ライフサイエンスコーパス: be controlled by

1 gulators of the cytoskeleton and, in humans, are controlled by 145 multidomain guanine nucleotide exc

2 e and positive selection, and both processes are controlled by a combination of HLA class I/II varian

3 the sensory panel, we demonstrated that VOCs are controlled by a few major genomic regions, some of w

4 Both, the laser and the camera are controlled by a Field Programmable Gate Array (FPGA)

5 onse to external environmental perturbations are controlled by a range of underlying factors such as

6 ovskite polymorph, where the growth kinetics are controlled by a synergistic effect between strain an

7 These processes are controlled by a tightly organized network of neurotr

8 s are induced by polariton hybridization and are controlled by a topological quantity.

9 SAA was recently shown to be controlled by a rapid systemic signaling mechanism te

10 Although the mammalian rest-activity cycle is controlled by a "master clock" in the suprachiasmatic

11 in apple leaf width with increasing altitude is controlled by a basic/helix-loop-helix transcription

12 Anthocyanin biosynthesis is controlled by a clade of R2R3 MYB transcription facto

13 DeltaH(diss) is controlled by a combination of cation solvation entha

14 els under conditions of pressure-driven flow is controlled by a combination of convection and diffusi

15 The development of primordial follicles is controlled by a complex network of interactions betwe

16 enes, the adaptive response to Mn limitation is controlled by a DtxR family metalloregulator, MtsR.

17 In Arabidopsis this process is controlled by a gene network, including components of

18 results suggest that digit tip regeneration is controlled by a gene regulatory network that recapitu

19 gral-threshold model in which the cell cycle is controlled by a licensing process, the rate of which

20 The tempo of somite formation is controlled by a molecular oscillator known as the seg

21 We show that VPO is controlled by a pair of female-specific descending ne

22 ATOH7 transcription is controlled by a promoter-adjacent primary enhancer an

23 production of secreted virulence factor SpeB is controlled by a quorum-sensing pathway and environmen

24 In Saccharomyces cerevisiae, it is controlled by a system of four methyltransferases (Se

25 tic process and that [Ca(2+)](i) oscillation is controlled by a threshold-regulating mechanism.

26 Ft virulence is controlled by a unique combination of transcription r

27 Escherichia coli RfaH action is controlled by a unique large-scale structural rearran

28 ent, which regulates gas exchange in plants, is controlled by a variety of environmental factors, inc

29 In contrast, infection was controlled by a combination of bNAbs targeting non-o

30 ss that followed the arylpalladium insertion was controlled by a fine-tuning of the reaction system,

31 All these phenotypes of this T/F variant were controlled by a genetic polymorphism located at the

32 gest algal growth and replication in hospite is controlled by access to nitrogen, which becomes limit

33 t the Smc3-Scc1 interface in a reaction that is controlled by acetylation and engagement of the Smc A

34 ted with SM increase and Cer decrease, which are controlled by acid sphingomyelinase (SMPD1).

35 Cytoneme formation and length are controlled by actin, intracellular calcium stores, a

36 pro-inflammatory or anti-inflammatory status is controlled by activating inflammatory signaling pathw

37 The polymer size can be controlled by adjusting temperature, reaction time, o

38 n vitro release rate of myrtle extract could be controlled by adjusting the lecithin concentration an

39 atterns of ventral midbrain dopamine neurons are controlled by afferent and intrinsic activity to gen

40 in aggregate stiffness, and regeneration can be controlled by altering stiffness.

41 Phosphene brightness was controlled by amplitude tuning, and color perception

42 oth required for normal host interaction and are controlled by an interrelated network that includes

43 hlore iridate and whose monopole density can be controlled by an external field.

44 m catalysts and alkyl/aryl electrophiles can be controlled by an OEEF applied along the direction of

45 suggests that orientation on first migration is controlled by an inherited navigational vector, a dir

46 The difference between the morphs is controlled by an S-locus "supergene" consisting of se

47 We identify transcriptional networks that are controlled by Arid1a and have an impact on endometri

48 Our results show that cortical state is controlled by behavioral demands and arousal by asymm

49 Overall enzyme activity can be controlled by both protein expression and various cel

50 Plant immunity is controlled by both positive regulators such as PBS3 a

51 he formation of these complicated structures is controlled by both the predetermined angles of the li

52 Ecosystems are controlled by 'bottom-up' (resources) and 'top-down'

53 t KCNQ channel assembly and heteromerization are controlled by C-terminal helices.

