ライフサイエンスコーパス: turnover rate

1 r higher ee, good regioselectivity, and high turnover rates).

2 s accompanied by an increase in the filament turnover rate.

3 like Na(+) and K(+) affinities and catalytic turnover rate.

4 f the host-specific variation in NS3 protein turnover rate.

5 ZSM-5 material, leading to a 460 times lower turnover rate.

6 viscosity that is inversely proportional to turnover rate.

7 and this protein possesses a relatively high turnover rate.

8 s and this protein displays a relatively low turnover rate.

9 site density and the species-specific sodium turnover rate.

10 nts for a second phase of the slow catalytic turnover rate.

11 increases in BZ contractile function and ATP turnover rate.

12 the human enzyme, indicated a reduced single turnover rate.

13 s but is caused by the significantly reduced turnover rate.

14 the increased hydrophobicity) decreased the turnover rate.

15 y differentiated and short-lived with a high turnover rate.

16 luence of cell-specific factors in dictating turnover rate.

17 lecules, ultimately increasing the enzymatic turnover rate.

18 light conditions increased SAUR63:HA protein turnover rate.

19 ased membrane expression because of a faster turnover rate.

20 for impaired mitochondrial function and high turnover rate.

21 by the complexity of water currents or slow turnover rate.

22 fatty acid hydroxylation at a >3,000 min(-1) turnover rate.

23 in the isotope envelope to calculate protein turnover rate.

24 eous plants showed little change in temporal turnover rates.

25 ong effect on H2 oxidation and H2 production turnover rates.

26 dominated by weak ties characterized by high turnover rates.

27 the same miRNA can possess vastly different turnover rates.

28 30 nucleotides or fewer at comparable single-turnover rates.

29 ort rates can be slow and comparable to mRNA turnover rates.

30 mation and compared with fluorescent product turnover rates.

31 range that strongly influenced CO oxidation turnover rates.

32 these mutants displayed a defect in protein turnover rates.

33 , di-, and tri-) is determined by nucleosome turnover rates.

34 different tradeoff conditions with different turnover rates.

35 d for their regulation rather than catalytic turnover rates.

36 from different networks, infection rates and turnover rates.

37 tial equations was used to calculate protein turnover rates.

38 ospinal fluid Abeta concentrations and Abeta turnover rates.

39 ed decomposition of SOC components with slow turnover rates.

40 exhibits an approximately 1,000-fold slower turnover rate (0.06-0.17 s(-1)), suggesting a potential

41 ed from cell growth and showed high specific turnover rates (~1 fmol/(cell h)), high conversion yield

42 tion between increasing age and slowed Abeta turnover rates (2.5-fold longer half-life over five deca

43 (1) the tumor niche (edge or core), (2) cell turnover rates, (3) the nature of the tradeoff between t

44 8 g m(-2) yr(-1) ), and a trend of decreased turnover rate (6 +/- 1 times yr(-1) ).

45 rylation of LmjAQP1 led to a decrease in its turnover rate affecting LmjAQP1 activity.

46 ite in the ATPase yielded enzymes with lower turnover rates, although Cu(+) transfer was minimally af

47 ly 70 most abundant proteins, variability in turnover rates among rats was low (median coefficient of

48 tes: an autoinhibited basal state with a low turnover rate and a low H(+)/ATP coupling ratio and an a

49 are a distinctive TRM population with a high turnover rate and a unique phenotype influenced by their

50 e APT2, that each species varies in terms of turnover rate and activity, altogether allowing the cell

51 ion is affected in two ways: by limiting the turnover rate and by a large overpotential requirement t

52 -fixing enzyme Rubisco, which exhibits a low turnover rate and can react with O2 instead of CO2 , lea

53 (2+) transport by improving both the SERCA2a turnover rate and catalytic efficacy.

54 so estimated lipolysis (from [(2)H5]glycerol turnover rate and circulating free fatty acids, glycerol

55 ositive charge of the residue) increased the turnover rate and decreased the Km of AdoMet but did not

56 roton transfer, leading to an overall faster turnover rate and exclusive cis-amidopalladation of alke

57 67 and annexin V stainings revealed a faster turnover rate and increased apoptosis of Raptor-deficien

58 conformation of SERT can explain the reduced turnover rate and increased association rate of inhibito

59 bility and found that the protein has a high turnover rate and is degraded by the proteasome 26S in a

60 re likely due to high biomass concentration, turnover rate and microbial activity in WWTPs, and likel

61 control alpha1beta1, FXYD1 reduces Vmax and turnover rate and raises K0.5Na.

