ライフサイエンスコーパス: wheel

1 d 'rest' when activity in the brain is 'free-wheeling'.

2 en mice were caged without access to running wheels).

3 s were categorized using the Behavior Change Wheel.

4 timed access to a palatable meal or running wheel.

5 individuals and different parts of the color wheel.

6 revented the mice from mastering the complex wheel.

7 pping or releasing DNA on either side of the wheel.

8 name 100 evenly sampled hues along the color wheel.

9 r when housed at 28 degrees C with a running wheel.

10 iation of color name density along the color wheel.

11 lexy in the presence of chocolate or running wheels.

12 nce can be restored by returning the running wheels.

13 or CTH-12 containing Cu(II) dinuclear paddle-wheels.

14 ive thresholds and distances run on exercise wheels.

15 oth the ABA and food-restricted mice without wheels.

16 of alpha-PtO2, either assembling into spoked wheels, 1-5 bar O2, or closely packed in parallel lines,

17 ane K(ass) values were obtained for calix[8]-wheels 2 and 3, with respect to calix[6]-host 1a, due to

18 monium axles 7(+) and 8(+) with the calix[6]-wheel 3 can occur by both routes of entering the macrocy

19 ed water maze performance, decreased running wheel ability, and altered auditory cue conditioning.

20 The CKD rats with voluntary wheel access also had reduced kidney cystic weight and r

21 body weight during scheduled fasting without wheel access and showed no changes in food intake.

22 o shorten free running period in response to wheel access in constant darkness and entrained more rap

23 However, voluntary running wheel access in our G9-10 LVRs uniquely increased their

24 ndritic spine density in the NAc showed that wheel access increased spine density (P < 0.001), wherea

25 -dwelling, Veh- and Tam-treated mice without wheel access served as activity controls.

26 ture remained stable after the first week of wheel access, despite further increases in wheel use.

27 eel exposure or sedentary conditions without wheel access.

28 Effects of METH on rectal temperature and wheel activity at 27 degrees C ambient temperature were

29 xpenditure, total cage activity, and running wheel activity were measured in the offspring at various

30 hed when wakefulness is dominated by running wheel activity.

31 [2]pseudorotaxane isomers in which the calix-wheel adopts 1,2,3-alternate and cone conformations, whi

32 ack and forth motions of a crown-ether based wheel along the axis of a bistable rotaxane are triggere

33 Rewarding stimuli (chocolate or running wheels) also increased cataplexy, but CNO produced no fu

34 ing this idea, we observed a decrease in off-wheel ambulation when mice were using the wheels, indica

35 s easy incorporation of results into well-to-wheel analyses.

36 ates of this type are necessary for "well-to-wheel" analyses of increased gasoline octane ratings in

37 Helical-wheel analysis revealed strict segregation of polar and

38 l task in a virtual corridor by running on a wheel and licking at a reward location.

39 We found that short-term OVL combined with wheel and long-term OVL did not worsen the deficit in sp

40 Interestingly, short-term OVL combined with wheel and long-term OVL markedly improved the susceptibi

41 from area V1 in mice head-fixed on a running wheel and monitored pupil diameter to assay arousal.

42 d the density of color names along the color wheel and observed that parts of the color wheel with hi

43 Comparing periods of running on a ladder wheel and periods of resting, we furthermore identified

44 s between two parallel arene moieties of the wheel and the pyridyl unit of axle are operative in addi

45 mance of pass vs marginal/fail and number of wheel and/or brake interventions were recorded.

46 ts of wheels including one set of tert-butyl wheels and another set of larger adamantane wheels on th

47 exhibited by rodents exposed to both running wheels and scheduled fasting, provides a model for aspec

48 ectron trajectories using spin as a steering wheel, and the discovery of new topological classes of m

49 The well-to-pump, pump-to-wheel, and vehicle cycle stages are modeled.

50 e that you can't drive a car with only three wheels, and you also cannot estimate a causal effect in

51 -management, coaching, and a behavior change wheel as lenses through which to consider the evidence f

52 e first examples of charge-neutral molybdate wheels as confirmed by BVS, solubility experiments, and

53 native conformationally mobile calix[6]arene wheel, as a consequence of their higher degree of preorg

54 neuroactive substances combined with running-wheel assays suggested that GABA, pigment-dispersing fac

55 The cone wheel-based pseudorotaxanes are 10-100 times more stable

56 average new light-duty vehicles on a tank-to-wheel basis between 2010 and 2050 that we call CO2 glide

57 ange from 71.7 to 95.7 gCO2e/MJ on a well to wheel basis, with the range in carbon intensity being de

58 d with an unlocked (U) or locked (L) running wheel before and during pregnancy.

