ライフサイエンスコーパス: GO

1 GO analysis revealed that these DEGs have putative funct

2 GO and NO-GO sequences differed only in that the order o

3 GO chemistry and morphology were controlled with easy-to

4 GO term enrichment, phosphorylation motif analyses, and

5 GO- Matryoshka yields green and orange fluorescence upon

6 GO-Al2O3 nanocomposite was synthesized using self-assemb

7 ar regression analysis was GO-peptide (1mM): GO-peptide (0.1mM): conventional chip (8-mercaptooctanoi

8 The N-doped 2D GO is also impermeable to small molecules, and hence a h

9 In total, 270 probes sets and 50 GO groups were differentially expressed (up-regulated or

10 There were 220 probe sets and 75 GO groups that were differentially expressed when compar

11 Under 0.82-sun illumination (825 W/m(2)), a GO leaf floating on water generated steam at a rate of 1

12 njugated QDs bind to the GO sheets to form a GO/aptamer-QDs ensemble.

13 ormalities at an early stage of pregnancy, a GO-peptide-based surface plasmon resonance (SPR) biosens

14 energy conversion efficiency of 54%, while a GO leaf lifted above water in a tree-like configuration

15 l molecule metabolic process, cell adhesion (GO IDs: 0030198, 0044281, 0007155) and pathways in cance

16 Meta-analysis across ADNI-GO/2 and ADNI-1 revealed a genome-wide significant inter

17 activity of the film with vertically aligned GO stems from an increased density of edges with a prefe

18 activity of the film with vertically aligned GO.

19 s a versatile approach to controllably alter GO band gap for optoelectronics and bio-sensing applicat

20 Although GO can be easily prepared by oxidation-exfoliation of gr

21 The 3D structure interconnected by ALG and GO ensures the high mechanical strength and good flexibi

22 nalysis biomechanics in peptide aptamers and GO sheets.

23 ies of free spore, olive oil formulation and GO formulation were 32.54%, 37.19%,and 45.20%, respectiv

24 er for free spore, olive oil formulation and GO formulation were 40%, 46.66%,and 56%, respectively.

25 ssect the effects of graphene oxide (GO) and GO functionalized with amino groups (GONH2) on 15 immune

26 Efficient MGO and GO detoxification can be controlled by a switch in metal

27 oxygen atoms form a bridged between MoSx and GO and play a crucial role in the fine dispersion of the

28 ation such as pathways, mouse phenotypes and GO-terms, stemming from MalaCards' affiliation with the

29 spiratory burst during defence response) and GO:0035556 (intracellular signal transduction) were sign

30 ltammetric measurements showed that TCNQ and GO triggered a synergistic effect and exhibited an unexp

31 as modified by a drop casting using TCNQ and GO.

32 GO contents as well as to pristine V2O5 and GO papers.

33 Antitumor GO peptides have been designed as dimerization inhibitor

34 ment were not significantly enriched for any GO-terms.

35 Ozone treatment in aqueous GO suspensions yields the addition/rearrangement of oxyg

36 ion of 1mug/ml for an Au/GO-COOH chip, an Au/GO chip and a traditional SPR chip are 35.5m degrees , 9

37 at a BSA concentration of 1mug/ml for an Au/GO-COOH chip, an Au/GO chip and a traditional SPR chip a

38 p to approximately 5.15 times that of the Au/GO chip.

39 verall affinity binding value, KA, of the Au/GO-COOH chip can be significantly enhanced by up to appr

40 f the antigen-antibody interaction of the Au/GO-COOH chip cause this chip to become four times as sen

41 ta-Amylase immobilization onto GO-CNT (bamyl@GO-CNT) and Fe3O4 (bamyl@Fe3O4), resulted into approxima

42 use is limited to aqueous solutions because GO membranes appear impermeable to organic solvents, a p

43 sh-like CO2-philic agent alternating between GO layers are prepared by a facile coating process for h

44 r the advantages of a strong bonding between GO and fiber device surface and a homogeneous GO overlay

45 the GO surface through the reaction between GO (size 240nm) and Co(2+) in basic solution at room t

46 derstand relationship and similarity between GO annotations of genes, it is important to have a conve

47 kS of (79.4+/-4.6)s(-1) was observed on BOD-GO composite having different negative charge density.

