ライフサイエンスコーパス: fluoride

1 oride, sodium monofluorophosphate, or sodium fluoride).

2 mercially available polymer, poly(vinylidene fluoride).

3 combination of oxalyl chloride and potassium fluoride.

4 p to four NH hydrogen-bond donors (HBDs) for fluoride.

5 lium atoms from an atomic lattice of lithium fluoride.

6 ediate that undergoes subsequent trapping by fluoride.

7 by desulfurative fluorination with silver(I) fluoride.

8 clinically relevant concentrations of (18)F-fluoride.

9 tries, attributable to the widespread use of fluoride.

10 valent hNE inhibitor: benzene-1,2-disulfonyl fluoride.

11 Ti(3+), d(1) site, and one type of bridging fluoride.

12 le organic iodides, bromides, chlorides, and fluorides.

13 used functional aryl substituents, including fluorides.

14 associated with the low reactivity of metal fluorides.

15 lization of the corresponding amino sulfonyl fluorides.

16 catalysts for fluorination with alkali metal fluorides.

17 to access both the E and Z isomers of vinyl fluorides.

18 emission tomography (PET) using (18)F-sodium fluoride ((18)F-fluoride) to detect microcalcification m

19 tion 1 h after the injection of (18)F-sodium fluoride ((18)F-NaF) at 248 +/- 10 MBq (mean +/- SD) and

20 Coronary (18)F-sodium fluoride ((18)F-NaF) positron emission tomography (PET)

21 ystal structures, we elaborated arylsulfonyl fluoride 2 to 12, which to our knowledge is the first co

22 showed large beneficial effects compared to fluoride (3.93; 0.34-7.53) with moderate certainty; for

23 Here we study sulfuramidimidoyl fluorides, a class of weak electrophiles that undergo su

24 fluorobenzyl palladium(II) complexes undergo fluoride abstraction followed by 1,1-migratory insertion

25 Silicon-mediated fluoride abstraction is demonstrated as a means of gener

26 study on the general suitability of silicon-fluoride-acceptor (SiFA)-conjugated radiopharmaceuticals

27 oach is presented to access arynes and their fluoride-activated precursors based on Ru-catalyzed C-H

28 on reagents and proceed in the presence of a fluoride activator at 80 degrees C.

29 an-rescan reproducibility of increased (18)F-fluoride activity in coronary atherosclerotic plaque.

30 At the segmental level, baseline (18)F-fluoride activity was an independent predictor of calciu

31 P.Fp(+) (i.e. 1b.Fp(+) ), which is inert to fluoride addition.

32 opening reaction in the presence of aluminum fluoride (AlF(3) ) to create SPEs inside LiNi(0.6) Co(0.

33 d evidence of superiority against placebo or fluorides (amine fluoride, sodium monofluorophosphate, o

34 its four NH groups in hydrogen bonding with fluoride, an arrangement that allows effective phase-tra

35 a non-enzymatic reaction between a sulfonyl fluoride and an amino group.

36 in magnesium flanking a core rich in sodium, fluoride and carbonate ions; this sandwich core is surro

37 luorspar (CaF(2)), the precursor to hydrogen fluoride and fluorine, has embarked on an industrial ini

38 e chloride (K~10(3) ) and to a lesser extent fluoride and iodide ions.

39 route to [(18)F]CF(3)SO(2)NH(4) from [(18)F]fluoride and its application to direct [(18)F]CF(3) inco

40 ance, which unequivocally identifies lithium fluoride and lithium alkylcarbonates as the main chemica

41 tonated form shows considerable affinity for fluoride and perchlorate, which in turn affects the isom

42 Besides fluoride and sulfate, short-chain perfluorinated carboxy

43 AS and suspect screening as well as hydrogen fluoride and total fluorine.

44 group (LG) in covalent reactions of sulfonyl fluorides and arylfluorosulfates.

45 he continuous growth of poorly conducting Li fluorides and carbonates to ensure efficient Li(+) trans

46 ifluoromethyl)sulfur oxyimines from sulfonyl fluorides and iminosulfur oxydifluorides, respectively.

