ライフサイエンスコーパス: forced

1 When plant growth forced a decision between the two arms of the maze, fans

2 he Northern Hemisphere, expanding ice sheets forced a large number of plants, including trees, to ret

3 d abstinence (shPKCdelta groups) or homecage forced abstinence (shSOM groups).

4 nd decreased incubated drug seeking after 15 forced abstinence days.

5 hereas Egr3 overexpression in D2-MSNs during forced abstinence facilitated extinction and blunted dru

6 A-seq) following differential housing during forced abstinence from cocaine self-administration for e

7 otein levels in the NAc following 20 days of forced abstinence from intravenous cocaine self-administ

8 ulated transcripts between rats of different forced abstinence length and housing environment, as wel

9 ally enriched based on housing condition and forced abstinence length including RELN, the Eif2 signal

10 We then exposed them to either homecage forced abstinence or voluntary abstinence induced by an

11 have used experimenter-imposed extinction or forced abstinence procedures.

12 Enriched, 21-day forced abstinence rats displayed a significant reduction

13 In contrast, incubation of craving after forced abstinence was associated with activation of CeL-

14 n gene expression associated with protracted forced abstinence.

15 ignaling pathways that occurs during cocaine forced abstinence.

16 ronger after voluntary abstinence than after forced abstinence.

17 ed oxycodone seeking after voluntary but not forced abstinence.

18 oxycodone seeking after either voluntary or forced abstinence.

19 5 receptor availability following 2 weeks of forced abstinence.

20 social choice-induced abstinence than after forced abstinence.

21 del, drug seeking is assessed after homecage forced abstinence.

22 ay 1 or after 15 days of either voluntary or forced abstinence.

23 uced only in female rodents after 20 days of forced abstinence.

24 point was also obtained following 2 years of forced abstinence.

25 eking behaviors in animals when given during forced abstinence.

26 Rats were exposed to forced activity, either in their rest-phase (simulating

27 nates from the novel formulation to prevent 'forced altruism' hidden in previous static algorithms wh

28 n of observational data and state-of-the-art forced and control climate model simulations to demonstr

29 series of GMSST over 1950-2010 is externally forced and largely linked to the representation of volca

30 Suppression of the APC/C or forced APC/C activation by targeting its repressor EMI1

31 Forced ASCL1 expression reversed the tumor-suppressive e

32 of undisturbed sleep (US) and two nights of forced awakening (FA) sleep disruption.

33 In both experiments, forced awakenings were applied to achieve rapid recovery

34 n cases were partitioned into 2 subgroups by forced binary clustering of cell counts: the inflamed de

35 Rather, it forced blood to flow peripherally to the gel.

36 Using a lake model forced by 21(st) century climate projections, we found t

37 the Benguela, a positive upwelling trend is forced by a global sea level pressure trend, which is co

38 show that the pause in circulation trends is forced by human activities, and has not occurred owing o

39 Model warming projections, forced by increasing greenhouse gases, have a large inte

40 he seasonal cycle of Arctic sea-ice that are forced by orbital variations and volcanic eruptions.

41 We use a dynamic bioclimate envelope model forced by physical-biogeochemical output from eight ocea

42 We infer that projections forced by RCP8.5 underestimate glacier mass loss which c

43 rced coupled climate model simulations, were forced by sea surface temperatures (SSTs) and exacerbate

44 further show the anomalous coastal winds are forced by the coastal warming.

45 We employed a simple two-alternative forced choice gambling task and quantified the frequency

46 In a forced choice matching task, humans but not great apes,

47 The forced choice procedure revealed that subjective ratings

48 Laboratory measures included a forced choice session (to measure reinforcement of nicot

49 the understanding of the emergent themes of forced choice, adjustment, gratitude, relationship chang

50 a standard psychophysical method (2-interval forced choice, in which the participant identifies which

51 Hence, performances on two, four-alternative forced-choice achromatic flicker fusion threshold tasks

52 ealthy participants (30 females) completed a forced-choice emotional face recognition task with stimu

53 rvers viewed stimulus videos and performed a forced-choice heading discrimination task.

54 find a robust sex difference in the classic forced-choice jealousy task.

55 he JND) were successfully discriminated in a forced-choice task.

56 During forced-choice trials, GCaMP6f transients shifted from pr

57 Here, we use a forced-choice, operant behavior assay to investigate rod

58 g the source of required action (free versus forced choices), outcome contingencies (low versus high

59 f 3.6, 2.5, and 1.5 mm on blink, gentle, and forced closures, respectively.

