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1 1 was only induced by functional p53 (at the permissive temperature).
2 ome lethal in the presence of the drug under permissive temperature.
3 ictive temperature, but arrests cells at the permissive temperature.
4 at the nonpermissive temperature than at the permissive temperature.
5 in silencing at the mating type loci at the permissive temperature.
6 when expressed in an ftsQ1(Ts) strain at the permissive temperature.
7 in tsBN67 cells restores splicing at the non-permissive temperature.
8 t restored significant growth ability at non-permissive temperature.
9 in transcripts in cells incubated at the non-permissive temperature.
10 PP2A decreased as cells were shifted to the permissive temperature.
11 d R-Ras and Src co-immunoprecipitated at the permissive temperature.
12 ectious virus is <1% of that obtained at the permissive temperature.
13 rad3, suggesting chromosomal defects even at permissive temperature.
14 sive conditions as well as some reduction at permissive temperature.
15 and G2/M cell cycle arrest upon shift to the permissive temperature.
16 emperature Resistant) that could grow at the permissive temperature.
17 ng the temperature-sensitive strain at a non-permissive temperature.
18 yeast topoisomerase II incubated at the non-permissive temperature.
19 of shift-down from the nonpermissive to the permissive temperature.
20 d from further growth by shifting to the non-permissive temperature.
21 All cells displayed enhanced growth at the permissive temperature.
22 t and slower progression into S phase at the permissive temperature.
23 strictive temperature if incorporated at the permissive temperature.
24 scherichia coli glnS strain UT172 at its non-permissive temperature.
25 ly reduced when assays were conducted at the permissive temperature.
26 temperature-sensitive FAB1 strain at the non-permissive temperature.
27 ly(A)+ RNA in nuclei when shifted to the non-permissive temperature.
28 cells accumulated uncapped mRNAs at the non-permissive temperature.
29 ells 6 h after shifting the cells to the non-permissive temperature.
30 lso display a complete increase in ploidy at permissive temperature.
31 (tsBN7) that undergoes apoptosis at the non-permissive temperature.
32 reappeared soon after switching back to the permissive temperature.
33 oxypeptidase Y and KKXX-tagged proteins at a permissive temperature.
34 na1-1, but not other mutant cells to the non-permissive temperature.
35 delay in mRNA production that occurs at the permissive temperature.
36 induced by ICE at permissive but not at non-permissive temperature.
37 l speckled distribution seen in cells at the permissive temperature.
38 us CKII, even when the cells were grown at a permissive temperature.
39 sec1 and end3 sort and mature ALP at the non-permissive temperature.
40 nt polypeptides from the ribosome at the non-permissive temperature.
41 defect in sense-codon translation at the non-permissive temperature.
42 emperature-sensitive p53, are shifted to the permissive temperature.
43 ing a splicing defect upon shift to the non- permissive temperature.
44 ransformed rat embryo fibroblasts at the non-permissive temperature.
45 d lethality to a tim10-1 yeast mutant at the permissive temperature.
46 for up to 36 h of estradiol treatment at the permissive temperature.
47 Rel-transformed cells are shifted to the non-permissive temperature.
48 eadthrough was observed in the mutant at the permissive temperature.
49 .5 degrees C followed by a shift down to the permissive temperature.
50 ut this mutation in E. coli is lethal at the permissive temperature.
51 e into Atp8p at nonpermissive but not at the permissive temperature.
52 icant activity on tRNA substrates at the non-permissive temperature.
53 profound defect in DNA synthesis at the non-permissive temperature.
54 completely inactivated upon shift to the non-permissive temperature.
55 lly affected when cells are grown at the non-permissive temperature.
56 tite genome distribution observed at the non-permissive temperature.
57 essing Cre recombinase was introduced at the permissive temperature.
58 cherichia coli results in inviability at the permissive temperature.
59 g an E. coli msbA missense mutant to the non-permissive temperature.
60 in the presence of high p53 activity at the permissive temperature.
61 lls and in dbf4 mutants incubated at the non-permissive temperature.
62 perature-sensitive (ts) mutants grown at the permissive temperature.
63 et and result in cell division arrest at non-permissive temperatures.
64 th arrest and increased subG1 phase cells at permissive temperatures.
