ライフサイエンスコーパス: Schizosaccharomyces pombe

1 ho8 alkaline phosphatase from fission yeast (Schizosaccharomyces pombe).

2 which is an intact homodimeric ATM/Tel1 from Schizosaccharomyces pombe.

3 ocess for proper actomyosin ring assembly in Schizosaccharomyces pombe.

4 etween PM and endosomes in the fission yeast Schizosaccharomyces pombe.

5 ct repeat recombination in the fission yeast Schizosaccharomyces pombe.

6 myces cerevisiae and the homologue, Eso1, in Schizosaccharomyces pombe.

7 scription factor, Sak1, in the fission yeast Schizosaccharomyces pombe.

8 n, genome-wide map of nucleosome turnover in Schizosaccharomyces pombe.

9 ncluding osmotic stress in the fission yeast Schizosaccharomyces pombe.

10 or telomere maintenance in the fission yeast Schizosaccharomyces pombe.

11 during histidine starvation in fission yeast Schizosaccharomyces pombe.

12 that found specifically in the fission yeast Schizosaccharomyces pombe.

13 l histone modifications in the fission yeast Schizosaccharomyces pombe.

14 east, including Saccharomyces cerevisiae and Schizosaccharomyces pombe.

15 ccharomyces cerevisiae and the fission yeast Schizosaccharomyces pombe.

16 ent of Set1C and H3K4me in the fission yeast Schizosaccharomyces pombe.

17 e played by ncRNAs in the stress response of Schizosaccharomyces pombe.

18 of synchronous meiosis in the fission yeast Schizosaccharomyces pombe.

19 niscent of the distantly related ascomycete, Schizosaccharomyces pombe.

20 Rhp26, which is the homolog of CSB/ERCC6 in Schizosaccharomyces pombe.

21 odel organism database for the fission yeast Schizosaccharomyces pombe.

22 wth characteristics of the unicellular yeast Schizosaccharomyces pombe.

23 ne Na(+)/H(+) exchanger of the fission yeast Schizosaccharomyces pombe.

24 t branch of homologous recombination (HR) in Schizosaccharomyces pombe.

25 one example being Cpc2p in the fission yeast Schizosaccharomyces pombe.

26 sure successful completion of cytokinesis in Schizosaccharomyces pombe.

27 row during cytokinesis of the fission yeast, Schizosaccharomyces pombe.

28 come from in vivo analysis in fission yeast Schizosaccharomyces pombe.

29 sculus and (ii) Saccharomyces cerevisiae and Schizosaccharomyces pombe.

30 phenomenon can occur in the sister species, Schizosaccharomyces pombe.

31 relationship between Spt6 and Set2 exists in Schizosaccharomyces pombe.

32 ntrinsic reproductive isolation in the yeast Schizosaccharomyces pombe.

33 chromosome condensation in the fission yeast Schizosaccharomyces pombe.

34 rmentation with Saccharomyces cerevisiae and Schizosaccharomyces pombe.

35 pic approaches to dissect their interplay in Schizosaccharomyces pombe.

36 elomeres 1) and Taz1 (telomere-associated in Schizosaccharomyces pombe 1) in vivo.

37 Here we report that in Schizosaccharomyces pombe a conserved DDB1-CUL4-associat

38 Here, using the fission yeast Schizosaccharomyces pombe (a classical model for closed

39 In the fission yeast Schizosaccharomyces pombe, a cortical gradient of pom1p

40 In Schizosaccharomyces pombe, a Hippo-related signaling pat

41 In Schizosaccharomyces pombe, a late mitotic kinase pathway

42 , little is known about replicative aging in Schizosaccharomyces pombe, a rod-shaped yeast that divid

43 In the fission yeast Schizosaccharomyces pombe, active Cdc42 and associated e

44 In Schizosaccharomyces pombe, alcohol dehydrogenase 1 (Adh1

45 is, Lachancea kluyveri, Lachancea waltii and Schizosaccharomyces pombe-also conform to these predicti

46 comprehensive profile of splicing events in Schizosaccharomyces pombe, amongst the simplest organism

