ライフサイエンスコーパス: GO

1 GO enrichment analysis, KEGG pathways and PPI network in

2 GO self-assembly can be controlled by changing the degre

3 GO terms statistically overrepresented within a set of a

4 069), regulation of cell death (GO: 0010941; GO: 0060548) and cell differentiation (GO: 0021861) were

5 ation of programmed cell death (GO: 0043067; GO: 0043069), regulation of cell death (GO: 0010941; GO:

6 mplicity and robustness of the hybrid MoS(2)-GO solid lubricant in mitigating wear-friction behavior

7 re randomly assigned (standard arm, n = 296; GO arm, n = 292).

8 arby genes were significantly enriched in 36 GO terms and 6 KEGG pathways including JAK/STAT signalin

9 ed magnetic graphene oxide (pectin/Fe(3)O(4)/GO) is presented.

10 zed (i.e., atomic layer oxidation) to form a GO layer, which acted as the bio-receptor, while retaini

11 We developed a variant of a GO/NOGO task that reveals important differences in these

12 -matched healthy controls (HC)] performed a 'GO'-commanded step initiation task on a force platform u

13 y clustered in olfactory receptors activity (GO:0004984, p = 4 x 10(- 10)) for PME traits.

14 revealed that the intravenously administered GO accumulated predominantly in the liver and spleen at

15 DNA-AuNPs) to selectively label administered GO in Solvable-treated tissue samples and (ii) construct

16 ng affinity for labeling of the administered GO (dissociation constant: 36.0 fM) and that the method'

17 either overlap of members or hierarchy among GO terms, and tables with depth and cluster information

18 associated with higher TMB (P < 0.0001) and GO (P = 0.003).

19 tween photoexcited fluorophores (donors) and GO (acceptor), we discovered that flurophore-labelled an

20 activity of MoSe(2) due to the Co doping and GO hybridization.

21 urrence of both sulfur functionalization and GO reduction.

22 artataWeb links targets to KEGG pathways and GO annotations, completing the bridge from drugs/chemica

23 rs, training datasets with varying sizes and GO terms form different levels.

24 mum performance is synthesized using ZOL and GO suspensions with the concentration of 50 uM and 2.91

25 oxide/poly(ethylenimine) support (denoted as GO-PEI-Carr).

26 Bio-affinity layers of protein-G (Pro-G) at GO-Ru(II) electrode interface promotes the localization

27 s network to predict the association between GO terms and isoforms, thus accomplishing the prediction

28 their activity determines the choice between GO and NO-GO pathways in the basal ganglia.

29 based on the overlap of gene members between GO terms.

30 this work analyses the relationship between GO terms and protein toxicity and builds predictor model

31 Both GO and MGO induced the formation of allysine in all test

32 In liquid assay system, both GO and MGO inhibited the target bacteria at concentratio

33 onnected, and further processed to make bulk GO and graphene materials of arbitrary form factors and

34 tion of MoS(2) layers that were protected by GO layers and, an absence of MoO(x) peaks indicate a str

35 led significantly higher response for m-Chit-GO (10pM) as compared to their bulk state (100 nM) on DA

36 med with three-electrode set-up using m-Chit-GO electrode as working electrode whereas Ag/AgCl and Gr

37 tained with particulate leaching, the m-chit-GO showed average pore size of 1mumwith slow (2 h) curin

38 The response of DA on m-Chit-GO was investigated and compared with their bulk counter

39 f mesoporous-chitosan-graphene oxide (m-Chit-GO) composite-based sensing electrode and graphene-based

40 Cistrome-GO has two working modes: solo mode for ChIP-seq peak an

41 Upon coating GO onto PLCL microfibers via a layer-by-layer (L-b-L) as

42 eating disordered macro and mesopores in COF-GO foams.