65 rm infectious virions following downshift to permissive temperatures.
66 were defective in chromosome segregation at permissive temperatures.
67 ss defects in cell shape and budding even at permissive temperatures.
68 e shows distinct replication defects even at permissive temperatures.
69 umor suppressor protein at permissive or non-permissive temperatures.
70 on at 498 K and was then quenched to folding-permissive temperatures.
71 en the cells were grown at permissive or non-permissive temperatures.
72 equency caused by a partial defect in MMR at permissive temperatures.
73 hr period length at both the restrictive and permissive temperatures.
74 re, induced apoptosis at restrictive but not permissive temperatures.
75 nication irreversibly at previously reported permissive temperatures.
76 ort substrate Pho4 within the nucleus at non-permissive temperatures.
77 d a synergistic mRNA-decapping defect at the permissive temperatures.
78 in defective pre-rRNA processing at the non-permissive temperatures.
79 L gene allowed 2-20/32 to grow at higher non-permissive temperatures.
80 ria that could not be recovered at the lower permissive temperatures.
81 larvae of mat-1/cdc-27 mutants grown at semi-permissive temperatures.
82 ts, respectively, under restrictive, but not permissive, temperatures.
83 moderate (rsw7) or negligible (rsw4) at the permissive temperature, 19 degrees C, and pronounced at
85 synthetic flagellar assembly defects at the permissive temperature, (2) heterozygous diploid strains
86 notype in the transheterozygotes at rsw1-1's permissive temperature (21 degrees C) and full complemen
90 ants arrest in G1 and G2/M when shifted from permissive temperatures (23 degrees C) to the restrictiv
95 he His343 to Gln (H343Q) mutant grown at the permissive temperature (30 degrees C) and was severely i
96 smid pWVO1 harboring Tn9l7, in JH1005 at the permissive temperature (30 degrees C) versus that at the
100 overexpression of the wild-type (wt) p53 at permissive temperature 32 degrees C leads to growth arre
103 that at 4-6 h after shifting cells from the permissive temperature (32.5 degrees C) to the restricti
104 bserved when the cells were incubated at the permissive temperature (32.5 degrees C), indicative that
105 as shifted from 37.5 degrees C to the wt-p53-permissive temperature (32.5 degrees C), the expression
106 The tsT/AC62 cells expressed TAg at the permissive temperature (32degrees C), and the loss of TA
107 s not detectable, in cell lines grown at the permissive temperature (33 degrees C) but after 5-14 day
116 but after 5-14 days of incubation at the non-permissive temperature (39.5 degrees C), MDP protein and
119 on of a vps41tsf mutant revealed that at non-permissive temperature ALP is mislocalized while vacuola
120 ell division cycle mutant with a G2 delay at permissive temperature and a terminal, mating-proficient
121 fission yeast, seem normal in mmd1 cells at permissive temperature and after several hours at the no
122 he enzyme activity to a certain level at the permissive temperature and aggravates the negative effec
123 128, defective for checkpoint control at the permissive temperature and essential for viability at 37
124 e oxidised in erv1-ts cells grown at the non-permissive temperature and in isolated mitochondria from
126 g the mutant protein can be generated at the permissive temperature and subsequently analyzed at the
127 ants have a petite-inducing phenotype at the permissive temperature and that a kgd2Delta mutation inc
129 Our analyses of mutant embryos generated at permissive temperature and then upshifted quickly just b
130 in the heat-sensitive tfa1 mutant at the non-permissive temperature and thereby prove that TCR does o
131 the distal one-third of the flagella at the permissive temperature and this phenotype is also rescue
132 ility promoter are conditionally immortal at permissive temperatures and produce monoclonal antibodie
133 cted 6 h after shifting the cells to the non-permissive temperature, and after 12 h they were synthes
134 alytic efficiency of the enzyme to 1% at the permissive temperature, and at the nonpermissive tempera
135 t the permissive temperature than at the non-permissive temperature, and R-Ras and Src co-immunopreci
136 ates is reduced 2-7-fold in cells grown at a permissive temperature, and the level of complex sphingo
138 sitive beta' mutant for cell growth at a non-permissive temperature, and those mutant enzymes that we
139 ichia coli nusA11(ts) mutant strains, at the permissive temperature, are highly sensitive to nitrofur
140 ns missegregate a chromosome fragment at the permissive temperature, are temperature sensitive for gr
