ライフサイエンスコーパス: CPP

1 CPP can be linked with various cargos like nanoparticles

2 CPP can enhance delivery of drugs to a targeted site whe

3 CPP FAP-310, a randomized, double-blind, Phase III trial

4 CPP have been effective for delivery of various chemothe

5 CPP sequence cyclisation or addition of a HA-sequence in

6 CPP-115 induced robust and significant increases in brai

7 CPP-115, a next-generation gamma-amino butyric acid (GAB

8 CPP-115-induced changes were exclusive to GABA and homoc

9 CPPs are known to be effective in promoting membrane tra

10 CPPs can also theoretically be used to modulate intracel

11 CPPs have tunable emission, possess large extinction coe

12 s carbonaceous analogues Mes-[10]CPP and [10]CPP.

13 While the photophysical properties of BN-[10]CPP remains similar to its carbonaceous analogues, the e

14 ically, Ir-catalyzed hydrogenation of BN-[10]CPP selectively reduces the BN heterocyclic ring, which

15 mple of a BN-doped cycloparaphenylene BN-[10]CPP was synthesized and characterized.

16 arison to its carbonaceous analogues Mes-[10]CPP and [10]CPP.

17 A bent 8H[12]CPP and a bent 12H[18]CPP, which were fused intramolecul

18 A molecule containing a bent 8H[12]CPP fused to a 4H[6]CPP was likewise constructed.

19 tronic properties of two different [2]DBP[12]CPP nanohoops with electronically modifying substituents

20 g two dibenzo[a,e]pentalene units: [2]DBP[12]CPP nanohoops.

21 Functionalized [12]cycloparaphenylenes ([12]CPPs) containing four alternating biphenyl and naphthyl

22 benzoquinone produced the functionalized [12]CPPs.

23 A bent 8H[12]CPP and a bent 12H[18]CPP, which were fused intramolecularly with two and thre

24 Inclusion of (Arg)9 or TAT(57-57) CPPs further modified the translation readouts, but vari

25 containing a bent 8H[12]CPP fused to a 4H[6]CPP was likewise constructed.

26 its of tetrahydro[6]cycloparaphenylene (4H[6]CPP) fused together through two 1,4-dimethoxybenzene uni

27 s as prototypical linear segments and [6]/[8]CPP as the radial segments, we demonstrate the formation

28 synthesis of two [8]cycloparaphenylenes ([8]CPP) derivatives, 1 and 2, bearing a monosubstituted ben

29 to synthesize a 2,2'-bipyridine-embedded [8]CPP, which we show can successfully coordinate to both P

30 planar chirality for the monosubstituted [8]CPP 1 and 2, whose configuration is here described by ap

31 olid-state structure of a monosubstituted [8]CPP derivative.

32 fine-tuning of the binding properties of [8]CPP 1 toward pyridinium cations due to the presence of t

33 e been investigated and compared with the [8]CPP macrocycle.

34 The [8]CPP ring of the alpha form encapsulates two dichlorometh

35 -embedded cycloparaphenylene nanohoop bipy[9]CPP to [Fe{H(2) B(pyz)(2) }] (pyz=pyrazolyl) produces th

36 the distorted octahedral complex [Fe(bipy[9]CPP){H(2) B(pyz)(2) }(2) ] (1).

37 Similarly, two 6H[9]CPPs were connected through three 1,4-dimethoxybenzene u

38 Aggressors develop a CPP, whereas non-aggressors develop a conditioned place

39 ion of a 1,2-azaborine BN heterocycle into a CPP scaffold enables facile and selective late-stage fun

40 e and determine the secondary structure of a CPP within cells is critical for clarifying the mechanis

41 e, we report on transcellular transport of a CPP, designated the CL peptide, that increases the deliv

42 Under a CPP paradigm, male BALB/c mice were intraperitoneally in

43 Treatment with systemic morphine abolished CPP to saphenous nerve block, demonstrating control of o

44 increases lHb neuronal firing and abolishes CPP to the intruder-paired context.

45 orophiles as innovative concepts to activate CPPs.

46 nicotine CPP reinstatement without affecting CPP acquisition.

