ライフサイエンスコーパス: growth

1 body weight in terms of phenotypic relative growth.

2 g mutations in the FGF receptor inhibit bone growth.

3 d reduces CD8+ T cells to promote lung tumor growth.

4 d even to efficiently block cancer stem cell growth.

5 diminished both lung MDSC presence and tumor growth.

6 trigger ferroptosis in vitro and slow tumour growth.

7 thus enable selective epitaxy during the VAN growth.

8 matal closure independently of its effect on growth.

9 e not known to be essential for phototrophic growth.

10 ssential bacterial gene product for mosquito growth.

11 d AR and AR-V7 levels to mitigate CRPC tumor growth.

12 cannot be given to induce such secretion and growth.

13 nd that PUM1/2 sustain myeloid leukemic cell growth.

14 easured repeatedly during the early stage of growth.

15 t a large part of its genome is dedicated to growth.

16 y to form lateral heterojunctions via direct growth.

17 inhibiting BRAF(V600E)-driven melanoma tumor growth.

18 ranscriptional targets to regulate human RMS growth.

19 efficient energy generation and reduced cell growth.

20 e cells, and supports cell proliferation and growth.

21 stinal epithelial cells did not affect tumor growth.

22 t essential role in polarity maintenance and growth.

23 a simple but widely applicable model of tip growth.

24 ecular mechanism measuring a fixed amount of growth.

25 s necessary for advanced monitoring of plant growth.

26 rm policy efforts to contain future spending growth.

27 ear group, experienced similar rates of cyst growth (19% vs. 20%; P= 0.95) and lower rates of cross-o

28 CTX014 decreased tumor growth, affected the accumulation and tolerogenic activi

29 erea showed a significant decrease in fungal growth after 7days at 5 degrees C.

30 ssociated with prematurity and reduced fetal growth, an issue of further interest given the mounting

31 Latent class growth analysis was applied to longitudinal data on soci

32 generally support the view that differential growth and actomyosin contraction drive formation of the

33 ) and El Tor (C6706) V. cholerae biotypes in growth and biochemical assays.

34 ed processes involved in mating, filamentous growth and biofilm formation, and also influences cAMP-r

35 and knockdown of circCCDC66 inhibited tumor growth and cancer invasion in xenograft and orthotopic m

36 Furthermore, we show that growth and cell cycle progression are arrested in cells

37 The depletion of KDM3 inhibits tumorigenic growth and chemoresistance of human colorectal CSCs.

38 odification was shown to be vital for axonal growth and dendritic branching.

39 which cytokinin regulates diverse aspects of growth and development as well as responses to biotic an

40 e suppresses host defences to facilitate the growth and development of the important rice pathogen Ma

41 TOR (Target of Rapamycin) pathway to balance growth and development with the available energy and nut

42 riched in functions associated with organism growth and development, suggesting an important role for

43 ral Gambia had a very small effect on linear growth and did not reduce morbidity compared to unfortif

44 s thus reveal a mechanism coordinating plant growth and drought tolerance.

45 te with free filament ends, preventing their growth and dynamically tethering the branched actin netw

46 ically initially, followed by further linear growth and eventual gradual saturation.

47 ution plays an immediate role, governing the growth and expansion speed of colonizing populations.

48 t infection with Zika virus impairs cortical growth and folding.

49 s a complex process that involves sequential growth and fusion of the facial prominences.

50 ndance of eIF4G and rates of cell population growth and global mRNA translation, with peak rates occu

51 esearch because of their importance for leaf growth and hence for plant fitness and crop yield.

52 veals a molecular link between thermosensory growth and immunity in plants.

53 at found in studies of Pt(111) homoepitaxial growth and ion erosion in ultrahigh vacuum.

54 f renewable bioproducts from atmospheric CO2 Growth and metabolism of cyanobacteria are inherently ti

55 which induces anoikis to suppress PDAC tumor growth and metastasis.