59 illar track complexes, in which two template wheels bind inside the nanoring.

60 linking was carried out by picturing "Aroma Wheels", built by Odour Activity Values (OAVs) of all th

61 lete threading of the axle fragment into the wheel cavity, where strong aromatic pi-pi stacking inter

62 MG491, two of the main components of the TO wheel complex that connects the TO with the cell body an

63 minal button, the electrodense core, and the wheel complex.

64 Chromium lanthanide heterometallic wheel complexes {Cr8 Ln8 } (Ln=Gd, Dy and Y) with altern

65 During constant access to food and running wheels, D2R-OE(NAc) mice of both sexes increased food in

66 for this cluster family-a new {Pd72 }(Prop) wheel decorated with propionate ligands.

67 rences, the density of color names along the wheel did not show any correlation with perceptual color

68 tantly, acute voluntary exercise in activity wheels did not increase the number of surviving cells.

69 Mice freely accessed a running wheel during three postnatal periods: the 4(th) postnata

70 ion), gestation trained (housed with running wheels during gestation), or sedentary (static cages).

71 ty-powered vehicles to have greater field-to-wheels efficiency (e.g., kilometers per gigajoule biomas

72 t range of heavy-duty vehicles, the field-to-wheels efficiency is higher for biofuels than for electr

73 Along a bus route in San Francisco, well-to-wheel emission factors ranged between 53 and 940 g of CO

74 hesis are modeled to estimate system well-to-wheel emissions and compare them to limits established b

75 ically calibrated fleet model, and a well-to-wheels emissions analysis.

76 4/72 eyes, 33.3%), displayed a radial "spoke-wheel" en face OCT pattern.

77 Accurate "tank-to-wheel" estimates of this type are necessary for "well-to

78 ormal chow, an HFD, or an HFD with voluntary wheel exercise for 6 weeks before and throughout pregnan

79 f transverse aortic constriction, or to free-wheel exercise, both of which promote adaptive cardiac m

80 ere randomly assigned to 3 weeks of activity wheel exposure or sedentary conditions without wheel acc

81 Use of a running wheel for 3 to 7 days increased daily energy expenditure

82 blated (VEGF(f/f) ) littermates with running wheels for 14 days.

83 four subgroups: trained (housed with running wheels for 2 weeks preconception and during gestation),

84 ), prepregnancy trained (housed with running wheels for 2 weeks preconception), gestation trained (ho

85 ousing in static cages or cages with running wheels for 2 weeks prior to breeding and throughout gest

86 ed in cages equipped with or without running wheels for 4 weeks.

87 can be utilized to selectively enrich Ln-MB wheels for effective separation of lanthanides.

88 osest packed structure, the mechanism of the wheel formation is proposed to depend on the delicate ba

89 pper prevents dethreading of the 30-membered wheel from the axle.

90 opment of safety-relevant components such as wheels from secondary material.

91 the Bakken well life cycle, then the well to wheel GHG emissions are estimated to be 89 g CO2eq/MJ (8

92 one pilot in a VTOL results in well-to-wing/wheel GHG emissions that are 35% lower but 28% higher th

93 In the OPT scenario, estimated well-to-wheels GHG emissions from full-size BEVs with 100-mile r

94 Well-to-wheel greenhouse gas emission factors for diesel trucks

95 who possess more names to describe the color wheel have a strong edge in color memorization over thos

96 Interacting gear wheels have evolved in some to give precise synchronizat

97 ence identity at corresponding polar helical-wheel heptad sites between vaccine and nonvaccine peptid

98 PAM-SCANR and the PAM wheel identified known functional PAMs while revealing c

99 nhalation also altered activity on a running wheel in a biphasic manner.

100 hree weeks of ad libitum access to a running wheel in their home cage increased galanin mRNA in the L

101 in," and on-time FCS, which was defined as "wheels in" within 6 minutes of the scheduled start time.