47 e-induced cross-sensitization of amphetamine CPP, DeltaFosB in the NAc and medial prefrontal cortex,

48 P10W, a peptide derived from the amphipathic CPP transportan 10; the second was based on DL1a, a synt

49 data suggest that cell uptake of amphipathic CPPs correlates with their adopted alpha-helix content i

50 Both endometriosis and CPP have significant negative impact.

51 cell type (10T1/2 > HepG2 > HeLa > HEK), and CPP sequence (Transportan > R8 > Penetratin~TAT > Xentry

52 ere exclusive to GABA and homocarnosine, and CPP-115 afforded brain GABA+ concentration changes compa

53 of AMPH-induced locomotor sensitization and CPP.

54 receiving injections of the NMDAr antagonist CPP immediately after four 45-min extinction sessions.

55 iginate from ionpair-pi interactions between CPP and activator implied that replacement of the pi-bas

56 However, accessing bright CPPs with emissions beyond 500 nm remains difficult.

57 Four candidate CPPs were discovered, and further study on one peptide (

58 hat cannot be accomplished with carbonaceous CPPs.

59 We found that after cocaine CPP and abstinence dynorphin attenuated inhibitory input

60 Moreover, after cocaine CPP and abstinence, the VP(VGluT2) input to the aversion

61 but this effect was abolished after cocaine CPP and abstinence.

62 Enhancement of LTP in the VTA and cocaine CPP in behaving rats both require glucocorticoid recepto

63 We report that attenuated cocaine CPP extinction in mice lacking Ca(v)1.2 channels in D1R-

64 ences are affected differentially by cocaine CPP and abstinence.

65 of the dDG, but not in the dCA1, for cocaine CPP extinction.

66 Cav1.2/CaMKII/S831 GluA1 pathway in cocaine CPP extinction, with data supporting contribution of hip

67 g in stress-induced reinstatement of cocaine CPP and provide insight into the impact of dose on the e

68 This stress-induced reinstatement of cocaine CPP depends on type 1 orexin receptors (OX1Rs), type 1 c

69 ing cells resulted in attenuation of cocaine CPP extinction and lack of extinction-dependent changes

70 hippocampus attenuated extinction of cocaine CPP.

71 of the hippocampus for extinction of cocaine CPP.

72 c disinhibition and reinstatement of cocaine CPP.

73 a genetic deletion strategy and the cocaine CPP procedure to first define the contributions of alpha

74 Thus, cocaine CPP followed by abstinence may allow VP(VGluT2) neurons

75 and knockout mice alike all acquired cocaine-CPP and exhibited increased levels of silent synapses af

76 quired for establishing or retaining cocaine-CPP.

77 the favoured candidate for high-conductance CPP single-molecule devices.

78 Changing the conjugated CPP resulted in a pronounced improvement in the antibact

79 a time-kill assay revealed three conjugated CPPs rapidly kill Listeria within 20 minutes without dis

80 A macrocyclic furan-containing CPP precursor was used for the Diels-Alder reaction with

81 rtion and enables more accurate controlling, CPP-based efficient virus-free delivery strategy has bee

82 Cycloparaphenylenes (CPP) can serve as both guest and host in a complex.

83 amolecular chemistries, cycloparaphenylenes (CPPs) have the potential to act as a new class of ligand

84 Here, cycloparaphenylenes (CPPs) are used as conjugated molecular additives to tune

85 al conjugation found in cycloparaphenylenes (CPPs) and other curved pai-surfaces.

86 oriented pai-system of cycloparaphenylenes (CPPs) gives rise to photophysical properties unlike any

87 ass of compounds termed cycloparaphenylenes (CPPs)-shape-persistent macrocycles with built-in cavitie

88 cdA and TcsL, uncovered two new TcdA-derived CPPs.

89 To screen for TcdB-derived CPPs, a panel of synthetic peptides was tested for the a

90 ase (ODC) using low-dose eflornithine (DFMO, CPP-1X), combined with maximal PA export using low-dose

91 was covalently conjugated to five different CPPs.

92 lar" monoterpenes chrysanthemyl diphosphate (CPP), lavandulyl diphosphate (LPP), and trace quantities

93 roduce the intermediate copalyl diphosphate (CPP), along with the more surprising finding of an atypi

94 e (LPP, TcCPS2) and (+)-copalyl diphosphate (CPP, TcCPS4), and three class-I diTPSs producing biforme

95 Further, a distinct CPP can enter cells through many mechanisms, often leadi

96 ween the evidence accumulation process (i.e. CPP) and subjective perceptual experience, suggesting th

97 ry and a basis for developing more efficient CPPs in the future.

