ライフサイエンスコーパス: forced

1 10(17) Previously, atomic interactions have forced a compromise between clock stability, which benef

2 thiophene units to the central borepin cores forced a high degree of local aromaticity within the bor

3 nd maintained similar levels of COC-SA, (ii) forced abstinence from COC-SA enhanced mPFC PN excitabil

4 Forced abstinence from higher preferred levels of drug t

5 them for relapse to aggression seeking after forced abstinence or punishment-induced suppression of a

6 higher after 21 days of either voluntary or forced abstinence than after 1 day (incubation of metham

7 ng signaling in D2-MSNs following 10-14 d of forced abstinence.

8 ated rats, this occurred after 14-18 days of forced abstinence.

9 palatable food; 20 trials/day) or home-cage forced abstinence.

10 fluctuation in Arabidopsis thaliana However, forced acidification through artificial proton pump acti

11 However, forced acidification through artificial proton pump acti

12 naling acts principally to activate AKT, and forced activation of AKT rescued GCB-DLBCL lines from kn

13 Forced activation of an FGF-ERK-ETV axis that is crucial

14 poxic GC cells that generates lethal ROS via forced activation of OXPHOS.

15 male Balb/c mice were exposed to 3 ppm O3 or forced air for 2 h and were studied after 6 or 24 h.

16 thods of relatedness estimation unusable, we forced all loci homozygous, in a process we refer to as

17 We demonstrate that forced apical localization of Par3, which is normally re

18 The stronger Asian lithosphere is also forced beneath the Indian lithosphere, forming a reverse

19 Doses of 25, 40, and 55 Gy were applied in forced-breath-hold to the atrioventricular junction, lef

20 on showed incubation of heroin craving after forced but not voluntary abstinence.

21 three climate models (GFDL, CCSM3, and CNRM) forced by a medium-high emission scenario (A2) in combin

22 SA partitioning and bioaccumulation modeling forced by changes in atmospheric inputs reasonably captu

23 Basin climate is sensitive to and indirectly forced by changes in the cryosphere, as evidenced by fas

24 ed an end-to-end ecosystem model (Atlantis), forced by downscaled global climate models and informed

25 r North Atlantic circulation changes, likely forced by increased southward flow of Arctic waters, con

26 owth of secondary vegetation and how much is forced by internal variability within the tropical ocean

27 We use a Lagrangian approach forced by modelled ocean circulation to simulate the cir

28 hanges, but is inconsistent with simulations forced by natural changes alone.

29 nary Research On Climate version 5 (MIROC5), forced by Representative Concentration Pathway 4.5 and 8

30 a numerical human dispersal model, which is forced by spatiotemporal estimates of climate and sea le

31 the relative roles of contemporaneous ocean-forced change and of ongoing glacier response to an earl

32 Importantly, forced changes in Erdr1 expression levels dictate the su

33 Anthropogenically-forced changes in ocean chemistry at both the global and

34 Next, a two-alternative forced choice perception experiment was performed (16 re

35 ts used pointing or left/right 2-alternative forced choice tasks to examine perceptual judgments of s

36 ith EEG as subjects performed a two-interval forced-choice contrast discrimination task.

37 check-all-that-apply questions, treating the forced-choice format as the "gold standard," ranged from

38 In Experiment 1, participants made forced-choice judgments of which of two tactile distance

39 s were apparent for all 4 outcomes, with the forced-choice questions yielding prevalence estimates ap

40 We developed a two-alternative forced-choice task in an automated modified T-maze.

41 In a forced-choice task, 2- to 4-year-olds successfully ident

42 ring a virtual memory-guided two-alternative forced-choice task.

43 , respectively, in a delayed two-alternative forced-choice task.

44 stions, with estimates measured by means of "forced-choice" questions.

45 Historically-forced climate models do not reproduce the observed tren

46 enhanced ice sheet runoff under volcanically forced conditions despite atmospheric cooling.

47 ee convection (at 50, 60, and 70 degrees C), forced convection at 40 degrees C and 315W microwave pow

48 volume and fuel plasma, while plasma-induced forced convection cools the substrate.

49 The column was cooled through forced convection inside the GC oven within the time fra

50 A laminar flow forced convection model was used in the design of a part

51 reduction of charge transfer resistance with forced convective flow of electrolytes as a result of be

52 It was discovered that forced convective flow of electrolytes greatly enhanced

53 nse to glutamate in a rat recombinant mGluR2 forced-coupled Ca(2+) mobilization assay.