62 signaling RNAs have high affinity and ATPase turnover rate and thus a high katpase/Kd.

63 of closed hexameric toroids capable of high turnover rates and amenable to allosteric regulation.

64 High C-turnover rates and cell abundances would have made these

65 oxic or volatile pathway intermediates, slow turnover rates and competing side reactions.

66 ed are thought to persist by slow population turnover rates and extremely low energy requirements.

67 se in turn determine plastid division and/or turnover rates and hence competitiveness.

68 d pulse-chase system, we measured population turnover rates and individual t1/2 of pre-established Ag

69 lity of pre-mRNA species with different high turnover rates and investigated potential correlations w

70 uman enzyme seems to restore both the single turnover rates and narrow distribution of fast dynamics.

71 noparticles with their support, so identical turnover rates and reaction selectivity is observed rega

72 he decomposition of SOC components with slow turnover rates and thus amplify the positive feedback to

73 Reversed phase HPLC provided multiple turnover rates and tryptophan fluorescence provided nucl

74 ing FGE with copper(II) is required for high turnover rates and yields.

75 owth rate, faster onset, higher steady-state turnover rate, and a greater volume of water collected c

76 ndon, with ~1000 fold differences in protein turnover rates, and overall faster protein turnover with

77 Both Npas4 mRNA and protein had high turnover rates, and, at the protein level, degradation w

78 from these conditions, they exhibit similar turnover rates, apparent activation energies and apparen

79 ietary intake over 2-3 y because of the slow turnover rate, appears promising but has so far been rar

80 is trafficking role, GRIP1b's palmitoylation turnover rate approaches the highest of all reported pro

81 timates of vegetation carbon pools and their turnover rates are central to understanding and modellin

82 Turnover rates are lower and kinetically relevant specie

83 stic interpretations of methanol dehydration turnover rates are used to assess how charge reorganizat

84 ons have a smaller SV pool size and a higher turnover rate as indicated by a younger pool of SV2.

85 eptidoglycan decomposition exhibited similar turnover rates as their l-enantiomers.

86 ivity genotype (contributing to low dopamine turnover rate) as well as the CDH13 gene (coding for neu

87 or ADF/cofilin1, which mediates high F-actin turnover rates, as an essential factor in this process.

88 ehavior directly competes with the enzymatic turnover rate at physiological glucose concentrations, t

89 d that Kv2.1, VAPA, and Nir2 have comparable turnover rates at ER-PM junctions, suggesting that they

90 ve rise to a large increase in CH4 oxidation turnover rates at oxygen chemical potentials leading to

91 Total ATP turnover rate (ATPtot) was estimated at exercise cessati

92 There is considerable heterogeneity of turnover rates between promoters in different tissues, b

93 tivity, protein interactions, targeting, and turnover rate, but despite their importance, they are st

94 and rehabilitation units had the lowest mean turnover rates, but most differences between service lin

95 l cortex exhibited diminished baseline spine turnover rates, but these rates were also enhanced by co

96 lication and increase the helicase-unwinding turnover rates by 1.7- and 3.5-fold, respectively, sugge

97 We characterized substrate turnover rates by following temporal changes in the enzy

98 is (mPDE), that resulted in decreased enzyme turnover rate compared with its unphosphorylated counter

99 filament subpopulations with very different turnover rates composed the actin cortex: one with fast

100 However, estimates of cardiomyocyte turnover rates conflict greatly, with a study employing

101 hat free F(1) was a newer pool with a faster turnover rate consistent with it being an assembly inter

102 Analysis of heavy water data sets yielded turnover rates consistent with a short blood half-life,

103 However, the single-turnover rate constant for alkylation does depend on the

104 t with the steady-state reaction, the single-turnover rate constant for dansyl-GCVLS alkylation was f

105 ease corresponds to the overall steady-state turnover rate constant, suggesting that product release

106 thenoadenine (epsilonA) from DNA with single-turnover rate constants that are 2.9 x 10(5)-fold greate

107 H, explains the structural origin of the ATP turnover rates detected in relaxed tarantula muscle by a

108 permanent extensive remodeling, but how the turnover rate differs between lipid classes and molecula

109 e shorter-lived, and exhibit higher baseline turnover rates distinct from AMs.