48 (23.6+/-0.9)pmolcm(-2) were obtained on BOD-GO composite having the same moderate negative charge de

49 ne groups reduce the perturbations caused by GO on cell metabolism and increase biocompatibility.

50 ectly exposed are expected to be quenched by GO, including the control line, made of bare QDs, report

51 anuscript (mixing images from the GO and Cds:GO samples).

52 luding calcium-activated potassium channels (GO:0016286; P=2.30 x 10(-5)), cognition (GO:0050890; P=1

53 Chemical GO modification allows for fine control of GO oxidation

54 (GO) terms, GO:0010200 (response to chitin), GO:0002679 (respiratory burst during defence response) a

55 of Gene Ontology-based term classification (GO), EuKaryotic Orthologous Groups (KOG) and Kyoto Encyc

56 ls (GO:0016286; P=2.30 x 10(-5)), cognition (GO:0050890; P=1.90 x 10(-6)), locomotion (GO:0040011; P=

57 d with the model bacterium Escherichia coli, GO nanosheets with vertical orientation exhibit enhanced

58 to Graphene oxide-carbon nanotube composite (GO-CNT), Graphene oxide nanosheets (GO) and Iron oxide n

59 led with glucose oxidase (GOD), the AR/CoOxH-GO system can determine glucose level in blood samples.

60 We fabricated a membrane-based CoOxH-GO probe for the visual detection of CN(-) by preparing

61 The peroxidase-like activity of CoOxH-GO is utilized herein for the quantitation of H2O2 in a

62 n of CN(-) by preparing a thin film of CoOxH-GO on a positively charged and porous nylon membrane (N(

63 (-) inhibits the catalytic activity of CoOxH-GO towards the H2O2-mediated oxidation of AR to form red

64 droxide/oxide-modified graphene oxide (CoOxH-GO) possessing peroxidase-like catalytic activity, and i

65 d the enzyme-mimicking activity of the CoOxH-GO nanohybrid in detail via the H2O2-mediated oxidation

66 inhibit the catalytic activity of the CoOxH-GO nanohybrid, which allows for the construction of a pr

67 The CoOxH-GO/N(+)M operates on the principle that CN(-) inhibits t

68 The PDI-HIS-Cu-GO (PCG) nanocomposite sensor provides a unique platform

69 The newly developed GO/pPG/anti-MBP/anti-Tau nanoimmunosensor has been estab

70 er for different un-doped and nitrogen doped GO membranes, and clarified the corresponding transfer m

71 Hypothesis-driven GO analysis suggests lower expression of genes involved

72 During GO:Nx synthesis, different nitrogen-bonding species, suc

73 Notably, during GO trials, MEPs increased to a similar extent in both gr

74 t interact in the antisaccade task: an early GO/NO-GO race decision process and a late GO/GO decision

75 tionally design more effective and efficient GO membranes.

76 gnificantly greater than observed for either GO or acid treated MWNTs.

77 patients, 60 patients (45%) required either GO or idarubicin for leukocytosis.

78 ific DEGs revealed 54 significantly enriched GO terms, including oxidation-reduction process, metabol

79 carbon materials in 3D printing, especially GO-based materials, have been extensively reported for e

80 : (i) using unified features (i.e. essential GO terms) to interpret why a prediction is made; (ii) be

81 With these essential GO terms, not only where a protein locates can be decide

82 Eventually, GO is added as a revealing agent and the photoluminescen

83 electively capture the biomarker-laden Fe3O4@GO particles, which subsequently catalyze hydrogen perox

84 This paramagnetic Fe3O4@GO composite (1microm size range) was decorated with ant

85 onto graphene oxide (GO) nano-sheets (Fe3O4@GO).