54 The CMIP5 externally forced decline in Barents Sea winter SIE is much weaker

55 n of the Southern Hemisphere westerly winds, forced deglaciation of this sector from at least 10,400

56 onitoring a continuous biologics process and forced degradation studies.

57 Second, a forced degradation study showed an increase in acidic sp

58 al dysfunction; circadian misalignment using forced desynchrony increases cardiovascular risk factors

59 The circadian and immune systems are linked; forced desynchrony of the circadian clock via nighttime

60 their free-running circadian periods using a forced desynchrony protocol with a 5-h day.

61 When forced detours require re-planning of the route to the g

62 In recent years, global forced displacement has reached record levels, with 22.5

63 espread genome CNAs that were independent of forced disruption of Tp53 and telomere shortening.

64 e changes in subseafloor carbon storage that forced distinct episodes of methane release due to natur

65 Forced Dnmt3b expression induced widespread DNA hypermet

66 a "rocket" natural draft stove (NDS), and a forced draft gasifier stove (FDGS), in order of increasi

67 es and include a low-cost ceramic model, two forced-draft cookstoves (FDCS; Philips HD4012LS and ACE-

68 After 6 months of forced drug abstinence, LgA rats returned to pre-escalat

69 These effects are inhibited by forced elevation of NADH, reduced expression of CtBP, or

70 to either submaximal exercise training or no forced exercise (untrained).

71 the humid air on the paper-sensor during the forced exhalation reduced the electrical resistance of t

72 ostbronchodilator FEV1 and prebronchodilator forced expiratory flow at 25% to 75% of forced vital cap

73 tion (FEV1, forced vital capacity [FVC], and forced expiratory flow between 25% and 75% [FEF25-75]) a

74 Percent predicted forced expiratory flow between the 25th and 75th percent

75 243250 was associated with increased FEV240 (Forced Expiratory Flow Volume after 240s of hypertonic s

76 al lung capacity) and lesser flows (FEV1 and forced expiratory flow, midexpiratory phase), and with i

77 FEV1/forced vital capacity (FVC) ratio, and forced expiratory volume after exhaling 75% of vital cap

78 point was change from baseline at week 12 in forced expiratory volume in 1 s (FEV1 in L) in patients

79 gnosis of cystic fibrosis, percent predicted forced expiratory volume in 1 s (FEV1) of 70 or more, an

80 d with a postbronchodilator reversibility in forced expiratory volume in 1 s (FEV1) of at least 12% a

81 gible patients had COPD, post-bronchodilator forced expiratory volume in 1 s (FEV1) of less than 50%,

82 lowed up by questionnaires until age 5, when forced expiratory volume in 1 s (FEV1) was measured by s

83 Among obese patients, the forced expiratory volume in 1 s (FEV1) was significantly

84 hen adjusted for sex, body-mass index (BMI), forced expiratory volume in 1 s (FEV1), and PA:A greater

85 ithin 1 year (defined as post-bronchodilator forced expiratory volume in 1 s [FEV1] to forced vital c

86 ung function measures sequentially (ratio of forced expiratory volume in 1 s [FEV1] to forced vital c

87 ase in FVC (forced vital capacity) and FEV1 (forced expiratory volume in 1 s) of 0.03 L [95% confiden

88 ng mass was the only measure associated with forced expiratory volume in 1 sec (FEV1) decline, with e

89 2) and 4.0 percentage points lower predicted forced expiratory volume in 1 second (95% CI, -6.6 to -1

90 flation, r = -0.8; 95% CI: -0.94, 0.42), and forced expiratory volume in 1 second (airway obstruction

91 re decline in lung function measurements for forced expiratory volume in 1 second (FEV1) (388 mL), fo

92 siblings (P = 0.010) and is associated with forced expiratory volume in 1 second (FEV1) (P = 0.030).

