ライフサイエンスコーパス: feed

1 In 90% of cases, the indication for DMEK was FED.

2 of animal origin for possible transfer from feed.

3 <30 days old prior to initiation of enteral feeding.

4 atory hormone response to hypoglycemia or on feeding.

5 de and suppress host immune responses during feeding.

6 Weight was kept constant throughout feeding.

7 ythrocytes decreased during tick acquisition feeding.

8 cuit to allow entrainment to time-restricted feeding.

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

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

11 th learning and memory processes to regulate feeding.

12 ment rates between the first and second tick feeding.

13 ess such as serum withdrawal and restrictive feeding.

14 Retinopathy was evaluated in rats fed a 45% kcal as fat diet for 8 weeks before administer

15 ntly improved glucose tolerance in aged mice fed a chow (~30% vs. saline) or HF (~50% vs. saline) die

16 RAP1-deficient and E85V knock-in mutant mice fed a chow diet manifested an increase in the length of

17 or HF (~50% vs. saline) diet and young mice fed a HFD (~30%).

18 ing were weaned at postnatal Day 21 and then fed a HFD for 9 weeks.

19 DUFB8 was significantly increased in WT mice fed a HFD, but remained unchanged in GCN5L1 cKO mice rel

20 ntent alters the metabolic phenotype in mice fed a high fat diet.

21 c acid improves metabolic parameters in mice fed a high fat diet.

22 In animals fed a high sugar diet, the response of PAM-beta'2 to swe

23 ificantly increased in KCs of wild-type mice fed a high-fat diet (HFD).

24 s sufficient to improve liver damage in mice fed a high-fat diet and in mice fed a methionine-choline

25 Diabetic mice fed a high-fiber diet were significantly less likely to

26 Dahl salt-sensitive rats were fed a high-salt diet (8% NaCl) from 7 weeks of age to in

27 -selective agonist G-1 at 0 or 1 mug/day and fed a lithogenic diet for 8 weeks.

28 tion was significantly lower when flies were fed a low-P high-C diet, revealing that flies shift thei

29 mage in mice fed a high-fat diet and in mice fed a methionine-choline-deficient diet.

30 In contrast, mice fed a Mn-supplemented diet showed slightly increased tol

31 CD1 female mice were acutely fed a standard breeding chow or HFD.

32 In mice fed a Western (high-fat/high-sucrose) diet for 16 weeks,

33 ETP (cholesteryl ester transfer protein) and fed a Western-type diet.

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

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

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

37 ied out with wild-type and CT-1 null mice in fed (ad libitum) and food-restricted conditions.

38 Flies fed after appetitive conditioning needed increased sleep

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

40 p production worldwide, particularly in rain-fed agricultural regions.

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

42 ndoxyl sulfate to the drinking water of rats fed an adenine-rich diet, we found an increase in indoxy

43 resulting in chronic infection, whereas mice fed an equivalent amount of nonfermentable fiber (cellul

44 Compared with littermate controls, cKO mice fed an HFD (16 weeks) had reductions in MDC (mainly CD11

45 renal cortex and medulla in SS(Nox4-/-) rats fed an HS diet.

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

47 urden of overnutrition was tested using chow-fed and high-fat (HF)-fed SkM-specific AMPKalpha1alpha2

48 Rain-fed and irrigated croplands had 328 and 730 Mg C/ha less

49 MTOR5 in regulating the mTORC1 pathway under fed and starved conditions.

50 ent on concentration equilibrium between the feed and draw solutions due to its ability to freely mov

51 he correct size while the larva continues to feed and gain body mass.

52 lipids have potential applications in food, feed and pharmaceutical industries, contributing to the

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

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

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

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

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

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

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

60 Feeding and suckling deficits in infants with PWS are re

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

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

63 ssembly allowed us to dissect the effects of feeds and eyestalk ablation and reveal their synergistic

64 the synergistic effects of feeding with live feeds and the ablation have never been elucidated at a t

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

66 12%) and BAT (278 +/- 19%) compared to warm/fed animals.