102 re TAT, whichwas defined as "wheels out" to "wheels in," and on-time FCS, which was defined as "wheel

103 loss rates, vehicle efficiency, and pump-to-wheels (in-use) methane emissions.

104 hort alkyne chassis, and combination sets of wheels including one set of tert-butyl wheels and anothe

105 ff-wheel ambulation when mice were using the wheels, indicating behavioral compensation.

106 al-inducible circadian oscillator (PICO) and wheel-inducible circadian oscillator (WICO) are generate

107 The {Pd84 }(Ac) wheel, initially discovered serendipitously, is the only

108 Glaucoma participants had a higher risk of wheel interventions than controls (OR, 4.67; 95% CI, 1.0

109 The {Cr8 Dy8 } wheel is a single-molecule magnet.

110 ary {Pd84} = [Pd84O42(PO4)42(CH3CO2)28](70-) wheel is explored.

111 A sensory water wheel is proposed to guide the training in bottled miner

112 the conrotatory rotation of the two template wheels is coupled to rotation of the nanoring track.

113 g-among the individuals and across the color wheel-is neither the cause nor the effect of variation i

114 amount of exercise, by removing the running wheels, leads to loss of scale-invariant properties in a

115 stewater-based algal biofuels with a well-to-wheel life cycle assessment (LCA).

116 spherical topologies may be more stable than wheel-like clusters, and DeltaH(f,(aq)) can be accuratel

117 n imaging, we uncover a centrosome-nucleated wheel-like microtubule configuration, aligned with the a

118 ided an unambiguous structural proof for the wheel-like molecule with a molar mass of 3815.4 g/mol.

119 The 186 CI is proposed to form a wheel-like oligomer that can mediate either wrapped or l

120 mes, but combinations of significant well-to-wheels methane emissions reductions and natural gas vehi

121 ate the assembly of gigantic molybdenum-blue wheel {Mo(154)} = [Mo(154)O(462)H(14)(H(2)O)(70)](14-),

122 y, 2 exhibits an elliptical lanthanide-doped wheel {Mo120 Ce6 } that is sealed by a {Mo10 } unit on o

123 f two new gigantic decameric molybdenum blue wheels, {Mo200Ce12} (1) and {Mo100Ce6} (2), by building

124 A-SPARKY plugin to seamlessly integrate PISA-wheel modeling into the NMRFAM-SPARKY platform.

125 egments using Polar Index Slant Angle (PISA)-wheel models.

126 the ring edge, with the ring sizes of the MB wheels modulated by the {Mo(2)} units.

127 tor in a single direction and to move a four-wheeled molecule across a surface.

128 Deaths among occupants of cars and three-wheeled motor vehicles constituted 48% and 20%, respecti

129 By changing the gain that couples the wheel movement to the virtual environment, we found that

130 d of bottlebrush arms and a molecular spoked wheel (MSW) core were prepared by atom transfer radical

131 firmed by colorimetric measurements on small wheels of Fuji apples treated with the hydroxyphenyl thi

132 and the relative orientations of the helical wheels of H-stems and oligomerization tags govern the ki

133 paralogs contribute to SMD by "greasing the wheels" of RNA-bound UPF1 so as to enhance its unwinding

134 played before and after an emotion-impacting wheel-of-fortune draw.

135 re carried out to locate the position of the wheel on the axle of the metal-free [2]rotaxane.

136 wheels and another set of larger adamantane wheels on the same car.

137 NL) were given access to a voluntary running wheel or standard cage conditions for 10 weeks starting

138 Outcomeswere TAT, whichwas defined as "wheels out" to "wheels in," and on-time FCS, which was d

139 for vehicular transportation, which field-to-wheels pathway is more efficient: that using biofuels or

140 ar degeneration, is characterized by a spoke-wheel pattern in the macular region of the retina and sp

141 A spoke-wheel pattern of high and low intensity was the most com

142 States today (e.g., 560-820 miles), field-to-wheels performance is similar, with some scenarios showi

143 Fluctuations in attention behind the wheel poses a significant risk for driver safety.

144 encies of bioethanol and photovoltaic sun-to-wheels process chains.

145 On an alpha helical wheel projection of TM2, the four positions where potent

146 y derived from their two-dimensional helical wheel projections, and the same is true for beta-sheets.

