaccharomyces pombe has grown to become one of the
151 lp14, a XMAP215 orthologue in fission yeast, Schizosaccharomyces pombe, has properties of a MT polyme
160 Est1 exists in multiple organisms, including Schizosaccharomyces pombe, humans, and Saccharomyces cer
161 nsive lipid homeostasis in the fission yeast Schizosaccharomyces pombe in a manner analogous to the m
162 al structures of the tRNA MTase spTrm10 from Schizosaccharomyces pombe in the presence and absence of
163 dao gene encoding D-amino acid oxidase from Schizosaccharomyces pombe in tobacco (Nicotiana tabacum)
164 ing formation has been well characterized in Schizosaccharomyces pombe, in which the cross-linking pr
166 1, a long-terminal repeat retrotransposon in Schizosaccharomyces pombe, integrates into promoters wit
169 determinants of aging, and the fission yeast Schizosaccharomyces pombe is a promising new system for
177 showed that drug tolerance in fission yeast Schizosaccharomyces pombe is controlled by lncRNA transc
179 anscriptional induction in the fission yeast Schizosaccharomyces pombe is currently a limitation of t
180 intermediates, we show that circular RNA in Schizosaccharomyces pombe is generated through an exon-c
181 hat site-specific replication termination in Schizosaccharomyces pombe is modulated by protein-mediat
182 evidence that cell size in the fission yeast Schizosaccharomyces pombe is regulated by a third strate
184 d26 in Saccharomyces cerevisiae and Rhp26 in Schizosaccharomyces pombe) is among the first proteins t
187 ammalian PtK1 cells and in the fission yeast Schizosaccharomyces pombe, kinetochores shortened after
188 ased on tRNA-mediated suppression (TMS) in a Schizosaccharomyces pombe La protein (Sla1p) mutant.
189 ro FRET-based assays, we show that human and Schizosaccharomyces pombe La proteins harbor RNA chapero
190 could complement the distantly related yeast Schizosaccharomyces pombe lacking its endogenous Dicer g
191 performed metabolic profiling on a strain of Schizosaccharomyces pombe lacking the zinc-responsive tr
197 A resolution cryo-electron microscopy map of Schizosaccharomyces pombe Mediator in which conserved Me
200 To understand their roles in fission yeast (Schizosaccharomyces pombe) mitochondria, we generated de
203 ion, we performed an unbiased screen to seek Schizosaccharomyces pombe mutants with reduced PM Ras.
205 ition of Arp2/3 complex in the fission yeast Schizosaccharomyces pombe not only depletes Arp2/3-compl
208 orthologs Pck1 and Pck2 in the fission yeast Schizosaccharomyces pombe operate in a redundant fashion
211 important for meiosis in the fission yeast, Schizosaccharomyces pombe Our genome-wide functional scr
215 his screen with the DNA-binding subdomain of Schizosaccharomyces pombe Pot1 (Pot1pN), which confers t
216 ain analysis of the evolutionarily conserved Schizosaccharomyces pombe pre-mRNA-processing factor, Sp
217 m inference of networks in the budding yeast Schizosaccharomyces pombe predicts a novel role in cell
219 nally, we used SIFTER to annotate all of the Schizosaccharomyces pombe proteins with experimental fun
220 epistasis map (E-MAP) for the fission yeast Schizosaccharomyces pombe, providing phenotypic signatur
221 -1-1 checkpoint clamp (ortholog of human and Schizosaccharomyces pombe Rad9), the replication initiat
222 nding proteins (SREBPs) in the fission yeast Schizosaccharomyces pombe regulate lipid homeostasis and
227 r quiescence (G0 phase of the cell cycle) in Schizosaccharomyces pombe RNAi mutants lose viability at
228 Here we show that, in the fission yeast Schizosaccharomyces pombe, RNAi and heterochromatin fact
229 a genome-wide map of nucleosomes in vivo in Schizosaccharomyces pombe (S. pombe) at base pair resolu
231 ustrial strains of Saccharomyces cerevisiae, Schizosaccharomyces pombe, Saccharomyces boulardii, Sacc
232 n in three distantly related fission yeasts: Schizosaccharomyces pombe, Schizosaccharomyces octosporu
235 biochemical studies on the Sen1 homolog from Schizosaccharomyces pombe showed that it can bind and un
237 xpression of the fungal Hsp104 homologs from Schizosaccharomyces pombe (Sp-Hsp104) or Candida albican
238 smic duplication cycle and regulation of the Schizosaccharomyces pombe SPB is analogous to centrosome
243 to varying degrees the growth defects of the Schizosaccharomyces pombe STUbL mutant rfp1/rfp2, and th
251 bed a mutant, pat1-as2, of the fission yeast Schizosaccharomyces pombe that undergoes synchronous mei
252 we find in Schizosaccharomyces japonicus and Schizosaccharomyces pombe that, during actomyosin ring c
268 sly shown that in the symmetrically dividing Schizosaccharomyces pombe there is a transition between
270 ia coli MiaA, Saccharomyces cerevisiae Mod5, Schizosaccharomyces pombe Tit1, and Caenorhabditis elega
271 dynamic cellular environments, here, we use Schizosaccharomyces pombe to characterize, both experime
272 biological information for the fission yeast Schizosaccharomyces pombe to effectively support both ex
273 ochromatin, conserved from the fission yeast Schizosaccharomyces pombe to humans, is its ability to s
275 Saccharomyces cerevisiae) to hetero-octamer (Schizosaccharomyces pombe) to hetero-nonamer (Metazoa).
276 t regulation of sterol response genes (Ofd1, Schizosaccharomyces pombe) to translation termination/mR
277 he Tetrahymena equivalent of mammalian TPP1, Schizosaccharomyces pombe Tpz1, and Oxytricha nova TEBPb
278 architecture of microtubules assembled from Schizosaccharomyces pombe tubulin, in the presence and a
279 activation at high H(2)O(2), showing that in Schizosaccharomyces pombe turning off peroxide defenses
281 performed mRNA profiling for splicing in the Schizosaccharomyces pombe U2AF(59) (prp2.1) temperature-
283 ed ribosome profiling with the fission yeast Schizosaccharomyces pombe under conditions of exponentia
285 A splicing using the intron-rich model yeast Schizosaccharomyces pombe Using epistatic miniarray prof
286 alyzed the consequences of Spt5 depletion in Schizosaccharomyces pombe using four genome-wide approac
287 sm of F-actin assembly during cytokinesis in Schizosaccharomyces pombe using lifeact as a probe to mo
288 resolution survey of genome interactions in Schizosaccharomyces pombe using synchronized cells to in
290 on properties of SpPot1, the POT1 homolog in Schizosaccharomyces pombe, we found an unanticipated ssD
293 hway for diamide-induced disulfide stress in Schizosaccharomyces pombe, where the nucleocytoplasmic H
294 calnexin-independence factor 1 (Cif1), from Schizosaccharomyces pombe, which has been implicated in
296 itotic and meiotic chromosome segregation in Schizosaccharomyces pombe, which has more than one kinet
297 ) and a modified version of TyrRS, AzFRS, in Schizosaccharomyces pombe, which is an attractive model
299 family member expressed in the fission yeast Schizosaccharomyces pombe, Zfs1, promotes the turnover o
300 ism, whereas the single protein expressed in Schizosaccharomyces pombe, Zfs1, regulates cell-cell int
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