ライフサイエンスコーパス: chloride

1 alladium(II) hydroxide and arylpalladium(II) chloride.

2 am and several anions, including nitrate and chloride.

3 s faster in the isomer with the NHC trans to chloride.

4 thermal gelation and the addition of sodium chloride.

5 tion and allosteric activation by low pH and chloride.

6 nt comprising magnesium chloride and choline chloride.

7 already be experiencing negative effects of chloride.

8 corporations of deuterated methyl-D9-choline chloride.

9 deprotonated and then titrated with ammonium chloride.

10 lysis device capable of selectively removing chloride.

11 and other C-O bonds in the presence of aryl chlorides.

12 of electron-deficient alkenes with sulfonyl chlorides.

13 thesis of bisphosphinates starting from acyl chlorides.

14 tones and regioselective acylation with acyl chlorides.

15 their intolerance of halides including aryl chlorides.

16 ling of unactivated alkyl chlorides and aryl chlorides.

17 enging for sulfamoyl chlorides than sulfonyl chlorides.

18 .55% cysteamine hydrochloride + benzalkonium chloride 0.01%) performed better in terms of decreasing

19 nated metal fragments and that they can bind chloride 1 to 2 orders of magnitude stronger than the re

20 In the presence of iron(III) chloride (1.5 equiv) and diorganyl diselenides (1.0 equi

21 diethylphenyl)acenaphtho[1,2-d] imidazolium} chloride (2) is used for the stabilization of the pallad

22 with a series of 5-substituted isophthaloyl chlorides (5-R'C(6)H(3)-2,6-{C(O)Cl}(2)) affords the dip

23 0%), Fe(III) (98%), COD (95%), BOD (94%) and Chloride (78%) was obtained at 15 min by kaolin/ZnO comp

24 n CCDs from aldosterone-treated mice reduced chloride absorption and epithelial sodium channel activi

25 mineralocorticoid receptor ablation reduces chloride absorption in the CCD and indirectly reduces pr

26 We measured CCD chloride absorption, transepithelial voltage, epithelial

27 CH(2)TMS, MgMe(2), and ZnMe(2) proceeds with chloride abstraction and alkane elimination to form the

28 Dp3sam with chloride, acetate and formate as counter ions were emplo

29 ion of hydrophosphorylic compounds in acetyl chloride/acetic anhydride mixture were found by (31)P NM

30 ity (ERH) of potassium sulfate and potassium chloride aerosol as well as the separation RH (SRH) for

31 x: an analogous reaction with toluylsulfenyl chloride affords the cluster [Fe(5) (mu(5) -C)(SC(7) H(7

32 mple, readily-accessible alkyl sulfinyl (IV) chloride allows formation of a trigonal bipyramidal sulf

33 th reduced PS exposure whilst chelerytherine chloride also reduced Yoda1-induced increases in [Ca(2+)

34 ls isostructural to caesium chloride, sodium chloride, aluminium diboride and K(4)C(60) are selected

35 tail-to-head cyclization reactions of neryl chloride analogues.

36 orination intermediate, LCuF, along with its chloride and bromide analogues, LCuCl and LCuBr, were pr

37 inhibitors were also tested, chelerytherine chloride and calphostin C.

38 s deep eutectic solvent comprising magnesium chloride and choline chloride.

39 In the case of chloride and humic acid, the calculated K(A) values of 9

40 II) bromide, nickel(II) chloride, cobalt(II) chloride and iron(II) chloride sheets through the periph

41 to investigate the prognostic value of serum chloride and its association with mortality in cirrhotic

42 rinating reagents by a combination of oxalyl chloride and potassium fluoride.

43 ndings signify the prognostic value of serum chloride and potential inclusion of chloride into future

44 lting anionic hemiaminal with trimethylsilyl chloride and subsequent coupling with nucleophilic reage

45 line chiral derivatization with (S)-naproxen chloride and subsequent preseparation.

