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1 inhibit apoptosis in ts13 cells grown at the nonpermissive temperature.
2 se activities for wt NSP2 were higher at the nonpermissive temperature.
3 lly reduced in the doubly tagged strain at a nonpermissive temperature.
4 d/or replication in the infected cell at the nonpermissive temperature.
5 hese improperly processed transcripts at the nonpermissive temperature.
6 e improperly 3' processed transcripts at the nonpermissive temperature.
7 cytes carrying wild-type protein even at the nonpermissive temperature.
8 ription defects and inhibit apoptosis at the nonpermissive temperature.
9 3 at various sites on the cell cortex at the nonpermissive temperature.
10 f the nucleolus is abnormal in ycs4-1 at the nonpermissive temperature.
11 ; this strain was also unable to grow at the nonpermissive temperature.
12 ke intermediate genes, were expressed at the nonpermissive temperature.
13 enzyme is further reduced at 42 degrees C, a nonpermissive temperature.
14 nsp5-mediated polyprotein processing at the nonpermissive temperature.
15 ubiquitinate or to internalize Ste2p at the nonpermissive temperature.
16 early viral gene expression occurred at the nonpermissive temperature.
17 2 cells in a dominant-negative manner at the nonpermissive temperature.
18 es were detected in tsH5-4 infections at the nonpermissive temperature.
19 in the ubiquitin-activating enzyme E1, at a nonpermissive temperature.
20 o NGF was absent in PC12(p53ts) cells at the nonpermissive temperature.
21 cells or Deltacdc6 null mutant cells at the nonpermissive temperature.
22 r viral gene expression were detected at the nonpermissive temperature.
23 unable to import Ran into the nucleus at the nonpermissive temperature.
24 cell cycle block in ts13 cells grown at the nonpermissive temperature.
25 MHV-Brts31-infected cells is reduced at the nonpermissive temperature.
26 ptive budding site did not take place at the nonpermissive temperature.
27 dding and actin polarization occurred at the nonpermissive temperature.
28 rature-sensitive pol III mutant (dnaE486) at nonpermissive temperature.
29 ochondrial inheritance and morphology at the nonpermissive temperature.
30 t defects have not been observed even at the nonpermissive temperature.
31 tin-activating enzyme (E1) upon shift to the nonpermissive temperature.
32 ture sensitive, forming small plaques at the nonpermissive temperature.
33 ambda gene rearrangement when shifted to the nonpermissive temperature.
34 ant cells appear to function normally at the nonpermissive temperature.
35 at least one round of DNA replication at the nonpermissive temperature.
36 so dramatically reduced in ts13 cells at the nonpermissive temperature.
37 with shorter poly(A) tails when grown at the nonpermissive temperature.
38 defect in NP protein)-infected cells at the nonpermissive temperature.
39 fected with a ts8 p35 deletion mutant at the nonpermissive temperature.
40 ls inhibited apoptosis of these cells at the nonpermissive temperature.
41 apidly undergo apoptosis when shifted to the nonpermissive temperature.
42 ive Ras GEF, Cdc25-2, allowing growth at the nonpermissive temperature.
43 in early but not late Golgi compartments at nonpermissive temperature.
44 ts showed reduced nuclear proteasomes at the nonpermissive temperature.
45 rp43 was sufficient to restore growth at the nonpermissive temperature.
46 romuscular junctions of csp mutant larvae at nonpermissive temperature.
47 ired less frequently in cdc45-1 cells at the nonpermissive temperature.
48 ript abundance when cells are shifted to the nonpermissive temperature.
49 ented E. coli strain sensitive to GFZ at the nonpermissive temperature.
50 PY and the secreted protein invertase at the nonpermissive temperature.
51 alize to a vacuolar membrane fraction at the nonpermissive temperature.
52 ature-sensitive mini-RK2 replicon grown at a nonpermissive temperature.
53 re selected based on colony formation at the nonpermissive temperature.
