ライフサイエンスコーパス: MIP

1 MIP's thickness and extraction duration were optimized b

2 MIP-7-hydroxycoumarin had greater selectivity and extrac

3 MIP-aripiprazole film-coated electrodes were used as ext

4 MIPs are a promising option for industrial packed and fl

5 MIPs are synthetic receptors that offer the advantages o

6 MIPs came into the spotlight in 1993 when they were dubb

7 MIPs have been intensively employed in classical solid-p

8 MIPs have been synthesized for targeting and visualizing

9 MIPs have been utilized as receptors in biosensing platf

10 MIPs synthesized by bulk polymerization using itaconic a

11 MIPs were formed by the anodic deposition of o-phenylene

12 MIPs were synthesized by bulk polymerization using metha

13 MIPs were synthesized under different polymerization pro

14 MIPs, implemented as a recognition element due to their

15 , 7.1] vs 32.6 pg/ml [7.1, 88.0]; p = .001), MIP-1beta (30.7 pg/ml [30.7, 30.7] vs 243.3 pg/ml [30.7,

16 serum IL-10 (p = 0.0001), IL-6 (p = 0.002), MIP-3alpha (p = 0.02) and CD40-L levels (p = 0.002) sign

17 uated the release of IL-6, IL-8, TNF, MCP-1, MIP-1alpha, IFN-gamma, LTB-4, MMP-8 and -9, and IL-1Ra w

18 Levels of IP-10, HGF, IL-6, MCP-1, MIP-1alpha, IL-12p70, IL-18, VEGF-A, PDGF-BB and IL-1RA

19 ory cytokines (IL-1beta, IL-6, IL-17, MCP-1, MIP-1alpha, MIP-2, RANTES, and TNF-alpha), inflammatory

20 associated with reduced inflammation (MCP-1, MIP-2, TNF-alpha, IL-6 and CD68), decreased accumulation

21 ins, including; IL-6, IL-10, MCP-1, sVCAM-1, MIP-1alpha, IP-10, GM-CSF, M-CSF, TNF-alpha, IFN-gamma,

22 -10, macrophage inflammatory protein-1alpha (MIP-1alpha), and MIP-1beta, the pattern of which varied

23 mmatory cytokine responses (e.g., IL-1alpha, MIP-1alpha, TNF, IL-6, and IL-8) as well as regulated a

24 acrophage inflammatory protein (MIP)-1alpha, MIP-1beta, monocyte chemoattractant protein (MCP)-1, int

25 IFN-gamma and TNF-alpha but not MIP-1alpha, MIP-1beta, and RANTES.

26 in pulmonary neutrophilia, IL-6, MIP-1alpha, MIP-1beta, CXCL1, and CXCL5 in AlloTbet mice.

27 s (IL-1beta, IL-6, IL-17, MCP-1, MIP-1alpha, MIP-2, RANTES, and TNF-alpha), inflammatory cell infiltr

28 to secret macrophage inflammatory protein 2 (MIP-2), which suggested that CXC ELR+ chemokines might b

29 including macrophage inflammatory protein-2 (MIP-2).

30 a, IL-1beta, IL-22, IL-33, IL-17alpha, IL-2, MIP-2, and MCP-1), and neutrophil infiltration (myeloper

31 ssion of chemokines/cytokines such as CCL-3 (MIP-1alpha) and granulocyte-macrophage colony-stimulatin

32 g reduction in pulmonary neutrophilia, IL-6, MIP-1alpha, MIP-1beta, CXCL1, and CXCL5 in AlloTbet mice

33 rein for the first time in the assembly of a MIP film, by electropolymerization, in the presence of C

34 y, excision of MANF from beta-cells of adult MIP-1Cre(ERT)::Manf(fl/fl) mice resulted in reduced beta

35 xing, overlap paired-end merging, alignment, MIP-arm trimming, variant calling, coverage analysis and

36 f chemokine ligand 10 [CXCL10], MIP-1 alpha [MIP-1alpha]/CCL3), which segregated participants who die

37 ignature (PS; IL-2(+)IFN-gamma(+)TNF-alpha(+)MIP-1beta(+)) found at low levels among NC.

