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1 cystis species with Taphrina, Saitoella, and Schizosaccharomyces, and divergence within Pneumocystis
2 e of centromere-binding protein-B (CENPB) in Schizosaccharomyces, as well as in metazoans.
3 erved, Tas3 is lost and Chp1 is truncated in Schizosaccharomyces cryophilus and Schizosaccharomyces o
4 hree additional Schizosaccharomyces species (Schizosaccharomyces cryophilus, Schizosaccharomyces japo
5 fission yeasts Schizosaccharomyces pombe and Schizosaccharomyces japonicus [1-3].
6 ces species (Schizosaccharomyces cryophilus, Schizosaccharomyces japonicus and Schizosaccharomyces oc
7                              Here we find in Schizosaccharomyces japonicus and Schizosaccharomyces po
8 dy, we have determined crystal structures of Schizosaccharomyces japonicus Mis16 alone and in complex
9 ut with loss of transposase function (except Schizosaccharomyces japonicus).
10                                           In Schizosaccharomyces japonicus, the conserved LEM-domain
11 on the cytokinetic ring in the fission yeast Schizosaccharomyces japonicus, unlike its role in S. pom
12 fission yeasts Schizosaccharomyces pombe and Schizosaccharomyces japonicus.
13 es pombe, Schizosaccharomyces octosporus and Schizosaccharomyces japonicus.
14  genes on chromosome 3 of the fission yeasts Schizosaccharomyces kambucha and S. pombe.
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
18 ryophilus, Schizosaccharomyces japonicus and Schizosaccharomyces octosporus).
19      Alkyltransferase-like (ATL) proteins in Schizosaccharomyces pombe (Atl1) and Thermus thermophilu
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
22 elomeres 1) and Taz1 (telomere-associated in Schizosaccharomyces pombe 1) in vivo.
23                       Here we report that in Schizosaccharomyces pombe a conserved DDB1-CUL4-associat
24                  Here we demonstrate that in Schizosaccharomyces pombe a DNA recognition protein, alk
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
29  broadly conserved between the fission yeast Schizosaccharomyces pombe and humans.
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
32                 As shown here when tested in Schizosaccharomyces pombe and mammalian HEK293T cells, t
33           Based on functional studies on the Schizosaccharomyces pombe and Neurospora crassa Nbp2p or
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
40                            The fission yeast Schizosaccharomyces pombe and the filamentous fungus Neu
41 bstrate for thioredoxin in the fission yeast Schizosaccharomyces pombe and, as such, competitively in
42                            The fission yeast Schizosaccharomyces pombe are rod-shaped cells that grow
43                                Fission yeast Schizosaccharomyces pombe are rod-shaped cells that grow
44                       In this study, we used Schizosaccharomyces pombe as a model to analyse mutants
45                Here we use the fission yeast Schizosaccharomyces pombe as a model to investigate UPD,
46                                        Using Schizosaccharomyces pombe as a model we show that the Ra
47                                Fission yeast Schizosaccharomyces pombe assembles actin into three dis
48                                 We show that Schizosaccharomyces pombe behaves similarly to metazoans
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
54                               Clp1/Flp1, the Schizosaccharomyces pombe Cdc14 orthologue, and Cdc14B,
55                                              Schizosaccharomyces pombe cdc15 homology (PCH) family me
56 omain of the essential cytokinetic scaffold, Schizosaccharomyces pombe Cdc15, during cytokinesis.
57 f the N-terminal homo-dimerization domain of Schizosaccharomyces pombe Cdc23 (Cdc23(Nterm)).
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
61                In this study, we report that Schizosaccharomyces pombe cells lacking efr3, which enco
62                                       Living Schizosaccharomyces pombe cells were loaded in a microfl
63                  In rod-shaped fission yeast Schizosaccharomyces pombe cells, division at midcell is
64 MD), is essential for spindle disassembly in Schizosaccharomyces pombe cells.
65 r model organism; however, the fission yeast Schizosaccharomyces pombe community currently lacks prot
66                                 In contrast, Schizosaccharomyces pombe contains two essential tRNase
67            The DNA replication checkpoint in Schizosaccharomyces pombe contains two major protein kin
68 ermine the nanoscale spatial organization of Schizosaccharomyces pombe contractile ring components re
69            Here, we report that deleting the Schizosaccharomyces pombe dcd1(+) dCMP deaminase gene (S
70 y and enzyme kinetics, we show that Trp43 of Schizosaccharomyces pombe Dcp2 is a conserved gatekeeper
71                                          Our Schizosaccharomyces pombe Deltapfh1 strain constitutes a
72 rmline mutations in DIS3L2, a homolog of the Schizosaccharomyces pombe dis3 gene, in individuals with
73                                              Schizosaccharomyces pombe displays a large transcription
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
76                                 Like humans, Schizosaccharomyces pombe encodes a single Pif1 family D
77                            The fission yeast Schizosaccharomyces pombe encodes homologs of HMGR and I
78                                    The yeast Schizosaccharomyces pombe expresses a single TTP family
79                                          The Schizosaccharomyces pombe fission yeast Tup family corep
80 /cell type has been demonstrated only in the Schizosaccharomyces pombe fission yeast.