98 e present a novel and bright orange-emitting CPP-based fluorophore showing a dramatic 105 nm red-shif

99 Here we show that monocytes engulf CPPs via macropinocytosis, and this process is strictly

100 iana benthamiana identified SdCPS1 as an ent-CPP synthase, which is prevalent in roots and, together

101 s (diTPSs), the ent-copalyl diphosphate (ent-CPP) synthase SdCPS1, and the clerodienyl diphosphate (C

102 ously acquired cocaine and alcohol (ethanol) CPP on subsequent days.

103 In this review, we summarize the existing CPP-based delivery system, emerging landscape of CPP app

104 l cargo to compare delivery capacity of five CPP sequences (Penetratin, R8, TAT, Transportan, Xentry)

105 we report a novel inactivation mechanism for CPP-115, a mechanism-based inactivator that undergoes GA

106 npointed an asparagine residue necessary for CPP activity.

107 We tested plausibility for CPP by combined mathematical modeling, comparison of pre

108 The computed (1)H NMR shifts of the guest CPP are shifted by about 1 ppm upfield relative to their

109 The guest CPP is modestly inclined relative to the plane of the ho

110 y inclined relative to the plane of the host CPP except when the host and guest differ by four phenyl

111 e structures of these partially hydrogenated CPPs were established by X-ray structure analysis, NMR s

112 optimal level to lower ICP without impairing CPP to counteract spaceflight-associated neuro-ocular sy

113 vasive method for lowering ICP and improving CPP for patients with pathologically elevated ICP on Ear

114 tion, and displayed no reward or aversion in CPP/CPA assays, suggesting that analogs might represent

115 However, the mice differed in CPP retention and CP-AMPAR incorporation.

116 ellular uptake of converting the residues in CPPs from l- to d-stereochemistry, but conflicting resul

117 and 17 +/- 4 mmHg; P < 0.0001) and increased CPP (P < 0.01).

118 rheumatoid arthritis (RA) exhibit increased CPP uptake and IL-1beta release in response to CaSR sign

119 the first time, we show that GBP can induce CPP through a dopaminergic-dependent mechanism.

120 cocaine (10 mg/kg, i.p.) was able to induce CPP in Wt but not in NOP (-/-).

121 ticity in the BNST following ethanol-induced CPP and CPA.

122 Ethanol-induced CPP was associated with increased neuronal excitability

123 ed using previously reported ethanol-induced CPP/CPA procedures.

124 receptor antagonist, attenuated GBP-induced CPP.

125 prevented the expression of morphine-induced CPP.

126 solated from SCI rats without TTA-P2-induced CPP (non-responders).

127 solated from SCI rats showing TTA-P2-induced CPP (responders) was ~6 fold greater than the interspike

128 hese results suggest that pregabalin-induced CPP was successfully modulated by CEF which could serve

129 knock-out mice prevented foot-shock-induced CPP reinstatement.

130 In addition, infusing CPP into the infralimbic medial prefrontal cortex (IL-mP

131 Interestingly, CPPs are also observed to improve the contact resistance

132 ating activity than several other well-known CPPs (TAT, penetratin, Pep-1, and TP10).

133 Many CPPs exhibit some sort of structural polymorphism, where

134 Inhibition of CaSR-mediated CPP uptake might be a therapeutic approach to treating R

135 mized to: CPP-1X 750 mg and sulindac 150 mg, CPP-1X placebo and sulindac 150 mg, or CPP-1X 750 mg and

136 Thus, CCS will likely be a minor CPP compliance strategy but may play a larger role under

137 e we use dimeric fluorescence TAT as a model CPP to explore the broader consequences of l- to d-stere

138 oherent Raman microscopy to localize a model CPP-penetratin-and determine its secondary structure in

139 mice were trained using an unpaired morphine CPP design and was absent when morphine was administered

140 Morphine-CPP acquisition increased the activity of the D1R-ERK-CR

141 Morphine-CPP reinstatement was associated with the D2R-mediated h

142 duced reinstatement of extinguished morphine-CPP in mouse models of opioid reward and relapse.

143 [ n]CPP molecules are nested in a unique fashion in the soli

144 ally pai-conjugated cycloparaphenylenes ([ n]CPPs) of various ring sizes ( n = 5-12, where n is the n

145 We predict that disordered [ n]CPPs exhibit hole mobilities as high as 2 cm(2)/(V.s).

146 As a result, the novel spiro[n,n]CPPs showed a remarkable performance as high affinity ma

147 (lemniscal) bismacrocycles, termed spiro[n,n]CPPs.

