ライフサイエンスコーパス: life cycle

1 istinct parasite migration events across the life cycle.

2 ed products and articles at the end of their life cycle.

3 transparent results across the data science life cycle.

4 for drug discovery and the study of the HBV life cycle.

5 fill its multifunctional role during the AAV life cycle.

6 growth and development at all stages of the life cycle.

7 ounds 46 and 47 suppress later steps of HAdV life cycle.

8 , supporting a specific role of VLCFA in HCV life cycle.

9 tuning of fatty acid supply during the plant life cycle.

10 der the lymphatic environment unique to KSHV life cycle.

11 te in the regulation of the tumorigenic KSHV life cycle.

12 nal targets to interfere with the spirochete life cycle.

13 dance at the different stages of the lamprey life cycle.

14 potential roles in the synaptic vesicle (SV) life cycle.

15 e causative agent of malaria, have a complex life cycle.

16 ns that promote late steps of the retroviral life cycle.

17 ubdue the erythrocytic phase of the parasite life cycle.

18 s of the LSD1 inhibitor SP-2509 on the HSV-1 life cycle.

19 virus infection at a late stage in the virus life cycle.

20 enhance the success of the wasps' parasitic life cycle.

21 splaying a dual functional role in the viral life cycle.

22 ry for the pathogen's obligate intracellular life cycle.

23 lar events occurring in the viral infectious life cycle.

24 to generate an optimal environment for their life cycle.

25 trol key replication events during the HIV-1 life cycle.

26 trid cell biology and development during its life cycle.

27 d, given their dependency on light for their life cycle.

28 that block multiple stages of the Plasmodium life cycle.

29 th to sporulation in a complex developmental life cycle.

30 tory syndrome (SARS) coronaviruses and their life cycle.

31 uzi and into its implication to the parasite life cycle.

32 ined periods of purine scarcity during their life cycle.

33 mmune responses to facilitate its productive life cycle.

34 latency and lytic replication stages in its life cycle.

35 a sensitive host: the lysogenic or the lytic life cycle.

36 hysiological processes throughout the fungal life cycle.

37 as a novel inhibitor for the influenza virus life cycle.

38 l cells, where it undergoes a complex sexual life cycle.

39 virus, harnesses the UPR to regulate its own life cycle.

40 o a virus factory, thus disrupting the viral life cycle.

41 -family kinase activity to enhance the viral life cycle.

42 growth and survival throughout their entire life cycle.

43 ely important for transmission and the viral life cycle.

44 ving to nourish the nematode over its 30-day life cycle.

45 establishment at the beginning of the plant life cycle.

46 ing physiological needs of each stage in the life cycle.

47 ract at crucial regulatory steps in the cell life cycle.

48 ple conformations in the course of the viral life cycle.

49 leads to larval arrest and disruption of the life cycle.

50 rdinate essential processes during the viral life cycle.

51 PROX1, regulated different steps of the KSHV life cycle.

52 erated during fundamental events in the cell life cycle.

53 juvenile and the adult stages of the lamprey life cycle.

54 for HPV-mediated carcinogenesis and the HPV life cycle.

55 ile not perturbing other stages of the virus life cycle.

56 uld be assigned a discrete role during their life cycle.

57 it of moulting continuously throughout their life-cycle.

58 anscript levels throughout the entire shrimp life-cycle.

59 ge acting widely across annual and migratory life cycles.

60 ive genes between the phases of the Chondrus life cycles.

61 xceptionally diverse in their morphology and life cycles.

62 dergoing similar physiologically challenging life cycles.

63 hybrids usually cannot complete their sexual life cycles.