43 engineered the 3D macro-architecture of COF-GO foams into complex geometries keeping their structura

44 e could integrate crystalline and porous COF-GO foams into self-supported three-dimensional (3D)-prin

45 macroporous volume (55%) throughout the COF-GO foam matrix enhances the flow of water (1.13 x 10(-3)

46 The interconnected 3D openings in these COF-GO foams further enhance the rapid and efficient uptake

47 The red color GO-AuNPs was changed to violet while adding 250 x 10(-5)

48 methylation-specific 5mC antibody conjugated GO(x) makes this assay relatively highly selective for D

49 get diazinon to the bioconjugates containing GO, photoluminescence recovery was detected due to detac

50 Most current GO composites use organic polymer as the matrix material

51 067; GO: 0043069), regulation of cell death (GO: 0010941; GO: 0060548) and cell differentiation (GO:

52 hat the regulation of programmed cell death (GO: 0043067; GO: 0043069), regulation of cell death (GO:

53 ical characteristic like bottleneck, degree, GO term/pathways analysis, bio-kinetics simulation, mole

54 me-wide experimental data, we have developed GO-CAM, a structured framework for linking multiple GO a

55 ociations among enriched but often different GO terms, demonstrating the usage of GO hierarchical rel

56 0941; GO: 0060548) and cell differentiation (GO: 0021861) were the main processes involved in adenoma

57 mutation profiles with nonrecurrent disease (GO, good outcome), recurrence (R), or progression (PD) i

58 Each GO cluster generated by GOMCL can be evaluated and furth

59 with depth and cluster information for each GO term.

60 Rgsepd computes significantly enriched GO terms for each experimental condition and generates m

61 O hierarchical structures among the enriched GO terms and their associated ancestor terms using GOfox

62 We conducted a randomized trial to evaluate GO in combination with intensive induction and consolida

63 regnancy, radioiodine therapy can exacerbate GO and surgery can result in hypoparathyroidism or laryn

64 )), beyond the capabilities of many existing GO composites.

65 FT-IR confirmed the formation of the Fc-GO nanocomposite and PEI deposition on the electrode sur

66 s (concentration loss: 11% for 3-DG, 24% for GO and MGO) and have an effect on the fermentative diges

67 o obtain a more accurate biodistribution for GO, we (i) developed a postadministration labeling strat

68 emission maximum was observed at 448 nm for GO while exciting at 335 nm.

69 Effective treatment for GO will modify one or more of these parameters.

70 e formation during laser processing used for GO reduction.

71 were ascribed to the leaching of AuNPs from GO.

72 l functional immuno-bioprobe translated from GO-Ru(II) conjugated nanostructures offers new insights

73 Further, GO is flexible and can be easily adapted to induce expre

74 ivities of the dicarbonyl compounds glyoxal (GO), methylglyoxal (MGO), 3-deoxyglucosone (3-DG) were a

75 nds (DCs), 3-deoxyglucosone (3-DG), glyoxal (GO) and methylglyoxal (MGO) during simulated gastrointes

76 The ability of alpha-dicarbonyls, glyoxal (GO) and methyl-glyoxal (MGO) (2 M), to induce the format

77 he dicarbonyls methylglyoxal (MGO), glyoxal (GO), and 3-deoxyglucosone (3-DG) in commonly-consumed pr

78 tabolites like methylglyoxal (MGO), glyoxal (GO), and 3-deoxyglucosone (3-DG).

79 aphene composite of graphene oxide/graphene (GO/G) for the detection of circulating miRNA-21, a relia

80 The visualization of the identified GO hierarchical structures among the enriched GO terms a

81 However, if GO and related derivatives are to become useful material

82 ] vs. 29% [8 of 28]), and the mean change in GO-QOL overall score (13.79 points vs. 4.43 points) (P<=

83 The most enriched DEGs in GO functional analysis were mainly associated with cell

84 lants show upregulation of genes enriched in GO terms related to oxidoreductase activity, respiratory

85 o muscle-invasive disease and was highest in GO, intermediate in PD, and lowest in R patients (P = 0.

86 Nanometer-sized pores are introduced in GO sheets by chemical etching.

87 dentification of potential quality issues in GO is a challenging and arduous task, given its growing

88 Quality issues in GO, if not addressed, can cause misleading results or mi

89 e number of GO terms by condensing them into GO clusters representing non-overlapping functional them

90 ers, such as the hydrated ion radius and ion-GO interactions, are currently lacking yet are needed to

91 to effectively separate the DNA-AuNP-labeled GO from the unbound DNA-AuNPs and the dissolved tissue m

92 A fluorescein dye labeled GO quenches the truncated aptamer by pai-stacking intera

93 Five-layer GO-based devices depicted complementary resistive switch

94 Tri-layer GO-based devices illustrated non-polar resistive switchi

95 es' ophthalmopathy-specific quality-of-life (GO-QOL) questionnaire across trial visits (from baseline

96 Meanwhile, GO@CoMoSe(2)-coated nickel foam (NF) achieved feasible s

97 MGO, GO, and 3-DG were about equally potent in the millimolar

98 The presented database of MGO, GO, and 3-DG opens the possibility to accurately estimat

99 idated a UHPLC-MS/MS method to quantify MGO, GO, and 3-DG.

