ライフサイエンスコーパス: growth

1 ostnatal role for EphA4 in adolescent muscle growth.

2 nto defined progenies and initiate the tumor growth.

3 es its stable accumulation at sites of polar growth.

4 sessing hypoxia, microvasculature, and tumor growth.

5 antitative longitudinal monitoring of tumour growth.

6 tionality not accessible by conventional CVD growth.

7 confirming the role of these genes in plant growth.

8 uffer from a challenging problem of dendrite growth.

9 ing cell migration and anchorage-independent growth.

10 on of these cells abrogated MI-induced tumor growth.

11 ncing ATP production efficiency and synaptic growth.

12 regulates mitochondrial biogenesis and cell growth.

13 inhibitor (GDC-0449) displays reduced tumor growth.

14 id metabolism in vegetative and reproductive growth.

15 lism and HSC senescence that promotes tumour growth.

16 be prevented by altering the temperature for growth.

17 pression and ablated FGF-mediated tumor cell growth.

18 dy of any kind of monolayer epithelial cells growth.

19 enzymes are strong promoters of microtubule growth.

20 by mutant KRAS, is essential for neoplastic growth.

21 d by the water decomposition and Zn dendrite growth.

22 sion clearly supported optimal S. islandicus growth.

23 of proline metabolism is critical for tumor growth.

24 roline biosynthesis and impairing spheroidal growth.

25 o measure the effect of policies on economic growth(5,6), to empirically evaluate the effect that the

26 etching of Au(0), which leads to nonuniform growths along different lateral directions to form six-p

27 eractions between maternal SDB and offspring growth and adiposity measurements after controlling for

28 tly influence the pace of tele-critical care growth and adoption.

29 icant environmental threat that limits plant growth and agricultural productivity.

30 ological model that represents the jellyfish growth and degrowth in laboratory conditions as well as

31 l for embryogenesis and normal postembryonic growth and development.

32 nmental factors to which plants adjust their growth and development.

33 y RNA polymerase (Pol) II and regulates cell growth and differentiation.

34 ted abundance of genes involved in bacterial growth and division.

35 tly interact with MM cells to increase tumor growth and expression of Ocy-derived factors that promot

36 -based approaches promote significant axonal growth and functional recovery in vivo in a spinal cord

37 The fundamental problem in axon growth and guidance is to understand how cytoplasmic sig

38 of actin in the growth cone to produce axon growth and guidance.

39 shows how much these animals changed during growth and has implications for ecology and skull develo

40 onomic conditions influence immune function, growth and health status.

41 APIO-EE-07 inhibited cell growth and induced apoptosis and also increased expressi

42 orally effectively inhibits xenograft tumor growth and induces survivin loss in tumors.

43 tently, GBP2 dramatically promotes GBM tumor growth and invasion in mice and significantly reduces th

44 -associated macrophages (TAMs) promote tumor growth and invasion.

45 aselective HDAC6 inhibitors can reduce tumor growth and invasiveness of breast cancer by noncanonical

46 ies have shed light on the genetics of early growth and its links with later-life health outcomes.

47 er, our understanding of the process of wood growth and its response to environmental drivers is limi

48 NCE, photosynthesis minus the C cost of leaf growth and maintenance) as a fitness proxy.

49 responds to long- and short-term changes in growth and measurement environmental conditions.

50 been implicated as critical drivers of cell growth and metastasis in numerous Ras-driven cancers.

51 colony formation in vitro, as well as tumor growth and metastasis in vivo.

52 Overexpression of Trop2 induces tumor growth and metastasis while loss of Trop2 suppresses the

53 enzymes have been linked to increased tumor growth and metastasis, largely on the basis of overexpre

54 mAb KU44.13A did not have any effect on the growth and migration of cancer cells nor did it induce r

55 tive proteins at 6 mo postpartum with infant growth and motor and cognitive development.

56 proteins and HMOs are associated with infant growth and motor and cognitive development.

57 Precise control of organ growth and patterning is executed through a balanced reg

58 n, tepary bean and guar for their vegetative growth and physiological responses to four different wat

59 IGF-1)/BP3 (binding peptide 3) improves lung growth and prevents PH in two antenatal models of BPD in

60 oids in ovarian cancer (OC) facilitate tumor growth and progression, and also pose major obstacles fo

61 ic acid synthesis required for anabolic cell growth and proliferation.

