ライフサイエンスコーパス: feeding

1 Weight was kept constant throughout feeding.

2 ythrocytes decreased during tick acquisition feeding.

3 cuit to allow entrainment to time-restricted feeding.

4 and interfering with host-seeking and blood-feeding.

5 ly injected in rats following 1-h restricted feeding.

6 emerge from the NAc normally act to restrict feeding.

7 orm crowns adapted to omnivorous/herbivorous feeding.

8 starvation, serum variation, and restrictive feeding.

9 similar metabolic effects caused by high-fat feeding.

10 wn whether muscle-secreted hormones regulate feeding.

11 intake, consistent with a permissive role in feeding.

12 neurons diminishes SF1 neural inhibition of feeding.

13 nt to nonphotic cues such as time-restricted feeding.

14 cognitive and psychopathological control of feeding.

15 asts, or soybean in the oral secretion after feeding.

16 th learning and memory processes to regulate feeding.

17 ment rates between the first and second tick feeding.

18 ess such as serum withdrawal and restrictive feeding.

19 <30 days old prior to initiation of enteral feeding.

20 atory hormone response to hypoglycemia or on feeding.

21 de and suppress host immune responses during feeding.

22 rrals (33.6%), parents uninterested in early feeding (28.2%), and lack of clinic time (20.9%).

23 Nevertheless, feeding a "very-low" protein infant formula may cause li

24 ls, administering alpha-naphtylisocyanate or feeding a 0.1% 3,5-diethoxycarbonyl-1,4-dihydrocollidine

25 Feeding a diet high in soluble oxalate or weekly injecti

26 hyperlipidemic blood from aged mice and upon feeding a high-fat diet (Apoe(-/-) mice).

27 evelopmental disability, muscular hypotonia, feeding abnormalities, recurrent fever episodes, and inf

28 cluding attack by arthropod herbivores whose feeding activity is often stimulated by rising temperatu

29 nges required for acetate and glycerol cross feeding affect dozens of chemical reactions, multiple bi

30 (i.e. carbohydrates, proteins, and lipids), feeding affected lipid metabolism the most.

31 Direct oral feeding after an esophagectomy does not affect functiona

32 cantly higher percentage of their encounters feeding after the storm than they did before or during.

33 ractices and promoted use of structure-based feeding among first-time parents compared with controls.

34 The evolution of cross-feeding among individuals of the same species can help g

35 s the first evolutionary evaluation of cycad-feeding among Lepidoptera along with a comprehensive rev

36 growth during maturation through continuous feeding (an "income" source).

37 m plays a fundamental role in the control of feeding and body weight.

38 cting tolerant cultivars from sting nematode feeding and could be targeted in breeding programs.

39 l role for involvement of Rgs4 in SP MSNs in feeding and DIO-susceptibility.

40 signals, which discourages the initiation of feeding and drinking (fully recapitulating the symptoms

41 er study of all conditions categorized under feeding and eating disorders.

42 RRs) to glucose deficit, including increased feeding and elevation of circulating corticosterone, epi

43 scribe metabolic interactions, such as cross-feeding and exchange of electron acceptors and small mol

44 s of bioluminescent bacteria for quantifying feeding and generating insights into the spatial pattern

45 , enriched in the ileum and colon, modulated feeding and glucose metabolism.

46 shaken drones were more likely to engage in feeding and grooming than a sham control.

47 GI tract and levels increase during high-fat feeding and gut infection and inflammation.

48 ty response; activation of the PVH decreases feeding and increases energy expenditure, thereby promot

49 veal that VAN GHSR knockdown induced various feeding and metabolic disturbances, including increased

50 infants with PWS are replaced with excessive feeding and obesity in childhood through adulthood.

51 desirable characteristic for poultry and pig feeding and represents a challenge for breeding programs

52 Feeding and suckling deficits in infants with PWS are re

53 ommon non-pharmacological technique included feeding and swaddling infants before imaging to encourag

54 V), a cranial nerve essential for suckling, feeding and swallowing (S/F/S), a key innate behavior co

55 aling is activated after acute high fat diet feeding and this effect is manifested through both UCP1-

56 gulating sleep/wake cycles, impact activity, feeding, and immunity.

