ライフサイエンスコーパス: desiccation

1 lent conditions of temperature, salinity and desiccation).

2 le for trehalose in protecting cells against desiccation).

3 se is essential for survival after long-term desiccation.

4 anisms to tolerate external hypertonicity or desiccation.

5 esistance to antibiotics, disinfectants, and desiccation.

6 halose during short-term, but not long-term, desiccation.

7 utant pollen collapsed at the time of anther desiccation.

8 tage of GC-rich DNA during cell freezing and desiccation.

9 alose is essential for survival to long-term desiccation.

10 ommonly used to prevent corneal exposure and desiccation.

11 area shrinkage between full turgor and oven desiccation.

12 escent spores that are resistant to heat and desiccation.

13 g seeds during embryogenesis, maturation and desiccation.

14 uctures and nutrients within the seed during desiccation.

15 transgenic flies also display resistance to desiccation.

16 is elevated during late seed maturation and desiccation.

17 in tear dynamics, leading to ocular surface desiccation.

18 ve a remarkable array of stresses, including desiccation.

19 Hsp12 functions to protect the membrane from desiccation.

20 tical to the survival of S. stapfianus under desiccation.

21 the plasma membrane to protect membrane from desiccation.

22 BI3) are required to protect the seed during desiccation.

23 wall to fold onto itself to prevent further desiccation.

24 icle, which protects A. gambiae embryos from desiccation.

25 enes involved in metabolic regulation during desiccation.

26 expands on long warm days, possibly to avoid desiccation.

27 involved in the response of B. japonicum to desiccation.

28 es than those transcriptionally activated by desiccation.

29 ate and protein synthesis or preparation for desiccation.

30 and embryos acquire the ability to withstand desiccation.

31 s, a related species with tolerance to rapid desiccation.

32 ich widespread fire activity depends on fuel desiccation.

33 s potentially novel mechanisms for surviving desiccation.

34 um during dehydration and upon recovery from desiccation.

35 gly induced in response to osmotic stress or desiccation.

36 es subjected to drought and seeds undergoing desiccation.

37 moist conditions is recommended followed by desiccation.

38 rrier function, which protects the body from desiccation.

39 maltose at conferring tolerance to long-term desiccation.

40 WSCP as interacting with RD21 (responsive to desiccation 21), a granulin domain-containing cysteine p

41 cysteine protease dubbed RD21 (RESPONSIVE TO DESICCATION-21).

42 uring ABA pretreatment and immediately after desiccation, a new target of ABI3 action appears to be i

43 Acute desiccation activates stress signaling pathways in the o

44 ed upon UV treatment, alkylation damage, and desiccation, also in a RecA-mediated manner.

45 at all three incubation times in response to desiccation, an additional 43 and 403 up-regulated genes

46 d Ranunculus bulbosus was less vulnerable to desiccation (analyzed via loss of kleaf and turgor loss

47 assive lipid oxidation initiated during seed desiccation and amplified during seed quiescence.

48 nfer resistance to stress conditions such as desiccation and antibiotics.

49 tion by increasing adhesion and tolerance to desiccation and antibiotics.

50 resting study on bacteria, which can survive desiccation and at the same time undergo the B-A-B trans

51 physiological mechanism during recovery from desiccation and cold stress.

52 opeptide gene and its encoded peptides alter desiccation and cold tolerance.

53 ned attached to the plant even after silique desiccation and dehiscence had taken place.

54 LK and DILP levels in neurons in response to desiccation and drinking.

55 ll land plants, providing protection against desiccation and external environmental stresses.

56 he McMurdo Dry Valleys of Antarctica support desiccation and freeze-tolerant microbial mats that are

57 nergy but also protects the mosquito against desiccation and heat stresses.

58 tes in the capa-expressing Va neurons during desiccation and nonlethal cold stress but is not release

59 ynthesis of the moss cuticle, which prevents desiccation and organ fusion.

60 evaporation-condensation processes and thus desiccation and osmolarity changes.

