ライフサイエンスコーパス: caged

1 Here we report Peroxy-Caged-[(18)F]Fluorodeoxy thymidine-1 (PC-FLT-1), an oxid

2 Photoactivation of nonfluorescent NQMP-caged 3-allyloxyfluorescein produces a highly emissive f

3 Caged nucleotides (caged-ADP and caged-ATP) were used to initiate nucleotid

4 The activity assay results suggest that the caged-ADP may interact with PGK substrate binding site(s

5 le PGK activity decreased in the presence of caged-ADP, the activity was not influenced by the additi

6 ase of caged glutamate and a newly developed caged AEA (anandamide), together with rapid [Ca2+]i meas

7 ctivation was examined using photolysis of a caged agonist, carboxynitrobenzyl-tyrosine-[Leu(5)]-enke

8 Chemical tools for optopharmacology include caged agonists and antagonists and reversibly photoswitc

9 gh activation kinetics can be assessed using caged agonists, deactivation kinetics are obscured by sl

10 The new caged alanine derivative will provide a useful tool for

11 ification of dozens of protein biomarkers in caged amphipods (Gammarus fossarum).

12 Carboxynitroveratryl-naloxone (CNV-NLX), a caged analog of the competitive opioid antagonist NLX, w

13 A corresponding caged analog of the sensor has been prepared, which is r

14 Opening of the coadded hairpin releases the caged analyte sequence, resulting in the dendritic RCA-i

15 s among unexplored inorganic crystals beyond caged and layered structures.

16 Ru(II) center, the nitriles of complex 2 are caged, and 2 does not act as a potent enzyme inhibitor.

17 entrality and hubness parameters in the home-caged animals.

18 Photolysis of a caged antagonist, carboxynitroveratryl-naloxone (caged n

19 Aldehydes and ketones caged as 4-(2,5-dihydroxyphenyl)-1,3-dioxolanes are effi

20 m infrared spectroscopy and UV photolysis of caged ATP.

21 Caged nucleotides (caged-ADP and caged-ATP) were used to initiate nucleotide binding to P

22 tivity was not influenced by the addition of caged-ATP.

23 nm, optically selective uncaging of DEAC450-caged biomolecules at 900 nm may allow facile two-color

24 Two-photon excitation (2PE) of "caged" biomolecules represents a powerful method to inve

25 Importantly, the caged-BK platform provided the first quantification of i

26 In summary, the caged-BK probe is a powerful tool to identify reactivity

27 The caged-BK probe was utilized to monitor cysteine reactivi

28 To overcome this limitation, a caged bromomethyl ketone (BK) electrophile was developed

29 surface coordinated by the ribose 3'-OH and caged by arginine and lysine side chains is a putative m

30 phous solids whose constituent particles are caged by their neighbours and thus cannot flow.

31 Biological messengers can be "caged" by adding a single photosensitive group that can

32 Moreover, photolysis of caged Ca elicits an inward current of similar size, time

33 In contrast, photolysis of caged Ca(2+) (o-nitrophenyl-EGTA) in astrocytes led to n

34 ncreasing [Ca(2+)](i) by flash photolysis of caged Ca(2+) also accelerated replenishment.

35 duced by flash-induced Ca(2+) release from a caged Ca(2+) buffer), which we had reported previously.

36 Photolysis of a caged Ca(2+) compound was used to characterize the depen

37 om extrasynaptic sources or by photolysis of caged Ca(2+) in astrocytes.

38 Photolysis of caged Ca(2+) in astrocytic endfeet ensheathing the vesse

39 l closure tissues, as UV-mediated release of caged Ca(2+) leads to cell contraction.

40 Photolysis of caged Ca(2+) loaded specifically into astrocytes evoked

41 otropic glutamate receptors or photolysis of caged Ca(2+) produced dilation of penetrating arterioles

42 ificial elevation of intracellular Ca(2+) by caged Ca(2+) release agents sensitizes hair cells to the

43 Accordingly, we applied flash photolysis of caged Ca(2+) to activate BK channels and determine their

44 uorometry and UV photolysis of intracellular caged Ca(2+), we optically resolved VSD activation promp

45 es of release, evoked by flash-photolysis of caged Ca(2+): exocytotic capacitance changes from indivi

46 Furthermore, localized photorelease of caged Ca2+ near the nuclear envelope resulted in a local

47 Using photolysis experiments of caged Ca2+, we demonstrate that asynchronous release dis

48 asing internal [Ca2+] by rapid photolysis of caged Ca2+.