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
83                        Using a non-essential Schizosaccharomyces pombe gene deletion collection, we i
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
86                  Their introduction into the Schizosaccharomyces pombe genome results in cell death o
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
89       Through transcriptome profiling of the Schizosaccharomyces pombe genome, we identified a natura
90 lore the high-resolution organization of the Schizosaccharomyces pombe genome, which despite its smal
91 matin, and origins of replication within the Schizosaccharomyces pombe genome.
92 copper is essential for spore germination in Schizosaccharomyces pombe Germinating spores develop a s
93                                              Schizosaccharomyces pombe harbors MTOCs at spindle pole
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
96                            The fission yeast Schizosaccharomyces pombe has six Rho GTPases (Cdc42 and
97                     Studies in fission yeast Schizosaccharomyces pombe have provided the basis for th
98                                          The Schizosaccharomyces pombe HDAC Clr6 (human HDAC1) binds
99                            The fission yeast Schizosaccharomyces pombe homologs of mammalian CENP-B p
100          Here, using Clr4, the fission yeast Schizosaccharomyces pombe homologue of mammalian SUV39H
101                         Here, we use the two Schizosaccharomyces pombe HP1 paralogs, Swi6 and Chp2, a
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)
105        Here we show that the Mst2 complex in Schizosaccharomyces pombe is a highly specific H3 lysine
106 determinants of aging, and the fission yeast Schizosaccharomyces pombe is a promising new system for
107                                              Schizosaccharomyces pombe is an attractive organism to s
108                                              Schizosaccharomyces pombe is an important experimental s
109                            The fission yeast Schizosaccharomyces pombe is an important model for euka
110                            The fission yeast Schizosaccharomyces pombe is an important model organism
111         Heterochromatin in the fission yeast Schizosaccharomyces pombe is clustered at the nuclear pe
112  showed that drug tolerance in fission yeast Schizosaccharomyces pombe is controlled by lncRNA transc
113                                      RNAi in Schizosaccharomyces pombe is critical for centromeric he
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
121              We found that the fission yeast Schizosaccharomyces pombe lacks both a Hac1/XBP1 ortholo
122                                We identified Schizosaccharomyces pombe mcb1(+) (Mcm-binding protein 1
123         Here, using the crystal structure of Schizosaccharomyces pombe MCC (a complex of mitotic spin
124 A resolution cryo-electron microscopy map of Schizosaccharomyces pombe Mediator in which conserved Me
125                                       During Schizosaccharomyces pombe meiotic prophase, homologous c
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
128                               We implicate a Schizosaccharomyces pombe nuclear envelope-spanning link
129          We present the crystal structure of Schizosaccharomyces pombe Nup37 in complex with Nup120,
130 orthologs Pck1 and Pck2 in the fission yeast Schizosaccharomyces pombe operate in a redundant fashion
131                        Here we show that the Schizosaccharomyces pombe ortholog of Nrd1, Seb1, does n
132  important for meiosis in the fission yeast, Schizosaccharomyces pombe Our genome-wide functional scr
133                                Fission yeast Schizosaccharomyces pombe P and M cells, which respectiv
134            WH domain mutation or deletion in Schizosaccharomyces pombe phenocopies the DNA-damage sen
135           The Loz1 transcription factor from Schizosaccharomyces pombe plays an essential role in zin
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
139                         In the fission yeast Schizosaccharomyces pombe proteins that contribute to th
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
143                  Preventing deSUMOylation in Schizosaccharomyces pombe results in slow growth and a s
144                One of these shuttle factors, Schizosaccharomyces pombe Rhp23, has an unusual domain a
145 r quiescence (G0 phase of the cell cycle) in Schizosaccharomyces pombe RNAi mutants lose viability at
146                               Similarly, the Schizosaccharomyces pombe Seg1-like protein Sle1 was nec
147                                          The Schizosaccharomyces pombe septation initiation network (
148 biochemical studies on the Sen1 homolog from Schizosaccharomyces pombe showed that it can bind and un
149                                          The Schizosaccharomyces pombe shu1(+) gene encodes a cell-su
150 smic duplication cycle and regulation of the Schizosaccharomyces pombe SPB is analogous to centrosome
151 in structure, and histone modifications in a Schizosaccharomyces pombe spt6 mutant.