47 Here, we describe the mobility of eight Schizosaccharomyces pombe AMR proteins at different stag

48 Schizosaccharomyces pombe, an organism containing numero

49 d its application to the unicellular fungus, Schizosaccharomyces pombe, an organism that shares many

50 from Homo sapiens, Drosophila melanogaster, Schizosaccharomyces pombe and Dictyostelium discoideum f

51 activities of two Dnmt2 homologs, Pmt1 from Schizosaccharomyces pombe and DnmA from Dictyostelium di

52 ere, we report the crystal structures of the Schizosaccharomyces pombe and Drosophila melanogaster CE

53 d in human cell lines, Arabidopsis thaliana, Schizosaccharomyces pombe and Escherichia coli and how i

54 RPS23 hydroxylases in S. cerevisiae (Tpa1p), Schizosaccharomyces pombe and green algae catalyze an un

55 broadly conserved between the fission yeast Schizosaccharomyces pombe and humans.

56 tance, and similar observations were made in Schizosaccharomyces pombe and in a mammalian cell line.

57 ents of a suppressor tRNA system specific to Schizosaccharomyces pombe and its adaptations for use to

58 As shown here when tested in Schizosaccharomyces pombe and mammalian HEK293T cells, t

59 Based on functional studies on the Schizosaccharomyces pombe and Neurospora crassa Nbp2p or

60 ions of retrotransposon Tf1 in the genome of Schizosaccharomyces pombe and obtained the first profile

61 two recently diverged fission yeast species Schizosaccharomyces pombe and S. kambucha, which mate to

62 the TATA element, transcription in the yeast Schizosaccharomyces pombe and Saccharomyces cerevisiae t

63 f RNA polymerase active sites genome-wide in Schizosaccharomyces pombe and Saccharomyces cerevisiae.

64 trategies between the related fission yeasts Schizosaccharomyces pombe and Schizosaccharomyces japoni

65 division site positioning in fission yeasts Schizosaccharomyces pombe and Schizosaccharomyces japoni

66 mental question using related fission yeasts Schizosaccharomyces pombe and Schizosaccharomyces japoni

67 bstrate for thioredoxin in the fission yeast Schizosaccharomyces pombe and, as such, competitively in

68 c shift in gene expression in fission yeast (Schizosaccharomyces pombe), and this response is driven

69 es of nucleosome occupancy in S. cerevisiae, Schizosaccharomyces pombe, and human cells.

70 genomic data from Saccharomyces cerevisiae, Schizosaccharomyces pombe, and Lachancea kluyveri, we ex

71 to two yeasts, Saccharomyces cerevisiae and Schizosaccharomyces pombe, and one filamentous fungus, N

72 anslation rates in Saccharomyces cerevisiae, Schizosaccharomyces pombe, Arabidopsis thaliana, Mus mus

73 Fission yeast Schizosaccharomyces pombe are rod-shaped cells that grow

74 The fission yeast Schizosaccharomyces pombe are rod-shaped cells that grow

75 om resolution cryo-EM structure of activated Schizosaccharomyces pombe Arp2/3 complex bound to the S.

76 In this study, we used Schizosaccharomyces pombe as a model to analyse mutants

77 Here we use the fission yeast Schizosaccharomyces pombe as a model to investigate UPD,

78 Using Schizosaccharomyces pombe as a model we show that the Ra

79 Alkyltransferase-like (ATL) proteins in Schizosaccharomyces pombe (Atl1) and Thermus thermophilu

80 We show that Schizosaccharomyces pombe behaves similarly to metazoans

81 5FU interferes with Pot1 (Pot1pN protein of Schizosaccharomyces pombe) binding.

