ライフサイエンスコーパス: temperature sensitivity

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

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

3 ies accounts for interspecific difference in temperature sensitivity.

4 by reduced enzymatic activity and increased temperature sensitivity.

5 including stress shielding, palpability and temperature sensitivity.

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

7 cation involves several steps with different temperature sensitivity.

8 C7 overexpression induced cell death or ipl1 temperature sensitivity.

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

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

11 oligodeoxynucleotide, blocked tumor-induced temperature sensitivity.

12 ctivation provides a mechanism for enhancing temperature sensitivity.

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

14 ted with seed priming effects on germination temperature sensitivity.

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

16 eterogeneity of soil C decomposition and its temperature sensitivity.

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

18 ,3-glucan synthesis and suppresses pgs1Delta temperature sensitivity.

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

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

21 one thread in a complex network that governs temperature sensitivity.

22 to the medium overcomes ethanol toxicity or temperature sensitivity.

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

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

25 ss TRPV1 orthologs with dramatically reduced temperature sensitivity.

26 gating and shed light on ancient origins of temperature-sensitivity.

27 Ms may have more accurately represented crop temperature sensitivities.

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

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

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 can lead to spurious differences in apparent temperature sensitivity and artificial spatial gradients

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

58 the PLP2 domain were not responsible for the temperature sensitivity but did reduce the frequency of

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

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

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

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

63 associated with several drawbacks, including temperature sensitivity, Ca(2+) dependence, and slow bin

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

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

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

67 ,634 plant species using a common measure of temperature sensitivity (change in days per degree Celsi

68 s of the CTD transforms TRPM8 into a reduced temperature-sensitivity channel (Q(10) ~4).

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

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

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

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

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

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

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

76 ew alternative approaches for characterizing temperature sensitivity, focusing on macromolecular rate

77 Although temperature sensitivities for bulk peat methanogenesis w

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

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

80 exhibits hypersensitivity to paclitaxel and temperature sensitivity for growth.

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

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

83 Along with temperature sensitivity found in the olfactory system of

84 strategies and tools for implementing a new temperature sensitivity framework; (c) develop thermal a

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

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

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

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

89 Improved understanding of temperature sensitivity in soils is particularly pertine

90 nd Arrhenius model are often poor metrics of temperature sensitivity in soils.

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

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

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

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

95 ents produce emergent ecosystem carbon stock temperature sensitivities inconsistent with emergent mul

96 This study characterized global impacts of temperature sensitivity-inducing missense mutations in t

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

98 The ice sheet's temperature sensitivity is 1.3 metres of sea-level equiv

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

100 Temperature sensitivity is evident in multiple periods o

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

102 This temperature sensitivity is remarkable considering that t

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

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

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

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

107 thermal ecology predictions that a species' temperature sensitivity matches the microclimate it expe

108 st alternative to the simple days-per-degree temperature sensitivity metric.

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

110 tory protein M2-2 and genetically stabilized temperature-sensitivity mutation 1030s in the RSV polyme

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

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

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

114 Different temperature sensitivities of carbonate properties and di

115 Despite these differences in the short-term temperature sensitivities of photosynthesis and respirat

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

117 e or highly restricted, but coordinating the temperature sensitivities of the Sodium activation gate

118 e efficacy of oxygen supply, and between the temperature sensitivities of these traits, which suggest

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

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

121 The temperature sensitivity of 22 fluorescent dyes was asses

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

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

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

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

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

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

128 Temperature sensitivity of anaerobic carbon mineralizati

129 We show that the apparent temperature sensitivity of animal production was consist

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

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

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

133 Temperature sensitivity of bovine milk beta-lactoglobuli

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

135 The temperature sensitivity of cell water transport in roots

136 The exceptionally high temperature sensitivity of certain transient receptor po

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

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

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

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

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

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

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

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

145 Temperature sensitivity of DNA polymerization and growth

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

147 mmer baseflow, we estimated variation in the temperature sensitivity of ecosystem respiration (R) amo

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

149 The temperature sensitivity of ELF3 is also modulated by the

150 es, no thermal compensation or change in the temperature sensitivity of enzyme activities, and no cha

151 The temperature sensitivity of expression of LsNCED4 may det

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

153 Little is known, however, on the temperature sensitivity of growth of microbial communiti

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

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

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

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

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

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

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

161 Temperature sensitivity of litter breakdown varied among

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

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

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

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

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

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

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

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

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

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

172 Temperature sensitivity of phenology might be greater in

173 Here, we examine the temperature sensitivity of phenology, and highlight cond

174 ues are rarely considered in analyses of the temperature sensitivity of phenology.

175 The high temperature sensitivity of pHi regulation in mammalian c

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

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

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

179 ociation between watershed geomorphology and temperature sensitivity of R was linked to the carbon qu

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

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

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

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

184 The temperature sensitivity of respiration in the plots was

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

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

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

188 The temperature sensitivity of Rsoil was strongly influenced

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

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

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

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

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

194 Despite much research, understanding of temperature sensitivity of SOC under long-term agricultu

195 The temperature sensitivity of soil carbon decomposition is

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

197 Here we show that the temperature sensitivity of soil microbial respiration (Q

198 The temperature sensitivity of soil processes is of major in

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

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

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

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

203 phic variation in the decomposition rate and temperature sensitivity of soils: soil C decomposition r

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

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

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

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

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

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

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

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

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

213 sensitivity is attenuated when we reduce the temperature sensitivity of the channel but not when we r

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

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

216 We show that differential temperature sensitivity of the female morphs and faster

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

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

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

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

221 illary and are evaluated with respect to the temperature sensitivity of the OH stretching vibration.

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

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

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

225 agents needed for the reaction steps and the temperature sensitivity of the phi29 polymerase.

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

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

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

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

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

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

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

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

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

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

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

237 rate the dramatic effect of restraint on the temperature sensitivity of these dyes.

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

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

240 IMS) single-cell analysis, we quantified the temperature sensitivity of these two taxonomic groups to

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

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

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

244 d that it may participate in controlling the temperature sensitivity of TRPV1.

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

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

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

248 We explored the temperature-sensitivity of individual saprotrophic basid

249 This phenomenon might partially explain the temperature-sensitivity of some transcriptional programs

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

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

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

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

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

255 ct on multicycle virus replication in vitro, temperature sensitivity, or specific infectivity.

256 r the temperature response of growth: Q(10) (temperature sensitivity over a given 10oC range) and T(m

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

258 Also, low-severity fires reduce the temperature sensitivity (Q(10) ) of peat, indicating tha

259 and (b) the importance of biotic factors for temperature sensitivity (Q(10) ) of SOM mineralization.

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

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

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

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

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

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

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

267 Further characterizations of temperature sensitivity quantitative trait loci that are

268 omorphic features imposed strong controls on temperature sensitivity; R in streams draining flat wate

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

284 c phenolate dye (PhOBtz) displays impressive temperature sensitivity to thiolate addition, with the b

285 MeBtz and PhNMe(2)Btz) display only moderate temperature sensitivity to thiolate capture and release.

286 Temperature sensitivity (ts) limits viral replication at

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

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

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

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

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

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

293 e the diversity of biophysical mechanisms of temperature-sensitivity, we characterized the temperatur

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

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

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

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

298 nology, researchers commonly use a metric of temperature sensitivity, which quantifies the change in

299 e conductance has a different characteristic temperature sensitivity, which raises the question of ho

300 hows similar secondary structure content and temperature sensitivity with other reported triose-phosp