47 tructures and chemical properties of complex fluorides and oxyfluorides.

48 (WFs) are a complex mix of metallic oxides, fluorides and silicates that can cause or exacerbate hea

49 uding nitrocellulose, nylon, poly(vinylidene fluoride), and cellulose.

50 efined Z- and E-alkenyl chlorides, bromides, fluorides, and boronates or Z-trifluoromethyl-substitute

51 PA, prevention alone (diet, plaque removal, fluorides, and fissure sealants).

52 uorination, using first-row transition-metal fluorides, and it overcomes these limitations.

53 We use fluoride- and hydroxide-doping to generate high concentr

54 or non- and microinvasive caries treatment (fluoride- and nonfluoride-based interventions) is to man

55 n-group cations are highly selective for the fluoride anion, which is transported more than 20 times

56 with Mo(6+) coordinated by two cis bridging fluoride anions that are trans to terminal oxide anions.

57 icaries mechanisms of action of arginine and fluoride are distinct.

58 s that the three hydrogen-bond contacts with fluoride are not equal in terms of their contribution to

59 ten leads to "over-reaction", where multiple fluorides are replaced.

60 [(18)F]-labeled aryl fluorides are widely used as radiotracers for positron e

61 sensitivity and DNA vectors enabling use of fluoride as a selection agent.

62 to a variety of (hetero)aryl carboxylic acid fluorides as well as diverse diboron reagents.

63 ng primary, secondary, and tertiary benzylic fluorides as well as unactivated tertiary fluorides, tha

64 ith relaxor-like behavior in poly(vinylidene fluoride), as required for high energy storage density,

65 talytic S(N) Ar reaction of unactivated aryl fluorides at ambient temperature without strong base is

66 Fluoride atoms and methoxy groups were also introduced t

67 olving alkyl-group migration, intermolecular fluoride attack is product- and enantio-determining.

68 owth, which is restored upon introduction of fluoride-based vectors.

69 is proposed to produce beta-poly(vinylidene fluoride) (beta-phase content: ~98%) with relaxor-like b

70 ation experiments, indicating that efficient fluoride binding also occurs in solution.

71 ea catalysts undergo urea isomerization upon fluoride binding and form dynamically rigid trifurcated

72 n/proton exchanger ClC-ec1 and observed that fluoride binds incoming protons within the selectivity f

73 eered P. putida is demonstrated with mineral fluoride both as only fluorine source (i.e. substrate of

74 on measurements, the partial substitution of fluoride by cyanide ligands leads to a marked increase i

75 nt functionality about the benzylic tertiary fluoride by virtue of the diversity of both reaction par

76 -PSMA-11 using direct labeling with aluminum fluoride can be produced in NH(4)OAc, pH 6.9; shows a hi

77 responded strongly to low concentrations of fluoride, carbonate, and acetate ions, weakly to phospha

78 terometallic {Cr(7)Ni} rings, are bound to a fluoride-centered {CrNi(2)} triangle.

79 Fluc family fluoride channels are assembled as primitive antiparalle

80 in solution, but with smaller halide anions (fluoride, chloride, and bromide), the catalysts fold aro

81 s on both the arene and the olefin including fluoride, chloride, trifluoromethyl, ester, nitro, aceta

82 oromethylsulfonyl)imide, and poly(vinylidene fluoride-co-hexafluoropropylene) as the ion exchange gel

83 An ion-gel composed of Poly(vinylidene fluoride-co-hexafluoropropylene), PVDF-co-HFP, a gelling

84 tructure and properties of the carbonic acid-fluoride complex, F(-)(H(2)CO(3)), and its deuterated is

85 ination reactivity of a formally copper(III) fluoride complex.

86 nsight into how the countercation influences fluoride complexation is provided based on NMR data char

87 ity of high-oxidation-state transition-metal fluoride complexes combined with the use of directing gr

88 ynamically rigid trifurcated hydrogen-bonded fluoride complexes that are structurally similar to thei

89 ey revealed the clear relation between water fluoride concentration, and therefore fluoride exposure,

90 Low fluoride concentrations severely inhibit biocontainment

91 s required for the channel to adopt an open, fluoride-conducting conformation.

