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1 pt4 in controlling elongation in budding and fission yeast.
2 nesis functions of Cdc14/Flp1 in budding and fission yeast.
3 recent experiments on histone methylation in fission yeast.
4 sure proper splicing of certain pre-mRNAs in fission yeast.
5 ce a robust anti-stress cellular response in fission yeast.
6 tromeres cluster at the spindle pole body in fission yeast.
7 dscapes of the distantly related budding and fission yeast.
8 nd is a key determinant of cohesive sites in fission yeast.
9 stinct action of its GEFs, Gef1 and Scd1, in fission yeast.
10  reminiscent of natural polarity patterns in fission yeast.
11  novel protein, Rng10, during cytokinesis in fission yeast.
12 iations mediated by condensin and cohesin in fission yeast.
13 nd its relationship with the Rho-GAP Rga7 in fission yeast.
14 increased gamete death after IR is innate to fission yeast.
15 se, is essential for acetyl-CoA synthesis in fission yeast.
16  Rgf3 is an essential GEF for Rho1 GTPase in fission yeast.
17 n-mediated actin assembly for cytokinesis in fission yeast.
18 spindle disassembly in the closed mitosis of fission yeast.
19 o coordinate mitotic progression and exit in fission yeast.
20 acterize the transcriptome in the meiosis of fission yeast.
21  and constriction of the contractile ring in fission yeast.
22 report how cell growth domains are shaped in fission yeast.
23 ion to isolate variants that support life in fission yeast.
24 t are anticorrelated at the two cell tips in fission yeast.
25 hase and mitotic chromosomal organization in fission yeast.
26 es Rho4 GTPase as a Rho GEF for septation in fission yeast.
27 y is a hallmark of aneuploidy in budding and fission yeast.
28 tics tools used to study protein function in fission yeast.
29 on and unlocks the CRISPR toolset for use in fission yeast.
30 RNAs), suggesting that dsRNAs form widely in fission yeast.
31 n in regulating DSB repair pathway choice in fission yeast.
32 ion and influences cell cycle progression in fission yeast.
33 ption of an lncRNA governs drug tolerance in fission yeast.
34 in RNAi-directed heterochromatin assembly in fission yeast.
35 ded for uptake of extracellular phosphate in fission yeast.
36 e isoform level in the sexual development of fission yeast.
37 ic tubule elongation and vesicle scission in fission yeast.
38 physical mechanism for typical conditions in fission yeast.
39 subunit and, thereby, controls exocytosis in fission yeast.
40  function of PS in the rod-shaped, polarized fission yeast.
41 ner similar to what has been demonstrated in fission yeast.
42 are coordinated to maintain lipid balance in fission yeast.
43 3 act in parallel to inhibit TOR function in fission yeast.
44 ut are conspicuously absent from budding and fission yeasts.
45 se transcript landscapes between budding and fission yeasts.
46  which are absent or divergent in budding or fission yeasts.
47                     In the closed mitosis of fission yeast, a microtubule-associated protein complex,
48 of this complexity, it is surprising that in fission yeast, a minimal Cdk network consisting of a sin
49 t during quiescence, the unicellular haploid fission yeast accumulates mutations as a linear function
50       Three 'killer genes' in one species of fission yeast act selfishly and keep it reproductively i
51                                          The fission yeast actin cytoskeleton is an ideal, simplified
52  Here, we develop a strategy for loading the fission yeast Ago1 with a single-stranded sRNA guide, wh
53                                   Whereas in fission yeast all kinetochores relaxed to a similar leng
54 ivity and resistance conferring mutations in fission yeast, along with biochemical assays with recomb
55                                              Fission yeast AMPK catalytic subunit Ssp2 is phosphoryla
56        A similar response can be observed in fission yeast and bacteria.
57 and regulatory basis of energy metabolism in fission yeast and beyond, and it pinpoints weaknesses of
58 ere spatially organized by eisosomes in both fission yeast and budding yeast cells.
59 -based systems analysis of CDK substrates in fission yeast and demonstrate that the phosphorylation o
60                             We purified both fission yeast and human Aip1 and investigated their bioc
61 fic manner in Schizosaccharomyces pombe Both fission yeast and human Sde2 are translated as inactive
62                                              Fission yeast and mammalian Rif1 proteins have also been
63 irth of synthetic centromeres in budding and fission yeast and mammals.