54 Regulated secretion is controlled by Ca(2+) sensors with different affinitie

55 ion of intermembrane space-localized MICU1/2 is controlled by Ca(2+)-regulatory mechanisms localized

56 ng in foods, the food carbonylome, which can be controlled by carbonyl-trapping agents, such as amine

57 the dimensionality of the obtained material is controlled by cation charge and size.

58 GO self-assembly can be controlled by changing the degree of oxidation, varyi

59 p to 162 pai-electrons (n = 40); aromaticity is controlled by changing the constitution, oxidation st

60 y the master regulator tra-1, whose activity is controlled by chromosomal sex and is necessary and su

61 otch activation has previously been shown to be controlled by cis-inhibition by Delta in the follicle

62 While plant species richness was controlled by climate and soil water availability, v

63 ccess to a drug after US regulatory approval is controlled by complex interactions between government

64 The inherent curvature in the CA tubes is controlled by conformational variability of residues

65 It is unknown whether and how osmoregulation is controlled by corticosteroid signaling in the phyloge

66 ytic core, cyclin-dependent kinase 8 (CDK8), is controlled by Cyclin C and regulatory subunit MED12,

67 B cell and plasma cell fates are controlled by different transcriptional networks, as

68 Inflammatory endotypes in CRSsNP were controlled by different molecular mechanisms.

69 ans and reproductive cycles, which in plants are controlled by differential DNA methylation.

70 Stage II is controlled by diffusion through a fused membrane stru

71 the system's stability at a molecular level is controlled by diminishing values of radiation [Formul

72 butions, suggesting different output modules are controlled by distinct inhibitory circuit motifs.

73 6)-linkages, suggest that enzymatic activity is controlled by distinct open and closed conformations

74 Sexual differentiation is controlled by diverse master regulatory factors acros

75 a key role in learning and decision-making, is controlled by dopamine and contributes to the pathoge

76 lar activity of active peptides in the brain is controlled by ectopeptidases.

77 e of GATA2 and SOX10, and in turn, these TFs are controlled by EDNRB and RET in a dose-dependent mann

78 The release of mito-DAMPs is controlled by efferocytosis of dying hepatocytes by p

79 a under disease and physiological conditions is controlled by either ubiquitin-dependent or receptor-

80 nnila LUCIFERASE reporter (Rluc) gene, which was controlled by either the ZmGH3.2- or ZmRAFS-promoter

81 excitons in OLEDs is spin dependent and can be controlled by electron-paramagnetic resonance, affect

82 overcome these challenges, drug activity can be controlled by employing delivery, targeting, or relea

83 heological properties of drilling fluids can be controlled by employing viscosifiers that should have

84 Blood pressure is controlled by endocrine, autonomic, and behavioral re

85 n and secretion of these homeostatic factors are controlled by endogenous purinergic signals.

86 nding how a broad-spectrum irritant receptor is controlled by endogenous and exogenous agents that el

87 olled by enthalpy (except the last step that is controlled by entropy).

88 We additionally show that p-Ezrin (T567) is controlled by epidermal growth factor receptor and ME

89 of dedicated spinal network components that are controlled by excitatory D(1) and inhibitory D(2) re

90 H-bonding was controlled by exposure to solvent vapor (solvatochro

91 mains unknown how bundle length and buckling are controlled by external physical factors.

92 Animal feeding is controlled by external sensory cues and internal meta

93 nt understanding of how force generation can be controlled by F-actin-myosin interactions.

94 Stage I is controlled by fiber swelling and diffusion according

95 volume of host rock involved, however, will be controlled by fluid-rock reactions.

96 such bonds, and hence the crosslinking rate, is controlled by force-dependent dissociation of a Diels

97 age zones, most of the permeability increase is controlled by fracture permeability, which is sensiti

98 We show that the ATF2 TAD is controlled by functionally distinct signaling pathway

99 1 is a neuronally enriched PP1 cofactor that is controlled by G-actin.

100 nd Consortium showed that gene transcription is controlled by genetic variants proximal to the gene (

101 A portion of the variation in the population is controlled by genetics as shown by the single-gene mu

102 hat this first cell fate specification event is controlled by glucose.