100 re, we report that the modulus of multilayer GO films can be significantly enhanced if some of the sh

101 a structured framework for linking multiple GO annotations into an integrated model of a biological

102 rpretation, and batch processing of multiple GO enrichment datasets.

103 involving graphene oxide-gold nanoparticles (GO-AuNPs) functionalized with capture probe 1 and gold n

104 raphene oxide stabilized gold nanoparticles (GO-AuNPs) was described.

105 n HRP@PGH NPs and graphene oxide nanosheets (GO NSs) were simultaneously electrodeposited onto the el

106 vity determines the choice between GO and NO-GO pathways in the basal ganglia.

107 our knowledge, the antibacterial activity of GO and MGO against Listeria innocua, Pseudomonas fluores

108 in MRD positive patients by the addition of GO led to a significantly lower CIR rate (4-year CIR, 29

109 In conclusion, the addition of GO to intensive chemotherapy in NPM1mut AML resulted in

110 HIF1A, VDR, and CLOCK, among others, and of GO term pathways related to ribosomal activity and infec

111 t it produces highly specific annotations of GO terms based on annotated reference phylogenetic trees

112 mportant for many commercial applications of GO composites.

113 lls, indicative of potential applications of GO for imaging MPO activity in live cells.

114 ed for thin-film or membrane applications of GO, dispersed nanoparticles for composite materials, and

115 The association of GO and labelled aptamer sensor platform has shown the ra

116 iles that are able to predict the benefit of GO on outcome.

117 sification, we confirmed that the benefit of GO was restricted to the favorable (hazard ratio [HR], 0

118 Interestingly, the benefit of GO was significant for patients with activating signalin

119 es with the surface oxygen dangling bonds of GO to form M O bonds.

120 unpredictable aggregation characteristics of GO and provide computational methods to design directed

121 importance of increasing the completeness of GO annotations to for supporting computational analyses

122 We prepared this layered composite of GO/G through low-damage plasma treatment of bilayer G.

123 pH-dependence of GO emission is utilized to provide the sensing of acidic

124 e recovery was detected due to detachment of GO from the aptamer as a result of the difference in aff

125 revealed a significant beneficial effect of GO in female, younger (<= 70 years), and FLT3 internal t

126 Interestingly, the emission of GO-AuNPs becomes "turn-on" after the addition of 75 x 10

127 n the work function and ionization energy of GO, supporting the functionalization of Ru(II).

128 and direct access to structural features of GO, (II) structure-based ranking of GO-terms, (III) mapp

129 been used to construct various bulk forms of GO and graphene-based materials through solution-based p

130 eractions with the oxygen functionalities of GO provide the benefit of higher capacitance but suffer

131 rmolecular bonding with functional groups of GO.

132 The inclusion of GO (0.1 wt.%) provided an approximate 20% enhancement of

133 The inclusion of GO in the polymer beads dramatically increased the poten

134 the utilization of structural information of GO and complement existing analysis tools.

135 identity, the blue fluorescence intensity of GO at 440 nm increases with the progression of oxidation

136 o 1125 x 10(-6) M, the emission intensity of GO-AuNPs linearly increases with the correlation coeffic

137 ciently identifies clusters within a list of GO terms using the Markov Clustering (MCL) algorithm, ba

138 any kind of analysis resulting in a list of GO-terms, e.g., from differentially expressed genes or g

139 to reduce redundancy and summarize lists of GO terms effectively and informatively.

140 e spent on manual curation of large lists of GO terms, minimize biases introduced by redundant GO ter

141 amics and newly developed accurate models of GO, the driving forces that lead to the various morpholo

142 the thermodynamically stable morphologies of GO and relevant dispersion mechanisms.

143 ological interpretation of a large number of GO terms by condensing them into GO clusters representin

144 ts is challenging due to the large number of GO terms, their hierarchical and connected organization

145 Additionally, the pathophysiology of GO (and likely pretibial myxoedema) involves the synergi

146 icroscopy to measure the ion permeability of GO films and evaluate its relationship with the measured

147 o exploit a graph-theoretical perspective of GO as manifested by its DAG-structure and the containing

148 oforms, thus accomplishing the prediction of GO annotations of isoforms.

