ライフサイエンスコーパス: starve

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

2 catecholate transport-deficient strain iron-starved.

3 of lysosomal membranes when cells are serum starved.

4 hus undergoes multicellular development when starved.

5 ending on the nutrient for which the cell is starved.

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

7 e indicates that the failing heart is energy starved.

8 ression changes during refeeding after being starved.

9 d from LDs into mitochondria when cells were starved.

10 thereby collectively lowering the chances of starving.

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

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

13 he surface of infected cells that were serum starved and had Akt activity inhibited.

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

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

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

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

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

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

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

21 t evidence that the failing heart is "energy starved" as it relates to CK.

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

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

24 Starving Bacillus subtilis cells execute a gene expressi

25 ferritin-like Dps (DNA-binding protein from starved bacteria) molecule, which has been shown to be i

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

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

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

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

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

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

32 211 renovates membrane lipids when phosphate starved by replacing a portion of its phospholipids with

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

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

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

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

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

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

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

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

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

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

43 lexes formed by the DNA-binding protein from starved cells (Dps), the only other stationary phase-spe

44 similarity to an archaeal DNA protection in starved cells (DPS)-like protein than to the 24-subunit

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

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

47 ng low luminescence with extracts from serum-starved cells and increased luminescence using extracts

48 ent initiation of replication in the thymine-starved cells and may be the underlying cause of TLD.

49 e ubiquitylated and endocytosed when glucose-starved cells are exposed to glucose.

50 Starved cells are not repelled by recombinant AprA, sugg

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

52 Adding methionine to S-starved cells causes a 50-fold decline (t(1/2) approxima

53 abolize SO(4)(=)), addition of SO(4)(=) to S-starved cells causes inactivation of (35)SO(4)(=) influx

54 All starved cells could oxidize exogenous glutamine, whereas

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

56 Furthermore, LT induction in serum-starved cells demonstrated gamma-H2AX accumulation in ce

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

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

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

60 T2 activities from purine-replete and purine-starved cells indicated that both transporters exhibited

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

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

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

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

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

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

67 able MT levels in proliferating cells and in starved cells stimulated with lysophosphatidic acid.

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

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

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

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

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

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

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

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

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

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

78 that replication slowly continues in thymine-starved cells, but the newly synthesized DNA becomes fra

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

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

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

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

83 on the repression of GCN4 translation in non-starved cells, nor on its derepression in response to hi

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

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

86 However, when glucose is added to prolonged starved cells, these enzymes are degraded in the vacuole

87 However, when glucose is added to prolonged-starved cells, these enzymes are degraded in the vacuole

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

89 ctivity upon adding glucose or tryptophan to starved cells.

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

91 d specifically phosphorylates 53BP1 in serum-starved cells.

92 co-localized with actin patches in prolonged-starved cells.

93 ify PUMA, NOXA, and TRB3 as executors of Gln-starved cells.

94 nd defects in Atg9 delivery and autophagy in starved cells.

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 interaction with Atg14L and other SNAREs in starved cells.

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

101 ctly released as was shown experimentally in starved cells.

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

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

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

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

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

107 Starving cells of manganese or zinc, but not copper, cau

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

109 Bacterial sporulation allows starving cells to differentiate into metabolically dorma

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

111 g processes relevant for the perseverance of starving cells.

112 widely expressed DNA-protective protein from starved-cells (Dps) family proteins are considered major

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

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

115 d specificity, better sensitivity for signal-starved compounds, and the ability to detect, quantify,

116 ment were employed: a closed heating (oxygen-starved condition) where the soil was heated under vacuu

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

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

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

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

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

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

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

124 in regulating LR development under phosphate-starved conditions.

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

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

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

128 These changes did not affect survival under starving conditions, but they significantly affected the

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

130 ersification in natural resources for energy-starved countries.

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

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

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

134 We show that, when starved, dividing S. meliloti bet hedge by forming two d

135 dividual honeybees was manipulated by either starving donor bees or feeding them sucrose or low doses

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

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

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

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

140 erculosis likely resides within the nutrient-starved environment of caseous lung granulomas.

141 at enhances B. anthracis replication in iron-starved environments.

142 ith DNA double-strand break repair in carbon-starved Escherichia coli result from error-prone DNA pol

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

144 dynamics of this highly macrotidal sediment starved estuary.

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

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

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

148 this same mechanism occurs in chromosomes of starving F(-) E. coli.

149 The readdition of an essential nutrient to starved, fermenting cells of the yeast Saccharomyces cer

150 nds, stimulated stable MT formation in serum-starved fibroblasts and caused a redistribution of mDia1

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

152 ress fiber formation when expressed in serum-starved fibroblasts.