60 ed an intervention, compared with 11% in the forced coagulation group (P = .006).

61 oved (96% in the Endocut group vs 95% in the forced coagulation group) or the proportion of polyps fo

62 he Endocut group and 7.9% of patients in the forced coagulation group, with no significant difference

63 current (Endocut Q) or coagulation current (forced coagulation) (Erbe Inc) (secondary intervention a

64 ction of large colorectal polyps (Endocut vs forced coagulation), we found no difference in risk of s

65 readings taking wind into account rely on a forced convection heat transfer coefficient.

66 on reservoirs expanded during astronomically-forced cool spells.

67 ional heatwaves, hotter than in historically forced coupled climate model simulations, were forced by

68 e, even though the expected pattern of tidal forced deformation should be symmetric between the north

69 h has been utilized to quantify the PTMs for forced degradation samples, comparability samples, and t

70 The results from forced degradation studies along with peak purity tests

71 the five most abundant oxidation products in forced degradation studies of two full-length therapeuti

72 r Executive Order 13688, which resulted in a forced demilitarization of several hundred departments.

73 intrinsic circadian period as measured under forced desynchrony protocols, the 'gold standard' for in

74 need for an effective SARS-CoV-2 vaccine has forced development to progress in the absence of well-de

75 ng concern to healthcare workers globally as forced displacement and migration from countries with hi

76 rriers to access among migrants experiencing forced displacement, particularly refugees and asylum se

77 the health needs of populations affected by forced displacement; the health systems-level barriers a

78 rus responsible for a worldwide pandemic has forced drastic changes in medical practice in an alarmin

79 s was confirmed intraoperatively by negative forced duction test and the characteristic appearance of

80 Here, we show that overexpression of a forced E2A homodimer is sufficient to drive robust neura

81 Forced E2F2 expression in the parental cells led to the

82 It is found to be essential to induce forced electrolyte convection into the thin electrolyte

83 ed out BCoV HE lectin function and performed forced evolution-population dynamics analysis.

84 Andrew Murray argues that you can use your forced exile from the lab to produce better future exper

85 efore (lag 2) were associated with lower mid-forced expiratory flow (FEF(25%-75%) ) and FEV(1) /FVC r

86 5% CI], -0.03 [-0.06 to -0.00]) but not with forced expiratory flow after exhaling 75% of FVC or asth

87 in prebronchodilator and postbronchodilator forced expiratory flow at 25% to 75% of vital capacity g

88 (1) and prebronchodilator/postbronchodilator forced expiratory flow at 25% to 75% of vital capacity o

89 d (FEV(1)), forced vital capacity (FVC), and forced expiratory flow at 25-75% of the pulmonary volume

90 ; n = 7) had lower FEV(1)/FVC (P = 0.02) and forced expiratory flow, midexpiratory phase (P = 0.009).

91 levels and growth rates of FVC, FEV(1), and forced expiratory flow, midexpiratory phase in both sexe

92 tcomes included percent-predicted one-second forced expiratory volume (FEV1%), forced vital capacity

93 All patients completed tests of preoperative forced expiratory volume capacity in 1 s (FEV1) and diff

94 al effects of 474 smoking-associated CpGs on forced expiratory volume in 1 s (FEV(1)) in UK Biobank (

95 etween DHEA-sulfate and percentage predicted forced expiratory volume in 1 s (FEV(1)PP).

96 Forced expiratory volume in 1 s/forced vital capacity (F

97 competence (OR, 3.58; 95% CI, 1.75 to 7.31); forced expiratory volume in 1 second < 80% (OR, 2.59; 95

98 bations, improved prebronchodilator (pre-BD) forced expiratory volume in 1 second (FEV(1) ) and quali

99 ose with severe persistent disease, can have forced expiratory volume in 1 second (FEV(1) ) values >=

100 measurements were positively correlated with forced expiratory volume in 1 second (FEV(1)) (r = 0.65,

101 relationship between longitudinal changes in forced expiratory volume in 1 second (FEV(1)) and CT-qua

102 inical prognostic scores (Liou and CF-ABLE), forced expiratory volume in 1 second (FEV(1)), and risk

103 iations of prematurity and birth weight with forced expiratory volume in 1 second (FEV(1)), forced vi

104 ow obstruction with lower values of ratio of forced expiratory volume in 1 second (FEV(1))-to-functio