38 gnature (NPS; IL-2(-)IFN-gamma(+)TNF-alpha(-)MIP-1beta(+)), found at increased levels among NC; and (

39 Proinflammatory cytokines (TNF-alpha, MIP-1, i-NOS) were decreased significantly and restorati

40 of 2,3'-bithiophene enables deposition of an MIP film in the form of an inverse opal.

41 putative cell-surface and membrane-anchored MIP virulence factors.

42 , including interleukin-12p70 (IL-12p70) and MIP-1alpha, which were positively correlated with the ma

43 ophage inflammatory protein (MIP)-1alpha and MIP-1beta at week 8.

44 eks post-surgery and those of MIP-1alpha and MIP-2alpha at 3 weeks.

45 nflammatory protein-1alpha (MIP-1alpha), and MIP-1beta, the pattern of which varied by stimulant.

46 ion inhibitory factor [MIF], MIP-1alpha, and MIP-2alpha) was measured using real-time PCR and western

47 ta, with IL-6, IL-8, IL-1alpha, IL-1beta and MIP-1alpha/beta production significantly elevated.

48 f proinflammatory cytokines (IL-6, IL-8, and MIP-1beta) by monocytes and DCs (IC50 < 1 muM) and preve

49 to syntheses of nanostructured MIP films and MIP nanoparticles.

50 It colocalized GABA and MIP but not AT or ORC immunoreactivity.

51 In contrast, when MIP-GlcA and MIP-NANA particles with a smaller size (125nm) were used

52 primary neutrophils in response to LTB4 and MIP-2 and in the migration of neutrophils during thiogly

53 IFN-gamma, IL-6, IL-8, IL-16, MCP-1, MIF and MIP-1 beta were significantly higher in all RD groups th

54 e, whereas the native chemokines (RANTES and MIP-1alpha) fail to displace bound fluorescent analogs e

55 ce, weight loss, neutrophil recruitment, and MIP-2 production.

56 he combination of a ratiometric strategy and MIP improves the sensitivity and selectivity of the sens

57 rnal and internal subdivisions of PEip), and MIPd.

58 iew, we summarize the integration of ILs and MIPs for biorecognition and biosensing.

59 ally overlaps with functionally defined area MIP, receives inputs from somatosensory (predominantly f

60 nfirming the high target selectivity of AuNP-MIP cavities.

61 The specificity of AuNP-MIP sensor was further investigated by studying with int

62 measurements for glucose binding on the AuNP-MIP sensor revealed a high affinity toward glucose with

63 The comparative rebinding studies with AuNP-MIP and non-imprinted polymer (AuNP-NIP) exhibited an ex

64 corated molecularly imprinted polymers (AuNP-MIPs).

65 The AuNP-MIPs were investigated by employing atomic force microsc

66 The AuNP-MIPs were synthesized on a gold surface by multistep amp

67 were compared against commercially available MIPs according to specificity and selectivity metrics; c

68 sted our pipeline using the hemophilia A & B MIP design from the "My Life, Our Future" initiative.

69 be readily adapted to design other PDA-based MIP sensors.

70 s for the design and development of IL-based MIPs and their applications in the biorecognition and bi

71 Then, specific applications of IL-based MIPs in peptide recognition, protein sensing, and food s

72 embly of inner-arm dynein IDA b and the beak-MIP structures.

73 The best MIP was morphologically characterized and equilibrium as

74 07a, macrophage inflammatory protein 1 beta (MIP-1beta), and TNF-alpha from NK cells.

75 L-8, macrophage inflammatory protein-1 beta [MIP-1beta]/C-C motif chemokine ligand 4 [CCL4], interfer

76 The combination of bio-MIP and photoelectrochemistry overcomes the defects of t

77 s strategies resulting in more biocompatible MIPs in the form of soluble nanogels, these synthetic an

78 Both MIPs were found to be highly selective towards their tar

79 MIP-1a, CXCL10/IP-10, CCL5/RANTES, and CCL20/MIP-3a.

80 wth factor), GM-CSF, IL-10, CCL2/MCP-1, CCL3/MIP-1a, CXCL10/IP-10, CCL5/RANTES, and CCL20/MIP-3a.

