ライフサイエンスコーパス: starve

1 hus undergoes multicellular development when starved.

2 e indicates that the failing heart is energy starved.

3 ression changes during refeeding after being starved.

4 d from LDs into mitochondria when cells were starved.

5 a nervosa (AN) are not motivated to eat when starved.

6 ing yeast, in which cells enter meiosis when starved.

7 thiolation deficient cells appear amino acid starved.

8 therefore, contrary to expectations, is gas-starved.

9 thereby collectively lowering the chances of starving.

10 f elevated water temperatures with voluntary starving.

11 Treatment of IL-3 and serum-starved 32D cells with 1 muM imatinib mysylate inhibited

12 rate (10 C, 16.7 mA cm(-2) ) and electrolyte-starved (4.7 muL mg(S) (-1) ) Li-S batteries.

13 nclude the idea that fasting when feverish ("starving a fever") can increase the pace of recovery, or

14 r low-glucose conditions, beta-cells adopt a starved adhesion phenotype consisting of actin stress fi

15 This starved adhesion phenotype prevented excessive insulin g

16 ed sleep for memory consolidation, but flies starved after training did not require sleep to form mem

17 rential expression analysis between nitrogen-starved and -repleted conditions (at stationary phase) f

18 brain increase significantly when flies are starved and decrease shortly after starved flies are ref

19 For sediment-starved and erosion-prone coasts, large-scale enhancemen

20 We show here that protein-free extracts of starved and high fat-fed livers contain metabolites that

21 ponding root parameters were quantified in K-starved and K-replete plants.

22 itions in light and dark as well as nitrogen-starved and phosphorus-starved conditions in light.

23 ters decreased if An. albimanus females were starved, and were reduced if insects emerged with low te

24 ehavior depending on their metabolic status; starved animals are eager to eat and satiated animals st

25 Moreover, we show that the F3 offspring of starved animals show an increased lifespan, corroboratin

26 rs the colitogenic phenotype from tryptophan starved animals to normally nourished mice.

27 E diet on FAM; in contrast to lipid-depleted starved animals, PE-fed caterpillars maintain lipid rese

28 spectively, restores negative thermotaxis in starved animals.

29 ative fuel usage may affect cell survival in starved animals.

30 reas octopamine promotes CO(2) attraction in starved animals.

31 e by directly promoting expression of Carbon Starved Anther (CSA) which encodes a MYB domain protein.

32 ponse invoked by paracrine signals from iron-starved astrocytes.

33 s, including C. elegans, survive longer when starved at higher densities, while for others survival i

34 ability of T7 phage to replicate in nitrogen-starved bacteria as a biological probe of E. coli cell f

35 Here, we show that starved bacteria encountering new resources can break th

36 neumophila as well as enhance growth of iron-starved bacteria.

37 nds Mn(2+) and Zn(2+) with high affinity and starves bacteria of these essential nutrients.

38 subsequent decomposition of MPn by phosphate-starved bacterioplankton may partially explain the exces

39 are similar to the phenotypes observed after starving beetles for 5 days PAE.

40 inhibition has a potential to provide tumour-starving benefits.

41 limited mitochondrial hyperfusion in glucose-starved breast cancer cells, as driven by downregulation

42 211 renovates membrane lipids when phosphate starved by replacing a portion of its phospholipids with

43 erium to resist superoxide stress when metal starved by the host, revealing that small changes in met

44 RNA-Seq analysis of iron-starved C. reinhardtii cells revealed notable changes in

45 rd extremes, particularly along the sediment-starved California coast.

46 that inhibit VEGFR2 trafficking and thereby starve cancer of blood supply.

47 rogrammed cell death known as ferroptosis in starved cancer cells and cancer-bearing mice.

48 o support mitochondrial energy production in starved cancer cells and causes autophagy-deficient cell

49 regulator of mitochondrial fusion in glucose-starved cancer cells.

50 switch in the survival versus death fate of starved cancer cells.