62 hrough the PI3K/Akt pathway, regulating cell growth and proliferation.

63 ave stimulatory effects on the activation of growth and reproductive axes, but the existence of gonad

64 le heterozygote showed defective pollen tube growth and seed development because of nonviable mutant

65 ietary intervention to block melanoma tumour growth and sensitize tumours to targeted therapy via epi

66 In this study, the influence of flow on the growth and shrinkage of a clot is investigated.

67 ing) suggest that sleep can promote synaptic growth and strengthening.

68 he miR-211-DUSP6-ERK5 axis in melanoma tumor growth and suggest a mechanism for the development of dr

69 uction, and coagulation, and harbors diverse growth and survival factors.

70 orter (bglP) was found to be crucial for GAS growth and survival in human blood and was validated in

71 y is the key factor limiting urban offspring growth and survival, at least in this well-studied speci

72 as insulin, IGF-1 and HGF support beta cell growth and survival, but in people with type 2 diabetes

73 liferative response, but also for tumor cell growth and survival.

74 endothelial cell (EC)-secreted IL6 on HNSCC growth and the CSC fraction.

75 f 2015/2016 led to a February onset of plant growth and the ecosystem became a sustained carbon sink

76 les that form undergo, possibly oscillatory, growth and then dissolve completely.

77 thesis is tightly coordinated with cell wall growth and turnover, and many of these control activitie

78 Here, we investigated the role of SpxA1 in growth and virulence by identifying genes regulated by S

79 ed germination and thus potentially increase growth and yield.

80 for observing and isolating microstructural growths and can supplement the current suite of techniqu

81 es are well known to control the metabolism, growth, and cell division.

82 (+) T and natural killer cells, slowed tumor growth, and improved mouse survival.

83 Depletion of Gln4p inhibited growth, and induced a GCN4 amino acid starvation respons

84 hate (Pi) is an essential nutrient for plant growth, and its availability strongly impacts crop yield

85 electronic transition and local Ge-Ge chain growth as well as locally enhanced bond alignment under

86 nd mechanism of generalism, we measured host growth benefits and functional traits.

87 of continued exposure, and further displayed growth benefits to at least 1 month post release.

88 were shown to ameliorate Plasmodium parasite growth, blood-brain barrier dysfunction, and mortality i

89 stence region are not only determined during growth but also at room temperature by post-processing.

90 ents to inhibit chemotherapy-resistant tumor growth by consuming intracellular glutathione and activa

91 RISC; rather, AGO1 controls cell and tissue growth by functioning as a direct transcriptional repres

92 LTRE analysis showed that population growth can be substantially affected by changes in trait

93 lso observe higher productivity and improved growth characteristics in specific clones.

94 howed a phthiocerol dimycocerosate-dependent growth compromise upon limitation of the corresponding s

95 488 growth conditions corresponding to 3,221 experimental da

96 ncer cells, and fibroblasts under unhindered growth conditions is dynamic.

97 (plant) under well watered and water-limited growth conditions, a high-throughput phenotyping facilit

98 dulates the cytoskeleton to produce directed growth cone motility.

99 sic, stochastic fluctuations of actin in the growth cone to produce axon growth and guidance.

100 hoprotein that plays a critical role in cell growth control as the central regulator of RNA polymeras

101 neration of the liver, where Hippo's role in growth control has been studied most intensely.

102 enrichment culture that exhibits exponential growth dependent on Mn(II) oxidation to a co-culture of

103 extrinsic doping techniques or bulk crystal growth, detrimentally affecting uniformity, scalability,

104 uring evolution into the regulation of plant growth, development and differentiation.

105 es (RLKs) play key roles in regulating plant growth, development and stress adaptations.

106 synthesis pathway may negatively impact fish growth due to its large energy expenditure, and future s

107 rown in this medium were severely stunted in growth due to removal of essential soluble nutrients - p

108 the zygote, affects embryonic viability and growth during gestation.

109 it will advance our understanding of cancer growth dynamics and response to therapies.