81 spinal fluid proteins including IL-12B, CD5, MIP-1a, and CXCL9 which had a combined diagnostic effica

82 in expression of neutrophil chemoattractants MIP-2alpha and CXCL5 in AAA lesions or macrophages from

83 cificity and selectivity metrics; commercial MIPs were characterized by quite broad cross-reactivity

84 We crossed MIP-TF mice with A(vy) mice which develop obesity and pr

85 0, IL-12, CRP, TNF-alpha, IFN-gamma, GM-CSF, MIP-1alpha, and Eotaxin-1 in patients with MDD based on

86 8 (95% CI: 0.98, 0.99); and (18)F-FDG PET/CT MIP atlas, 0.99 (95% CI: 0.98, 1.00).

87 0]/C-X-C motif chemokine ligand 10 [CXCL10], MIP-1 alpha [MIP-1alpha]/CCL3), which segregated partici

88 veral proinflammatory genes (CXCL1/KC, CXCL2/MIP-2, MCP-1/CCL2, CXCR2, IL-6, ICAM-1, P-selectin, and

89 The deposited MIP and non-imprinted polymer (NIP) films were character

90 ated and optimized using fabricated MOF- DES/MIPs monolithic fiber.

91 nts/molecularly imprinted polymers (MOF- DES/MIPs) and were used for microextraction of phthalate est

92 ming the strong binding between the designed MIP and the protein as predicted by the computational st

93 he best of our knowledge, both the developed MIPs towards BMK and the electrochemical sensor for its

94 d when labeling vertebrae on two-dimensional MIPs.

95 tvax vaccine induced anti-Dn-ACP and anti-Dn-MIP antibodies.

96 ozyme inhibitor function, and homology of Dn-MIP to other putative cell-surface and membrane-anchored

97 Finally, the medial bank of the IPS (i.e., MIP) projects solely to the dorsalmedial stream (PO).

98 ovides a general overview of electrochemical MIP-based sensors that have been reported for the detect

99 epi-detected mid-infrared photothermal (epi-MIP) microscope at a spatial resolution of 0.65 mum.

100 on of molecular cavities, the hybrid epitope-MIPs, particularly with the inclusion of AuNPs have prov

101 best of our knowledge there are no existing MIPs-based sensors toward amphetamine-type stimulants (A

102 n with a molecularly imprinted polymer film (MIP), viz., myoglobin-imprinted electropolymerized poly(

103 cosystem Model Intercomparison Project (Fish-MIP) to analyze responses of marine animal biomass in al

104 Following, MIPs were synthesized in the presence of TBZ as a templa

105 otocin, RGWamide, DLamide, FLamide, FVamide, MIP, and serotonin were present in fewer cells in demarc

106 The expressed G212R-MIP was diminished and almost exclusively cytoplasmic in

107 of maximal uptake on PET/CT-derived MR(gluc)MIP images.

108 Glucose uptake on MR(gluc)MIP was found to correlate positively with a change in T

109 We will end the review by reporting how MIPs themselves can act as therapeutics by inhibiting ca

110 le epitope imprints, whereas the AuNP-hybrid MIPs enhanced the sensitivity level to a great extent an

111 The AuNPs decorated epitope-mediated hybrid MIPs, as well as the standard hybrid MIPs, were utilized

112 he biomarker assay using the standard hybrid MIPs resulted in 2.5-fold higher sensitivity compared to

113 hybrid MIPs, as well as the standard hybrid MIPs, were utilized for the preparation of electrochemic

114 developed on a surface molecular imprinted (MIP) polydopamine-coated CdS/CdSe/Zn heterojunction.

115 was not affected by p-synephrine binding in MIP-film molecular cavities.

116 advantages, they have found intensive use in MIPs by remedying the latter's shortcomings.

117 ted RAW macrophages, both alarmins increased MIP-2 (macrophage inflammatory protein-2) chemokine expr

118 al Impact Model Intercomparison Project (ISI-MIP, including HYBRID4, JeDi, JULES, LPJml, ORCHIDEE, SD

119 olated from beta-cell-specific Ghsr knockout MIP-Cre/ERT;Ghsr(f/f) mice.