64 -mediated antioxidant response affects viral life cycles, a number of viruses deregulate Nrf2 pathway

65 The parasite has a digenetic life cycle alternating between mammalian and insect host

66 Chondrus has a complex haplodiplontic life cycle, alternating between male and female gametoph

67 Technoeconomic and life-cycle analyses are presented for catalytic conversi

68 Applying our observations to life-cycle analyses, we found that switching to NGVs fro

69 ontributions using other assessments such as life cycle analysis (LCA) would allow dentistry to ident

70 t a hump-shaped performance profile over the life cycle and a long-run shift in the profile toward yo

71 f Darwinian evolution onto the bacteriophage life cycle and allows directed evolution to occur on muc

72 nd, accordingly, also change during the cell life cycle and at differentiation.

73 e human-relevant stages of the P. falciparum life cycle and describes how licensed antimalarials, cli

74 ew of SARS-CoV-2 and its uniquely aggressive life cycle and discuss the interactions of various viral

75 ment of an optimal environment for the SFTSV life cycle and efficient pathogenesis.IMPORTANCE Tick-bo

76 ntiation is a central aspect of the parasite life cycle and encompasses adaptation to both host and e

77 may harness this activity to regulate viral life cycle and host cell response to viral infection.

78 t cell energy metabolism important for viral life cycle and HPV-mediated tumorigenesis.

79 unctions related to enhancement of the viral life cycle and immune escape.

80 ots grow and accumulate biomass during plant life cycle and in relation to shoot growth phenology rem

81 d peripheral homeostasis in the CD4+ Th cell life cycle and invariant NK (iNK) T cell development and

82 In Saccharomyces cerevisiae, the complex life cycle and maturation of telomerase includes a cytop

83 utilized by the virus during its vegetative life cycle and offers insights into the host-virus inter

84 response that critically controls the viral life cycle and pathogenesis.

85 is a key question in understanding the HSV-1 life cycle and pathogenesis.

86 additional direction of research into their life cycle and pathogenesis.

87 y, mutations are a natural part of the virus life cycle and rarely impact outbreaks dramatically.

88 expression throughout its aquatic and aerial life cycle and specific organs.

89 hts for the understanding of the coronavirus life cycle and the development of host-directed therapie

90 o complete the liver stage of the parasite's life cycle and the subsequent transition to asexual bloo

91 etween different trypanosomatids, with their life cycles and ecological niches likely influencing the

92 We comprehensively surveyed helminth life cycles and transmission involving ungulates.

93 of XBP1s and ATF6 as activators of the viral life cycle, and an unexpected role of XBP1u as a potent

94 ic reticulum (ER) membranes throughout their life cycle, and degradation of ER membranes restricts fl

95 eplication and successive steps in the virus life cycle, and further highlight the promising potentia

96 rypanosoma cruzi has a complicated dual-host life cycle, and starvation can trigger transition from t

97 Their central role in metabolism, complex life cycle, and unique lipid monolayer surface have garn

98 nants associated with different host ranges, life cycles, and distributions.

99 environmental (extrahost) stages in nematode life cycles, and that filarial worms contain compact and

100 Given their catadromous life-cycle, and global commercial and cultural importanc

101 erations thought to be important for the HPV life cycle are actually late events that may reflect imm

102 elated to thermal energy, water end use, and life cycle are cost-effective with significant abatement

103 pre-erythrocytic stages of the P. falciparum life cycle are the most advanced to date, affording mode

104 ed modelling of human behaviour and pathogen life-cycle are required in order to produce accurate res

105 Yersinia remodels its membrane during its life cycle as it alternates between mammalian hosts (37

106 Even so, a life cycle assessment (LCA) case study illustrates pract

107 Decision support tools such as life cycle assessment (LCA) increasingly aim to account

108 Life cycle assessment (LCA) is a reference methodology f

109 We present a global, locally resolved life cycle assessment (LCA) model to assess the potentia

110 Seventy-one unique life cycle assessment (LCA) studies that quantify the en

111 This study uses Life Cycle Assessment (LCA) to investigate the environme

112 This paper conducts a life cycle assessment and cost-benefit analysis for city

113 This paper presents a life cycle assessment for three stationary energy storag

114 Environmental indicators based on the life cycle assessment method are integrated into an ener

115 Policy Integrated Climate and process-based life cycle assessment models to quantify life cycle glob

116 Life cycle assessment of electricity generation should m

117 odel with field experiments; (b) make a full life cycle assessment of the potential for greenhouse ga