86 ered in serum samples by adjusting the Fe3O4@GO Concentration.

87 To produce the films, GO nanosheets are aligned in a magnetic field, immobiliz

88 main, which is the antibody-binding site for GO, as well as diagnostic immunophenotypic panels.

89 Methylglyoxal (MGO) and glyoxal (GO) are toxic reactive carbonyl species generated as by-

90 After the Apt-GMNPs-GO-L-AgNPs were introduced to a gold anodic BPE array, t

91 bases of the immobilized aptamer (Apt-GMNPs-GO-L-AgNPs).

92 performance, compared to papers with higher GO contents as well as to pristine V2O5 and GO papers.

93 O and fiber device surface and a homogeneous GO overlay with desirable stability, repeatability and d

94 gate how individual GO properties can impact GO membrane characteristics and water permeability.

95 NOGO trials and decreased in both groups in GO trials.

96 omitantly it leads to an initial increase in GO fluorescence intensity and significant (100 nm) blue

97 n or/and lattice structure reorganization in GO:Nx.

98 New tools include GO, metabolic pathway and word enrichment analyses plus

99 rches against annotation databases including GO and KEGG.

100 decrease in Young's modulus with increasing GO content.

101 Thus, here we investigate how individual GO properties can impact GO membrane characteristics and

102 trols needed to suppress (NOGO) or initiate (GO) ballistic index finger isometric voluntary contracti

103 y influenced by the amount of the integrated GO phase.

104 g induction and once during intensification (GO arm, n = 408) as per the Children's Oncology Group AA

105 ly GO/NO-GO race decision process and a late GO/GO decision process.

106 n (GO:0050890; P=1.90 x 10(-6)), locomotion (GO:0040011; P=6.70 x 10(-5)) and Stat3 protein regulatio

107 ivative that emits fluorescence, which makes GO an attractive material for optoelectronics and biotec

108 icantly, we further identify that N-mediated GO can be built into a highly efficient PEM with a proto

109 ng mesenchyme (GM) were enriched in multiple GO terms and KEGG pathways, including many biological pr

110 ges by employing a single FP-cassette, named GO-(Green-Orange) Matryoshka.

111 mposite (GO-CNT), Graphene oxide nanosheets (GO) and Iron oxide nanoparticles (Fe3O4).

112 A new GO deposition technique based on chemical-bonding in con

113 standard five-course chemotherapy alone (No-GO arm, n = 408) or chemotherapy with the addition of tw

114 GO and NO-GO sequences differed only in that the order of their co

115 ract in the antisaccade task: an early GO/NO-GO race decision process and a late GO/GO decision proce

116 er relapse risk in the GO arm than in the No-GO arm (26% v 49%; P < .001).

117 the CC genotype in the GO arm than in the No-GO arm (65% v 46%, respectively; P = .004), but this ben

118 The ds-DNA/p(L-Cys)/Fe3O4 NPs-GO/CPE exhibited an increase in peak currents and the el

119 es-graphene oxide (ds-DNA/p(L-Cys)/Fe3O4 NPs-GO/CPE) for sensitive detection of adenine (A) and guani

120 n this study we demonstrate that activity of GO peptides is independent of the level of cellular expr

121 e target hCG protein, the major advantage of GO-peptide-based SPR sensors was their reduced nonspecif

122 TEM analyses of GO flakes confirm the size decrease of ordered sp(2) dom

123 osite was synthesized using self-assembly of GO and Al2O3 and characterized using the scanning electr

124 of functional similarity and associations of GO terms and genes.

125 es functional similarity and associations of GO terms and genes.