120 rred in obese A(vy)/MIP-TF mice but not lean MIP-TF mice.

121 The LSPR/MIP sensor provided a linear response for astringency ex

122 surface of the magnetic particles (magnetic MIPs).

123 The magnetic-MIP showed a significant immobilization capacity of biot

124 necessity to develop new strategies to make MIP sensors more specific if practical applications are

125 p70, IL-13, IL-16, IP-10, MCP-1, MCP-4, MDC, MIP-1a, TARC, TNFB) was associated with diminished quali

126 Meanwhile, MIP-1404, PSMA-11, 2-(3-{1-carboxy-5-[(6-fluoro-pyridine

127 ssed this possibility using transgenic mice (MIP-TF mice) whose B-cells express enhanced green fluore

128 acrophage migration inhibitory factor [MIF], MIP-1alpha, and MIP-2alpha) was measured using real-time

129 IPva, LIPvp, LIPda, LIPdp, PIPv, PIPd, MIPv, MIPd, AIPda, AIPdp, and AIPv.

130 line (AN) m-aminobenzenesulfonic acid (MSAN) MIP polymers.) Composition of the imprinted polymer, (th

131 otential (P, V), were measured for the MWCNT/MIP-sensors after their incubation with non-diluted plas

132 has been paid to syntheses of nanostructured MIP films and MIP nanoparticles.

133 boronate ester bond-mediated, thin (~75 nm) MIP-based biomimetic recognition layer was electrodeposi

134 roduction of IFN-gamma and TNF-alpha but not MIP-1alpha, MIP-1beta, and RANTES.

135 genetic and functional evidence for a novel MIP mutation of G212R, which leads to congenital progres

136 Using this novel MIP-based method, it was possible to detect bacteria in

137 ted ADCC and antibody-mediated activation of MIP-1beta in NK cells as the four immunological paramete

138 arkers, an emerging and fast-growing area of MIP applications.

139 will discuss the current state-of-the-art of MIP synthesis and applications in the context of food an

140 This combination of MIP nanoparticles with micromechanical sensors is one of

141 w surveys novel achievements in the field of MIP nanostructures and their application for determinati

142 otein expression level of the mutant form of MIP was remarkably reduced compared with that of the wil

143 kely to damage the structure and function of MIP.

144 were employed to improve the performance of MIP sensors.

145 Novel techniques of MIP deposition as thin films, surface development, and i

146 creased at 2 weeks post-surgery and those of MIP-1alpha and MIP-2alpha at 3 weeks.

147 The costs and time of MIP production were substantially low due to selection o

148 After the best batch of MIPs was chosen, different strategies for immobilizing t

149 rent limitations in the commercialisation of MIPs technology.

150 This work describes the development of MIPs, based on the epitope approach, synthesized from th

151 roles of ILs in improving the performance of MIPs are firstly summarized, including serving as solven

152 at have been employed for the preparation of MIPs destined for in vitro and in vivo targeting and bio

153 These works mark a new opening in the use of MIPs for antibody therapy and even immunotherapy, as mat

154 of right and left breasts were evaluated on MIP and post-contrast T1-weighted magnetic resonance ima

155 roscopic analysis were performed to optimize MIP synthesis.

156 Surprisingly, two other MIPs are Mck1 and Mkk2 that are the upstream kinases of

157 e glycol dimethacrylate)] polymer particles (MIPs) for CO2 capture were synthesized by suspension pol

158 t-dispersing factor, myoinhibitory peptides (MIPs), and orcokinins (ORCs) were part of both entrainme

159 bination of a molecularly-imprinted polymer (MIP) and a natural antibody for the accurate surface-enh

160 liquid-based molecularly imprinted polymer (MIP) and gold nanoparticles/graphene oxide (Au/GO).

161 by the layer of molecular imprinted polymer (MIP) as the recognition medium.

162 is to develop molecularly imprinted polymer (MIP) based micromechanical cantilever sensor system that

163 ally friendly molecularly imprinted polymer (MIP) coated on silica-carbon quantum dots (SiCQDs).

