ライフサイエンスコーパス: temperature-sensitive

1 e modification of OsFIE1 were observed to be temperature sensitive.

2 aeruginosa chronic infection isolate 2192 is temperature sensitive.

3 morphic alleles, and another two mutants are temperature sensitive.

4 other key biochemical processes appear more temperature sensitive.

5 g315Leu, indicating that these mutations are temperature sensitive.

6 development rate, and vector competence are temperature sensitive.

7 renders yeast cells rapamycin resistant and temperature sensitive.

8 pathogenic Cx31 mutants are un/misfolded and temperature sensitive.

9 136 kJ mol(-1), HMF formation being the most temperature sensitive.

10 The mutant phenotype is also temperature-sensitive.

11 We allowed all five steps in the cycle to be temperature-sensitive.

12 dization processes, which are expected to be temperature-sensitive.

13 ed (CPD) versions of RSV were attenuated and temperature-sensitive.

14 Subsequently, 10 lethal, 1 severely temperature-sensitive, 2 quasi-infectious, and 3 wild ty

15 The concept utilizes temperature-sensitive absorption of a suitable solvent f

16 ase A (ACA) with SQ22536 and incubation of a temperature-sensitive ACA mutant at the restrictive temp

17 Mutants screened for temperature-sensitive activity had mutations clustered a

18 Temperature-sensitive aep3 mutants are selectively block

19 Based on these data, we suggest that temperature-sensitive age 0 bass constrain the upstream

20 lement the growth of Escherichia coli with a temperature-sensitive AK identified functional proteins

21 We isolated a temperature-sensitive allele (rsw12) of the gene in a sc

22 in S. pombe We show that the lethality of a temperature-sensitive allele of eso1 (eso1-H17) is due t

23 A temperature-sensitive allele of the EGFR ligand Spitz (S

24 Utilizing a temperature-sensitive allele, spt6-1004, we show that Sp

25 d a robust system that serves the purpose of temperature-sensitive alleles in other model organisms,

26 We isolated temperature-sensitive alleles of all three and investiga

27 P417L or P417S as the only copy of Ssa were temperature sensitive and exhibited defects in Ssa1-depe

28 stabilized vaccine candidate was moderately temperature sensitive and had a level of restriction in

29 g evidence that mutations at these sites are temperature sensitive and highlighting the importance of

30 tures at low temperature, as inactivation of temperature-sensitive and cold-sensitive ded1 mutants ga

31 es were poorly tolerated, conferring extreme temperature-sensitive and lethal phenotypes.

32 The ambisense viruses were temperature sensitive, and NSs was shown to localize to

33 ver, Ca(2+) dissociation from TnC was not as temperature-sensitive as cross-bridge detachment.

34 are nonviable except for P2(Min), a variant temperature-sensitive at 33 and 39.5 degrees C.

35 nuclear migration in unc-84 null animals is temperature sensitive; at 25 degrees migration fails in

36 function of inner hair cell ribbon synapses (temperature-sensitive auditory neuropathy) or auditory n

37 A mutant screen with an Arabidopsis thaliana temperature-sensitive autoimmune mutant bonzai1 revealed

38 of TRPC5 in 129S1/SvImJ mice resulted in no temperature-sensitive behavioral changes, TRPM8 and/or o

39 omyces cerevisiae that allowed a recovery of temperature-sensitive but respiratory competent zim17 mu

40 1 neurons) were artificially activated via a temperature-sensitive cation channel (dTRPA1), males fol

41 lation of the DPM neurons by activation of a temperature-sensitive cation channel between acquisition

42 Therefore, we investigated if TRPV4, a temperature-sensitive cation channel, plays an important

43 er release, or activated them with dTrpA1, a temperature-sensitive cation channel.

44 anilloid 1 and 4 genes (trpv1, trpv4) encode temperature-sensitive cation channels hypothesized to me

45 Temperature-sensitive cdc1(ts) mutants are reported to s

46 lement a growth defect in yeast containing a temperature-sensitive Cdc7 mutant.