110 xia, can produce spheroids with similar bulk growth dynamics but differing internal compositions (the

111 pevine rootstocks are coupled with fine root growth dynamics during drought and return of soil moistu

112 amino acid variants in Hsp90 and quantified growth effects under standard conditions and under five

113 ude upon T cell activation to support T cell growth even under amino acid (AA) replete conditions.

114 Fibroblast growth factor (FGF) signaling plays pivotal roles in gen

115 Heparin-binding epidermal growth factor like growth factor (HB-EGF), a crucial regulator of heart val

116 Nerve growth factor (NGF) regulates many aspects of neuronal b

117 -function mechanism, augmenting transforming growth factor (TGF) beta signaling.

118 Third, we uncovered that insulin-like growth factor 1 (IGF1) is produced by tumor-associated m

119 ncluding significantly elevated insulin-like growth factor 1 levels, larger weight and body length, h

120 urite markers betaIII tubulin and fibroblast growth factor 12, with differential effects in patients

121 ession of the metabolic regulator fibroblast growth factor 21 (FGF21) was blunted by TCS.

122 Treatment with anti-vascular endothelial growth factor agents.

123 -stimulating factor (GM-CSF), a myelopoietic growth factor and pro-inflammatory cytokine, plays a cri

124 Here, we found transforming growth factor beta (TGFbeta) and bone morphogenetic prot

125 FA) had decreased expression of transforming growth factor beta 1 (TGF-beta1) because of interleukin-

126 In the adult brain, vascular endothelial growth factor D (VEGFD) is required for structural integ

127 We find that Vgf nerve growth factor inducible gene up-regulation is a common t

128 y of ADAM17 toward Heparin-binding epidermal growth factor like growth factor (HB-EGF), a crucial reg

129 Inhibition of multiple growth factor pathways may postpone resistance and exten

130 The human hepatocyte growth factor receptor (c-MET) signaling pathway is dysr

131 rosine kinases (RTKs), such as the epidermal growth factor receptor (EGFR), locally increases the abu

132 Hypoxia induced increased fibroblast growth factor receptor 1 (FGFR1) expression in NSCLC cel

133 Other anti-fibroblast growth factor receptor 3 (FGFR3) compounds are showing p

134 Fibroblast growth factor receptor 3 (FGFR3) was also identified as

135 gesterone receptor (PR), and human epidermal growth factor receptor-2 (HER2) are the three crucial bi

136 PEA-OXA administration enhanced neurotrophic growth factor release and decreased the astroglial and m

137 d a minimal mathematical model demonstrating growth factor signaling is sufficient to guarantee this

138 Upon growth factor stimulation, the guanine-nucleotide exchan

139 ed regions with distinct microstructures and growth factor types.

140 s into latent GDF9 generated a highly potent growth factor, called hereafter Super-GDF9.

141 IGF-1 (insulin-like growth factor-1) is markedly decreased in normal preterm

142 ith reduced hippocampal vascular endothelial growth factor-A (VEGF-A) in both male and female mice, a

143 ther macrophage-derived vascular endothelial growth factor-A (Vegf-A) is crucial to establishing NMJ

144 Here we show that depletion of transforming growth factor-beta receptor 2 (TGFBR2) in CD4(+) T cells

145 Transforming growth factor-beta1 (TGF-beta1) plays a premier role in

146 itor of metalloproteinase-2 and insulin-like growth factor-binding protein 7 was measured at H0, H6,

147 ound that EC-specific YY1 ablation inhibited growth factor-induced angiogenesis.

148 Modulation of vascular endothelial growth factor-mediated immune suppression via angiogenes

149 It is known that growth factors such as insulin, IGF-1 and HGF support be

150 that sequential inputs from amino acids and growth factors trigger PA production required for mTORC1

151 ility, and decreases dependence on exogenous growth factors.

152 rate populations relative to undisturbed old-growth forests.