149 zation capabilities and (IV) prioritizing of GO-terms.

150 ications due to the attractive properties of GO, such as high strength and high electrical conductivi

151 ique combination of mechanical properties of GO/Mfp films will be attractive for a range of applicati

152 nsitive, interference-free quantification of GO through measurement (inductively coupled plasma mass

153 tures of GO, (II) structure-based ranking of GO-terms, (III) mapping to reduced GO-DAGs including vis

154 fter subsequent electrochemical reduction of GO NSs into graphene nanosheets (GNSs) and following pho

155 lying SSIF to the October 3, 2018 release of GO suggested 1938 unique potentially missing is-a relati

156 on top of a sequence-based representation of GO concepts along with three conditional rules (monotoni

157 estingly, the photoluminescence responses of GO and SWCNTs to enzymatic degradation are counterposed.

158 to participate in the immunological stage of GO, but whether they can directly affect the fibroblasts

159 ange in annotation completeness and types of GO classes.

160 fferent GO terms, demonstrating the usage of GO hierarchical relations enhance data analysis.

161 healthy cells suggesting a potential use of GO as a non-invasive optical sensor for cancer microenvi

162 s "turn-off" after the formation of AuNPs on GO surface due to masking of oxygen functional groups re

163 cripts, most with a biological role based on GO analysis.

164 es are obtained by varying the IO content on GO.

165 acidic conditions, the adsorption of HSA on GO led to the formation of protein layers with a high de

166 alidated against the extensive literature on GO systems in organic solvents-furnish quantitative expl

167 h the instructive stimuli (lever pressing on GO, withholding on NOGO) did not.

168 etal precursors with defined atomic ratio on GO support during solvent sublimation, which is not affo

169 Turn-on GO fluorescence is also observed with neutrophil-like HL

170 Here we report a 'Gene On' (GO) reporter system that indicates precise cytosine or a

171 base was then used to perform Gene ontology (GO) analysis and Kyoto Encyclopedia of Gene and Genome p

172 Gene ontology (GO) analysis highlighted genes relating to nuclear struc

173 Gene Ontology (GO) analysis of DEG that were higher or lower in PVEC vs

174 Gene Ontology (GO) analysis of FIR up-regulated genes indicated that th

175 Gene Ontology (GO) and MapMan pathway analyses underlined that flavanoi

176 functional categories such as gene ontology (GO) and other databases.

177 detect potentially incorrect Gene Ontology (GO) annotations by comparing the ratio of annotation rat

178 re significantly enriched for Gene Ontology (GO) categories mainly related to social behavior, functi

179 Clustering and gene ontology (GO) enrichment analyses of radish datasets followed by a

180 Moreover, gene ontology (GO) enrichment analysis of salt responsive target genes

181 f genes and pathways based on Gene Ontology (GO) has been widely used to describe the results of vari

182 Gene ontology (GO) is an eminent knowledge base frequently used for pro

183 The Gene Ontology (GO) is the unifying biological vocabulary for codifying,

184 s uncovered the activation of Gene Ontology (GO) pathways relevant to the human disease, such as type

185 Based on the gene ontology (GO) term analysis, six promising candidate genes were si

186 Moreover, Gene Ontology (GO) term enrichment enabled identification of the biolog

187 yTP) genes categorized in the Gene Ontology (GO) term of "Xenobiotic Detoxification Program" (XDP).

188 ber of significantly enriched gene ontology (GO) terms that are related to the cytoskeleton, cell adh

189 nt (nr) protein database, and Gene Ontology (GO) terms were assigned based on the top BLAST hit using

190 tool provides annotations to Gene Ontology (GO) terms, and PANTHER family and subfamily.

191 ly (p < 0.05) enriched in 279 gene ontology (GO) terms, including those related to photosynthesis, me

192 d with chondrogenesis-related gene ontology (GO) terms.

193 ion, and the structure of the Gene Ontology (GO) to best utilize sparse input labels and make consist

194 sources like gene expression, Gene Ontology (GO), and protein-protein interaction network (PPIN) are

195 sed genes (DEGs), followed by gene ontology (GO), Hallmark pathway enrichment and protein-protein int

196 of radiotherapy for Graves' ophthalmopathy (GO) has not been established convincingly.

197 so performed using formulations with pMPO or GO omitted.

198 ntibodies also underlie Graves' orbitopathy (GO) and pretibial myxoedema.