56 ssion of IL-6 and IL-8 and rescued the tumor growth and migratory phenotypes of ovarian cancer cells

57 ovided important adaptations with respect to growth and morphogenesis and defense against biotic and

58 gy homeostasis were found to relate to fetal growth and neonatal body composition and thus may be amo

59 me3 domain that is established during oocyte growth and persists through preimplantation development

60 s salmon, where distinct temporal changes in growth and physiology during development are critical fo

61 AUXIN UP RNA (SAUR) genes promote elongation growth and play a key role in PM H(+)-ATPase activation

62 ates PI3Kalpha/Akt signaling, promoting cell growth and proliferation.

63 acterial growth using multigenerational cell growth and shape data for single Caulobacter crescentus

64 stem cell scaling is maintained during organ growth and shrinkage.

65 eedback mechanism to optimize the balance of growth and stress responses.

66 Autophagy supports cell growth and survival autonomously by recycling intracellu

67 nsporters are essential players in bacterial growth and survival, since they are key for uptake of nu

68 r, MYCN was essential to retinoblastoma cell growth and tumor formation, and ectopic MYCN partially r

69 tributions CHY4 and MMSD make to the overall growth and viability of plants.

70 reasing MMP activation, airway smooth muscle growth, and airway responsiveness.

71 e plant strategies for resource acquisition, growth, and competition, as well as plant impacts on eco

72 N on HCC tumor angiogenesis as well as tumor growth, and indicate that SFN has potential for the prev

73 er a retrograde extension mechanism for axon growth, and reveal the aetiology of axon-guidance defect

74 decreased B16-F10 metastasis and s.c. tumor growth, and this was IFN-gamma dependent.

75 al processes including reproduction, somatic growth, and tissue maintenance.

76 ition is required for apoptosis, but not for growth arrest, through a mechanism involving the derepre

77 red early vascularization and stromal tissue growth as well as reduced glandular secretory activity o

78 , and thoroughly exploits the nucleation and growth as well as subsequent superlattice transformation

79 ers discuss approaches to fetal and neonatal growth assessment.

80 d rates of vessel recanalization and infarct growth at 24 hours and occurrence of large parenchymal h

81 er coalignment and orientation to the cell's growth axis.

82 ich enhanced subsequent airway smooth muscle growth by 1.5-fold (P < 0.05), which was dependent on MM

83 at HOXA4 may play a role in regulating human growth by epigenetic mechanisms.

84 Indeed, TrxR1 depletion reduces myoblasts growth by inducing an early myogenesis -related gene exp

85 remodeler subunit, BAF60, represses seedling growth by modulating DNA accessibility of hypocotyl cell

86 ar adhesion contributes to uncontrolled cSCC growth by preventing inhibition of YAP/WBP2.

87 ng images revealed unexpected differences in growth characteristics among strains of B. anthracis, wh

88 help regulate DNA replication in response to growth conditions.

89 ay periodicity can be tuned by adjusting the growth conditions.

90 nce between the two proteomes under standard growth conditions.

91 n guidance that mediates opposing effects on growth cone motility.

92 ides an improved theoretical basis for tumor growth control and may also find utility in therapeutic

93 of BaP, with subsequent mutation of critical growth control genes.

94 re assessed using longitudinal random-effect growth curve models.

95 K, AKT and PAK1 as well as regulation of the growth, cytoskeleton remodeling and motility, invasion o

96 orrelated with plant mass, compatible with a growth-defence trade-off.

97 eport a tumor-suppressive mode of action for growth-differentiation factor 11 (GDF11) and an unusual

98 es can account for the discrepancies between growth dynamics in the notch-drives-growth model and rea

99 Fibroblast growth factor (Fgf) receptors have a recognized role in

100 glycolytic enzymes downstream of fibroblast growth factor (FGF) signaling.

101 the N-terminal prodomain from the C-terminal growth factor (GF) domain in each monomer, pro-TGF-beta

102 hese endothelial cells supply the hepatocyte growth factor (HGF) required for the chemotactic gradien

103 mutants of ATL1 in PC-12 cells inhibit nerve growth factor (NGF)-induced neurite outgrowth.