49 ne capacitance together with photorelease of caged-Ca2+ and membrane depolarization to study exocytos

50 alized calcium transients with photolysis of caged calcium induced rapid outgrowth of axonal processe

51 The caged calcium probe o-nitrophenyl EGTA and UV uncaging w

52 d during activation in situ by photolysis of caged calcium using bifunctional fluorescent probes in t

53 We developed a "caged calcium" molecule by conjugation of BIST to a Ca(2

54 used this chromophore to synthesize DEAC450-caged cAMP and found this probe was very stable toward a

55 Localized UV photolysis of caged cAMP triggered gradients of PKA-mediated phosphory

56 upled receptor stimuli and UV photolysis of "caged" cAMP.

57 these questions, we used flash photolysis of caged-cAMP (DMNB-cAMP) to provide high temporal resoluti

58 The local photolysis of caged carbachol demonstrated that the functional express

59 Using local photolysis of caged carbachol, a broad-spectrum cholinergic agonist, w

60 Prepared caged carbons could regain their emission only through i

61 Caged carbonyl compounds are prepared by their acetaliza

62 S release kinetics from a series of isomeric caged-carbonyl sulfide (COS) compounds, including thioca

63 The ability of the "caged" ceramide 1-phosphate analogues to release the bio

64 Photolysis of caged-cGMP enhanced current through Ca(2+)-activated K(+

65 n control samples where either UVA light, or caged-chelator is absent.

66 d intracellular LIP following irradiation of caged-chelator-treated cells, but not in control samples

67 ntracellular Ca(2+) elevation through either caged chelators or pharmacological inhibitors of Ca(2+)

68 ecules loaded with a photocleavable peptide (caged Class II MHC molecules) enabled synchronous and ve

69 Here, we present caged collagen mimetic peptides (CMPs) that can be photo

70 kinetics of opioid signaling we developed a caged competitive antagonist that can be quickly photore

71 of the pair of radicals forming the solvent-caged complex is caused by the reduced stability (high r

72 When coordinated as the caged complex, copper has diminished reactivity to produ

73 hole substrate, or the substrate pieces in a caged complex.

74 The caged compound has a major absorption band with a maximu

75 validate that the inhibitory activity of the caged compound is dependent on exposure to light.

76 have recently utilized a new ruthenium-based caged compound, ruthenium-bipyridine-triphenylphosphine-

77 photolysis of many widely used nitroaromatic caged compounds (e.g., 4-carboxymethoxy-5,7-dinitroindol

78 mooth muscle cells using local photolysis of caged compounds and Ca2+ imaging.

79 mit UV light locally, for photoactivation of caged compounds and, in particular, used for photo-contr

80 Caged compounds are light-sensitive probes that function

81 Caged compounds are molecules rendered functionally iner

82 Since many nitroaromatic caged compounds are two-photon active at 720 nm, optical

83 Photosensitive caged compounds have enhanced our ability to address the

84 Photolysis of caged compounds is a powerful tool for studying subcellu

85 ed to striatal cholinergic interneurons, the caged compounds were photolyzed in an chromatically orth

86 Such cloaked caged compounds will enable the study of the signaling o

87 We combined local photolysis of caged compounds with fluorescence imaging to visualize m

88 To test this hypothesis without using caged compounds, force responses and individual sarcomer

89 I describe important examples of widely used caged compounds, their design features and synthesis, as

90 ents and the loading with indicator dyes and caged compounds.

91 hange and a pulsed laser system for uncaging caged compounds.

92 th sufficient sensitivity to 2PE for use in "caged" compounds.

93 s (skilled reaching, unskilled reaching, and caged control).

94 A photosensitive caged copper complex has been prepared from a tetradenta

95 oxymethyl ester); (ii) locally photolyzing a caged coumarin in one cell of a coupled cell pair to rel

96 s and photochemical properties of a coumarin-caged cyclic RGD peptide and demonstrate that uncaging c

97 ion, a conjugate between the dicyanocoumarin-caged cyclic RGD peptide and ruthenocene, which was sele

98 We designed a protein that includes a caged cysteine and a buried disulfide.

99 Saturation of transporters by photolysis of caged D-aspartate failed to elicit transporter currents

100 The substrate, a caged D-luciferin-galactoside conjugate, must first be c

101 N-protected p-hydroxyphenacyl (pHP) ammonium caged derivatives at 313 nm releases primary and seconda

102 is- (photo-DIBOD, 1) and mono-cyclopropenone-caged dibenzocyclooctadiynes (MC-DIBOD, 5) allows for se

103 In the caged diffusion model, the vesicles diffuse in small cir

104 verage number of cooperative duplexes, these caged dimers constitute the first example of cooperative

105 ly route to a variety of discrete cyclic and caged disulfide structures, which can then be kineticall

106 This is the first example of a caged DNA decoy for the photochemical regulation of gene

107 ntisense agents through the preparation of a caged DNA phosphoramidite and its site-specific incorpor

108 xed but rather maintained within ellipsoidal caged domains, similar to eukaryotic interphase chromoso

109 lly by directly characterizing flows using a caged dye imaging method.