82 ed pre-mRNAs in an intron-specific manner in Schizosaccharomyces pombe Both fission yeast and human S

83 jump in yeast and the Tf1 retrotransposon of Schizosaccharomyces pombe, both of which prefer nucleoso

84 posttranslational modification in eEF1A from Schizosaccharomyces pombe but not in various other eukar

85 dida albicans, Saccharomyces cerevisiae, and Schizosaccharomyces pombe, but not zymosan preparations

86 ct in a ded1 temperature-sensitive strain of Schizosaccharomyces pombe, but the cancer-associated mut

87 ith the Mre11-Rad50-Nbs1 nuclease complex in Schizosaccharomyces pombe, but the mechanism by which Ct

88 etic calcium transients in the fission yeast Schizosaccharomyces pombe by adopting GCaMP, a genetical

89 s activation of the DNA damage checkpoint in Schizosaccharomyces pombe by physically coupling the Rad

90 heptapeptide repeat of the CTD of RNAP II in Schizosaccharomyces pombe by substituting non-phosphoryl

91 pressure on endocytosis in the fission yeast Schizosaccharomyces pombe by time-lapse imaging of indiv

92 s the 12 species in MitoMiner (now including Schizosaccharomyces pombe) by homology mapping.

93 t mRNA deadenylation by purified recombinant Schizosaccharomyces pombe CCR4/NOT complexes, although t

94 Schizosaccharomyces pombe cdc15 homology (PCH) family me

95 omain of the essential cytokinetic scaffold, Schizosaccharomyces pombe Cdc15, during cytokinesis.

96 f the N-terminal homo-dimerization domain of Schizosaccharomyces pombe Cdc23 (Cdc23(Nterm)).

97 n to a set of time-course experiments on the Schizosaccharomyces pombe cell-cycle gene expression.

98 we show that upon quiescence establishment, Schizosaccharomyces pombe cells drastically rearrange bo

99 In this study, we report that Schizosaccharomyces pombe cells lacking efr3, which enco

100 In rod-shaped fission yeast Schizosaccharomyces pombe cells, division at midcell is

101 For example, rod-shaped fission yeast Schizosaccharomyces pombe cells, which divide at a fixed

102 MD), is essential for spindle disassembly in Schizosaccharomyces pombe cells.

103 cent findings show that in the fission yeast Schizosaccharomyces pombe, cleavage furrow ingression is

104 r model organism; however, the fission yeast Schizosaccharomyces pombe community currently lacks prot

105 In the fission yeast Schizosaccharomyces pombe, conserved protein complexes e

106 In contrast, Schizosaccharomyces pombe contains two essential tRNase

107 ermine the nanoscale spatial organization of Schizosaccharomyces pombe contractile ring components re

108 In Schizosaccharomyces pombe, copper is transported by thre

109 ta from 116 transcriptomes in fission yeast (Schizosaccharomyces pombe), covering multiple physiologi

110 In Schizosaccharomyces pombe, cytokinesis requires the asse

111 During mitosis in fission yeast Schizosaccharomyces pombe, cytoplasmic microtubule nucle

112 In Schizosaccharomyces pombe, deletion of the ATPase vps4 l

113 Our Schizosaccharomyces pombe Deltapfh1 strain constitutes a

114 c chromosome movements in the fission yeast, Schizosaccharomyces pombe, depend on astral microtubule

115 complementation group M (FANCM)-ortholog of Schizosaccharomyces pombe, directs the formation of NCOs

116 rmline mutations in DIS3L2, a homolog of the Schizosaccharomyces pombe dis3 gene, in individuals with

117 Schizosaccharomyces pombe displays a large transcription

118 In Schizosaccharomyces pombe, division plane positioning is

119 epair and Tel1 (ATM) checkpoint signaling in Schizosaccharomyces pombe, double-strand break resection

120 stand the morphogenesis of the fission yeast Schizosaccharomyces pombe drove us to investigate cellul

121 In the fission yeast Schizosaccharomyces pombe, dynamic cytoplasmic MT bundle

122 Here we show that, in the fission yeast Schizosaccharomyces pombe, ectopically induced domains o

123 Like humans, Schizosaccharomyces pombe encodes a single Pif1 family D

124 microbial cellular discrimination assay for Schizosaccharomyces pombe, Escherichia coli and Staphylo

125 re has also successfully processed data from Schizosaccharomyces pombe, Escherichia coli, and Zymomon

126 Upon nitrogen starvation, Schizosaccharomyces pombe exit the mitotic cell cycle an

127 The yeast Schizosaccharomyces pombe expresses a single TTP family

128 The Schizosaccharomyces pombe fission yeast Tup family corep

129 Pho7 is the Schizosaccharomyces pombe fission yeast Zn(2)Cys(6) tran

130 /cell type has been demonstrated only in the Schizosaccharomyces pombe fission yeast.

