ライフサイエンスコーパス: temperature sensitivity

1 cation involves several steps with different temperature sensitivity.

2 C7 overexpression induced cell death or ipl1 temperature sensitivity.

3 g to a 7-fold improvement in the NV center's temperature sensitivity.

4 s, in contrast, the pore domain lacks robust temperature sensitivity.

5 oligodeoxynucleotide, blocked tumor-induced temperature sensitivity.

6 ctivation provides a mechanism for enhancing temperature sensitivity.

7 modalities, including touch, pain, itch, and temperature sensitivity.

8 ted with seed priming effects on germination temperature sensitivity.

9 rise to the large entropy that defines high temperature sensitivity.

10 ycle checkpoint activation, and, ultimately, temperature sensitivity.

11 ,3-glucan synthesis and suppresses pgs1Delta temperature sensitivity.

12 the reductions in base respiration and FCO2 -temperature sensitivity.

13 udied, mitigates nearly all of the estimated temperature sensitivity.

14 while mutations in the C-terminus conferred temperature sensitivity.

15 on, into the dnaX(Ts) mutant exacerbated its temperature sensitivity.

16 the supD allele in this strain had lost its temperature sensitivity.

17 f Elp3 confer typical elp phenotypes such as temperature sensitivity.

18 e 5'-untranslated region were sufficient for temperature sensitivity.

19 ss TRPV1 orthologs with dramatically reduced temperature sensitivity.

20 mbrane, reduced lipid droplet formation, and temperature sensitivity.

21 reveals that the channel can have a dynamic temperature sensitivity.

22 ies accounts for interspecific difference in temperature sensitivity.

23 by reduced enzymatic activity and increased temperature sensitivity.

24 including stress shielding, palpability and temperature sensitivity.

25 g that the HA and NA influence the degree of temperature sensitivity.

26 Ms may have more accurately represented crop temperature sensitivities.

27 istribution simultaneously with a comparable temperature sensitivity (0.2 K) to that of existing conv

28 ved residues resulted in loss-of-function or temperature sensitivity, accompanied by telomere shorten

29 Using isogenic strains that carry a temperature sensitivity allele of the gene that encodes

30 riguing phenotypes as cell division defects, temperature sensitivity, altered membrane lipid composit

31 Viral multiplication and temperature sensitivity analyses in avian and mosquito c

32 suppressors of muk mutants: they suppressed temperature sensitivity and anucleate cell production of

33 s was constructed and demonstrated increased temperature sensitivity and attenuation relative to eith

34 eptor potential channels display outstanding temperature sensitivity and can be directly gated by low

35 specific high copy suppressor of cdc28(CST) temperature sensitivity and chromosome instability.

36 l that elevated levels of PCNA rescue pds5-1 temperature sensitivity and cohesion defects, but do not

37 didates exhibited the in vitro phenotypes of temperature sensitivity and cold adaptation and were res

38 pared Pdot-RhB nanoparticle showed excellent temperature sensitivity and high brightness because it t

39 t for cellular function, as we find that the temperature sensitivity and histone H2B deubiquitination

40 opic expression of Mge1p also suppressed the temperature sensitivity and initiation defect conferred

41 ure dependence of Rsoil by assuming constant temperature sensitivity and linearly interpolating refer

42 idase, as a high copy suppressor of both the temperature sensitivity and precocious sister dissociati

43 kened cell wall, including sorbitol-remedial temperature sensitivity and sensitivities to calcofluor

44 IG4 in vac7Delta mutant cells suppresses the temperature sensitivity and vacuolar morphology defects,

45 apacity (DeltaCp), can determine a channel's temperature sensitivity and whether it is activated by c

46 loci in mukB cells, despite suppressing the temperature-sensitivity and production of anucleate cell

47 dihydroxyacetone phosphate and polymixin B, temperature sensitivity, and ability to be activated by

48 s characterized by incomplete cell division, temperature sensitivity, and altered phospholipid levels

49 th single copy Ser(301) homozygotes, reduced temperature sensitivity, and altered RNA editing associa

50 standing of the sensory modalities of touch, temperature sensitivity, and pain.

51 mbination with nup1Delta, suppress nup1Delta temperature sensitivity, and partially suppress the nucl

52 mposition, causing lower observed 'apparent' temperature sensitivity, and these constraints may, them

53 e sensitivity, two mutants exhibited partial temperature sensitivity, and two mutants formed no plaqu

54 RESs, established that the IRES strength and temperature sensitivity are mediated by the ribosome bin

55 olecular mechanism giving rise to their high temperature sensitivity are not fully understood.