104 nted protein known to stimulate transforming growth factor (TGF)-beta1 to -beta3 translation in vitro

105 ular density (MVD), and vascular endothelial growth factor (VEGF) expression) from 9 patients with pr

106 Vascular endothelial growth factor (VEGF) is implicated in the peritoneal mem

107 We also show how vascular endothelial growth factor (VEGF) regulates PRKCB promoter function i

108 trate the importance of Vascular Endothelial Growth Factor (VEGF) secretion for this pathway of hypox

109 factor 1 (SDF-1alpha), vascular endothelial growth factor (VEGF), hypoxia-inducible factor 1-alpha (

110 Vascular endothelial growth factor (VEGF)-A has been implicated in this conte

111 licing in the exon-8 of vascular endothelial growth factor (VEGF)-A results in production of proangio

112 ebrand factor (vWF) and vascular endothelial growth factor (VEGF)-C expression were measured.

113 Vascular endothelial growth factor (VEGF)-D is capable of inducing angiogenes

114 rculating levels of insulin and insulin-like growth factor 1 (IGF-1).

115 of inflammation, serum levels of fibroblast growth factor 21 (FGF21), and activation of signaling pa

116 (PDGFRalpha) and its ligand platelet-derived growth factor A (PDGF-A) are co-expressed in migrating c

117 a2SP(+/-) LSCs was activated by transforming growth factor beta (TGFbeta)-activated kinase 1 (TAK1; M

118 pic chondrogenic induction with transforming growth factor beta to set up a dual-compartment culture.

119 ation-progenitor, proliferation-transforming growth factor beta, and Wnt-catenin beta1.

120 , but surprisingly, more active transforming growth factor beta.

121 maximal thrombospondin and platelet-derived growth factor D expression.

122 We find that platelet-derived growth factor evokes transient oxidation on or close to

123 Vascular endothelial growth factor has emerged as a significant contributor t

124 Inhibition of the insulin-like growth factor I receptor (IGF-IR) is a new therapeutic s

125 es, including glucose, insulin, insulin-like growth factor I, triglycerides, cholesterol, cortisol, a

126 erate when challenged with stressors such as growth factor insufficiency.

127 Current anti-epidermal growth factor receptor (EGFR) therapy for oral cancer do

128 ported to regulate the function of epidermal growth factor receptor (EGFR), the effect of protein met

129 ed ALL proliferation in ABL/platelet-derived growth factor receptor (PDGFR)-mutant models with mean 6

130 sed on estrogen receptor and human epidermal growth factor receptor 2 status was also assessed.

131 Here, we show that platelet-derived growth factor receptor alpha (PDGFRalpha) and its ligand

132 Here we report that platelet-derived growth factor receptor alpha (PDGFRalpha) positive ( + )

133 Activation of the fibroblast growth factor receptor FGFR4 by FGF19 drives hepatocellu

134 iate the increase independently of epidermal growth factor receptor transactivation.

135 Epidermal growth factor receptor tyrosine kinase inhibitors, inclu

136 Many receptor systems, notably including growth factor receptors and G protein-coupled receptors,

137 mportance of posttranslational regulation of growth factor signaling in this process.

138 ecialized processes such as neurogenesis and growth factor signaling.

139 if the up-regulation of vascular endothelial growth factor strengthens the protective effect of amnio

140 ipants who received antivascular endothelial growth factor therapies for neovascular AMD had decrease

141 ding the highly cancer relevant insulin-like growth factor type 1 receptor (IGF-1R).

142 Insulin-like growth factor type 2 (IGF2) receptor (IGF2R) recognizes

143 n CTS SSCT and that the presence of fibrotic growth factor, PDGF-AA, results in increased proliferati

144 metabolites in combination with insulin-like growth factor-1 are shown to promote the corneal epithel

145 In activation of the transforming growth factor-beta1 precursor (pro-TGF-beta1), integrins

146 t enrichment analysis uncovered transforming growth factor-beta1 signaling activation in vastus later

147 Soluble klotho down-regulates growth factor-driven PI3K signaling, contributing to ext

148 omain, apply force, and release the TGF-beta growth factor.

149 ganoids, PPAR agonism is sufficient to drive growth-factor-independent growth in the context of concu

150 ins, matrix-bound chemokines, cytokines, and growth factors (GFs) influence functional properties of

151 Genetic assays revealed that Abl allows growth factors and Semaphorin/Plexin repellents to combi

152 Angiopoietins are a family of growth factors that are ligands for the tyrosine kinase

153 mphiphiles (PAs) that encapsulates cells and growth factors within a muscle-like unidirectionally ord

154 s to use naturally occurring combinations of growth factors.