46 red third group consisting of cyanobacterial chloride and sulfate ion-pumping rhodopsins, the Mastigo

47 ble with a role in influencing intracellular chloride and thereby neuronal parameters such as membran

48 using the relative variations of Sodium and Chloride and using a neighbouring pristine catchment as

49 ncluding polyester, polypropylene, polyvinyl chloride and vinyl chloride copolymers.

50 Passive reabsorption of chloride and water also increases.

51 s method permits methylation of (hetero)aryl chlorides and acyl chlorides at an early and late stage

52 Alkyl chlorides and aryl chlorides are among the most abundant

53 s-electrophile coupling of unactivated alkyl chlorides and aryl chlorides.

54 C-N coupling of hydrazine with (hetero)aryl chlorides and bromides to form aryl hydrazines with cata

55 ism of the reaction between cyclopropyl acid chlorides and imines to form 1,3-oxazin-4-enones was pro

56 sociated with fatty acid phosphate, sulfate, chloride, and carboxylate ions.

57 tor (HIF), including desferrioxamine, cobalt chloride, and dimethyloxalylglycine, raised NCOA4 messen

58 oxide, cyclodextrin, Citrox, cetylpyridinium chloride, and essential oils.

59 been validated commercially to produce vinyl chloride, and here we show that this facile synthesis me

60 concentration of sodium, potassium, calcium, chloride, and nitrite in urine, accurately quantified us

61 n urine, such as sodium, potassium, calcium, chloride, and nitrite, has significant diagnostic value

62 (polyethylene terephthalate (PET), polyvinyl chloride, and polypropylene carbonate), were identified

63 e-4,5-dicarboxylic acid functionalized Allyl chloride, and significant improvement of its performance

64 t biomarkers including glucose, lactate, pH, chloride, and volume.

65 ilies of valuable organic iodides, bromides, chlorides, and fluorides.

66 bromides and electron-deficient (hetero)aryl chlorides, and significantly reduced reaction times (10

67 rotein, encoded by SLC26A3, a key intestinal chloride anion exchanger, has recently been identified a

68 ocyclization reaction, and surprisingly, the chloride anion had a negative template effect in opposit

69 ansported more than 20 times faster than the chloride anion.

70 oup of the lactam ring, hydrogen bond to the chloride anion.

71 ded antiparallel beta-sheet dimer that binds chloride anions.

72 abscisic acid (ABA), Ca(2+), protons (H(+)), chloride (anions), the glutathione redox potential, and

73 Alkyl chlorides and aryl chlorides are among the most abundant and stable carbon

74 Alkyl chlorides are bench-stable chemical feedstocks that rema

75 Sulfonyl chlorides are inexpensive reactants extensively explored

76 This process utilizes rhodium(III) chloride as a commercially available, high-oxidation sta

77 rogen bond donor and methyltriocthylammonium chloride as a hydrogen bond acceptor.

78 E) modified with 1-ethyl-3-methylimidazolium chloride as an ionic liquid (IL) and NiFe(2)O(4)-rGO nan

79 d by using glutathione (GSH) and copper (II) chloride as precursors via a facile hydrothermal method.

80 s solution using dioctadecyldimethylammonium chloride as the structure-directing agent.

81 the etherification of aryl bromides and aryl chlorides as well as sulfonates with a wide range of pri

82 Herein, we present a pyrrole and chloride assisted photochromic structure to address this

83 a homogeneous alkalization process driven by chloride-assisted glycidol rupture (the Epoxide Route) a

84 A second infusion of methyl-D9-choline chloride at day 5 clearly indicated continued activity o

85 thylation of (hetero)aryl chlorides and acyl chlorides at an early and late stage with broad function

86 yte-based molten lithium-molybdenum-iron(II) chloride battery (denoted as Li-Mo-FeCl(2) ) operated at

87 bial agents triclosan (TCS) and benzalkonium chloride (BC) can contribute to bacterial resistance to

88 tor directly regulates the intercalated cell chloride/bicarbonate exchanger pendrin is unclear, as ar