164 e developed a molecularly imprinted polymer (MIP) electrode for the detection of perfluorooctanesulfo

165 or conductive molecularly imprinted polymer (MIP) film coated electrodes was investigated in detail.

166 the deposited molecularly imprinted polymer (MIP) film on three length scales.

167 us conducting molecularly imprinted polymer (MIP) films are deposited by electropolymerization at rel

168 coupled with a molecular imprinted polymer (MIP) for imidacloprid (IMI) determination.

169 to prepare a molecularly imprinted polymer (MIP) layer on the surface of multi-walled carbon nanotub

170 ently-labeled molecularly imprinted polymer (MIP) particles for bioimaging of fixed and living human

171 A molecularly imprinted polymer (MIP) recognition system was devised for selective determ

172 ed core-shell molecularly imprinted polymer (MIP) was applied as a sorbet in solid phase extraction c

173 anosheets and molecularly imprinted polymer (MIP) was presented for etoposide (ETO) detection.

174 A molecularly-imprinted polymer (MIP) was produced at the working electrode by direct ele

175 ypyrrol (PPy) molecularly-imprinted polymer (MIP), assembled in-situ.

176 and sensitive molecularly imprinted polymer (MIP)-based electrochemical sensor was fabricated for the

177 ic assay with molecularly imprinted polymer (MIP)-based ELISA for the detection of methyl parathion (

178 s to engineer molecularly imprinted polymer (MIP)-based synthetic receptors for the molecular recogni

179 nce (LSPR) and molecular imprinted polymers (MIP) at gold nanodisks as an alternative to sensorial an

180 lypyrrol (PPy) molecular imprinted polymers (MIP) for proteins detection.

181 The lab-made molecularly imprinted polymers (MIP), selective for simple coumarins, were used in three

182 Molecularly imprinted polymers (MIPs) are biomimetics which can selectively bind to anal

183 Molecularly imprinted polymers (MIPs) are tailor made recognition materials that can mim

184 Molecularly imprinted polymers (MIPs) are tailor-made chemical receptors that recognize

185 cations with molecularly imprinted polymers (MIPs) as recognition elements.

186 A series of molecularly imprinted polymers (MIPs) comprising reactionary sites which are complementa

187 Molecularly imprinted polymers (MIPs) emerged thanks to the low-cost and long-term stabi

188 ication with molecularly imprinted polymers (MIPs) for determination of thiabendazole (TBZ).

189 ing based on molecularly imprinted polymers (MIPs) has become an interesting field for environmental

190 Molecularly imprinted polymers (MIPs) have been developed to replace antibodies for the

191 , artificial molecularly imprinted polymers (MIPs) have received great attention in biotechnology.

192 electrode with molecular imprinted polymers (MIPs) immobilized on its surface.

193 ly selective molecularly imprinted polymers (MIPs) towards benzyl methyl ketone (BMK) were synthesize

194 s to prepare molecularly imprinted polymers (MIPs) with ampicillin (AMP) and to evaluate the feasibil

195 re report on molecularly imprinted polymers (MIPs) with an external phospho-sulpho switch driven by s

196 We combine a molecularly imprinted polymers (MIPs) with surface enhanced Raman spectroscopy (SERS) to

197 eparation of molecularly imprinted polymers (MIPs), adsorption performance, adsorption kinetic, and s

198 d (RA) using molecularly imprinted polymers (MIPs).

199 device using molecularly imprinted polymers (MIPs).

200 ed anti-FLAG molecularly imprinted polymers (MIPs).

201 ncentration in solution at the polythiophene MIP-film coated electrode did not originate from swellin

202 In addition to sample preparation, MIPs have also been viewed as promising alternatives to

203 a generated using molecular inversion probe (MIP) capture.

204 following the sad mood induction procedure (MIP).

