ライフサイエンスコーパス: Schizosaccharomyces

1 cystis species with Taphrina, Saitoella, and Schizosaccharomyces, and divergence within Pneumocystis

2 e of centromere-binding protein-B (CENPB) in Schizosaccharomyces, as well as in metazoans.

3 erved, Tas3 is lost and Chp1 is truncated in Schizosaccharomyces cryophilus and Schizosaccharomyces o

4 hree additional Schizosaccharomyces species (Schizosaccharomyces cryophilus, Schizosaccharomyces japo

5 fission yeasts Schizosaccharomyces pombe and Schizosaccharomyces japonicus [1-3].

6 ces species (Schizosaccharomyces cryophilus, Schizosaccharomyces japonicus and Schizosaccharomyces oc

7 Here we find in Schizosaccharomyces japonicus and Schizosaccharomyces po

8 dy, we have determined crystal structures of Schizosaccharomyces japonicus Mis16 alone and in complex

9 ut with loss of transposase function (except Schizosaccharomyces japonicus).

10 In Schizosaccharomyces japonicus, the conserved LEM-domain

11 on the cytokinetic ring in the fission yeast Schizosaccharomyces japonicus, unlike its role in S. pom

12 fission yeasts Schizosaccharomyces pombe and Schizosaccharomyces japonicus.

13 es pombe, Schizosaccharomyces octosporus and Schizosaccharomyces japonicus.

14 genes on chromosome 3 of the fission yeasts Schizosaccharomyces kambucha and S. pombe.

15 ication of an ancestral anillin early in the Schizosaccharomyces lineage may have led to subfunctiona

16 d fission yeasts: Schizosaccharomyces pombe, Schizosaccharomyces octosporus and Schizosaccharomyces j

17 ncated in Schizosaccharomyces cryophilus and Schizosaccharomyces octosporus We show that truncated Ch

18 ryophilus, Schizosaccharomyces japonicus and Schizosaccharomyces octosporus).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

40 The fission yeast Schizosaccharomyces pombe and the filamentous fungus Neu

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

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

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

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

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

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

47 Fission yeast Schizosaccharomyces pombe assembles actin into three dis

48 We show that Schizosaccharomyces pombe behaves similarly to metazoans

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

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

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

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

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

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

55 Schizosaccharomyces pombe cdc15 homology (PCH) family me

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

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

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

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

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

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

62 Living Schizosaccharomyces pombe cells were loaded in a microfl

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

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

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

66 In contrast, Schizosaccharomyces pombe contains two essential tRNase

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

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

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

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

71 Our Schizosaccharomyces pombe Deltapfh1 strain constitutes a

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

73 Schizosaccharomyces pombe displays a large transcription

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

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

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

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

78 The yeast Schizosaccharomyces pombe expresses a single TTP family

79 The Schizosaccharomyces pombe fission yeast Tup family corep

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

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

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

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

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

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

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

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

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

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

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

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

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

93 Schizosaccharomyces pombe harbors MTOCs at spindle pole

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

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

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

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

98 The Schizosaccharomyces pombe HDAC Clr6 (human HDAC1) binds

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

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

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

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

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

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

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

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

107 Schizosaccharomyces pombe is an attractive organism to s

108 Schizosaccharomyces pombe is an important experimental s

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

110 The fission yeast Schizosaccharomyces pombe is an important model organism

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

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

113 RNAi in Schizosaccharomyces pombe is critical for centromeric he

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

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

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

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

118 ro FRET-based assays, we show that human and Schizosaccharomyces pombe La proteins harbor RNA chapero

119 could complement the distantly related yeast Schizosaccharomyces pombe lacking its endogenous Dicer g

120 performed metabolic profiling on a strain of Schizosaccharomyces pombe lacking the zinc-responsive tr

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

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

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

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

125 During Schizosaccharomyces pombe meiotic prophase, homologous c

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

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

128 We implicate a Schizosaccharomyces pombe nuclear envelope-spanning link

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

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

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

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

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

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

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

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

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

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

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

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

141 -1-1 checkpoint clamp (ortholog of human and Schizosaccharomyces pombe Rad9), the replication initiat

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

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

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

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

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

147 The Schizosaccharomyces pombe septation initiation network (

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

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

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

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

152 Schizosaccharomyces pombe Sre1 is a membrane-bound trans

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

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

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

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

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

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

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

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

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

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

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

164 In Schizosaccharomyces pombe the Tf2 LTR retrotransposons a

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

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

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

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

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

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

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

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

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

174 The Schizosaccharomyces pombe TUT Cid1 is a model enzyme tha

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

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

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

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

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

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

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

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

183 The Schizosaccharomyces pombe WISH/DIP/SPIN90 ortholog dip1p

184 5FU interferes with Pot1 (Pot1pN protein of Schizosaccharomyces pombe) binding.