103 propose that SNHG7 is a lncRNA oncogene that is controlled by growth factor signaling in a feedback m

104 onstrate that the metabolic shift to the PPP is controlled by heme oxygenase-dependent generation of

105 Back-to-front MPA density gradients were controlled by higher cofilin-mediated turnover of F

106 e lifetime (from ca. 300 to ca. 600 mus) can be controlled by host differential sensitization and ene

107 We further describe how the activity of RLRs is controlled by host regulatory mechanisms, including R

108 ation of cell wall composition and structure are controlled by hundreds of enzymes and have a direct

109 We find that at low velocities, friction is controlled by hydrodynamic flow through the porous hy

110 fertilizer residues, and their concentration is controlled by hydrological processes, in particular e

111 are restricted by IFN-I via IRF5(13,14), and are controlled by IFN-I and IFN-gamma in vivo(15-17).

112 endent on IgG2, whereas type I IFN responses are controlled by IgG3, and IgG1 is able to regulate bot

113 The inflammatory effects of IL-1alpha/beta are controlled by IL-1R antagonist (IL-1Ra).

114 e reveal that lymphocyte environment sensing is controlled by immune activation, and that CD4(+) and

115 Meanwhile, transport depth and speed can be controlled by infiltration time and applied voltage.

116 The deposition mechanism is controlled by interaction forces between particles an

117 suggests that adaptation to matrix rigidity is controlled by internal mechanical properties of the c

118 els are voltage independent and their gating is controlled by intracellular [Ca(2+) ] in a biphasic m

119 The timing of this switch is controlled by intracellular Cl- concentrations, but f

120 ity measurements showed that conductivity is being controlled by ion mobility over these RH.

121 derstanding of the biological processes that are controlled by IP(3)Rs.

122 trated that IRT1 endocytosis and degradation are controlled by IRT1 non-iron metal substrates in a ub

123 n unstructured bimetallic Zn(II) complex can be controlled by its inclusion in the cavity of a gamma-

124 a directed Ni-catalyzed alkene arylation can be controlled by judicious tuning of the coordination en

125 h scenarios and show how these distributions are controlled by key biochemical parameters through a d

126 ween these pathogens, we found infections to be controlled by largely non-overlapping subsets of miRN

127 helves is through ocean-driven melting which is controlled by largely unobserved oceanic thermodynami

128 However, how these events are controlled by light is largely unknown.

129 covalent bis-functionalization of C(60) can be controlled by light.

130 As diapause may be controlled by lipid accumulation, our findings may co

131 Replication is controlled by loading of helicases at origins of repl

132 do not exhibit a simple spatial pattern and are controlled by local physical and net biological proc

133 er species richness of individual grid cells is controlled by local factors, or reflects larger-scale

134 rential expression of a network predicted to be controlled by low TXN activity, resulting in activati

135 We find that obesity-repressed LincIRS2 is controlled by MAFG and observe that genetic and RNAi-

136 denaturation and formation of aggregates can be controlled by manipulating feed moisture content duri

137 pecies and smaller inactive species that can be controlled by manipulating the identity and concentra

138 Epithelial apicobasal polarity is controlled by many polarity genes, including the crb

139 Ty3/Gypsy retrotransposons and host defense are controlled by master meiotic regulators.

140 ograms that define the identity of each cell are controlled by master transcription factors (TFs) tha

141 em and prodigiosin antibiotics, and motility are controlled by master transcriptional and post-transc

142 The variable air cavity is controlled by means of a piezoelectric actuator that

143 n a periodic array and a ground plane, which is controlled by means of a piezoelectric actuator.

144 This response to Hg(II) is controlled by MerR and genetic evidence suggests that

145 mRNA code into protein, and this process can be controlled by metabolites that bind to the translatin

146 Their spatiotemporal activity is controlled by molecular layer interneurons (MLIs) thr

147 or of gene translation and protein function, is controlled by mTORC1 and EIF-4E Binding Proteins (EIF

148 We found that 56% of yeast genes are controlled by multiple core promoters, and alternati

149 Profibrotic mechanisms are controlled by multiple regulatory molecules, includi

150 Sex expression of homosporous ferns is controlled by multiple factors, one being the antheri

151 formation of mammalian dendritic cells (DCs) is controlled by multiple hematopoietic transcription fa

152 Moreover, the ion selectivity of bBest2 is controlled by multiple residues, including those invo

153 Finally, we show that Phospho1 expression is controlled by myogenin, which binds to the promoter o

154 s suggest that growth hormone (GH) secretion is controlled by negative-feedback loops mediated by GH-

155 hat binding specificity of DIP/Dpr subgroups is controlled by "negative constraints", which interfere

156 soform abundance across multiple tumor types are controlled by NMD.

