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1 cystis species with Taphrina, Saitoella, and Schizosaccharomyces, and divergence within Pneumocystis
3 erved, Tas3 is lost and Chp1 is truncated in Schizosaccharomyces cryophilus and Schizosaccharomyces o
4 hree additional Schizosaccharomyces species (Schizosaccharomyces cryophilus, Schizosaccharomyces japo
6 ces species (Schizosaccharomyces cryophilus, Schizosaccharomyces japonicus and Schizosaccharomyces oc
8 dy, we have determined crystal structures of Schizosaccharomyces japonicus Mis16 alone and in complex
11 on the cytokinetic ring in the fission yeast Schizosaccharomyces japonicus, unlike its role in S. pom
15 ication of an ancestral anillin early in the Schizosaccharomyces lineage may have led to subfunctiona
16 d fission yeasts: Schizosaccharomyces pombe, Schizosaccharomyces octosporus and Schizosaccharomyces j
17 ncated in Schizosaccharomyces cryophilus and Schizosaccharomyces octosporus We show that truncated Ch
20 a genome-wide map of nucleosomes in vivo in Schizosaccharomyces pombe (S. pombe) at base pair resolu
21 xpression of the fungal Hsp104 homologs from Schizosaccharomyces pombe (Sp-Hsp104) or Candida albican
25 omplex Set1C purified from the fission yeast Schizosaccharomyces pombe and chromatin substrates that
26 from Homo sapiens, Drosophila melanogaster, Schizosaccharomyces pombe and Dictyostelium discoideum f
27 activities of two Dnmt2 homologs, Pmt1 from Schizosaccharomyces pombe and DnmA from Dictyostelium di
28 RPS23 hydroxylases in S. cerevisiae (Tpa1p), Schizosaccharomyces pombe and green algae catalyze an un
30 tance, and similar observations were made in Schizosaccharomyces pombe and in a mammalian cell line.
31 ents of a suppressor tRNA system specific to Schizosaccharomyces pombe and its adaptations for use to
34 ions of retrotransposon Tf1 in the genome of Schizosaccharomyces pombe and obtained the first profile
35 two recently diverged fission yeast species Schizosaccharomyces pombe and S. kambucha, which mate to
36 the TATA element, transcription in the yeast Schizosaccharomyces pombe and Saccharomyces cerevisiae t
37 f RNA polymerase active sites genome-wide in Schizosaccharomyces pombe and Saccharomyces cerevisiae.
38 division site positioning in fission yeasts Schizosaccharomyces pombe and Schizosaccharomyces japoni
39 trategies between the related fission yeasts Schizosaccharomyces pombe and Schizosaccharomyces japoni
41 bstrate for thioredoxin in the fission yeast Schizosaccharomyces pombe and, as such, competitively in
49 ed pre-mRNAs in an intron-specific manner in Schizosaccharomyces pombe Both fission yeast and human S
50 posttranslational modification in eEF1A from Schizosaccharomyces pombe but not in various other eukar
51 s activation of the DNA damage checkpoint in Schizosaccharomyces pombe by physically coupling the Rad
52 heptapeptide repeat of the CTD of RNAP II in Schizosaccharomyces pombe by substituting non-phosphoryl
53 pressure on endocytosis in the fission yeast Schizosaccharomyces pombe by time-lapse imaging of indiv
56 omain of the essential cytokinetic scaffold, Schizosaccharomyces pombe Cdc15, during cytokinesis.
58 n to a set of time-course experiments on the Schizosaccharomyces pombe cell-cycle gene expression.
59 We observe the dynamic behavior of Wee1 in Schizosaccharomyces pombe cells and manipulate its local
60 we show that upon quiescence establishment, Schizosaccharomyces pombe cells drastically rearrange bo
65 r model organism; however, the fission yeast Schizosaccharomyces pombe community currently lacks prot
68 ermine the nanoscale spatial organization of Schizosaccharomyces pombe contractile ring components re
70 y and enzyme kinetics, we show that Trp43 of Schizosaccharomyces pombe Dcp2 is a conserved gatekeeper
72 rmline mutations in DIS3L2, a homolog of the Schizosaccharomyces pombe dis3 gene, in individuals with
74 ular fungi like Saccharomyces cerevisiae and Schizosaccharomyces pombe do not harbor genes coding for
75 stand the morphogenesis of the fission yeast Schizosaccharomyces pombe drove us to investigate cellul
81 rs in Smc5/6 hypomorphs in the fission yeast Schizosaccharomyces pombe following genotoxic and replic
82 calization and silencing when transformed in Schizosaccharomyces pombe Furthermore, multiple copies o
84 d its loader complex, Mis4(Scc2)-Ssl3(Scc4) (Schizosaccharomyces pombe gene names appear throughout w
85 mere repeat and the promoter regions of many Schizosaccharomyces pombe genes, including all of those
87 We report a systematic reappraisal of the Schizosaccharomyces pombe genome that ignores thresholds
88 egration events within silent regions of the Schizosaccharomyces pombe genome, we focused on performi
90 lore the high-resolution organization of the Schizosaccharomyces pombe genome, which despite its smal
92 copper is essential for spore germination in Schizosaccharomyces pombe Germinating spores develop a s
94 genome editing system in the model organism Schizosaccharomyces pombe has been hampered by the lack
95 es in the 1940s and 1950s, the fission yeast Schizosaccharomyces pombe has grown to become one of the
102 nsive lipid homeostasis in the fission yeast Schizosaccharomyces pombe in a manner analogous to the m
103 al structures of the tRNA MTase spTrm10 from Schizosaccharomyces pombe in the presence and absence of
104 dao gene encoding D-amino acid oxidase from Schizosaccharomyces pombe in tobacco (Nicotiana tabacum)
106 determinants of aging, and the fission yeast Schizosaccharomyces pombe is a promising new system for
112 showed that drug tolerance in fission yeast Schizosaccharomyces pombe is controlled by lncRNA transc
114 anscriptional induction in the fission yeast Schizosaccharomyces pombe is currently a limitation of t
115 intermediates, we show that circular RNA in Schizosaccharomyces pombe is generated through an exon-c
116 evidence that cell size in the fission yeast Schizosaccharomyces pombe is regulated by a third strate
117 ased on tRNA-mediated suppression (TMS) in a Schizosaccharomyces pombe La protein (Sla1p) mutant.