57 regulation in sexually mature animals, after feeding, and in specific lunar phases.

58 area (LH) is a vital controller of arousal, feeding, and metabolism [1, 2], which integrates externa

59 n of POMC neurons upon HFD exposure, reduces feeding, and protects from obesity, but it does not affe

60 reef sharks, Carcharhinus melanopterus, from feeding, and to minimise injuries from shark bites.

61 Our results reveal a feeding- and circadian-regulated dynamic neuroimmune cir

62 es such as pain, respiration, addiction, and feeding; and how receptor signaling and circuits are alt

63 Under- and over-feeding are both commonplace in the beef and dairy indus

64 ng to ask whether acetate and glycerol cross-feeding are especially likely to evolve, perhaps because

65 st that these seamounts likely are important feeding areas for dolphins.

66 ear rate ( Y ), and vascular function in the feeding arteries of the stretched muscle have been exten

67 ce was found between CT and MRI in AVM size, feeding artery and draining vein diameter, and artifact

68 Twenty-two AVMs had a feeding artery diameter of less than or equal to 2 mm, o

69 owever, little is known about sleep in blood-feeding arthropods, which have a critical role in public

70 ditional feeding).Most studies defined early feeding as feeds commenced <=24 hours postoperatively (r

71 tility associated genes responding to xylose feeding, as well as widely varying gene expression in th

72 sponses as measured in the standard membrane feeding assay (SMFA).

73 Standard and direct membrane-feeding assays (SMFA and DMFA) are fundamental assays to

74 Direct feeding assays resulted in mosquito infections from 9/12

75 ns and afferent pathways in mice during free feeding assays.

76 lete the two-injection regimen with mosquito feeding at day 42, but were included in the safety analy

77 as is the case for gleaning bats and nectar-feeding bats.

78 mation plays an important role in disrupting feeding behavior and energy homeostasis as well as in th

79 itive processes contribute to the control of feeding behavior and help organism's survival when they

80 essing neurons in Drosophila adults regulate feeding behavior and metabolism.

81 ion, we found that neuronal xbp-1s modulates feeding behavior and reproduction, dependent upon tyrami

82 c nociceptin neurons may act as a gateway to feeding behavior by connecting AgRP neurons to both home

83 In animals, the brain regulates feeding behavior in response to local energy demands of

84 Discovery of such a feeding behavior in this ancient, terrestrial, and omniv

85 to the pPVT was sufficient to elicit robust feeding behavior in well fed mice, inhibition of VLM(CA)

86 or how these interactions lead to changes in feeding behavior is not well-understood.

87 al nervous system responsible for regulating feeding behavior, coupled with metabolic changes due to

88 ating changes that influence their activity, feeding behavior, metabolism, egg production and gene ex

89 ds caused by pentatomids is related to their feeding behavior, morphology of mouth parts, and saliva,

90 sary and sufficient to stimulate a reflexive feeding behavior, the proboscis extension reflex (PER),

91 e maintenance of cellular representations of feeding behavior.

92 use of a poor understanding of how different feeding behaviors impact feeding system design (form-fun

93 The feeding behaviors of extinct cave bears living during Pl

94 This work suggests that feeding behaviors should be an intrinsic part of future

95 ehaviors from more than 1400 observations of feeding behaviors video-recorded in a wild population of

96 edonic brain nuclei can lead to pathological feeding behaviors, namely overconsumption of highly pala

97 al basis for an interplay between stress and feeding behaviors.

98 neuroanatomical basis of the stress-related feeding behaviors.

99 th well defined roles in producing different feeding behaviors.

100 cate that the interaction of temperature and feeding behaviour could be a major ecological determinan

101 bsorption and motility(2,3), and brain-wired feeding behaviour(2).

102 y and quantity of prey might influence their feeding behaviours.

103 eeding between AOB and NOB and induced cross-feeding between AOB and nitrite reducing organisms.