110 To facilitate conjugation of the caged dye to the substrate of interest via click chemist

111 tion in vivo, we developed a bioconjugate of caged dye, named dextran-CANPE-HCC, for imaging cell cou

112 er pipet spritzing and photolytic release of caged effectors, each is limited in key respects.

113 Three months after the spill, caged embryos at oiled sites showed sublethal cardiac to

114 The network acts as a caged entrapment for lithium metal that prevents dendrit

115 egy for the construction of a profluorescent caged enzyme is described.

116 s and carbonyls from loop 6 to stabilize the caged enzyme-substrate complex.

117 a polluted section of the river for a 28 day caged exposure.

118 tumor cell line) were microinjected with the caged FAK peptide and locally photoactivated using a foc

119 ch decays to [Fe(3+)-O-Fe(3+)] precursors of caged ferritin biominerals.

120 s of Lygus spp. up to 30-fold in whole-plant caged field trials.

121 PCL-1 is a boronic acid-caged firefly luciferin molecule that selectively reacts

122 the separation capillary by photolysis of a caged-fluorescein label using the 351-364 nm irradiation

123 We describe a method based on a caged fluorescent molecule that can act as a chemical tw

124 ZE) based upon photophysical activation of a caged, fluorogenic label covalently attached to the targ

125 Vinyl ether caged fluorophores and tetrazine partners are conjugated

126 s tetrazine reactivity to unmask vinyl ether caged fluorophores spanning the visible spectrum, includ

127 espread used indicator of live bacteria is a caged form of carboxyfluorescein in which 3' and 6' hydr

128 Here we report that photolysis of a double-caged form of the second messenger inositol 1,4,5-trisph

129 rs, which hold TIM in a catalytically active caged form.

130 izontal lineNOR' are of interest as prodrug (caged) forms of the bioeffectors nitric oxide (NO) and n

131 We developed a caged GABA (gamma-aminobutyric acid), which, when combin

132 d application of a practically useful doubly caged GABA analog, termed bis-alpha-carboxy-2-nitrobenzy

133 njugation of a large, neutral dendrimer to a caged GABA probe we introduce a "cloaking" technology th

134 ght penetration from an LED and diffusion of caged GABA to quickly terminate intense focal seizures.

135 tiated response to laser photostimulation of caged GABA when placed in the nRT.

136 GABA), has been limited by the propensity of caged GABAs to interact with GABA receptors.

137 trifluoromethylated p-hydroxyphenacyl (pHP)-caged gamma-aminobutyric acid (GABA) and glutamate (Glu)

138 ysiological recording, photolytic release of caged glutamate and a newly developed caged AEA (anandam

139 also used laser scanning photostimulation of caged glutamate and whole cell recordings to map excitat

140 Photolysis of caged glutamate evoked GABAergic IPSCs and/or depolarizi

141 o acid carrier 1) through photo-release from caged glutamate generated a transient inward current, as

142 ed laser scanning photostimulation (LSPS) of caged glutamate in conjunction with whole-cell patch-cla

143 the preBotC using holographic photolysis of caged glutamate in medullary slices from neonatal mice.

144 nation with minimal and maximal stimulation, caged glutamate photolysis, and single axon tracing.

145 we used laser-scanning photostimulation with caged glutamate to characterize the spatial distribution

146 l apical dendrites using focal photolysis of caged glutamate triggered abnormally prolonged plateau p

147 d), which, when combined with an appropriate caged glutamate, allows bimodal control of neuronal memb

148 e were stimulated by using the photolysis of caged glutamate, and in vitro whole-cell patch-clamp rec

149 -photon calcium imaging, flash photolysis of caged glutamate, and patch-clamp electrophysiology in co

150 ial CSF (23 degrees C) containing 100 microM caged glutamate, APV (2-amino-5-phosphonovaleric acid),

151 Here, using fast 3D two-photon imaging and a caged glutamate, we challenge this classical view by dem

152 Using laser-pulse photolysis of caged glutamate, we determined the pre-steady-state kine

153 Using two-photon photolysis of caged glutamate, we found that activation of stubby dend

154 recordings, and scanning photostimulation of caged glutamate, we report first that principal neurons

155 receptor responses using focal photolysis of caged glutamate.