92 f using tetralactam macrocycles to stabilize fluoride-containing liquid electrolytes within redox dev

93 ified for dental fluorosis were ingestion of fluoride-containing toothpaste, water fluoridation, fluo

94 (test) or (2) toothpaste containing 1450 ppm fluoride (control), and were instructed to brush with th

95 tertiary alkyl bromide, chloride, ester, and fluoride could therefore be easily prepared in only thre

96 chiral microenvironment for enantioselective fluoride delivery to the electrophile.

97 but low control over enantioselectivity for fluoride delivery.

98 A subsequent intramolecular fluoride displacement reaction provides a functionalized

99 This approach utilizes glycosyl fluoride donors and silyl ether acceptors while tolerati

100 ental fluorosis occurs from overingestion of fluoride during tooth formation.

101 covalent bond formation by an aryl sulfonyl fluoride electrophile at a tyrosine residue (Tyr-82) inh

102 molecules, each bearing a sulfuramidimidoyl fluoride electrophile, with human cell lysate, and the p

103 de range of gem-difluoroalkenes through beta-fluoride elimination of the generated alpha-CF(3) carban

104 al approach to O-sulfation by the sulfur(VI) fluoride exchange (SuFEx) reaction between aryl fluorosu

105 f weak electrophiles that undergo sulfur(VI) fluoride exchange chemistry.

106 In enamel cells, fluoride exposure affected the functioning of the ER-loc

107 Fluoride exposure did not alter Ca(2+) homeostasis or in

108 Policies were introduced to reduce excessive fluoride exposure during the period of tooth development

109 Sources of fluoride exposure have been documented in most of the mo

110 dental fluorosis, we analyzed the effects of fluoride exposure in enamel cells to assess its impact o

111 water fluoride concentration, and therefore fluoride exposure, and prevalence and severity of dental

112 irreversible and potentially severe forms of fluoride (F(-)) toxicity such as skeletal fluorosis bein

113 transport various ions of interest, such as fluoride (F(-)), potassium (K(+)), calcium (Ca(++)), and

114 Fluoride facilitates the remineralization of dental hard

115 lyl pyrrole latent nucleophiles with allylic fluorides followed by hydrogenation and diastereoselecti

116 get to increase the S. mutans sensitivity to fluoride for a better prevention of dental caries.

117 The activation of potassium fluoride for nucleophilic fluorination of alkyl halides

118 f the number and magnitude of HB contacts to fluoride for thirteen bisurea catalysts.

119 ary drinks between meals, 4) receive topical fluoride from a health professional, 5) visit the dentis

120 served steps including elution of the [(18)F]fluoride from an anion exchange cartridge with a basic s

121 n site and an industry lab purchasing [(18)F]fluoride from an outside vendor), and provides [(18)F]FD

122 h strength of the C-F bond, the departure of fluoride from metabolic intermediates can be facile.

123 date, the direct preparation of [(18)F]-aryl fluorides from aryl halides remains limited to S(N)Ar re

124 l, and practical procedures to prepare vinyl fluorides from readily available precursors remains a sy

125 click derivatization of the pendant sulfonyl fluoride group in 96 well-plates-demonstrating the versa

126 nucleophilic fluorination with metal alkali fluoride has been accomplished with BINAM-derived bisure

127 Allyl fluorides have been shown to be superior precursors for

128 High-entropy perovskite fluorides (HEPFs) have great potential in electrocatalys

129 e fed low dose fluoride (LF(-)) or high dose fluoride (HF(-)) and given intrauterine injections of li

130 biofluorination are wired to the presence of fluoride (i.e. circumventing the need of feeding expensi

131 total fluorine (TF) analysis, and inorganic fluoride (IF) analysis was applied to disclose the chemi

132 of cyclic enediynes using tetrabutylammonium fluoride in an acetone/water mixture and the investigati

133 ing aluminum nitrate, potassium and ammonium fluoride in an acid medium, with reduction of the reagen

134 e resulted in decreased cell viability under fluoride in both the planktonic state and single-/dual-s

135 nformation on hydrogen-bonding networks with fluoride in solution, as well as how these arrangements

136 stigate experimentally, forms a complex with fluoride in the gas phase.