157 indicating that firing rate homeostasis can be controlled by non-transcriptional mechanisms.

158 of sparseness of the recalled sequences can be controlled by nonlinearities in the learning rule.

159 budding yeast, the decision to enter meiosis is controlled by nutrient and mating-type signals that r

160 The IPR is controlled by PALS-22 and PALS-25, proteins of unknow

161 d carbonate mineral saturation state (Omega) are controlled by partial equilibrium with the atmospher

162 mechanism of tumour growth by pericytes that is controlled by pericyte FAK.

163 4-phosphate 5-kinase (PIP5KI), which in turn is controlled by phosphatidic acid (PA), the product of

164 hibition of microtubule-sliding by Pavarotti is controlled by phosphorylation.

165 s suggest that plant transport of soil gases is controlled by plant hydraulics, whether by diffusion

166 Stage III is controlled by polymer degradation and involves releas

167 Heart muscle contractility and performance are controlled by posttranslational modifications of sar

168 e results confirm that Rad53 phosphorylation is controlled by PP4 during the repair of a DNA lesion a

169 Reactivation from latency is controlled by processes that restrict or activate the

170 The temporal and spatial expression of genes is controlled by promoters and enhancers.

171 bellar nuclear neurons of the medial nucleus are controlled by Purkinje cells, the sole output of the

172 whose room-temperature transport properties are controlled by quantum interference (QI), is an essen

173 Mammalian gene expression patterns are controlled by regulatory elements, which interact wi

174 sive intensity of the coordination cages can be controlled by restricting the dynamics of AIE-active

175 This process is controlled by secreted RALF signaling peptides, which

176 y and kinetics of the reassembly process can be controlled by selecting appropriate buffer conditions

177 Bile acid metabolism, in turn, is controlled by several nutrient-sensitive transcriptio

178 a model in which multiple body size factors are controlled by signaling through the DBL-1 pathway an

179 macrophages, and classical dendritic cells) are controlled by signals from the M-CSF receptor (CSF1R

180 This effect can be controlled by similar means in both VO(2) and V(2)O(3

181 ouble bonds, where onset of the reaction can be controlled by simply tuning the spray voltage.

182 toxicity of Cyt1Aa crystals grown in Bti can be controlled by single atom substitution.

183 burden when compared to wild-type and burden was controlled by SKAP2 expression in innate immune cell

184 The eukaryotic endomembrane system is controlled by small GTPases of the Rab family, which

185 nt switch in how V1 processes head movements is controlled by somatostatin-expressing (SOM) inhibitor

186 nudation across an erosional catchment, P(v) is controlled by spatially variable erosion that occurs

187 psis thaliana and demonstrate that each gene is controlled by specific sets of transcriptional regula

188 This phenotypic shift was controlled by stearoyl-CoA desaturase-1 (SCD1), an e

189 formation of hapalindoles and fischerindoles is controlled by Stig cyclases through a three-step casc

190 The contraction and relaxation of the heart is controlled by stimulation of the beta1-adrenoreceptor

191 rther found that the variation in N fixation was controlled by substrate carbon(C) : N and C : (N : P

192 On the transcriptional level, this response is controlled by SULFUR LIMITATION1 (SLIM1), a member of

193 lithography, the bending of the actuator can be controlled by switching the laser polarization.

194 r, the direction and magnitude of the change was controlled by taxonomic identity.

195 al genes whose expression does not appear to be controlled by TFEB.

196 age in Gimap5-deficient CD4(+) T cells could be controlled by TGF-beta, thereby promoting T(H)17 pola

197 e pancreas size and islet beta-cell function are controlled by the ATP-dependent Swi/Snf chromatin re

198 to identifying the biological pathways that are controlled by the circadian clock, an important regu

199 Timing and duration of sleep are controlled by the circadian system, which keeps an ~

200 exhibit unique transcriptional profiles that are controlled by the combined effects of host genetic p

201 he population ratio of the exchanging states are controlled by the concentration and pH of the buffer

202 n ecotypic differences in seed dormancy that are controlled by the DOG1 locus.