54 BHK tsBN7) induce CHOP when cultured at the nonpermissive temperature.
55 n binding to Spc110-220p is defective at the nonpermissive temperature.
56 markedly inhibited following incubation at a nonpermissive temperature.
57 partial restoration of nsp5 activity at the nonpermissive temperature.
58 ssed a differentiation phenotype only at the nonpermissive temperature.
59 titution of amino acid 186, binds p53 at the nonpermissive temperature.
60 ribosomal protein genes is repressed at the nonpermissive temperature.
61 ort of poly(A)+ RNA following a shift to the nonpermissive temperature.
62 host cell but had an uncoating defect at the nonpermissive temperature.
63 dentical to that of Alb/ts/nsp5/V148A at the nonpermissive temperature.
64 d fewer myxospores than the wild type at the nonpermissive temperature.
65 is mutant also fails to enter S phase at the nonpermissive temperature.
66 pro, blocking its function completely at the nonpermissive temperature.
67 5 with the U(L)28 and U(L)33 proteins at the nonpermissive temperature.
68 m10 in mcm10-1 mutants that are grown at the nonpermissive temperature.
69 nts after 24 h of incubation in LB medium at nonpermissive temperature.
70 ants, even after prolonged incubation at the nonpermissive temperature.
71 ally assumes that the protein is inactive at nonpermissive temperature.
72 mutant FabG proteins may be disrupted at the nonpermissive temperature.
73 in mutant, and the VSV-G ts045 mutant at the nonpermissive temperature.
74 rain JN394top2-4 expressing betaE522K at the nonpermissive temperature.
75 ured in vivo was inhibited upon shift to the nonpermissive temperature.
76 2 viral DNA replication is unimpaired at the nonpermissive temperature.
77 undergo rapid apoptosis after a shift to the nonpermissive temperature.
78 ject its virion DNA into the nucleus at this nonpermissive temperature.
79 islocalized to the vacuole in neo1-ts at the nonpermissive temperature.
80 he viral life cycle that was affected at the nonpermissive temperature.
81 ast-acting mei-1(ts) mutant was shifted to a nonpermissive temperature.
82 n mutant cells before and after the shift to nonpermissive temperature.
83 erature-sensitive mutant when shifted to the nonpermissive temperature.
84 use dramatic cellular phenotypes observed at nonpermissive temperatures.
85 E. coli strain that lacks BCCP when grown at nonpermissive temperatures.
86 scue the tsBN67 cell proliferation defect at nonpermissive temperatures.
87 d for enhanced survival during incubation at nonpermissive temperatures.
88 or no proteolytic activity at permissive and nonpermissive temperatures.
89 that rapidly blocks synaptic transmission at nonpermissive temperatures.
90 ions to trigger exocytosis in csp mutants at nonpermissive temperatures.
91 t of a temperature-sensitive sec31 mutant at nonpermissive temperatures.
92 e inactivated MGMT protein at permissive and nonpermissive temperatures.
93 ature-sensitive mutation in the UL15 gene at nonpermissive temperatures.
94 NA (rnpB709) subunits lead to inviability at nonpermissive temperatures.
95 generate the TS phenotype at permissive and nonpermissive temperatures.
96 cally defective in Sir2-Sir4 interactions at nonpermissive temperatures.
97 itro, but only the rice isoforms denature at nonpermissive temperatures.