104 ds, sulfide likely disrupted microbial cross-feeding between AOB and NOB and induced cross-feeding be

105 We then manipulated the gut microbiome by feeding birds one of two diets that differed in their re

106 ts on microphytobenthos (MPB), a key deposit-feeding bivalve, Macomona liliana, and sediment nutrient

107 During stimulation feeding, blood samples were collected daily to determine

108 A combination of pair-feeding, bone marrow-transplant, and microglial ablation

109 saliva from Anopheles mosquitoes facilitates feeding by blocking production of the anaphylatoxins C3a

110 Feeding by invertivores declines across all latitudes in

111 y to occur in the northern hemisphere, where feeding by tropical herbivores is predicted to expand fr

112 Access to the circuit controlling feeding can help determine the logic and cellular mechan

113 to a defined daily interval (time-restricted feeding) can synchronize the central and peripheral circ

114 nted with quantitative RT-PCR, we found that feeding causes substantial and transient changes in gene

115 ique organs that provide them with food from feeding cells.

116 However, the feeding circuit for the VMH regulation of food intake re

117 an MXene patch antenna array with integrated feeding circuits on a conformal surface has comparable p

118 ly modulate the organization of hypothalamic feeding circuits.

119 ondition, suggesting a significant effect of feeding competition alone on social structure.

120 y creates an increasing period of suboptimal feeding conditions for zooplankton at a time of year whe

121 xin within the mPFC mediates cue potentiated feeding (CPF).

122 sion during the normal physiological fasting-feeding cycle in nutrient-sensitive and -insensitive mic

123 tood about the mechanisms involved in nectar-feeding decisions, or how this sensory information is pr

124 tify Ap as the bacterium altering the host's feeding decisions.

125 HF/HC feeding decreased ALR expression in all groups of mice.

126 an experimental manipulation that imposed a feeding delay (Experiment 2), which increased their own

127 e progression is stereotyped and occurs in a feeding-dependent manner.

128 Secoiridoid glycosides are anti-feeding deterrents of the Oleaceae family recently highl

129 group may provide a robust reservoir of anti-feeding deterrents to mitigate future herbivore threats

130 speech delay, autistic features, hypotonia, feeding difficulties, spasticity or ataxic gait, and abn

131 We have shown that high-fat (HF) feeding during pregnancy significantly reduces maternal

132 describing the locomotion, pose, biting, and feeding dynamics of Aedes aegypti, Aedes albopictus, Ano

133 contributes to a better understanding of the feeding ecology of oceanic dolphins and provides new ins

134 ributed to neck elongation and its impact on feeding efficiency.

135 intrinsic hepatocyte clock mechanism and the feeding environment.

136 Cross-feeding Escherichia coli strains, where one strain feeds

137 to earlier in the day [early time-restricted feeding (eTRF)] is a novel type of IF.

138 associated with food availability can induce feeding even in satiated subjects.

139 In response to animal feeding, evolutionarily conserved growth signaling pathw

140 urons, offspring from mothers exposed to HFD feeding exhibited a sexually dimorphic expression of DA-

141 Here, we performed a controlled feeding experiment, where developing eggs of two cosmopo

142 Through stable isotope feeding experiments, we demonstrate the in vivo activity

143 resent study was to elucidate the effects of feeding flaxseed meal (FSM) and turmeric rhizome powder

144 ming instead of tethered since the resulting feeding flow past the cell body is stronger, leading to

145 estigates the effect of direct start of oral feeding following minimally invasive esophagectomy (MIE)

146 stomosis or to receive nil-by-mouth and tube feeding for 5 days postoperative (control group).

147 In response to high fat diet (HFD) feeding for 6 or 18 weeks, WT and AIF1L deficient mice g

148 nce generates predictions that attenuate the feeding forward of predicted stimuli while passing forwa

149 ncy of visits to a veterinarian (P = 0.026), feeding frequency (P = 0.033), and higher snack intake (

150 reproduction were offset by the benefits of feeding from the carcass during an initial breeding atte

151 st feed was significantly lower in the early feeding group, but not significantly lower for the mean

152 e that was 2.3-fold greater than the formula-feeding group.