67 dentify different insect species in food and feed are a necessity.

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

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

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

71 ut without predictable additive effects when fed as a mixture.

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

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

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

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

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

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

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

79 targeting methanol formation from CO(2)/H(2) feeds at 170 degrees C and 1-8 bar pressure.

80 g were quantified with land requirements and feed availability around forests.

81 e model reveals that behavior and demography feed back on one another to determine how the ecosystem

82 g., Wnts, Bmps, inflammatory mediators) that feed back to regulate the epithelial cells themselves.

83 olic evolution (anaerobic methanotrophy) may feed back to the atmosphere and destabilize the climate,

84 of information flow (e.g., feed-forward, or feed-back).

85 Fed-batch fermentations using concentrated green seaweed

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

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

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

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

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

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

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

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

94 The feeding behaviors of extinct cave bears living during Pl

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

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

97 neuroanatomical basis of the stress-related feeding behaviors.

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

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

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

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

102 ult in invertebrate-fed bulbuls, while fruit-fed bulbuls maintained body mass despite variation in im

103 body mass and delayed moult in invertebrate-fed bulbuls, while fruit-fed bulbuls maintained body mas

104 -PB neurons led to reduced sleep in normally fed but not yeast-deprived males.

105 ings demonstrate that high-elevation streams fed by snow and other cold-water sources continue to ser

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

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

108 subcamps with greater average infectiousness fed cases to those with a lower transmission rate.

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

110 ly modulate the organization of hypothalamic feeding circuits.

111 The direct coupled, vapor-fed CO(2)R cell yields a total Faradaic efficiency of up

112 eding).Most studies defined early feeding as feeds commenced <=24 hours postoperatively (range 2-72 h

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

114 The optimal feed composition yielding a theoretical maximal amount o

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

116 e on the Western-style diet compared to mice fed control bacteria and had alterations in hepatic lipi

117 F0 females were fed control diet (CD; 10%kcal from fat) or HFD (60%kcal

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

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

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

121 annabinol and other cannabinoids in food and feed derived from hemp and in food of animal origin for

122 In addition, birds fed diets APS21 and CTL19 showed significantly increased

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

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

125 s from wild-type (WT) or TLR2(-/-) dams were fed either by their biologic dam or a dam of the alterna

126 le C57BL/6 mice were divided into groups and fed either i) control, CON (45% fat diet) ii) CON + MINO

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

128 Plaques of APOA1 (tg/tg)/Apoe (-/-) mice fed F1394 showed a 60% reduction of macrophages accompan

129 Memory in fed flies is mediated by the anterior-posterior alpha'/b

130 exists in the EU to ensure the safety of the feed-food chain, while such an integrated system for com

131 gh (HD) or low (LD) expression of fads2 were fed for three months during the spawning season with two

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

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

134 a-band (40 to 90 Hz) power/connectivity that fed forward up the cortical hierarchy via superficial-la

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

136 s that these epigenetic alterations act in a feed-forward fashion to promote aberrant DNA methylation

137 iology and optogenetics to study vHPC-evoked feed-forward inhibition in the mouse PFC.

138 uence opiate use, suggesting a bidirectional feed-forward interaction between poor sleep and opioid u

139 and mechanical changes create a progressive feed-forward loop in which enhanced matrix deposition an

140 kine interleukin-2 (IL-2) through a positive feed-forward loop involving increased expression of the

141 urther impairs local microcirculation with a feed-forward loop of organ damage, due to vasoconstricti

142 echanism of organ crosstalk is mediated by a feed-forward regulatory loop caused by JNK-regulated FGF

143 lucocorticoid receptor (GR) and KLF15 form a feed-forward transcription loop that cooperatively trans

144 These core TFs form interconnected feed-forward transcriptional loops to establish and rein

145 ng, and direction of information flow (e.g., feed-forward, or feed-back).