61 mosphere: pavement cells protect plants from desiccation and other environmental stresses, while stom

62 y provides food, habitat and protection from desiccation and predation.

63 comial, opportunistic pathogen that survives desiccation and quickly acquires resistance to multiple

64 osing cells or not to Mars-related stresses (desiccation and radiation).

65 we investigated the effects of environmental desiccation and recovery on the sperm cells of three mos

66 ts reconcile MSC events and demonstrate that desiccation and refilling were timed by the interplay be

67 double-strand breaks caused by the frequent desiccation and rehydration characteristic of bdelloid h

68 t for stabilizing lipid droplets during seed desiccation and rehydration.

69 their ability to survive repeated cycles of desiccation and rehydration.

70 ave a limited shelf life, due to postharvest desiccation and senescence, which limits their global di

71 Insect cuticular hydrocarbons (CHCs) prevent desiccation and serve as chemical signals that mediate s

72 m corneum serves to protect the body against desiccation and simultaneously limits the passage of dru

73 cells to understand the stresses imposed by desiccation and their stress response pathways.

74 reduced in cutin and were less resistant to desiccation and to infection by the fungus Alternaria br

75 f a balance of trehalose stockpiled prior to desiccation and trehalose degradation by trehalases in d

76 ven the abilities of mycobacteria to survive desiccation and trehalose in solution to protect biomole

77 tive propagules and provided protection from desiccation and UV-B radiation.

78 at reveal that treatments ranged from simple desiccation and wrapping in bandages to, in the case of

79 e hygrosensation (humidity sensing) to avoid desiccation and, in vectors such as mosquitoes, to locat

80 es: physical damage to hindwings, predation, desiccation, and cold shock.

81 lies and monitored food intake, responses to desiccation, and peptide expression levels.

82 ccation resistance in species which adapt to desiccation, and rainforest restricted species which can

83 AAs) also contributes to alternative energy, desiccation, and seed vigor; thus, manipulating FAA leve

84 icle that provides essential protection from desiccation, and so its evolution is believed to have be

85 eme environments that exert low-temperature, desiccation, and starvation stress on bacteria over thou

86 -crystalline amorphous solids (vitrify) upon desiccation, and this vitrified state mirrors their prot

87 uticular hydrocarbons, highly susceptible to desiccation, and with reduced viability upon adult emerg

88 the capability (capa) neuropeptide gene is a desiccation- and cold stress-responsive gene in diverse

89 By analogy with the desiccation- and radiation-resistant bacterium Deinococc

90 of a deadly fungal parasite through complete desiccation (anhydrobiosis) and disperse by wind to esta

91 ecent climatic warming and resultant wetland desiccation are causing severe declines in 4 once-common

92 During desiccation, assimilation and (13)CO(2) discrimination i

93 transcript abundance of genomic 'clusters of desiccation-associated genes' (CoDAGs), reflecting the c

94 ty, the ability to resume reproduction after desiccation at any life stage, and a paucity of transpos

95 gests that plants actively promote localized desiccation at the infection site and thus restrict path

96 iency might be in offsetting warming-induced desiccation because higher CO(2) also leads to higher pl

97 ons, we manipulated mosquito egg exposure to desiccation before inducing hatching and allowing surviv

98 ggest that B. japonicum directly responds to desiccation by adapting to changes imparted by reduced w

99 ecies from all kingdoms of life, can survive desiccation by entering a state with no detectable metab

100 Dehydration can be due to desiccation caused by a lack of environmental water or t

101 on cells from an exponential culture survive desiccation compared with one in five cells in stationar

102 fixative and duration of sample storage via desiccation contribute to minor spectral changes only.

103 fixative and duration of sample storage via desiccation contribute to minor spectral changes where s

104 Desiccation costs are high for harvester ants foraging i

105 bination of intense solar radiation and soil desiccation creates a short circuit in the biogeochemica

106 upply (upward growth) with avoidance of root desiccation (downward growth).