155 cancer progression, such as the insulin-like growth factors.

156 acclimation and by facilitating compensatory growth following drought.

157 out after fire and/or have graminoid or herb growth forms were particularly affected by postfire weat

158 ignificant differences in photosynthesis and growth from a population maintained in ambient CO2 and t

159 Models projecting population growth from different starting seed densities showed tha

160 perennial weed that maintains its perennial growth habit through generation of underground adventiti

161 o quantify growth under conditions for which growth has a specific functional form.

162 onstrated functional complexation with human growth hormone binding protein (hGHBp) to the different

163 Growth hormone receptor deficiency (GHRD) results in sho

164 therapeutic effects of agonistic analogs of growth hormone-releasing hormone (GHRH) and their mechan

165 Such changes occur as growth improves at the poleward edge of a species distri

166 nctional contributions of P. simiae genes to growth in 90 distinct in vitro conditions by RB-TnSeq, h

167 ive sites can abolish Pseudomonas aeruginosa growth in a defined medium with malonate as the sole car

168 hat LF-W271A blocked ERK phosphorylation and growth in a melanoma cell line, suggesting that it may p

169 erest given the mounting evidence that fetal growth in general is linked to degrees of risk of common

170 highlight the importance of postmitotic cell growth in gut epithelial repair.

171 However, despite the huge growth in knowledge and advances in prevention and treat

172 export from vacuoles and inhibits Salmonella growth in macrophages.

173 quired for oncogenic transcription and tumor growth in non-small-cell lung cancer (NSCLC).

174 lacebo, bosutinib at 200 mg/d reduced kidney growth in patients with ADPKD.

175 Mycobacterial growth in peripheral blood mononuclear cells (PBMC) from

176 prove essential to accurately modeling yeast growth in response to different environments.

177 erally increased with age which showed rapid growth in severe cases.

178 tter (DOM) levels due to ash input and algal growth in source waters, and consequently impacting disi

179 ufficient to drive growth-factor-independent growth in the context of concurrent tumor suppressor los

180 Quantitative analysis of hypocotyl cell growth in the nek6-1 mutant demonstrated that NEK6 suppr

181 has shown that glacial Ca limits vegetative growth in the wild progenitors of both C3 and C4 founder

182 s were essential for fitness during in vitro growth in three C. jejuni strains, revealing that a larg

183 alciparum PKG, inhibits blood stage parasite growth in vitro and in mice and blocks transmission to m

184 nes and promote cell proliferation and tumor growth in vivo Taken together, our findings reveal a nov

185 nes correlated positively with mycobacterial growth in whole blood from UK/Asian adults and, to a les

186 The growth increase at warmer sites was due almost entirely

187 of CSF, and tested 0.5 mL with mycobacteria growth indicator tube culture, 1 mL with Xpert, and cryo

188 pression of membrane proteins often leads to growth inhibition and perturbs central metabolism and th

189 ehydrogenase complex, caused a profound cell growth inhibition in tumour cells harbouring KRAS mutati

190 In vitro studies demonstrate that Ct growth inhibition occurs by interferon-gamma (IFN-gamma)

191 ic oil, as a combination of terpenes, exerts growth inhibitory effects against colon carcinoma, sugge

192 derlying the effect of ILT3.Fc on tumor cell growth involves inhibition of the p70S6K signaling pathw

193 Moreover, tumor growth is accelerated, not only in tristetraprolin-defic

194 1 disruption and at early times net G-strand growth is apparent, indicating telomerase-mediated G-str

195 g mouse models, we demonstrate that melanoma growth is drastically reduced in mice lacking c-Rel, but

196 ation and are where much of the future urban growth is expected to occur.

197 s a topic of intense debate as proliferative growth is homogenous.

198 ce of the effect of refugee rations on fetal growth is limited.

199 Muscle growth is negatively regulated by myostatin (MSTN) and a

200 While quasicrystal growth is predominantly dominated by the attachment kine

201 Further development and growth is proposed to rely on layer-restricted progenito

202 How synaptic growth is terminated after reaching proper size remains

203 n P2 nucleotide receptor expression and hCPC growth kinetics revealed downregulation of select P2 rec

204 selective exclusion of molecules needed for growth may contribute to regeneration decline.