47 rkably, deletion of mdbA results in a severe temperature-sensitive cell division phenotype.

48 utants were viable at 32 degrees C, showed a temperature-sensitive cell entry defect, and, after prot

49 tied to enhanced chromosome instability and temperature-sensitive cell growth.

50 By generating clones of cells that carry a temperature-sensitive cell-lethal mutation, we condition

51 We decorated a modified temperature-sensitive channel, TRPV1, with antibody-coat

52 formed temperature-insensitive isoforms into temperature-sensitive channels and significantly perturb

53 olecular basis of the thermal sensitivity of temperature-sensitive channels appears to arise from a s

54 at may underlie the function of a variety of temperature-sensitive channels.

55 This study reports that metastable and temperature-sensitive chemically exfoliated MoS2 (ce-MoS

56 the Fe-S cluster domain, which renders cells temperature sensitive, closely mimics the global defects

57 he six internal protein gene segments of the temperature sensitive, cold-adapted (ca) A/Ann Arbor/60

58 es low surfactant emulsion formulations with temperature-sensitive compounds, is scalable to industri

59 In a screen for temperature-sensitive conditional seizure mutants, we id

60 ility and conduction that safeguards against temperature-sensitive conduction failure.

61 ites for transport inhibitors have specific, temperature-sensitive conformations.

62 Here we investigated the critical period for temperature-sensitive courtship rate plasticity in the b

63 We deployed temperature-sensitive crayons throughout the burn site,

64 at 4 degrees C displayed ADP-insensitive but temperature-sensitive decay.

65 ydomonas reinhardtii mutant (dhc1b-3) with a temperature-sensitive defect in DHC1b, enabling inducibl

66 This is the first time that a temperature-sensitive defect in O-antigen production has

67 exploit Varshavsky's N-end rule to create a temperature-sensitive degron form of avian Orc6.

68 d against deattenuation, specifically, a non-temperature-sensitive deletion mutation involving 6 nucl

69 two orders of magnitude, owing to the highly temperature-sensitive diffusion between aggregated DNA-c

70 ell extravasation within tumors treated with temperature-sensitive doxorubicin and ultrasound hyperth

71 Previous studies with the temperature-sensitive dpb11-1 allele, truncated at amino

72 for image-guided drug delivery in bone with temperature-sensitive drug carriers.

73 We attached the temperature sensitive dye-Rhodamine B (RhB), whose emiss

74 Temperature-sensitive dynamin (shi(ts1)) mutations in Dr

75 TEs of >600 mRNAs, whereas inactivation of a temperature-sensitive eIF4A variant encoded by tif1-A79V

76 L-1 fragment, show an incompletely penetrant temperature-sensitive embryonic lethality.

77 sion in hamster (ldlF) cells depleted of the temperature-sensitive epsilon-COP subunit.

78 acid changes is able to rescue growth of the temperature-sensitive Escherichia coli glnS strain UT172

79 sential gene deletion mutants, as well as in temperature-sensitive essential gene mutants.

80 , the observation of striking differences in temperature-sensitive expressions, testicular physiology

81 tional mutation in the cdkg1 gene leads to a temperature-sensitive failure of meiosis in late Zygoten

82 mito-nuclear incompatibility causes a severe temperature-sensitive female infertility.

83 we screened for extragenic suppressors of a temperature-sensitive fission yeast strain mutated in th

84 ne conductance regulator (CFTR) results in a temperature-sensitive folding defect that impairs protei

85 on human CFTR, the F508del mutation caused a temperature-sensitive folding defect, which disrupted ov

86 molecular analyses identified p.R3277C as a temperature-sensitive folding/trafficking mutant, and le

87 arly interesting as Asp-302 is the site of a temperature-sensitive-folding mutation.