153 e or decline was consistent across arthropod feeding groups and was similar for heavily disturbed ver

154 these great apes to understand better their feeding habits and habitats.

155 We studied polar bear feeding habits with bulk stable isotope ratios of carbon

156 In contrast, early feeding has become well established in the adult populat

157 ain plant resistance against chewing and sap-feeding herbivores than classic diversity indices.

158 Homeostatic feeding (i.e. titration of caloric intake), is typically

159 rives heat seeking and heat-stimulated blood feeding in Anopheles At a cellular level, Ir21a is essen

160 acquired by CxD7L1 evolved to enhance blood-feeding in mammals, where ADP plays a key role in platel

161 ters (opportunists) are organisms adapted to feeding in nutritionally poor and rich environments, res

162 s aimed at investigating the safety of early feeding in pediatric GI surgery, with or without a fast-

163 aptive, such as when learned food cues drive feeding in the absence of hunger.

164 The role of breast-feeding in the development of oral tolerance and allergi

165 (SAT) varies dynamically during naturalistic feeding in tufted capuchins (Sapajus apella).

166 However, most methods of measuring feeding in worms quantify either foraging behavior or fo

167 e multiple purposes, including to facilitate feeding, in predation, and in defence when attacked [4].

168 For most animals, feeding includes two behaviors: foraging to find a food

169 Coconut oil, but not C(8)/C(10) feeding, induced periportal macrovesicular steatosis in

170 ins used here exhibit several differences in feeding-induced hepatic responses in gene expression, es

171 uard induced > 80% mortality and > 90% blood-feeding inhibition of An. gambiae sl mosquitoes before a

172 variety of behaviors in Drosophila including feeding initiation, locomotion, aggression, and courtshi

173 The peritrophic matrix of blood-feeding insects is a chitinous structure that forms a pr

174 tion of the lipogenic program in response to feeding/insulin, and its contribution to development of

175 Here we show that modeling cross-feeding interactions at an intermediate level between ge

176 discuss possible reasons why only two cross-feeding interactions have been discovered during experim

177 evolution and argue that multiple new cross-feeding interactions may await discovery.

178 observed for multiple other of the 56 cross feeding interactions we study.

179 ps also less genetic change than other cross-feeding interactions.

180 trial were randomized to directly start oral feeding (intervention) after a MIE with intrathoracic an

181 ssign to future rewards, yet, the components feeding into this appraisal of value remain unclear.

182 Further, although female blood-feeding is essential for anautogenous mosquito reproduct

183 odification and supervision requirements for feeding, is used for clinical research but has limited p

184 valuated the impact of an infant young child feeding (IYCF)-SQ-LNS intervention on anemia and growth

185 ill SCC function may be important during the feeding juvenile and the adult stages of the lamprey lif

186 nhibition of the NAc shell induces voracious feeding, leading to the hypothesis that the inhibitory p

187 rall, KEGG pathway analysis revealed that GB feeding led to the enriched accumulation of proteins imp

188 iesis, we induced iron deficiency in mice by feeding low iron diet.

189 Feeding males with stable-isotope-labelled glucose revea

190 Feeding may also be influenced by environmental cues, se

191 As infant feeding may influence allergy development, we aimed to i

192 exclusivity and duration but not breastmilk feeding mode (nursing versus pumping).

193 In membrane feeding mosquito infection experiments, we found that ga

194 ange of host environments, both within blood-feeding mosquitoes, their definitive hosts, and in verte

195 f vector control may involve targeting sugar-feeding mosquitoes.

196 s were fed in a traditional way (traditional feeding).Most studies defined early feeding as feeds com

197 women who were lactating (n = 12) or formula-feeding (n = 6) their infants and who were closely match

198 buscular mycorrhizal fungi and reduced plant-feeding nematodes.