131 rs in Smc5/6 hypomorphs in the fission yeast Schizosaccharomyces pombe following genotoxic and replic

132 Previously we established assays in Schizosaccharomyces pombe for studying recombination ind

133 calization and silencing when transformed in Schizosaccharomyces pombe Furthermore, multiple copies o

134 Using a non-essential Schizosaccharomyces pombe gene deletion collection, we i

135 d its loader complex, Mis4(Scc2)-Ssl3(Scc4) (Schizosaccharomyces pombe gene names appear throughout w

136 mere repeat and the promoter regions of many Schizosaccharomyces pombe genes, including all of those

137 In fission yeast (Schizosaccharomyces pombe), genetic screens have previou

138 Yeast cells (Saccharomyces cerevisiae and Schizosaccharomyces pombe) genetically depleted of La gr

139 Their introduction into the Schizosaccharomyces pombe genome results in cell death o

140 egration events within silent regions of the Schizosaccharomyces pombe genome, we focused on performi

141 Through transcriptome profiling of the Schizosaccharomyces pombe genome, we identified a natura

142 lore the high-resolution organization of the Schizosaccharomyces pombe genome, which despite its smal

143 matin, and origins of replication within the Schizosaccharomyces pombe genome.

144 copper is essential for spore germination in Schizosaccharomyces pombe Germinating spores develop a s

145 In Schizosaccharomyces pombe, H3K9me deposition depends on

146 In the fission yeast Schizosaccharomyces pombe, H3K9me heterochromatin can be

147 ng the tested transporters, the Mae1(p) from Schizosaccharomyces pombe had the highest activity towar

148 Schizosaccharomyces pombe harbors MTOCs at spindle pole

149 genome editing system in the model organism Schizosaccharomyces pombe has been hampered by the lack

150 es in the 1940s and 1950s, the fission yeast Schizosaccharomyces pombe has grown to become one of the

151 The fission yeast Schizosaccharomyces pombe has six Rho GTPases (Cdc42 and

152 lp14, a XMAP215 orthologue in fission yeast, Schizosaccharomyces pombe, has properties of a MT polyme

153 Studies in fission yeast Schizosaccharomyces pombe have provided the basis for th

154 The Schizosaccharomyces pombe HDAC Clr6 (human HDAC1) binds

155 velop a strategy for the isolation of native Schizosaccharomyces pombe heterochromatin and euchromati

156 In Schizosaccharomyces pombe, heterochromatin assembly on t

157 In the fission yeast Schizosaccharomyces pombe, heterochromatin formation inv

158 In Schizosaccharomyces pombe, heterochromatin spread, which

159 CLEAR AUTOANTIGENIC SPERM PROTEIN (NASP) and Schizosaccharomyces pombe histone chaperone Sim3 is a so

160 The fission yeast Schizosaccharomyces pombe homologs of mammalian CENP-B p

161 Here, using Clr4, the fission yeast Schizosaccharomyces pombe homologue of mammalian SUV39H

162 Mal3p and Tip1p are the fission yeast (Schizosaccharomyces pombe) homologues of EB1 and CLIP-17

163 uring AMR formation has been well studied in Schizosaccharomyces pombe; however, the corresponding ef

164 Here, we use the two Schizosaccharomyces pombe HP1 paralogs, Swi6 and Chp2, a

165 ere we show that chromatin compaction by the Schizosaccharomyces pombe HP1 protein Swi6 results in ph

166 Est1 exists in multiple organisms, including Schizosaccharomyces pombe, humans, and Saccharomyces cer

167 In Schizosaccharomyces pombe, important membrane-CR scaffol

168 nsive lipid homeostasis in the fission yeast Schizosaccharomyces pombe in a manner analogous to the m