64 s with sensitivity to DNA-damaging agents in fission yeast and reduced viability in human cells.
65 led previously undetected origin clusters in fission yeast and shows that in human cells replication
66 r target recognition in the TORC2 complex in fission yeast and the mTORC2 complex in mammals.
67 ed up to the length of entire chromosomes in fission yeast and up to 12 Mb fragments in human cells.
68 studies of Cdc42 polarization in budding and fission yeasts and demonstrate that models describing sy
69  confidence SUMO-modified target proteins in fission yeast, and a robust method for future analyses o
70 pe in mammals, spindle pole body dynamics in fission yeast, and surveillance of defective nuclear por
71 nderstand the mechanism of cytokinesis using fission yeast as a favorable model system.
72                                        Using fission yeast as a model, we report here that DBAN delay
73 oles of GR in cellular stress response using fission yeast as a model.We surprisingly discovered mark
74 motes epigenetic stability of centromeres in fission yeast, at least in part via recruitment of the C
75 ere we present a mechanism for aneuploidy in fission yeast based on spindle pole microtubule defocusi
76 found previously that upon disruption of the fission yeast bouquet, centrosomes failed to insert into
77 ve species-specific network rewiring between fission yeast, budding yeast, and human.
78 rtholog) are required for both activities in fission yeast but whether they are genetically separable
79 points contributes to kinetochore capture in fission yeast, but the relative contributions of dynamic
80 daptor Nro1 regulate the hypoxic response in fission yeast by controlling activity of the sterol regu
81          We report here that Rga6 is another fission yeast Cdc42 GAP which shares some functions with
82  only GAP described as negative regulator of fission yeast Cdc42.
83                                        Using fission yeast cell cycle as an example, we uncovered tha
84 g the stability, speed and robustness of the fission yeast cell cycle oscillations.
85 equentiality, as observed in the budding and fission yeast cell- cycle.
86 In further investigations of the budding and fission yeast cell-cycle, we identify two generic dynami
87 opy (FPALM), we probed this question in live fission yeast cells at unprecedented resolution.
88 s required for oxidative stress responses in fission yeast cells by promoting transcription initiatio
89                           Here, we show that fission yeast cells carrying a mutation in the DNA-bindi
90                                 We show that fission yeast cells deficient in ER-PM contacts exhibit
91                               Cytokinesis in fission yeast cells depends on conventional myosin-II (M
92              We study cell polarization when fission yeast cells exit starvation.
93 inuous replication of hundreds of individual fission yeast cells for over seventy-five generations.
94                                   Rod-shaped fission yeast cells grow in a highly polarized manner, a
95                                        Using fission yeast cells lacking the debranching enzyme Dbr1,
96 erresolution localization microscopy of live fission yeast cells to improve the spatial resolution to
97                                              Fission yeast cells use Arp2/3 complex and formin to ass
98     In this issue, Dudin et al. image mating fission yeast cells with unprecedented spatiotemporal re
99                                           In fission yeast cells, a microtubule-dependent network has
100 which distributes homogeneously in wild-type fission yeast cells, can be made to concentrate at cell
101                                           In fission yeast cells, the formin Fus1, which nucleates li
102 okinesis nodes and contractile rings in live fission yeast cells.
103             Here, we employ the well-studied fission yeast centromere [13-16] to investigate the func
104 ton and cytoskeleton (LINC) complex connects fission yeast centromeres and the centrosome, across the
105 to contribute to heterochromatin assembly at fission yeast centromeres.
106 lectable kanMX reporter gene embedded within fission yeast centromeric heterochromatin.
107 g genome-wide methods, here we show that the fission yeast CID-protein Seb1 is essential for terminat
108                           Here, we show that fission yeast Cki3 (a casein kinase 1gamma homolog) is a
109                         In this work, we use fission yeast co-expression networks before and after ex
110 tute cohesin loading onto DNA using purified fission yeast cohesin and its loader complex, Mis4(Scc2)
111                Using biochemical analysis of fission-yeast cohesin, we find that a similar series of
112       PomBase provides a central hub for the fission yeast community, supporting both exploratory and
113 similar structures appear to be conserved in fission yeast, computational modeling and analysis of hi
114                                          The fission yeast contractile ring has been proposed to asse
115             Using in vitro reconstitution of fission yeast contractile ring precursor nodes containin
116 ly analyse the requirements of the different fission yeast cyclins for meiotic cell cycle progression
117 ivered by myosin-V on linear actin cables in fission yeast cytokinesis.