51 native paradigm of acute glucose oxidase for starving cancer cells and sensitizing them to thermal ab

52 can oxidize ethene to epoxyethane, and that starved Carver etheneotrophs exhibit significantly reduc

53 By feeding starved CAX larvae for various durations, we found that

54 However, in 2-h or 16-h starved cell cultures, JAK3 switches to a PLD2-enhancing

55 Herein, we deploy a genetic system to starve cells of an essential ribosomal protein, which re

56 Here, we show that DNA-binding protein from starved cells (Dps) - the extremely small archaeal antio

57 urans contains two DNA-binding proteins from starved cells (Dps): Dps1 (DR2263) and Dps2 (DRB0092).

58 t can provide a new carbon source to glucose-starved cells and enhance growth of yeast.

59 We show that these starved cells are not dormant but are growing and dividi

60 t, thioridazine did not generate DD Mtb from starved cells but killed those generated by rifampin.

61 All starved cells could oxidize exogenous glutamine, whereas

62 itial chromosomal replication in thymine (T)-starved cells could reflect a considerable endogenous dT

63 n the absence of hpf, the rRNA abundances of starved cells decrease to levels that cause them to lose

64 n leads to stalling at G0/G1 Moreover, serum-starved cells display reduced hRpn13 and Uch37 protein l

65 on storage protein, DNA-binding protein from starved cells from E. coli.

66 ns, including in a subpopulation of nutrient-starved cells in vitro and in hippocampal neurons of neo

67 Finally, some of the factors released from starved cells induced chemotaxis of B cells, macrophages

68 ovel mechanism by which protein synthesis in starved cells is down-regulated by phosphorylation of th

69 ate micro-lipophagy for energy production in starved cells is relevant for studies on aging and evolu

70 Starved cells lacking Grh1 are metabolically active, but

71 f mutations (hisC952, metB5, and leuC427) in starved cells of the Bacillus subtilis YB955 strain.

72 Lysosomes from amino acid-starved cells possess greater V-ATPase-dependent proton

73 nfocal microscopy, demonstrate that nitrogen-starved cells produce NO only when the cytochrome b6f de

74 Autophagy in starved cells replenished LDs with FAs, increasing LD nu

75 Methane reintroduction to starved cells stimulates a rapid, transient extracellula

76 c reduction of fungal CFI proteins in carbon-starved cells suggests that the pre-mRNA processing path

77 nditions using either freshly grown cells or starved cells to explain reactor performance.

78 Starved cells treated with exopolyphosphatase failed to

79 compartments immunoisolated from amino acid-starved cells was performed.

80 Meanwhile, the metabolomic data showed serum-starved cells were clearly separated with control cells,

81 wn by inducing autophagy, which provides the starved cells with amino acids for protein synthesis and

82 Consistent with these results, serum-starved cells with high ST6Gal-I expression maintain a g

83 rexpression or knockdown, we find that serum-starved cells with high ST6Gal-I levels exhibit increase

84 Dps (DNA-binding protein from starved cells) are dodecameric assemblies belonging to t

85 an NAP called Dps (DNA-binding protein from starved cells) becomes highly up-regulated and can massi

86 . coli Dps protein (DNA-binding protein from starved cells).

87 teins are recruited to the ERGIC membrane in starved cells, dependent on active PI3K.

88 they mobilize and move into mitochondria in starved cells, driving oxidative respiration, is unclear

89 When mitochondrial fusion was prevented in starved cells, FAs neither homogeneously distributed wit

90 In serum-starved cells, increased IRSp53 phosphorylation triggers

91 However, when glucose is added to glucose-starved cells, levels of extracellular FBPase decrease r

92 In prolonged starved cells, substantial amounts of the key gluconeoge

93 ighly regulated by iron and abundant in iron-starved cells, suggesting a role in iron acquisition.

94 teins with a high N content are reduced in N-starved cells, while the proteins that are increased hav

95 od of producing cultures of >/=90% DD Mtb in starved cells.

96 rous cancers, promotes the survival of serum-starved cells.

97 uted to maintenance of ATP levels in glucose-starved cells.

98 lites were identified between ADMA and serum-starved cells.

99 ut were enriched during phage infection of P-starved cells.

100 e metabolism and avoidance of FA toxicity in starved cells.

101 ctivity upon adding glucose or tryptophan to starved cells.

102 ial steps of LD formation occurring in lipid-starved cells.