110 erary of the cadherin, resulting in a higher turnover rate due to decreased recycling and increased d

111 otein levels while intact exhibited a higher turnover rate during activation of switching to IgG3 and

112 of cell turnover, with tissues with low cell turnover rates (e.g. the adult central nervous system) s

113 e.g., growth rate), community (e.g., biomass turnover rates), ecosystem (e.g., trophic pyramids), and

114 O-GlcNAcylation, which maintained the rapid turnover rate even in the presence of GlcN and increased

115 K(+)-ATPase retained a wild-type-like enzyme turnover rate for ATP hydrolysis and rate of cellular K(

116 We compare turnover rates for 1-octene epoxidation and H(2)O(2) dec

117 This enrichment resulted in turnover rates for an additional 17 proteins.

118 A comparison of the turnover rates for H2 and O2 revealed that in the presen

119 ied nitrogen (N), phosphorus (P) and caloric turnover rates for Lake Huron lake trout, and reveal how

120 Turnover rates for mixed alkenes give relative alkoxide

121 regional differences, and the high regional turnover rates found challenge the universal concept of

122 hosphatidylcholine increases the Na,K-ATPase turnover rate from 5483 +/- 144 to 7552 +/- 105 (p < 0.0

123 ution of forward ET rates is higher than the turnover rate from ensemble steady-state measurements an

124 ng a reference dataset of 496 plasma protein turnover rates from 4 healthy adults.

125 generated DNA oxidation and adduct formation turnover rates from the array correlated very well with

126 Estimates of isotopic turnover rate further confirmed incomplete turnover of R

127 i) a nonsense mutation (R150*) or (iii) high turnover rates (G134W).

128 edicted to experience >10% increases in root turnover rates given potential shifts in tree species co

129 r ammonia emissions than if historical fleet turnover rates had prevailed.

130 tion in skeletal muscle, a tissue with a low turnover rate, has never been investigated.

131 ing network and its parameters (mean degree, turnover rate) have a strong adverse effect on the abili

132 We observed that Rad17 protein turnover rate in breast epithelial cells is much faster

133 thways results in an increased mitochondrial turnover rate in GCN5L1(-/-) cells.

134 probably results from more rapid increase of turnover rate in leaves than in fine roots.

135 s, and quantitative RT-PCR revealed a higher turnover rate in the humerus than in lumbar vertebrae, s

136 hols, while numerous steps contribute to the turnover rate in the oxidation of aliphatic alcohols.

137 rats in vivo, measure variability of protein turnover rates in any animal model, and utilize activity

138 etermine hepatitis B surface antigen (HBsAg) turnover rates in chronic hepatitis B (CHB) patients.

139 Previously, we analyzed protein turnover rates in cultured brain cells under basal neuro

140 de copy numbers, mRNAs, proteins and protein turnover rates in each cell line.

141 We measured miRNA turnover rates in eight mammalian cell types with a comb

142 a, possibly relating to the modified protein turnover rates in heterotrophic plastids.

143 This paper focuses on new nurses' unit-level turnover rates in hospitals.

144 on under future climate scenarios while root turnover rates in other portions of the eastern US were

145 slide to observe their individual substrate turnover rates in parallel by fluorescence microscopy.

146 s the first to measure global plasma protein turnover rates in rats in vivo, measure variability of p

147 inant processes that shape vegetation carbon turnover rates in real forest ecosystems at a large spat

148 le of the polymerase fidelity and nucleotide turnover rates in recombination.

149 We sought to measure the global protein turnover rates in the eye using nitrogen-15 labeling of

150 CO2 was also associated with faster nutrient turnover rates in the first six months of the experiment

151 e to <1% per year in adulthood, with similar turnover rates in the major subdivisions of the myocardi

152 ned model identified patterns of faster root turnover rates in the North Central US and slower turnov

153 ver rates in the North Central US and slower turnover rates in the Southeastern US.

154 hotometric measurements suggest that aqueous turnover rates in TSP1-null and TSP2-null mice are great

155 is of in vitro degradation rates and protein turnover rates in vivo of specific proteins indicated th

156 TECs; 2) whereas cTECs and mTECs had similar turnover rates in young mice, the turnover of mTECs was

157 A submodule attenuates supercomplex I+III(2) turnover rate, indicating an unexpected molecular adapta

158 We found that differences in biomass turnover rates influenced F : B under conditions of C li

159 on for a wide range of conditions, but their turnover rate is high.