199 icantly clustered in organelle organization (GO:0004984, p = 3.9 x 10(- 2)) for valeric acid, and 17

200 too large and contains redundant overlapping GO terms hindering informative functional interpretation

201 However, these lists of overrepresented GO terms are often too large and contains redundant over

202 ine myeloperoxidase (pMPO), glucose oxidase (GO), glucose, sodium chloride, and specific amino acids

203 For any degree of oxidation, GO does not disperse in PVA as a thermodynamic equilibri

204 The effects of graphene oxide (GO) addition in the PVC gel were also investigated.

205 arch has revealed the use of graphene oxide (GO) and its derivatives as a potential biomaterial becau

206 e MPO-catalyzed oxidation of graphene oxide (GO) and surfactant-coated pristine (6,5) single-walled c

207 ing the interactions between graphene oxide (GO) and the biological milieu, including cells and tissu

208 ce quenching capabilities of graphene oxide (GO) and the versatile format offered by the famous micro

209 udies have demonstrated that graphene oxide (GO) based polymer beads cannot only adsorb Cr (VI) via e

210 rostatic printing (NFEP) and graphene oxide (GO) coating.

211 switching characteristics in graphene oxide (GO) have been extensively studied in recent years, where

212 Graphene oxide (GO) is an antimicrobial agent with tunable surface chemi

213 In this study, graphene oxide (GO) is conjugated with ZOL, and the nanostructured mater

214 utilizing silver (Ag) and Ag-graphene oxide (GO) is designed and developed for the detection of adult

215 and membrane applications of graphene oxide (GO) materials are dictated by its intrinsic material pro

216 ethersulfone (PES)-supported graphene oxide (GO) membrane has been developed by a simple casting appr

217 eered Au-nano-Dendroids, and graphene oxide (GO) nanocomposite.

218 graphene derivatives such as graphene oxide (GO) or reduced graphene oxide (rGO), which suffers from

219 he structure of graphene and graphene oxide (GO) phases is vitally important for any of its widesprea

220 ld nanoparticles (AuNPs) and graphene oxide (GO) sheets are representative zero- and two-dimensional

221 Graphene oxide (GO) sheets have been used to construct various bulk form

222 we are able to functionalize graphene oxide (GO) to produce phosphate graphenes (PGs) with unpreceden

223 Graphene oxide (GO) was used as a platform for screening of the minimal-

224 n coating a layer of coupled graphene oxide (GO) with sensitive chemical compounds along with gold na

225 The direct treatment of graphene oxide (GO) with the commercially available Lawesson's reagent p

226 x (Ru(II)) on the surface of graphene oxide (GO), enabling a dual-functional immunoprobe for the dete

227 both disordered proteins and graphene oxide (GO), we report a disordered protein-GO co-assembling sys

228 Graphene oxide (GO)-based composite materials have become widely popular

229 brid SERS substrate based on graphene oxide (GO)-supported l-cysteine-functionalized starlike gold na

230 anic frameworks (Fe-MOF) and graphene oxide (GO).

231 2D-molybdenum disulfide and graphene-oxide (GO) that can be deposited on to stainless steel substrat

232 thermodynamically stable for highly oxidized GO.

233 for the evaluation of gemtuzumab ozogamicin (GO) in this AML entity.

234 MRD and the effect of gemtuzumab ozogamicin (GO) on NPM1mut TLs and the cumulative incidence of relap

235 it of the addition of gemtuzumab ozogamicin (GO) to standard front-line chemotherapy.

236 In this technique latex particles, GO nanosheets, olive oil, ethanol, and water were used t

237 ork model, named NNTox, which uses predicted GO terms for a target protein to further predict the pos

238 based green synthesis strategy for preparing GO/Mfp film composites.

239 ound for both traits with biological process GO terms that were involved in pathways related to prote

240 We include the bulk-RNA tools PROGENy, GO enrichment, and DoRothEA that estimate pathway and tr

241 e oxide (GO), we report a disordered protein-GO co-assembling system that through a diffusion-reactio

242 d a 36% increase in power output for the PVC/GO gel over traditional plasticizer only PVC gel.

243 Plating assays show that as-received GO (ARGO) and TGO200, TGO500, and TGO800 reduce Escheric

244 an hierarchical clustering in reconstructing GO both when the data are complete, and incomplete.

245 n's reagent produced sulfur-enriched-reduced GO (S-rGO).