126 respectively; P = .004), but this benefit of GO addition was not seen in patients with the CT or TT g

127 The combination of GO and olive oil revealed the highest viabilities of 50.

128 is is the first time that the combination of GO and TCNQ have been successfully employed to construct

129 l of GO oxidation state, allowing control of GO architectural laminate (GOAL) spacing and permeabilit

130 l GO modification allows for fine control of GO oxidation state, allowing control of GO architectural

131 nomic data) and introduce a novel dataset of GO-disease inferences (that identify common molecular un

132 der to identify an optimal charge density of GO for BOD-ErGO composite preparation, several GO fracti

133 onsider the influence of a charge density of GO on direct bioelectrochemistry/bioelectrocatalysis of

134 y) and ATO (0.15 mg/kg daily) with a dose of GO (9 mg/m(2) on day 1) added to high-risk patients (whi

135 emotherapy with the addition of two doses of GO once during induction and once during intensification

136 ensitive population showed downregulation of GO processes like photosynthesis, ATP biosynthesis and i

137 eatment to controllably tune the band gap of GO, which can significantly enhance its applications.

138 ime visualization of functional groupings of GO terms and genes as well as statistical analysis of en

139 Based on the model of GO fluorescence originating from sp(2) graphitic islands

140 The surface morphology of GO overlay was characterized by Atomic force microscopy,

141 s develop an understanding of the origins of GO fluorescence emission.

142 perties and enables controlled processing of GO.

143 ining the chemical and optical properties of GO with the versatility of the VHH scaffold in the conte

144 reaction, thereby inducing the reduction of GO and simultaneous doping of heteroatoms on the GO.

145 The results of GO and KEGG pathways associated proteomics analysis indi

146 Moreover, the reusability of GO-dLPG biosensor has been facilitated by a simple regen

147 Similarity of GO terms and gene functions is quantified with six diffe

148 new chapter in the long and unusual story of GO, which was the first antibody-drug conjugate approved

149 Understanding the structure of GO allows further reliable interpretation of its optical

150 ant plants conversely showed upregulation of GO terms like G-protein coupled receptor pathway, membra

151 icantly expands possibilities for the use of GO membranes in purification and filtration technologies

152 The IgG was covalently immobilized on GO-dLPG via EDC/NHS heterobifunctional cross-linking che

153 xidation, compared to GCE modified with only GO, TCNQ or TCNQ/electrochemically reduced GO.

154 beta-Amylase immobilization onto GO-CNT (bamyl@GO-CNT) and Fe3O4 (bamyl@Fe3O4), resulted

155 r >5000 mRNAs we determined gene ontologies (GO).

156 d 4 (CCL4), while exploratory gene ontology (GO) analyses revealed lower expression of immune-related

157 Gene Ontology (GO) analysis and Kyoto Encyclopedia of Genes and Genomes

158 Gene ontology (GO) analysis of the co-expression modules suggested that

159 nes/proteins, diseases, taxa, Gene Ontology (GO) annotations, pathways, and gene interaction modules.

160 hierarchical structure of the Gene Ontology (GO) data dramatically improves prediction accuracy.

161 racterized using the MetaCore Gene Ontology (GO) enrichment analysis algorithm.

162 Gene ontology (GO) enrichment analysis of nod+ specific DEGs revealed 5

163 ct directions in stage-2, the gene ontology (GO) enrichment analysis showed several significant resul

164 Additional evaluations using gene ontology (GO) indicate that significant enrichment occurred in the

165 tructure and manual curation, Gene Ontology (GO) is the most frequently used vocabulary for represent

166 d untreated C. albicans using Gene Ontology (GO) revealed a large cluster of down regulated genes tha

167 mic features, here defined by gene ontology (GO) terms, enriched for causal variants affecting a quan

168 Gene ontology (GO) terms, GO:0010200 (response to chitin), GO:0002679 (

169 nd we assessed enrichment for gene ontology (GO) terms.

170 ate functional annotations in Gene Ontology (GO).

171 ene expression (fold-change), gene ontology (GO; biological process) and pathway analyses were perfor

172 fficiency in comparison with graphene oxide (GO) and exhibited excellent radiostability in vivo.