169 al structures of the tRNA MTase spTrm10 from Schizosaccharomyces pombe in the presence and absence of

170 ing formation has been well characterized in Schizosaccharomyces pombe, in which the cross-linking pr

171 at mediate epigenetic inheritance, we used a Schizosaccharomyces pombe inducible heterochromatin form

172 1, a long-terminal repeat retrotransposon in Schizosaccharomyces pombe, integrates into promoters wit

173 In fission yeast, Schizosaccharomyces pombe, interactions between the shel

174 determinants of aging, and the fission yeast Schizosaccharomyces pombe is a promising new system for

175 Schizosaccharomyces pombe is an attractive organism to s

176 Schizosaccharomyces pombe is an important experimental s

177 The fission yeast Schizosaccharomyces pombe is an important model for euka

178 The fission yeast Schizosaccharomyces pombe is an important model organism

179 Heterochromatin in the fission yeast Schizosaccharomyces pombe is clustered at the nuclear pe

180 showed that drug tolerance in fission yeast Schizosaccharomyces pombe is controlled by lncRNA transc

181 RNAi in Schizosaccharomyces pombe is critical for centromeric he

182 The Ctp1 protein in Schizosaccharomyces pombe is essential for DNA double-st

183 intermediates, we show that circular RNA in Schizosaccharomyces pombe is generated through an exon-c

184 evidence that cell size in the fission yeast Schizosaccharomyces pombe is regulated by a third strate

185 d26 in Saccharomyces cerevisiae and Rhp26 in Schizosaccharomyces pombe) is among the first proteins t

186 Cut7, the sole kinesin-5 in Schizosaccharomyces pombe, is essential for mitosis.

187 In the fission yeast Schizosaccharomyces pombe, it is well established that m

188 ammalian PtK1 cells and in the fission yeast Schizosaccharomyces pombe, kinetochores shortened after

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

192 We found that the fission yeast Schizosaccharomyces pombe lacks both a Hac1/XBP1 ortholo

193 In Schizosaccharomyces pombe, late mitotic events are coord

194 Heterologous expression in Schizosaccharomyces pombe, LC-MS analyses, and kinetic s

195 Here, using the crystal structure of Schizosaccharomyces pombe MCC (a complex of mitotic spin

196 A resolution cryo-electron microscopy map of Schizosaccharomyces pombe Mediator in which conserved Me

197 During Schizosaccharomyces pombe meiotic prophase, homologous c

198 canonical architecture and mechanochemistry, Schizosaccharomyces pombe microtubules were stabilized b

199 In fission yeast (Schizosaccharomyces pombe), mitochondria are organized a

200 In the fission yeast Schizosaccharomyces pombe, mitotic entry is orchestrated

201 ion, we performed an unbiased screen to seek Schizosaccharomyces pombe mutants with reduced PM Ras.

202 y we established an assay for studying TS in Schizosaccharomyces pombe (Nguyen et al., 2015).

203 ition of Arp2/3 complex in the fission yeast Schizosaccharomyces pombe not only depletes Arp2/3-compl

204 We implicate a Schizosaccharomyces pombe nuclear envelope-spanning link

205 ring functions of the evolutionarily distant Schizosaccharomyces pombe Num1 homologue.

206 orthologs Pck1 and Pck2 in the fission yeast Schizosaccharomyces pombe operate in a redundant fashion

207 Here we show that the Schizosaccharomyces pombe ortholog of Nrd1, Seb1, does n

208 important for meiosis in the fission yeast, Schizosaccharomyces pombe Our genome-wide functional scr

209 Fission yeast Schizosaccharomyces pombe P and M cells, which respectiv

210 WH domain mutation or deletion in Schizosaccharomyces pombe phenocopies the DNA-damage sen

211 The Loz1 transcription factor from Schizosaccharomyces pombe plays an essential role in zin

212 his screen with the DNA-binding subdomain of Schizosaccharomyces pombe Pot1 (Pot1pN), which confers t

213 ain analysis of the evolutionarily conserved Schizosaccharomyces pombe pre-mRNA-processing factor, Sp