107 olutionary adaptation to survive episodes of desiccation encountered in their characteristic habitats

108 As desiccation extends, the activities of the protein chape

109 f sperm cells were tolerant to environmental desiccation for extended periods (d) and that tolerance

110 the ability of Acanthamoeba cysts to survive desiccation for more than 20 years.

111 A-sensitive COLD REGULATED and RESISTANCE TO DESICCATION genes was diminished in Arabidopsis during i

112 Adaptation to extreme desiccation has conferred extraordinary radiation resist

113 How tardigrades survive desiccation has remained a mystery for more than 250 yea

114 and many repeated instances of evolution to desiccation have been observed among Drosophila populati

115 the form of spores were highly resistant to desiccation, heat, and UV light.

116 y protecting spore DNA against damage due to desiccation, heat, toxic chemicals, enzymes, and UV radi

117 Exposure to desiccation, high UV, and daytime temperature regimes ar

118 During desiccation, homoiochlorophyllous resurrection plants re

119 g environmental constraints such as seasonal desiccation imposed by living on land.

120 , S. lepidophylla appears poised to tolerate desiccation in a constitutive manner using a wide range

121 adly, the patterns of deformation induced by desiccation in both mesophyll and xylem suggest that cel

122 Tolerance to desiccation in cultures of Saccharomyces cerevisiae is i

123 (RFOs) accumulate in seeds during maturation desiccation in many plant species.

124 Global warming is predicted to induce desiccation in many world regions through increases in e

125 y expressed at high levels or induced during desiccation in multiple tardigrade species.

126 croclimates in winter and greater host plant desiccation in summer.

127 the human host, losing infectivity following desiccation in the environment.

128 y experiences high osmolarity as a result of desiccation in the soil.

129 y reduced carotenoid degradation during seed desiccation, increasing beta-carotene content 8.4-fold r

130 gly protects cells against disinfectants and desiccation, indicating its potential significance for l

131 o make dividing yeast tolerant to short-term desiccation, indicating that other disaccharides have st

132 Desiccation-induced change in corneal fluorescein staini

133 ufficiency of trehalose as an antagonizer of desiccation-induced damage in yeast emphasizes its poten

134 ratio (3.59 +/- 0.94) observed after the air desiccation-induced injury.

135 f DNA Pol V genes may directly contribute to desiccation-induced mutagenesis.

136 Sequences of the rpoB gene from desiccation-induced Rif(r) mutants showed a signature th

137 We show that desiccation induces protein misfolding/aggregation of cy

138 , as well as mediating adaptive responses to desiccation, injury, and pathogen infection in vegetativ

139 ty was sufficient for complementation of the desiccation intolerant seed phenotype of abi3.

140 chlanis dilatata, a rotifer belonging to the desiccation-intolerant and facultatively sexual class Mo

141 by knockout mutants and overexpression in a desiccation-intolerant mutant background to play an impo

142 ies showed increased frond temperature, high desiccation levels and reduced photophysiological perfor

143 However, most organisms are sensitive to desiccation, likely due to an assortment of different st

144 ation (6-10 daa), grain fill (12-21 daa) and desiccation/maturation (28-42 daa) and were associated w

145 eason for a better fungal adaptation to soil desiccation may be hydraulic redistribution of water by

146 Alginate deficiency decreased survival of desiccation not only by P. putida but also by Pseudomona

147 tains sufficient water, indicating that leaf desiccation occurs in the natural progression of a flood

148 atherosclerotic-like lesions induced by air desiccation of a femoral artery, followed by balloon ove

149 Desiccation of cells resulted in the differential expres

150 graphy), biophysical (evapotranspiration and desiccation of invertebrates) and ecological (food chain

151 uted low CH4 oxidation rates in dry soils to desiccation of MOB, we present several lines of evidence

152 However, we demonstrate that the final desiccation of the Bodele Basin occurred around 1 ka.

153 We show that desiccation of the corneal surface due to nerve damage a

154 s an extended history of hydrogen escape and desiccation of the planet.

155 The desiccation of upper soil horizons is a common phenomeno

156 ided with protective mechanisms to cope with desiccation or cold stress.