118 ro FRET-based assays, we show that human and Schizosaccharomyces pombe La proteins harbor RNA chapero
119 could complement the distantly related yeast Schizosaccharomyces pombe lacking its endogenous Dicer g
120 performed metabolic profiling on a strain of Schizosaccharomyces pombe lacking the zinc-responsive tr
124 A resolution cryo-electron microscopy map of Schizosaccharomyces pombe Mediator in which conserved Me
126 ion, we performed an unbiased screen to seek Schizosaccharomyces pombe mutants with reduced PM Ras.
127 ition of Arp2/3 complex in the fission yeast Schizosaccharomyces pombe not only depletes Arp2/3-compl
130 orthologs Pck1 and Pck2 in the fission yeast Schizosaccharomyces pombe operate in a redundant fashion
132 important for meiosis in the fission yeast, Schizosaccharomyces pombe Our genome-wide functional scr
136 his screen with the DNA-binding subdomain of Schizosaccharomyces pombe Pot1 (Pot1pN), which confers t
137 ain analysis of the evolutionarily conserved Schizosaccharomyces pombe pre-mRNA-processing factor, Sp
138 m inference of networks in the budding yeast Schizosaccharomyces pombe predicts a novel role in cell
140 nally, we used SIFTER to annotate all of the Schizosaccharomyces pombe proteins with experimental fun
141 -1-1 checkpoint clamp (ortholog of human and Schizosaccharomyces pombe Rad9), the replication initiat
142 nding proteins (SREBPs) in the fission yeast Schizosaccharomyces pombe regulate lipid homeostasis and
145 r quiescence (G0 phase of the cell cycle) in Schizosaccharomyces pombe RNAi mutants lose viability at
148 biochemical studies on the Sen1 homolog from Schizosaccharomyces pombe showed that it can bind and un
150 smic duplication cycle and regulation of the Schizosaccharomyces pombe SPB is analogous to centrosome
154 to varying degrees the growth defects of the Schizosaccharomyces pombe STUbL mutant rfp1/rfp2, and th
161 bed a mutant, pat1-as2, of the fission yeast Schizosaccharomyces pombe that undergoes synchronous mei
162 we find in Schizosaccharomyces japonicus and Schizosaccharomyces pombe that, during actomyosin ring c
165 sly shown that in the symmetrically dividing Schizosaccharomyces pombe there is a transition between
167 ia coli MiaA, Saccharomyces cerevisiae Mod5, Schizosaccharomyces pombe Tit1, and Caenorhabditis elega
168 dynamic cellular environments, here, we use Schizosaccharomyces pombe to characterize, both experime
169 biological information for the fission yeast Schizosaccharomyces pombe to effectively support both ex
170 ochromatin, conserved from the fission yeast Schizosaccharomyces pombe to humans, is its ability to s
171 he Tetrahymena equivalent of mammalian TPP1, Schizosaccharomyces pombe Tpz1, and Oxytricha nova TEBPb
172 architecture of microtubules assembled from Schizosaccharomyces pombe tubulin, in the presence and a
173 activation at high H(2)O(2), showing that in Schizosaccharomyces pombe turning off peroxide defenses
176 ed ribosome profiling with the fission yeast Schizosaccharomyces pombe under conditions of exponentia
178 A splicing using the intron-rich model yeast Schizosaccharomyces pombe Using epistatic miniarray prof
179 alyzed the consequences of Spt5 depletion in Schizosaccharomyces pombe using four genome-wide approac
180 sm of F-actin assembly during cytokinesis in Schizosaccharomyces pombe using lifeact as a probe to mo
181 resolution survey of genome interactions in Schizosaccharomyces pombe using synchronized cells to in
186 Yeast cells (Saccharomyces cerevisiae and Schizosaccharomyces pombe) genetically depleted of La gr
188 d26 in Saccharomyces cerevisiae and Rhp26 in Schizosaccharomyces pombe) is among the first proteins t