152                                              Schizosaccharomyces pombe Sre1 is a membrane-bound trans
153                      We previously developed Schizosaccharomyces pombe strains that report on two pol
154 to varying degrees the growth defects of the Schizosaccharomyces pombe STUbL mutant rfp1/rfp2, and th
155               We then analyzed N. crassa and Schizosaccharomyces pombe telomerase reconstituted in vi
156                                The 3' end of Schizosaccharomyces pombe telomerase RNA (SpTER1) is gen
157                           We report that the Schizosaccharomyces pombe telomerase RNA, TER1 (telomera
158                  MtgA is the ortholog of the Schizosaccharomyces pombe telomere-anchoring inner nucle
159 ignificantly less toxic to the fission yeast Schizosaccharomyces pombe than unstimulated OSPW.
160                 We isolated C11 mutants from Schizosaccharomyces pombe that cause pol III to readthro
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
163                         In the fission yeast Schizosaccharomyces pombe the activation of the G2/M CDK
164                                           In Schizosaccharomyces pombe the Tf2 LTR retrotransposons a
165 sly shown that in the symmetrically dividing Schizosaccharomyces pombe there is a transition between
166         We examined the function of i6A37 in Schizosaccharomyces pombe tit1+ and tit1-Delta cells by
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
174                                          The Schizosaccharomyces pombe TUT Cid1 is a model enzyme tha
175              Here, we present a structure of Schizosaccharomyces pombe Uba1 in which the second catal
176 ed ribosome profiling with the fission yeast Schizosaccharomyces pombe under conditions of exponentia
177                            The fission yeast Schizosaccharomyces pombe undergoes "closed" mitosis in
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
182                                   Until now, Schizosaccharomyces pombe was known to use reductive iro
183                                          The Schizosaccharomyces pombe WISH/DIP/SPIN90 ortholog dip1p
184  5FU interferes with Pot1 (Pot1pN protein of Schizosaccharomyces pombe) binding.
185 s the 12 species in MitoMiner (now including Schizosaccharomyces pombe) by homology mapping.
186    Yeast cells (Saccharomyces cerevisiae and Schizosaccharomyces pombe) genetically depleted of La gr
187       Mal3p and Tip1p are the fission yeast (Schizosaccharomyces pombe) homologues of EB1 and CLIP-17
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
194                            In fission yeast (Schizosaccharomyces pombe), RNA interference (RNAi)-medi
195                            In fission yeast (Schizosaccharomyces pombe), the E3 ubiquitin ligase Dma1
196                         In the fission yeast Schizosaccharomyces pombe, a cortical gradient of pom1p
197                                           In Schizosaccharomyces pombe, a Hippo-related signaling pat
198                                           In Schizosaccharomyces pombe, a late mitotic kinase pathway
199 , little is known about replicative aging in Schizosaccharomyces pombe, a rod-shaped yeast that divid
200                         In the fission yeast Schizosaccharomyces pombe, active Cdc42 and associated e
201                                           In Schizosaccharomyces pombe, alcohol dehydrogenase 1 (Adh1
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
205 es of nucleosome occupancy in S. cerevisiae, Schizosaccharomyces pombe, and human cells.
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
215                         In the fission yeast Schizosaccharomyces pombe, conserved protein complexes e
216                                           In Schizosaccharomyces pombe, copper is transported by thre
217                         In the fission yeast Schizosaccharomyces pombe, cytokinesis also involves a c
218                                           In Schizosaccharomyces pombe, cytokinesis requires the asse
219              During mitosis in fission yeast Schizosaccharomyces pombe, cytoplasmic microtubule nucle
220                                           In Schizosaccharomyces pombe, deletion of the ATPase vps4 l
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
223                                           In Schizosaccharomyces pombe, division plane positioning is
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
226                                           In Schizosaccharomyces pombe, H3K9me deposition depends on
227 lp14, a XMAP215 orthologue in fission yeast, Schizosaccharomyces pombe, has properties of a MT polyme