160 ) and closed (active) state, and the overall turnover rate is inversely proportional to the lifetime

161 The turnover rate is mainly determined by the alkene coordin

162 knowledge of the root carbon pool sizes and turnover rates is limited.

163 he large number of single molecule substrate turnover rates is representative of the activity distrib

164 Depending on the myosin turnover rate, junctions either preserve stable length o

165 re primarily due to changes in the catalytic turnover rate (k(cat)) and not in the affinity for the s

166 PR by an order of magnitude, affecting both turnover rate (k(cat)) and substrate affinity (K(m)).

167 VISIT) using estimates of vegetation carbon turnover rate (k) derived from a combination of remote s

168 Apparent turnover rates (k(cat,app)) of the reconstituted enzymes

169 he binding constant (K(D)) and the catalytic turnover rate, k(cat).

170 At -1 degrees C, the Rubisco turnover rate, kcat (c) , was 0.4 C s(-1) per site and t

171 Irreversible and turnover-rate limiting reaction with pinacolborane (k ~

172 on the reaction, catalyst resting state, and turnover-rate limiting step has been examined.

173 tification of the catalyst resting state and turnover-rate limiting step.

174 light-harvesting and surface-area-normalized turnover rates, making Y2 Ti1.94 Rh0.06 O7 an excellent

175 rity exhibit dynamic instability with higher turnover rates nearer to the midzone.

176 y of the inhibition and the very low protein turnover rate observed for the enzyme are particularly r

177 imethylsilyl)amine is formed with an initial turnover rate of 1 N(TMS)3/min, ultimately reaching a tu

178 lar system is 1.1 min(-1), comparable to the turnover rate of a truncated trimodular derivative (2.5

179 show that the Leu-Phe substitution increases turnover rate of acetaldehyde but decreases turnover rat

180 f the postsynaptic apparatus is altered, the turnover rate of AChRs increases significantly, and the

181 how that actin phosphorylation increases the turnover rate of actin filaments and promotes the short-

182 ctin can work in concert to increase the ATP turnover rate of actin.

183 f guppies (Poecilia reticulata) to study the turnover rate of alleles (temporal genetic differentiati

184 o-photon microscopy and determined the spine turnover rate of apical dendrites of layer 5 (L5) and L2

185 A mutant exhibited an increase in the single-turnover rate of correct nucleotide insertion.

186 gap junction communication by increasing the turnover rate of Cx43 from the plasma membrane.

187 The K m value and turnover rate of CYP71AN24 for phenylacetaldoxime were 3

188 ent of particulate antigen secretion and the turnover rate of cytoplasmic protein.

189 ations dramatically reduced the biosynthetic turnover rate of DE-Cad during apical-basal polarization

190 lear bomb test-derived (14)C revealed a high turnover rate of endothelial cells throughout life (>15%

191 F-actin, wherein the steady-state length and turnover rate of F-actin are controlled by the actin reg

192 growth and root respiration, as well as the turnover rate of fine-root C fixed during [CO(2)] fumiga

193 absolute (molar) abundance and determine the turnover rate of glycerophospholipids and sphingolipids

194 Using electrochemical measurements of the turnover rate of hydrogenase, we could resolve the first

195 turnover rate of acetaldehyde but decreases turnover rate of larger aldehydes.

196 Because of the rapid turnover rate of membrane Hsp70, fluorescently labeled T

197 We measured the nucleotide turnover rate of myosin in tarantula leg muscle fibers b

198 y after photobleaching (FRAP) to examine the turnover rate of myosin VI during endocytosis.

199 ceptor density was dramatically reduced, the turnover rate of receptors at synaptic sites was signifi

200 ne bilayer as a mechanism for increasing the turnover rate of SERCA.

201 munities, with possible consequences for the turnover rate of soil carbon (C) pools and feedbacks to

202 individual site, indicating that the spatial turnover rate of soil microbial communities was accelera

203 (2+) and Mn(2+) were comparable, whereas the turnover rate of SPCA1a in Ca(2+) was 2-fold higher.

