戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 s, neurons cells from mice, and yeast cells (S. pombe).
2  plays a central role in zinc homeostasis in S. pombe.
3 d examining salt tolerance in sod2-deficient S. pombe.
4 activities between two different proteins in S. pombe.
5 confer salt tolerance when reintroduced into S. pombe.
6 sion yeasts Schizosaccharomyces kambucha and S. pombe.
7 ill be a valuable tool for future studies in S. pombe.
8  integrity and cellular stress resistance in S. pombe.
9  histone expression at the end of S phase in S. pombe.
10 quired for proper cell fate determination in S. pombe.
11 ences that contained 31% of the promoters of S. pombe.
12 en the CPC and the process of cytokinesis in S. pombe.
13 eb in mammals, and Tsc1/Tsc2 inhibit Rhb1 in S. pombe.
14 on similarly as an export carrier of mRNA in S. pombe.
15 tor 1 (Tbf1), a second TRF1/TRF2 ortholog in S. pombe.
16 nstream components of the meiotic pathway in S. pombe.
17 uble mutant generation in the fission yeast, S. pombe.
18 itotic DSB repair and crossover formation in S. pombe.
19 ity of cleaving nicked HJs during meiosis in S. pombe.
20 the hermes transposon from the housefly into S. pombe.
21 epair to ensure accurate nuclear division in S. pombe.
22 -NXT pathway, is required for mRNA export in S. pombe.
23 tial for efficient nuclear protein import in S. pombe.
24 y species and in heterochromatin assembly in S. pombe.
25  Rae1p is an essential mRNA export factor in S. pombe.
26 sulting from loss of Rho1 GTPase function in S. pombe.
27 , for the coordination of DNA replication in S. pombe.
28 E expansion required for "closed" mitosis in S. pombe.
29 REBP activation and low-oxygen adaptation in S. pombe.
30 terest in developing research projects using S. pombe.
31 osaccharomyces japonicus, unlike its role in S. pombe.
32  mitochondrial proteins in S. cerevisiae and S. pombe.
33  related mutant has only a mild phenotype in S. pombe.
34 oles for Smc5/6 are genetically separable in S. pombe.
35 were most homologous to molecules present in S. pombe (52% identical and 67% homologous for PCRan1 an
36 sis also identified 24 SNPs between ours and S. pombe 972h- strain yFS101 that was recently sequenced
37 ations and down-regulated WEE1 (WEE1 homolog-S. pombe), a kinase that blocks cell-cycle progression.
38      Here, we show that in the fission yeast S. pombe, a relatively small number of CENP-A/Cnp1 nucle
39            Systematic analysis of the entire S. pombe ABC transporter family identified Abc2 as a ful
40                                          The S. pombe abc1 abc2 abc3 abc4 hmt1 quintuple and abc2 hmt
41 , the septation initiation network (SIN), in S. pombe act through an unknown mechanism to keep the ph
42                                              S. pombe actin shares many properties with skeletal musc
43        Heterologous expression of cehmt-1 in S. pombe alleviates the Cd2+-hypersensitivity of hmt- mu
44                              The response of S. pombe, also known as fission yeast, to misfolded prot
45 ASs) in two yeast species, S. cerevisiae and S. pombe Although >80% of the mRNA genes in each species
46 cerol and glycerophospholipid homeostasis in S. pombe, analogous to mammalian SREBP-1.
47 -modifying enzymes (a PtdIns(4)P-5-kinase in S. pombe and a PI-4-kinase in D. melanogaster) that inte
48  Whereas studies of Mre11 complex mutants in S. pombe and A. thaliana indicate that the complex has o
49 ghly active in inhibiting PCNA function both S. pombe and human cells and showed a high affinity for
50 tural differences are also conserved between S. pombe and humans, suggesting that the S. pombe struct
51 and S. cerevisiae, but are conserved between S. pombe and humans.
52 esolution map of transcription elongation in S. pombe and identify divergent roles for Spt4 in contro
53 nd process for crossover formation exists in S. pombe and is consistent with our finding that deletio
54 dated three functional repurposing events in S. pombe and mammalian cells and discovered that (1) two
55 ds containing candidate insertion sites into S. pombe and mapped the positions of integration.
56  duplication in Saccharomyces cerevisiae and S. pombe and PcpA, the anchor for gamma-TuSCs at the SPB
57 ous assays of recombination intermediates in S. pombe and provide new information on the mechanism of
58 er, our data indicate that APA mechanisms in S. pombe and S. cerevisiae are largely different: S. pom
59 n, a section on some key differences between S. pombe and S. cerevisiae is included for readers with
60 ighly purified factors between reconstituted S. pombe and S. cerevisiae transcription systems, we con
61 f the transcription mechanism differ between S. pombe and S. cerevisiae, but are conserved between S.
