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 revented the mice from mastering the complex wheel.

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

5 o one of the two subcavities of the calix[8]-wheel.

6 k-donation from the Ru(5) ring to the La(14) wheel.

7 s the "rolling" motion, similar to a rolling wheel.

8 a 1,10-phenanthroline containing crown ether wheel.

9 late the assembly of the surrounding {Mo150} wheel.

10 s were categorized using the Behavior Change Wheel.

11 timed access to a palatable meal or running wheel.

12 te in the {Mo(36)} templated synthesis of MB wheels.

13 iction conditions, or in mice housed without wheels.

14 out reducing survival in mice housed without wheels.

15 s as a new class of novel aromatic molecular wheels.

16 e, half of the mice were housed with running wheels.

17 lexy in the presence of chocolate or running wheels.

18 nce can be restored by returning the running wheels.

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

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

21 ted diaminoalkane axles with cucurbit[6]uril wheels, (2) 1,2-bis(4,4'-bipyridinio)ethane axles with d

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

23 nzyl one, was observed by threading calix[8]-wheel 3 with the directional n-butylbenzylammonium axle

24 ridinio)ethane axles with dibenzo[24]crown-8 wheels, (3) 2,6-naphthalene dicarboxylate axles with tet

25 the desired coordination-driven bicycle-like wheel (90 % yield).

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

27 We then tested whether scheduled wheel access could improve deficits observed in vasointe

28 We found that scheduled wheel access during the late night improved many of the

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

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

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

32 sensitive to stress prior to and during the wheel access period.

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

34 In wild-type mice, scheduled wheel access was able to increase ambulatory activity, i

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

36 Following 3 weeks of wheel access, the anxiolytic effect of exercise was asse

37 eel exposure or sedentary conditions without wheel access.

38 In our studies, we used four wheel-access conditions (no access; free access; early n

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

40 er, OLZ did not alter food intake or running wheel activity during ad-lib feeding (baseline) or restr

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

42 disruption, as assessed by circadian running-wheel activity.

43 hed when wakefulness is dominated by running wheel activity.

44 [2]pseudorotaxane isomers in which the calix-wheel adopts 1,2,3-alternate and cone conformations, whi

45 g/kg), or EX (3 weeks of access to a running wheel), alone or in combination, reduced rearing behavio

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

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

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

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

50 Helical-wheel analysis revealed strict segregation of polar and

51 the presence of nitroxide labels both at the wheel and at the dumbbell.

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

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

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

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

56 e of the unsymmetrical structure of both the wheel and the axle, two different geometrical isomers co

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

58 lf-assembly process for both the face of the wheel and the side of the axle.

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

60 late axles with tetra-imidazolium macrocycle wheels and (4) a Cu(I) complex of a 1,10-phenanthroline

61 ates), {Mo(154)}, {Mo(176)}, {Mo(248)} ("big wheels"), and {Mo(368)} ("blue lemon") - all having the

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

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

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

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

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

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

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

69 Reinventing the wheel: Bimetallic AuPd nanowheels, a freestanding form o

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

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

72 ions and to observe the templation of the MB wheel by {Mo(36)} directly.

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

74 e benefits on all time frames if the well-to-wheels CH(4) leakage were capped at a level 45-70% below

75 osition of the [Rh(2)(O(2)CCF(3))(4)] paddle-wheel complex is associated with a dominant donation fro

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

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

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

79 osed of viologen-type axle and calix[6]arene wheel components.

80 ry or activity (voluntary access to activity wheel) conditions.

81 l fuel requirements of five different sun-to-wheels conversion pathways for every county in the conti

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

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

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

85 ly); differences in well-to-pump and pump-to-wheel efficiencies can largely offset each other.

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

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

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

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

90 high degree of variability exists in well-to-wheel emissions due to differences in technologies emplo

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

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

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

94 ll exercise group, and the voluntary running wheel exercise group.

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

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

97 ith continuous voluntary access to a running wheel for either 2 or 5 weeks exhibited dramatic leftwar

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

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

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

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

102 rats with or without free access to running wheels for 3 weeks.

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

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

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

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

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

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

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

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

111 HF diet given access to a voluntary running wheel (HF-RUN).

112 service use included regular use of Meals on Wheels, Home Care, or community nurse services.

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

114 tive generation of a highly symmetric spoked wheel in 94% isolated yield via geometric and thermodyna

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

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

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

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

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

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

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

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

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

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

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

126 dimensional D(6h) supramacromolecular spoked wheel is reported.