89 4% yield, by atomic manipulation on a sodium chloride bilayer on Cu(111) at 5 K, and imaged by high-r

90 The chloride binding constants for thioureas and croconamide

91 art (the protonated DMAP) in the presence of chloride binding Schreiner's thiourea have been discusse

92 The structure reveals that the chloride-binding mode is more similar to HRs than chlori

93 ctions in Li- and Na-containing sulfides and chlorides by applying thermodynamic analyses based on a

94 role for this cocatalyst to recycle an allyl chloride byproduct generated in the course of the reacti

95 ng ionic liquid (1-butyl-3-methylimidazolium chloride ([C(4)mim]Cl)).

96 Chloride can be toxic, and water quality guidelines have

97 these tactics, aryl boronic esters and aryl chlorides can be carried through the reaction untouched.

98 osed to increasing concentrations of choline chloride (CC) and D,L-methionine (DLM).

99 hloride (OMe) and 4-(trifluoromethyl)benzoyl chloride (CF(3)) were studied.

100 C(2)Cl(4)), chloroform (CHCl(3)), and methyl chloride (CH(3)Cl), are gases not regulated by the Montr

101 Accounting for chloride changes resulted in substantial alterations in

102 unction of intracellular transporters of the Chloride Channel (CLC) family in eukaryotes: not only co

103 AtCLCa (Arabidopsis thaliana Chloride Channel a) is a vacuolar NO(3) (-)/H(+) exchang

104 C-RPE fully restored BEST1 calcium-activated chloride channel activity and improved rhodopsin degrada

105 rated that in mouse, genetic inactivation of chloride channel Ano1/Tmem16a compromises airway barrier

106 ate the involvement of the calcium-activated chloride channel anoctamin 1 (ANO1) in esophageal prolif

107 We tested the effect of the chloride channel blocker 9-anthracenecarboxylic acid (9A

108 ) transmembrane conductance regulator (CFTR) chloride channel has been argued to be critical for effi

109 LRP3 activation, this was still sensitive to chloride channel inhibitors, suggesting there are additi

110 The ClC-2 chloride channel is expressed in the plasma membrane of

111 ally overlaps with the cohort expressing the chloride channel OCA2.

112 CLC-2 is a voltage-gated chloride channel that is widely expressed in mammalian t

113 ate that Hodor is a pH-sensitive, zinc-gated chloride channel that mediates a previously unrecognized

114 mate transporter and also as glutamate-gated chloride channel, the chloride conductance being large e

115 tein Kinase A (PKA)-mediated facilitation of chloride channel-7 (ClC-7) delivery to lysosomes which r

116 F transmembrane conductance regulator (CFTR) chloride channel.

117 d of five subunits arranged around a central chloride channel.

118 These results suggest that chloride channels (or transporters) provide the main pat

119 ominated by the activity of Ca(2+)-activated chloride channels (TMEM16A), including the cystic fibros

120 les for Ano1 in organogenesis, and show that chloride channels are essential for mammalian airway for

121 mportant step in NLRP3 activation, but which chloride channels are involved is still unknown.

122 tive allosteric modulator of glutamate-gated chloride channels found in nematodes and insects.

123 pports allosteric binding to glutamate-gated chloride channels similar to ivermectin.

124 is the accessory subunit of the human ClC-K chloride channels, which are expressed in both the kidne

125 While the influence of chloride (Cl(-)) and natural organic matter on Cu specia

126 trophin family of calcium (Ca(2+))-activated chloride (Cl(-)) channels, which mediate the influx and

127 to lysosomes which reverses markedly lowered chloride (Cl(-)) content in PSEN1 KO lysosomes.