148 e probed: previously reported hoop-shaped [n]CPPs and a novel family of all-phenylene figure-8 shaped

149 The new CPP 2 exhibits peculiar optoelectronic properties: (i) f

150 LA neurons was sufficient to induce nicotine CPP reinstatement, identifying an anatomically specific

151 the BLA prevented yohimbine-induced nicotine CPP reinstatement without affecting CPP acquisition.

152 ity is necessary for stress-induced nicotine CPP reinstatement.

153 g/kg, i.p.) induce reinstatement of nicotine CPP in a norbinaltorphimine (norBNI, a KOR antagonist)-s

154 naling cascades on reinstatement of nicotine CPP.

155 Notably, CPP forms at a temperature of 90 degrees C, much lower t

156 Notably, CPP thus extinguished cannot be reinstated by drug re-ex

157 The sequence of a novel CPP sequence, termed 'Cupid', was identified from the ge

158 e sequence requirements for developing novel CPPs for transcellular delivery of cargo.

159 NP-[CPP] is formed by PEG-PLA chains modified with a cell pe

160 When loaded with doxorubicin, irradiated NP-[CPP] significantly reduces neovascular lesion size.

161 Here we develop nanoparticles (NP-[CPP]) that can be administered intravenously and allow l

162 er-induced CNV, intravenous injection of NP-[CPP] coupled to irradiation of the eye allows NP accumul

163 p to the CPP inhibits cellular uptake of NP-[CPP].

164 The pharmacodynamic characteristics of CPP-115 remain to be evaluated.

165 nd increase the local interfacial density of CPP on the surface of the cargo.

166 o receive either single daily 80 mg doses of CPP-115 (n=4) or placebo (n=2) for 6, 10, or 14 days.

167 althy subjects receiving oral daily doses of CPP-115 or placebo.

168 cterize the acute pharmacodynamic effects of CPP-115 with additional dose-descending measures.

169 if there was any difference in the impact of CPP in those with vs. those without a confirmed diagnosi

170 based delivery system, emerging landscape of CPP application in stem cell manipulation and reprogramm

171 uisition of FPPase activity for synthesis of CPP, LPP, and MPP.

172 It is observed that the addition of CPPs results in significant improvement in the stretchab

173 d 2,2'-bipyridine units into the backbone of CPPs.

174 er, very little is known about the design of CPPs for efficient transcellular transport.

175 onal materials has driven the development of CPPs as versatile platforms for applications including (

176 Enhanced macropinocytosis of CPPs results in increased lysosomal activity, NLRP3 infl

177 The cross-linked nature of CPPs means that they have permanent intrinsic porosity (

178 d information on the relative performance of CPPs in delivering proteins to cells, specifically the c

179 In our detailed investigation, two series of CPPs were probed: previously reported hoop-shaped [n]CPP

180 ess is known about the fate and structure of CPPs within cells largely due to measurement difficulty.

181 rally associated with an increased uptake of CPPs.

182 al class I (di)terpene synthase that acts on CPP to produce the abietane olefin miltiradiene, but als

183 Here, we focus on CPP mediated delivery of drugs to the tumor sites, deliv

184 this review is to highlight select works on CPPs, including basic structural design principles, vari

185 distinct TF families: one TCP (OsPCF2), one CPP (OsCPP5) and three NIN-like (OsNIN-like2, OsNIN-like

186 distinct TF families: one TCP (OsPCF2), one CPP (OsCPP5) and three NIN-like (OsNIN-like2, OsNIN-like

187 l ionpair-pi interactions afford operational CPP activators in model membranes and cells.

188 compound, Cs(7)(H(4)PO(4))(H(2)PO(4))(8), or CPP, which forms at elevated temperatures from the react

189 0 mg, CPP-1X placebo and sulindac 150 mg, or CPP-1X 750 mg and sulindac placebo once daily for 24 mon

190 ased efficiently from endosomes, while other CPPs are not.

191 Chronic pelvic pain (CPP) affects a significant number of women worldwide.

192 4 potently stabilizes calciprotein particle (CPP) growth, consistently demonstrates low micromolar ac

193 0 nm-sized colloidal calciprotein particles (CPPs).