228                                           In Schizosaccharomyces pombe, heterochromatin assembly on t
229                                           In Schizosaccharomyces pombe, heterochromatin spread, which
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
233                            In fission yeast, Schizosaccharomyces pombe, interactions between the shel
234                  Cut7, the sole kinesin-5 in Schizosaccharomyces pombe, is essential for mitosis.
235                         In the fission yeast Schizosaccharomyces pombe, it is well established that m
236 ammalian PtK1 cells and in the fission yeast Schizosaccharomyces pombe, kinetochores shortened after
237                                           In Schizosaccharomyces pombe, late mitotic events are coord
238                   Heterologous expression in Schizosaccharomyces pombe, LC-MS analyses, and kinetic s
239                         In the fission yeast Schizosaccharomyces pombe, mitotic entry is orchestrated
240                                           In Schizosaccharomyces pombe, Myosin Vs transport secretory
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
243          The fission yeast clade--comprising Schizosaccharomyces pombe, S. octosporus, S. cryophilus,
244 ustrial strains of Saccharomyces cerevisiae, Schizosaccharomyces pombe, Saccharomyces boulardii, Sacc
245 n in three distantly related fission yeasts: Schizosaccharomyces pombe, Schizosaccharomyces octosporu
246                         In the fission yeast Schizosaccharomyces pombe, the CaMKK-like protein kinase
247                         In the fission yeast Schizosaccharomyces pombe, the cell integrity MAPK pathw
248                         In the fission yeast Schizosaccharomyces pombe, the centromeres of each chrom
249                                              Schizosaccharomyces pombe, the fission yeast, cells alte
250                                           In Schizosaccharomyces pombe, the H3-K9 methyltransferase C
251                                 In the yeast Schizosaccharomyces pombe, the mitochondria are pushed t
252                         In the fission yeast Schizosaccharomyces pombe, the multi-BRCT domain protein
253                                           In Schizosaccharomyces pombe, the myo2-E1 mutation affects
254                         In the fission yeast Schizosaccharomyces pombe, the protein kinase Cdr1 is a
255                         In the fission yeast Schizosaccharomyces pombe, the proteins Mto1 and Mto2 fo
256                                           In Schizosaccharomyces pombe, the RNAi pathway is required
257                         In the fission yeast Schizosaccharomyces pombe, the SREBP-2 homolog Sre1 regu
258 on properties of SpPot1, the POT1 homolog in Schizosaccharomyces pombe, we found an unanticipated ssD
259                                           In Schizosaccharomyces pombe, we found that the iss1(+) gen
260                      Using the fission yeast Schizosaccharomyces pombe, we show that a proper force b
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
263                                           In Schizosaccharomyces pombe, which has epigenetically defi
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
269 ncluding osmotic stress in the fission yeast Schizosaccharomyces pombe.
270 or telomere maintenance in the fission yeast Schizosaccharomyces pombe.
271 that found specifically in the fission yeast Schizosaccharomyces pombe.
272 l histone modifications in the fission yeast Schizosaccharomyces pombe.
273 east, including Saccharomyces cerevisiae and Schizosaccharomyces pombe.
274 ccharomyces cerevisiae and the fission yeast Schizosaccharomyces pombe.
275 ent of Set1C and H3K4me in the fission yeast Schizosaccharomyces pombe.
276 e played by ncRNAs in the stress response of Schizosaccharomyces pombe.
277  of synchronous meiosis in the fission yeast Schizosaccharomyces pombe.
278 niscent of the distantly related ascomycete, Schizosaccharomyces pombe.
279  Rhp26, which is the homolog of CSB/ERCC6 in Schizosaccharomyces pombe.
280 odel organism database for the fission yeast Schizosaccharomyces pombe.
281 wth characteristics of the unicellular yeast Schizosaccharomyces pombe.
282 ne Na(+)/H(+) exchanger of the fission yeast Schizosaccharomyces pombe.
283 t branch of homologous recombination (HR) in Schizosaccharomyces pombe.
284 one example being Cpc2p in the fission yeast Schizosaccharomyces pombe.
285 sure successful completion of cytokinesis in Schizosaccharomyces pombe.
286 f nucleosome positions in the fission yeast, Schizosaccharomyces pombe.
287 eplication origin sites in the fission yeast Schizosaccharomyces pombe.
288 ion between transcription and replication in Schizosaccharomyces pombe.
289 ntrinsic reproductive isolation in the yeast Schizosaccharomyces pombe.
290 chromosome condensation in the fission yeast Schizosaccharomyces pombe.
291 which is an intact homodimeric ATM/Tel1 from Schizosaccharomyces pombe.
292 ocess for proper actomyosin ring assembly in Schizosaccharomyces pombe.
293 ct repeat recombination in the fission yeast Schizosaccharomyces pombe.
294 myces cerevisiae and the homologue, Eso1, in Schizosaccharomyces pombe.
295 scription factor, Sak1, in the fission yeast Schizosaccharomyces pombe.
296 rmentation with Saccharomyces cerevisiae and Schizosaccharomyces pombe.
297 n, genome-wide map of nucleosome turnover in Schizosaccharomyces pombe.
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
300 s changed essential residues conserved among Schizosaccharomyces species.

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