103 interaction with Atg14L and other SNAREs in starved cells.

104 ctly released as was shown experimentally in starved cells.

105 We observe two subpopulations of glucose-starved cells: recoverers, which rapidly adapt and resum

106 nto a multicellular organism when individual starving cells aggregate and form a mound.

107 Starving cells also accumulate extracellular polyphospha

108 The results show that the assumption--starving cells die exponentially--is true only at high c

109 cific time point provided insights as to how starving cells obtain energy and precursors necessary fo

110 ting glucose addiction, while simultaneously starving cells of glucose, EA proves to be synthetically

111 Starving cells of leucine or treating them with leucyl-t

112 At low density, starving cells persevere for extended periods of time, b

113 Bacterial sporulation allows starving cells to differentiate into metabolically dorma

114 sion constitutes a strategic reserve kept by starving cells to quickly meet demand upon sudden improv

115 g processes relevant for the perseverance of starving cells.

116 ns that adapt COPII vesicles to the needs of starving cells.

117 proximately 200 nm) dominating under hot air starved combustion and a larger sized mode dominating un

118 were found during fast burning under hot air starved combustion conditions, in both stoves.

119 k as well as nitrogen-starved and phosphorus-starved conditions in light.

120 with E. coli cells undergoing division under starved conditions producing 66% fewer secreted protein

121 xamined in RAW 264.7 macrophages under serum-starved conditions that trigger apoptosis.

122 LDLR led to decreased cell survival in serum-starved conditions, associated with Caspase 3 cleavage.

123 so induces autophagy in nutrient-replete or -starved conditions, but depletion of the related kinase

124 Leu) is a critical mTORC1 regulator under AA-starved conditions, how Leu regulates autophagy is poorl

125 idual Znu component are unable to grow in Zn-starved conditions, including in the presence of the hos

126 pment and auxin accumulation under phosphate-starved conditions, suggesting a role for autophagy in r

127 AMPK signaling in muscle was impaired under starved conditions, while mTORC1 signaling remained acti

128 regulating the mTORC1 pathway under fed and starved conditions.

129 in regulating LR development under phosphate-starved conditions.

130 uxin-mediated LR development under phosphate-starved conditions.

131 erely reduced LRs when grown under phosphate-starved conditions.

132 rsus those transitioning from P-replete to P-starved conditions.

133 ivity is critical for sleep regulation under starved conditions.

134 However, under starving conditions, the maintenance of stress fibers an

135 loratory behavior is suppressed less than in starved control males.

136 showed fitness metrics no different from the starved control.

137 The dominant communities in starved copepods were Vibrio spp. and related Gammaprote

138 In this work, we demonstrate that energy-starved cultures of Pyrinomonas methylaliphatogenes, an

139 ction of cathodic electron uptake by lactate-starved D. ferrophilus IS5 cells resulted in the express

140 rthermore, 80% (25 million) live on sediment-starved deltas, which cannot naturally mitigate flooding

141 Here, we examine cell shape and movement in starved Dictyostelium amoebae during migration toward a

142 Thus, HIV-1 variants that attempt to "starve" DIPs to escape interference would be selected ag

143 es upon loss of the Ccz1-Mon1-Rab7 module in starved Drosophila fat cells.

144 In addition, nitrogen-starved E. coli cells synthesize a signal molecule, guan

145 d modifications were investigated in glucose starved E. coli cultures and compared to a DeltarelADelt

146 racterized dynamics of survival and death of starving E. coli cells.

147 ial mats to support their growth in a carbon-starved ecosystem.

148 n of single-cell lag times of populations of starved Escherichia coli and show that population growth

149 se is an adaptive mechanism used by nitrogen-starved Escherichia coli to scavenge for alternative nit

150 that epoxyethane stimulated the activity of starved etheneotrophs by inducing the enzyme alkene mono

151 del for TRAPPIII function in both normal and starved eukaryotic cells.

152 Today's Sargasso Sea is nutrient starved, except for episodic upwelling events caused by

153 ts differentiated in vitro, but not in serum starved fibroblasts, suggesting that their expression is

154 flies are starved and decrease shortly after starved flies are refed.