118 nsumption and carbon emission estimates with life cycle assessment to calculate the energy and greenh

119 at the University of Tennessee-Knoxville, a life cycle assessment was performed to calculate the ove

120 Life cycle assessment was used to compare environmental

121 etween sending and receiving systems), using life cycle assessment, model scenarios, and the framewor

122 g techno-economic analysis and time-resolved life cycle assessment.

123 erent practices were also considered using a life-cycle assessment approach.

124 This study presents a comprehensive life-cycle assessment, using reported and measured data,

125 However, policies are based on attributional life cycle assessments (LCAs) that do not account for ma

126 To factor this effect into life cycle assessments, location-specific models of the

127 these models reveals that in every case the life cycle assumptions entail local reproduction and loc

128 We estimate a complete life cycle at 3-4 months.

129 tage (and perhaps other stages) of the viral life cycle, based on several lines of evidence.

130 Life cycle-based analyses are considered crucial for des

131 hallmark of the Trypanosoma brucei digenetic life cycle because the insect stage utilizes a cost-effe

132 ulation process, completing the Streptomyces life cycle by facilitating dispersal of spores by soil a

133 one auxin controls many aspects of the plant life cycle by regulating the expression of thousands of

134 ewly translated viral proteins and the viral life cycle cannot be completed without protease activity

135 ughput sequencing and a method for promoting life cycle changes in vitro to assess the mechanisms and

136 To successfully complete its life cycle, Chlamydia must evade both intracellular inna

137 we show that ORM1 and ORM2 are essential for life cycle completion in Arabidopsis (Arabidopsis thalia

138 The model predicts the number of life-cycle completions (LCC) for a given location per un

139 r crescentus employs a specialized dimorphic life cycle consisting of two differentiated cell types.

140 es between the studies which look beyond the life cycle context, and apply other biodiversity metrics

141 al ability of aquatic parasites with complex life cycles differs strongly across scales, meaning that

142 8), PMR per life-cycle (PMRLC), and parasite life-cycle duration.

143 tes constitute a critical stage of the plant life cycle during which the genome undergoes reprogrammi

144 arvest losses and did not increase the total life-cycle enegy and GHGE.

145 erstanding spatially and temporally explicit life cycle environmental impacts is critical for designi

146 However, annual life cycle environmental impacts of crop production at c

147 superior fouling resistance will reduce the life cycle environmental impacts of ultrafiltration by 2

148 ve the spatial and temporal heterogeneity of life cycle environmental impacts.

149 t (i.e., Ecodesign), this study assesses the life cycle environmental performance of drinking water t

150 ritized in future R&D to further improve the life cycle environmental performance of LFMs.

151 to 22.0 kg CO(2)-eq kg soybean(-1), whereas life cycle EU and AD impacts varied by factors of 302 an

152 on rate were the top influencing factors for life cycle EU and AD impacts.

153 imate change causes changes in the timing of life cycle events across all trophic groups.

154 the interplay between C(i) availability and life cycle evolution.

155 inae) bore into tree xylem to complete their life cycle, feeding on symbiotic fungi.