93 solute change in the percentage of predicted forced expiratory volume in 1 second (FEV1) from the bas

94 eal-life study was to compare the changes in forced expiratory volume in 1 second (FEV1) of omalizuma

95 te change in the percentage of the predicted forced expiratory volume in 1 second (FEV1) through week

96 .77; P < .0001) with percentage predicted of forced expiratory volume in 1 second (FEV1) was observed

97 effect of either benralizumab regimen on the forced expiratory volume in 1 second (FEV1), as compared

98 h and decline on the basis of graphs showing forced expiratory volume in 1 second (FEV1), representin

99 ficant correlation (P < .01) with changes in forced expiratory volume in 1 second (r = 0.70), forced

100 year, asthma hospitalization in prior year, forced expiratory volume in 1 second [FEV1 ; FEV1 <65% v

101 y history of lung cancer, and lung function (forced expiratory volume in 1 second [FEV1]).

102 The prebronchodilator forced expiratory volume in 1 second at week 52 was high

103 ion of methacholine required to decrease the forced expiratory volume in 1 second by 20% (PC20).

104 e model that predicted PRM gas trapping, the forced expiratory volume in 1 second normalized to the f

105 difference in the z scores for the ratio of forced expiratory volume in 1 second to forced vital cap

106 ity of the lungs for carbon monoxide (DLCO), forced expiratory volume in 1 second, and forced vital c

107 x, estimated glomerular filtration rate, and forced expiratory volume in 1 second.

108 alth care use and lung function, measured by forced expiratory volume in 1 second.

109 /= 0.35 kUA /L) (n = 418) and lung function [forced expiratory volume in one second (FEV1 ) and force

110 ization, serum total immunoglobulin E (IgE), forced expiratory volume in one-second (FEV1) and forced

111 de Park led to an increase in lung function (forced expiratory volume in the first second [FEV1] and

112 mean BMI of 21.6 [IQR, 18.2-26.1], mean [SD] forced expiratory volume in the first second of expirati

113 high-density lipoprotein (HDL) cholesterol, forced expiratory volume, grip strength, HbA1c, longevit

114 ene, has been previously associated with the forced expiratory volume/forced vital capacity ratio.

115 logical measurements of lung function (i.e., forced expiratory volumes and diffusing capacities).

116 Moreover, forced expression and knockdown of SPZ1 in hepatoma cell

117 This is rescued by forced expression of a deacetylated CTTN mimetic.

118 Forced expression of Amigo2 in QRsP-11 cells increased l

119 the survival and growth of T-ALL cells, and forced expression of ARID5B in immature thymocytes resul

120 not expressed in mammalian MG after injury, forced expression of Ascl1 in mouse MG induces a neuroge

121 Forced expression of bta-miR-23a mimics reduced lipid ac

122 Forced expression of Cxcl12, Fzd2, or Ifi27l2a increases

123 expression, migration and invasion, whereas forced expression of EpCAM resulted in decreased ERK pat

124 Forced expression of EphA4 reversed the effects of miR-5

125 Here we show that forced expression of FGFR3b-S249C, the most prevalent FG

126 Moreover, forced expression of forkhead box protein O1 (FoxO1), an

127 We found that forced expression of GAS5 blocked, but knockdown of GAS5

128 Forced expression of hsa-miR-125b in these cells resulte

129 actions was restricted to myogenic cells, as forced expression of ICAM-1 by fibroblasts did not augme

130 Our analysis revealed that forced expression of Irf4 repressed ES-DC development, w

131 Direct reprogramming can be achieved by forced expression of master transcription factors.

132 Forced expression of MCM8 in RWPE1 cells, the immortaliz

133 s (iCPCs) from mouse adult fibroblasts using forced expression of Mesp1, Tbx5, Gata4, Nkx2.5 and Baf6

134 'missing-self' response can be prevented by forced expression of minimally polymorphic HLA-E molecul

135 Forced expression of miR-23b cluster or miR-125a-5p enha

136 Forced expression of MIST1 in PCs caused them to expand

137 tiation of primary human skin fibroblasts by forced expression of myogenic transcription factor MyoD,

138 Forced expression of necdin enhances mitochondrial funct

139 Forced expression of NUMBL inhibits osteoclast different

140 However, forced expression of pneumococcal NanA in GBS removed te

141 Forced expression of recombinant afadin in pulmonary end

142 Forced expression of SAP in SLE T cells normalized IL-2

143 Forced expression of Six1 in the postnatal retina was su

144 Forced expression of STIM1 in cultured adult feline vent

145 We found that forced expression of the Notch inhibitor NUMB in HepaRG

146 Forced expression of the WT1(-KTS) isoform, which functi

147 Forced expression of these novel genes resulted in IL3-i

148 Further, the forced expression of TRPM2 mutant channel (C1008-->A) or

149 Forced expression of Vsig4 in mice ameliorates MHV-3-ind

150 Using a combination of protein silencing and forced expression of wild-type/constitutively active var

151 e1 and Prickle2 in individual cells or local forced expression of Wnt5a perturbed polarization of nei