156 each genotype following brief photolysis of caged glutamate.

157 or specifically by local flash photolysis of caged glutamate.

158 Under physiological conditions, DECM-caged glycine is water soluble and stable.

159 ental results demonstrated that neither DECM-caged glycine nor its byproduct inhibits or activates hu

160 w photolabile precursor of glycine (coumarin-caged glycine) are reported.

161 Calcium release using caged gPIP2 was inhibited by the addition of single-cage

162 PgammaS) in solution, and caged GTPgammaS or caged GTP loaded on the RhoA.RhoGDI complex to show that

163 iotriphosphate) (GTPgammaS) in solution, and caged GTPgammaS or caged GTP loaded on the RhoA.RhoGDI c

164 We used photolysis of caged phenylephrine, caged guanosine 5'-O-(thiotriphosphate) (GTPgammaS) in s

165 ate a fluorescence response and also release caged H2S, thus addressing challenges of analyte homeost

166 at bristles with ethyl groups mounted onto a caged heterotricyclic core.

167 ional alterations of eight selected genes in caged honey bees exposed to different concentrations of

168 n (Kcat and kcat/Km), DFP decay, and protein-caged hydrated ferric oxide accumulation decreased in fe

169 drug discovery, and entertains the classical caged hydrocarbon systems potentially missing from the c

170 ds, and reptiles that maintain their nucleus caged in a network of intermediate filaments.

171 At the Dhaka Zoo, multiple NHP species are caged in close proximity.

172 ion of fathead minnows (Pimephales promelas) caged in four Nebraska, USA watersheds - the Niobrara an

173 osphotriesterase (a bioremediation catalyst) caged in GSBs and isolate a 20-fold faster mutant in les

174 tem consists of the analyte-sequence that is caged in the stem region and a single-stranded loop doma

175 benzyl trimethylammonium hydroxide (PVBTAH) caged in ZIF-8 is synthesized in steps of chloro-monomer

176 NAzyme) linked to a G-rich domain, which is "caged" in the complex structure, is assembled on Au-coat

177 sign of a hairpin structure that includes a "caged" inactive G-quadruplex sequence.

178 d one-fourth of the HRP-mimicking DNAzyme in caged, inactive configurations are used as functional el

179 be a concise, modular synthesis of InsP7 and caged InsP7.

180 nonhydrolyzable IP(3), and by photolysis of caged IP(3) in the MN.

181 Inside cells, the caged IP(3) is inert until activated by two-photon excit

182 ormer describes the organic synthesis of the caged IP(3), which requires 12 d, and the latter an appl

183 aded with the Ca(2+) indicator Fluo-4/AM and caged-IP(3).

184 By focally photolyzing a novel caged IP3 compound in dendritic spines, we find that pai

185 of single-caged IP3, suggesting that single-caged IP3 is an antagonist of calcium release.

186 Unexpectedly, single-caged IP3 led to less release in somata and was ineffect

187 Spine photolysis of double-caged IP3 led to local calcium release.

188 energy with higher cooperativity for double-caged IP3 than for conventional single-caged IP3, consis

189 isphosphate (IP3) receptors by photolysis of caged IP3 The rate of Ca(2+) removal from the cytosol wa

190 ouble-caged IP3 than for conventional single-caged IP3, consistent with a chemical two-photon effect.

191 PIP2 was inhibited by the addition of single-caged IP3, suggesting that single-caged IP3 is an antago

192 Flash photolysis of caged IP3/GPIP2 (glycerophosphoryl-myo-inositol 4,5-bisp

193 receptors stimulated with IP3 released from caged-IP3 .