56 dues in the rat alpha2C-AR restored the same temperature sensitivity as in the human receptor.

57 This second step exhibits remarkable temperature sensitivity, as illustrated by numerous nonc

58 akdown in streams and rivers to quantify its temperature sensitivity, as measured by the activation e

59 m GG-actin is cold-sensitive, reflecting the temperature sensitivity associated with mutations that d

60 ur at 67.0 +/- 1.2 degrees C and the maximum temperature sensitivity at 41.4 +/- 0.7 degrees C from M

61 a number of intriguing phenotypes, including temperature sensitivity at 42 degrees C, altered membran

62 polymorphic phenotypic effects on sex ratio, temperature sensitivity, behavior, and fitness.

63 nteraction, showing significant variation in temperature sensitivity between months.

64 with an artificial pore turret sequence lose temperature sensitivity but maintain normal ligand respo

65 ower earliest in the spring have the highest temperature sensitivities, but this trend was not reflec

66 expression of cut15 partially suppresses the temperature sensitivity, but not the mitotic delay in im

67 we generated cdc31 mutations chosen only for temperature sensitivity, but otherwise unbiased as to ph

68 on, whereas binding of vanilloids influences temperature-sensitivity by largely affecting the open/cl

69 Furthermore, their temperature sensitivity can be highly dynamic and use-de

70 the levels in wild-type cells and the stu1-5 temperature sensitivity can be rescued by additional cop

71 Thus geographic variation in body temperature sensitivity can modulate species' experience

72 identified as a multicopy suppressor of the temperature sensitivity caused by deletion of the genes

73 e C-terminal activator of HSF and rescue the temperature sensitivity caused by its deletion.

74 ,634 plant species using a common measure of temperature sensitivity (change in days per degree Celsi

75 P2, but found a lack of the strong intrinsic temperature sensitivity common to other thermosensitive

76 ed potassium (Kv) channels also exhibit high temperature sensitivity comparable to that of TRPV1, whi

77 All depths responded to warming with similar temperature sensitivities, driven by decomposition of de

78 hly damped volume fluctuations and their low temperature sensitivity, echo that PLFE liposomes are ri

79 rtial loss-of-function mutant suppressed the temperature sensitivity, endocytic phenotypes, and actin

80 t differ in autologous serum neutralization, temperature sensitivity, entry kinetics, intrinsic infec

81 without symbionts reflects local SSTs with a temperature sensitivity equivalent to that of laboratory

82 he United States, more than the conventional temperature sensitivity estimated from T(mean).

83 trosylation of the mutant RyR1 increases its temperature sensitivity for activation, producing muscle

84 d more than a decade ago was the same as the temperature sensitivity for carbon fixed less than 10 y

85 s similar to that reported for E. coli, with temperature sensitivity for growth and enhanced sensitiv

86 exhibits hypersensitivity to paclitaxel and temperature sensitivity for growth.

87 A single point mutation in gene 5 confers temperature sensitivity for phage growth.

88 sition was not affected, suggesting that the temperature sensitivity for resistant organic matter poo

89 We find, however, that the temperature sensitivity for SOM decomposition was not af

90 Along with temperature sensitivity found in the olfactory system of

91 easurements and rewarming distinguished true temperature sensitivity from amplitude reduction due to

92 Three phenotypes of the cdc31 mutants, temperature sensitivity, G2/M arrest, and cell lysis, we

93 The dnaK mutant exhibited temperature sensitivity, grew more slowly than C. diffic

94 ts do not exhibit mucoidy, phage resistance, temperature sensitivity, growth rate defects, or antibio

95 in the yeast homologue SEC9 also results in temperature sensitivity, implying a conserved role for t

96 inished stress response validates reports of temperature sensitivity in B. aphidicola and suggests th

97 attenuation markers of small plaque size and temperature sensitivity in LLC-MK(2) cells, less efficie

98 attenuation, including small plaque size and temperature sensitivity in LLC-MK(2) cells, limited repl

99 Moreover, the neurons exhibited intrinsic temperature sensitivity in patch-clamping experiments, p

100 Interestingly, the rescue of temperature sensitivity in strains having both pif1-m2 a

101 vation and found that TRPM3 exhibited slight temperature sensitivity in the bilayers.