141 an be bypassed by maintaining mutants at the permissive temperature at stages commensurate with synap
142 eloped as normal fertile XX and XY adults at permissive temperatures below 20 degrees C, but at highe
145 HCF-1 is chromatin bound in tsBN67 cells at permissive temperature but dissociates from chromatin be
146 nd produces wild-type amounts of p60v-src at permissive temperatures but becomes p60v-src-resistant a
147 ar association and E2F regulation at the non-permissive temperature, but regains these properties at
148 defective for growth at 30 degrees C, a non-permissive temperature, but resumed growth and DNA synth
149 d, this defect in the OST complex at the non-permissive temperature caused also the underglycosylatio
150 ing of single-cell clonal populations to the permissive temperature caused the p53-/-mdm2-/- fibrobla
151 fter IR exposure at both the restrictive and permissive temperatures, Cdkn1/p21 was only induced by f
153 (Asp) formation in vivo by growth at the non-permissive temperature, codons for seven other amino aci
154 essential, conditional alleles grown at the permissive temperature complement the essential function
156 rain harboring a mutation of Kap121p, at the permissive temperature, confirming an essential role for
158 lly similar in magnitude to wild type at the permissive temperature despite defects in the structure
159 f eIF2 phosphorylation (Gcd- phenotype) at a permissive temperature, directly implicating eIF5-CTD in
160 dicate that aberrant tal-1 expression at the permissive temperature does not exert a proliferative ef
161 R in a heat-sensitive tfa1 mutant at the non-permissive temperature during which growth is inhibited
165 the transfected FDCP-Mix cells grown at the permissive temperature for Bcr-Abl tyrosine kinase activ
168 pre-rRNA processing was not affected at the permissive temperature for growth, but dimethylation was
171 work [3] was performed at 25 degrees C, the permissive temperature for myo2-E1, we compared cytokine
174 its wild-type parent even at 30 degrees C, a permissive temperature for the strain, and its activity
175 lso is sensitive to 38 degrees C, which is a permissive temperature for wild-type and loss-of-functio
178 served that the dnaB107(ts) mutation, at its permissive temperature, greatly stimulated deletion even
179 in ring contraction when rings isolated from permissive temperature-grown cells are incubated with AT
182 und that the interval between initiations at permissive temperature, i.e., the eclipse period, was no
183 ormed clones, and detectable only at the non-permissive temperature in a clone which was cold-sensiti
184 n 10(3)-fold reduction in replication at the permissive temperature in both mouse and human neuroblas
185 idine, which augments transmitter release at permissive temperature in csp mutants, fails to reverse
186 mperature-sensitive p53 protein (p53 val) at permissive temperature in M1-t-p53 cells results in rapi
187 m) proteins, and it is stabilized at the non-permissive temperature in mutants of the anaphase-promot
188 ested, transcription is inhibited at the non-permissive temperature in temperature-sensitive kin28 mu
189 lipopolysaccharides, accumulates at the non-permissive temperature in the inner membrane of either h
190 growth and severe delays in septation at the permissive temperature, indicating that expression of an
191 cells, under normoxic conditions, to the non-permissive temperature induced a rapid and progressive a
192 e BHK21 hamster cell line tsBN67, at the non-permissive temperature, inhibits the protein's interacti
193 allele is dnaA46; its inactivity at the non-permissive temperature is due to a specific defect in AT
194 p53 mutant, activation of p53 by shifting to permissive temperatures leads to MDM2 induction and degr
196 shifting cells from the nonpermissive to the permissive temperature) led to an increase in the tyrosi
198 f conditional top2 mutants grown at the semi-permissive temperature; most notably, a reduced fidelity
200 oncluded that degradation of DAD1 at the non-permissive temperature not only affects the stability of
201 nts harboring these alleles grew well at the permissive temperature of 20 degrees C to 25 degrees C b
202 utant cells (ssa1ts ssa2 ssa3 ssa4) from the permissive temperature of 23 degrees C to the nonpermiss
204 nized in G(1) phase with alpha-factor at the permissive temperature of 24 degrees C and then released
206 oth chloroquine and growing the cells at the permissive temperature of 27 degrees C restored expressi
208 nt wild-type (WT) RSV, even at the typically permissive temperature of 32 degrees C (growth efficienc