153 is view, emerging research suggests that old-growth grasslands support substantial biodiversity and a

154 of microbes in sustaining agricultural plant growth has great potential consequences for human prospe

155 s important to tumorigenesis and cancer cell growth, here we report a chemoproteomic analysis of a ki

156 ure was negatively correlated with fine-root growth, highlighting that drying of these typically wate

157 emonstrated to significantly boost microbial growth; however, the microbial community response has no

158 patients were less likely to present Candida growth in all 3 sets of blood cultures (15.4% vs 45.1%;

159 of techniques utilised to analyse dendritic growth in all-solid-state cells.

160 etabolism, energy conservation, and filament growth in cable bacteria remains enigmatic.

161 Thus, Rb dilution through cell growth in G(1) provides one of the long-sought molecular

162 es water and provides a means of maintaining growth in hot, water-limited environments.

163 We examined how birth size and growth in infancy and childhood were associated with IQ

164 , as well as attenuated suppression of tumor growth in mice.

165 with anti-PD1 therapy in suppressing tumour growth in mouse models of cancer.

166 a combination with anti-PD1, SG7 slows tumor growth in multiple syngeneic mouse models.

167 ression that leads to an inhibition of shoot growth in response to ethylene.

168 at mutant strains lacking gigC have impaired growth in the absence of the amino acid cysteine and tha

169 panion cells caused strongly reduced rosette growth in the absence of wounding.

170 used on diversity and inclusion will promote growth in the field of cell biology and enable scientist

171 train had an increased Cu load and decreased growth in the presence of Cu, which was abrogated by the

172 ct which mutations are selected during viral growth in the presence of single antibodies.

173 onstrated dose-dependent inhibition of tumor growth in the PSMA(+) flank tumor model.

174 K3 in leukemic stem cell (LSC) retention and growth in the remodeled tumor-promoting BM is unclear.

175 The rapid growth in U.S. unconventional oil and gas has made energ

176 se in metagenomics has led to an exponential growth in virus discovery.

177 cterial species, or model conditions such as growth in vitro, in macrophages and in the mouse.

178 onal activity and is required for TNBC tumor growth in vivo using an orthotopic xenograft model in im

179 ed rates of protein synthesis, which lead to growth inhibition and hypersensitivity to osmotic stress

180 The mechanism for growth inhibition does not, however, involve canonical r

181 though beneficial for plant survival, active growth inhibition is often undesirable for crop producti

182 26a was able to induce an 80% tumor growth inhibition of xenografts derived from the enzalut

183 In xenografts, a significant tumor growth inhibition was seen after twice-weekly intravenou

184 d decreases sensitivity to cytokinin-induced growth inhibition.

185 n of dapF(Ct) allowed the mutant to overcome growth inhibition.

186 Considering that the biggest urban growth is projected to occur in these smaller-scale citi

187 der periods when AMP synthesis and bacterial growth is slow and pathogen pressure from this cool-adap

188 Oocyte growth is triggered at the transition from primordial to

189 -type HVT and HVT-DeltavNr-13 showed similar growth kinetics; however, at early time points, HVT-Delt

190 Although microbes influence plant growth, little is known about the impact of microbial di

191 Parieto-frontal growth, mainly between 7 and 13 years in FT children, wa

192 tions and measured a suite of morphological (growth, mass allocation, plant and leaf morphology) and

193 ndent gene expression and neuronal dendritic growth mediated by the CREB transcription factor.

194 rilized (8 J/cm(2)) and monomer extracted in growth medium (1, 3 or 7 days).

195 uppresses their production when added to the growth medium.

196 tone of dendroecology, Cook's 1987 aggregate growth model, and the great potential to use tree-ring n

197 orne fungal ecology of homes with known mold growth ("moldy") differs from the normal airborne fungal

198 ozyme-functionalized origami slows bacterial growth more effectively than treatment with free lysozym

199 last 50 years, mainly due to city population growth, more frequent travels and ecological changes.

200 ontinues to serve as an influential model of growth, morphogenesis and pattern formation.

201 ptional repressor of the master regulator of growth, Myc.

202 This microbial growth occurs despite unfavourable conditions associated

203 results show that CsrA is essential for the growth of A. baumannii on host-derived substrates and is

204 ve important implications for nucleation and growth of atmospheric secondary organic aerosols and atm

205 vide explanations for the puzzling fact that growth of B. subtilis does not result in the significant

206 inal succinate, a crucial metabolite for the growth of C. difficile, and therefore prevented the grow

207 of C. difficile, and therefore prevented the growth of C. difficile.