102 lly, residue 310 modulated antibody blockade temperature sensitivity in the tested strains.

103 The mechanism that underlies the temperature sensitivity in thermo-transient receptor pot

104 1,2-dioxygenase, previously found to convey temperature sensitivity in vivo because of a methionine-

105 electivity, voltage-dependent gating, strong temperature sensitivity, inhibition by Zn(2+), and gatin

106 We find that variability in CO2 and temperature sensitivity is attributable, in part, to the

107 Temperature sensitivity is evident in multiple periods o

108 Therefore, high temperature sensitivity is intrinsic to both TRP and Kv

109 This temperature sensitivity is remarkable considering that t

110 osphatidylinositol (GPI) precursors, and its temperature sensitivity is suppressed differentially by

111 onors, demonstrating altered cell integrity, temperature sensitivity, lack of growth in an animal mod

112 e impaired HA acid and thermal stability and temperature sensitivity likely contributed to the restri

113 its thermosensory system exhibits exquisite temperature sensitivity, long-term plasticity, and the a

114 Using a tumor-induced temperature sensitivity model, we showed that in vivo ad

115 nsation defect, but importantly, neither the temperature sensitivity nor cohesion defects exhibited b

116 h1Delta nem1Delta mutant phenotypes, such as temperature sensitivity, nuclear/endoplasmic reticulum m

117 nction, explaining the marked differences in temperature sensitivity observed between recombinant and

118 The rise in air temperature suggested by the temperature sensitivities of glaciers in cold regions is

119 pect to MAT by counterbalancing the apparent temperature sensitivities of the component processes.

120 The resonators exhibit temperature sensitivity of -1.8 GHz K(-1) and can be con

121 ce yield loss under warming, with an average temperature sensitivity of -5.2 +/- 1.4% K(-1).

122 The temperature sensitivity of 22 fluorescent dyes was asses

123 r, only CDC37 was capable of suppressing the temperature sensitivity of a cka2-13 strain, implying th

124 sensitivity and the ability to suppress the temperature sensitivity of a degP null mutation.

125 solated as a cDNA capable of suppressing the temperature sensitivity of a Saccharomyces cerevisiae cd

126 VRK1 can complement the temperature sensitivity of a vaccinia B1 mutant, implyin

127 wall defects of pgs1Delta and suppressed the temperature sensitivity of all CL-deficient mutants.

128 The definition of Q10 is a measure of the temperature sensitivity of an enzymatic reaction rate or

129 es the spindle checkpoint and suppresses the temperature sensitivity of an ipl1-2 mutant.

130 Temperature sensitivity of anaerobic carbon mineralizati

131 This study characterizes the temperature sensitivity of Arabidopsis using a chlorophy

132 sion of PDE2 or deletion of RAS2 rescued the temperature sensitivity of ask1-3 mutants.

133 However, the addition of RNA reduced the temperature sensitivity of assembly reactions.

134 rmal cell division but does not suppress the temperature sensitivity of BC202, indicating that YghB a

135 Temperature sensitivity of bovine milk beta-lactoglobuli

136 ure, factors that can influence the apparent temperature sensitivity of breakdown and the relative pr

137 The temperature sensitivity of cell water transport in roots

138 The exceptionally high temperature sensitivity of certain transient receptor po

139 Variation in the temperature sensitivity of CO2 and CH4 production and in

140 In contrast, SMT4 does not suppress temperature sensitivity of cohesin complex mutants.

141 e of crd1Delta, strongly suggesting that the temperature sensitivity of crd1Delta is a consequence of

142 ons of fresh litter accurately represent the temperature sensitivity of Cs decomposition.

143 At the global scale, the apparent temperature sensitivity of CUEh with respect to mean ann

144 there is a lack of studies investigating the temperature sensitivity of decomposition for decadally c

145 Results indicated that the temperature sensitivity of decomposition for decadally c

146 find that modulation of PIF4 function alters temperature sensitivity of defense.

147 w that reduction of gating charges amplifies temperature sensitivity of designer channels, which acco

148 sely, this CTD mutation was able to suppress temperature sensitivity of DNA binding by the cts62 repr

149 Temperature sensitivity of DNA polymerization and growth

150 Temperature sensitivity of DNA polymerization and growth

151 solated and characterized suppressors of the temperature sensitivity of dnaD and dnaB mutant cells.