152 Forced expression of WT or variant Kcnj2 changes the nor

153 Forced-expression of MICU1 in normal cells phenocopies t

154 n analysis of the critical properties in the forced ferromagnetic region yields 3D Heisenberg exponen

155 fect on biliary cholesterol excretion, while forced GATA4 expression increases cholesterol excretion

156 oci homozygous, in a process we refer to as "forced homozygote approach".

157 The evolution to bipedalism forced humans to develop suitable strategies for dynamic

158 Climate-forced ice losses are increasing potential for iceberg-s

159 Interestingly, the forced inhibition of miR-23a and miR-23b during C2C12 di

160 Using novel real-time MRI, forced inspiration has been identified recently as a mai

161 CSF movement toward the brain in response to forced inspiration was seen in all subjects at the aqued

162 moved upward toward the head in response to forced inspiration.

163 for time-to-event analyses with age and sex forced into all models and additional covariates evaluat

164 can become responsive to the treatment when forced into cycle via granulocyte colony-stimulating fac

165 We review the high pressure forced intrusion studies of water in hydrophobic micropo

166 It includes forced labor and sexual exploitation of both U.S. and no

167 g of mutant LDB1 to the beta-globin promoter forced LCR loop formation in the absence of mediator or

168 The Earth's rotation forced life to evolve under cyclic day and night environ

169 ems and predict their dynamics in terms of a forced linear model.

170 decomposition of chaos as an intermittently forced linear system.

171 Furthermore, forced localization of the D252G and W274L mutations int

172 d by Col17a1 deficiency and prevented by the forced maintenance of COL17A1 in HFSCs, demonstrating th

173 We find that forced maintenance of CRISPR targets induces a fitness c

174 Forced MCPH1 expression causes cell death, underlining t

175 Microfibril movements during forced mechanical extensions differ from those during cr

176 he transatlantic slave trade was the largest forced migration in world history.

177 ern Hemisphere represents one of the largest forced migrations in history and had a profound impact o

178 ghlights the decisive role of astronomically forced "Milankovitch" climate change in timing and pacin

179 pper surface of the deep brine layer by wind-forced mixing.

180 of-function mouse models to demonstrate that forced MSI2 expression retards anagen entry and conseque

181 And also, the forced oscillation technique (FOT) is a noninvasive meth

182 nd impaired lung mechanics determined by the forced oscillation technique and plethysmography.

183 thematical models including free-running and forced oscillators and signalling systems.

184 Finally, forced overexpression of full-length KRT7-AS or OL KRT7-

185 ificant reduction in cell proliferation, and forced overexpression of JunD increased the proliferatio

186 Forced overexpression of MGLL in human HCC cells resulte

187 Forced overexpression of miR-218 in NK cells knocked dow

188 Forced overexpression of miR-34a in CCA cells inhibited

189 Forced overexpression of MYBL1 led to a reduced populati

190 he recently proposed theoretical approach of forced partitioning for three structurally different bet

191 Commensurately, forced PHLPP2 expression ameliorates hepatic steatosis i

192 hat incursions of warm Atlantic bottom water forced rapid gas hydrate dissociation and enhanced metha

193 udied by means of Infrared Thermal Diffusion Forced Rayleigh Scattering.

194 A forced reduction in intracellular iron reduces the proli

195 nted the abuses they had suffered, including forced religious conversion, torture, and sex slavery.

196 ations and CMIP5 multi-model mean externally forced response.

197 Forced retention of NPM1 in the nucleus, as well as inhi

198 cally-loading hat-shaped specimens to induce forced shear localization.

199 Forced SHP expression normalizes lipoprotein secretion w

200 prevalence among renal failure patients has forced some centers to carefully consider such candidate

201 in Europe with temperate distributions were forced south, becoming distributed among the isolated pe

202 tween a feeding gravid state and a period of forced starvation while they brood developing young insi

203 AR levels increased in TNBC cells grown in forced suspension culture compared with those in attache

204 indicated by reduced immobility time in the forced swim and tail suspension tasks, as well as reduce

205 abolite ratio which strongly correlated with forced swim test (FST) floating time.