88 In the ftsZ84 strain, which is temperature sensitive for filamentation due to a mutatio

89 dbp5-R256D/R259D nup42Delta double mutant is temperature-sensitive for mRNA export.

90 rprisingly, the recombinant CPD viruses were temperature-sensitive for replication in vitro (level of

91 BSI: 5 have been previously described in non-temperature-sensitive forms of congenital ichthyosis (Ar

92 ly time points following treatment with this temperature sensitive formulation.

93 ow an elongated cell division phenotype in a temperature-sensitive FtsA background, demonstrating the

94 rA and DrrB proteins expressed together in a temperature-sensitive ftsH mutant strain of Escherichia

95 Here, we combined the Gal4/UAS system and a temperature-sensitive Gal80 molecule to induce RNAi-medi

96 The physicochemical underpinnings of this temperature-sensitive gating have proven difficult to pa

97 onally complement the S. cerevisiae ScAlg2-1 temperature sensitive growth phenotype.

98 10, Saccharomyces cerevisiae cells exhibit a temperature-sensitive growth defect under oxidative grow

99 biosynthesis mutant (rer2) complemented the temperature-sensitive growth defect.

100 sensitivity to the herbicides and rescuing a temperature-sensitive growth defect.

101 We identified a temperature-sensitive growth mutant, FV-P6, which irreve

102 hosphomimetic cse4-4SD mutant suppresses the temperature-sensitive growth of ipl1-2 and Ipl1 substrat

103 Furthermore, the temperature-sensitive growth of ypk1(ts) ypk2 cells is s

104 rms based on their ability to complement the temperature-sensitive growth phenotype of Escherichia co

105 BI in the context of a bcmd-RGFlu carrying a temperature-sensitive H1N1 virus resulted in protection

106 , we report the generation of a recombinant, temperature-sensitive H3N8 CIV as a live-attenuated infl

107 10-bp gene that codes for a homologue of the temperature-sensitive hemagglutinin (Tsh) autotransporte

108 ers of photo-crosslinkable copolymers with a temperature-sensitive hydrogel as the middle layer.

109 Temperature-sensitive hydrogel polymers are utilized as

110 le copy, including constructs expressing the temperature-sensitive inactivator of neuronal function S

111 arge peptide pool, subsequently refined by a temperature-sensitive induced-fit mechanism to retain th

112 n of Escherichia coli, which is dependent on temperature-sensitive interdomain unfolding and cis-tran

113 or 555-conjugated human transferrin revealed temperature-sensitive internalisation indicating the BBB

114 The biophysical basis of temperature-sensitive ion channel gating has been a toug

115 ce of modular temperature-sensing domains in temperature-sensitive ion channels.

116 For Cu-azurin, a temperature-sensitive IR mode involving Cu(II)-His vibra

117 In yeast, a temperature-sensitive L4,5 mutation (E467A) disrupts bid

118 Specifically, we used a temperature-sensitive lactose repressor mutant that lose

119 as better than that conferred by the current temperature-sensitive LAIV.

120 We isolated a temperature-sensitive lethal mtDNA allele, mt:CoI(T300I)

121 here the isolation and characterization of a temperature-sensitive lethal mutation, bamAE373K, which

122 all of that chromosome's essential genes by temperature-sensitive lethal mutations.

123 ted recessive lethality, with one displaying temperature-sensitive lethality.

124 duced levels of Mitf activity using an mitfa temperature-sensitive line results in a dramatic increas

125 diated nanoparticles were quantified using a temperature sensitive lipid-based assay and compared to

126 oteridol was enhanced in tumors treated with temperature-sensitive liposomal doxorubicin and ultrasou

127 Temperature-sensitive liposomal formulations of chemothe

128 Clinical-grade doxorubicin encapsulated low temperature sensitive liposomes (LTSLs) were combined wi

129 on-thermosensitive liposomes (NTSLs) and low temperature sensitive liposomes (LTSLs).