156 emperate bacteriophages can enter one of two life cycles following infection of a sensitive host: the

157 During its entire life cycle from 2002 to 2012, iWiW reached up to 300 mil

158 include the entirety of the medical imaging life cycle from image creation to diagnosis to outcome p

159 the cytoplasm, during all phases of the cell life cycle (from development to senescence), under a var

160 We explore the economic and life-cycle GHG impacts of biogas upgrading and CO(2) cap

161 sed life cycle assessment models to quantify life cycle global warming (GWP), eutrophication (EU) and

162 icity source, recycling, and efficiency, the life cycle global warming potential for LFP ranges from

163 extured and more realistic assessment of the life cycle greenhouse gas emissions outcomes, using a ca

164 Models that characterize life cycle greenhouse gases from electricity generation

165 n their achieving much greater reductions in life-cycle greenhouse gas emissions than corn starch eth

166 Life cycle GWP impacts ranged from -11.4 to 22.0 kg CO(2

167 texture were the top influencing factors for life cycle GWP impacts.

168 cated that significant variations existed in life cycle GWP, EU, and AD among counties and across yea

169 o establish infection and complete the viral life cycle, human papillomavirus (HPV) needs to alter th

170 tion to housing important steps in the viral life cycle, IBs protect new viral RNA from innate immune

171 haracterization factors that can be used for life cycle impact assessment (LCIA) and risk assessment.

172 Currently, a generally accepted life cycle impact assessment (LCIA) framework for assess

173 r- and polyfluoroalkyl substances (PFASs) in life cycle impact assessment (LCIA) is proposed.

174 There are currently limited life cycle impact assessment methods existing for assess

175 alternatives assessments considering use and life cycle impacts or additionally prioritizing transfor

176 cts can have higher influence in determining life cycle impacts.

177 igate functions of this protein in the viral life cycle.IMPORTANCE Crimean-Congo hemorrhagic fever vi

178 ral genome determines the phase of the viral life cycle in the host.

179 iruses, we examined key aspects of the viral life cycle in three-dimensional (3-D) human airway tissu

180 in a consistent decrease in the C. difficile life cycle in vivo, it was able to attenuate an overly r

181 otein ICP22 plays several roles in the virus life cycle, including downregulation of cellular gene ex

182 host proteins for various steps of the virus life cycle, including entry, replication, and egress.

183 engthening distance decay of spread over the life-cycle indicating high fraction of distant diffusion

184 We demonstrate that life cycle influences cranial shape diversity and rate o

185 site, which spends a substantial part of its life cycle inside erythrocytes as rings, trophozoites, a

186 acilitate the use of the model, we provide a life cycle inventory tool with information on salts emit

187 lants flower a single time during their 1-yr life cycle, investing much of their energy into rapid re

188 parasitic protozoan that undergoes a complex life cycle involving insect and mammalian hosts that pre

189 Babesia spp. have complex life cycles involving multiple stages in the tick and th

190 ding the cellular factors involved in the PV life cycle is another important area of investigation.

191 Although disrupting the viral life cycle is critical for limiting viral spread and dis

192 stratified squamous epithelia, and the viral life cycle is linked to epithelial differentiation.

193 protozoan parasite Plasmodium falciparum Its life cycle is regulated by a cGMP-dependent protein kina

194 The choice between the two alternative life cycles is dependent upon a tight regulation of prom

195 reservoir hosts and the Ixodes tick vectors' life cycle, long-term studies are required to better und

196 ae phylogeny to date suggests that an annual life cycle may have contributed to domestication.

197 t important to understand virus assembly and life cycle mechanisms that offer distinct targets for th

198 g the impacts of packaging across its entire life cycle, most of the focus is on packaging waste or f

199 Here, we report the first complete life cycle of a luminous ostracod (Vargula tsujii Kornic

200 tor of innate immunity to DNA viruses in the life cycle of a small pathogenic RNA virus.

201 important yet poorly understood facet of the life cycle of a successful pathogen is host-to-host tran

202 plex plant-mediated mechanism regulating the life cycle of arbuscules in AM symbiosis.

203 During the natural enzootic life cycle of Borrelia burgdorferi (also known as Borrel

204 Previous work described that the life cycle of C. owczarzaki (hereafter, Capsaspora) incl

205 rphology and dynamics of chromatin along the life cycle of cells.