62 ing the distinct initiation patterns between S. pombe and S. cerevisiae, but rather, these patterns a
63 us, whereas m(7)G caps are essential in both S. pombe and S. cerevisiae, m(2,2,7)G caps are not.
64                                Therefore the S. pombe and S. japonicus mating systems provide the fir
65 ucleosome-excluding sequences functioning in S. pombe and S. octosporus, and binding sites for trans-
66 nscriptional interference are shared between S. pombe and the highly divergent budding yeast Saccharo
67 r and Tc5 elements by horizontal transfer in S. pombe (and humans) is accompanied by alteration of th
68  pianissimo from D. discoidieum, STE20p from S. pombe, and AVO3p from S. cerevisiae.
69 Cdc15, which is essential for cytokinesis in S. pombe, and in the related PCH protein, Imp2.
70             We propose that many hotspots in S. pombe, and perhaps other organisms, result from simpl
71            Human Rab6 can substitute Ryh1 in S. pombe, and therefore Rab6 may be a potential activato
72 cts affect but do not deplete nucleosomes in S. pombe, and they prefer special rotational positions w
73 species approximately 350 million years ago, S. pombe appears to have evolved less rapidly than S. ce
74 sidues involved in binding each substrate of S. pombe Aps1 are unknown.
75                      Since S. cerevisiae and S. pombe are evolutionary distant, this methodology will
76                            The popularity of S. pombe as a model organism suggests that this augmente
77 ome lies at the heart of the exploitation of S. pombe as a model system.
78 able at http://cerevisiae.oridb.org/ and for S. pombe at http://pombe.oridb.org/.
79 osomes in vivo in Schizosaccharomyces pombe (S. pombe) at base pair resolution.
80 cts the kinase activity and stability of the S. pombe Aurora B homologue, Ark1, colocalizes with know
81                We estimate that dispersal of S. pombe began during human antiquity ( approximately 34
82 gamma-H2A/X phosphate is likely conserved in S. pombe Brc1 and human Mdc1 genome maintenance proteins
83 iated heavy metal detoxification not only in S. pombe but also in some invertebrates while at the sam
84 ng is highly predictable by A/T frequency in S. pombe but not in S. cerevisiae, suggesting that the g
85 rved biological pathways that are present in S. pombe, but not S. cerevisiae, and will enable a compr
86                       This Primer introduces S. pombe by describing the yeast itself, providing a bri
87 aneous phenotypic mutations can be mapped in S. pombe by Solexa sequencing.
88 - and Q-independent tRNA methylation site in S. pombe, C34 of tRNA(Pro).
89 ine the three-dimensional arrangement of the S. pombe Ccq1-Tpz1-Poz1 (CTP) complex.
90 us by the FEAR network and Cdk1, whereas the S. pombe CDC14-like phosphatase Clp1p (also known as Flp
91              DCAF2/Cdt2, which is related to S. pombe Cdt2, functions in Xenopus egg extracts and hum
92 ion by competitive binding in both human and S. pombe cells as EGFP fusion proteins.
93         Our work demonstrates that quiescent S. pombe cells assemble specific cytoskeleton structures
94                   IR exposure of sporulating S. pombe cells induced misrepair and irreparable DNA dou
95                                              S. pombe cells lacking tit1+ exhibit slow growth in glyc
96 A damage sites could provide a mechanism for S. pombe cells to arrest at G(2)/M boundary in response
97                                              S. pombe cells treated with a lethal concentration of av
98                       Indeed, Rho1-deficient S. pombe cells were strongly hypersensitive to avicin G,
99 osynthesis is selectively blocked in mutated S. pombe cells, their ability to acquire exogenous hemin
100 ade by mathematical models of endocytosis in S. pombe cells.
101 peraccumulation of ubiquitinated proteins in S. pombe cells.
102 scopic observation of hundreds of individual S. pombe cells.
103 vious studies have suggested that functional S. pombe centromeres lack regularly positioned nucleosom
104 nteractions were captured between and within S. pombe chromosomes.