194 The mean difference between the patients' CPP and their CPPopt was related to outcome for both cal

195 peptide containing cell-penetrating peptide (CPP) and collagen (COLL) domains is designed to undergo

196 e have developed a cell-penetrating peptide (CPP) conjugate of the HIV TAT protein that is fused to a

197 these approaches, cell penetrating peptide (CPP) is promising and affords widely used vector for eff

198 ridize it with the cell penetrating peptide (CPP) that allows for effective penetration of biological

199 ntified as a novel cell-penetrating peptide (CPP) that is able to efficiently internalize into human

200 rotamine (LMWP), a cell penetrating peptide (CPP), insulin showed greatly improved permeability throu

201 , enzyme-triggered cell penetrating peptide (CPP)-mediated systems seem to be a feasible approach.

202 ns modified with a cell penetrating peptide (CPP).

203 Cell penetrating peptides (CPP) have the ability to rapidly internalize across biol

204 be conjugated to cell penetrating peptides (CPP) to overcome challenging delivery barriers.

205 oes into cells by cell-penetrating peptides (CPPs) and the bactericidal activity of antimicrobial pep

206 Although cationic cell-penetrating peptides (CPPs) are able to bind to cell membranes, thus promoting

207 Cell-penetrating peptides (CPPs) are short peptide sequences that can translocate a

208 Cell-penetrating peptides (CPPs) are well established as delivery agents for otherw

209 Many cell-penetrating peptides (CPPs) fold at cell surfaces, adopting alpha- or beta-str

210 antimicrobial and cell-penetrating peptides (CPPs) form amphipathic alpha-helices when bound to lipid

211 TDs), also called cell-penetrating peptides (CPPs), can promote uptake of macromolecules via endocyto

212 Like many cell-penetrating peptides (CPPs), CPMPs enter the endocytic pathway; the difference

213 iii) inclusion of cell penetrating peptides (CPPs).

214 that function as cell-penetrating peptides (CPPs).

215 ify BBB-penetrant cell-penetrating peptides (CPPs).

216 ate arginine-rich cell-penetrating peptides (CPPs).

217 t to a variety of cell-penetrating peptides (CPPs).

218 is conjugation to cell-penetrating peptides (CPPs); however, very little is known about the design of

219 Cell permeating peptides (CPPs) are attracting great interest for use as molecular

220 , and normal CCS under the Clean Power Plan (CPP) and a hypothetical more stringent CO2 emission redu

221 ate that current-perpendicular-to-the-plane (CPP) junctions have three-orders-of-magnitude higher ele

222 Conjugated porous polymers (CPPs) are a class of amorphous polymer networks that are

223 f the broad-band centro-parietal positivity (CPP) and limb-selective beta-band (8-16 and 18-30 Hz) EE

224 G potential (the Centro-Parietal Positivity, CPP) to be a correlate of the accumulation of sensory ev

225 ce accumulation (centro-parietal positivity; CPP) show that predicted confidence affects neural prepa

226 that perfluorinated fatty acids are powerful CPP activators in HeLa cells but not in model membranes.

227 h-pull aromatics should afford more powerful CPP activators.

228 Conditioned place preference (CPP) and saccharin (0.2% w/v) self-administration were a

229 acute morphine-conditioned place preference (CPP) and stress-induced reinstatement of extinguished mo

230 ent of cocaine conditioned place preference (CPP) and the effects of low dose guanfacine on BNST acti

231 cues (ie, the conditioned place preference (CPP) apparatus) triggers a significant decrease in the n

232 In a conditioned place preference (CPP) assay, we observed that menthol plus nicotine produ

233 ion of cocaine conditioned place preference (CPP) in adult male mice.

234 on, of cocaine conditioned place preference (CPP) in male mice increased Cav1.2 L-type Ca(2+) channel

235 codone-induced conditioned place preference (CPP) in rats.

236 y, we used the conditioned place preference (CPP) model to investigate the involvement of the dopamin

237 nduce a strong conditioned place preference (CPP) or aversion (CPA) in rodents.

238 bined with the conditioned place preference (CPP) paradigm to determine the relationship between the

239 sessed using a conditioned place preference (CPP) paradigm.

240 sessed using a conditioned place preference (CPP) paradigm.

241 egabalin using conditioned place preference (CPP) paradigm.

242 Using a conditioned place preference (CPP) reinstatement procedure in mice, we show that both

243 /kg) using the conditioned place preference (CPP) test.

244 Studies using conditioned place preference (CPP) tests of reward indicate that song production in gr

245 d that cocaine conditioned place preference (CPP) training followed by abstinence selectively potenti

246 Combining-conditioned place preference (CPP) with molecular analyses, we investigated the DA D1

247 ion in cocaine-conditioned place preference (CPP).