208 that transition metal nucleated, high yield growth of carbon nanotubes (CNTs) is inhibited in electr

209 VT-DeltavNr-13 showed 1.3- to 1.7-fold-lower growth of cell-associated virus and 3- to 6.2-fold-lower

210 ll-associated virus and 3- to 6.2-fold-lower growth of cell-free virus.

211 inhibitor of RSK1 and MSK2, can suppress the growth of colon cancer by attenuating RSK1 and MSK2 sign

212 demic many countries showed an almost linear growth of confirmed cases for extended time periods.

213 MDs, we precisely control the nucleation and growth of diverse m-TMDs with designable periodic arrang

214 Here, we evaluate the growth of genetically defined renal tumors and their ass

215 is, which creates a microenvironment for the growth of hepatic progenitor cells (HPCs) at the peripor

216 ed a compound, BCH070, that inhibits asexual growth of multiple antimalarial-resistant strains of Pla

217 mmunodeficient mice, mAb treatment inhibited growth of mutant TP53, WT PTEN LN-229 tumors, and sensit

218 er, the high processing temperatures prevent growth of other Janus materials and their heterostructur

219 duced buffer layers that can be used for the growth of other noble-metal-based delafossites, which ar

220 We demonstrate the growth of single-crystal layers of hexagonal boron nitri

221 ds (mainly acetate and lactate) and favoring growth of the beneficial genera Bifidobacterium (bread c

222 in vitro and complemented biotin-independent growth of the M. smegmatis tam deletion mutant strain.

223 Addition of excess mDAP inhibited growth of this strain, but overexpression of dapF(Ct) al

224 This dietary pattern also promotes the growth of unhealthful gut bacteria, fostering, among oth

225 d that Trem2(-/-) mice are more resistant to growth of various cancers than wild-type mice and are mo

226 es to a halt for the foreseeable future, the growth of virtual conferences has highlighted many of th

227 could be broadly used as a tool to increase growth of virus stocks for research and for the generati

228 rant mismatch between E. coli physiology and growth on citrate.

229 Within the second phase of polymer growth, opened hGBP1 molecules can be incorporated in th

230 aracterize hyperacusis as increased loudness growth over a wide-frequency range, decreased tolerance

231 During their first year of growth, overwintering biennial plants transport Suc thro

232 e will provide a critical comparison between growth pathways in vapour- and liquid-phase synthesis te

233 lity of yeast during the initial exponential growth phase and throughout fermentation.

234 g the transcriptome to degrade RNAs encoding growth-phase factors and, thus, support the maturation p

235 ured in different time points throughout the growth phases of 4469 Scottish Blackface sheep and weath

236 VOCs emitted over the course of the growth phases were collected from the headspace above th

237 mutants showed no discernible morphological growth phenotype.

238 ne marrow but also within the periosteum and growth plate reserve zone.

239 cholesterol levels and a higher frequency of growth plate thickening in comparison to Aip+/, Prkar1a+

240 th the mTORC1/4E-BP/eIF4E axis inhibited the growth potential endowed by accumulation of multiple dri

241 most commonly employed model for biological growth processes.

242 factor HY5 controlling a complex downstream growth program.

243 fails to form spores, does not confer plant growth-promoting effect, and displays altered colony and

244 n and cell division during sorghum internode growth, providing insight into the regulation of monocot

245 The impacts on M. smegmatis growth range from mild to severe, but many cause irrever

246 [18%, 62%]), and a 11% decrease of the viral growth rate (95% credible interval: [4%, 20%]).

247 compiled 644 paired values of the population growth rate (lambda) from high and low levels of an iden

248 ion of the thermal sensitivity of population growth rate across phytoplankton (Cyanobacteria and euka

249 This phenotype resulted from enhanced growth rate and a delay in ecdysteroid elevation during

250 and tested for predicted trade-offs between growth rate and efficiency.