204 strate that extramatrix Ca(2+) modulates the turnover rate of the APC and not the binding affinity of

205 The maximum turnover rate of the complete hexamodular system is 1.1

206 n the mammalian circadian clock involves the turnover rate of the repressors CRY and PER.

207 These findings indicate a low basal turnover rate of the total KCC2 protein pool.

208 verall catalytic cycle and hence governs the turnover rate of this industrially important enzyme.

209 ubstrates, lysozyme exhibited processive low turnover rates of 20-50 s(-1) and rapid (200-400 s(-1))

210 of (14)N-labeled proteins, we calculate the turnover rates of 508 different proteins in barley and s

211 oaches to compare the relative abundance and turnover rates of 848 and 196 proteins, respectively, in

212 Turnover rates of A(g7) and H2-A(d) were indistinguishab

213 f Fe and Zn per polypeptide and demonstrates turnover rates of approximately 3 s(-1) Similar rates ar

214 rates (r(2) = 0.68, P < 0.05), and that the turnover rates of both leaf (r(2) = 0.63, P < 0.05) and

215 abolic scaling theory, we show that isotopic turnover rates of carbon and nitrogen in whole organisms

216 Our findings suggest that the higher turnover rates of carbon pools in semi-arid biomes are a

217 erived 14C in genomic DNA, we determined the turnover rates of CD4+ and CD8+ naive T-cell populations

218 el regularities: condition invariant in vivo turnover rates of enzymes and the correlation of protein

219 Measuring whole-body turnover rates of glucose and FFAs in L-AktFoxo1TKO mice

220 Steady-state kinetic analyses show that the turnover rates of His-257 mutants are significantly smal

221 main largely undefined, as do differences in turnover rates of individual proteins in the collagen an

222 pectrometry and bioinformatics, we calculate turnover rates of individual proteins within rat Achille

223 l properties depend strongly on the relative turnover rates of its constituents, but quantitative dat

224 ce times around 1 to 2 s, and similarly high turnover rates of membrane-associated proteins in CME.

225 beling allowed the concurrent measurement of turnover rates of multiple natural products from small a

226 Because increased turnover rates of new soil C limit the potential for add

227 and suggest that elevated CO2 might increase turnover rates of new soil C.

228 of supporting productive T cell development, turnover rates of niche occupancy, and feedback mechanis

229 Here, turnover rates of plasma proteins in rats were measured

230 protein-protein interactions, and control of turnover rates of proteins.

231 Remarkably, the turnover rates of SPCA1a in the presence of Mn(2+) and S

232 ation in synaptic plasticity, as well as the turnover rates of specific neuronal proteins.

233 is demonstrated by the determination of the turnover rates of the enzyme using the Michaelis-Menten

234 nt choice significantly affected binding and turnover rates of the recombinant enzymes with various x

235 perties that determine the selectivities and turnover rates of these catalysts have not yet been eluc

236 iggers an increase in the specific activity (turnover rate) of the membrane-bound kinase molecule.

237 irements, pathway delineation and metabolite turnover rates) of Clostridium carboxidivorans P7, a mod

238 n hydrophilic Sn-Beta, giving rise to higher turnover rates on hydrophobic Sn-Beta.

239 ncomitant reduction of the maximal catalytic turnover rate or expression level.

240 nergy reserve) and the digestive gland (fast turnover rate organ, reflecting recent consumption).

241 Turnover rates (per H(+) ) for methanol and ethanol dehy

242 esolved issue whether differences in Aux/IAA turnover rates played a significant role in plant respon

243 ), while the linear rise was associated with turnover rates (r = 0.28; P < .05).

244 tive relationship between leaf and fine root turnover rates (r(2) = 0.68, P < 0.05), and that the tur

245 The channel/PDE5 tandem encodes cGMP turnover rates rather than concentrations.

246 ms, the accumulation of N in pools with slow turnover rates reduces N available for plant uptake and

247 Ca(2+), and its mutation lowered the Ca(2+) turnover rate relative to that of Mn(2+), increased subs

248 Spontaneous spine turnover rates remain high in older Tg1 animals compared

249 Increasing cell turnover rates slightly slows tumor growth but accelerat

250 tments, in-stream PUCs characterized by fast turnover rates, such as filamentous algae, showed the hi

251 Production and turnover rates suggest that day/night Abeta patterns are

252 deletion of Lynx1 doubled the baseline spine turnover rate, suggesting that the spine dynamics in the

253 Follicular B cells had higher turnover rates, survived poorly after adoptive transfer,

254 gradual slowing of the RC electron transport turnover rate (tau(QA)) from ~1.6 to 6.4 ms and an ~3-fo

255 ted a higher physiological baseline monocyte turnover rate than adults.