105                          Thus, the impact of S. pombe CLASP on interphase microtubule behavior is mor
106        Third, Peg1 antagonized the action of S. pombe CLIP170 (Tip1) and EB1 (Mal3).
107 proteome-wide binary protein interactome for S. pombe, comprising 2,278 high-quality interactions, of
108                                              S. pombe contains a single Mis18 isoform that forms a ho
109 logous end joining to be largely faithful in S. pombe, contrary to current belief.
110          Significantly, 3' UTR shortening in S. pombe coordinates with up-regulation of expression fo
111                         We isolated multiple S. pombe ctp1 mutants deficient in clipping but proficie
112 nitiator Dpb11 (ortholog of human TopBP1 and S. pombe Cut5), and the multifunctional nuclease/helicas
113 bers, Cdc15 and Imp2, play critical roles in S. pombe cytokinesis.
114 s of tRFs for eight species: R. sphaeroides, S. pombe, D. melanogaster, C. elegans, Xenopus, zebra fi
115 e switch-activating protein Sap1 is a GRF in S. pombe, demonstrating the general applicability of our
116 rticle outlines the way in which interest in S. pombe developed and spread from Europe to Japan, Nort
117          Upon mitotic checkpoint activation, S. pombe Dma1 concentrates at spindle pole bodies (SPBs)
118                                              S. pombe does not have a well-defined nucleosome-deplete
119                            Comparison of the S. pombe E-MAP to an analogous genetic map from the budd
120                       Although comparable to S. pombe eMTOCs, A. nidulans sMTOCS are permanent septum
121 ound with mutations affecting the same gene, S. pombe erf2 (sp-erf2), encoding sp-Erf2, a palmitoyltr
122                    Here, we demonstrate that S. pombe Est1 was required for the telomere association
123           Our results reveal that the UPR in S. pombe executes RIDD in an intricate interplay between
124 An alanine scan of 11 conserved positions of S. pombe Fcp1 identifies Thr(174), Tyr(237), Thr(243), a
125  have observed the growth characteristics of S. pombe for N=100 cells to determine the growth phenoty
126 the Cdc14-family phosphatase, called Clp1 in S. pombe, from being sequestered and inhibited in the nu
127 e than cells lacking zwf1 We propose that in S. pombe Gcd1 and Idn1 act together to shunt glucose int
128 hese studies reveal that convergent genes in S. pombe generate overlapping transcripts in the G1 phas
129 nts, we identified Cdc48-binding proteins in S. pombe, generating a list of many previously unknown p
130  including approximately 40% of nonessential S. pombe genes.
131 26 heptamer sequence occurs in the wild-type S. pombe genome approximately 300 times, but it has been
132 on for each intergenic region and ORF in the S. pombe genome.
133 gest that Hsp90 plays a specific role in the S. pombe glucose/cAMP pathway.
134    Thus, Git1 is a critical component of the S. pombe glucose/cAMP pathway.
135                                     Although S. pombe growth is resistant to rapamycin, sla1-Delta ce
136  APA features of higher species, and Pab2 in S. pombe has a different role in APA regulation than its
137                  This is the first time that S. pombe has been utilized for isolating and characteriz
138 mbe and S. cerevisiae are largely different: S. pombe has many of the APA features of higher species,
139  major motor involved in ring contraction in S. pombe." Here, we show that most of the differences ob
140              Our findings identified a novel S. pombe histone demethylase with specificity toward di-
141 MT-1 suppresses the Cd2+ hypersensitivity of S. pombe hmt-1 mutants and localizes to the vacuolar mem
142               Crucially, similar analyses of S. pombe hmt-1 mutants extend this finding to show that
143                      Genetic ablation of the S. pombe homologs, splsd1 and splsd2, resulted in slow g
144               Msc1 co-precipitates Rhp6, the S. pombe homologue of the human ubiquitin-conjugating en
145 alian XPG (also known as ERCC5) and ERCC1 in S. pombe homologues Rad13 and Swi10 and biochemical inte
146 together with previous observations made for S. pombe homologues tea1p and tea3p, they have broad imp
147         Here we show that binding of the key S. pombe HP1 protein, Swi6, to methylated nucleosomes dr
148                                    Using the S. pombe HP1 protein, Swi6, we show that recognition of
149 hich is identical to swo1(+) and encodes the S. pombe Hsp90 chaperone protein.
150 thaliana OXS3 to enhance stress tolerance in S. pombe, indicating a role in stress tolerance for the
151 nes are better conserved between the yeasts, S. pombe interactions are significantly better conserved
152 r data argue that trans-histone crosstalk in S. pombe involves direct enhancement of Set1C methyltran
153 orter linker length previously identified in S. pombe is due to a preponderance of nucleosomes separa
154 hat, in contrast to S. cerevisiae, Uap56p in S. pombe is not required for pre-mRNA splicing.