152 imum temperature) rather than changes in the temperature sensitivity of ecosystem respiration.

153 The temperature sensitivity of expansin-mediated wall extens

154 The temperature sensitivity of expression of LsNCED4 may det

155 reasing faster than ET because of the higher temperature sensitivity of GPP relative to ET.

156 Supplementation with inositol alleviated the temperature sensitivity of gsk-3Delta.

157 positions previously reported to affect the temperature sensitivity of influenza A viruses.

158 C and 36 degrees C, one should consider the temperature sensitivity of IP3-mediated signal amplitude

159 The temperature sensitivity of ipl1-2 can also be suppressed

160 everal mutant GLC7 alleles that suppress the temperature sensitivity of ipl1-2 exhibit negative synth

161 use of inappropriate comparisons between the temperature sensitivity of IR snake reception and imagin

162 Such convergence in the temperature sensitivity of leaf respiration suggests tha

163 rature and thus compensates for the inherent temperature sensitivity of ligand-induced activation.

164 Temperature sensitivity of litter breakdown varied among

165 ressor mutations in MCM2, which suppress the temperature sensitivity of mcm10-1, fail to overcome the

166 ) with K(d) 9.2 and 92 microm, showed strong temperature sensitivity of MgATP binding and equal disso

167 Both Kv11 channels exhibited an overall high temperature sensitivity of most gating parameters, with

168 ed seasonal and elevational variation in the temperature sensitivity of mountain vegetation activity.

169 some condensation by MukB did not rescue the temperature sensitivity of MukEF-deficient cells, nor di

170 Thus, the temperature sensitivity of muscle force is markedly incr

171 e also examined the treatment effects on the temperature sensitivity of net N mineralization and net

172 , we identified multicopy suppressors of the temperature sensitivity of new conditional alleles of SW

173 y on evoked release, and the reported higher temperature sensitivity of osmotic enhancement.

174 orders of magnitude, limited only by the low-temperature sensitivity of our spectroscopic thermometry

175 s revealed that ELG1 deletion suppresses the temperature sensitivity of pds5 mutant cells.

176 Temperature sensitivity of phenology might be greater in

177 The high temperature sensitivity of pHi regulation in mammalian c

178 To do this we determined the temperature sensitivity of pHi, intracellular buffering

179 Strophanthidin reduced the temperature sensitivity of post-stimulus recovery of [K+

180 int is the major reason of low stability and temperature sensitivity of promoter complexes formed by

181 ons, PLFE liposomes exhibit a remarkably low temperature sensitivity of proton permeation and dye lea

182 The temperature sensitivity of R was greater in darkness tha

183 ilT and vegetation greenness on the apparent temperature sensitivity of Reco and to the effects of an

184 The level of temperature sensitivity of replication in vitro did not

185 re response curve, and thus in the intrinsic temperature sensitivity of respiration across the globe.

186 metabolic constraint imposed by the greater temperature sensitivity of respiration and more efficien

187 microbial community responses increased the temperature sensitivity of respiration in high-latitude

188 The temperature sensitivity of respiration in the plots was

189 ial to fungal ratios were related to greater temperature sensitivity of respiration, which was amplif

190 than reduces the mid- to long-term (90 days) temperature sensitivity of respiration.

191 iously isolated suppressor of cbp1ts-induced temperature sensitivity of respiratory growth.

192 The temperature sensitivity of Rsoil was strongly influenced

193 -forward cyclic mechanism that increases the temperature sensitivity of RyR1 activation and underlies

194 The results of this study explain the temperature sensitivity of SA11-tsC and shed new light o

195 ion of both Sec24p and Sec23p suppressed the temperature sensitivity of sec16-2.

196 Overproduction of Sec24p suppressed the temperature sensitivity of sec23-2, and overproduction o

197 and temperature, we are able to estimate the temperature sensitivity of selection on lay date (B), bu

198 The temperature sensitivity of severing by adseverin and gel

199 librations to fossil corals assumes that the temperature sensitivity of skeletal Sr/Ca is conserved,

200 SUMO ligase Mms21p partially suppresses the temperature sensitivity of smc5 strains and increases th

201 The temperature sensitivity of soil carbon decomposition is

202 arch, a consensus has not yet emerged on the temperature sensitivity of soil carbon decomposition.