205 ere performed to understand the ion-molecule growth mechanism of small acetylene clusters (up to hexa

206 between growth dynamics in the notch-drives-growth model and real plants following excision.

207 In an alternative "notch-pre-patterns-growth" model, a persistently acting growth regulator wh

208 out childhood, identified using latent class growth modeling.

209 With the growth of 3D packaging technology and the development of

210 hesized through a one-step compartmentalized growth of a mesoporous organosilica sphere attached to a

211 ics largely restricted by the nucleation and growth of a new phase.

212 ctron-microscopic observations of deposition growth of aligned ice crystals on feldspar, an atmospher

213 fields, A. rabiei effectively suppressed the growth of all competing fungi, such as Alternaria, Epico

214 ge state of color centers based on epitaxial growth of an inorganic passivation layer is presented.

215 e effect on the photosynthetic processes and growth of Arabidopsis (Arabidopsis thaliana).

216 he fat-derived hormone leptin stimulates the growth of axons from the arcuate nucleus of the hypothal

217 this pathway has been shown to suppress the growth of bacterial pathogens; however, the identificati

218 up to 263-fold more potent at inhibiting the growth of breast cancer cell lines (MCF7, MCF7/VP16, BT4

219 rstanding of what triggers and maintains the growth of cancerous cells.

220 Neurons promote the growth of cancers of the brain, skin, prostate, pancreas

221 the addition of antifungal agents decreased growth of Candida species in optisol-GS and should be fu

222 l prefrontal cortex (PFC) tracked the latent growth of cumulative economic outcomes.

223 d the hypothesis that reduced root secondary growth of dicotyledonous species improves phosphorus acq

224 the nonlinear HCR, forming a chain-branching growth of DNA dendrimer by self-assembly.

225 There were also significant differences in growth of EFW between countries.

226 y peptide nucleic acid (PNA) and the in situ growth of electroactive polymers through the surface-ini

227 during the deposition process to promote the growth of inclined ZnO microcrystals.

228 e telomestatin derivative (6OTD), limits the growth of intractable glioblastoma (grade IV glioma) and

229 to be effective in selectively promoting the growth of Lactobacillus reuteri C1 strain as evidenced b

230 ase, low Coulombic efficiency, and dendritic growth of Li.

231 evented Ser118 phosphorylation and inhibited growth of MCF7-Y537S cells.

232 ethacin yielded an additive reduction in the growth of MDA-MB-231 tumor xenografts.

233 istration of S17 significantly inhibited the growth of MGC803 cells in vivo in a xenograft mouse mode

234 However, the growth of MRSA was inhibited, and a significant protecti

235 oP, phoQ or Sant_4061 completely retards the growth of S. praecaptivus in the presence of an antimicr

236 , and diminished clonogenicity and malignant growth of SCLC cells in vivo Collectively, our studies v

237 a need to anticipate supply given the rapid growth of specialty and subspecialty fellowships.

238 The reaction proceeds through nucleation and growth of the new phase in corners of the nanocubes.

239 al cord appears to be related to anisotropic growth of the somatic and neural elements following earl

240 approach has been to make use of frustrated growth of the supramolecular assembly by tuning the bala

241 phoP and Sant_4061 is necessary to abrogate growth of this bacterium in an insect host.

242 extracts heme from hemoglobin (Hb) to enable growth on Hb as a sole iron source.

243 utcomes were repeat clinic presentations and growth over 24 wk.

244 noted secular improvements in all postnatal growth parameters (except weight-for-length), accompanie

245 ence of the Sb composition in the NWs on the growth parameters investigated has been explained by an

246 cant differences between groups in patients' growth parameters, use of 3-dimensional imaging, and typ

247 sembly chemistries and processes.Probing the growth pathways of quasicrystalline materials, where til

248 omic DNA methylation levels as a function of growth phase in Escherichia coli.

249 entose phosphate pathway, have a more severe growth phenotype than cells lacking zwf1 We propose that

250 ignaling lowers cyclic GMP production in the growth plate, which counteracts bone elongation.

251 changes have driven major reductions in reef growth potential, which have declined from an average 4.

252 and yet produce significantly more accurate growth predictions.