173 ry to dissect the effects of graphene oxide (GO) and GO functionalized with amino groups (GONH2) on 1

174 d its two major derivatives, graphene oxide (GO) and reduced graphene oxide (rGO) have played an impo

175 de (PDI-HIS), copper ion and graphene oxide (GO) and that could be utilized as a highly effective sen

176 Given the fact that graphene oxide (GO) can act as an electron acceptor, we used iron(II) an

177 Graphene oxide (GO) can be considered as one of the most visible outcome

178 (BOD)-based biocathode using graphene oxide (GO) could be prepared in 2 steps.

179 anoquinodimethane (TCNQ) and graphene oxide (GO) for low-potential amperometric detection of reduced

180 Recently, graphene oxide (GO) has been suggested as an adsorbent; however, a suppo

181 stigating the performance of graphene oxide (GO) in the protective effect of olive oil on Bacillus th

182 epared through incorporating graphene oxide (GO) into alginate (ALG) matrix by using a facile combine

183 Graphene oxide (GO) is a graphene derivative that emits fluorescence, wh

184 Graphene oxide (GO) membranes continue to attract intense interest due t

185 emerging example consists of graphene oxide (GO) membranes for separation processes.

186 O4 nanoparticles loaded onto graphene oxide (GO) nano-sheets (Fe3O4@GO).

187 We explore graphene oxide (GO) nanosheets functionalized dual-peak long period grat

188 kly Zn-CuO nanoparticles and graphene oxide (GO) nanosheets on a Ni porous electrode.

189 ules, are complemented by 2D graphene oxide (GO) nanosheets.

190 imensional (2D) graphene and graphene oxide (GO) offer great potential as a new type of cost-efficien

191 lene dioxythiophene) (PEDOT)/graphene oxide (GO) onto the CFE surface is shown to increase the sensit

192 of carbon nanotube (CNT) or graphene oxide (GO) particles on the FN layer.

193 The pH sensor, based on a graphene oxide (GO) sensitive layer, had a sensitivity of 40+/-4mV/pH in

194 designed based on decorated graphene oxide (GO) sheet with alumina (Al2O3) nanocrystals.

195 Graphene oxide (GO) sheets are mixed with the aptamer-QDs.

196 We combined graphene oxide (GO) sheets with a specific peptide aptamer to create a n

197 prised of two functionalized graphene oxide (GO) surfaces that allow the capture of distinct leukocyt

198 pired synthetic leaf made of graphene oxide (GO) thin film material, which exhibited broadband light

199 d simultaneous derivation of graphene oxide (GO) to form a biocompatible polymeric matrix on RGO nano

200 ed by a partial reduction of graphene oxide (GO) using urea [CO(NH2)2].

201 materials as fillers such as graphene oxide (GO), carbon nanotubes (CNT), carbon blacks, and solvent,

202 tation of GBNs, most notably graphene oxide (GO), in previous experimental studies obscured the inter

203 rodes (carbon, graphene (G), graphene oxide (GO), single wall carbon nanotube (SWCNT), multi-wall car

204 routes for the production of graphene oxide (GO), such as the Hummers' method, suffer from environmen

205 dy, sub-20-nm thick, layered graphene oxide (GO)-based hollow fiber membranes with grafted, brush-lik

206 icus whole cells adsorbed on graphene oxide (GO)-coated Surface Plasmon Resonance (SPR) interfaces.

207 carbon nanotubes (CNTs), and graphene oxide (GO).

208 l of carboxyl-functionalized graphene oxide (GO-COOH) composites to form biocompatible surfaces on se

209 ilver nanoparticle-decorated graphene oxide (GO-L-AgNPs) participates in pi-pi interactions with the

210 Nitrogen-doped graphene oxides (GO:Nx) were synthesized by a partial reduction of graphe

211 ration (FDA) approved gemtuzumab ozogamicin (GO) for the treatment of adults with newly diagnosed CD3

212 is regimen with added gemtuzumab ozogamicin (GO) in high-risk patients.

