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

1 that found specifically in the fission yeast Schizosaccharomyces pombe.

2 l histone modifications in the fission yeast Schizosaccharomyces pombe.

3 east, including Saccharomyces cerevisiae and Schizosaccharomyces pombe.

4 ccharomyces cerevisiae and the fission yeast Schizosaccharomyces pombe.

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

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

7 of synchronous meiosis in the fission yeast Schizosaccharomyces pombe.

8 niscent of the distantly related ascomycete, Schizosaccharomyces pombe.

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

10 odel organism database for the fission yeast Schizosaccharomyces pombe.

11 wth characteristics of the unicellular yeast Schizosaccharomyces pombe.

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

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

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

15 sure successful completion of cytokinesis in Schizosaccharomyces pombe.

16 ntrinsic reproductive isolation in the yeast Schizosaccharomyces pombe.

17 f nucleosome positions in the fission yeast, Schizosaccharomyces pombe.

18 eplication origin sites in the fission yeast Schizosaccharomyces pombe.

19 ion between transcription and replication in Schizosaccharomyces pombe.

20 re required for heterochromatic silencing in Schizosaccharomyces pombe.

21 chromosome condensation in the fission yeast Schizosaccharomyces pombe.

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

23 ocess for proper actomyosin ring assembly in Schizosaccharomyces pombe.

24 ct repeat recombination in the fission yeast Schizosaccharomyces pombe.

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

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

27 rmentation with Saccharomyces cerevisiae and Schizosaccharomyces pombe.

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

29 ncluding osmotic stress in the fission yeast Schizosaccharomyces pombe.

30 or telomere maintenance in the fission yeast Schizosaccharomyces pombe.

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

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

33 Here we demonstrate that in Schizosaccharomyces pombe a DNA recognition protein, alk

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

35 In Schizosaccharomyces pombe, a Hippo-related signaling pat

36 In Schizosaccharomyces pombe, a late mitotic kinase pathway

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

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

39 In Schizosaccharomyces pombe, alcohol dehydrogenase 1 (Adh1

40 e and mouse, a tra1Delta mutant is viable in Schizosaccharomyces pombe, allowing us to test these iss

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

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

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

44 omplex Set1C purified from the fission yeast Schizosaccharomyces pombe and chromatin substrates that

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

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

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

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

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

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

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

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

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

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

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

56 y modulating proteins from Escherichia coli, Schizosaccharomyces pombe and Saccharomyces cerevisiae,

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

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

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

60 The fission yeast Schizosaccharomyces pombe and the filamentous fungus Neu

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

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

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

64 ESR, in the distantly related fission yeast, Schizosaccharomyces pombe, and in humans can explain gen

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

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

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

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

69 Here we introduce the fission yeast Schizosaccharomyces pombe as a model organism to elucida

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

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

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

73 Fission yeast Schizosaccharomyces pombe assembles actin into three dis

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

75 We show that Schizosaccharomyces pombe behaves similarly to metazoans

76 5FU interferes with Pot1 (Pot1pN protein of Schizosaccharomyces pombe) binding.

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

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

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

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

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

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

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

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

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

86 logue of the human RNA-binding protein La in Schizosaccharomyces pombe, causes irregularities in tRNA

87 Clp1/Flp1, the Schizosaccharomyces pombe Cdc14 orthologue, and Cdc14B,

88 Schizosaccharomyces pombe cdc15 homology (PCH) family me

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

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

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

92 We observe the dynamic behavior of Wee1 in Schizosaccharomyces pombe cells and manipulate its local

93 We show that in the absence of telomerase, Schizosaccharomyces pombe cells can survive telomere seq

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

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

96 Schizosaccharomyces pombe cells switch mating type by re

97 Living Schizosaccharomyces pombe cells were loaded in a microfl

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

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

100 We show here that the Schizosaccharomyces pombe CLASP, Cls1p, is a homodimer t

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

102 ifferent stress conditions in fission yeast, Schizosaccharomyces pombe, combining dynamic genome-wide

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

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

105 In contrast, Schizosaccharomyces pombe contains two essential tRNase

106 The DNA replication checkpoint in Schizosaccharomyces pombe contains two major protein kin

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 the fission yeast Schizosaccharomyces pombe, cytokinesis also involves a c

111 In Schizosaccharomyces pombe, cytokinesis requires the asse

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

113 Here, we report that deleting the Schizosaccharomyces pombe dcd1(+) dCMP deaminase gene (S

114 y and enzyme kinetics, we show that Trp43 of Schizosaccharomyces pombe Dcp2 is a conserved gatekeeper

115 In Schizosaccharomyces pombe, deletion of the ATPase vps4 l

116 Our Schizosaccharomyces pombe Deltapfh1 strain constitutes a

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

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

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

120 Schizosaccharomyces pombe displays a large transcription

121 In Schizosaccharomyces pombe, division plane positioning is

122 ular fungi like Saccharomyces cerevisiae and Schizosaccharomyces pombe do not harbor genes coding for

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

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

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

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

127 The fission yeast Schizosaccharomyces pombe encodes homologs of HMGR and I

128 sponding iron-binding position, with that of Schizosaccharomyces pombe Epe1, which plays an essential

129 The yeast Schizosaccharomyces pombe expresses a single TTP family

130 The Schizosaccharomyces pombe fission yeast Tup family corep

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

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

133 For example, in Schizosaccharomyces pombe, four septins localize to the

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

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

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

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

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 We report a systematic reappraisal of the Schizosaccharomyces pombe genome that ignores thresholds