253 nucleation process followed by a subsequent growth process.

254 iomas are brain tumors characterized by slow growth, progressive loss of vision, and limited therapeu

255 een plant roots, mycorrhizal fungi and plant growth-promoting rhizobacteria (PGPR) can improve plant

256 baspirillum rubrisubalbicans is a well-known growth-promoting rhizobacteria that can also act as a mi

257 to influence the transcription of hypocotyl growth-promoting SAUR19 subfamily members.

258 g demographic rates contribute to population growth rate (lambda) is key to understanding how animal

259 We found that ATP supported a similar growth rate and cell yield as L1 medium and observed DIP

260 R037 and MDR045, colonisation also increased growth rate and reproductive success of S. avenae on the

261 hat would otherwise have an average negative growth rate by increasing the duration of favorable envi

262 are still necessary to recover the observed growth rate distribution in SD medium.

263 in plant longevity, reproductive output and growth rate is fundamental to effective predictions of v

264 sh maintaining a standard metabolic rate and growth rate lower than expected when fed on a diet diffe

265 . jejuni physiology were studied at constant growth rate using carbon (serine)-limited continuous che

266 ligomers with tailored structures and a high growth rate would greatly facilitate research into the s

267 r incorporating experimental measurements of growth rates and extracellular fluxes from a set of pert

268 ted tumor-initiating frequencies, as well as growth rates of BCSC-derived tumor xenografts in immunod

269 omplex 1 (mTORC1) protein kinase is a master growth regulator that becomes activated at the lysosome

270 mTOR complex I (mTORC1) is a central growth regulator that senses amino acids through a pathw

271 atterns-growth" model, a persistently acting growth regulator whose distribution is pre-patterned by

272 ection fish dramatically suppressed tapeworm growth relative to high-infection fish, and parasite siz

273 n, such as physiologic or pathologic cardiac growth, remain elusive.

274 f the Hippo pathway involved in development, growth, repair and homeostasis.

275 We find the transcription factor early growth response 3 (EGR3) is increased in D1 receptor con

276 e context-dependent information to calibrate growth responses to temperature signals.

277 maternal age (AMA) are susceptible to fetal growth restriction (FGR) and stillbirth.

278 lacental vessel networks in normal and fetal growth restriction (FGR) complicated pregnancies.

279 th preterm delivery, low birth weight, fetal growth retardation and developmental defects.

280 enotype, and correlated with the severity of growth retardation and the in vitro cellular phenotype.

281 Severe growth retardation, distorted branches and up-curled lea

282 ight and number of leaves were higher at 4th growth stage; however, at this stage the end-use is not

283 001 which is of particular interest for bone growth stimulation is achievable by this assembly.

284 Based on the in vitro growth study, MOS-III and MOS-IV was found to be effecti

285 expressing PEX1 in wild-type plants impaired growth, suggesting that excessive PEX1 can be detrimenta

286 6SrRNA genes demonstrated that plants in the growth system support a microbial rhizosphere effect.

287 s the interplay between tissue asymmetry and growth that helps our hearts take shape.

288 gf10Fgf10(+) progenitors undergo anisotropic growth: those displaced rostrally differentiate into ant

289 tides activate P2Y6 receptors to suppress GC growth through a novel SOCE/Ca(2+)/beta-catenin-mediated

290 ver, current models are designed to quantify growth under conditions for which growth has a specific

291 TCP20 and NLP6&7 also support root meristem growth under N starvation.

292 l and the cell cycle dependence of bacterial growth using multigenerational cell growth and shape dat

293 lood depressing substance II suppresses axon growth via an increase in the amplitude and frequency of

294 Decreased growth was associated with reductions in vascular densit

295 UR expression and auxin-dependent elongation growth were closely correlated.

296 PDZK1 on SHP-1 phosphorylation and the tumor growth were verified in vivo by xenograft tumor studies.

297 genes, during multiple rounds of vegetative growth when sporulation is not required.

298 particles (MPs), supported accelerated tumor growth which was halted by PMP transfusion.

299 tion of nanoparticles in the early stages of growth with unobtrusive laser probes should give insight

300 ibiting cytokinesis in the liver slows tumor growth without compromising the health of normal hepatoc