203 Our observations indicate that the temperature sensitivity of soil respiration decreases--o

204 ource quality and biological activity on the temperature sensitivity of soil respiration under differ

205 Finally, the temperature sensitivity of soil respiration was not infl

206 , depending on the mechanisms underlying the temperature sensitivity of soil respiration.

207 robial community-level responses control the temperature sensitivity of soil respiration.

208 more general mechanism that establishes the temperature sensitivity of somatosensory neurons.

209 We observed distinct patterns of temperature sensitivity of splicing to acceptors A1 and

210 y in space (SpaceSens) model for calculating temperature sensitivity of spring plant phenophases acro

211 s (D8N, K69Q, D174N, D203N) complemented the temperature sensitivity of sse1Delta and lethality of ss

212 refore reexamined the molecular basis of the temperature sensitivity of strain AS17.

213 The temperature sensitivity of stu1-5 can be suppressed by d

214 uspecting biogeochemist focused primarily on temperature sensitivity of substrate decay thus cannot m

215 ironmental constraints obscure the intrinsic temperature sensitivity of substrate decomposition, caus

216 pic spectrum of BSI and the understanding of temperature sensitivity of TGM1 mutations.

217 e BSI genotypes to draw inferences about the temperature sensitivity of TGM1 mutations.

218 This is in accord with a higher temperature sensitivity of the apparent rate constants i

219 with global ecosystem model predictions, the temperature sensitivity of the carbon fixed more than a

220 Given the strong temperature sensitivity of the dominant lawn fluxes, and

221 -1-Pase but fully functional in changing the temperature sensitivity of the E. coli double mutant str

222 creased with incubation temperature, but the temperature sensitivity of the enzymes did not differ be

223 It was further observed that the temperature sensitivity of the ffh mutant was suppressed

224 There was no difference in temperature sensitivity of the metabolic and structural

225 ariation and compelled an examination of the temperature sensitivity of the model that revealed a nar

226 GLEBS domain of SONB1(NUP98) suppresses the temperature sensitivity of the nimA1 allele and compromi

227 f expression of dinB or umuDC suppresses the temperature sensitivity of the nusA11 strain, requiring

228 t substitutes space for time to estimate the temperature sensitivity of the optimum timing of 22 plan

229 at SAS2 deletion (sas2Delta) exacerbates the temperature sensitivity of the ORC mutants orc2-1 and or

230 rotein Stm1 as a multicopy suppressor of the temperature sensitivity of the pat1Delta strain.

231 The reduced HA stability and temperature sensitivity of the pLAIV viruses may account

232 s of soil warming affected the rates and the temperature sensitivity of the soil CO2 efflux, extracel

233 The temperature sensitivity of the strain, in media of all o

234 By measuring the different pressure and temperature sensitivity of the tested PrP oligomers, we

235 utilizing collection records to compare the temperature sensitivity of the timing of adult flight in

236 hesized that its extension would relieve the temperature sensitivity of the ts3813 mutation.

237 dence of transformation in R6 to result from temperature sensitivity of the uptake apparatus and not

238 This paper discusses the efficiency and temperature sensitivity of the VCSELs emitting at 2.6 mu

239 cavity mode de-tuning determines the overall temperature sensitivity of the VCSELs.

240 reased stringency may be explained by a mild temperature sensitivity of the wild-type F10 kinase, whi

241 cle checkpoints and the subsequent rescue of temperature sensitivity of the yku70Delta strain.

242 helicase yeast homolog Sgs1 exacerbated the temperature sensitivity of the yku70Delta strain.

243 ic properties, which determine the intrinsic temperature sensitivity of their decomposition.

244 , deletion of CDC55 partially suppresses the temperature sensitivity of these mutants.

245 re soil carbon stock will mainly rely on the temperature sensitivity of these resistant carbon pools.

246 ction mechanism that explains the intriguing temperature sensitivity of this motility.

247 l diffusion model that may explain the large temperature sensitivity of TRP channels.

248 ly, either form of adaptation does not alter temperature sensitivity of TRPM8 but does lead to a chan

249 These findings demonstrate that the temperature sensitivity of TRPV3 is separable from all o

250 These findings demonstrate that the temperature sensitivity of TRPV3 is separable from all o

251 r basis that underlies the use dependence of temperature sensitivity of TRPV3.