155                          Based on studies of S. pombe, it has been proposed that SpHMT-1 transports h
156                                           In S. pombe, it is known that Rhb1 binds Tor2, and Tor2 inh
157                                          The S. pombe JmjC family protein Epe1 prevents the ectopic s
158                        We show here that the S. pombe JmjC-domain protein Lid2 is a trimethyl H3K4 de
159 ons with the S. japonicus lipin acquiring an S. pombe-like mitotic phosphorylation pattern.
160        Rec10 protein is a major component of S. pombe LinEs and is required for their development.
161                         CENP-B homologues of S. pombe localize at and recruit histone deacetylases to
162 ponse, we show that modest overexpression of S. pombe los1(+) (also known as Xpo-t), encoding the nuc
163  subtilis lumazine synthase (Ki 2.6 microM), S. pombe lumazine synthase (Ki 0.16 microM), M. tubercul
164                                           In S. pombe, many actomyosin ring components assemble at th
165   These results suggest that PDE activity in S. pombe may be coordinately regulated with adenylate cy
166          A point mutant within this motif of S. pombe Mcm10p was defective in primer synthesis in vit
167                               In contrast to S. pombe, medial assembly of the actomyosin ring in mito
168 cuoles and abrogates (35)S-PC(2) uptake into S. pombe microsomal vesicles.
169 at Mal3 makes a distinctive footprint on the S. pombe microtubule lattice and that unlike mammalian m
170 tice and that unlike mammalian microtubules, S. pombe microtubules do not show the longitudinal latti
171 stituted dynamically unstable single isoform S. pombe microtubules with full length Alp14/TOG and Alp
172 and functional analysis of human anillin and S. pombe Mid1.
173 is I and to suppress merotelic attachment in S. pombe mitosis, and crosslinking rDNA repeats to aid r
174  of Rab-GTPase activity is a property of the S. pombe MOP essential for the initiation of membrane fo
175  providing the first identification of these S. pombe mtDNA discrepancies.
176  sufficient for polar cell extension, but in S. pombe, MTs are in addition required for the establish
177 n approach to directly select for long-lived S. pombe mutants from a random DNA insertion library.
178                                              S. pombe mutants lacking a new factor described here, Er
179          Interestingly, proteasome-defective S. pombe mutants were not markedly hypersensitive to avi
180                          In vitro studies of S. pombe MYH identified residues I261 and E262 of the ID
181                  Here, we show that the sole S. pombe myosin I, myo1p, is required for proper organiz
182 E1-Sup1 cells depend on the late cytokinetic S. pombe myosin II isoform, Myp2p, a non-essential prote
183 e localization to nuclei and mitochondria in S. pombe, neither of the S. cerevisiae homologs, nor hum
184 rs of low oxygen adaptation, we screened the S. pombe nonessential haploid deletion collection and id
185 ns of the chromosome organization within the S. pombe nuclei were made by polymer modeling.
186                         In the fission yeast S. pombe, nuclei are actively positioned at the cell cen
187 revisiae, A/T-rich sequences are enriched in S. pombe nucleosomes, particularly at +/-20 bp around th
188                         We conclude that the S. pombe nucleus is spatially divided into functional su
189 t levels have preferred positions within the S. pombe nucleus.
190               Because all well characterized S. pombe origins are located in intergenic regions, we a
191 formation of stable protein-DNA complexes at S. pombe origins of replication involves binary interact
192                             We show that the S. pombe ortholog Seb1 is associated with pericentromeri
193  Oxs1 and Pap1-homologues can substitute for S. pombe Oxs1 and Pap1 to enhance stress tolerance.
194 f transcriptional interference involving the S. pombe pho1(+) gene.
195 ogether, results reported here revealed that S. pombe possesses an unexpected pathway for heme assimi
196                                   Studies of S. pombe Pot1-DBD and its individual OB-fold domains rev
197 domain (residues 1-187) found in full-length S. pombe Pot1.
198                    Two crystal structures of S. pombe profilin and homology models of S. pombe profil
199  of S. pombe profilin and homology models of S. pombe profilin bound to actin show how the two profil
200                         Human profilin-I and S. pombe profilin have similar affinities for actin mono
201 in filament elongation by formin Cdc12p like S. pombe profilin.