157 protein-loaded material without the need for desiccation or freeze-drying.

158 mosquitoes succumb sooner after exposure to desiccation or heat.

159 ically protected from degradation during the desiccation period and conserved in dry seeds to allow i

160 and declines during the late maturation and desiccation phase when dormancy is induced.

161 tion is a response trait that influences the desiccation phenotype by increasing survivorship, shifti

162 itical during preparation of worms for harsh desiccation (preconditioning) and during the entry of ye

163 pidly accumulated before the seed begins the desiccation process.

164 lso plays a unique role in the regulation of desiccation processes during seed formation.

165 These changes imply that stronger desiccation processes occur during seed development.

166 During periods of dehydration and/or desiccation, proteomes struggle to maintain adequate cyt

167 majority of Cupressaceae species, uses leaf desiccation rather than high ABA levels to close stomata

168 Deinococcus radiodurans (Dr) withstands desiccation, reactive oxygen species, and doses of radia

169 reatment categories with different hydration/desiccation regimes.

170 t Shock Proteins, aquaporins, expansins, and desiccation related proteins (DRPs), which are highly di

171 Conventional CO(2) insufflation leads to desiccation-related peritoneal inflammation and injury,

172 expansion at 6 Ma coincident with major MSC desiccation; relative sea-level modelling indicates a pr

173 (mbCHCs) are a dual trait that affects both desiccation resistance and mate choice in Drosophila ser

174 produce cuticular hydrocarbons required for desiccation resistance and pheromonal communication.

175 experiment, suggesting that pigmentation and desiccation resistance are not unequivocally linked in a

176 igate this relationship further, we examined desiccation resistance attributable to an allele that da

177 CHC evolution may be a common mechanism for desiccation resistance in D. melanogaster.

178 map of population level genetic variation in desiccation resistance in D. melanogaster.

179 ing to compare patterns of CHC variation and desiccation resistance in species which adapt to desicca

180 und no significant effect of pigmentation on desiccation resistance in this experiment, suggesting th

181 One general mechanism for desiccation resistance is Cuticular Hydrocarbon (CHC) me

182 At most desiccation resistance loci there was a significant asso

183 s a significant association between CHCs and desiccation resistance of the sort predicted from clinal

184 neurons diminished LK expression, increased desiccation resistance, and diminished food intake.

185 icification provides viruses with remarkable desiccation resistance, which could allow extensive aeri

186 in both sexes, CHCs correlated strongly with desiccation resistance.

187 ing metabolic rate reduction associated with desiccation resistance.

188 cular hydrocarbons have been shown to confer desiccation resistance.

189 ssociated with venation features that affect desiccation resistance.

190 deserts of North America, is one of the most desiccation resistant in the genus, surviving low humidi

191 Its eggs are desiccation resistant, and the larvae develop rapidly in

192 The formation of a highly desiccation-resistant endospore might serve as a logical

193 n the potential roles of sncRNA in mediating desiccation-responsive pathways in early land plants.

194 Preventing corneal desiccation results in a milder and more transient HSK w

195 -tolerant (DT) Sporobolus stapfianus and the desiccation-sensitive (DS) Sporobolus pyramidalis formed

196 One protein prevents desiccation-sensitive enzymes from aggregating during dr

197 genomes of P. vanderplanki and a congeneric desiccation-sensitive midge P. nubifer.

198 The exact stress(es) that cause lethality in desiccation-sensitive organisms and how the lethal stres

199 lls that produce CHCs) of a closely related, desiccation-sensitive species, D. birchii, due in part t

200 ant species, Selaginella lepidophylla, and a desiccation-sensitive species, Selaginella moellendorffi

201 Here we exploit the desiccation sensitivity of exponentially dividing cells

202 t from the media converts yeast from extreme desiccation sensitivity to a high level of desiccation t

203 ecies provides evidence for the existence of desiccation-specific gene expression systems in P. vande

204 now allow pathogenic enterococci to survive desiccation, starvation, and disinfection in the modern

205 microenvironment, protecting residents from desiccation stress and increasing survival.