130 ted whether enhanced therapeutic activity of temperature sensitive liposomes (TSL) could be obtained

131 (Free-DOX), Stealth liposomes (Stealth-DOX), temperature sensitive liposomes (TSL) with intra-vascula

132 (CuDox) in the core of lysolipid-containing temperature-sensitive liposomes (LTSLs).

133 doxorubicin (CuDox) cargo in lysolipid-based temperature-sensitive liposomes (LTSLs).

134 design principles around the construction of temperature-sensitive liposomes (TSL) and their use in c

135 n, hyperthermia-triggered drug delivery from temperature-sensitive liposomes (TSLs), and combinations

136 Temperature-sensitive liposomes are an especially attrac

137 Further, doxorubicin delivery by temperature-sensitive liposomes can reliably cure local

138 Here, we explore the application of temperature-sensitive liposomes that have been formulate

139 behavior, and clinical potential of various temperature-sensitive liposomes, as well as the various

140 r and doxorubicin (CuDox) was created within temperature-sensitive liposomes.

141 ne expression on virus pathogenesis, using a temperature-sensitive, live-attenuated 2009 pandemic H1N

142 Mutations in rumi result in a temperature-sensitive loss of Notch signaling in Drosoph

143 Mutations in Drosophila rumi result in a temperature-sensitive loss of Notch signaling.

144 eal of work has been dedicated to developing temperature sensitive macromolecules that can be crafted

145 ted nuclei regulate their volume in a highly temperature-sensitive manner.

146 n-coding gene segments from the cold-adapted temperature-sensitive master donor virus A/Ann Arbor/6/1

147 Thermal stability of channel function and temperature-sensitive maturation of the mutant protein a

148 Mathematical modeling further supports a temperature-sensitive mechanism to protect a subset of t

149 ser beam at-a-distance was found to activate temperature-sensitive membrane receptors, resulting in a

150 We then validated and narrowed our list of temperature-sensitive microbes by comparing the results

151 Dual pH and temperature sensitive microgel-based etalons were fabric

152 rticular, the Northern Hemisphere network of temperature-sensitive millennial tree-ring chronologies,

153 eveloped plasmid constructs that overexpress temperature sensitive miRNAs: miR-34a, miR-451, and miR-

154 The fabrication makes use of the temperature-sensitive miscibility of hydrocarbon, silico

155 pen reading frames (ORFs) (C(Delta170)) or a temperature-sensitive missense mutation in the L ORF (L(

156 Here, we use a temperature-sensitive mitf zebrafish mutant to condition

157 Selection drove complete replacement of the temperature-sensitive mitochondrial genome by a wild-typ

158 may serve as the basis for developing other temperature-sensitive models for the study of recessive

159 Inactivation of E1 in E1 temperature-sensitive mouse embryonic fibroblast (MEF) c

160 edimentation of mitochondrial ribosomes from temperature-sensitive mtg3 mutants grown at the permissi

161 Using a temperature sensitive mutant of the p53 (Trp53) gene, we

162 spatial and temporal control of Filamenting temperature sensitive mutant Z (FtsZ) Z-ring formation i

163 ees C with those in the widely used pat1-114 temperature-sensitive mutant at 34 degrees C, a temperat

164 s to complement fission yeast profilin SpPRF temperature-sensitive mutant cdc3-124 cells.

165 Indeed, in pkh-ts temperature-sensitive mutant cells and in cells expressi

166 tivity on the functional conformation of the temperature-sensitive mutant cystic fibrosis channel (F5

167 Genetic analysis of the outer core in a temperature-sensitive mutant demonstrated this core func

168 The dnaN159 allele encodes a temperature-sensitive mutant form of the beta sliding cl

169 ROS is not observed in cells infected with a temperature-sensitive mutant of Ad2, ts1, which is defec

170 ream region of highly transcribed genes in a temperature-sensitive mutant of Clp1 at elevated tempera

171 Using a temperature-sensitive mutant of Pkc1p revealed a high le

172 Use of a temperature-sensitive mutant of ubiquitin-conjugating en

173 e characterized the growth of a B1-deficient temperature-sensitive mutant virus (Cts2 virus) in U2OS

174 actor for virion morphogenesis by studying a temperature-sensitive mutant with a lesion in A6.