105 Forced expiratory volume in 1 second (FEV1) and forced v

106 Forced expiratory volume in 1 second (FEV1), forced vita

107 pid decline in lung function, as measured by forced expiratory volume in 1 second (FEV1), forced vita

108 A priori determined covariates were forced expiratory volume in 1 second and diffusion capac

109 d greater improvement relative to placebo in forced expiratory volume in 1 second at Day 28 (102 mL [

110 Kaplan-Meier curves showed patients with forced expiratory volume in 1 second decline >=5% and >=

111 Oxygen requirement >2 L/min at diagnosis and forced expiratory volume in 1 second decline >=5% postin

112 HSV or T2-weighted VIP were associated with forced expiratory volume in 1 second percentage predicte

113 ut airway obstruction, defined by a ratio of forced expiratory volume in 1 second to the forced vital

114 Greater effects on forced expiratory volume in 1 second were observed in th

115 were 92% for forced vital capacity, 93% for forced expiratory volume in 1 second, 116% for total lun

116 dence interval [CI], 67-345 mL; P = .004 and forced expiratory volume in 1 second, 143 mL higher; 95%

117 Safety, pharmacokinetics, forced expiratory volume in 1 second, asthma control que

118 , IQR(N) correlated with obstruction markers forced expiratory volume in 1 second-to-forced vital cap

119 n defect percentage were correlated with the forced expiratory volume in 1 second.

120 atment failure, asthma control days, and the forced expiratory volume in 1 second; a two-sided P valu

121 Airway obstruction was defined as forced expiratory volume in 1-second (FEV1)/forced vital

122 ilution) in eight patients with severe COPD (forced expiratory volume in 1s (FEV(1) ) +/- SEM = 0.9 +

123 sease and whether the first treatment year's forced expiratory volume in one second (FEV(1) ) predict

124 les, the Forced Vital Capacity (FVC) and the Forced Expiratory Volume in one second (FEV(1)) can be i

125 hat were found to be associated with similar forced expiratory volume in one second (FEV(1)) measurem

126 levels of these six genes and lung function (Forced Expiratory Volume in one second (FEV(1)), Forced

127 ancer is genetically correlated with reduced forced expiratory volume in one second (FEV(1): r(g) = 0

128 Forced expiratory volume in one second accounted for les

129 In 12 COPD patients (forced expiratory volume in one second: 58 +/- 17%pred.)

130 ratio values correlated positively with the forced expiratory volume in the first second (FEV(1), %)

131 COPD defined by postbronchodilator ratio of forced expired volume in the first second to vital capac

132 Forced expression of a constitutively active isoform of

133 vage of Septin-2 occurred at residue 306 and forced expression of a non-cleavable Septin-2 restored c

134 Interestingly, forced expression of a stabilized derivative of beta-cat

135 Forced expression of all four strands show cooperativity

136 Previous studies have shown that forced expression of core cardiogenic transcription fact

137 Importantly, forced expression of Hspa1a or inhibition of NF-kappaB s

138 Forced expression of miR-486-5p enhanced the self-renewa

139 sease phenotype, we evaluated the effects of forced expression of MNRR1 on the mitochondrial disease

140 muscle cells directly into myogenic cells by forced expression of MyoD represents one route to obtain

141 Forced expression of NO66 promoted cell survival and inv

142 Forced expression of NRARP reduced the abundance of NICD

143 Forced expression of plasmids expressing mutant Ezrin (T

144 ocopies deficiency of calsyntenin 3beta, and forced expression of S100b in brown adipocytes rescues t

145 Forced expression of SHANK2 in neuroblastoma cells resul

146 Forced expression of SOCS1 in macrophages depleted of ME

147 omyelinated; this defect could be rescued by forced expression of SOX10 and MYRF by mHTT hGPCs.

148 Forced expression of Tfap2 in i-cells converted them to

149 Forced expression of the irisin precursor Fndc5 in trans

150 or example, in Drosophila female germ cells, forced expression of the testis-specific PHD finger prot

151 Intracerebroventricular infusion or forced expression of this protein exacerbates neuroinfla

152 eobox 1 (ZEB1) in claudin-low tumor cells or forced expression of ZEB1 in basal-like tumor cells, two

153 Forced expression of ZFP36L1 in cancer cells markedly re

154 suppression of proliferation and invasion by forced expression, and significant stimulation of invasi

155 included lagophthalmos on blink, gentle and forced eyelid closure, upper eyelid margin-to-reflex dis

156 ction by promoting Fto mRNA degradation, and forced FTO expression in macrophages mimics the phenotyp

157 , it computes their numbers by averaging the forced-fusion and segregation estimates weighted by the

158 To assess their feasibility, a forced gradient cross-borehole tracer experiment was con

159 e Southwest in a context when climate change forced growing Ancestral Puebloan populations to exploit

160 Forced heterochromatin formation at implicated loci conf

161 size that this hiatus was climate-driven and forced hunter-gatherers to abandon the lakes.