206 accumulation and has a reduced tolerance of desiccation stress compared with the wild type.

207 transporting tissue to regulate responses to desiccation stress in the fly.

208 l in response to temperature, oxidative, and desiccation stress.

209 This approach has broad use in desiccation studies to carefully investigate the relatio

210 /3.0 degrees C day/night warming resulted in desiccation, such that combined CO(2) enrichment and war

211 emes of physical and biological stress (e.g. desiccation, temperature, UV radiation and microbial inf

212 Diverse organisms capable of surviving desiccation, termed anhydrobiotes, include species from

213 re less sensitive and better adapted to soil desiccation than bacterial-based food webs.

214 and preparation for hyperosmotic stress and desiccation that begin at sunrise.

215 hen the same groups of cells were exposed to desiccation, the aggregates survived better, and the com

216 sic acid at the same rate, but, after 4 h of desiccation, the jasmonic acid level was much higher in

217 In response to desiccation, the mutant and WT leaves produced abscisic

218 enudation of the right femoral artery by air desiccation to induce an atherosclerotic-like lesion and

219 yperosmotic barrier presenting the threat of desiccation to reach a source of food odor.

220 In seeds, desiccation tolerance (DT) and the ability to survive th

221 Desiccation tolerance (DT) is a remarkable process that

222 e mosses (Selaginellaceae) that have evolved desiccation tolerance (DT) or the ability to 'resurrect'

223 ar plants in which some species have evolved desiccation tolerance (DT).

224 chaperones, explaining its important role in desiccation tolerance and emphasizing the translational

225 that there is an inverse correlation between desiccation tolerance and growth rate in glucose-, ammon

226 Correlations between desiccation tolerance and potential effectors have been

227 ith carbon reserves possibly contributing to desiccation tolerance and resumption of metabolism upon

228 g support for the hypothesis that vegetative desiccation tolerance arose by redirection of genetic in

229 Knockdown of the capa gene increases desiccation tolerance but lengthens chill coma recovery

230 nch of the TOR and Ras-cAMP pathway inhibits desiccation tolerance by inhibiting the stress response

231 The time frame for maintaining long-term desiccation tolerance consists of a balance of trehalose

232 ant (LEA) proteins is highly correlated with desiccation tolerance in anhydrobiotic animals, selected

233 a prominent and important role in promoting desiccation tolerance in B. japonicum.

234 Loss of the GS dramatically decreased desiccation tolerance in both organisms.

235 LEA proteins dramatically enhance desiccation tolerance in mammalian cells and offer the o

236 nderstanding the networks that regulate seed desiccation tolerance in model plant systems would provi

237 ion of transcripts typically associated with desiccation tolerance in seeds and involvement of orthol

238 Vegetative desiccation tolerance in X. viscosa was found to be unco

239 fective in 60S showed a dramatic increase in desiccation tolerance independent of growth rate.

240 We found that induction of desiccation tolerance is cell autonomous and that there

241 Desiccation tolerance is common in seeds and various oth

242 Respiration as a prerequisite for acquiring desiccation tolerance is corroborated by respiration inh

243 geneous nature of dryland landscapes and the desiccation tolerance of biocrusts, which leaves them fr

244 yed a stable expression, suggesting that the desiccation tolerance of T. gelatinosa mostly relies on

245 a conserved metabolic rewiring that confers desiccation tolerance on organisms as diverse as worm an

246 e functional link between ABA, ABI3, and the desiccation tolerance phenotype that is found in angiosp

247 rs bypassing the respiration requirement for desiccation tolerance reveal at least two pathways, one

248 in yeast emphasizes its potential to confer desiccation tolerance to otherwise sensitive organisms.

249 ccharide trehalose is a major determinant of desiccation tolerance via unresolved mechanisms.

250 nhanced relative to pro and a defect in seed desiccation tolerance was uncovered.