251 clinical dose of Abraxane reduces the tumor growth rate as effectively as the standard clinical dose

252 ow that crystals accelerated from an initial growth rate of 10(-6)-10(-7) m s(-1) to 10(-5)-10(-4) m

253 Rt, is a key time-varying prognostic for the growth rate of any infectious disease epidemic.

254 hese anti-contagion policies have had on the growth rate of infections.

255 Growth rate of malaria parasites in the blood of infecte

256 The measured GA growth rate was consistent across studies using color fu

257 Despite an increased growth rate, virulence was still dependent on the mevalo

258 Across all coral taxa, projected stochastic growth rates (lambda(s) ) were found to be lowest under

259 eaction-diffusion model, we demonstrate that growth rates are inextricably coupled with effective spa

260 h effective spatial scales, such that higher growth rates cause more localized competition.

261 Across experimental trials, growth rates differed among family lineages, and the hig

262 owever, there are indications that increased growth rates may shorten trees' lifespan and thus recent

263 andom effects meta-analysis to determine the growth rates of GA.

264 iversity of approaches to quantify intrinsic growth rates of plant populations, including experiments

265 at plant traits can predict mean annual tree growth rates with moderate explanatory power.

266 an predict the activation energy for crystal growth rates, including activation energies significantl

267 rinsic oncogenic properties, decreased tumor growth, reduced the incidence of lung metastasis and inc

268 n within isobaths that likely influenced the growth regime of H. tuna.

269 t phasiRNAs are critical for fertility under growth regimes for optimal yield.

270 pression of a fusion protein combining wheat GROWTH-REGULATING FACTOR 4 (GRF4) and its cofactor GRF-I

271 gene regulatory network that controls oocyte growth remains unknown.

272 Biotrophic growth requires maintaining metabolic homeostasis while

273 exerts a central function in coupling these growth responses and maintaining auxin levels in the roo

274 In vitro and in vivo growth responses of Abi-/Enza-resistant LNCaP-95 cells i

275 correlation between calendar-dated tree-ring growth responses to climatically effective volcanism in

276 an understand how tree size and traits shape growth responses to droughts.

277 Here, we found that shoot and root growth responses to high ambient temperature are coordin

278 Fetal growth restriction (FGR) and pre-eclampsia are severe, a

279 Fetuses with intrauterine growth restriction (IUGR) have reduced muscle mass that

280 ith pregnancy disorders such as intrauterine growth restriction and preeclampsia, which are character

281 l pH upregulation to sustain elevated tissue growth, resulting in a porous and fragile skeleton.

282 iabetes, lipodystrophy, hepatosteatosis, and growth retardation.

283 tions and mutations leading to excessive pro-growth signaling pathway activations frequently occurs i

284 implication of these genes into A. thaliana growth, six of them were further studied by phenotyping

285 ness will alter sorghum (Sorghum bicolor L.) growth, soil nutrient dynamics and interactions (antagon

286 Remarkably, despite this exuberant growth, stable neurotransmission is maintained throughou

287 gation treatments at different physiological growth stages (before flowering, beginning of flowering,

288 X in order to form heme that is required for growth stimulation and survival in vivo Consequently, B.

289 Specifically, we found stem growth stops at soil moisture potentials of -0.47 MPa fo

290 lly arrested, we have characterized synaptic growth, structure and function at the neuromuscular junc

291 hanges within bacteria in environments where growth substrate availability is difficult to quantify c

292 feasible to experimentally determine optimal growth temperature (OGT) for every known microbial speci

293 constitutively transcribed during vegetative growth, their effects are suppressed by strong and const

294 Kinetic crystal growth theory is used to show that crystals accelerated

295 ely, we propose that EXOSC10 promotes normal growth-to-maturation transition in mouse oocytes by scul

296 exhibit organ sparing at the level of arbor growth: Under nutrient stress, sensory dendrites prefere

297 AL growth was analyzed relative to treated vs fellow eye, c

298 ssimilation, pssm2-Fd complemented bacterial growth when coexpressed with a P. marinus sulfite reduct

299 microscopy to yield nearly pinhole-free film growth while maintaining epitaxy and high crystal qualit

300 /PARP-2-deficiency in T cells promotes tumor growth while single deficiency of each protein limited t

301 hen grown in the presence of OTC compared to growth without OTC.