98 emperature (30 degrees C) and shifted to the nonpermissive temperature (16 degrees C) form tumor-like
101 e in virus yields between the permissive and nonpermissive temperatures (2.2 x 10(6) and 3 x 10(3), r
103 hat sec14-3 cells could grow at an otherwise nonpermissive temperature (34 degrees C) when carrying a
104 clear gene (MNA6), which lose mt 15S rRNA at nonpermissive temperature (36 degrees C), were previousl
110 eplication immediately after transfer to the nonpermissive temperature [37 degrees C]) and three (1-2
112 f the second splicing reaction, while at the nonpermissive temperature (39 degrees C), both splicing
113 tential at 33 degrees C, but on shift to the nonpermissive temperature (39 degrees C), they show dimi
114 activating enzyme E1, were incubated at the nonpermissive temperature (39.5 degrees C) in the presen
116 cells, stably expressing human iNOS, at the nonpermissive temperature (40 degrees C) resulted in inh
117 s aligned by a shift of dnaC2(Ts) mutants to nonpermissive temperature (40 degrees C), mioC transcrip
118 ensitive VSV mutant (ts045) and grown at the nonpermissive temperature (40.5 degrees C), cells transi
122 emperature (30 degrees C) versus that at the nonpermissive temperature (45 degrees C); (ii) transposi
123 120/R273K mutant suppressed apoptosis at the nonpermissive temperature, a phenotype correlated with i
125 Dts38], Dts12, and Dts56) and shown that at nonpermissive temperature all of the tsD5 viruses exhibi
127 fect in the accumulation of viral DNA at the nonpermissive temperature, although both the A20 protein
128 Upon shifting the vam3(tsf) mutant cells to nonpermissive temperature, an immediate block in protein
130 mutations was inhibited upon a shift to the nonpermissive temperature and in the latter case decline
131 ks PBP1b and has a thermosensitive PBP1a, at nonpermissive temperature and induced a mild cell-chaini
132 ed in as little as 30 s after a shift to the nonpermissive temperature and is accompanied by a dramat
133 cells in a G(0)-like state when grown at the nonpermissive temperature, and the same domain interacts
134 hat capsids present within cells infected at nonpermissive temperatures are also cryosensitive and di
135 Synchronized mutant cells incubated at the nonpermissive temperature arrest as large budded cells w
137 causing a delayed entry into S phase at the nonpermissive temperature, as well as a high plasmid los
139 Aspergillus, their growth is arrested at the nonpermissive temperature, because the scNek2/Kin3 (D55G
140 a temperature-sensitive VSV-M mutant at the nonpermissive temperature both substantially reversed th
141 have the wild-type sequence; however, at the nonpermissive temperature, both E1 and PE2 are retained
145 M failed to accumulate in the nucleus at the nonpermissive temperature but did accumulate when the pe
146 e temperature and after several hours at the nonpermissive temperature but display aberrant organizat
147 rly proteins were detected at permissive and nonpermissive temperatures, but one mutant showed an abs
150 e protected from cell death on incubation at nonpermissive temperature by mutation in the cydA gene c
151 201 is reversible, and capsids formed at the nonpermissive temperature can undergo maturational cleav
152 synthesis, and thus lack of function at the nonpermissive temperature cannot be attributed to a lack
154 on of cells with thermosensitive Sec17-1p at nonpermissive temperature causes SNARE complex disassemb
158 ouble-mutant phenotype indicated that at the nonpermissive temperature, cells failed to undergo cytok
160 ar-targeted proteins in the cytoplasm at the nonpermissive temperature consistent with a defect in nu
161 ccumulate poly(A)+ RNA in the nucleus at the nonpermissive temperature, consistent with a failure to
162 Cells infected with tsE and maintained at nonpermissive temperature contain few replication-assemb
163 plasm of cells that had been infected at the nonpermissive temperature contained large granular areas
164 prepared from these cells, when grown at the nonpermissive temperature, contained about 5% SecY and s
165 strong mouse-specific defect of PV1(RIPO) at nonpermissive temperature correlated with the translatio
166 the dam1-1 allele becomes delocalized at the nonpermissive temperature, correlating with the subseque
170 vam7(tsf) mutant cells incubated at the nonpermissive temperature displayed rapid defects in the
172 cdc5-1 mutants arrest at telophase at the nonpermissive temperature due to the failure of CDK inac
173 that in ts23-infected cells incubated at the nonpermissive temperature, E1 folding is disrupted early
175 e mutant proteins were largely stable at the nonpermissive temperature except the A68T/N73D mutant pr
176 or olsA gene products supported growth at a nonpermissive temperature, exhibited AGPAT activity in v
177 sion of ORF P; (ii) in cells infected at the nonpermissive temperature for ICP4, ORF O protein is mad
179 ibroblast growth factor at 39 degrees C, the nonpermissive temperature for T function, resulted in th
182 cantly reduced if assayed at 30 degrees C, a nonpermissive temperature for Ty1 retrotransposition, or
184 lication immediately halts upon a shift to a nonpermissive temperature, growth and DNA replication of
185 archaeal and bacterial cysS genes grew at a nonpermissive temperature, growth was also supported by
186 uses (2B33F and 2B20L) at the permissive and nonpermissive temperatures have been compared with that
187 Instead of a cell division defect at the nonpermissive temperature, however, revertants displayed
188 factor) were completely blocked in the ER at nonpermissive temperature; however, other proteins (i.e.