137 col that allows a single substitution of one fluoride in trifluoromethyl groups with neutral phosphin

138 rovides access to a broad range of aliphatic fluorides, including primary, secondary, and tertiary be

139 mes limit the scope and efficiency of [(18)F]fluoride incorporation chemistry.

140 )) give insight into how multiple H bonds to fluoride influence reaction performance.

141 In contrast, excessive fluoride intake causes dental fluorosis, visually recogn

142 rting ligands, diamagnetic Ni(IV) sigma-aryl fluoride intermediates can be detected spectroscopically

143 ) at super-concentration, leading to lithium fluoride interphase formation, while precipitation of th

144 Fluoride ion (F(-)) is one of the most harmful elements

145 as proposed for the on-site determination of fluoride ion (F(-)) with high sensitivity and accuracy.

146 orination promoted decomposition occurs with fluoride ion acting as a base.

147 Fluoride ion affinity (FIA) calculations reveal a soluti

148 ynthesis of [(18)F]fluoromethane from [(18)F]fluoride ion and then cobalt(III) fluoride mediated gas

149 Biological fluoride ion channels are sub-1-nanometer protein pores

150 ors: Michael addition, enamine addition, and fluoride ion elimination followed by conjugate addition.

151 e efficacy of the dyes as probes, a turn-off fluoride ion probe was prepared from 3C, which consisted

152 s consistent with results showing incomplete fluoride ion release (up to 53% of the F content in AFFF

153 ectrometry-based analysis of metabolites and fluoride ion release experiments.

154 ithin redox devices such as room-temperature fluoride-ion batteries.

155 onged consumption of water contaminated with fluoride ions (F(-)) at concentrations exceeding 1.5 ppm

156 Elevated concentrations of fluoride ions (F(-)) in natural groundwater are a worldw

157 Fluoride ions are highly reactive, and their incorporati

158 ounds, few reactions are able to incorporate fluoride ions directly into alkyl C-H bonds.

159 acid causing cell membrane leakage allowing fluoride ions easy access to urease.

160 s been observed in the presence of acids and fluoride ions, respectively.

161 These results suggest that (18)F-fluoride is a non-invasive imaging biomarker of active c

162 boronates bearing a Z-trisubstituted alkenyl fluoride is disclosed.

163 The ammonium salt tetra-n-butylammonium fluoride is simply admixed with the conjugated polymer p

164 Potassium fluoride (KF) is an ideal reagent for fluorination becau

165 n ascribed principally to stabilization of a fluoride leaving group (LG) in covalent reactions of sul

166 Pregnant mice were fed low dose fluoride (LF(-)) or high dose fluoride (HF(-)) and given

167 Enriching the SEI with lithium fluoride (LiF) has recently gained popularity to improve

168 ium anode is suppressed by forming a lithium fluoride (LiF)-enriched solid electrolyte interphase (SE

169 The (18)F-fluoride ligand bound to microcalcifications formed by c

170 Additionally, the (18)F-fluoride ligand identified micro and macrocalcifications

171 Baseline coronary (18)F-fluoride maximum tissue-to-background ratio correlated w

172 rom [(18)F]fluoride ion and then cobalt(III) fluoride mediated gas phase fluorination.