162 combinant form of the ZIKV E protein that is forced in a covalently stable dimeric conformation (cvD)

163 ; however, current approaches typically used forced injections of synthetic cannabinoids or isolated

164 expiration (LES pressure) and at the peak of forced inspiration (hiatal contraction).

165 ure profile of the EGJ at end-expiration and forced inspiration revealed marked differences between t

166 By interfacing the i-motif with a forced-intercalation readout, we introduce a quencher-fr

167 e undetected in young adult mouse HSCs until forced into cycle.

168 issue-specific stem cell presumed to only be forced into self-renewal and differentiation by injury.

169 f concept for using remote sensing to detect forced labor abuses.

170 g data, we show that vessels reported to use forced labor behave in systematically different ways fro

171 While forced labor in the world's fishing fleet has been widel

172 on these vessels, many of whom may have been forced labor victims.

173 responded to the health system challenges of forced migration and refugee-related health including th

174 rds have fueled a broad understanding of the forced migration from Africa to the Americas yet remain

175 onflict and violence, nuclear proliferation, forced migration, globalisation, and climate change are

176 Mic60 can uniquely redistribute adjacent to forced mitochondria-vacuole contact sites.

177 However, the forced MMM only accounts for a small fraction of observe

178 It forced most institutions to shut down nearly every aspec

179 lice correcting oligomer was chosen to treat forced-myogenic cells, derived from fibroblasts from nin

180 Conversely, forced notch signaling in all TECs resulted in widesprea

181 Forced nuclear accumulation of PHB1 in human RKO or SW48

182 d ocean-atmosphere climate model simulations forced only by SC irradiance variations.

183 l/biogeochemical simulations of a seasonally-forced, open-Southern-Ocean ecosystem reveal that mesosc

184 Between tests, the rats underwent either forced or social choice-induced abstinence.

185 function was measured by a spirogram and the forced oscillation technique.

186 These findings are relevant to low-frequency forced oscillations in power grids and will help advance

187 Forced overexpression of active YAP (YAP5SA) in KCs enha

188 n mature Tregs, and ex vivo data reveal that forced overexpression of GILZ in mature Tregs inhibits t

189 mation, male and female transgenic mice with forced overexpression of Mfn2 specifically in neurons we

190 We observed that forced overexpression of Sox2 in TICs increased transcri

191 gene networks than parental Suit2 cells, and forced overexpression of ST6Gal-I in the Suit2 line was

192 Widespread use of these medications forced overwhelmed health care systems to search for way

193 However, forced PGC-1alpha over-expression rescued the deficits i

194 PR-based gene drive system can allow for the forced propagation of a genetic element that bypasses Me

195 ed already limited health care resources and forced rationing, triage, and prioritization of care in

196 Both forced reaggregation and endogenous cell mixing reveals

197 iation of hiPSC in 2D cultures followed by a forced reaggregation step that leads to highly enriched

198 rating foreign sequences in the viral genome forced researchers to select a fluorescent or a lucifera

199 oop measured while the patient is performing forced respiratory cycles, the Forced Vital Capacity (FV

200 nic forcing may overestimate the size of the forced response relative to natural ENSO variability.

201 n simulating multidecadal variability in the forced response, internal variability, or both.

202 up a biorefinery process to produce DFC from forced roots of Belgian endive (DFC-BE) and characterise

203 As a control, non-treated forced roots powder (FRP-BE) was tested.

204 and volcanic aerosols over GHG in generating forced Sahel rainfall variability in models.

205 The COVID-19 pandemic is causing deaths with forced separations that deny final goodbyes and traditio

206 s the relationship between the properties of forced, sheared, stratified turbulence (as found in ocea

207 depended on ST6Gal-I overexpression, because forced ST6Gal-I overexpression in normal gastric stem ce

208 eated rice bran protected RP the best during forced storage, with a 35% recovery after 8 weeks.