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

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

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

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

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

146 In Schizosaccharomyces pombe, H3K9me deposition depends on

147 Schizosaccharomyces pombe harbors MTOCs at spindle pole

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

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

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

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

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

153 The Schizosaccharomyces pombe HDAC Clr6 (human HDAC1) binds

154 In Schizosaccharomyces pombe, heterochromatin assembly on t

155 In Schizosaccharomyces pombe, heterochromatin spread, which

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

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

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

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

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

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

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

163 dao gene encoding D-amino acid oxidase from Schizosaccharomyces pombe in tobacco (Nicotiana tabacum)

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

165 The transposon Tf1 of Schizosaccharomyces pombe integrates with a strong prefe

166 1, a long-terminal repeat retrotransposon in Schizosaccharomyces pombe, integrates into promoters wit

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

168 Here we show that the Mst2 complex in Schizosaccharomyces pombe is a highly specific H3 lysine

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

170 The fission yeast Schizosaccharomyces pombe is a rod-shaped cell that grow

171 Schizosaccharomyces pombe is an attractive organism to s

172 Schizosaccharomyces pombe is an important experimental s

173 Fission yeast Schizosaccharomyces pombe is an important genetic model

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

175 The fission yeast Schizosaccharomyces pombe is an important model organism

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

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

178 RNAi in Schizosaccharomyces pombe is critical for centromeric he

179 anscriptional induction in the fission yeast Schizosaccharomyces pombe is currently a limitation of t

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

181 hat site-specific replication termination in Schizosaccharomyces pombe is modulated by protein-mediat

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

183 A major role of the RNAi pathway in Schizosaccharomyces pombe is to nucleate heterochromatin

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

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

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

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

188 ased on tRNA-mediated suppression (TMS) in a Schizosaccharomyces pombe La protein (Sla1p) mutant.

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 We identified Schizosaccharomyces pombe mcb1(+) (Mcm-binding protein 1

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

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

198 During Schizosaccharomyces pombe meiotic prophase, homologous c

199 In the rod-shaped fission yeast Schizosaccharomyces pombe, microtubules regulate polariz

200 To understand their roles in fission yeast (Schizosaccharomyces pombe) mitochondria, we generated de

201 sis I and inhibiting merotelic attachment in Schizosaccharomyces pombe mitosis.

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

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

204 In Schizosaccharomyces pombe, Myosin Vs transport secretory

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

206 We implicate a Schizosaccharomyces pombe nuclear envelope-spanning link

207 We present the crystal structure of Schizosaccharomyces pombe Nup37 in complex with Nup120,

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

209 Rad3, the Schizosaccharomyces pombe ortholog of human ATR and Sacc

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

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

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

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

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

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

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

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

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

219 nally, we used SIFTER to annotate all of the Schizosaccharomyces pombe proteins with experimental fun

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

221 -1-1 checkpoint clamp (ortholog of human and Schizosaccharomyces pombe Rad9), the replication initiat

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

223 Cytokinesis in Schizosaccharomyces pombe requires the function of Cdc15

224 Preventing deSUMOylation in Schizosaccharomyces pombe results in slow growth and a s

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

226 In fission yeast (Schizosaccharomyces pombe), RNA interference (RNAi)-medi

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

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

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

230 The fission yeast clade--comprising Schizosaccharomyces pombe, S. octosporus, S. cryophilus,

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

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

233 Similarly, the Schizosaccharomyces pombe Seg1-like protein Sle1 was nec

234 The Schizosaccharomyces pombe septation initiation network (

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

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

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

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

239 Here, we report that in Schizosaccharomyces pombe splicing also enhances NMD, bu

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

241 Schizosaccharomyces pombe Sre1 is a membrane-bound trans

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

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

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

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

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

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

248 erevisiae and ~40-fold more CENP-A (Cnp1) in Schizosaccharomyces pombe than predicted.

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

250 We isolated C11 mutants from Schizosaccharomyces pombe that cause pol III to readthro

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

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

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

254 In Schizosaccharomyces pombe the Tf2 LTR retrotransposons a

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

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

257 In the fission yeast Schizosaccharomyces pombe, the cell integrity MAPK pathw

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

259 Schizosaccharomyces pombe, the fission yeast, cells alte

260 In Schizosaccharomyces pombe, the H3-K9 methyltransferase C

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

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

263 In Schizosaccharomyces pombe, the myo2-E1 mutation affects

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

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

266 In Schizosaccharomyces pombe, the RNAi pathway is required

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

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

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

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

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

272 biological information for the fission yeast Schizosaccharomyces pombe to effectively support both ex

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

274 We used Schizosaccharomyces pombe to investigate the role of sep

275 Saccharomyces cerevisiae) to hetero-octamer (Schizosaccharomyces pombe) to hetero-nonamer (Metazoa).

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

277 he Tetrahymena equivalent of mammalian TPP1, Schizosaccharomyces pombe Tpz1, and Oxytricha nova TEBPb

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

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

280 The Schizosaccharomyces pombe TUT Cid1 is a model enzyme tha

281 performed mRNA profiling for splicing in the Schizosaccharomyces pombe U2AF(59) (prp2.1) temperature-

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

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

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

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

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

287 sm of F-actin assembly during cytokinesis in Schizosaccharomyces pombe using lifeact as a probe to mo

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

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

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

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

292 Using the fission yeast Schizosaccharomyces pombe, we show that a proper force b

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

294 calnexin-independence factor 1 (Cif1), from Schizosaccharomyces pombe, which has been implicated in

295 In Schizosaccharomyces pombe, which has epigenetically defi

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 The Schizosaccharomyces pombe WISH/DIP/SPIN90 ortholog dip1p

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