147 Pump-to-wheels (PTW) methane emissions from the heavy-duty (HD)

148 e residues in the Schiffer-Edmundson helical wheel representation, hydrophobic residues consisting of

149 g animals were either subjected to voluntary wheel running (exercised mice) or remained in sedentary

150 followed by stepwise exposures to voluntary wheel running (HFD+Ex) and then 25% caloric restriction

151 as well as in rats after 6 days of voluntary wheel running (LVR(run) and HVR(run)).

152 We used voluntary wheel running (VWR) in mice to test the prevailing hypot

153 ore, we investigated the impact of voluntary wheel running (VWR) on the abundance of endothelial nitr

154 ice showed a profound reduction in voluntary wheel running activity at both 6 and 12 months of age.

155 uterine histology, serum hormone levels, and wheel running activity were evident in Pgr null female r

156 Wheel running also has longer-term effects on spiking ac

157 th high arousal and positive emotions (i.e., wheel running and chocolate).

158 haviors characterized by decreased voluntary wheel running and exploratory activity.

159 avior deficits including decreased home-cage wheel running and increased immobility in both tail susp

160 Moreover, we find that voluntary wheel running and muscle-specific peroxisome proliferato

161 results during nonspatial behaviors such as wheel running and rapid eye movement (REM) sleep.

162 fluence rewarding behaviour) with respect to wheel running and sedentary female Wistar rats at 8 and

163 based locomotor behaviors, such as voluntary wheel running and the accelerating rotarod, but show onl

164 ant relationship between the amount of daily wheel running and total daily energy expenditure or ener

165 cted, but treated mice were less active in a wheel running assay.

166 Female mice underwent forced wheel running at 37.5 degrees C/40% relative humidity un

167 re and reward 'hub' in the brain) influences wheel running behaviour in rodents.

168 Conversely, decreased wheel running by adult female WD offspring was associate

169 Here we report the effect of voluntary wheel running during wakefulness on neuronal activity in

170 We find that one week of voluntary wheel running enhances the acquisition of motor skills i

171 Here, we show that voluntary wheel running exercise, which is a low stress exercise,

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

173 e also showed normal adaptation to voluntary wheel running for 4 weeks, including the glycolytic-to-o

174 experiments, voluntary exercise training by wheel running for only 11 days resulted in profound chan

175 Voluntary wheel running has long been known to induce precursor ce

176 Wheel running improved serum biochemistry with decreased

177 Increased wheel running in juvenile female WD offspring was associ

178 We show that chronic voluntary wheel running in mice increases stress resilience and in

179 Voluntary wheel running in mice scaled the GABAergic input to abDG

180 humans, on energy expenditure, and voluntary wheel running in mice.

181 rAAV) leptin antagonism in the VTA decreased wheel running in standard diet but not in WD F1 female o

182 ot affect diaphragm adaptations to voluntary wheel running in young or aged mice.

183 ration of dexamethasone did not suggest that wheel running increases HPA-axis negative feedback throu

184 We find that stereotypic wheel running is associated with a substantial reduction

185 However, whether voluntary wheel running is associated with enkephalinergic activit

186 pe and alphaCGRP(-/-) sedentary or voluntary wheel running mice were treated with vehicle, alphaCGRP,

187 ich may explain the increased motivation for wheel running observed in the HCR line.

188 Decreased wheel running occurred prior to Il1b detection in the br

189 Reduced wheel running occurs when mice are fed a high-fat diet b

190 There was no effect of wheel running on ENK mRNA expression.

191 We then measured the effects of wheel running on serum biochemistry, tissue weight, volu

192 vivo electrophysiology, the consequences of wheel running on VTA dopamine (DA) neuronal activity wer

193 ysis of F2 offspring found no differences in wheel running or adiposity in male or female offspring,

194 criptomic changes between 8- and 14-week-old wheel running rats, and select transcripts were later an

195 er, expected adaptations to a 20 d voluntary wheel running regime were not compromised in mKO mice.

196 Voluntary wheel running resulted in multiple beneficial systemic e

197 g) inhibited light induced phase advances of wheel running rhythms by 55%, but had no effect on light

198 duced phase advances and delays of circadian wheel running rhythms.

