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 , despite the lack of sequence conservation, Schizosaccharomyces centromere DNA possesses intrinsic c

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

5 hree additional Schizosaccharomyces species (Schizosaccharomyces cryophilus, Schizosaccharomyces japo

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

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

8 Here we find in Schizosaccharomyces japonicus and Schizosaccharomyces po

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

10 with scaling in the rod-shaped fission yeast Schizosaccharomyces japonicus that relies on cellular ge

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

12 y such mechanisms, we studied NE assembly in Schizosaccharomyces japonicus, a fission yeast that unde

13 Schizosaccharomyces japonicus, a member of the fission y

14 assembly and integrity in its close relative Schizosaccharomyces japonicus, revealing a remarkable ev

15 In Schizosaccharomyces japonicus, the conserved LEM-domain

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

17 undamental questions using the fission yeast Schizosaccharomyces japonicus, which breaks and reforms

18 fission yeasts Schizosaccharomyces pombe and Schizosaccharomyces japonicus.

19 fission yeasts Schizosaccharomyces pombe and Schizosaccharomyces japonicus.

20 es pombe, Schizosaccharomyces octosporus and Schizosaccharomyces japonicus.

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

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

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

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

25 ryophilus, Schizosaccharomyces japonicus and Schizosaccharomyces octosporus).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

54 We show that Schizosaccharomyces pombe behaves similarly to metazoans

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

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

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

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

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

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

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

62 Schizosaccharomyces pombe cdc15 homology (PCH) family me

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

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

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

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

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

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

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

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

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

72 In contrast, Schizosaccharomyces pombe contains two essential tRNase

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

74 Our Schizosaccharomyces pombe Deltapfh1 strain constitutes a

75 Schizosaccharomyces pombe displays a large transcription

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

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

78 The Schizosaccharomyces pombe fission yeast Tup family corep

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

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 Previously we established assays in Schizosaccharomyces pombe for studying recombination ind

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

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

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

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

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

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

94 Schizosaccharomyces pombe harbors MTOCs at spindle pole

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

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

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

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

99 The Schizosaccharomyces pombe HDAC Clr6 (human HDAC1) binds

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

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

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

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

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

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

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

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

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

109 Schizosaccharomyces pombe is an attractive organism to s

110 Schizosaccharomyces pombe is an important experimental s

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

112 The fission yeast Schizosaccharomyces pombe is an important model organism

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

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

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

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

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

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

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

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

121 During Schizosaccharomyces pombe meiotic prophase, homologous c

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

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

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

125 We implicate a Schizosaccharomyces pombe nuclear envelope-spanning link

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

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

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

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

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

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

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

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

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

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

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

137 -1-1 checkpoint clamp (ortholog of human and Schizosaccharomyces pombe Rad9), the replication initiat

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

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

140 In Schizosaccharomyces pombe rod-shaped cells, Pom1 kinase

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

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

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

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

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

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

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

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

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

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

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

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

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

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

155 In Schizosaccharomyces pombe the Tf2 LTR retrotransposons a

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

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

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

159 /3 complex is activated at cortical sites in Schizosaccharomyces pombe to assemble branched actin net

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

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

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

163 The Schizosaccharomyces pombe TUT Cid1 is a model enzyme tha

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

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

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

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

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

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

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

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

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

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

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

175 5FU interferes with Pot1 (Pot1pN protein of Schizosaccharomyces pombe) binding.

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

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

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

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

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

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

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

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

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

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

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

187 In Schizosaccharomyces pombe, a Hippo-related signaling pat

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

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

190 In Schizosaccharomyces pombe, alcohol dehydrogenase 1 (Adh1

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

192 Schizosaccharomyces pombe, an organism containing numero

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

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

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

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

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

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

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

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

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

202 In Schizosaccharomyces pombe, copper is transported by thre

203 In Schizosaccharomyces pombe, cytokinesis requires the asse

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

205 In Schizosaccharomyces pombe, deletion of the ATPase vps4 l

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

207 In Schizosaccharomyces pombe, division plane positioning is

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

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

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

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

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

213 In Schizosaccharomyces pombe, H3K9me deposition depends on

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

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

216 In Schizosaccharomyces pombe, heterochromatin assembly on t

217 In the fission yeast Schizosaccharomyces pombe, heterochromatin formation inv

218 In Schizosaccharomyces pombe, heterochromatin spread, which

219 In Schizosaccharomyces pombe, important membrane-CR scaffol

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

221 1, a long-terminal repeat retrotransposon in Schizosaccharomyces pombe, integrates into promoters wit

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

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

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

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

226 In Schizosaccharomyces pombe, late mitotic events are coord

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

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

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

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

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

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

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

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

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

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

237 In Schizosaccharomyces pombe, the expression of the zrt1 zi

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

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

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

241 In Schizosaccharomyces pombe, the myo2-E1 mutation affects

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

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

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

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

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

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

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

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

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

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

252 Using Schizosaccharomyces pombe, we show that the distance bet

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

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

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

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

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

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

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

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

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

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

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

264 ocess for proper actomyosin ring assembly in Schizosaccharomyces pombe.

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

266 ct repeat recombination in the fission yeast Schizosaccharomyces pombe.

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

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

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

270 ncluding osmotic stress in the fission yeast Schizosaccharomyces pombe.

271 during histidine starvation in fission yeast Schizosaccharomyces pombe.

272 or telomere maintenance in the fission yeast Schizosaccharomyces pombe.

273 that found specifically in the fission yeast Schizosaccharomyces pombe.

274 l histone modifications in the fission yeast Schizosaccharomyces pombe.

275 east, including Saccharomyces cerevisiae and Schizosaccharomyces pombe.

276 ccharomyces cerevisiae and the fission yeast Schizosaccharomyces pombe.

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

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

279 of synchronous meiosis in the fission yeast Schizosaccharomyces pombe.

280 niscent of the distantly related ascomycete, Schizosaccharomyces pombe.

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

282 odel organism database for the fission yeast Schizosaccharomyces pombe.

283 wth characteristics of the unicellular yeast Schizosaccharomyces pombe.

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

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

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

287 sure successful completion of cytokinesis in Schizosaccharomyces pombe.

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

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

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

291 relationship between Spt6 and Set2 exists in Schizosaccharomyces pombe.

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

293 ntrinsic reproductive isolation in the yeast Schizosaccharomyces pombe.

294 chromosome condensation in the fission yeast Schizosaccharomyces pombe.

295 rmentation with Saccharomyces cerevisiae and Schizosaccharomyces pombe.

296 pic approaches to dissect their interplay in Schizosaccharomyces pombe.

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

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.