199 Competitive interactions in the feeding niches during the low water season, plus tempora

200 HFD feeding of CysC-deficient (CysC knockout [KO]) mice wors

201 xity: uni-, bi-, and multi-directional cross-feeding of either substitutable metabolic byproducts or

202 Thus, regulating the production and feeding of ER membranes into NE holes together with ESCR

203 We further found that the feeding of meat preparations with added nitrate to rats

204 We find that short-term high-fat-diet (HFD) feeding of mice activates prepronociceptin (PNOC)-expres

205 rough-legged hawks and long-tailed jaegers) feeding on a pulsed resource (brown and collared lemming

206 sylvaticus hirtensis may also play a role by feeding on adults, chicks or eggs.

207 nificantly increased in carnivores regularly feeding on birds.

208 livary glands from nymphs, males and females feeding on genetically susceptible and resistant bovine

209 When not feeding on human blood bed bugs aggregate in refuges clo

210 However, we caution that opportunistic blood feeding on humans by sylvatic Ae. malayensis may occasio

211 ound in the alpine, but that are generalists feeding on many plant genera.

212 nto tree xylem to complete their life cycle, feeding on symbiotic fungi.

213 During simultaneous feeding on the different substrate types, Fe deficiency

214 ER) and the effect of sub-optimal restricted feeding on the rumen microbiome of African Zebu cattle r

215 ity of spirochetes to colonize the tick when feeding on these animals.

216 sfer from prey to predator, through D. magna feeding on virus-loaded T. pyriformis.

217 gLONs directly into the brain and monitoring feeding, only NEGR1 altered food intake significantly.

218 Concentrated animal feeding operations (CAFOs) are major emitters of both am

219 urnus vulgaris) found on concentrated animal feeding operations (CAFOs).

220 in response to environmental inputs such as feeding or exercise.

221 ably by efficient restoration of the central feeding organ (manubrium).

222 ts by supplying food and nutrients to filter-feeding organisms such as cold-water corals.

223 s metabolic changes and interdependent cross-feeding pathways occur in neighboring non-mannanolytic p

224 rcadian differences in physical activity and feeding pattern is unclear.

225 the existence of an extra-European reservoir feeding plague into Western Europe in multiple waves.

226 fe events including mode of delivery, infant feeding practice, antibiotics exposure, and other events

227 Infant feeding practices (i.e., food to soothe, structure vs. c

228 vented the use of nonresponsive, controlling feeding practices and promoted use of structure-based fe

229 aimed to identify groups of infants based on feeding practices and to examine their associations with

230 eses, no differences were detected in bottle-feeding practices such as putting to bed with a bottle/s

231 t the use of some nonresponsive, controlling feeding practices while establishing consistent feeding

232 her this process is influenced by breastmilk feeding practices.

233 the mediating effect of low birthweight and feeding practices.

234 that sulfated salicinoids do not affect the feeding preference of the generalist caterpillar Lymantr

235 mic dysfunction (neonatal bradycardia/apnea, feeding problems, hyperactive startle reflex), severe po

236 ecause each meal promotes mutually exclusive feeding programs with distinct sensory appendages, meal

237 fed via these catheters using a standardized feeding protocol.

238 Likewise, feeding protocols were optimized to recapitulate longevi

239 beaver engaged in woodcutting behaviour for feeding purposes.

240 age 1 y, the Structure and Control in Parent Feeding Questionnaire revealed that the mothers in the R

241 ire, and the Structure and Control in Parent Feeding Questionnaire.

242 Nonfederal feeding recommendations exist for children <2 y, but lim

243 When the pig feeding regime was disrupted, we automatically detected

244 es (defined by a combination of genotype and feeding regime).

245 on efficiencies vary across diurnal time and feeding regimen, codon dwell times were highly stable an

246 strial purposes must therefore consider both feeding regimes and the light environment.

247 derstanding the neural components modulating feeding-related behavior and energy expenditure is cruci

248 Furthermore, these cross-feeding relationships were spatially distributed between

249 ly emerged as a brain region that integrates feeding-relevant biological signals with learning and me

250 the spread of mosquito-borne diseases, blood feeding remains poorly understood due to technological l

251 [(13)C(6)]-glucose feeding revealed that GCBCs generate significantly less

252 ected the expected deviations from the daily feeding routine in standing, lateral lying and drinking

253 mothers in the RP group used more consistent feeding routines (4.19 [0.43] compared with 3.77 [0.62],

254 ding practices while establishing consistent feeding routines in subsequent siblings.