214 m inference of networks in the budding yeast Schizosaccharomyces pombe predicts a novel role in cell

215 In the fission yeast Schizosaccharomyces pombe proteins that contribute to th

216 Two new studies using Schizosaccharomyces pombe provide insight into how compa

217 epistasis map (E-MAP) for the fission yeast Schizosaccharomyces pombe, providing phenotypic signatur

218 -1-1 checkpoint clamp (ortholog of human and Schizosaccharomyces pombe Rad9), the replication initiat

219 nding proteins (SREBPs) in the fission yeast Schizosaccharomyces pombe regulate lipid homeostasis and

220 One of these shuttle factors, Schizosaccharomyces pombe Rhp23, has an unusual domain a

221 r quiescence (G0 phase of the cell cycle) in Schizosaccharomyces pombe RNAi mutants lose viability at

222 Here we show that, in the fission yeast Schizosaccharomyces pombe, RNAi and heterochromatin fact

223 In Schizosaccharomyces pombe rod-shaped cells, Pom1 kinase

224 a genome-wide map of nucleosomes in vivo in Schizosaccharomyces pombe (S. pombe) at base pair resolu

225 tion, but not sequence, is conserved between Schizosaccharomyces pombe, S. octosporus and S. cryophil

226 ustrial strains of Saccharomyces cerevisiae, Schizosaccharomyces pombe, Saccharomyces boulardii, Sacc

227 n in three distantly related fission yeasts: Schizosaccharomyces pombe, Schizosaccharomyces octosporu

228 The Schizosaccharomyces pombe septation initiation network (

229 biochemical studies on the Sen1 homolog from Schizosaccharomyces pombe showed that it can bind and un

230 The Schizosaccharomyces pombe shu1(+) gene encodes a cell-su

231 xpression of the fungal Hsp104 homologs from Schizosaccharomyces pombe (Sp-Hsp104) or Candida albican

232 smic duplication cycle and regulation of the Schizosaccharomyces pombe SPB is analogous to centrosome

233 in structure, and histone modifications in a Schizosaccharomyces pombe spt6 mutant.

234 Schizosaccharomyces pombe Sre1 is a membrane-bound trans

235 We previously developed Schizosaccharomyces pombe strains that report on two pol

236 to varying degrees the growth defects of the Schizosaccharomyces pombe STUbL mutant rfp1/rfp2, and th

237 In the rod-shaped fission yeast Schizosaccharomyces pombe, symmetric division is achieve

238 We then analyzed N. crassa and Schizosaccharomyces pombe telomerase reconstituted in vi

239 The 3' end of Schizosaccharomyces pombe telomerase RNA (SpTER1) is gen

240 We report that the Schizosaccharomyces pombe telomerase RNA, TER1 (telomera

241 MtgA is the ortholog of the Schizosaccharomyces pombe telomere-anchoring inner nucle

242 ignificantly less toxic to the fission yeast Schizosaccharomyces pombe than unstimulated OSPW.

243 bed a mutant, pat1-as2, of the fission yeast Schizosaccharomyces pombe that undergoes synchronous mei

244 The wtf4 gene is a meiotic driver in Schizosaccharomyces pombe that uses a poison-antidote me

245 we find in Schizosaccharomyces japonicus and Schizosaccharomyces pombe that, during actomyosin ring c