155 Starved flies exhibit enhanced sensitivity to attractive

156 Starved flies exhibit increased sugar and decreased bitt

157 show taste aversion to acetic acid, whereas starved flies show a robust appetitive response.

158 ns respond to food presentation, but only in starved flies.

159 inhibited sugar sensitivity in satiated and starved flies.

160 ed onto collagen-coated biosensors and serum-starved, followed by exposure to agonistic compounds tar

161 say on cultured goblet cells that were serum-starved for 2 hours before stimulation with VIP, VPAC1-,

162 gical relevance of this process in vivo Mice starved for 48 h exhibited a sharp decrease in overall c

163 for TORC1 activation in cells that have been starved for a significant period of time.

164 with expression patterns observed in plants starved for carbon or energy supply.

165 t, they raise the pH of the environment when starved for glucose or when grown strictly with non-ferm

166 oli in stationary phase as a result of being starved for glucose, not on the genetic adaptation of E.

167 When starved for iron, E. coli tolC mutants synthesize but ca

168 tabolically to increase H2 yields when it is starved for N2, and thus not growing, we tracked changes

169 hat occurs when Chlamydomonas reinhardtii is starved for nitrogen in the presence of acetate and unde

170 When starved for nitrogen, non-growing cells of the photosynt

171 become dormant or form spores when they are starved for nutrients.

172 rted to nonphosphorus lipids when cells were starved for phosphate, or when growing on methylphosphon

173 oichiometric to phosphorus consumption, when starved for phosphate.

174 and C. pneumoniae are Trp auxotrophs and are starved for this essential nutrient when the human host

175 ars fed honeycomb, fed polyethylene (PE), or starved for up to 72 h.

176 ned >95% viability, whereas the viability of starving, freely suspended (planktonic) cells decreased

177 S-starved ggct2;1 primary roots grow longer than the wild-

178 ged antibodies to activate MET in live serum-starved glioblastoma cells and monitor the fate of antib

179 rated a low death profile in stressed cells (starved + H(2)O(2)), while cell proliferation was stagna

180 Proteoid roots from Pi-starved harsh hakea were analyzed over 20 d of developme

181 d upon the addition of ammonium to glutamine-starved Hep3B cancer cells.

182 GC-1 overexpression was sufficient to rescue starved hlh-30 mutant worms, demonstrating a critical ne

183 Moreover, we show that starved human fibroblasts secrete matrix proteins that m

184 at retinal ganglion cells (RGC-5), and serum-starved human retinal pigment epithelial cells (ARPE-19)

185 the filamentous growth program when nitrogen starved if they had been previously exposed to this cond

186 ome indicates that these cells are reductant-starved in the dark, likely because enzymes of the prima

187 When males are starved in the presence of inedible food, they become nu

188 ring oral processing of foods and drinks and starves in between times.

189 We observed that reducing serum (starved) induced reactive oxygen species which provided

190 ease in infectious virus production, whereas starving infected cells of exogenous glucose had no sign

191 inositol and similarly observed in inositol-starved ino1Delta cells.

192 MP1 removes Mn and other essential metals to starve intracellular pathogens; in the extracellular spa

193 mmunity." This chelation strategy ultimately starves invading pathogens, limiting their growth within

194 tebrates limit access to manganese and zinc, starving invading pathogens, such as Staphylococcus aure

195 CD4 T cells attempt to contain Mtb growth by starving it of tryptophan--a mechanism that successfully

196 nucleotide pools is a critical challenge for starving Kras-driven tumor cells.

197 the primordial germ cells (PGCs) of emergent starved L1 larvae that correlate with compromised reprod

198 regulate expression of insulin-like genes in starved L1 larvae.

199 vior in C. elegans nematodes, aggregation of starved L1 larvae.

200 tably, the majority of genes dysregulated in starved L1 Rb(-) animals were not found to be dysregulat

201 n apparent correlation between propensity of starved L1s to aggregate and density dependence of their

202 Conversely, refeeding the starved larvae strongly reduces CDK8 levels but increase

203 autophagy causes dysregulated pupariation of starved larvae, which leads to pupal lethality, whereas

204 Loss of HLH-30 markedly impaired survival in starved larval worms and recovery upon refeeding bacteri

205 ant was able to stimulate the growth of iron-starved legionellae.