251 , and these genes are sufficient to increase desiccation tolerance when expressed in heterologous sys

252 oration of genes involved in photosynthesis, desiccation tolerance, alkane production, and other feat

253 on is tightly correlated with acquisition of desiccation tolerance, and data support their capacity t

254 TDPs are required for tardigrade desiccation tolerance, and these genes are sufficient to

255 s TDPs as functional mediators of tardigrade desiccation tolerance, expanding our knowledge of the ro

256 st Saccharomyces cerevisiae exhibits extreme desiccation tolerance, its usefulness has been hampered

257 pair nevertheless retain wild-type levels of desiccation tolerance, suggesting that this trait involv

258 Desiccation tolerance, the ability to survive nearly tot

259 r and genetic mechanisms enabling vegetative desiccation tolerance, we produced a high-quality whole-

260 t heat shock induces a 5000-fold increase in desiccation tolerance, whereas hyper-ionic, -reductive,

261 examining the genomic background of extreme desiccation tolerance, which is exclusively found in lar

262 d range of carbon sources, including several desiccation tolerance-promoting sugars and unusually lar

263 rty of trehalose is directly responsible for desiccation tolerance.

264 sordered proteins, which play major roles in desiccation tolerance.

265 ssential role in seed maturation, conferring desiccation tolerance.

266 at shock and nutrient deprivation, increases desiccation tolerance.

267 disordered proteins (TDPs) are essential for desiccation tolerance.

268 This is accompanied by increased desiccation tolerance.

269 ortant clues to the sensors and effectors of desiccation tolerance.

270 a few angiosperm species possess vegetative desiccation tolerance.

271 f moss (Physcomitrella patens) cells confers desiccation tolerance.

272 ng as a model system for studying vegetative desiccation tolerance.

273 of growth that allows for the expression of desiccation tolerance.

274 esting that they could potentially influence desiccation tolerance.

275 e desiccation sensitivity to a high level of desiccation tolerance.

276 ydrobiotes has been strongly correlated with desiccation tolerance.

277 ranscriptomes in B. argenteum to establish a desiccation-tolerance transcriptomic atlas.

278 restrial green algae and all its species are desiccation tolerant (DT).

279 The desiccation tolerant bryophyte Bryum argenteum is an imp

280 Remarkably, desiccation tolerant organisms can survive years without

281 We identify that desiccation tolerant seeds exhibit a striking transcript

282 ions that facilitated efficient dispersal of desiccation tolerant spores, evolved in the ancestral la

283 Diverse organisms across taxa are desiccation tolerant, capable of surviving extreme water

284 The desiccation-tolerant (DT) Sporobolus stapfianus and the

285 d to plants; multiple forms are expressed in desiccation-tolerant animals from at least four phyla.

286 ralea3m mRNA is expressed manyfold higher in desiccation-tolerant embryonic stages when compared with

287 whole-genome sequencing and assembly of the desiccation-tolerant grass Oropetium thomaeum.

288 Experiments on the desiccation-tolerant moss Syntrichia ruralis assessed th

289 and how the lethal stresses are mitigated in desiccation-tolerant organisms remain poorly understood.

290 eversible recovery of hydraulic conductance, desiccation-tolerant seeds, or rhizomes may allow them t

291 e by redirection of genetic information from desiccation-tolerant seeds.

292 etabolic basis of DT was conducted between a desiccation-tolerant species, Selaginella lepidophylla,

293 * The observation of desiccation-tolerant sperm in multiple moss species has

294 low temperature in buds and leaves, whereas desiccation treatment induces PpeS6PDH in buds and repre

295 ies in sperm cell tolerance to environmental desiccation was observed, suggesting selection could pot

296 cines, including additives, temperature, and desiccation, were determined and their protective effica

297 ndance during maturation and decrease during desiccation, when plastids dedifferentiate/degenerate.

298 ates maintained a constant level during seed desiccation, whereas the fatty alcohols and saturated om

299 rom low-density logarithmic cultures survive desiccation, while 20-40% of cells from saturated cultur

300 We hypothesized that reduced peritoneal desiccation would improve patient-centered outcomes in c