246 In the fission yeast Schizosaccharomyces pombe the activation of the G2/M CDK

247 In Schizosaccharomyces pombe the Tf2 LTR retrotransposons a

248 In fission yeast (Schizosaccharomyces pombe), the E3 ubiquitin ligase Dma1

249 In the fission yeast Schizosaccharomyces pombe, the CaMKK-like protein kinase

250 In the fission yeast Schizosaccharomyces pombe, the centromeres of each chrom

251 In Schizosaccharomyces pombe, the CR forms mid-cell during

252 In Schizosaccharomyces pombe, the expression of the zrt1 zi

253 In the fission yeast Schizosaccharomyces pombe, the formin For3 nucleates act

254 In Schizosaccharomyces pombe, the H3-K9 methyltransferase C

255 In the yeast Schizosaccharomyces pombe, the mitochondria are pushed t

256 In the fission yeast Schizosaccharomyces pombe, the multi-BRCT domain protein

257 In Schizosaccharomyces pombe, the myo2-E1 mutation affects

258 In the fission yeast Schizosaccharomyces pombe, the protein kinase Cdr1 is a

259 In the fission yeast Schizosaccharomyces pombe, the proteins Mto1 and Mto2 fo

260 In the fission yeast Schizosaccharomyces pombe, the SREBP-2 homolog Sre1 regu

261 sly shown that in the symmetrically dividing Schizosaccharomyces pombe there is a transition between

262 We examined the function of i6A37 in Schizosaccharomyces pombe tit1+ and tit1-Delta cells by

263 ia coli MiaA, Saccharomyces cerevisiae Mod5, Schizosaccharomyces pombe Tit1, and Caenorhabditis elega

264 /3 complex is activated at cortical sites in Schizosaccharomyces pombe to assemble branched actin net

265 dynamic cellular environments, here, we use Schizosaccharomyces pombe to characterize, both experime

266 ochromatin, conserved from the fission yeast Schizosaccharomyces pombe to humans, is its ability to s

267 Here, we utilize the fission yeast Schizosaccharomyces pombe to investigate how lncRNAs eng

268 t regulation of sterol response genes (Ofd1, Schizosaccharomyces pombe) to translation termination/mR

269 In the fission yeast Schizosaccharomyces pombe, TORC1 is essential for vegeta

270 architecture of microtubules assembled from Schizosaccharomyces pombe tubulin, in the presence and a

271 activation at high H(2)O(2), showing that in Schizosaccharomyces pombe turning off peroxide defenses

272 The Schizosaccharomyces pombe TUT Cid1 is a model enzyme tha

273 In Schizosaccharomyces pombe, two SAD kinases (Cdr1/Nim1 an

274 Here, we describe the structures of Schizosaccharomyces pombe Ub E1 in these two states, cap

275 Here, we present a structure of Schizosaccharomyces pombe Uba1 in which the second catal

276 ed ribosome profiling with the fission yeast Schizosaccharomyces pombe under conditions of exponentia

277 kinase of the DNA replication checkpoint in Schizosaccharomyces pombe Under replication stress, it i

278 The fission yeast Schizosaccharomyces pombe undergoes "closed" mitosis in

279 from Saccharomyces cerevisiae and Pfh1 from Schizosaccharomyces pombe, unwind double-stranded DNA by

280 A splicing using the intron-rich model yeast Schizosaccharomyces pombe Using epistatic miniarray prof

281 alyzed the consequences of Spt5 depletion in Schizosaccharomyces pombe using four genome-wide approac

282 resolution survey of genome interactions in Schizosaccharomyces pombe using synchronized cells to in

283 found transposable element (TE) mobility in Schizosaccharomyces pombe was greatly increased when cel

284 Until now, Schizosaccharomyces pombe was known to use reductive iro

285 la melanogaster, Caenorhabditis elegans, and Schizosaccharomyces pombe was significantly less efficac

286 Here, motivated by work in fission yeast (Schizosaccharomyces pombe), we generated a fluorescent m

287 tigate these features for the fission yeast, Schizosaccharomyces pombe, we developed an integrative m

288 on properties of SpPot1, the POT1 homolog in Schizosaccharomyces pombe, we found an unanticipated ssD

289 Through genetic analyses in Schizosaccharomyces pombe, we found that myo2-S1 (myo2-G

290 In Schizosaccharomyces pombe, we found that the iss1(+) gen

291 Using Schizosaccharomyces pombe, we show that the distance bet

292 Here, in fission yeast Schizosaccharomyces pombe, we successfully implemented t

293 hway for diamide-induced disulfide stress in Schizosaccharomyces pombe, where the nucleocytoplasmic H

294 ample of sizer behavior is in fission yeast, Schizosaccharomyces pombe, which enters mitosis at a min

295 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

298 Although human mtSSBs and those from Schizosaccharomyces pombe, Xenopus laevis, and Xenopus t

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