252 Mutant channels have high temperature sensitivity of voltage activation, specifica

253 in a screen for multicopy suppressors of the temperature-sensitivity of a mutant allele of S. cerevis

254 We explored the temperature-sensitivity of individual saprotrophic basid

255 endence on the PI surface concentration, and temperature sensitivity) of the LSB6-encoded enzyme were

256 emperature range of synaptic output, but not temperature sensitivity, of the AFD thermosensory neuron

257 ulin can confer both colcemid resistance and temperature sensitivity on a mammalian cell line.

258 which attenuation is generated by conferring temperature sensitivity onto the virus.

259 al plate screen for suppressors of rrp6Delta temperature sensitivity or a novel microarray enhancer/s

260 o not exhibit alterations in cell integrity, temperature sensitivity, or cellular morphology.

261 The temperature sensitivity (Q 10) of Rs increased after the

262 fected CO2 and N2 O fluxes and altered their temperature sensitivities (Q10 ) over successive DW cycl

263 The temperature sensitivities (Q10) of RS and RH were higher

264 erstanding the spatial patterns of Nmin, its temperature sensitivity (Q10 ) and regulatory mechanisms

265 SUE and its temperature sensitivity (Q10 warmed: 0.84 +/- 0.03, cont

266 ncubation temperature, but the rates and the temperature sensitivity (Q10 warmed: 2.54 +/- 0.23, cont

267 adapted to higher temperature with a higher temperature sensitivity (Q10(5-15 degrees C) increased b

268 mbient level, the soil moisture, Rs, and the temperature sensitivity (Q10) values increased by an ave

269 Further characterizations of temperature sensitivity quantitative trait loci that are

270 R101S-R105S was synergistic and resulted in temperature sensitivity reflected by reduced viral repli

271 and mechanisms mediating TRPV1's pronounced temperature sensitivity remain unclear.

272 ymous mutations in 9 of 11 ORFs did not lose temperature sensitivity, remained genetically stable, an

273 omplement the pah1Delta mutant phenotypes of temperature sensitivity, respiratory deficiency, nuclear

274 tion, we identified three suppressors of the temperature sensitivity resulting from deletion of the R

275 ties of films of both materials show extreme temperature sensitivity, resulting in the formation of v

276 e STT3 was identified in a staurosporine and temperature sensitivity screen of yeast.

277 ophysical components of the final model have temperature sensitivities similar to those found in natu

278 l have recently emerged that offer excellent temperature sensitivity, spatial resolution, or cellular

279 , and Ca(2+) buffering each have independent temperature sensitivities, suggesting that the balance o

280 These residues were mutated and tested for temperature sensitivity, taking advantage of the excepti

281 to warmer temperatures caused a reduction in temperature sensitivity that resulted in slower rates at

282 rotein-B) dimerization domain suppressed the temperature sensitivity, the benomyl sensitivity, and th

283 ird, and sixth positions conferred increased temperature sensitivity: this was greatest for the third

284 ation, we were able to systematically confer temperature sensitivity to a canonical voltage-gated ion

285 ommunity Climate System Model shows the same temperature sensitivity to changes in insolation as does

286 Despite this temperature sensitivity, transcription of the heat shock

287 Temperature sensitivity (ts) limits viral replication at

288 This study determined the temperature sensitivity (ts) of MP-12 vaccine to underst

289 andidates exhibited phenotypic properties of temperature sensitivity (ts), ca, and attenuation (att)

290 verexpression of any cyclophilin resulted in temperature sensitivity (TS).

291 al control, we isolated mutations leading to temperature sensitivity (Ts- phenotype) targeted at TIF5

292 t they were lethal, two mutants exhibited no temperature sensitivity, two mutants exhibited partial t

293 ele in vac7Delta mutant cells suppresses the temperature sensitivity, vacuolar morphology, and PtdIns

294 ition and SOM formation are expected to have temperature sensitivity varying with the lability of pla

295 Consistent with this model, rsp5-1 temperature sensitivity was suppressed by either ubp2Del

296 conductance-based model in which exponential temperature sensitivities were given by Q10 parameters.

297 The largest fraction of loci associated with temperature sensitivity were involved in the biosynthesi

298 the telomeres, which are the major cause of temperature sensitivity, were slightly increased.

299 nce of interactions between N deposition and temperature sensitivity, which could influence C storage

300 A third region conferred temperature sensitivity without affecting cell lysis or