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

154 Starved flies exhibit enhanced sensitivity to attractive

155 Starved flies exhibit increased sugar and decreased bitt

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

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

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

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

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

161 or survival of Saccharomyces cerevisiae when starved for either of two nutrients: phosphate or leucin

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

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

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

165 e-wide gene expression as these strains were starved for methionine.

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

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

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

169 extracts but is absent in yeast abz1 mutants starved for pABA.

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

171 oichiometric to phosphorus consumption, when starved for phosphate.

172 respond to methionine starvation like yeast starving for natural nutrients such as phosphate or sulf

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

174 ero-calorie) sugar (sucralose or L-glucose), starved Gr5a; Gr64a double mutants preferred metabolizab

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

176 xpression of 75 kinases in cultures of serum-starved (HCF) were investigated using protein kinase scr

177 Furthermore, activation of mTORC1 in starved HEK-293 cells stimulated by amino acids requires

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

179 that apoptosis triggered by BIK in estrogen-starved human breast cancer cells is suppressed by GRP78

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

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

182 that these two hormones prolong survival in starved humans as they do in mice.

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

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

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

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

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

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

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

190 ease of mRNA and protein expression in serum-starved islets compared with controls.

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

192 Serum-starved JB6 cells contain very little endogenous H2BS32

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

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

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

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

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

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

199 Starved larvae can survive L1 arrest for weeks, but grow

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

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

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

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

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

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

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

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

208 olism of methylphosphonic acid by phosphorus-starved marine microbes, with concomitant release of met

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

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

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

212 shortly after adding >0.02 mM SO(4)(=) to S-starved met3Delta cells.

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

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

215 Starving microalgae for nitrogen sources is commonly use

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

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

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

219 We found that starved mouse embryonic fibroblasts lacking the essentia

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

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

222 Starved Myxococcus xanthus cells glide to aggregation ce

223 Starving Myxococcus xanthus bacteria use their motility

224 o a similarly generated data set of nitrogen-starved N. punctiforme resulting in hormogonium formatio

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

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

227 d was essential for heme utilization by iron-starved NTHI.

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

229 When Saccharomyces cerevisiae are starved of glucose for a prolonged period of time, gluco

230 re induced when Saccharomyces cerevisiae are starved of glucose.

231 is induced when Saccharomyces cerevisiae are starved of glucose.

232 When either starved of glutamine or rendered IDH2-deficient by RNAi,

233 have been performed wherein the dumbbell is starved of the macrocyclic components, and up to five ti

234 ability in bacterial, yeast, and human cells starved of thymine.

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

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

237 dead splenocytes and to apoptotic cells from starved or irradiated lymphocytic cell lines, an observa

238 extend to the entire cell periphery in serum-starved or nonmotile fibroblasts.

239 ouble-stranded RNA into the previtellogenic, starved, or JH-deficient female adults increased Vg mRNA

240 ignificantly disrupted when for(R) flies are starved overnight.

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

242 Isoleucine-starved parasites remain viable for 72 h and resume rapi

243 Microarray analysis of starved parasites revealed a 60% decrease in the rate of

244 circadian rhythms as shown by the fact that starved period mutants sleep like wild-type flies.

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

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

247 nditions and during the recovery of nitrogen-starved plants.

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

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

250 blotting of p85-associated proteins in serum-starved PTEN-deficient LNCaP and C4-2 PCa cells showed a

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

252 athways with bafilomycin A1 sensitized serum-starved quiescent cells to MG132-induced apoptosis.

253 he autophagy/lysosomal pathway protect serum-starved quiescent fibroblasts from proteasome inhibition

254 e phages are infecting host cells that are P starved, relative to P-replete control cells.

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

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

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

258 Addition of glucose to starved Saccharomyces cerevisiae initiates collective NA

259 tioxidant enzymatic systems in nutritionally starving Salmonella.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

276 emoglobin (Hb)-derived oligopeptides, likely starving the parasite resulting in death.

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

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

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

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

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

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

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

284 When starved, these bacteria coordinate their gliding movemen

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

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

287 monstrated a protein profile similar to iron-starved Trichodesmium in culture, suggestive of acclimat

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

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

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

291 ic therapies are being pursued as a means of starving tumors of their energy supply.

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

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

294 alysis of pho85Delta mutant cells, phosphate-starved wild type cells, and cells expressing phosphoryl

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 From reporter gene studies in glucose-starved yeast, it was proposed that translationally sile

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

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