203 viously that oral cancer metastasis and pain are controlled by the endothelin axis, which is a pathwa

204 f Drosophila neural stem cells (neuroblasts) are controlled by the highly conserved RNA binding prote

205 dsRNA sensing and gene-regulatory roles and are controlled by the HUSH complex.

206 wetting properties of vermiculite laminates are controlled by the hydrated cations on the surface an

207 ring the juvenile phase of plant development are controlled by the maize (Zea mays) transcription fac

208 a wide range of spatial arrangements, which are controlled by the MOF topology.

209 ins involved in plant growth and development are controlled by the NADPH/NADPH thioredoxin reductase

210 inct proinflammatory profiles of macrophages are controlled by the natural genetic polymorphism in an

211 W) or clockwise (CW) senses, and transitions are controlled by the phosphorylated form of the respons

212 In insects, TEs are controlled by the Piwi-interacting small interfering

213 addition, the steady-state levels of Nup188 are controlled by the sensitivity of the PCM pool, but n

214 rate the local density variations near voids are controlled by the unique ring structures as voids op

215 son, the properties of the doped crystal can be controlled by the amount and state of the JT complexe

216 properties since the pore size and shape can be controlled by the application of external stimuli.

217 in which the volume of sampled solution can be controlled by the applied pressure.

218 properties of transition metal complexes can be controlled by the appropriate choice of the metal, it

219 in that the position of the equilibrium can be controlled by the concentration of exogeneous ligand

220 growth and shrinkage and is hypothesized to be controlled by the conformation and nucleotide state o

221 energy of the lowest unoccupied orbital can be controlled by the degree of bending in the structures

222 e of this adaptive response is postulated to be controlled by the endothelium, although the underlyin

223 ehavioral and cognitive functions thought to be controlled by the PFC dose-dependently.

224 he size of the subnanometric Ir clusters can be controlled by the post-synthesis treatments and maint

225 size of the prepared porous materials could be controlled by the proportion of PBS and the degradati

226 systems, in which the onset of functions can be controlled by the protonation state of embedded resid

227 n and the matter-light quantum coherence can be controlled by the two-qubit coupling, initial cavity-

228 Maturation of lymphoid cells is controlled by the action of stage and lineage-restric

229 caffold protein multi-sex combs (Mxc), which is controlled by the activity of cyclin-dependent kinase

230 and the final step in this canonical pathway is controlled by the activity of the hydroxysteroid-dehy

231 EAEC virulence gene expression is controlled by the autoactivated AraC family transcrip

232 Bacterial flagellar motility is controlled by the binding of CheY proteins to the cyt

233 scriptional control in which mRNA production is controlled by the binding of specific transcriptionfa

234 aL_2 domain and the ECF core, SigG1 activity is controlled by the cognate anti-sigma protein RsfG, en

235 the temperature of the water, which in turn is controlled by the combination of the thermal structur

236 Results show that avulsion frequency is controlled by the competition between relative sea-le

237 The pH-stimulated release of insulin is controlled by the concentration of glucose.

238 ll cycle is a tightly regulated process that is controlled by the conserved cyclin-dependent kinase (

239 Cell-cycle progression in eukaryotes is controlled by the conserved family of cyclin-dependen

240 We show that the fracture strain is controlled by the coordination number of the network

241 network bound to the surface per unit area) is controlled by the duration of the functionalization r

242 The regioselectivity is controlled by the electron-donating alkoxy group, whe

243 te synaptic transmission and their abundance is controlled by the fine balance between endocannabinoi

244 matic red siskin and monochromatic canaries, is controlled by the gene that encodes the carotenoid-cl

245 e complex molecular systems, whose structure is controlled by the geometrical preferences of the meta

246 n the hexosamine biosynthetic pathway, which is controlled by the glutamine:fructose-6-phosphate amid

247 lude that proliferation of commensal vibrios is controlled by the host immune system, preventing syst

248 mechanism through which S. aureus infection is controlled by the immune system(2).