206 ial products, waste is the last stage of the life cycle of engineered nanomaterials, which are then i

207 ost cell is one of the critical steps in the life cycle of enveloped viruses.

208 rom latency is a key transition point in the life cycle of herpesviruses.

209 ' end of the HIV-1 genome in controlling the life cycle of HIV-1 indicates that this region significa

210 ctomotor pathways are present throughout the life cycle of lampreys, but olfactory-driven behaviors d

211 ude the strong cyclophilin dependency of the life cycle of many coronaviruses, including severe acute

212 The life cycle of many organisms includes a quiescent stage,

213 is a critical developmental decision in the life cycle of many plant species.

214 ication of important areas during the annual life cycle of migratory animals, such as baleen whales,

215 ito to a host is an essential process in the life cycle of mosquito-borne flaviviruses.

216 environmental impacts throughout the entire life cycle of packaging and FSW were analyzed.

217 The complex life cycle of Plasmodium parasites is shared between two

218 conditions are maintained over the hazardous life cycle of radioactive wastes (some ~10,000 years).

219 lease HO plays a central role in the natural life cycle of Saccharomyces cerevisiae, but its evolutio

220 summary, single-molecule imaging unveils the life cycle of telomerase RNA and provides a framework to

221 By describing the life cycle of the newly emergent coronavirus, SARS-CoV-2

222 er net environmental impacts across the full life cycle of the packaging and FSW.

223 have a significant role in the intracellular life cycle of the parasite.

224 it awareness of the location and within-host life cycle of the pathogen are shedding light on how hum

225 gument proteins pUL47 and pUL48 in the whole life cycle of the virus.

226 s enhances our understanding of the cellular life cycle of this medically important family of emergin

227 This review summarises the knowledge of the life cycle of this therapeutic target, including its bio

228 Reflecting the complex life cycle of V. cholerae, this organism has three diffe

229 The life cycles of many highly pathogenic RNA viruses like i

230 The life cycles of the tick vectors and spirochete pathogen

231 ze and complexity, little is known about the life cycles of these viruses.

232 oxycholic acid (UDCA; ursodiol) inhibits the life cycles of various strains of C. difficile in vitro,

233 o host chromosomes is a critical step in the life-cycle of retroviruses, including an oncogenic delta

234 Their complex life cycles - often heteroxenous with sexual and asexual

235 d carbon turnover from a speeding up of tree life cycles, or increased biomass from trees reaching la

236 study presents evidence for the dynamics of life cycle patterns of cognitive performance over the pa

237 into better context, integrating a holistic, life cycle perspective into research efforts and discuss

238 This review analyses studies which, using a life cycle perspective, assess the impacts of products'

239 uring the erythrocytic phase of the parasite life cycle, Plasmodium falciparum invades red blood cell

240 plication rate per 48 hours (PMR48), PMR per life-cycle (PMRLC), and parasite life-cycle duration.

241 omplexity of the Plasmodium parasite and its life cycle poses a challenge to our understanding of the

242 hitecture in controlling gene regulation and life cycle progression in Plasmodium spp.

243 eir roles in restricting the influenza virus life cycle remain mostly unknown.

244 tis worldwide, yet basic questions about its life cycle remain unanswered due to an historical lack o

245 ed during SARS-CoV-2 and related coronavirus life cycles remain ill defined.

246 anscription, an essential event in the HIV-1 life cycle, requires deoxynucleotide triphosphates (dNTP

247 Life cycle results suggest that optimization models that

248 h impacts of fluoropolymers throughout their life cycle(s).

249 iophage switch is unable to choose the lytic life cycle showing that the CI:MOR complex is essential

250 ng dispersion, the final step of the biofilm life cycle, single cells egress from the biofilm to resu

251 tion of resting spores, a heavily silicified life cycle stage associated with carbon export due to ra

252 ole of these stem cells during this critical life cycle stage remains unclear.

253 t switch their host range according to their life cycle stage.