118  in turn modulates active Rho1 levels during fission yeast cytokinesis.
119                                           In fission yeast, cytokinesis involves the type II myosins
120 icient contractile ring assembly in vivo.The fission yeast cytokinetic ring assembles by Search-Captu
121 rchers, to support community curation in the fission yeast database, PomBase.
122  a GFP-based protein reporter and screened a fission yeast deletion collection using flow cytometry.
123 l to analyze these results, we conclude that fission yeast does not age and that cellular aging and r
124                 The related SHREC complex in fission yeast drives transcriptional gene silencing in h
125                                          The fission yeast Dsc E3 ligase is a Golgi-localized complex
126                      In the absence of mga2, fission yeast exhibited growth defects under both normox
127 hat during transcriptional activation of the fission yeast fbp1 gene, binding of Rst2 (a critical C2H
128                                           In fission yeast, force balance is restored when both kines
129 d facultative heterochromatin islands in the fission yeast genome and found that RNA elimination mach
130                                          The fission yeast genome, which contains numerous short intr
131               Micro-C XL maps of budding and fission yeast genomes capture both short-range chromosom
132                                           In fission yeast, glucose starvation triggers lncRNA transc
133                                              Fission yeast GTase binds the Spt5 CTD at a separate doc
134                                              Fission yeast has a single H3K9 methyltransferase, Clr4,
135                    The anaphase B spindle in fission yeast has a slender morphology and must elongate
136                                    Using the fission yeast, here, we track G0-associated chromatin an
137 ith each other in vitro, and at least in the fission yeast, heterologous Oxs1 and Pap1-homologues can
138                                           In fission yeast, histone H3 lysine 9 (H3K9) is methylated
139                                    Erh1, the fission yeast homolog of Enhancer of rudimentary, is imp
140                    Here, we identify Fft3, a fission yeast homolog of the mammalian SMARCAD1 SNF2 chr
141  of the SMN.Gemin2 complexes from humans and fission yeast (hSMN.Gemin2 and ySMN.Gemin2).
142 d mitogen activated protein kinase (MAPK) in fission yeast, inhibits TORC2-dependent Gad8 phosphoryla
143                         Here we show that in fission yeast, introducing the K9M mutation into one of
144 t early divergence from a common ancestor in fission yeast involved important changes in the mechanis
145                          Like budding yeast, fission yeast is an important and popular model organism
146 is type of non-canonical fork convergence in fission yeast is prone to trigger deletions between repe
147 hods also show that the number of patches in fission yeast is proportional to cell length and that th
148  Mer2, identified so far only in budding and fission yeasts, is in fact evolutionarily conserved from
149                                  However, in fission yeast it has been shown that a single CDK comple
150 s effective in predicting the DNA content of fission yeast, it is likely to have a broad application
151             JMJ24 functionally resembles the fission yeast JmjC protein Epe1.
152 hanism underlying nuclear congression during fission yeast karyogamy upon mating of haploid cells.
153  for the bidirectional motility mechanism of fission yeast kinesin-5 and provide insight into the fun
154 s, we studied the effects of deletion of the fission yeast kinesin-8 proteins Klp5 and Klp6 on chromo
155                                              Fission yeast lacking Aip1 are viable and assemble cytok
156                                           In fission yeast lacking Nup132 (Sc/HuNUP133), Ulp1 is delo
157  fork blockage at a site-specific barrier in fission yeast, leading to a restarted fork within approx
158              Here, we describe a multiplexed fission yeast lifespan micro-dissector (multFYLM) and an
159                   Myo51, a class V myosin in fission yeast, localizes to and assists in the assembly
160          Here, we show that insertion of the fission yeast LTR retrotransposon Tf1 is guided by the D
161 rminant of chromosome segregation defects in fission yeast may be microtubule dynamic defects.