209 ur initial findings reveal that horizontally forced subduction zone initiation is dominant over the l

210 ) concentration coincide with supraglacially forced subglacial flushing events, confirming a subglaci

211 time-dependent antidepressant effects in the forced swim and novelty suppressed feeding tests, and in

212 tests) and depression-like (measured via the forced swim and saccharin preference tests) behaviors in

213 itor into the dorsal raphe prior to repeated forced swim stress decreased resulting stress-induced an

214 and altered stress-coping strategies in the forced swim task.

215 ress-induced depressive-like behavior in the forced swim test (FST), but prevented anxiety-like behav

216 d by increased duration of immobility in the forced swim test and decreased sucrose preference.

217 inetic evaluation, and in vivo efficacy in a forced swim test resulted in identification of 3-(6-chlo

218 of rat LHb neurons reduced immobility in the forced swim test, but the downstream target of these neu

219 ed a reduction in baseline immobility in the forced swim test, mimicking an antidepressant effect.

220 Using the forced swim test, we found that chemogenetic inhibition

221 that led to depressive-like behaviour in the forced swim test.

222 y times decreased on the tail suspension and forced swim tests; and sucrose preference increased.

223 g-lasting antidepressant-like effects in the forced swim, novelty-suppressed feeding, female urine sn

224 CORT increased immobility in the forced-swim test and impaired object-location memory.

225 Antidepressant activity was tested using the forced-swim test and tail suspension tests.

226 an antidepressant-like effect in the Porsolt forced swimming test in rats.

227 oTyper), the Elevated Plus Maze test and the Forced Swimming tests.

228 mobility time during the tail suspension and forced swimming tests.

229 as measured with the sucrose preference, and forced swimming tests.

230 ) were not affected after one or two days of forced swimming.

231 Disruption of shieldin or forced targeting of PALB2 to ssDNA in BRCA1(D11)53BP1(S2

232 Forced Tgfbr2 also rescued P2RX7-deficient Trm cell mito

233 Forced Tgfbr2 expression rescued P2RX7-deficient Trm cel

234 We forced the budding yeast, Saccharomyces cerevisiae, to u

235 , a number of factors have shifted that have forced the cardiology community to reconsider the role o

236 ngoing coronavirus disease 2019 pandemic has forced the clinical and scientific community to try drug

237 eatures of both naive and effector cells has forced the field to struggle with several conceptual que

238 e matter emission limit value that typically forced the introduction of a diesel particulate filter.

239 resistance against life-saving medicines has forced the scientific community and pharmaceutical indus

240 ders were thrust into unchartered waters and forced them to make unprecedented decisions.

241 ear signal that behaviour is environmentally forced through optimisation of gain, provides an integra

242 When people are forced to be isolated from each other, do they crave soc

243 The extended coastlines of Oman have been forced to change in the last few decades because of urba

244 elements of the feeding apparatus in fishes forced to employ alternate foraging modes.

245 Commissioner for Refugees, 44,000 people are forced to flee their homes every day due to conflict or

246 ncy of PRC2 increases drastically when it is forced to form PRC2.1.

247 be fused by deliberate genome engineering or forced to fuse spontaneously by blocking the replication

248 ted infection (1.57, 1.20-2.06); having been forced to have sex (1.82, 1.38-2.42); having experienced

249 west available states once two materials are forced to reach atomically close distance so that electr

250 tourist season, suggesting stingrays may be forced to rely on native prey items to supplement the de

251 during each expiration so that they are not forced to rerecruit during the subsequent inspiration.

252 tes, the cases of Leopold Lichtwitz, who was forced to resign as elected chairman in 1933, and commit

253 ally expressed the original association when forced to respond rapidly (~300-600 ms).

254 logical protection disappears when birds are forced to stay awake at other times of the year; thus th

255 Cells may naturally proceed or be forced to transition to a state with a radically lower b

256 laced on an atomically flat substrate can be forced to undergo a buckling transition(7-9), resulting

257 It is only when MEFs are forced to use mitochondrial oxidative metabolism for ATP

258 ave solidified important emerging trends and forced us to further innovate to get the most out of wor

259 scale score >1), and impaired lung function (forced vital capacity <=75% predicted) conducted in 39 U

260 ciated with reduced prebronchodilator FEV(1)/forced vital capacity (beta coefficient, -0.10; 95% CI,

261 Forced expiratory volume in 1 s/forced vital capacity (FEV(1)/FVC) but not FVC was relat

262 p = 2.3 x 10(-8)) and the ratio of FEV(1) to forced vital capacity (FEV(1)/FVC: r(g) = 0.137, p = 2.0

263 one-second forced expiratory volume (FEV1%), forced vital capacity (FVC%), and the FEV1/FVC ratio.