199 In these mice, voluntary wheel running significantly improved myocardial phenotyp

200 Wheel running was also associated with increased adrenal

201 ere we demonstrate that 4 weeks of voluntary wheel running was anxiolytic in C57BL/6J mice and result

202 In female mice, voluntary wheel running was decreased (P < .05) in the HET vs WT a

203 Voluntary wheel running was greatest at 8 weeks and had significan

204 Voluntary wheel running was increased in juvenile (4-7 wk of age),

205 We tested the hypothesis that voluntary wheel running would improve musculoskeletal health in a

206 s can be improved by activity (ie, voluntary wheel running) in mdx mice.

207 estigated whether physical activity (chronic wheel running) increases stress resilience and galanin e

208 dentary or physically active (10-12 weeks of wheel running) rats.

209 tic background (strain), voluntary exercise (wheel running), and their interaction on azoxymethane (A

210 ion (e.g. rotarod, treadmill, grip test, and wheel running), we observed that mTORC1 activity was sig

211 sis, and abolished activity (e.g., voluntary wheel running)-induced anxiolytic effect and adult DG ne

212 ot protected from tumor-induced decreases in wheel running, despite attenuated cytokine action and ex

213 lphaCGRP treatment, in contrast to voluntary wheel running, improved myocardial phenotype and functio

214 After 3 weeks of activity-wheel running, rats were decapitated and brains were ext

215 ermined whether short-term OVL combined with wheel running, short-term OVL combined with irradiation,

216 ence (sedentary, SED) or presence (voluntary wheel running, VWR) of aerobic exercise.

217 Despite a large variation in wheel running, we did not observe a significant relation

218 etween a rodent model of voluntary exercise- wheel running- and total daily energy expenditure.

219 ibed above) in the nucleus accumbens reduced wheel running.

220 ic inputs at 7 dpi are modified by voluntary wheel running.

221 cose tolerance as was four days of voluntary wheel running.

222 transmission, and age-related reductions in wheel running.

223 ich were completely ameliorated by voluntary wheel running.

224 ng from 3, 5, 7, 14 and 28 days of voluntary wheel running.

225 TA DA neuronal activity after acute/repeated wheel running.

226 d allodynia and increases the motivation for wheel running.

227 ced food intake, and substantially increased wheel running.

228 itor roscovitine, dose-dependently decreased wheel running.

229 eletal muscle mass after weaning and reduced wheel-running activity but normal forced treadmill perfo

230 Shank3 mutants also have trouble regulating wheel-running activity in constant darkness.

231 ated differences in cortical Abeta42 levels, wheel-running activity, and circadian free-running perio

232 matic nucleus (SCN), determine the period of wheel-running activity.

233 -deficient backgrounds, circadian rhythms of wheel-running and SCN bioluminescence showed increased p

234 knock-out (KO) mice failed to phase advance wheel-running behavior in response to 3 d subcutaneous i

235 ing on a treadmill (HCR; LCR) also differ in wheel-running behavior, but whether wheel-running can be

236 nucleus accumbens, partly explain divergent wheel-running behavior.

237 d gene expression causing abnormal circadian wheel-running behavior.

238 iffer in wheel-running behavior, but whether wheel-running can be explained by intrinsic or adaptive

239 age), F1 female WD offspring In contrast, no wheel-running differences in F1 male offspring were obse

240 tary and active rats after chronic voluntary wheel-running exercise.

241 ervations revealed that fathers subjected to wheel-running for 12 wk produced offspring that were mor

242 estigated the effects of long-term voluntary wheel-running in C57BL/6J male mice on their offspring's

243 al populations or from astrocytes, decreased wheel-running performance in mice.

244 nhibitory transmission as a prerequisite for wheel-running performance in mice.

245 mutations and of CB(1) receptor blockade on wheel-running performance.

246 al area (VTA) CB(1) receptor blockade on the wheel-running performances of wildtype (gamma-aminobutyr

247 suprachiasmatic nuclei (SCN) and behavioural wheel-running rhythms.

248 Food anticipatory (wheel-running) activity in all Period mutant mice was al

249 er than normal SCs with or without a running wheel (RW).

250 stimuli [methamphetamine (Meth) and running wheel (RW)] restores autonomous circadian activity in ar

251 lecules possessing an unconventional "roller-wheel" shaped structure that is distinctly different fro

252 In these cart-wheel-shaped arrays, coordination of ditopic perylenedii

253 late (tdc) MOFs based on novel dodecanuclear wheel-shaped building blocks has been synthesized in alm

254 e fusion of 10 U(6) and 10 U monomers into a wheel-shaped cluster (U(70)).