254 a role during an early, prereplication virus life-cycle stage.

255 The Chondrus life cycle stages are isomorphic; however, a major pheno

256 gical differentiation between the isomorphic life cycle stages of Chondrus.

257 we studied endogenous TcHTE in the different life cycle stages of the parasite to gain insight into i

258 he native protein was expressed by the three life cycle stages of the parasite.

259 a company had reported a PCF's breakdown to life cycle stages or only the total emissions (10.9% ave

260 Multiple hosts and various life cycle stages prompt the human malaria parasite, Pla

261 to appropriately differentiate into distinct life cycle stages, such as the transition from its repli

262 o interrogate U-indel editing in EMF and MCF life cycle stages.

263 y contributing to the formation of different life-cycle stages, tissue differentiation and metabolism

264 , there were significant differences between life-cycle stages.

265 v10 on HCV infection and determine the virus life cycle steps affected by changes in Mov10 overexpres

266 to either direct-developing or paedomorphic life cycle strategies.

267 hich extent evolutionary transitions between life-cycle strategies are internally constrained at the

268 Here we study the evolution of life-cycle strategies in the grass subfamily Pooideae an

269 ich may explain the ubiquity of this complex life cycle strategy across disparate organisms.

270 We integrate ecological, life-cycle strategy and growth data in a phylogenetic fr

271 nging external conditions by switching their life-cycle strategy, likely due to the presence of evolu

272 We conducted a life cycle study using measurements from a nine-year Iow

273 and egress are essential steps in the viral life cycle that govern pathogenesis and spread.

274 Toxoplasma has a multistage life cycle that is intimately linked to environmental st

275 We highlight aspects of the viral life cycle that may be amenable to antiviral targeting a

276 replication, housing key steps in the virus life cycle that warrant further investigation.

277 for HEV infection, the analysis of the viral life cycle, the development of effective antivirals and

278 milarities influence the Tombusviridae viral life cycles, the structures of cucumber leaf spot virus

279 Due to their long and unique life cycles, these arthropods likely evolved robust epig

280 bition of virus at a later time in the virus life cycle through the suppression of nuclear export of

281 yte algae produce a siliceous stage in their life cycle, through either asexual or sexual reproductio

282 any organisms enter a dormant state in their life cycle to deal with predictable changes in environme

283 that TORC1 is required at each stage of the life cycle to progress to the next stage.

284 pathogens are able to compartmentalize their life cycle to provide favorable conditions for replicati

285 eciated role of viruses in regulating diatom life cycle transitions and ecological success.

286 ns targeting multiple stages of the P. vivax life cycle.TRIAL REGISTRATIONACTRN12614000930684 and ACT

287 How this life cycle unfolds and how host and parasite interact re

288 ther environmental factors (G x E), and host life-cycle variation may contribute to the maintenance o

289 ect effects of warmer temperatures on beetle life cycles versus indirect effects of drought on host s

290 C was 16.4 (95% CI, 15.1-17.8), and parasite life-cycle was 38.8 hours (95% CI, 38.3-39.2 hours).

291 tive and reproductive stages of the chickpea life cycle were obtained.

292 Most basics of the hepadnaviral life-cycle were unraveled using duck HBV (DHBV) as a mod

293 rily been driven by warming-amplified beetle life cycles whereas drought-weakened host defenses appea

294 CHIKV inhibits different stages of the viral life cycle, which could inform vaccine and therapeutic d

295 le body plans while navigating their complex life cycle, which involves two different hosts: a mammal

296 geny compared with species with single-phase life cycles, which may drive divergent evolutionary dyna

297 Malaria-causing parasites have a life cycle with unique cell-division cycles, and a reper

298 -added product at the end of the coffee pods life cycle, with nutrient-rich compost being recirculate

299 recapitulating different steps of the viral life cycle without using the virus' genetic material cou

300 oot system growth for most if not all of the life cycle, yet light enough (approximately 21 kg when f