249 The number of hydrogen atoms in a metal is controlled by the interaction of hydrogens with the m

250 Assembly of the brush border is controlled by the intermicrovillar adhesion complex (

251 Finally, we show that the extent of curling is controlled by the interplay between in-plane and out-

252 e loading of MHCII in the endosomes of cells is controlled by the interplay of the nonclassical MHCII

253 r procentriole assembly, and its recruitment is controlled by the kinase activity of Plk4, but how th

254 tic activation of isoform gamma (AtLEGgamma) is controlled by the latency-conferring dimer state, the

255 Delayed segregation is controlled by the MatP protein, which binds to specif

256 gap phase of the cell cycle in budding yeast is controlled by the Mitotic Exit Network (MEN).

257 een the electromagnetic and mechanical modes is controlled by the optical steady-state amplitude.

258 pid coaggregates, which we term "messicles," is controlled by the peptide:lipid (P:L) ratio and by th

259 Self-incompatibility in Petunia is controlled by the polymorphic S-locus, which contains

260 recycling or degradation of these receptors is controlled by the Rab GTPase family of proteins.

261 V-ATPase activity is controlled by the regulated assembly of the enzyme fr

262 icate once per cell cycle, in a process that is controlled by the serine/threonine protein kinase PLK

263 The energy balance of the Earth is controlled by the shortwave and longwave radiation em

264 MCP-1-induced Pyk2 tyrosine phosphorylation is controlled by the Src family kinase.

265 Degradation of the yeast HMGR isozyme Hmg2 is controlled by the sterol pathway intermediate GGPP, w

266 Cell shape is controlled by the submembranous cortex, an actomyosin

267 us system of the Caenorhabditis elegans male is controlled by the temporally regulated miRNA let-7 an

268 ransformation has a thermodynamic origin and is controlled by the terminations of the (111) surfaces

269 The long term marine primary productivity is controlled by the terrestrial input of phosphorus (P)

270 ivate or not to activate the immune response is controlled by the time to reach the stationary concen

271 hoinositide-binding protein whose expression is controlled by the UPR through the IRE1-bZIP60 pathway

272 iquid interface metamaterial, whose geometry is controlled by the wave phase shift.

273 MYRF expression was controlled by the epithelial identity TF HNF1B, and

274 Thus, the reactivity of 6:2 FTS was controlled by the factors affecting the production a

275 acteria-associated sepsis in 7 Gy GIARS mice was controlled by the GL through the inhibition of M2bM

276 everal methods, and the false discovery rate was controlled by the NestBoot framework.

277 We found that peatland GEP was controlled by the same mechanisms across all sites:

278 he GTP-dependent signaling of these proteins is controlled by their regulators; guanine nucleotide ex

279 ise patterns of gene expression in metazoans are controlled by three classes of regulatory elements:

280 The equilibrium is controlled by three residues positioned around the ac

281 that spindle length and microtubule mass can be controlled by titrating the ratios of the tubulins fr

282 Critically, we observe a shift from growth being controlled by traits related to carbon cycling (as

283 Sterol biosynthesis is controlled by transcription factor SREBP in many euka

284 Cell identity in eukaryotes is controlled by transcriptional regulatory networks tha

285 rst, it is shown that the inflated shape can be controlled by tuning the geometric parameters of the

286 The dynamics are controlled by two dimensionless numbers relating the

287 Expression of genes encoding these proteins is controlled by two integral membrane proteins, BlaR1 a

288 anions whose hierarchical assembly in water is controlled by two parameters: acidity and the lanthan

289 vules in the developing gynoecium and fruits is controlled by two secreted peptides, EPFL2 and EPFL9

290 l antimicrobial and metabolic responses that are controlled by type-3 innate lymphoid cells (ILC3)(1-

291 Oil yield is controlled by variant alleles of a type II MADS-box g

292 The kinetics of this process is controlled by various environmental factors, yet the

293 t the effectiveness of postharvest processes is controlled by various factors and that understanding

294 nzyme kinetics and final hydrogel properties are controlled by varying the initial ultrasound exposur

295 nity, optical, and electrical properties can be controlled by varying fs-PLD process parameters to pr

296 tency of TRPV1-mediated Ca(2+) responses can be controlled by varying the applied voltage.

297 The release profile can be controlled by varying the size of the hole and/or the

298 thermore, the helical sense of chirality can be controlled by varying the wavelength of UV irradiatio

299 Moreover, the phosphorylation of TRIM28 was controlled by VEGF and Notch1 through a mechanism in

300 suggests that the in-plane elastic response is controlled by water molecules whereas the transverse