248 d AMPH-induced conditioned place preference (CPP).

249 ion of cocaine conditioned place preference (CPP).

250 development of conditioned place preference (CPP).

251 or amphetamine conditioned place preference (CPP).

252 uished cocaine-conditioned place preference (CPP).

253 e retention of conditioned place preference (CPP).

254 relief (i.e., conditioned place preference, CPP), revealing the presence of ongoing pain.

255 he mathematical model predicted preferential CPP into cells with lower cell stiffness, expected from

256 determined the cerebral perfusion pressure (CPP) at which the pressure reactivity (PRx or wPRx) was

257 until negative cerebral perfusion pressure (CPP) was obtained.

258 Cerebral perfusion pressure (CPP), calculated as mean arterial blood pressure at midb

259 ) decreases lHb neuronal firing and promotes CPP to the intruder-paired context.

260 We propose CPP as a potentially novel mechanism in mammalian interc

261 By conjugating EEDs to a TAT-PTD/CPP spilt-GFP peptide complementation assay, we were abl

262 We hypothesize "cell-projection pumping" (CPP), in which cytoplasm in retracting cell projections

263 e productive mode of action of arginine-rich CPPs.

264 Our results provide a guide to select CPP for endosomal/lysosomal delivery and a basis for dev

265 In conclusion, we have identified six CPPs from large clostridial toxins and have demonstrated

266 han redispatching under the CPP and stronger CPP, respectively.

267 ent CO2 emission reduction target ("stronger CPP").

268 subsequent 90-min extinction retention test, CPP-treated rats lever pressed less than saline-treated

269 We show here that CPP binding to lipid bilayers, a simple model of the cel

270 ght cleaves DEACM from the CPP, allowing the CPP to migrate from the NP core to the surface, renderin

271 With foreknowledge, the CPP and beta-band signals exhibited a similar gradual bu

272 Without foreknowledge, the CPP exhibited identical dynamics, whereas choice-selecti

273 ation with blue light cleaves DEACM from the CPP, allowing the CPP to migrate from the NP core to the

274 idence accumulation signal (reflected in the CPP amplitude) is mediated by the level of subjective ex

275 pth of insertion or membrane fluidity in the CPP vicinity.

276 w illustrates the role of cholesterol in the CPP/lipids interaction.

277 self-assembly the cargo-induced loss of the CPP affinity to bio-membranes.

278 mics, and proton transport properties of the CPP phase is discussed.

279 NA interference targeting either both of the CPP synthases, TwTPS7v2 and TwTPS9v2, or the subsequentl

280 spectra, giving access to information on the CPP/lipid interaction at a molecular level such as depth

281 persisted up until the delayed response, the CPP dropped toward baseline after peaking.

282 Once accumulated at the targeting site, the CPP modified drug is released from the blockage by a sec

283 This shows that the CPP closely tracks the subjective perceptual evidence, o

284 hment of a DEACM photocleavable group to the CPP inhibits cellular uptake of NP-[CPP].

285 cost effective than redispatching under the CPP and stronger CPP, respectively.

286 dicates that optimal binding occurs when the CPP nanohoops differ by five phenyl rings.

287 hould aid in experimental detection of these CPP planetary orbit complexes.

288 ion of polyhistidine peptides is critical to CPP-mediated protein transduction.

289 improving and developing PNAs conjugated to CPPs to better target intracellular pathogens.

290 e pathways, attachment of cargo molecules to CPPs invariably reduces their cellular uptake.

291 gible adults with FAP will be randomized to: CPP-1X 750 mg and sulindac 150 mg, CPP-1X placebo and su

292 a randomized controlled single-blind trial (CPP 2009-A00346-51).

293 g loaded applications, i.e. enzyme-triggered CPP-mediated systems in drug delivery were reviewed.

294 nt types of applications of enzyme-triggered CPP-mediated systems in tumor imaging were illustrated.

295 An enzyme-triggered, CPP-mediated system would combine these advantages to yi

296 ransistors are subsequently fabricated using CPP/semiconductor composites as active layers.

297 tate and singing behavior, as revealed using CPP tests of song-associated reward.

298 l manipulation and reprogramming, along with CPP contributions to gene editing techniques.

299 Our results suggested that conjugation with CPP followed by encapsulation in MNPs provides an effect

300 People with CPP, regardless of diagnosis, reported moderate to sever