173 Here, a fluoride-mediated desilylation (FMDS) (11)C-labeling app

174 tasurface of microstructured poly(vinylidene fluoride) membrane, referred to as a "meta-skin" insulat

175 cused chemical screen revealed that the aryl fluoride motif on YJH08 is essential for high-affinity G

176 the interobserver agreement in (18)F-sodium fluoride (NaF) PET/CT for the detection of bone metastas

177 ts, and changes in quantitative (18)F-sodium fluoride (NaF) positron emission tomography/computed tom

178 )F-fluorodeoxyglucose (FDG) and (18)F-sodium fluoride (NaF) uptake in culprit versus nonculprit carot

179 Fluoride negatively affected mitochondrial respiration,

180 cetuximab was performed, and (18)F-aluminium fluoride-NOTA-Z(EGFR:03115) (12 mug, 1.5-2 MBq/mouse) wa

181 ater had been the only significant source of fluoride, now there are many, and this led to an increas

182 insoluble CsF and KF into solution, control fluoride nucleophilicity, and provide a chiral microenvi

183 can be achieved from the free alcohols using fluoride or silanolate, allylic acetate precursors to 5-

184 um salts with in situ formed carboxylic acid fluorides or 2-pyridyl esters under reducing conditions

185 an amine (propargylamine and ethanolamine), fluoride, or a nucleoside monophosphate (uridine monopho

186 in 3 allows for an exclusive selectivity for fluoride over other competing halides.

187 Our results suggest that (18)F-fluoride PET signal in PET-positive, CT-negative regions

188 enerate bioprosthetic valves displayed (18)F-fluoride PET uptake that colocalized with tissue degener

189 sel coronary atherosclerosis underwent (18)F-fluoride PET-computed tomography angiography and compute

190 was to determine if additional (18)F-sodium fluoride PET/CT (NaF PET/CT) improves the prognostic acc

191 This study tested the hypothesis that (18)F-fluoride PET/CT can identify early microcalcifications.

192 Static (18)F-fluoride PET/CT scans were acquired 60 min after injecti

193 t broadly cover metal oxides, chalcogenides, fluorides, phosphides, nitrides, and silicates with spec

194 The authors sought to assess whether (18)F-fluoride positron emission tomography (PET)-computed tom

195 with increased morbidity and mortality.(18)F-fluoride positron emission tomography (PET)/computed tom

196 Coronary (18)F-fluoride positron emission tomography identifies rupture

197 ronary artery disease underwent serial (18)F-fluoride positron emission tomography.

198 or 16 different substituents, by determining fluoride production rates, quantum yields, and half-live

199 id fluoride substitution to generate allylic fluoride products with excellent levels of branched-to-l

200 igh Lewis basicity and small ionic radius of fluoride promote the formation of strong ionic hydrogen

201 rinciple of sensing strategy is based on the fluoride-promoted Si-O bond cleavage of 2-(tert-butyldip

202 [(11) C]carbonyl difluoride over silver(II) fluoride provides easy access to this new synthon in rob

203 phate) (PB2MP) functionalised polyvinylidene fluoride (PVDF) track-etched membranes, PB2MP-g-PVDF, wa

204 focus on materials involving polyvinylidene fluoride (PVDF), and also discussed both their current a

205 R mutant was used for RNA-sequencing and the fluoride related permease gene (frtP) was found as 1 of

206 was constructed and the transcription factor fluoride related transcriptional regulator (FrtR) was id

207 Fluoride release at pH 7 was greatest after 24 h for the

208 echanical properties, biofilm formation, and fluoride release.

209 ubations, while total fluorine (organic plus fluoride) remained constant throughout the incubations.

210 yster shells can be an effective sorbent for fluoride removal, with the added benefit of re-use of a

211 g carbanions to undergo alpha-elimination of fluoride renders this process highly challenging.

212 rategies for unmodified peptides with [(18)F]fluoride require (18)F-labeled prosthetics for bioconjug

213 By harnessing fluoride-responsive riboswitches and the orthogonal T7 R

214 olabeled IL2 variants, namely aluminum (18)F-fluoride-(restrained complexing agent)-IL2 ((18)F-AlF-RE

215 on particle RNA and the Bacillus cereus crcB fluoride riboswitch.

216 In the presence of a highly concentrated, fluoride-rich electrolyte, the inner SEI layer has an el

217 granular corrosion of Ni-Cr alloys in molten fluoride salt at 650 degrees C.