206 ubstantially up-regulated proteins in purine-starved Leishmania donovani parasites.

207 toxic H2 O2 , a novel treatment paradigm of starving-like therapy is developed for significant tumor

208 irst time constructed for synergistic cancer starving-like/gas therapy without the need of external e

209 A on gene expression and metabolism in serum-starved LoVo cells with gene microarray and metabolomic

210 Pi-starved M. mazei cells increased transcript abundance of

211 Subsequent incubation of Pi-starved M. mazei cells under Pi replete conditions, led

212 icin against the nonreplicating streptomycin-starved M. tuberculosis 18b-Lux strain, and therefore, t

213 rescue cell survival and mTORC1 activity in starved macrophages and tumor cells.

214 matrix proteins that maintain the growth of starved mammary epithelial cells contingent upon epithel

215 System's terrestrial planets formed from gas-starved mass-depleted debris that remained after the pri

216 ay data from MATa cells, MATa/alpha cells, a starving MATalpha/alpha control, and a meiosis-impaired

217 Attachment of serum-starved MCF-10A cells to fibronectin, but not poly-d-lys

218 Livers of starved mice also had increased levels of Ppargc1a mRNA

219 important regulator of iron homeostasis, in starving mice (a model of persistently activated glucone

220 Starving microalgae for nitrogen sources is commonly use

221 immune system employs multiple strategies to starve microbes of metals.

222 n the upper, aerobic ocean, where phosphorus-starved microbes catabolize methylphosphonate for its ph

223 ight into how the human innate immune system starves microbes of essential metal nutrients.

224 s commonly assumed that survival kinetics of starving microbes follows exponential decay.

225 acrophages with conditioned media from serum-starved mouse proximal tubule cells.

226 iron donor and supports replication of iron-starved mycobacteria.

227 Starved Myxococcus xanthus cells glide to aggregation ce

228 studied unfolded protein response in energy-starved neurons during stroke, which is relevant to the

229 ]), (2) light-limited (LL), and (3) nitrogen-starved (NS) conditions.

230 lls die a "thymineless death" since they are starved of a crucial DNA synthesis precursor.

231 During infection, pathogens are starved of essential nutrients such as iron and tryptoph

232 re induced when Saccharomyces cerevisiae are starved of glucose.

233 Prior work has shown that P. aeruginosa is starved of iron in the presence of CP.

234 ogenic, are sensitive to host processes that starve or swamp the prokaryote with large fluctuations i

235 iol utilization (PDU) microcompartments when starved or grown on 1,2-propanediol (1,2-PD) or rhamnose

236 In rats which had been starved overnight, Acipimox caused a fall in ejection fr

237 and paired-end Illumina reads for phosphorus-starved (P-) and phosphorus-treated (P+) genovars of tol

238 size only in a nutrient-rich environment; in starved planarians, silencing results in a decrease in c

239 ssion that differed markedly from growing or starving planktonic cells, highly expressing genes in gl

240 We also show that Pi-starved plants increase the cis-zeatin (cZ) : trans-zeat

241 We propose that Pi-starved plants increase the cZ : tZ ratio to maintain ba

242 rboxylase (PEPC) in inorganic phosphate (Pi)-starved plants.

243 PI3K/AKT signaling was reduced in serum-starved Psen1-/- cells, and this was associated with ele

244 However, PAD is also suppressed in nitrogen-starved pt4 pt8 double mutants, negating this hypothesis

245 under challenging conditions, such as photon-starving quantum applications.

246 Re-feeding starved retinas in vitro rescues both proliferation and

247 ening of a cDNA library derived from sucrose-starved rice suspension cells.

248 Starving rodents, for example, will forage in areas that

249 f reciprocity, vampire bats share blood with starving roost-mates.