162                                           In fission yeast, Mcp5 is the anchor protein of dynein and
163                                           In fission yeast, medial division is controlled through neg
164                                           In fission yeast, meiosis-specific transcripts are selectiv
165      In contrast, distinct pathways activate fission yeast Mga2 and Sre1.
166 n telomere dispersion and disjunction during fission yeast mitosis.
167  chromosome territories are organized in the fission yeast model organism.
168                                 We analyze a fission yeast mutant that is unable to complete S phase
169 we analyzed the poly(A)(+) transcriptomes of fission yeast mutants that lack each of the four inessen
170 , we discovered that the myosin I protein in fission yeast, Myo1, which is required for organization
171 r previous work suggested, however, that the fission yeast myosin-V (Myo52p) is a nonprocessive motor
172                                           In fission yeast, nitrogen stress results in sustained prol
173 ysical model of kinetochore capture in small fission-yeast nuclei using hybrid Brownian dynamics/kine
174 the degradation pathways for Sdj1-L169P, the fission yeast orthologue of the disease-causing DJ-1 L16
175  suggests a mechanistic conservation between fission yeast PAF1 repressing AGO1/small interfering RNA
176 hat the greatwall-endosulfine (Ppk18-Igo1 in fission yeast) pathway couples the nutritional environme
177                                          The fission yeast plasma membrane is highly compartmentalize
178              Besides the Cdk7 ortholog Mcs6, fission yeast possesses a second CAK, Csk1.
179 ing yeast profilin ScPFY fails to complement fission yeast profilin SpPRF temperature-sensitive mutan
180                               A new study in fission yeasts promotes the notion that transient polari
181                        Here, we identify the fission yeast protein Sdj1 as the orthologue of DJ-1 and
182       To isolate ring mechanisms, we studied fission yeast protoplasts, in which constriction occurs
183   As a model for cellular energy regulation, fission yeast provides an attractive and complementary s
184              This analysis of H3-G34R mutant fission yeast provides mechanistic insight into how G34R
185 parts list of genes important for meiosis in fission yeast, providing a valuable resource to advance
186                                              Fission yeast Rec12 (Spo11 homolog) initiates meiotic re
187 ed Mst2 histone acetyltransferase complex in fission yeast regulates histone turnover at heterochroma
188                        Here, we identify new fission yeast regulatory lncRNAs that are targeted, at t
189                                The growth of fission yeast relies on the polymerization of actin fila
190                   Unlike S. pombe, two other fission yeasts rely on hyperstabilization of the U6 snRN
191 viding a brief description of the origins of fission yeast research, and illustrating some genetic an
192 in inhibitors Sml1p and Spd1p in budding and fission yeast, respectively.
193 y, a superresolution microscopy study of the fission yeast ring revealed that myosins and formins tha
194                                    Thus, the fission yeast ring sets its own tension, but other proce
195 e a coarse-grained mathematical model of the fission yeast ring to explore essential consequences of
196                                           In fission yeast, RNAi machinery and RNA elimination factor
197          Using a genome-wide approach in the fission yeast S. pombe, we have found that Dcr1, but not
198    We examine the function of Swi1 and Swi3, fission yeast's primary FPC components, to elucidate how
199                                          The fission yeast scaffold molecule Sid4 anchors the septum
200 oes not position the cytokinetic ring in the fission yeast Schizosaccharomyces japonicus, unlike its
201 nce, RNAi, are broadly conserved between the fission yeast Schizosaccharomyces pombe and humans.