256 0.9-kDa subunits, had a significantly higher turnover rate than intact CI or CI+CIII(2).

257 r nicotinamide adenine dinucleotide (NAD(+)) turnover rate than normal cells, making this biosyntheti

258 apparent Ca(2+) affinity and a lower maximal turnover rate than the purified sarco(endo)plasmic retic

259 reactivity, with up to 4 times higher local turnover rates than those of the parent H-ZSM-5 crystals

260 ize may be related to changes in the subunit turnover rate that are independent of the GTP hydrolysis

261 und pool, and a dynamic bound pool with high turnover rate that exchanges with the cytoplasmic pool.

262 he most hydrophilic Ti-BEA gives epoxidation turnover rates that are 100 times larger than those in d

263 y influenced by steric constraints, yielding turnover rates that increase by up to two orders of magn

264 Conversely, IMs exhibited higher turnover rates that were similar to those of blood monoc

265 n ergosterol accrual in ingrowth cores), and turnover rate (the quotient of annual production and ave

266 led that SOS samples a broad distribution of turnover rates through stochastic fluctuations between d

267 of AMs, and these cells maintained the lower turnover rate throughout the duration of infection.

268 he ovary to those of the mantle muscle (slow turnover rate tissue, representing an energy reserve) an

269 ied a suppressor mutation that increases the turnover rate to restore the specific activity of the hi

270 also allow plant carbon pool sizes and their turnover rates to be predicted from the single readily q

271 e A673T substitution modulates the catalytic turnover rate (V(max)) of APP by the BACE1 enzyme, witho

272 lgeranyl diphosphate was 18.7 microm, with a turnover rate value of 6.85 s(-1).

273 Turnover rates vary widely among Pol II promoters in a m

274 oduction was 279 +/- 63 g m(-2) yr(-1) , and turnover rate was 10 +/- 3 times yr(-1) .

275 e the enzymatic reduction of N2 into NH3 The turnover rate was 75 per minute, 63% of the ATP-coupled

276 xposure to glucose, a steady-state enzymatic turnover rate was detected through amperometric oxidatio

277 Mean ATP turnover rate was not different between protocols ( appr

278 iously that a high peripheral blood monocyte turnover rate was predictive for the onset of disease pr

279 type control mice, whereas the GI eosinophil turnover rate was unaltered in the absence of CD22.

280 Based on the measured turnover rates we have established a quantitative, singl

281 Based on global population sizes and turnover rates, we estimate that these species have the

282 In contrast, when particles were labile and turnover rates were high, aggregation promoted competiti

283 elial cells (ECs), and fibroblasts and their turnover rates were measured by retrospective (14)C birt

284 nursing staff turnover and registered nurse turnover rates were modeled as dependent variables in hi

285 rred among some microbial additions, similar turnover rates were observed, and in general, results do

286 on differentiation, numerous changes in H3.3 turnover rates were observed, the majority of which occu

287 approach, 273 proteins were identified, and turnover rates were quantified for 157 plasma proteins w

288 The higher TG turnover rates were significantly correlated with higher

289 Lipid turnover rates were studied by pulse-chase experiments a

290 new nurses work in hospitals and have higher turnover rates when compared to experienced nurses.

291 nkton communities displayed slower community turnover rates when dominated by few genera.

292 ved NK cell expansion was not due to altered turnover rate, whereas it was associated with preferenti

293 endocytic receptor correlate with different turnover rates which, together with differences in their

294 variants is impaired mainly by limiting the turnover rate, which drops sharply as the pH is raised,

295 -specific isotope discrimination, and tissue turnover rates, which are typically species- and tissue-

296 anisms may be used in cells to tune filament turnover rates, which can vary widely for different acti

297 Measured protein turnover rates will be important for understanding of th

298 The plot was characterized by high AMF turnover rates with a positive spatiotemporal relationsh

299 that S. pyogenes has an unusually high mRNA turnover rate, with median and mean half-lives of 0.88 m

300 through which cells can maintain high actin turnover rates without having to alkalinize cytosol, whi