189 sis of independently isolated mutants at the nonpermissive temperature identified a variety of well-d
192 ystem in Escherichia coli, was depleted at a nonpermissive temperature in a strain which had a temper
193 regulator of chromosome condensation) at the nonpermissive temperature in the thermosensitive mutant
194 nt in releasing mRNA from the spliceosome at nonpermissive temperature in vitro, the suppressor prote
195 e tested was impaired at both permissive and nonpermissive temperatures in secY40 cells grown in eith
196 ty to substrate stiffness during upshifts to nonpermissive temperatures in temperature-sensitive muta
197 coat protein mutants which can be rescued at nonpermissive temperatures in vivo by the overproduction
198 hibited upon shift of mutant cultures to the nonpermissive temperature, indicating blockage of the sy
199 n ts v-G37E-transformed cells shifted to the nonpermissive temperature, indicating that an ICE-like p
200 nt mutation are strongly bactericidal at the nonpermissive temperature, indicating that this pathway
202 risingly, certain ftsZ84 strains lyse at the nonpermissive temperature instead of filamenting, and in
203 ous ts alleles of spe-9, loss of function at nonpermissive temperatures is not due to protein misloca
204 ediate-early transcripts and proteins at the nonpermissive temperature, it did not produce any early
205 1% at the permissive temperature, and at the nonpermissive temperature, it renders further deteriorat
206 ion of this conditional-lethal mutant at the nonpermissive temperature led to aggregated mitochondria
207 train carrying an ftsZ84(Ts) mutation to the nonpermissive temperature led to loss of Z rings within
208 inhibition of leaf development in lem7 under nonpermissive temperatures may serve as a useful tool fo
210 in virus-infected cells showed that, at the nonpermissive temperature, MHV-Brtsc31 was not able to p
212 of temperature-conditional vps9 cells to the nonpermissive temperature, newly synthesized carboxypept
219 rphology seen in rat7-1 cells shifted to the nonpermissive temperature of 37 degrees C and, thus, res
220 ermissive temperature of 23 degrees C to the nonpermissive temperature of 37 degrees C on the process
228 that the cells rapidly lose viability at the nonpermissive temperature of 42 degrees C as well as sho
229 affect the mutant protein's stability at the nonpermissive temperature or its ability to associate wi
231 their only carbon source, and accumulate at nonpermissive temperatures predominantly as large-budded
232 7 hamster cell line arrests proliferation at nonpermissive temperatures, primarily in a G(0)/G(1) sta
233 ibits a loss of silencing when raised to the nonpermissive temperature regardless of cell-cycle posit
234 entous phenotype following incubation at the nonpermissive temperature, reminiscent of a defect in ce
235 tions in proteins produced at or heated to a nonpermissive temperature render the proteins defective
239 RNA obtained from the ts strain shifted to a nonpermissive temperature revealed accumulation of unspl
240 xamination of ts1249 capsids produced at the nonpermissive temperature revealed that, in comparison w
241 plating analysis performed at permissive and nonpermissive temperatures revealed that changes in the
242 wth at 37 degrees C, and upon a shift to the nonpermissive temperature show an accumulation of large
244 sI temperature-sensitive mutant grown at the nonpermissive temperature, some filaments displaying a s
245 in translation of the tap42-11 mutant at the nonpermissive temperature, suggest that Tap42, Sit4, and
246 st in mitosis with monopolar spindles at the nonpermissive temperature, suggesting a defect in SPB du
247 d processes at the permissive as well as the nonpermissive temperature, suggesting that cells express