206 ice using the sucrose preference test (SPT), forced swim test (FST), and tail suspension test (TST).

207 dels: the tail suspension test (TST) and the forced swim test (FST).

208 assessed their behavioral response with the forced swim test (FST).

209 t, increased depression-like behavior in the forced swim test was observed in all mice, regardless of

210 ssive-like behavior (via tail suspension and forced swim test) was assessed.

211 We used the forced swim test, a standardized behavioral approach to

212 s well as an increase in floating during the forced swim test, indicative of a depression-like phenot

213 amine blocked stress-induced behavior in the forced swim test, novelty suppressed feeding paradigm, a

214 ory bulbectomy, chronic mild stress, chronic forced swim test, novelty-induced hypophagia (NIH), nove

215 aired responses to ketamine treatment in the forced swim test.

216 nteraction and reduced passive behavior in a forced swim test.

217 ed zero maze, acoustic startle response, and forced swim test.

218 eased immobility in both tail suspension and forced swim tests.

219 d in the open-field, elevated-plus-maze, and forced swim tests.

220 was observed in the prepulse inhibition and forced swim tests.

221 sing novelty suppressed feeding, splash, and forced swim tests.

222 ts biochemically and behaviorally, using the forced swim, tail suspension, and novelty suppressed fee

223 atment during CUS blocked the changes in the forced-swim test and deficits in memory recall.

224 phetamine hydrochloride into the mPFC before forced-swim testing.

225 ice, assessed by tail suspension test (TST), forced swimming test (FST), novelty suppressed feeding (

226 essed feeding and the immobility time in the forced swimming test in BDNF(Val/Val) but not in BDNF(Me

227 nalysis of tipping phenomena in periodically forced systems and show that, when limit cycles are cons

228 reduced the impairment in motor function on forced tasks, such as rotarod and treadmill tests, cause

229 covers from significant perturbations, e.g., forced temporary switching off aimed at utilizing the fl

230 It is generally assumed that as more heat is forced through the thermoelectric legs, their performanc

231 ing fired at 90 m.s(-1) through fish scales, forced through vial septa, and employed in a targeted st

232 As a consequence, alphaS molecules are forced to access a hidden conformational state on the ph

233 Many models of morphogenesis are forced to assume specific mechanical properties of cells

234 A protein forced to be continuously unfolded completely loses its

235 In order to maintain yields, farmers may be forced to change cultivation practices, the timing of cu

236 variant analysis to their investigations is forced to explore the literature for mtDNA pipelines, ev

237 xpress ICAM-1, and myoblasts and fibroblasts forced to express full length ICAM-1 or a truncated form

238 hospitals in the United States, ASPs will be forced to find ways to provide more efficient, impactful

239 es, tens to hundreds million people could be forced to leave the Sahel by the end of this century.

240 e to stroke decreasing, more individuals are forced to live with crippling disability resulting from

241 eductible insurance plans, many patients are forced to pay high retail prices to obtain their medicat

242 AMD patients read slower than controls when forced to read out loud.

243 We are now forced to reconsider this definition by the avalanche of

244 elded between 19 and 47% more oil than crops forced to remain erect.

245 e inhospitable environments, tumor cells are forced to remodel their signaling pathways by altering t

246 e efficiently, we observe that when fish are forced to swim fast-well above their free-swimming typic

247 e future payoffs will occur and (ii) are not forced to take the immediate reward out of financial nee

248 ly, these phenotypes could be rescued by the forced transcription of TERRA independent of CTCF bindin

249 LD) or high intensity, short duration (HISD) forced treadmill regimen.

250 in West Antarctica is part of a climatically forced trend that was triggered in the 1940s.

251 lates the local concentration of tPA through forced unbinding via degradation of fibrin and tPA relea

252 recancerous adenomatous polyps and show that forced upregulation of CBS in an adenoma-like colonic ep

253 levels of TNFalpha associated with VHL loss forced VHL-deficient cells to rely on intact RIPK1 to in

254 ren with asthma and airway obstruction (FEV1/forced vital capacity < 0.85 and FEV1 < 100% predicted)

255 piratory volume in 1 second (FEV1) (388 mL), forced vital capacity (298 mL), and the FEV1/forced vita

256 ate pregnancy was negatively associated with forced vital capacity (difference in standard deviation

257 year, was defined as a decrease in predicted forced vital capacity (FVC) by 10% or more, a decrease i

258 CNV association (discovery P = 0.0007) with Forced Vital Capacity (FVC) downstream of BANP on chromo

259 riants associated with FEV1 and its ratio to forced vital capacity (FVC) in never-smokers.