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

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

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

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

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

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

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

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

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

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

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

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

197 In Schizosaccharomyces pombe, a Hippo-related signaling pat

198 In Schizosaccharomyces pombe, a late mitotic kinase pathway

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

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

201 In Schizosaccharomyces pombe, alcohol dehydrogenase 1 (Adh1

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

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

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

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

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

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

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

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

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

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

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

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

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

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

216 In Schizosaccharomyces pombe, copper is transported by thre

217 In the fission yeast Schizosaccharomyces pombe, cytokinesis also involves a c

218 In Schizosaccharomyces pombe, cytokinesis requires the asse

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

220 In Schizosaccharomyces pombe, deletion of the ATPase vps4 l

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

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

223 In Schizosaccharomyces pombe, division plane positioning is

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

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

226 In Schizosaccharomyces pombe, H3K9me deposition depends on

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

228 In Schizosaccharomyces pombe, heterochromatin assembly on t

229 In Schizosaccharomyces pombe, heterochromatin spread, which

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

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

232 1, a long-terminal repeat retrotransposon in Schizosaccharomyces pombe, integrates into promoters wit

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

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

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

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

237 In Schizosaccharomyces pombe, late mitotic events are coord

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

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

240 In Schizosaccharomyces pombe, Myosin Vs transport secretory

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

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

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

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

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

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

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

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

249 Schizosaccharomyces pombe, the fission yeast, cells alte

250 In Schizosaccharomyces pombe, the H3-K9 methyltransferase C

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

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

253 In Schizosaccharomyces pombe, the myo2-E1 mutation affects

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

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

256 In Schizosaccharomyces pombe, the RNAi pathway is required

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

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

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

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

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

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

263 In Schizosaccharomyces pombe, which has epigenetically defi

264 itotic and meiotic chromosome segregation in Schizosaccharomyces pombe, which has more than one kinet

265 ) and a modified version of TyrRS, AzFRS, in Schizosaccharomyces pombe, which is an attractive model

266 family member expressed in the fission yeast Schizosaccharomyces pombe, Zfs1, promotes the turnover o

267 ism, whereas the single protein expressed in Schizosaccharomyces pombe, Zfs1, regulates cell-cell int

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

269 ncluding osmotic stress in the fission yeast Schizosaccharomyces pombe.

270 or telomere maintenance in the fission yeast Schizosaccharomyces pombe.

271 that found specifically in the fission yeast Schizosaccharomyces pombe.

272 l histone modifications in the fission yeast Schizosaccharomyces pombe.

273 east, including Saccharomyces cerevisiae and Schizosaccharomyces pombe.

274 ccharomyces cerevisiae and the fission yeast Schizosaccharomyces pombe.

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

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

277 of synchronous meiosis in the fission yeast Schizosaccharomyces pombe.

278 niscent of the distantly related ascomycete, Schizosaccharomyces pombe.

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

280 odel organism database for the fission yeast Schizosaccharomyces pombe.

281 wth characteristics of the unicellular yeast Schizosaccharomyces pombe.

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

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

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

285 sure successful completion of cytokinesis in Schizosaccharomyces pombe.

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

287 eplication origin sites in the fission yeast Schizosaccharomyces pombe.

288 ion between transcription and replication in Schizosaccharomyces pombe.

289 ntrinsic reproductive isolation in the yeast Schizosaccharomyces pombe.

290 chromosome condensation in the fission yeast Schizosaccharomyces pombe.

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

292 ocess for proper actomyosin ring assembly in Schizosaccharomyces pombe.

293 ct repeat recombination in the fission yeast Schizosaccharomyces pombe.

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

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

296 rmentation with Saccharomyces cerevisiae and Schizosaccharomyces pombe.

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

298 ata sets and the genomes of three additional Schizosaccharomyces species (Schizosaccharomyces cryophi

299 c1/mariner and Tc5 transposons, occur in all Schizosaccharomyces species, as well as in humans, but w

300 s changed essential residues conserved among Schizosaccharomyces species.