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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.
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
52 Here, we develop a strategy for loading the fission yeast Ago1 with a single-stranded sRNA guide, wh
54 ivity and resistance conferring mutations in fission yeast, along with biochemical assays with recomb
57 and regulatory basis of energy metabolism in fission yeast and beyond, and it pinpoints weaknesses of
59 -based systems analysis of CDK substrates in fission yeast and demonstrate that the phosphorylation o
61 fic manner in Schizosaccharomyces pombe Both fission yeast and human Sde2 are translated as inactive
65 led previously undetected origin clusters in fission yeast and shows that in human cells replication
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
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
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
86 In further investigations of the budding and fission yeast cell-cycle, we identify two generic dynami
88 s required for oxidative stress responses in fission yeast cells by promoting transcription initiatio
93 inuous replication of hundreds of individual fission yeast cells for over seventy-five generations.
96 erresolution localization microscopy of live fission yeast cells to improve the spatial resolution to
98 In this issue, Dudin et al. image mating fission yeast cells with unprecedented spatiotemporal re
100 which distributes homogeneously in wild-type fission yeast cells, can be made to concentrate at cell
104 ton and cytoskeleton (LINC) complex connects fission yeast centromeres and the centrosome, across the
107 g genome-wide methods, here we show that the fission yeast CID-protein Seb1 is essential for terminat
110 tute cohesin loading onto DNA using purified fission yeast cohesin and its loader complex, Mis4(Scc2)
113 similar structures appear to be conserved in fission yeast, computational modeling and analysis of hi
116 ly analyse the requirements of the different fission yeast cyclins for meiotic cell cycle progression
120 icient contractile ring assembly in vivo.The fission yeast cytokinetic ring assembles by Search-Captu
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
127 hat during transcriptional activation of the fission yeast fbp1 gene, binding of Rst2 (a critical C2H
129 d facultative heterochromatin islands in the fission yeast genome and found that RNA elimination mach
137 ith each other in vitro, and at least in the fission yeast, heterologous Oxs1 and Pap1-homologues can
142 d mitogen activated protein kinase (MAPK) in fission yeast, inhibits TORC2-dependent Gad8 phosphoryla
144 t early divergence from a common ancestor in fission yeast involved important changes in the mechanis
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
150 s effective in predicting the DNA content of fission yeast, it is likely to have a broad application
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
157 fork blockage at a site-specific barrier in fission yeast, leading to a restarted fork within approx
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
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
179 ing yeast profilin ScPFY fails to complement fission yeast profilin SpPRF temperature-sensitive mutan
183 As a model for cellular energy regulation, fission yeast provides an attractive and complementary s
185 parts list of genes important for meiosis in fission yeast, providing a valuable resource to advance
187 ed Mst2 histone acetyltransferase complex in fission yeast regulates histone turnover at heterochroma
191 viding a brief description of the origins of fission yeast research, and illustrating some genetic an
193 y, a superresolution microscopy study of the fission yeast ring revealed that myosins and formins tha
195 e a coarse-grained mathematical model of the fission yeast ring to explore essential consequences of
198 We examine the function of Swi1 and Swi3, fission yeast's primary FPC components, to elucidate how
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.
204 cts of turgor pressure on endocytosis in the fission yeast Schizosaccharomyces pombe by time-lapse im
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
213 e oxygen-responsive lipid homeostasis in the fission yeast Schizosaccharomyces pombe in a manner anal
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
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
233 In both mammalian PtK1 cells and in the fission yeast Schizosaccharomyces pombe, kinetochores sh
238 The single family member expressed in the fission yeast Schizosaccharomyces pombe, Zfs1, promotes
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
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
264 putative chromatin remodeling subunit of the fission yeast Snf2/histone deacetylase (HDAC) repressor
267 genic suppressors of a temperature-sensitive fission yeast strain mutated in the exocyst subunit Sec3
270 Therefore, knowledge from the budding and fission yeast systems illuminates highly conserved molec
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.
284 ools to track and count endocytic patches in fission yeast to increase the quality of the data extrac
286 and FPALM superresolution microscopy of live fission yeast to investigate the structures and assembly
290 Here, we report the crystal structure of the fission yeast Tpz1(475-508)-Poz1-Rap1(467-496) complex t
292 mic bundling is important for cytokinesis in fission yeast, we created the less dynamic bundling muta
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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