255 are summarized, showing that the assembly of wheel-shaped complexes with the high symmetry of the mol

256 ngth magnetic fields can reversibly assemble wheel-shaped devices in situ from individual colloidal b

257 he self-assembly process of two enantiomeric wheel-shaped macroanions, [Fe28(mu3-O)8(Tart)16(HCOO)24]

258 X-ray diffraction data revealed an unusual wheel-shaped node of 18 neptunyl polyhedra stabilized in

259 The wheel-shaped orb web is primitive to this clade, but mos

260 tures a hat-shaped structure with the parent wheel-shaped {Mo150 } being capped by a {Mo30 } unit on

261 binations of structural features: tert-butyl wheels, short alkyne chassis, and combination sets of wh

262 l, tumor-bearing mice with access to running wheels showed reduced growth of MCF-7 (-36%, P < 0.05) a

263 The "OAVs' Aroma Wheels" showed that the classes of sensory descriptors a

264 lization clearly revealed the defined spoked wheel structure of the molecule with six internal pores.

265 nthesis of a defined, rigid molecular spoked wheel structure with the sum formula C1878H2682 and a di

266 hape-persistent polyphenylene with a "spoked wheel" structure was synthesized as a subunit of an unpr

267 MB wheels such as {Mo(176)} and {Mo(154)} are made from pen

268 ompare attributes of the microjet and coated-wheel techniques, developed by Manfred Faubel and John F

269 d to a liquid sample chamber with a rotatory wheel that presents the liquid to the laser beam as a th

270 Where there's a wheel, there's a way: The terpyridine-based title system

271 Using silicone-based wheels, these motors enable a new class of soft locomoti

272 eractive visualization scheme termed the PAM wheel to convey individual PAM sequences and their activ

273 riched environments with access to a running wheel to determine whether enrichment increased the surv

274 016, and roughly half of the energy spent in wheeled transportation and the majority of energy spent

275 two "embracing" Tri2 conformers and a "third-wheeling" Tri1, fasten the capsid floor.

276 ly, we asked whether individual variation in wheel use within a group of mice would be associated wit

277 f wheel access, despite further increases in wheel use.

278 simulation, patients showed greater steering wheel variability (p = 0.0001) and lateral acceleration

279 Greater steering wheel variability was independently associated with OU-V

280 ateral acceleration variability and steering wheel variability, were calculated from vehicle sensor d

281 The PAM wheel was also readily applicable to existing high-throu

282 spontaneous locomotion activity on a running wheel was measured chronologically at 50, 65, 72 and 80

283 mice performing self-initiated walking on a wheel were studied.

284 n HRT rats that ran voluntarily on a running wheel, whereas HIT on the treadmill had a smaller, stati

285 e housed in larger cages fitted with running wheels, whereas rats in the SED group remained in standa

286 work proposes a cholesterol detection color wheel which is used along with cost effective cholestero

287 th an average of 2.1 K within the {Cr8 Gd8 } wheel, which leads to a large ground spin state (ST =16)

288 uctural analogue of the existing {Pd84 }(Ac) wheel with glycolate ligands, {Pd84 }(Gly) , and the nex

289 r wheel and observed that parts of the color wheel with higher density of color names are held in mem

290 l side chains of different length thread the wheel with the shorter chain.

291 Molecular spoked wheels with an all-phenylene backbone and different alko

292 The threading of the calix[5]arene wheels with the asymmetric pentylbenzylammonium axle 2c(

293 hat learn a new skill (running on a "complex wheel" with irregularly spaced rungs).

294 Whereas running wheel withdrawal quickly reverses leptin levels, the imp

295 ric strain induced by long-term running in a wheel worsened the dystrophic process.

296 A well-to-wheel (WTW) life cycle assessment (LCA) model is develop

297 -induced GHG emissions, we estimated well-to-wheels (WTW) GHG emissions of U.S. production of gasolin

298 In this paper, we compared the well-to-wheels (WTW) greenhouse gases (GHGs) and criteria air po

299 rgy Technology Laboratory produced a well-to-wheels (WTW) life cycle greenhouse gas analysis of petro

300 n also be perceived on the afterimage of the wheel, yet by definition this afterimage is stationary o