248 n strains carrying ftsW(Ts) mutations at the nonpermissive temperature, suggesting that FtsW is unlik
249 efore tsBN67 cells stop proliferating at the nonpermissive temperature, suggesting that loss of HCF-1
250 m wild-type virus in assays performed at the nonpermissive temperature, suggesting that the ts mutati
251 ion that was transcriptionally silent at the nonpermissive temperature, suggesting that thermoregulat
252 isiae dna2-1 mutant strain for growth at the nonpermissive temperature, suggesting that XDna2p is a f
253 the lethal phenotype of smc1-2 and smc2-6 at nonpermissive temperatures, suggesting that the interact
254 layed a modestly increased Cse4 half-life at nonpermissive temperatures, suggesting that turnover of
255 of temperature-sensitive E. coli Y815 at the nonpermissive temperature, supporting its biological act
256 s of tsE NSP2 were significantly less at the nonpermissive temperature than at the permissive tempera
257 mutations were more rapidly degraded at the nonpermissive temperature than were the wild-type protei
258 rat8-2p localized to cytoplasmic granules at nonpermissive temperature that are distinct from P-bodie
262 In an ipl1-2 yeast strain, shifted to the nonpermissive temperature, the chromosomes and plasmid a
264 when unfolded by a shift from permissive to nonpermissive temperature, the G protein was reglucosyla
265 nt 143ala revealed that at 32 degrees C, the nonpermissive temperature, the growth of breast epitheli
271 shown that these cells enter mitosis at the nonpermissive temperature upon incubation with okadaic a
272 formed growth-based selection experiments at nonpermissive temperatures using a library of random bet
275 cause thermolability of the protein; at the nonpermissive temperature, virion morphogenesis arrests
276 cells transfected with the ts mutant at the nonpermissive temperature was comparable to that of wild
278 lude viral DNA cleavage and packaging at the nonpermissive temperature was identified as a change fro
279 ntegrase in mutant particles produced at the nonpermissive temperature was inconsistent with defectiv
280 Overexpression of topoisomerase III at the nonpermissive temperature was shown subsequently to rest
281 removal of the inhibitors and a shift to the nonpermissive temperature, we assayed for protein transp
283 cted for defective ribosome synthesis at the nonpermissive temperature were also found to have defect
284 rs accumulated in sec31-sec35 mutants at the nonpermissive temperature were core-glycosylated but lac
285 nfectivity of mutant virions produced at the nonpermissive temperature were greatly reduced when assa
286 ol) were detected in virions produced at the nonpermissive temperature when the HIV-1 protease was in
287 istribute back to the ER upon a shift to the nonpermissive temperature, where they misfolded and were
288 pendent leader peptidase is inhibited at the nonpermissive temperature, whereas the insertion of the
289 her (i) a temperature-sensitive virus at its nonpermissive temperature which does not inject viral DN
290 had decreased levels of 60S subunits at the nonpermissive temperature which resulted in the formatio
291 ressors of dnaN5 that restored growth at the nonpermissive temperature while maintaining an increase
292 e prevented by the infection of cells at the nonpermissive temperature with a mutant virus defective
293 mosome maintenance defect and arrests at the nonpermissive temperature with dumbbell morphology and 2
294 All five mutant T antigens bind pRb at the nonpermissive temperature with efficiencies similar to t
298 ere also isolated from cells infected at the nonpermissive temperature with the HSV-1 mutant tsProt.A
299 e yip1-4 allele accumulate ER membranes at a nonpermissive temperature, with no apparent accumulation
300 rently normal distribution at permissive and nonpermissive temperatures, yet mitosis appears to be ab