213 Purpose Gemtuzumab ozogamicin (GO), a CD33-targeted immunoconjugate, is a re-emerging t

214 s surface charge density of these particular GO nanosheets was developed.

215 cell group- and condition-specific pathways, GO-Terms and transcription factors.

216 PEDOT/GO coated electrodes rapidly and robustly detect DA, bot

217 sing the electrode surface area with a PEDOT/GO coating and improved adsorption of DA's oxidation pro

218 sulting from 25 s electrodeposition of PEDOT/GO produces the optimal electrode, exhibiting an 880% in

219 Thicker PEDOT/GO coatings demonstrate higher sensitivities for DA, but

220 isease Neuroimaging Initiative (ADNI) phases GO/2 (n=678).

221 e enriched Gene Ontology Biological Process (GO BP) terms, actin cytoskeleton organization, actin fil

222 ercalation and oxidation approach to produce GO on the large laboratory scale (tens of grams) compris

223 Moreover, the as-produced GO can be subsequently deeply reduced (3.2 at.

224 the protective effect of two UV protectant; GO and olive oil and also the combination of both, on th

225 or intracellular signaling cascade proteins (GO: 0007242) and Ras protein signal transduction (GO: 00

226 scaffolds such as reduced graphene oxide (r-GO) films.

227 lently anchored to reduced graphene oxide (r-GO) via a simple one-pot reaction, thereby inducing the

228 With the bending-tolerant r-GO/Li-metal anode, bendable lithium-sulfur and lithium-o

229 By simultaneously reconstructing GO term-gene associations and HPO phenotype-gene associa

230 and glucose as co-reducing agents to reduce GO under mild reaction conditions without introducing to

231 ld highly conductive (54600 S m(-1)) reduced GO.

232 y GO, TCNQ or TCNQ/electrochemically reduced GO.

233 ombustion yields freestanding CNT or reduced GO microtubular fibers.

234 ctrochemical capacitors based on the reduced GO showed an ultrahigh rate capability of up to 10 V s(-

235 LCC9-sepecific miR-29b-1/a-regulated GO processes include oxidative phosphorylation, ATP meta

236 6.70 x 10(-5)) and Stat3 protein regulation (GO:0042517; P=6.4 x 10(-5)).

237 Also, defense-related GO terms of 'translational elongation', 'translation fac

238 T (MT-CVAT) identified functionally relevant GO categories associated with the quantitative trait, ch

239 for BOD-ErGO composite preparation, several GO fractions differing in an average flake size and zeta

240 sensor employing graphene oxide nano-sheets (GO), multiwalled carbon nanotubes (MWCNTs), and pyrogall

241 A combination of PolyPhen-2, SNPs&GO, MutPred, MutationTaster2 and FATHMM was found to per

242 e popular prediction tools (PolyPhen-2, SNPs&GO, MutPred, SIFT, MutationTaster2, Mutation Assessor an

243 constructed by coating graphene oxide/ssDNA (GO-ssDNA) on an Au-electrode for VEGF detection, and inc

244 Additionally, we find substantial GO-induced oxidation of glutathione, a model intracellul

245 tively low fabrication cost of the synthetic GO leaf could potentially unlock a new generation of des

246 H sensitively using a GCE modified with TCNQ/GO at -0.05V.

247 Gene ontology (GO) terms, GO:0010200 (response to chitin), GO:0002679 (respiratory

248 LGO has a much lower density of defects than GO prepared using the conventional Hummers' method and c

249 ng and atomic force microscopy confirms that GO nanosheets align progressively well with increasing m

250 vesicles as a model system, we observe that GO nanosheets induce physical disruption of the lipid bi

251 The GO linking layer provides a remarkable analytical platfo

252 The GO-dLPG based biosensor demonstrates an ultrahigh sensit

253 The GO-peptide-based chip (1mM) had a high affinity (KA) of

254 The GO/aptamer-QDs ensemble assay acts as a "turn-on'' fluor

255 the size of graphitic islands affecting the GO band gap and emission energies.