210 ransport to melanosomes were promoted at the permissive temperature of 32 degrees C, but not at the n
212 and morphological changes efficiently at the permissive temperature of 32.5 degrees C, but is weakly
214 s near-normal levels of RNA synthesis at the permissive temperature of 33 degrees C but is unable to
215 Once the cell culture is returned to the permissive temperature of 33 degreesC, these same cells
221 ly with POL1 and CTF4 mutations; the maximum permissive temperature of double mutants was lower than
222 Lawns of transformants were grown at the permissive temperature on kanamycin-supplemented agar an
223 tionally, growth of patient fibroblasts at a permissive temperature or with chemical chaperones incre
224 reatment with chemical chaperones, growth at permissive temperature, or inhibition of proteasomal deg
225 served in the COS-1 p53Val(135) cells at the permissive temperature, overexpression of bax, but not p
229 ion defects after just 30 minutes at the non-permissive temperature, prior to any detectable change i
231 Fluctuating temperatures that remain within permissive temperature ranges generally improve performa
232 n in five different temperature ranges, with permissive temperatures ranging from 18 degrees to 30 de
233 ing overall levels of Cdc7 by growth at semi-permissive temperature reduced activation at early and l
235 Shifting the G(2) arrested cells back to the permissive temperature resulted in a reversal of the cel
236 temperature-sensitive v-Src proteins to the permissive temperature resulted in concomitant associati
238 xhibited a drastic reduction in the range of permissive temperature, resulting in a severe lysis defe
240 Quantitative hormone binding studies at the permissive temperature revealed the presence of both hig
241 g the ts mutant grown at the restrictive and permissive temperatures revealed that whereas erythrocyt
243 or novel cDNAs which rescue yeast at the non-permissive temperature should provide a powerful approac
244 50% reduction of total protein synthesis at permissive temperatures, slows run-off of polyribosomes,
248 ell lysates showed that after 6 h at the non-permissive temperature, steady-state levels of the ribop
249 from occurring following arrest even at the permissive temperature, suggesting a role for DnaB prior
250 undergo development when it was shifted to a permissive temperature, suggesting that cells had the ca
251 lost as oligomer formation took place at the permissive temperature, suggesting that temperature sens
252 ay is specifically elevated in ycs4-1 at the permissive temperature, suggesting that the Ycs4p plays
253 o be markedly thermolabile when grown at the permissive temperature, suggesting that there was a flaw
254 ti-microtubule agent thiabendazole at a semi-permissive temperature, suggesting that TRF4/5 function
257 rmed with temperature-sensitive v-Src at the permissive temperature than at the non-permissive temper
263 altered growth rate and colony morphology at permissive temperatures; the severity of these phenotype
265 fected cells were incubated initially at the permissive temperature to allow uncoating of the viral g
266 ve Sce VMA mutations that splice only at the permissive temperatures to generate intact host proteins
267 ells were shifted from 38 degrees C (the non-permissive temperature) to 28 degrees C, at which the p5
274 n for cells that become permeabilized at non-permissive temperature was used to isolate in vitro-gene
275 utants that were also sensitive to TPCK at a permissive temperature, we isolated three tsm (TPCK-sens
276 oplasmic-nuclear movement occurs by shift to permissive temperature, we show that p53 movement is imp
277 lling forces in gpa-16(it143) embryos at the permissive temperature were attributable to GOA-1 functi
279 ound that (i) mutant virions produced at the permissive temperature were indistinguishable from wild-
281 All of the mutant proteins once folded at permissive temperature, were functional at restrictive t
282 NA synthesis when shifted to 37 degrees C, a permissive temperature, were subsequently selected.
283 and restrictive temperature, diploidizes at permissive temperature when combined with the mps1-1 mut
284 mplex was approximately 2-fold slower at non-permissive temperatures when compared with the release o
286 23 into export-competent heterodimers at the permissive temperature while concurrently blocking their
287 to the vitality of cdc13-1 strains grown at permissive temperatures, while Din7, Msh2, Nuc1, Rad2, R
288 sitive allele sir3-8 has an eso phenotype at permissive temperature, yet acts as a null allele at res
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