175 direct inhibitor of the E. coli filamenting temperature-sensitive mutant Z division protein.

176 eukaryotic tubulin and bacterial filamenting temperature-sensitive mutant Z protein (FtsZ) polymers.

177 thesized Gp0.4 binds to purified filamenting temperature-sensitive mutant Z protein and directly inhi

178 Utilizing temperature sensitive mutants of tor2 and tap42, we exam

179 The loss of Srp1 is lethal, although several temperature-sensitive mutants have been described.

180 Temperature-sensitive mutants in both pUL25 and pUL36 do

181 We show that rescue of temperature-sensitive mutants in parE and parC (encoding

182 In the nematode Caenorhabditis elegans, temperature-sensitive mutants of emb-1 arrest as one-cel

183 Here, using temperature-sensitive mutants of trz1 and trz2, we provi

184 Temperature-sensitive mutants were defective in RNA repl

185 Characterization of two temperature-sensitive mutants, nse5-ts1 and nse5-ts2, de

186 ased temperature imposed selection against a temperature-sensitive mutation affecting cytochrome oxid

187 A temperature-sensitive mutation in TFC3 that weakens DNA

188 the flagella of fla10-1 cells, which carry a temperature-sensitive mutation in the anterograde motor

189 Viruses carrying temperature-sensitive mutations are good candidates for

190 otypes, multiple cold-adaptive mutations and temperature-sensitive mutations arose.

191 ypomorphic mutations that behave as apparent temperature-sensitive mutations due to the additive effe

192 f the UTRs together with the introduction of temperature-sensitive mutations in both the nucleocapsid

193 subgenic M polypeptides, by incorporation of temperature-sensitive mutations in the N and L genes, an

194 hing suit ichthyosis is caused by recessive, temperature-sensitive mutations in the transglutaminase-

195 onditional loss-of-function reagents such as temperature-sensitive mutations is that the resulting ph

196 encoding the NSs protein and introduction of temperature-sensitive mutations, in the design of attenu

197 To take full advantage of fast-acting temperature-sensitive mutations, thermal control must be

198 n also suppress aurora protein kinase, ipl1, temperature-sensitive mutations.

199 Temperature-sensitive mzt1 mutants display varying degre

200 lobal transcriptome analysis reveals a major temperature-sensitive node of SA signalling, impacting

201 Specifically, we used a temperature-sensitive Notch allele to drive germ-line st

202 ctionally complement the defect in the yeast temperature-sensitive nucleoporin mutant nup159.

203 tion mutant of stO1, we demonstrate that the temperature-sensitive O-antigen production defect in 219

204 RFP-GRalpha translocation was temperature sensitive, occurring at 37 degrees C but not

205 tations at key residues of this site lead to temperature-sensitive or null phenotypes.

206 varian tumor cells expressed a heterozygous, temperature-sensitive p53(V172F) mutation, which reduced

207 ecreased life span, locomotor abnormalities, temperature-sensitive paralysis, and defects of neuromus

208 e find that the drug-metal complex formed in temperature-sensitive particles can be internalized by c

209 der to design protocols for the use of these temperature-sensitive particles in cancer treatment, the

210 is required to inactivate the commonly used temperature-sensitive Pat1 kinase mutant (pat1-114).

211 the incubation temperature during a critical temperature sensitive period (TSP) determines sexual fat

212 of female-biased gene expression in the post-temperature sensitive period gonads.