218 scourage the dissolution of Cr in the molten fluoride salts which is widely recognized as the mechani

219 We showcase 2-Substituted-Alkynyl-1-Sulfonyl Fluorides (SASFs) as a new class of connective hub in co

220 Silver diamine fluoride (SDF) is used topically to prevent or arrest de

221 iocontainment strategy leveraging engineered fluoride sensitivity and DNA vectors enabling use of flu

222 hat frtP upregulation led to the increase of fluoride sensitivity.

223 a highly selective, sensitive, and reliable fluoride sensor was then developed.

224 lls and an enamel cell line (LS8) exposed to fluoride showed decreased internal Ca(2+) stores and sto

225 (18)F-fluoride signal amplification derived from microcalcific

226 evidence (SMD; 95% CI): potassium + stannous fluoride (SnF(2)) (3.05; 1.69-4.41), calcium sodium phos

227 eriority against placebo or fluorides (amine fluoride, sodium monofluorophosphate, or sodium fluoride

228 electrospray ionization of an aqueous sodium fluoride solution in the presence of gas-phase carbon di

229 e of an iridium(I) catalyst and nucleophilic fluoride source (Et(3)N.3HF), allylic trichloroacetimida

230 -bromostyrenes, utilizing HF-pyridine as the fluoride source and m-CPBA as the stoichiometric oxidant

231 Using CsF as the fluoride source in CH(3)CN, the N-H benzotriazoles are f

232 or-E behaves as the activating agent and the fluoride source.

233 ith KF, as an inexpensive, abundant and safe fluoride source.

234 t ages 9, 13, 17, and 23 as part of the Iowa Fluoride Study, which has followed a cohort from birth.

235 Single fluoride substitution in trifluoromethylarenes is an ong

236 allylic trichloroacetimidates undergo rapid fluoride substitution to generate allylic fluoride produ

237 to make a prediction on whether a given aryl fluoride substrate favors a concerted or stepwise mechan

238 electrolytes on a hydrophobic polyvinylidene fluoride substrate.

239 of this study was to explore the effects of fluoride supplementation using a mouse model of preterm

240 ound state hydrogen molecules with a lithium fluoride surface.

241 r combo consisting of tannic acid and sodium fluoride (TA-NaF), which exhibits clear synergistic inhi

242 e-containing toothpaste, water fluoridation, fluoride tablets (which were sometimes ingested in areas

243 bisurea catalyst with tetra-n-butylammonium fluoride (TBAF) or CsF.

244 Hydroxide and fluoride terminations are identified, found to be intima

245 triclosan + 2.0% PVM/MA copolymer + 1450 ppm fluoride (test) or (2) toothpaste containing 1450 ppm fl

246 catalytic decarbonylative borylation of acid fluorides that proved applicable to a variety of (hetero

247 ed covalent docking to identify arylsulfonyl fluorides that target a noncatalytic lysine (Lys162) in

248 ic fluorides as well as unactivated tertiary fluorides, that are typically inaccessible by nucleophil

249 ence of external stimuli (tetrabutylammonium fluoride), the organogel of 1 disassembles into sol.

250 In the absence of fluoride, the biocontainment strain exhibits phenotypes

251 erstanding Streptococcus mutans' response to fluoride, the mechanism regulating intrinsic fluoride to

252 agnetic ordering of U(IV) atoms in a complex fluoride through the incorporation of 3 d transition met

253 d electrolyte interphase composed of lithium fluoride, tin, and the tin-lithium alloy is formed, whic

254 35 (33.7%) patients who had increased (18)F-fluoride (tissue-to-background ratio, 2.32 [95% CI, 1.81

255 catalyst system requires tetramethylammonium fluoride (TMAF) and [Fp(THF)][BF(4)] (Fp = Fe(eta(5)-C(5

256 t equilibrium binding of a sulfuramidimidoyl fluoride to a protein can allow nucleophilic attack by a

257 rained linker, which orients an arylsulfonyl fluoride to react rapidly and enantioselectively with Ly

258 t has been demonstrated that the addition of fluoride to the resulted complex induces the release of

259 phy (PET) using (18)F-sodium fluoride ((18)F-fluoride) to detect microcalcification may provide insig

260 was to evaluate whether they are related to fluoride tolerance in S. mutans.