246 technique and in situ reduction into reduced GO (rGO), the obtained conductive scaffolds, with 25-50

247 the water permeability of thermally reduced GO membrane was increased by a factor of 26 times by cre

248 anking of GO-terms, (III) mapping to reduced GO-DAGs including visualization capabilities and (IV) pr

249 rms, minimize biases introduced by redundant GO terms in data interpretation, and batch processing of

250 M promoters were enriched for immune-related GO categories; this enrichment was not observed for gene

251 ntial gene expression patterns with reported GO function terms and quantitative trait loci, a total o

252 ratio of annotation rates (RAR) for the same GO term across different taxonomic groups, where those w

253 twork analysis as well as improving standard GO annotations for traditional GO-based applications.

254 quickly and strongly quenched by the studied GO-coated microwell, whereas Fl-Abs complexed with the r

255 onstruct two ratiometric sensors using SWCNT/GO nanoscrolls by incorporating surfactant-wrapped prist

256 In agarised assay system, GO and MGO exhibited antimicrobial activity, with higher

257 We test GO using an activatable GFP and use it to measure the ki

258 We expect that GO-CAM will enable new applications in pathway and netwo

259 We previously showed that GO adipogenic and fibrotic phenotypes could be modelled

260 een these photoluminescent complexes and the GO-coated surface.

261 surface due to the low affinity between the GO-coated surface and the relatively long distance betwe

262 As expected, the GO@CoMoSe(2) modified glassy carbon electrode exhibited

263 However, the GO emission was "turn-off" after the formation of AuNPs

264 Lipase immobilized in the GO aerogel exhibits a 5 to 10-fold increase in apparent

265 te during induction therapy was 10.3% in the GO arm and 5.7% in the standard arm (P = .05).

266 overy (CRi) was significantly reduced in the GO arm compared with the standard arm (P = .005), with n

267 EFS in the GO arm was not significantly different compared with tha

268 a result of a higher early death rate in the GO arm.

269 significantly fewer relapses occurred in the GO compared with the standard arm.

270 NPM1mut TLs were significantly lower in the GO-Arm across all treatment cycles, resulting in a signi

271 xploration and use of the information in the GO.

272 multicellular organism process branch of the GO biological process ontology is more challenging to re

273 mulation reveals that the sensitivity of the GO integrated device (in terms of RIU/nm) is enhanced by

274 ited ion mobility due to constriction of the GO interlayer spacing.

275 of the adsorption of bacterial cells on the GO material.

276 ty database of carbon variables based on the GO-SHIP A25 section (1997-2018).

277 These GO-based devices with Au Nps comprising different config

278 These GO/Mfp films display high tensile strength (134-158 MPa)

279 The 5.0 um thick GO film coated on PES support membrane showed a long-ter

280 Thirty-three GO, 10 R, 18 PD, and 1 unknown outcome patients were ana

281 Thus, GO provides a powerful approach to increase the practica

282 nocytes and neurons, bone and heart tissues; GO: 0009653).

283 to the competitive binding of the aptamer to GO.

284 The DNA-AuNPs can bind to GO in a concentration- and time-dependent manner.

285 With these tools, GO can be exploited to functionally link BE events at en

286 ving standard GO annotations for traditional GO-based applications.

287 The study confirms that using GO modified fiber optic probe, the sensitivity is enhanc

288 It enables visualizing GO clusters as a heatmap, networks based on either overl

289 When GO was omitted from the formulation, no antimicrobial ac

290 ng to specific experimental conditions, when GO-cell interactions occur.

291 mutant tumors (COSMIC5) were associated with GO (P = 0.047; P = 0.0002).

292 ile later stages were mostly associated with GO terms relevant to organ development and morphogenesis

293 CC2 and BRCA2 mutations were associated with GO.

294 he nutrient medium reacted quickly both with GO and MGO, interfering with the antibacterial potential

295 be 2 is fabricated by modifying Ag film with GO for sensitivity improvement.

296 ond to transcriptionally silenced genes with GO enrichment for neuronal function and protein kinase A

297 tion of allysine in all tested proteins with GO being more reactive (23.8 and 8.6 nmoles/mg protein i

298 and all-trans-retinoic acid with or without GO.

299 ZOL-GO nanostructures can facilitate the mineralization of B

300 Nanostructured ZOL-GO with an optimum performance is synthesized using ZOL

301 ults obtained confirm the performance of ZOL-GO nanostructures as promising drug complexes for the tr