260 SAMS scores were associated with changes in forced vital capacity (FVC) in two cohorts.

261 COPD was defined as FEV1/forced vital capacity (FVC) of less than 70% and less th

262 ed with PEA showed a lower decrease in their forced vital capacity (FVC) over time as compared with u

263 bject pollutant concentrations with FEV1 and forced vital capacity (FVC) percent predicted, FEV1/FVC

264 unger gestational age had a lower FEV1, FEV1/forced vital capacity (FVC) ratio, and forced expiratory

265 truction phenotype (A Trpg) was defined as a forced vital capacity (FVC) z score of less than -1.64 o

266 Exploratory efficacy measurements included forced vital capacity (FVC), carbon monoxide diffusing c

267 Lung function parameters (forced vital capacity (FVC), pre- and postbronchodilator

268 Eligible patients, stratified by baseline forced vital capacity (FVC), serum LOXL2 (sLOXL2) concen

269 d expiratory volume in one-second (FEV1) and forced vital capacity (FVC).

270 expiratory volume in one second (FEV1 ) and forced vital capacity (FVC)] (n = 414).

271 of dysphagia (OR=10.67; p=0.03) and reduced forced vital capacity (p=0.005).

272 V values of patients with CF correlated with forced vital capacity (r = 0.7; 95% confidence interval

273 ed expiratory volume in 1 second (r = 0.70), forced vital capacity (r = 0.84), and %VV (r = 0.56).

274 iratory volume in 1 second normalized to the forced vital capacity (standardized coefficients [betaS]

275 of forced expiratory volume in 1 s [FEV1] to forced vital capacity [FVC] <70%, bronchodilator reversi

276 or forced expiratory volume in 1 s [FEV1] to forced vital capacity [FVC] ratio <0.7 in patients with

277 ratory volume in the first second [FEV1] and forced vital capacity [FVC]) and a decrease in pulse wav

278 Measures of lung function (FEV1, forced vital capacity [FVC], and forced expiratory flow

279 ts negatively and positively correlated with forced vital capacity and age, respectively.

280 The rate of progression of the forced vital capacity and of the ALS Functional Rating S

281 The primary endpoint, change in forced vital capacity as a percentage of the predicted n

282 a statistically significant increase in ALS-forced vital capacity decline in SOD1(A4V) compared with

283 forced vital capacity (298 mL), and the FEV1/forced vital capacity ratio (3.7%) over the follow-up, c

284 el was associated with a 5% decrease in FEV1/forced vital capacity ratio (beta = -0.05; 95% CI, -0.08

285 , and IL4R were associated with reduced FEV1/forced vital capacity ratio (beta = -0.11, -0.08, and -0

286 associated with the forced expiratory volume/forced vital capacity ratio.

287 None of the SNPs identified for FEV1/forced vital capacity replicated in the independent coho

288 o of forced expiratory volume in 1 second to forced vital capacity was -0.75 (95% confidence interval

289 flow between the 25th and 75th percentile of forced vital capacity was also inversely associated with

290 ), forced expiratory volume in 1 second, and forced vital capacity were performed systematically befo

291 ation was associated with a decrease in FVC (forced vital capacity) and FEV1 (forced expiratory volum

292 Pseudomonas aeruginosa infection, FEV1/FVC (forced vital capacity), PA:A greater than 1, and previou

293 o phenotypes used to assess asthma severity: forced vital capacity, a sensitive measure of airway obs

294 ither ALS Functional Rating Scale-Revised or forced vital capacity, having at least 25% improvement a

295 om -5.1% to -1.2%/month percentage predicted forced vital capacity, P < .04 and from -1.2 to 0.6 ALS

296 ator forced expiratory flow at 25% to 75% of forced vital capacity.

297 nd we found some evidence of less decline in forced vital capacity.

298 decade(-1)) compared with the ensemble mean (forced) warming rate projected by Coupled Model Intercom

299 When forced with common environmental drivers, the soil model

300 from a large ensemble of climate simulations forced with natural and anthropogenic changes, but is in