202 an bind and unwind both DNA and RNA, but the S. pombe protein is not essential and has not been demon
203                                The essential S. pombe protein Teb1 contains two Myb-like DNA binding
204 cterized fungal proteins, including a second S. pombe protein that is not functionally redundant with
205 ere, we isolate a previously uncharacterized S. pombe protein through association with the Cdc14 phos
206 at one of the AT-STUbLs least related to the S. pombe protein, AT-STUbL4, has acquired a plant-specif
207 occurs in the 5' to 3' direction, as for the S. pombe protein.
208 n of this new technology for the analysis of S. pombe proteins.
209 minished for Atl1 R69A and R69F mutants, and S. pombe R69A and R69F mutants are more sensitive toward
210 verified utility by C-terminally tagging the S. pombe rad4 and swi1 genes with yEGFP and the yEGFP de
211 e been able to identify homologous motifs in S. pombe Rad9 that can activate Mec1.
212              When the mammalian homologue of S. pombe Rad9 was inactivated, increases in chromosome e
213                      zfs1 and its targets in S. pombe represent a useful model system for studies of
214                        However, we find that S. pombe requires cap guanine-N7 methylation catalyzed b
215 dition to the endoribonuclease Dcr1, RNAi in S. pombe requires two interacting protein complexes, the
216                 We describe the expansion of S. pombe research during this period with an emphasis on
217 emperature-sensitive and knockout strains of S. pombe, respectively, further verified the functions o
218 than deleting their singleton counterpart in S. pombe, revealing post-duplication adaptation.
219 ns identified here as subject to skipping in S. pombe reveals high sequence conservation and perfect
220 isome component C20orf43/RTF2 (homologous to S. pombe Rtf2) must be removed for fork restart to be op
221 s ability to insert within silent regions of S. pombe's genome.
222 genome-scale cell-cycle mRNA expression from S. pombe, S. cerevisiae and human.
223                          Purification of the S. pombe SAGA complex showed that its subunit compositio
224                                  Analysis of S. pombe SAGA mutants revealed that SAGA has two opposin
225 , Pidoux et al. and Williams et al. identify S. pombe Scm3 as the proximate factor in the Cnp1/CENP-A
226 romeric nucleosomes, the dynamic behavior of S. pombe Scm3 suggests that it acts as a Cnp1 assembly/m
227  factors, deletion of the SpELL gene renders S. pombe sensitive to the drug 6-azauracil.
228                                To ask if the S. pombe septins function redundantly in cytokinesis, we
229 Taken together, our results suggest that the S. pombe septins participate redundantly in one or more
230                We found that the activity of S. pombe Set1C toward nucleosomal histone H3 is directly
231 d Spt8 have opposing regulatory roles during S. pombe sexual differentiation.
232       Global analysis of tRNA methylation in S. pombe showed a striking selectivity of Pmt1 for tRNA(
233 s in each species were found to display APA, S. pombe showed greater 3' UTR size differences among AP
234 lease expression in cells harbouring a novel S. pombe single-strand annealing (SSA) assay.
235 erevisiae SIR2 gene can function in place of S. pombe sir2(+), suggesting overlapping deacetylation s
236 ith single-particle averaging to localize 14 S. pombe SPB components and regulators, determining both
237 e first comprehensive molecular model of the S. pombe SPB, resulting in structural and functional ins
238 mental role for Ppc89 in organization of the S. pombe SPB.
239 ich is highly diverged from the well-studied S. pombe species (with 44% GC content).
240 S. japonicus differ vastly from those of the S. pombe species.
241          Here we report that deletion of the S. pombe Spt5 CTD results in slow growth and aberrant ce
242                                    Thus, the S. pombe STE, although distant from the template, ensure
243         The laboratory strain and most other S. pombe strains contain three chromosomes, but one rece
244                                        Using S. pombe strains deficient for Pcf11 or Pab2, we show th
245 ed mmd4 in a screen of temperature-sensitive S. pombe strains for aberrant mitochondrial morphology a
246 SVs in the genomes of a worldwide library of S. pombe strains, including duplications, deletions, inv
247 cript levels in wild-type and zfs1-deficient S. pombe strains; those elevated in the zfs1-deficient s
248                                          The S. pombe stress response pathway (SRP) also promotes com
249                                           In S. pombe, strong motifs surrounding distal PASs lead to
250 een S. pombe and humans, suggesting that the S. pombe structure may be a good surrogate for that of t
251               Functions for RNAi revealed in S. pombe, such as heterochromatic silencing and chromoso
252 s observed in B. subtilis, S. cerevisiae and S. pombe, such as the tendency of FRS to increase from t
253                             Recent data from S. pombe suggest an alternative possibility: that the re
254                                           In S. pombe, Swi1 and Swi3 form the replication fork protec
255 ntriguingly, unlike their human counterpart, S. pombe SWIRM complex contains neither a histone deacet
256                                    Thus, the S. pombe system can be used to identify novel, evolution
257 ken together, these results suggest that the S. pombe system described here can be employed for compa
258 ctions that are important in maintaining the S. pombe telomere in a non-extendible state.