194 siologically relevant doses of UVA, such as "caged-iron chelators", may provide dose- and context-dep

195 The caged kinase displays analogous behavior in living cells

196 Here, a new lanthanide-chelating NMR probe, Caged Lanthanide NMR Probe-7 (CLaNP-7), is presented.

197 An acid-degradable polymer-caged lipoplex (PCL) platform consisting of a cationic l

198 , and in vivo imaging applications of Copper-Caged Luciferin-1 (CCL-1), a bioluminescent reporter for

199 t the synthesis and characterization of iron-caged luciferin-1 (ICL-1), a bioluminescent probe that e

200 ynthesis, and in vivo applications of Peroxy Caged Luciferin-1 (PCL-1), a chemoselective bioluminesce

201 lish this approach, we have developed Peroxy Caged Luciferin-2 (PCL-2), a H(2)O(2)-responsive boronic

202 sualizing cellular networks, we developed a "caged" luciferin that produces light only when cells are

203 through the site-specific installation of a caged lysine amino acid.

204 We employed caged major histocompatibility complex molecules to gene

205 Caged male and female FHMs were deployed at a Great Lake

206 Ferritin biominerals are protein-caged metabolic iron concentrates used for iron-protein

207 Here we describe a strategy for the use of a caged metabolic precursor that is activated for cellular

208 HC products loaded with conditional ligands (caged MHC molecules) provides a fast and straightforward

209 ational change that locks the substrate in a caged Michaelis complex that provides optimal stabilizat

210 ianion activation by stabilization of active caged Michaelis complexes may be generalized to the many

211 The caged molecule is stable and releases InsP7 only on irra

212 manipulations, as exemplified by the use of caged morpholino (cMO) oligonucleotides to inactivate ge

213 Spectrally differentiated caged morpholino oligonucleotides (cMOs) and wavelength-

214 d antagonist, carboxynitroveratryl-naloxone (caged naloxone), blocked the current induced by a series

215 Modularly clickable polymer-caged nanobins (PCNs) were prepared from liposome templa

216 enes; however, the formation of these carbon-caged nanomaterials still remains a mystery.

217 By photolyzing caged neurotransmitter in brain slices we can generate p

218 These caged neurotransmitters are currently the most chemicall

219 Thus, the synthesis of dinitroindolinyl-caged neurotransmitters is within the scope of a modestl

220 ray of strategies, including photorelease of caged neurotransmitters, engineered light-gated receptor

221 Caged neurotransmitters, in combination with focused lig

222 Photoactivatable "caged" neurotransmitters allow optical control of neural

223 ng two-photon activation of an intracellular caged NMDA receptor antagonist (tc-MK801), we found that

224 oscopy and laser-triggered NO release from a caged NO compound, we found that both free hemoglobin an

225 gh tissue phantoms and in vivo activation of caged nucleic acids were also accomplished.

226 Caged nucleotides (caged-ADP and caged-ATP) were used to

227 ity assays were performed in the presence of caged-nucleotides.

228 present investigation used photolysis of two caged opioid ligands to examine the kinetics of MOR-indu

229 Caged (or bridged) bicyclic structural elements offer a

230 350 nm irradiation of a cyclopropenone caged oxo-dibenzocyclooctyne (photo-ODIBO) biotin yields

231 lculations, grows rapidly with the number of caged p-H(2) molecules and is a significant fraction of

232 This caged pair reacts mainly via internal return with a rate

233 drazone to (1)O(2) leading to an ion-radical caged pair.

234 For both methods and for all the radical caged pairs investigated, there were no observable heavy

235 n can be efficiently performed both with the caged peptide and with its ruthenocenoyl bioconjugate re

236 farnesyltransferase; irradiation of the NDBF-caged peptide in the presence of the enzyme resulted in

237 Photolysis of this caged peptide in the squid giant presynaptic terminal ca

238 onjugate reveals great potential for DEAdcCE-caged peptide sequences as selective drug carriers in th

239 es the DEACM group without affecting the NPE-caged peptide.

240 We used photolysis of caged phenylephrine, caged guanosine 5'-O-(thiotriphosph

241 c force decay upon release of phosphate from caged phosphate was previously interpreted as a signatur

242 Although studies with NPE-caged phosphoamino acids have provided valuable informat

243 Exposure of DEACM- and NPE-caged phosphopeptides to 420 nm light selectively releas

244 h lacks the temporal control afforded by the caged phosphopeptides.

245 7-(diethylamino)coumarin-4-yl]methyl (DEACM)-caged phosphorylated serine, threonine, and tyrosine bui

246 Microinjection of a non-caged phosphorylated tyrosine 397 FAK peptide into migra

247 ing 'click' chemistry to couple biotin to a 'caged' photocleavable (PC) guanosine monophosphate (GMP)

248 We allocated 48 caged populations initiated with homozygous GA and WT ad

249 3-3%) suggests that photolysis of 200 microm caged precursor is sufficient for full PKA activation.