264 mild restrictive spirometric pattern [60 <= forced vital capacity (FVC) < 80% predicted] vs. 21.2% w

265 ed Expiratory Volume in one second (FEV(1)), Forced Vital Capacity (FVC) and FEV(1)/FVC).

266 y reduced decline in percentage of predicted forced vital capacity (FVC) and stabilised 6-min walking

267 is performing forced respiratory cycles, the Forced Vital Capacity (FVC) and the Forced Expiratory Vo

268 sing unclassifiable ILD, a percent predicted forced vital capacity (FVC) of 45% or higher and percent

269 lmonary fibrosis and percentage of predicted forced vital capacity (FVC) of 55% or greater were enrol

270 ssociation of alpha-T levels with FEV(1) and forced vital capacity (FVC) percent predicted.

271 forced expiratory volume in 1-second (FEV1)/forced vital capacity (FVC) ratio <0.7.

272 ced expiratory volume in 1 second (FEV1) and forced vital capacity (FVC) were lower in the HIV+ compa

273 rced expiratory volume in 1 second (FEV(1)), forced vital capacity (FVC), and forced expiratory flow

274 Forced expiratory volume in 1 second (FEV1), forced vital capacity (FVC), and physical activity were

275 forced expiratory volume in 1 second (FEV1), forced vital capacity (FVC), and their ratio (FEV1:FVC).

276 end point was the annual rate of decline in forced vital capacity (FVC), assessed over a 52-week per

277 th older age, being HIV+, and having reduced forced vital capacity (FVC).

278 y volume in the first second (FEV(1), %) and forced vital capacity (FVC, %) values.

279 ssociated with mortality after adjusting for forced vital capacity (HR 2.47, 95% CI 1.48-4.15; p=0.00

280 oved patients' HRCT scan scores (P < .0001), forced vital capacity (P = .0017), FEV(1) (P = .037), an

281 Jacobian values correlated with changes in forced vital capacity (R = -0.38; 95% CI: -0.25, -0.49;

282 or carbon monoxide, total lung capacity, and forced vital capacity (rho = -0.76, -0.70, and -0.62, re

283 t respiratory-related events, lung function (forced vital capacity and gas transfer), and patient-rep

284 %, A/C 5.2%, and C/C 9.5%; p = 0.003), lower forced vital capacity at diagnosis (median percentage A/

285 forced expiratory volume in 1 second to the forced vital capacity greater than or equal to 70% (HR,

286 er, measures of pulmonary dysfunction (PaO2, forced vital capacity percentage predicted, total lung c

287 with FEV(1) (r = -0.35; P = .04) and FEV(1)/forced vital capacity ratio (r = -0.41; P = .01).

288 kers forced expiratory volume in 1 second-to-forced vital capacity ratio (r = -0.70; 95% confidence i

289 (FEV(1)) (r = 0.65, P < .001), the FEV(1)-to-forced vital capacity ratio (r = 0.81, P < .001), and di

290 Subjects with preserved FEV(1)-to-forced vital capacity ratio and reduced FEV(1) percentag

291 ed FEV(1) percent predicted and an FEV(1)-to-forced vital capacity ratio at age 50 years (-3.36% [95%

292 , and the mean (SD) prebronchodilator FEV(1)/forced vital capacity ratio was 80.2% (9.0%).

293 or carbon monoxide, total lung capacity, and forced vital capacity were rho = -0.65, -0.70, and -0.57

294 patients up to 48 weeks post-ART initiation (forced vital capacity, 206 mL higher; 95% confidence int

295 centage of predicted values and were 92% for forced vital capacity, 93% for forced expiratory volume

296 either signal associated with FEV(1), FEV(1)/forced vital capacity, atopy, and age of asthma onset.

297 ocker-at the cholinergic synapse, suppressed forced water uptake by desiccated ticks, while injection

298 Female mice underwent forced wheel running at 37.5 degrees C/40% relative humi

299 Male and female C57bl/6J mice underwent forced wheel running for 1.5-3 h in a 37.5 degrees C/40%

300 Using an atmospheric model forced with observed SSTs, we also find that remote SST