189 To understand their roles in fission yeast (Schizosaccharomyces pombe) mitochondria, we generated de
190 Saccharomyces cerevisiae) to hetero-octamer (Schizosaccharomyces pombe) to hetero-nonamer (Metazoa).
191 t regulation of sterol response genes (Ofd1, Schizosaccharomyces pombe) to translation termination/mR
192 c shift in gene expression in fission yeast (Schizosaccharomyces pombe), and this response is driven
193 ta from 116 transcriptomes in fission yeast (Schizosaccharomyces pombe), covering multiple physiologi
199 , little is known about replicative aging in Schizosaccharomyces pombe, a rod-shaped yeast that divid
202 e and mouse, a tra1Delta mutant is viable in Schizosaccharomyces pombe, allowing us to test these iss
203 comprehensive profile of splicing events in Schizosaccharomyces pombe, amongst the simplest organism
204 d its application to the unicellular fungus, Schizosaccharomyces pombe, an organism that shares many
206 ESR, in the distantly related fission yeast, Schizosaccharomyces pombe, and in humans can explain gen
207 genomic data from Saccharomyces cerevisiae, Schizosaccharomyces pombe, and Lachancea kluyveri, we ex
208 to two yeasts, Saccharomyces cerevisiae and Schizosaccharomyces pombe, and one filamentous fungus, N
209 jump in yeast and the Tf1 retrotransposon of Schizosaccharomyces pombe, both of which prefer nucleoso
210 dida albicans, Saccharomyces cerevisiae, and Schizosaccharomyces pombe, but not zymosan preparations
211 ct in a ded1 temperature-sensitive strain of Schizosaccharomyces pombe, but the cancer-associated mut
212 logue of the human RNA-binding protein La in Schizosaccharomyces pombe, causes irregularities in tRNA
213 cent findings show that in the fission yeast Schizosaccharomyces pombe, cleavage furrow ingression is
214 ifferent stress conditions in fission yeast, Schizosaccharomyces pombe, combining dynamic genome-wide
221 c chromosome movements in the fission yeast, Schizosaccharomyces pombe, depend on astral microtubule
222 complementation group M (FANCM)-ortholog of Schizosaccharomyces pombe, directs the formation of NCOs
224 epair and Tel1 (ATM) checkpoint signaling in Schizosaccharomyces pombe, double-strand break resection
225 Here we show that, in the fission yeast Schizosaccharomyces pombe, ectopically induced domains o
227 lp14, a XMAP215 orthologue in fission yeast, Schizosaccharomyces pombe, has properties of a MT polyme
230 Est1 exists in multiple organisms, including Schizosaccharomyces pombe, humans, and Saccharomyces cer
231 ing formation has been well characterized in Schizosaccharomyces pombe, in which the cross-linking pr
232 1, a long-terminal repeat retrotransposon in Schizosaccharomyces pombe, integrates into promoters wit
236 ammalian PtK1 cells and in the fission yeast Schizosaccharomyces pombe, kinetochores shortened after
241 epistasis map (E-MAP) for the fission yeast Schizosaccharomyces pombe, providing phenotypic signatur
242 Here we show that, in the fission yeast Schizosaccharomyces pombe, RNAi and heterochromatin fact
244 ustrial strains of Saccharomyces cerevisiae, Schizosaccharomyces pombe, Saccharomyces boulardii, Sacc
245 n in three distantly related fission yeasts: Schizosaccharomyces pombe, Schizosaccharomyces octosporu
258 on properties of SpPot1, the POT1 homolog in Schizosaccharomyces pombe, we found an unanticipated ssD
261 hway for diamide-induced disulfide stress in Schizosaccharomyces pombe, where the nucleocytoplasmic H
262 calnexin-independence factor 1 (Cif1), from Schizosaccharomyces pombe, which has been implicated in
264 itotic and meiotic chromosome segregation in Schizosaccharomyces pombe, which has more than one kinet
265 ) and a modified version of TyrRS, AzFRS, in Schizosaccharomyces pombe, which is an attractive model
266 family member expressed in the fission yeast Schizosaccharomyces pombe, Zfs1, promotes the turnover o
267 ism, whereas the single protein expressed in Schizosaccharomyces pombe, Zfs1, regulates cell-cell int
268 is, Lachancea kluyveri, Lachancea waltii and Schizosaccharomyces pombe-also conform to these predicti
298 ata sets and the genomes of three additional Schizosaccharomyces species (Schizosaccharomyces cryophi
299 c1/mariner and Tc5 transposons, occur in all Schizosaccharomyces species, as well as in humans, but w
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