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

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

148 The growth pressure of the nitrogen feed gas was varied while the growth temperature remaine

149 ficiency of 71 % with 10 % O(2) in the CO(2) feed gas.

150 KO mice fed GC-1 diet for 2 and 4 weeks had decreased serum alka

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

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

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

154 Furthermore, fish-free feed had the highest degree of in-vitro protein hydrolys

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

156 the second protocol, sensitized animals were fed HEWP for 28 days.

157 In addition, Leg5,7Ac(2)-fed human cells did not display this NulO on their surfa

158 up to a control group in which patients were fed in a traditional way (traditional feeding).Most stud

159 o the season when right whales congregate to feed in CCB.

160 The findings show that including green feed in the diet of dairy buffaloes enhances health-prom

161 onic acid without affecting the digestion of feed in the rumen.

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

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

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

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

166 amino acid levels in a singular manner when fed individually but without predictable additive effect

167 ium concentrations were detected in workers, fed individually once per os with 10 uL of 25 mM LiCl in

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

169 In conclusion, alternative feed ingredients (protein sources) in broiler finisher d

170 d, land use, and dependency on animal-source feed inputs per kg of fillet.

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

172 Relative to CON, pigs fed with LP had lower feed intake (FI) and body weight (BW) throughout the stu

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

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

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

176 agnetic space groups, we generate data to be fed into the algorithm of MTQC to determine the topology

177 n and (iii) the obtained feature vectors are fed into XGBoost to predict protein submitochondrial loc

178 tion performances once a pure carbon dioxide feed is restored, indicating a negligible long-term impa

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

180 and improved survival of high-lysine/low PN fed KO mice.

181 Sequencing of gut transcripts revealed PE-fed larvae retain an expression profile consistent with

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

183 , to improve their ability to grow fast when fed low fish meal (FM) and FO diets during grow-out phas

184 In well-fed males, insulin-like (insulin/IGF-1 signaling [IIS])

185 Feeding males with stable-isotope-labelled glucose revea

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

187 n L. vannamei (Pacific whiteleg shrimp) were fed mealworm biomass grown with PS containing HBCD.

188 romoted steatosis-to-NASH progression in HFD-fed mice by inducing liver inflammation, injury, and p38

189 Alcohol-fed mice demonstrated increased hepatic expression of th

190 Furthermore, high-fat diet (HFD)-fed mice exhibit the downregulation of FABP5 and ST2 exp

191 Analysis of fecal samples revealed that HFD-fed mice exhibited a reduction in fecal species richness

192 urthermore, rm-resistin-injected normal chow-fed mice showed upregulated blood glucose level by incre

193 ium-specific knockout mice and high-fat diet-fed mice to assess the role of endothelial AKAP150-TRPV4

194 defensin 5 (HD5) was orally given to alcohol-fed mice to test the therapeutic potential.

195 After 12 weeks, WDSW fed mice were randomized to receive (1) WDSW alone, (2)

196 ious reports showed that high-fat-diet (HFD)-fed mice with liver-specific knockout of both AMPK catal

197 Treatment of HFD-fed mice with verteporfin inhibited KC activation, reduc

198 human islets transplanted into high-fat diet-fed mice.

199 IgE production and worm expulsion in inulin-fed mice.

200 e lung tissue compared with normal diet (ND)-fed mice.

201 aggregates can be controlled by manipulating feed moisture content during extrusion, with 49.3% feed

202 oisture content during extrusion, with 49.3% feed moisture prompting favourable partial denaturation

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

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

205 s prediction capability of LoopPredictor, we fed mouse multi-omics features into a model trained on h

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

207 buscular mycorrhizal fungi and reduced plant-feeding nematodes.

208 ial fibrosis compared with diabetic controls fed normal chow or a zero-fiber diet.

209 efficiently remove cobalt and cesium from a feed of dissolved lithium, cobalt, cesium, and boric aci

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

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

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

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

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

215 Mice fed omega3-rich or omega6-rich diets were treated with T

216 Thus, Rhamphorhynchus apparently fed on aquatic animals by grabbing prey whilst flying di

217 ratio) during the gape cycle while subjects fed on foods of different mechanical properties.