128 reaction of oxidized soybean oil with acetyl chloride clarified assignments of proton signals, confir

129 us acid (HOCl), chlorine (Cl(2)), and nitryl chloride (ClNO(2)) reached part-per-billion by volume le

130 changes in expression of GABA(A)R or of the chloride co-transporter KCC2, but rather with inhibition

131 cally defined nickel(II) bromide, nickel(II) chloride, cobalt(II) chloride and iron(II) chloride shee

132 actions are catalyzed by a ruthenium hydrido chloride complex (1), supported by a chelating P^N ligan

133 In contrast, the selectivity of the chloride complex closely matched that of the catalytic r

134 ation of a hydrazine-bound arylpalladium(II) chloride complex to give an arylpalladium(II) hydrazido

135 diaryl hydrazine was lower than that of the chloride complex, as well as the catalytic reaction.

136 l pathways for the in situ formation of lead chloride compounds are discussed.

137 targeted dendritic inhibition where dynamic chloride compromised the ability of inhibition to offset

138 ory acidosis, electrodialysis reduced plasma chloride concentration by 26 +/- 5 mEq/L within 6 hours

139 Consequently, dynamics in the neuronal chloride concentration can alter the functional properti

140 We hypothesized that the reduction of plasma chloride concentration could be an alternative strategy

141 sing the load from 200 W to 100 W, the sweat chloride concentration decreased from 27.7 +/- 10.5 to 1

142 In this work, we recorded real-time sweat chloride concentration for 12 healthy subjects in three

143 rces and processes governing the groundwater Chloride concentration in agricultural catchments, using

144 exercise load from 100 W to 200 W the sweat chloride concentration increased from 12.0 +/- 5.9 to 31

145 lations revealed that progressive changes in chloride concentration mean that the neuronal input-outp

146 n r(2) of 0.86 for predictions of the median chloride concentration observed at each lake.

147 e information from 2773 lakes to predict the chloride concentration of all 49 432 lakes greater than

148 chemically-induced sweating where the sweat chloride concentration was almost independent of sweat r

149 nificant formation of Cl(2)(g) even when the chloride concentration was more than 2 orders of magnitu

150 Increasing specific conductance (SC) and chloride concentrations [Cl] negatively affect many stre

151 Almost 2000 lakes are predicted to have chloride concentrations above 50 mg L(-1) and should be

152 22.7% of recreational lakes in Ontario have chloride concentrations between 5 and 40 mg/L suggesting

153 coordinated with large shifts in proton and chloride concentrations during the synaptic vesicle cycl

154 f NaCl for road deicing has caused increased chloride concentrations in lakes near urban centers and

155 redictors with the largest influence on lake chloride concentrations were low and medium intensity de

156 ts showed that Daphnia were sensitive to low chloride concentrations with decreased reproduction and

157 lso as glutamate-gated chloride channel, the chloride conductance being large enough for EAAT5 to ser

158 t United States are at risk of anthropogenic chloride contamination, but there is little knowledge of

159 polypropylene, polyvinyl chloride and vinyl chloride copolymers.

160 ios of the K(+)/Cl(-) transporters potassium-chloride cotransporter 2 (KCC2) and sodium-potassium-chl

161 ne point variation in the neuronal potassium-chloride cotransporter 2 (KCC2).

162 crease in the expression ratio of the cation-chloride cotransporters (CCCs) NKCC1 and KCC2.

163 The secondary active cation-chloride cotransporters (CCCs) utilize the existing Na(+

164 t factors determining local levels of cation-chloride cotransporters remain elusive.

165 foaming dental gel containing cetylpridinium chloride (CPC), hydrogen peroxide (H(2) O(2) ), sodium b

166 showed normal surface expression but reduced chloride currents, and accelerated whole-cell desensitiz

167 alf-time associated with the change in sweat chloride, defined as the time at which the concentration

168 Both the hydride and chloride derivatives, (X=H(-) , Cl(-) ), underwent excha

169 PSCs, but endosulfan sulfate and tributyltin chloride did not.

170 a kinetic analysis of reductively triggered chloride dissociation, revealing that chloride loss is 1

171 In this work, 311 cesium chloride double perovskites (Cs(2)BB'Cl(6)) were selecte

172 r understanding the computational effects of chloride dynamics on dendritically targeted synaptic inh

173 ibitory synapses interact with intracellular chloride dynamics to modulate the input-output function

174 s transported 10 times more efficiently than chlorides (EC(50) =0.47 mum).