205 identified that the melanoma immune profile (MIP), an IFN-based gene signature, and the ratio of CD8(

206 Coronal maximum intensity projection (MIP) images of both hips were automatically reconstructe

207 8)F-FDG PET/CT maximum intensity projection (MIP), 0.98 (95% CI: 0.98, 0.99); and (18)F-FDG PET/CT MI

208 l and coronal maximum intensity projections (MIPs) and augmented it with two additional components: s

209 and week 8; macrophage inflammatory protein (MIP)-1alpha and MIP-1beta at week 8.

210 -2 R, IL-8, macrophage inflammatory protein (MIP)-1alpha, MIP-1beta, monocyte chemoattractant protein

211 in (IP)-10, macrophage inflammatory protein (MIP)-3alpha, and monokine induced by gamma interferon (M

212 let linkages and microtubule inner proteins (MIPs).

213 ns, including 33 microtubule inner proteins (MIPs).

214 Reading of the different protocols (MIP, abbreviated and full) was made by an expert radiolo

215 differences between the different protocols (MIP, abbreviated and full), which places the abbreviated

216 d by mass spectrometry the performance of pY-MIP for enrichment and sequencing of phosphopeptides obt

217 The combination of pY-MIP- and TiO2-based phosphopeptide enrichment provided m

218 analysis of physicochemical properties of pY-MIP-TiO2-enriched phosphopeptides demonstrated that this

219 t using inexpensive pY-imprinted polymer (pY-MIP).

220 The pY-MIP-TiO2 and the TiO2 protocols yielded comparable numbe

221 ptides (approximately 70%) when using the pY-MIP-TiO2 combination as compared to TiO2 alone.

222 pY constituted up to 8% of the pY-MIP-TiO2-enriched phosphopeptide fractions.

223 r imaging with the two different colored QDs-MIPs was demonstrated.

224 es (IL-1beta, IL-5, IL-6, TNF-alpha, RANTES, MIP-1beta, MCP-1, KC and IL-10).

225 More recently, MIPs have been combined with magnetic bead extraction, w

226 uction, high selectivity and rapid response, MIPs combined with miniaturized electrochemical transduc

227 The performance of the resulting MIP electrode was evaluated by the current obtained from

228 ed integration site and proviral sequencing (MIP-Seq), an experimental approach involving multiple di

229 Several MIPs are conserved hypothetical proteins and may be invo

230 by integration of the fluorescent core-shell MIP sensor particles into a modular microfluidic platfor

231 , low cost and highly sensitive CPX specific MIP nanoparticle based nanosensor developed in this rese

232 ighly fluorescence SiCQDs and, subsequently, MIP formed on surface (MIP@SiCQDs) using a sol-gel metho

233 Subsequently, MIPs were used for extraction of S. aureus from milk and

234 Ds and, subsequently, MIP formed on surface (MIP@SiCQDs) using a sol-gel method.

235 aphyseal angle were measured on coronal SWMR MIP-images, T1weighted MIP-images and radiographs.

236 dsorption of thiabendazole using synthesized MIPs via precipitation polymerization.

237 y of muscles and bone on SWMR and T1weighted MIP-images was calculated and compared between these two

238 sured on coronal SWMR MIP-images, T1weighted MIP-images and radiographs.

239 r on SWMR (2.00 and 2.02) than on T1weighted MIP-images (1.6 and 1.42; p < 0.001).

240 rface was coated with the PQQPFPQQ-templated MIP film, by electropolymerization, to result in a compl

241 Studies have consistently shown that MIPs can effectively minimize complex food matrix effect

242 The MIP electrode was able to detect PFOS with a detection l

243 The MIP material acted as a pre-concentration scheme for the

244 The MIP membrane, as a molecular recognition receptor, has a

245 The MIP sensor can detect allergenic soy markers at concentr

246 The MIP synthetic receptor was deposited by potentiodynamic

247 The MIP was evaluated as a sorbent for extraction and precon

248 The MIP-film coated electrode was examined with cyclic volta

249 The MIP-film thickness in the absence and in the presence of

250 The MIP/Au/GO nanocomposite was synthesized through non-cova

251 As proof-of-concept, the MIP film was tailored for chloramphenicol (CAP), a commo

252 biomarker for heart failure, by coupling the MIP biosensor with surface plasmon resonance (SPR) detec

253 For a sensitive SERS detection, the MIP film was first incubated in sample containing CEA an

254 luorooctanesulfonate (PFOS) and explored the MIP surface and the effects of interfering molecules.