256 e interaction of AFM1 with the aptamers, the GO-L-AgNPs detach from the aptamer; the resulting ECL of

257 By depositing the GO with a thickness of 49.2nm, the sensitivity in refrac

258 on of the manuscript (mixing images from the GO and Cds:GO samples).

259 ll is affected and the cells detach from the GO based interfaces, causing a characteristic decrease i

260 Furthermore, the GO leaf can be easily restored to its pristine condition

261 had significantly lower relapse risk in the GO arm than in the No-GO arm (26% v 49%; P < .001).

262 gher in patients with the CC genotype in the GO arm than in the No-GO arm (65% v 46%, respectively; P

263 tal electric field intensity (DeltaE) in the GO-based sensing interfaces was significantly enhanced b

264 t, is introduced as a carrier-brush into the GO nanochannels with chemical bonding.

265 Interactive navigation of the GO function space provides intuitive and effective real-

266 CoOxH is formed and deposited in situ on the GO surface through the reaction between GO (size 240nm

267 nd simultaneous doping of heteroatoms on the GO.

268 experiment with a 15 wt % NaCl solution, the GO leaf demonstrated stable performance despite gradual

269 No study has taken the GO hierarchy into account together with the protein netw

270 al structure that largely corresponds to the GO biological process hierarchy, allowing the user to na

271 ntly, the aptamer-conjugated QDs bind to the GO sheets to form a GO/aptamer-QDs ensemble.

272 e energy transfer (FRET) from the QDs to the GO sheets, quenching the fluorescence of QDs.

273 er, previous methods usually either used the GO hierarchy to refine the prediction results of multipl

274 Thus, using the GO-Al2O3 nanocomposite modified electrode, the cell viab

275 pipeline that quantifies and visualizes the GO function analyses in a systematic fashion.

276 t to be significantly more potent than their GO prototypes.

277 This GO-based aptasensor under the optimum conditions exhibit

278 We expect this GO-based membrane structure combined with the facile coa

279 nd specificity suggest the potential of this GO-peptide-based SPR chip detection method in clinical a

280 Moreover, the transfer learning through GO term-gene associations significantly improved associa

281 fast filtration of organic solutions through GO laminates containing smooth two-dimensional (2D) capi

282 ents with the CT or TT genotype, exposure to GO did not influence relapse risk (39% v 40%; P = .85).

283 This two-step approach leads to GO with a high yield (>70 wt %), good quality (>90%, mon

284 or rs12459419 have a substantial response to GO, making this a potential biomarker for the selection

285 with a likelihood of significant response to GO.

286 as a hub transcription factor within the top GO term, and a potential drug target.

287 007242) and Ras protein signal transduction (GO: 0007265), and contain active Ras.

288 The potential of ultrathin GO laminates for organic solvent nanofiltration is demon

289 s to facilitate the development of ultrathin GO-based membranes for CO2 capture.

290 dent interaction of GBNs with bacteria using GO composite films.

291 nd blue-light response were identified using GO and KEGG databases.

292 ial structure and cell cycle processes using GO analysis.

293 tein assay in linear regression analysis was GO-peptide (1mM): GO-peptide (0.1mM): conventional chip

294 When GO was replaced by EDI, the fluorescence of QDs was rest

295 al organic self-assembled spheres along with GO proved very valuable for the detection of PPi in unpr

296 ssociations indirectly through relation with GO terms.

297 lymorphism in patients with AML treated with GO-containing chemotherapy.

298 combination of ATRA and ATO, with or without GO.

299 l that the ceramic-based papers with 0.5 wt% GO show superior in-plane mechanical performance, compar

300 f EmuPAD integrated with nanocrystalline Zeo-GO for detection of ketamine has immense prospective for

301 oflakes and graphene-oxide nanocrystals (Zeo-GO).