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

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

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

130 ed Ru(5) ring embedded in a La(14) hexagonal wheel-like cage, an incommensurate combination of the tw

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

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

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

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

135 nd 1 and the archetypal Molybdenum Blue (MB) wheel, {Mo(150)}, identified compound 1 as a likely inte

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

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

138 about whether some impaired persons who need wheeled mobility devices may now be inappropriately deni

139 A transparent, evidence-based approach to wheeled mobility service delivery (the matching of mobil

140 This review describes the process of wheeled mobility service delivery for long-term wheelcha

141 base for the effectiveness of approaches to wheeled mobility service delivery is insufficient, and a

142 ntified 24 studies that evaluated aspects of wheeled mobility service delivery.

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

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

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

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

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

148 the effects of prolonged access to a running wheel on electrical self-stimulation of the lateral hypo

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

150 en performed either 10 or 6 weeks of running wheel or treadmill exercise, respectively.

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

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

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

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

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

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

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

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

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

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

161 levels of BDNF mRNA in CA1 were elevated in wheel runners compared to sedentary rats and this differ

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

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

164 d from a line selectively bred for increased wheel running (high runner) and the C57BL/6J inbred stra

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

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

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

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

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

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

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

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

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

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

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

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

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

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

179 esis was assessed after 20 days of voluntary wheel running by measuring electron transport chain prot

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

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

182 is increased by unlimited access to activity wheel running for 3 weeks but is not dependent upon accu

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

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

185 Increased wheel running in juvenile female WD offspring was associ

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

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

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

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

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

191 reased incidence of knee OA with obesity, as wheel running is protective rather than damaging.

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

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

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

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

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

197 ained for 6 weeks by treadmill and voluntary wheel running or housed normally.

198 After 6 weeks of voluntary wheel running or sedentary conditions, the selective 5-H

199 Similarly, voluntary wheel running produces anxiolytic- and antidepressant-li

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

201 We found that voluntary wheel running reduced the behavioral effects of CP-80910

202 studies tested the hypothesis that voluntary wheel running reduces the behavioral consequences of 5-H

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

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

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

206 Wheel running was also associated with increased adrenal

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

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

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

210 liably predict elapsed time (15-20 s) during wheel running with a precision of 0.5 s.

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

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

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

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

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

218 tron transport chain activity, and voluntary wheel running-induced mitochondrial biogenesis were not

219 ich were completely ameliorated by voluntary wheel running.

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

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

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

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

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

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

226 itor roscovitine, dose-dependently decreased wheel running.

227 In contrast, the periods of wheel-running activity in Kv4.3(-/-) mice and firing in

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

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

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

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

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

233 hibited extremely disrupted daily rhythms in wheel-running behavior.

234 nockout mice show markedly altered circadian wheel-running behaviour and deregulated lipid metabolism

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

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

237 Wheel-running exercise reduced progression of OA in the

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

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

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

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

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

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

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

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

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

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

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

249 at detected curves from sensors on the front wheel set, and a predictive mode that determined curves

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

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

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

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

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

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

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

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

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

259 vel illusion in which the center of a static wheel stimulus (with 30-40 spokes) is experienced as fli

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

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

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

263 rating the template effect of {Mo(36)} to MB wheel synthesis was indicated by an increase in the yiel

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

265 To date, four different, axle - wheel templating motifs have been used to create the [2]

266 e role for IsdC is acting as the central cog-wheel that facilitates heme transfer from IsdA to IsdE.

267 emissive (quantum yield = 27%) heptanuclear wheel that is the largest example of a chiral luminescen

268 by synthesizing a spin labeled alpha-CD (the wheel) that was mechanically blocked on a thread contain

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

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

271 oborate the mechanism of formation of the MB wheels through observation of the individual cluster spe

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 7 days prior to the introduction of running wheels to assess the impact of prior and concurrent stre

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

276 y of different properties of the sphere- and wheel-type metal-oxide-based clusters can directly be re

277 The wheel-type molybdenum-oxide clusters exhibiting complex

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

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

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

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

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

283 osure, functioning or nonfunctioning running wheels were introduced into stressed and unstressed grou

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

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

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

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

293 s the need for researchers to 're-invent the wheel' with each new project, accelerating the rate of p

294 access reduced survival in mice housed with wheels without reducing survival in mice housed without

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

296 generation supply interact to impact well-to-wheel (WTW) energy use and greenhouse gas (GHG) emission

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

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

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