213 t in formation of noncytopathic viruses or a temperature sensitive phenotype cluster at the nsP2/nsP3

214 specifically to determine if the attenuating temperature-sensitive phenotype can revert and, if so, t

215 type mammalian PRDX4 into the ER rescued the temperature-sensitive phenotype of an ero1 yeast mutatio

216 n allele-specific manner, (b) suppresses the temperature-sensitive phenotype of both groES and groEL

217 Deletion of DIA2 partially suppresses the temperature-sensitive phenotype of tom1 mutants.

218 ns and PVR-Tg21 transgenic mice, loss of the temperature-sensitive phenotype, and the capacity for su

219 ng the H3N2 NS1-V194I protein demonstrated a temperature-sensitive phenotype, further attenuating the

220 sequences partially suppresses the bdf1Delta temperature-sensitive phenotype, suggesting that maintai

221 e wild-type BUNV, resulted in a virus with a temperature-sensitive phenotype.

222 t, we found that all three segments encode a temperature-sensitive phenotype.

223 phenotype, and mutants A49, A52 and A53 had temperature-sensitive phenotypes.

224 sect pest, Drosophila suzukii, by creating a temperature-sensitive point mutation in the sex-determin

225 e metal-free purely organic phosphors in the temperature-sensitive polymer matrix.

226 Using E. coli harboring a temperature-sensitive polymerase I allele, we establishe

227 ted with the use of lysolipids and synthetic temperature-sensitive polymers.

228 temperatures above 30 degrees C suggesting a temperature-sensitive process that slows impulse propaga

229 change is likely to increase the rate of the temperature-sensitive processes that decompose stored or

230 s can exploit degenerate relationships among temperature-sensitive processes to achieve robust functi

231 We show that R1108C and R1129C are both temperature-sensitive processing mutants that engage the

232 ccharide-based systems with inherent pH- and temperature-sensitive properties, as well as enzyme-clea

233 We crossed any1 with the temperature-sensitive radial swelling1-1 (rsw1-1) CesA1

234 A temperature-sensitive receptor prevents mosquitoes from

235 riple charged-to-alanine mutation produced a temperature-sensitive replication phenotype with no dete

236 Temperature-sensitive rho1 mutants (rho1(ts)) are hypers

237 A temperature-sensitive secA mutant of E. coli was strongl

238 n SCN1A mutation in a child with early-onset temperature-sensitive seizures.

239 ationale for understanding the phenotypes of temperature-sensitive Sgt1 mutants and for linking Skp1-

240 In Drosophila melanogaster, temperature-sensitive silencers and activators are widel

241 o alpine areas should not be based solely on temperature-sensitive, site-specific upper-treeline stud

242 emperature window, which correlates with the temperature-sensitive size transition of the molecular a

243 rate that the phosphoswitch is intrinsically temperature sensitive, slowing down PER2 degradation as

244 The ability of these forests to buffer temperature-sensitive species from climate warming will

245 buffering, and subsequent ability to retain temperature-sensitive species under climate change.

246 Such changes may threaten temperature-sensitive species, causing local extinctions

247 have implications for the interpretation of temperature-sensitive, speleothem climate proxies such a

248 Accordingly, we find that previously known temperature-sensitive splicing mutants become lethal in

249 ay not be necessary to include an additional temperature-sensitive step.

250 anifested by their inability to complement a temperature-sensitive strain of FtsW.

251 DX3X complements the growth defect in a ded1 temperature-sensitive strain of Schizosaccharomyces pomb

252 Starting with a conditional strain (i.e., a temperature-sensitive strain), we describe how to effici

253 AF-C phosphorylation from wild-type and CKII temperature-sensitive strains (cka1Delta cka2-8) showed

254 d MDCK cells is defective, possibly due to a temperature-sensitive structural or functional property

255 cessing of high-performance transistors onto temperature sensitive substrates such as plastic.

256 ze the conserved GII.4 blockade epitope were temperature sensitive, suggesting that particle conforma

257 E. coli DeltafliL cells also exhibit temperature-sensitive swarming.

258 nt temperature window which coincides with a temperature-sensitive switch in seed dormancy state.