218 nt loads than coastal bears because (1) they feed on a higher proportion of marine and higher trophic

219 s, are intravascular flatworm parasites that feed on blood and lay eggs, resulting in pathology.

220 . macellaria, that invade necrotic wound and feed on dead tissue.

221 es are rare, particularly among species that feed on highly mobile prey across broad landscapes.

222 rage in the marginal ice zones, and (4) they feed on prey located closer to pollutant emission source

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

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

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

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

227 ther removal of the reactant ketone from the feed, or its substitution with a similarly structured sp

228 oplands had 402 Mg C/ha less than their rain-fed pairs (p < .0001).

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

230 n ring muscles defines tentacle primordia in fed polyps.

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

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

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

234 the mediating effect of low birthweight and feeding practices.

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

236 ier fly as a tool for waste valorization and feed production has primarily been investigated at the b

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

238 fed via these catheters using a standardized feeding protocol.

239 Likewise, feeding protocols were optimized to recapitulate longevi

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

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

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

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

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

245 oalgae have great potential as an energy and feed resource.

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

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

248 d MCDI systems-in addition to using the same feed salinity, salt removal, water recovery, and product

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

250 was tested using chow-fed and high-fat (HF)-fed SkM-specific AMPKalpha1alpha2 knockout (mdKO) mice a

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

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

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

254 In both fasted and fed states, both mouse strains shared common expression

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

256 Plant-eating dinosaurs evolved varied feeding strategies.

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

258 ing early intervention to effectively adjust feeding strategy.

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

260 ata, outperforming TDFs derived from captive feeding studies.

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

262 ll mannan and is widely used as prebiotic in feed supplements for poultry and aquaculture.

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

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

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

266 Moreover, birds fed test diet containing APS21 recorded better (P < 0.05

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

268 that appear more often within users' social feeds than they do globally among all posts.

269 Mice fed the L lactis subsp cremoris had increased glucose to

270 However, dams fed the low protein diet showed extensive bone loss by t

271 ation method to impute missing data and then fed the selected variables to multiple machine learning

272 splantation of microbiota from feces of mice fed the wheat- or ATI-containing diets to intestines of

273 ral systems, P fertilisation is essential to feed the world.

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

275 d-use of herring by-products from being 100% feed, to include also high-quality minces, protein isola

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

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

278 e even in the unlikely event that a mosquito fed upon a viremic host.

279 xhibited lateralized behavior, preferring to feed using the right side of the jaw.

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

281 All patients were fed via these catheters using a standardized feeding pro

282 aw solution and river water (0.017 M) as the feed water at an applied hydraulic pressure difference o

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

284 Three experimental feeds were tested, differing in ethylenediaminetetraacet

285 ransplants for Fuchs' endothelial dystrophy (FED) were analyzed using Kaplan-Meier survival curves wi

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

287 s they produced in a concentration flow cell fed with 0.02 and 0.5 M NaCl solutions.

288 andomly divided into three groups and gavage fed with 0.7 and 2.8 g/kg/day ethanol or volume-matched

289 The material consisted of eggs from hens fed with a mixture without oil and with the addition of

290 ectron microscopic studies performed in mice fed with cuprizone and treated with anacardic acid showe

291 Rats (n = 32) were fed with either normal diet (ND) or HFD for 20 weeks.

292 weight (BW) throughout the study, but those fed with LP + BCAA improved overall FI computed for 4 we

293 Relative to CON, pigs fed with LP had lower feed intake (FI) and body weight (

294 ng surfactant-containing saline water as the feed with low surface tension, experiments reveal that t

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

296 Feeding with breastmilk as opposed to formula reduces in

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

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

299 te and chronic leptin treatment of chow diet-fed WT mice decreased MTP expression in the intestine, i

300 toxic levels of pesticides from beef cattle feed yards.