175 Chloride efflux is suggested as an important step in NLR

176 ased on a silver wire with a layer of silver chloride electroplated onto the surface.

177 tion of aquaporin water channels by mercuric chloride eliminates XA21-mediated dehydration survival,

178 iomerically enriched tertiary alkyl bromide, chloride, ester, and fluoride could therefore be easily

179 Sorbic chloride evaporate without condensation, on dynamic heat

180 Although hyperfiltration restores sodium and chloride excretion it imposes added physical stress on t

181 that activating a hemiacetal with a sulfonyl chloride, followed by treating the resultant glycosyl su

182 de-based perovskites and then employ organic chlorides for dynamic treatment, inserting and in situ i

183 the catchment scale, about 60 percent of the Chloride found in groundwater originates from fertilizer

184 Currents were recorded in chloride-free Ringer's solution with low or high concent

185 adsorption of Cr(VI), Fe(III), COD, BOD, and chloride from tannery wastewater were investigated.

186 water, polyglycerol polyricinoleate, sodium chloride, gallic acid and pH 5.0 sodium acetate buffer s

187 n of sodium azide with 2H-azirine-2-carbonyl chlorides, generated by the Fe(II)-catalyzed isomerizati

188 the reaction of [Ni(I)(IMes)(2)Cl] with aryl chlorides generating additional aryl radicals and [Ni(II

189 of a bis(arylethynyl phenylurea) host with a chloride guest in eight solvents spanning E(T)(30) value

190 mophysical results, the solvent with choline chloride had the most compact fluid structure.

191 ophile coupling of aryl chlorides with alkyl chlorides has remained a challenge.

192 (19) F NMR titrations with chloride highlight that the HBeXB analogue exhibits stro

193 n an N-alkoxyphthalimide-based oxidant and a chloride hydrogen atom transfer catalyst.

194 Here, we report that local abundance of the chloride importer NKCC1 and timely emergence of GABAergi

195 gar, ascorbic acid in vitamin C tablets, and chloride in soy sauces and saline inhalation solutions w

196 ng, specifically the concentration of sodium chloride in the immediate vicinity of the wound.

197 es from the droplets, solutes such as sodium chloride in the media become more concentrated.

198 Trapping the sulfinyl chlorides in situ with a variety of nitrogen nucleophile

199 oline supplementation (ChS; 5.0 g/kg choline chloride) in two generations (Gen) of APP/PS1 mice.

200 ogy was applied to a variety of (hetero)aryl chlorides including biologically relevant derivatives.

201 We found that it reduces ferric-chloride-induced experimental thrombosis in mice and sup

202 use hemophilia model, when assayed as ferric chloride-induced thrombosis.

203 Hyperreabsorption of sodium and chloride induces tubuloglomerular feedback from the macu

204 ted with thionyl chloride to form a sulfinyl chloride intermediate.

205 A potential permeation pathway for chloride intersects with the glutamate binding site.

206 of serum chloride and potential inclusion of chloride into future cirrhosis prognostic scores.

207 xazolo[5,4-b]pyridines treated with aluminum chloride into synthetically hard-to-reach benzo[c][1,7]n

208 irus (HCMV) and identified the voltage-gated chloride ion channel inhibitor 4,4'-diisothiocyano-2,2'-

209 ctance regulator (CFTR) gene, encoding for a chloride ion channel.

210 ofiling ion flux through human intracellular chloride ion channels using live-cell based techniques,

211 n aqueous media is particularly sensitive to chloride ion concentration and propose that this sensiti

212 n the Pieta indicates the conditions of high chloride ion concentrations (i.e., activities) and/or lo

213 ](-2) with AlCl(3) and (2) coordination of a chloride ion to a coordinatively unsaturated vanadium ce

214 motif, which is involved in the binding of a chloride ion.

215 ation by the nucleophilic olefin facilitates chloride ionization and thereby circumvents simple elimi

216 e active transport of sodium, potassium, and chloride ions across cell membranes.