250 a sensitizing antenna from a nonsensitizing caged precursor.

251 of firefly luciferin from two complementary caged precursors that can be unmasked by different bioch

252 e been extended to allow the introduction of caged proteins into cells by permeabilization or microin

253 ver, the chemical or genetic construction of caged proteins is nontrivial, with subsequent laborious

254 Analogous to self-caged proteins, installation of this linker shifts the e

255 Light-activatable ("caged") proteins have been used to correlate, with exqui

256 ording is combined with UV photolysis of NPE-caged proton.

257 o muscle contraction and that the release of caged protons is sufficient to induce muscle contraction

258 c and protein-based photoactivatable probes, caged QDs can confer increased spatial and temporal reso

259 ovel optical properties, we have synthesized caged quantum dots, which are nonluminescent under typic

260 products evolve from initial formation of a caged radical intermediate [Fe(IV)=O *NO(2)].

261 O proceed through the same [Fe(IV)=O *NO(2)] caged radical intermediate and lead to similar outcomes.

262 decomposition in water and the nature of the caged radical pair.

263 Subsequent processes include solvent-caged radical recombination to afford the major aminatio

264 gery control squirrels were presented with a caged rattlesnake pre- and postsurgery.

265 II directly or through photo-release of the caged Rho kinase inhibitor also reduced the rate of VE-c

266 st bioadhesion, were internally labeled with caged rhodamine to make the particles photoactivatable.

267 and a late-stage cyclization to complete the caged ring scaffold.

268 ferent approaches were investigated with the caged RNA molecules: the light-regulation of catalytic R

269 bitor of Rho kinase, Rockout, to generate a 'caged Rockout' derivative.

270 d a synthetic approach to the preparation of caged secondary amines by acid-catalyzed rearrangement o

271 transmission model, in which guinea pigs are caged separately, the oseltamivir-resistant viruses tran

272 This probe is the first example of a "caged" Si-rhodamine, exhibits higher photon counts compa

273 ons have been limited to the use of only one caged species in a single experiment.

274 us elevation of intracellular Sph levels via caged Sph leads to a significant and transient calcium r

275 rization of small molecular equivalents of a caged Src kinase.

276 In the 'caged' state, the sODN blocked hybridization of the asOD

277 line-earth complexes prefer a highly compact caged structure with both phenyl rings providing cation-

278 product of the tight framework of the rigid caged system.

279 ons, are akin to those of rattling guests in caged-systems.

280 A caged T7 RNA polymerase was expressed in cells with an e

281 exemplify the utility of this amino acid, we caged the nuclear localization sequences (NLSs) of nucle

282 orpholino-based antisense reagents have been caged through oligonucleotide cyclization, enabling phot

283 e was developed through the incorporation of caged thymidine nucleotides into a DNA-based logic gate.

284 However, most caged transmitters are, surprisingly, severe antagonists

285 HPLC is used to purify the caged transmitters at the end of the syntheses.

286 ation experiments on the recently discovered caged type superconductor Y5Rh6Sn18 ( TC= 3.0 K).

287 w (Pimephales promelas), a small-bodied fish caged upstream and downstream of a local wastewater trea

288 combination with 1- or 2-photon excitation, caged vanilloids are a powerful tool for probing morphol

289 oton excitation with red light (720 nm), the caged vanilloids can be photoreleased in situ to activat

290 The two caged vanilloids, Nb-VNA and Nv-VNA, are photoreleased w

291 synthesis and biological application of two caged vanilloids: biologically inert precursors that, wh

292 ovarian carcinoma (SKOV3) cells with an NDBF-caged version of a farnesylated peptide followed by UV i

293 However, the development of caged versions of the chief vertebrate inhibitory neurot

294 ter male mosquitoes can efficiently suppress caged wild-type mosquito populations, providing the foun

295 An N-azidoacetylmannosamine derivative caged with a peptide substrate for the prostate-specific

296 /6J female mice were randomly assigned to be caged with an unlocked (U) or locked (L) running wheel b

297 e cycles of CIH mimicking OSAS in humans, or caged with room air (handled controls [HC]).

298 of alcohols, phenols, and carboxylic acids "caged" with the (3-hydroxy-2-naphthalenyl)methyl group r

299 of alcohols, phenols, and carboxylic acids "caged" with the 2,5-dihydroxybenzyl group or its naphtha

300 which MP(TVCV) and SYTA directly interacted caged within ER membrane.

301 were observed at later ages (when mice were caged without access to running wheels).