255 This approach provided clear views of feeding sites and surrounding tissues, with resolution s

256 deer characterised by a high preference for feeding sites exhibited more pronounced behavioural adju

257 nects the patch to the leaky-wave open-ended feeding slot-lines running underneath the patches.

258 suggest a niche partitioning of habitat and feeding sources amongst the three Typhlatya species inve

259 Feeding state does not alter the activity of the core th

260 position by observing their associations at feeding stations and monitored the number of days surviv

261 pots of marine life in the Azores, acting as feeding stations for top predators, including cetaceans.

262 r, how neck elongation influenced exactly on feeding strategies is subject of debate.

263 icroplastics, our findings highlight how the feeding strategies of different zooplankton species may

264 Plant-eating dinosaurs evolved varied feeding strategies.

265 auropod species which evolved lower browsing feeding strategies: the antero-dorsal sloping caused by

266 ing early intervention to effectively adjust feeding strategy.

267 discrimination factors derived from captive feeding studies are highly variable, and it is challengi

268 Last, feeding studies using male rats demonstrate that intra-N

269 ata, outperforming TDFs derived from captive feeding studies.

270 eedle inoculations in naive animals for tick feeding studies.

271 Our artificial diet-feeding study indicates that dsRNAs greater than or equa

272 was considered by examining the fraction of feeding study intake variation explained by these regres

273 : Babies Need Soothing Questionnaire, Infant Feeding Styles Questionnaire, and the Structure and Cont

274 NOS1(PVH) neurons contribute to PVH-mediated feeding suppression.

275 ng of how different feeding behaviors impact feeding system design (form-function relationships).

276 this study, we describe a new in vitro tick feeding system that facilitates the study of ticks and t

277 monstrates the utility of an artificial tick feeding system to directly study the association between

278 modified proteome of milk from two different feeding systems.

279 maze, light-dark box, and novelty-suppressed feeding test revealed no differences between the offspri

280 ts in the forced swim and novelty suppressed feeding tests, and increased synaptic plasticity.

281 nutrient needs, environmental cues can drive feeding through hedonic and cognitive processes.

282 rcadian clock disarrangement, alterations in feeding time or content, or epithelial-specific MHC clas

283 Restricting feeding to a defined daily interval (time-restricted fee

284 DAF-7 likely acts upstream of IIS and links feeding to odr-10 only in males, due in part to the male

285 ke activities against adjustable load during feeding, to investigate the resistance exercise-induced

286 logic impairment, and presence of an enteral feeding tube.

287 Percutaneous Endoscopic Gastrostomy (PEG) feeding tubes are frequently placed in patients to provi

288 the prevalence of mutualism and pollinators feeding upon resources in addition to rewards.

289 Aspergillus strain expressing CndF and CndE, feeding various alkyl-beta-keto esters led to the biosyn

290 e chemoreceptor expression and influence the feeding-versus-exploration decision.

291 ressful environment is a potent modulator of feeding, we seek in the present work to decipher the neu

292 ion, and later introduction of complementary feeding were associated with more energy from the "neutr

293 Furthermore, daytime-restricted feeding, which affects the phase of the skin circadian c

294 ity was established by prepregnant HF (ppHF) feeding, which avoided the dietary effect during pregnan

295 pheles gambiae initiated shortly after blood-feeding, which stimulates immune induction and promotes

296 ignificantly impaired glucoprivation-induced feeding while leaving other major counterregulatory resp

297 re randomly assigned to 8 weeks of monitored feeding with a control diet typical of what many America

298 Feeding with breastmilk as opposed to formula reduces in

299 m from mice that were previously infected by feeding with DC-microinjected nymphal ticks.

300 various aspects, the synergistic effects of feeding with live feeds and the ablation have never been