217 ial generated by the transport of sodium and chloride ions across the skin.

218 he lumen is dependent on apical secretion of chloride ions, most notably by the CFTR channel, which h

219 opening of unsymmetrical phenonium ions with chloride ions.

220 Serum chloride is independently and inversely associated with

221 eaction of naphthoquinone with arenesulfonyl chlorides is revealed.

222 lectropositive hydrogen face can co-ordinate chloride (K~10(3) ) and to a lesser extent fluoride and

223 between diorganyl diselenides and iron(III) chloride leading to the formation of 4-methylene-3-(orga

224 ropose that this sensitivity originates from chloride ligand displacement by hydroxide or H(2)O at th

225 ggered chloride dissociation, revealing that chloride loss is 1000 times faster in the isomer with th

226 Ammonium chloride-mediated trifluoromethylthiolation of p-quinone

227 What is more, trisubstituted Z-alkenyl chloride moiety can be accessed with similar efficiency

228 educing, with high pH (>7.5) and high sodium/chloride (Na/Cl) ratios resulting from cation exchange.

229 ng and those of two Hofmeister salts, sodium chloride (NaCl) as kosmotrope and sodium thiocyanate (Na

230 on the sample of electron irradiated sodium chloride (NaCl) crystals, a well-studied sample with low

231 le of SnCl(4) and TiCl(4) as Lewis acids and chloride nucleophiles.

232 odel predictions had an r(2) of 0.94 for all chloride observations, and an r(2) of 0.86 for predictio

233 the hydrolysis reactions of 4-methoxybenzoyl chloride (OMe) and 4-(trifluoromethyl)benzoyl chloride (

234 e found that the observed effects of dynamic chloride on neuronal output were mediated by changes in

235 n blood, and the in vivo fate of neat (64)Cu-chloride or (64)Cu-CA003 were determined to prove whethe

236 ell culture medium was adjusted using sodium chloride or water.

237 ed with this process, large concentration of Chloride originating from rain was found only in these a

238 PEM comprising poly(diallyldimethylammonium chloride) (PDADMAC) and poly (sodium 4-styrenesulfonate)

239 synaptic inhibition is primarily mediated by chloride-permeable Type A GABA receptors.

240 The presence of lead chloride phases in the Pieta indicates the conditions of

241 Choline chloride:phenol-based DES showed the best results.

242 with various Pb compounds (i.e., carbonate, chloride, phosphate [P], or sulfate) to convert native P

243 ed mono-alpha-arylation of acetone with aryl chlorides, pivalates, and carbamates has been achieved f

244 ion and by the metabolic byproducts of vinyl chloride pollutants.

245 tion of polystyrene, polyethylene, polyvinyl chloride, polypropylene, and poly(methyl methacrylate) i

246 ling shows can be explained by intracellular chloride processing.

247 iNP), a common plasticizer used in polyvinyl chloride products, exhibits endocrine-disrupting capabil

248 The chloride-proton exchanger CLC-7 plays critical roles in

249 drochloride (PubChem CID: 66449); Poly(vinyl chloride) (PubChem SID: 24864273); Tricresyl phosphate (

250 hy this point mutation can convert the MastR chloride pump into a proton pump but cannot in HRs.

251 Chloride-pumping MastR contains in its ion transport pat

252 ide-binding mode is more similar to HRs than chloride-pumping rhodopsins, but the overall structure m

253 archaeal halorhodopsins (HRs) and bacterial chloride-pumping rhodopsins, have been structurally char

254 lular side more similar to BR than the other chloride pumps.

255 predict plasticizer emission from polyvinyl chloride (PVC) products, based on group contribution met

256 ally, blank (undoped) plasticized poly(vinyl chloride) (PVC) membranes mounted into an electrode body

257 Extracorporeal chloride removal by electrodialysis proved to be feasibl

258 y to correct acidemia through extracorporeal chloride removal by electrodialysis.Methods: Ten swine (

259 tions with a series of nine different cation chloride salts as a function of salt concentration.