202                                              Fission yeast Schizosaccharomyces pombe are rod-shaped c
203                              Here we use the fission yeast Schizosaccharomyces pombe as a model to in
204 cts of turgor pressure on endocytosis in the fission yeast Schizosaccharomyces pombe by time-lapse im
205                                In rod-shaped fission yeast Schizosaccharomyces pombe cells, division
206 ant and popular model organism; however, the fission yeast Schizosaccharomyces pombe community curren
207 quest to understand the morphogenesis of the fission yeast Schizosaccharomyces pombe drove us to inve
208 This also occurs in Smc5/6 hypomorphs in the fission yeast Schizosaccharomyces pombe following genoto
209 ean laboratories in the 1940s and 1950s, the fission yeast Schizosaccharomyces pombe has grown to bec
210                                          The fission yeast Schizosaccharomyces pombe has six Rho GTPa
211                                   Studies in fission yeast Schizosaccharomyces pombe have provided th
212                        Here, using Clr4, the fission yeast Schizosaccharomyces pombe homologue of mam
213 e oxygen-responsive lipid homeostasis in the fission yeast Schizosaccharomyces pombe in a manner anal
214                                          The fission yeast Schizosaccharomyces pombe is an important
215                                          The fission yeast Schizosaccharomyces pombe is an important
216                       Heterochromatin in the fission yeast Schizosaccharomyces pombe is clustered at
217    We recently showed that drug tolerance in fission yeast Schizosaccharomyces pombe is controlled by
218 re we present evidence that cell size in the fission yeast Schizosaccharomyces pombe is regulated by
219 how that inhibition of Arp2/3 complex in the fission yeast Schizosaccharomyces pombe not only deplete
220   The two PKC orthologs Pck1 and Pck2 in the fission yeast Schizosaccharomyces pombe operate in a red
221                                              Fission yeast Schizosaccharomyces pombe P and M cells, w
222                                       In the fission yeast Schizosaccharomyces pombe proteins that co
223 ory element-binding proteins (SREBPs) in the fission yeast Schizosaccharomyces pombe regulate lipid h
224 ted OSPW was significantly less toxic to the fission yeast Schizosaccharomyces pombe than unstimulate
225 viously described a mutant, pat1-as2, of the fission yeast Schizosaccharomyces pombe that undergoes s
226 sue we performed ribosome profiling with the fission yeast Schizosaccharomyces pombe under conditions
227                                          The fission yeast Schizosaccharomyces pombe undergoes "close
228                                       In the fission yeast Schizosaccharomyces pombe, active Cdc42 an
229             Recent findings show that in the fission yeast Schizosaccharomyces pombe, cleavage furrow
230                                       In the fission yeast Schizosaccharomyces pombe, conserved prote
231                            During mitosis in fission yeast Schizosaccharomyces pombe, cytoplasmic mic
232                    Here we show that, in the fission yeast Schizosaccharomyces pombe, ectopically ind
233      In both mammalian PtK1 cells and in the fission yeast Schizosaccharomyces pombe, kinetochores sh
234                                       In the fission yeast Schizosaccharomyces pombe, the CaMKK-like
235                                       In the fission yeast Schizosaccharomyces pombe, the multi-BRCT
236                                       In the fission yeast Schizosaccharomyces pombe, the protein kin
237                                       In the fission yeast Schizosaccharomyces pombe, the SREBP-2 hom
238    The single family member expressed in the fission yeast Schizosaccharomyces pombe, Zfs1, promotes
239 study mitotic chromosome condensation in the fission yeast Schizosaccharomyces pombe.
240 motion of direct repeat recombination in the fission yeast Schizosaccharomyces pombe.
241 w mitotic transcription factor, Sak1, in the fission yeast Schizosaccharomyces pombe.
242 l conditions including osmotic stress in the fission yeast Schizosaccharomyces pombe.
243 is essential for telomere maintenance in the fission yeast Schizosaccharomyces pombe.
244 distinct from that found specifically in the fission yeast Schizosaccharomyces pombe.
245 transcriptional histone modifications in the fission yeast Schizosaccharomyces pombe.
246 dding yeast Saccharomyces cerevisiae and the fission yeast Schizosaccharomyces pombe.
247 rgely independent of Set1C and H3K4me in the fission yeast Schizosaccharomyces pombe.
248  for induction of synchronous meiosis in the fission yeast Schizosaccharomyces pombe.