255 Following the MIP, there was a robust induction of depressed mood in t

256 e PQQPFPQQ epitope, and its removal from the MIP film.

257 (p.G212R) substitution was identified in the MIP gene through target region capture sequencing.

258 better understand PFOS association into the MIP, a Langmuir binding model was developed based on the

259 akly, confirming the high selectivity of the MIP cavities.

260 Integration of the MIP film as a recognition unit with a sensitive extended

261 AFM imaging of the MIP film surface indicated changes in mechanical propert

262 over, it was demonstrated that doping of the MIP film was not affected by p-synephrine binding in MIP

263 The rebinding features of the MIP film were evaluated by electrochemical impedance spe

264 originate from swelling or shrinking of the MIP film, as it was previously postulated, but from chan

265 Combination of the MIP signature with the CTL/macrophage ratio stratified p

266 An apparent imprinting factor of the MIP-1 was IF = 4.95.

267 the sensor is the resistive component of the MIP-functionalized titanium electrodes as derived from t

268 changes in electrochemical responses of the MIP.

269 e resulted with 18.4-48.9pg mass load on the MIP modified cantilever.

270 compared in order to study the effect on the MIP performance and characteristics.

271 onsible to signal the presence of CEA on the MIP platform.

272 vely weak adsorption of these species on the MIP.

273 The results indicate that the MIP based AFM nanosensor has high sensitivity for the CP

274 tem showed decreased power values due to the MIP layer interfaced in the electrical circuit, also dis

275 In this specific case, the MIPs were synthesized from acryclic acid monomers, which

276 When loaded with drugs, the MIPs could locally kill the tumor cells, making them eff

277 Importantly, the MIPs were not cytotoxic and did not affect cell viabilit

278 approach by homogenizing the content in the MIPs.Supplemental material is available for this article

279 Two of the MIPs are Mst11 and Mst7 that are known to interact with

280 Characterization of the MIPs were carried out by Fourier-transform infrared spec

281 , in combination with the versatility of the MIPs, will make this sensor platform a versatile diagnos

282 s with a smaller size (125nm) were used, the MIPs being synthesized as thin shells around green and r

283 constant (K(d)) of 3 x 10(-8) M whereas the MIPs without AuNPs could not detect even the highest con

284 Unlike their MIP-TF littermates, MHV68-EGFP-infected A(vy)/MIP-TF mic

285 For that, a thin MIP film was devised, guided by density functional theor

286 cross-linker was co-polymerized into a thin MIP layer grafted from the surface of silica micropartic

287 ndicate future possible applications of this MIPs-based capacitive biosensor for environmental and fo

288 5-fold decrease in kidney uptake relative to MIP-1095.

289 cularly imprinted poly(vinylimidazole-TRIM) (MIP-1VN) at pH 4.0, followed by elution with 2.0 mL of M

290 al from the mutant compared to the wild-type MIP.

291 ates, summarize the recent progress in using MIPs for preparing and analysing food samples, and discu

292 -alpha, IL-6, IL-12p70, IL-10, GM-CSF, VEGF, MIP-1beta, TNF-beta, IFN-alpha2 and IL-7 in response to

293 intra-insulitis and occurred in obese A(vy)/MIP-TF mice but not lean MIP-TF mice.

294 IP-TF littermates, MHV68-EGFP-infected A(vy)/MIP-TF mice developed moderate intra-insulitis and trans

295 Moreover, in MHV68-EGFP-infected A(vy)/MIP-TF mice, Th1 reactivity spread from EGFP to other B-

296 intra-insulitis in older, more obese, A(vy)/MIP-TF mice.

297 In contrast, when MIP-GlcA and MIP-NANA particles with a smaller size (125

298 One of the most interesting areas where MIPs have shown the biggest potential is food analysis.

299 Batch extraction with MIP coated on to magnetic particles was relatively time-

300 ytoplasmic in the HeLa cells; whereas the WT-MIP was stable dispersed throughout the cytoplasm, and i