250 ng ratiometric imaging, we delineate that Pi-starved roots have a normal response to extracellular AT

251 Addition of glucose to starved Saccharomyces cerevisiae initiates collective NA

252 the global ocean floor is draped by nutrient-starved sediments characterized by deep oxygen penetrati

253 However, when nitrogen-starved, seedling growth is severely arrested, and as th

254 For the wild type, only S-starved seedlings benefited from DMDS exposure.

255 se, we devised an experimental procedure for starving single Escherichia coli bacteria in microfluidi

256 also takes place at the surface of nutrient-starved, sPLA(2) overexpressing hyphae, may strengthen a

257 (GDP):RagC(GTP) GTPases as they exist in the starved state with their lysosomal anchor Ragulator comp

258 However, FISH analysis of the starved stringent response mutant showed a bimodal respo

259 e F display sleep-dependent memory even when starved, suggesting that circuit selection is determined

260 , induced a fed fly to eat as though it were starved, suggesting that these neurons are downstream of

261 , cell migration, and proliferation in serum-starved Swiss 3T3 cells.

262 any point by exogenous arginine, suggesting starved T cells remain poised awaiting nutrients.

263 nce imaging is an inherently signal-to-noise-starved technique that limits the spatial resolution, di

264 rom smoking and/or microbial infections that starve the biofilm and epithelial attachment of lysine.

265 the possibility that E. coli Nissle 1917 can starve the O157:H7 E. coli strain EDL933 of gluconeogeni

266 logical basis of such a strategy would be to starve the tumor cells of an important class of nutrient

267 uced ribosome stalling at specific codons by starving the bacterium Escherichia coli for the cognate

268 o hydrolyze asparagine to aspartate, thereby starving the cancer cells of this amino acid.

269 sition in reservoirs, which is thought to be starving the coast of sediment and decreasing the resili

270 egulate carbohydrate metabolism, essentially starving the heart of fuel.

271 N-glycan branching in mouse T cell blasts by starving the hexosamine pathway of glucose and glutamine

272 This simple act of nutritional warfare, starving the invader of an essential element, is an effe

273 ter rodentium by consuming amino acids, thus starving the invading organism of essential nutrients.

274 on blocking these transporters as a means of starving the tumor cells of amino acids, but their poten

275 of the V1 and VO regions of the V-ATPase by starving the yeast Saccharomyces cerevisiae, allowing us

276 When starved, the Gram-positive bacterium Bacillus subtilis f

277 interior cells from external attack but also starve them through nutrient consumption.

278 ein that binds to bacterial siderophores and starves them for iron, thus representing a novel host de

279 nergy, in such a way that blocking lipolysis starves them to death.

280 ng effects, more effective than conventional starving therapy by only cutting off the energy supply.

281 When starved, these bacteria coordinate their gliding movemen

282 s cell death, an alternative to G0, in serum-starved THP1 cells.

283 oocytes and hastens early G0 arrest in serum-starved THP1 cells.

284 gene that is highly up-regulated in nutrient-starved tuberculosis models and codes for l-alanine dehy

285 l describe a new method to screen drugs that starve tumors by using umbilical cords, which allow nour

286 Because it is not possible to starve tumors of glucose in vivo, here we sought to iden

287 ntiangiogenic agents--originally designed to starve tumors--could transiently normalize tumor vascula

288 meostasis helps to nourish hypoxic, nutrient-starved tumors and protects them from chemotherapy-induc

289 cular endothelial growth factor A (Vegfa) by starved Vldlr(-/-) photoreceptors, leading to neovascula

290 ation of HCO(3)(-) in the high pH and carbon-starved water.

291 otic cells in higher eukaryotes often do not starve, we developed a model yeast system to study cells

292 However, these cells, when starved, were impeded in the epimastigote to trypomastig

293 S-starved wild-type plants also produce longer primary roo

294 starvation causes glutathione depletion in S-starved wild-type seedlings, but higher glutathione is m

295 Well-fed worms migrated up, while starved worms migrated down.

296 ectively stimulated and inhibited feeding in starved worms, but not in worms lacking NPR-17, which en

297 Nitrogen replenishment of nitrogen-starved yeast cells resulted in substantial transcriptom

298 Furthermore, in copper-starved yeast, the response of the Rad53 pathway to MMS

299 f 28 transcription factors (TFs) in nitrogen-starved yeast.

300 In starving yeast exposed to thermal stress, a transient dr