260 The presence of the rare lead chloride salts cotunnite (PbCl(2)) and challacolloite (K

261 However, we find that the addition of chloride salts dramatically improves ROMP conversion and

262 Increases in CFTR chloride secretion also induced YAP signaling and cellul

263 hBE cells, as demonstrated by a recovery of chloride secretion and apical membrane conductance.

264 that the ASO is more effective at recovering chloride secretion in our assay than ivacaftor, the pote

265 ing adenosine induced a robust CFTR-mediated chloride secretory response together with cAMP-mediated

266 suggesting there are additional and specific chloride sensing and regulating mechanisms controlling N

267 ) chloride, cobalt(II) chloride and iron(II) chloride sheets through the peripheral coordination of s

268 s, and small stellate cells, the site of the chloride shunt conductance, with these AQPs localizing t

269 )O(2) layers in Bi(2)O(2)Se and the terminal chloride sites that produce the van der Waals gap in BiO

270 colloidal crystals isostructural to caesium chloride, sodium chloride, aluminium diboride and K(4)C(

271 ensor was suspended in a sterile 0.9% sodium chloride solution and placed in a water bath at 37 degre

272 out aqueous ROMP in the presence of various chloride sources such as NaCl, KCl, or tetrabutylammoniu

273 This sodium chloride-specific wound detection mechanism is independe

274 Chloride-substituted variants of the Lindqvist vanadium-

275 reduction is more challenging for sulfamoyl chlorides than sulfonyl chlorides.

276 halen-2-ylmethyl)phenylamino] cyclopropenium chloride (TNTPC) displayed a strong photophysical profil

277 etal sulfinate which is reacted with thionyl chloride to form a sulfinyl chloride intermediate.

278 with diorganyl dichalcogenides and iron(III) chloride to give selectively three different types of co

279 reatment, inserting and in situ immobilizing chlorides to blue-shift and stabilize the emission.

280 oselective isomerization of acyclic cinnamyl chlorides to strained cyclopropanes.

281 entral for understanding proton, sodium, and chloride transport mechanisms of microbial rhodopsins.

282 system hereditary disease caused by abnormal chloride transport.

283 cotransporter 2 (KCC2) and sodium-potassium-chloride transporter (NKCC1).

284 had significantly reduced expression of the chloride transporter, KCC2, suggesting less effective GA

285 that depends on the regulated expression of chloride transporters NKCC1 and KCC2.

286 the arene and the olefin including fluoride, chloride, trifluoromethyl, ester, nitro, acetate, cyanid

287 approach for the methylation of (hetero)aryl chlorides using nickel/photoredox catalysis wherein trim

288 Results indicated that ~4.3% of the initial chloride was converted to inorganic byproducts (free Cl(

289 Serum chloride was independently associated with 180-day morta

290 :2:3 M ratio), XoCH, and citric acid:choline chloride:water (1:1:6 M ratio), CiCH.

291 gro-food field were studied: xylitol:choline chloride:water (1:2:3 M ratio), XoCH, and citric acid:ch

292 s have been characterized: d-glucose:choline chloride:water (GCH) and d-glucose:citric acid:water (GC

293 ces such as NaCl, KCl, or tetrabutylammonium chloride, we show that diblock copolymers can be readily

294 r(VI), 91% Fe(III), 91% COD, 89% BOD and 73% Chloride were removed by kaolin under the same condition

295 While the changes in sweat chloride were statistically significant, there was no co

296 salts used as food preservatives and sorbic chloride were submitted to thermal analysis in order to

297 ng an alkyne, an alpha,beta-unsaturated acid chloride, which serves as both the alkene and carbon mon

298 The second is structurally bound chloride with delta(37)Cl values averaging 7.3 +/- 3.5 p

299 ped, the cross-electrophile coupling of aryl chlorides with alkyl chlorides has remained a challenge.

300 The mild borylation of alkyl bromides and chlorides with bis(neopentylglycolato)diborane (B(2)neop