259 eotide consisting of two conserved hexameric S. pombe telomere repeats, d(GGTTACGGTTAC), with an affi
260                   The identified Tbf1p binds S. pombe telomeric DNA with high sequence specificity in
261                     We further show that the S. pombe telomeric protein Tpz1, like its mammalian homo
262 the heterogeneous spacers that occur between S. pombe telomeric repeats, and it also has implications
263                                    While the S. pombe TER intron contains the canonical 5'-splice sit
264 d by Tgs2 can be converted to m(2,2,7)GDP by S. pombe Tgs1 in the presence of excess AdoMet.
265                        A genetic analysis of S. pombe Tgs1 showed that it is nonessential.
266                                           An S. pombe tgs1Delta strain grows normally, notwithstandin
267  is a TOG-family microtubule polymerase from S. pombe that tracks plus ends and accelerates their gro
268 ify a pause in early elongation, specific to S. pombe, that requires the conserved elongation factor
269 at for two distant yeasts (S. cerevisiae and S. pombe), the only other organisms comprehensively exam
270                                           In S. pombe, the ER membrane-resident kinase/endoribonuclea
271               Remarkably however, similar to S. pombe, the S. japonicus cells switch cell/mating type
272                                           In S. pombe, the SIN and Clp1 act as part of a cytokinesis
273 hat sla1(+) regulates AAM mRNA production in S. pombe through its effects on nuclear tRNA processing
274 tch from proliferation to differentiation in S. pombe through the dynamic and opposing activities of
275 s scenario may principally be conserved from S. pombe to filamentous fungi.
276  shu1(+) that encodes a protein that enables S. pombe to take up extracellular heme for cell growth.
277                                   Studies of S. pombe, together with studies of its distant cousin, S
278 hat Rhb1 interacts with Tor2, one of the two S. pombe TOR (Target of Rapamycin) proteins.
279                                A screen with S. pombe transcription factor mutant strains for growth
280 phy reveals that microtubules assembled from S. pombe tubulin have predominantly B-lattice interproto
281                                       Unlike S. pombe, two other fission yeasts rely on hyperstabiliz
282 leavage mechanism is more ancestral than the S. pombe-type.
283 s could completely substitute for the native S. pombe TZF domain, as determined by measurement of tar
284             Here, we report the structure of S. pombe Uba1 in complex with Ubc15, a Ub E2 with intrin
285 of protein SUMOylation, and we identified an S. pombe Ulp2/Smt4 homolog that, when overexpressed, red
286 -specific transcriptome of the fission yeast S. pombe under multiple growth conditions using a novel
287                 The cassette consists of the S. pombe ura4(+) selectable marker flanked by a wild-typ
288                                        Thus, S. pombe uses a universally conserved stress-sensing mac
289 reas both species divide in the middle, only S. pombe uses the anillin Mid1 as a primary nucleus-deri
290 SINaTRA by predicting synthetic lethality in S. pombe using S. cerevisiae data, then identify over on
291 ters abolishes phytochelatin accumulation in S. pombe vacuoles and abrogates (35)S-PC(2) uptake into
292 are lethal in S. cerevisiae, they are not in S. pombe We show that the lethality of a temperature-sen
293 rgosterol with respect to wild-type Dap1p in S. pombe, we find that Dap1pY138F expression is still su
294  a genome-wide approach in the fission yeast S. pombe, we have found that Dcr1, but not other compone
295 nes suggests Tf1 may improve the survival of S. pombe when cells are exposed to environmental stress.
296 port a novel mechanism for oxygen-sensing in S. pombe, whereby the 2-OG-Fe(II) dioxygenase Ofd protei
297                     Our results suggest that S. pombe will be a useful model organism for elucidating
298  mouse, rat, mouse-ear cress, fruit fly, the S. pombe yeast, the E. coli bacterium and the M. jannasc
299                            When expressed in S. pombe, YopJ sensitized cells to osmotic and oxidative
300 in techniques, we replaced the TZF domain of S. pombe Zfs1 with the equivalent domains from human TTP

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top