259 d-site mutation that enhances lethality of a temperature sensitive tbx-2 mutant and show that this mu

260 Increased awareness of temperature-sensitive TGM1 genotypes should aid in genet

261 ge upstream of the second AAA+ domain in the temperature sensitive TgNoAP1 allele leads to conditiona

262 d that the rate of dissociation was far more temperature-sensitive than the rates of both association

263 ral of these TRP channels on macrophages are temperature sensitive, they may comprise the link for hy

264 monstrate that human alpha2C-AR has a unique temperature-sensitive traffic pattern within the G prote

265 Temperature-sensitive transient receptor potential (TRP)

266 ilic supramolecular assemblies with a unique temperature-sensitive transition have been investigated.

267 e systems are known to exhibit a macroscopic temperature-sensitive transition, where the assembly pha

268 dence of the coupling between gating and the temperature-sensitive transitions, as well as the DeltaH

269 tivity to drive channel activation, allowing temperature-sensitive TRP channels to function as polymo

270 Here, we determined that a temperature sensitive (ts) PSD1 allele is autocatalytica

271 tates are derived from a human virus that is temperature sensitive (ts), characterized by restricted

272 cted mutagenesis, we have discovered 12 taf2 temperature-sensitive (ts) alleles.

273 ive attenuated influenza vaccines (LAIVs) on temperature-sensitive (ts) backbones derived from animal

274 ising live-attenuated vaccine candidate is a temperature-sensitive (ts) cDNA-derived virus named rA2c

275 and yielded variants with wild-type (wt) or temperature-sensitive (ts) growth phenotypes or had a le

276 The temperature-sensitive (ts) mutant Dts57, which was gener

277 The use of a temperature-sensitive (TS) mutant of Cns1p in yeast reve

278 Four rotavirus SA11 temperature-sensitive (ts) mutants and seven rotavirus R

279 Temperature-sensitive (ts) mutants of simian rotavirus (

280 atitis virus (MHV) nsp5, we identified a new temperature-sensitive (ts) mutation in D2 of nsp5 (Ser13

281 Conditional temperature-sensitive (ts) mutations are important reage

282 have shown previously that incorporation of temperature-sensitive (ts) mutations into the PB1 and PB

283 is exquisitely bleach-sensitive, displays a temperature-sensitive (ts) phenotype during aerobic grow

284 ng the H3N2 NS1-V194I protein demonstrated a temperature-sensitive (ts) phenotype, providing a most l

285 hal mutants, bearing cold-sensitive (cs) and temperature-sensitive (ts) point mutations, were more am

286 n Mediator integrity is compromised in med17 temperature-sensitive (ts) yeast, demonstrating the modu

287 This mutation conferred temperature-sensitive uncoordination in a gain-of-functi

288 Alternatives to the widely used but highly temperature-sensitive uzu1.a allele of HvBRI1 represent

289 the activation segment of PINK1 uncovered a temperature-sensitive variant of PINK1 (tsPINK1).

290 nents and the rationale behind the design of temperature-sensitive vesicle systems, as well as the cr

291 Using a temperature-sensitive viral glycoprotein folding mutant,

292 Here, we isolated a temperature-sensitive virescent (tsv) mutant that is ext

293 Rhodopsin (RH1), the temperature-sensitive visual pigment mediating dim-light

294 gnificantly perturbed temperature sensing in temperature-sensitive wild-type channels.

295 the cpSRP receptor, chloroplast filamentous temperature-sensitive Y (cpFtsY).

296 ruction and characterization of a useful new temperature-sensitive YRA1 allele (R107A/F126A).

297 is specified by placement of the Filamentous temperature sensitive Z (FtsZ) ring, and the Min system

298 The cytoskeletal Filamenting temperature-sensitive Z (FtsZ) ring is critical for cell

299 acterial cytoskeletal protein FtsZ (filament temperature-sensitive Z) formed on a mica surface.

300 FtsZ (filamentation temperature-sensitive Z) is the bacterial homolog of tub