249 f meiotic drive genes on chromosome 3 of the fission yeasts Schizosaccharomyces kambucha and S. pombe
250 NE management strategies between the related fission yeasts Schizosaccharomyces pombe and Schizosacch
251 e plasticity of division site positioning in fission yeasts Schizosaccharomyces pombe and Schizosacch
252 he most dramatic shift in gene expression in fission yeast (Schizosaccharomyces pombe), and this resp
253 lyze RNA-seq data from 116 transcriptomes in fission yeast (Schizosaccharomyces pombe), covering mult
254 atalog of genes important for meiosis in the fission yeast, Schizosaccharomyces pombe Our genome-wide
255          Meiotic chromosome movements in the fission yeast, Schizosaccharomyces pombe, depend on astr
256                                           In fission yeast, Schizosaccharomyces pombe, interactions b
257                                           In fission yeast, Scm3sp and the Mis18 complex, composed of
258              Similar to the human shelterin, fission yeast shelterin is composed of telomeric sequenc
259                           Elimination of the fission yeast shelterin subunit Ccq1 causes progressive
260                                           In fission yeast, shelterin is comprised of five proteins.
261  In contrast, previous work with budding and fission yeast showed that some outer kinetochore protein
262 ypotheses, yielding additional evidence that fission yeast siRNA-Argonaute silencing complexes are re
263 inding mutant shows a reduced association of fission yeast SMC5/6 with chromatin.
264 putative chromatin remodeling subunit of the fission yeast Snf2/histone deacetylase (HDAC) repressor
265                                          The fission yeast specific chaperone Rng3 was thus not requi
266                       Proteolytic release of fission yeast SREBPs from the membrane in response to lo
267 genic suppressors of a temperature-sensitive fission yeast strain mutated in the exocyst subunit Sec3
268                        Here we show that the fission yeast stress-activated protein kinase Sty1, a ho
269  coupled with mass spectrometry, to identify fission yeast SUMO conjugates.
270    Therefore, knowledge from the budding and fission yeast systems illuminates highly conserved molec
271                                           In fission yeast, Tel1(ATM)/Rad3(ATR)-mediated phosphorylat
272                                           In fission yeast, telomerase is recruited through an intera
273 p1, an uncharacterized NAP family protein in fission yeast that antagonizes CENP-A loading at both ce
274 sight into the role of H3-G34R, we generated fission yeast that express only the mutant histone H3.
275                                   We show in fission yeast that, at low Cdc20 concentrations, Cdc20(M
276                                           In fission yeast, the conserved telomeric shelterin complex
277                                           In fission yeast, the kinesin-14 Pkl1 binds the gamma-tubul
278                                           In fission yeast, the Rpa1-D223Y mutation provokes telomere
279                                           In fission yeast, the ste11 gene encodes the master regulat
280           Here we address these questions in fission yeast through proteome-wide analyses of SUMO mod
281                  Here we show that Tts1, the fission yeast TMEM33 protein that was previously implica
282 , showing tetrameric Mis18 is conserved from fission yeast to humans.
283            We screened deletion libraries of fission yeast to identify over 200 genes required for re
284 ools to track and count endocytic patches in fission yeast to increase the quality of the data extrac
285                                 Here, we use fission yeast to investigate how phosphatase activity pa
286 and FPALM superresolution microscopy of live fission yeast to investigate the structures and assembly
287                                         From fission yeast to mammals, heterochromatin assembly at DN
288                                           In fission yeast, TORC2 is dispensable for proliferation un
289                                           In fission yeast, TORC2 is dispensable for proliferation un
290 Here, we report the crystal structure of the fission yeast Tpz1(475-508)-Poz1-Rap1(467-496) complex t
291                The Schizosaccharomyces pombe fission yeast Tup family corepressors Tup11 and Tup12 (T
292 mic bundling is important for cytokinesis in fission yeast, we created the less dynamic bundling muta
293                                   Here using fission yeast, we identify Fun30(Fft3) as a chromatin re
294                                        Using fission yeast, we report the first genome-wide analysis
295                   To characterize R-loops in fission yeast, we used the S9.6 antibody-based DRIPc-seq
296 l1p, the main eisosome BAR-domain protein in fission yeast, we visualized whole eisosomes and, after
297 ibe a functional fluorescent Cdc42 allele in fission yeast, which demonstrates Cdc42 dynamics and pol
298  cytokinesis arrest in the erg11-1 mutant of fission yeast, which has a partial defect in the biosynt
299 rding the human gene homologs in budding and fission yeast, worm, fly, fish, mouse, and rat on a sing
300 antified the localization pattern of Mcp5 in fission yeast zygotes and show by perturbation of phosph

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