261 fluoride, the mechanism regulating intrinsic fluoride tolerance is not yet clear.

262 n in S. mutans, thus affecting the intrinsic fluoride tolerance.

263 triclosan was more effective than a regular fluoride toothpaste in improving the periodontal clinica

264 hing mechanism involving direct and indirect fluoride transfer from a CF(3) anionoid to TMSCF(3) (1)

265 ormed in situ, allows effective nucleophilic fluoride transfer to a range of primary and secondary al

266 tive of endoplasmic reticulum (ER) stress in fluoride-treated LS8 cells.

267 achieve high EC strength in poly(vinylidene fluoride-trifluoroethylene-chlorofluoroethylene)-based n

268 for determining total (TF) and total soluble fluorides (TSF) in 5 child formula dentifrices (CFD) usi

269 nts, irrespective of the model, measure, and fluoride type (p < 0.001).

270 ssion of sub-15 nm alkaline-earth rare-earth fluoride UCNPs (M(1-x) Ln(x) F(2+x,) MLnF) with a CaF(2)

271 tor AEBSF (4-[2-aminoethyl] benzene sulfonyl fluoride) up-regulated full-length Dicer, both in MM6 ce

272 remained unchanged in segments without (18)F-fluoride uptake (from 46 [16-113] to 49 [20-115] AU; P=0

273 ly increased in coronary segments with (18)F-fluoride uptake (from 95 [30-209] to 148 [61-289] AU; P<

274 , and to categorize increased coronary (18)F-fluoride uptake and determine its reproducibility has ye

275 o investigate the relationship between (18)F-fluoride uptake and progression of coronary calcificatio

276 Areas of (18)F-fluoride uptake are associated with osteopontin, an infl

277 Indeed (18)F-fluoride uptake correlated with deterioration in all the

278 Individuals with increased (18)F-fluoride uptake demonstrated more rapid progression of c

279 Patients with increased (18)F-fluoride uptake exhibited more rapid deterioration in va

280 Specifically, coronary (18)F-fluoride uptake had a high signal to noise ratio compare

281 Conclusions Coronary (18)F-fluoride uptake identifies both patients and individual

282 ale), 116 (63%) patients had increased (18)F-fluoride uptake in at least one vessel.

283 The synthesis of acyl fluorides using the deoxofluorination reaction of carbox

284 electrochemical approach to prepare sulfonyl fluorides using thiols or disulfides, as widely availabl

285 Other potential color centers based on fluoride vacancies with multiple potential charge states

286 are regimen (periodic prophylaxis and serial fluoride varnish applications) appropriate for the manag

287 bent dose) when the initial concentration of fluoride was 10 mg/L.

288 A highly selective recognition of fluoride was achieved through the design of a small hemi

289 the non-invasive imaging radiotracer, (18)F-fluoride, was highly selective for hydroxyapatite deposi

290 , and multifunctional cyclic alkenylsulfonyl fluorides were efficiently prepared from the correspondi

291 A wide range of acyl fluorides were obtained in moderate to excellent yields

292 rious kinds of anions, with the exception of fluoride, which acts as an effective inhibitor.

293 A high quality factor magnesium fluoride whispering gallery mode resonator enables both

294 showed large beneficial effects compared to fluoride with moderate certainty of evidence (SMD; 95% C

295 showed large beneficial effects compared to fluoride with moderate to high certainty.

296 ionic hydrogen bonds in the complexation of fluoride with protic molecules.

297 decarbonylative coupling of carboxylic acid fluorides with diboron reagents to selectively afford ar

298 or-like behavior observed in poly(vinylidene fluoride) with high molecular weight > 534 kg mol(-1), w

299 .F(-)] reveals that the encapsulation of one fluoride, within 3, occurs through NH...F(-) H-bonding w

300 tterbium ions doped within a yttrium-lithium-fluoride (YLF) host crystal.

301 The high efficiency of the hydrogen fluoride zipping makes our approach attractive for the r