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1 nteraction energies of dimethylphosphate and tetramethylammonium.
2 tants were also estimated in the presence of tetramethylammonium.
3 competitive with a small cholinergic ligand, tetramethylammonium.
4 sis ALF5 cDNA in yeast confers resistance to tetramethylammonium.
5 tely, we demonstrate that the combination of tetramethylammonium 2,6-dimethylphenoxide and sulfuryl f
6 functionalized polyacetylene analogues poly(tetramethylammonium 2-cyclooctatetraenylethanesulfonate)
7 rs, a 1H NMR observable leading electrolyte, tetramethylammonium acetate, is employed here to better
10 ptor ligands it was found that block by CCh, tetramethylammonium and phenyltrimethylammonium can be a
12 When residue 430 was Phe, the effects of tetramethylammonium and tetrapropylammonium were not alt
13 affinities of three agonists, acetylcholine, tetramethylammonium, and succinyldicholine 170-560-fold.
14 molecules were observed for all ions except tetramethylammonium, and the BIRD results indicate that
15 , extracellular tetraethylammonium (TEA) and tetramethylammonium application produces potent, voltage
17 as nonclathrate structures are indicated for tetramethylammonium as well as ions at the other cluster
18 in the real-time iontophoresis method using tetramethylammonium, as well as earlier radiotracer meth
19 size of the quaternary ammonium; the smaller tetramethylammonium blocked with similar properties, whe
20 ons of phase-transfer catalysis (CHCl3, KOH, tetramethylammonium bromide), with sonication, gives exc
21 methanol the tetrakis(benzoxazines) complex tetramethylammonium cation within the cavity, and the ca
22 represent metal ions, tetrabutylammonium and tetramethylammonium cations were studied to represent qu
23 um chloride (moderate ion-lipid binding) and tetramethylammonium chloride (low ion-lipid binding) sol
25 dolomite were exposed to sodium chloride and tetramethylammonium chloride (TMACl) aqueous solutions w
29 s, locked nucleic acid substituted dT's, and tetramethylammonium chloride salts were characterized.
30 tion for several different analytes, namely, tetramethylammonium chloride, tetrabutylammonium chlorid
33 xic propargyl alcohol (corrosion inhibitor), tetramethylammonium (clay stabilizer), biocides or stron
34 r dynamics simulations of the simple ligand, tetramethylammonium, crossing this bottleneck region are
35 3)(-), OH(-), tetrabutyl-, tetrapropyl-, and tetramethylammonium, Cs(+), Na(+), Li(+), H(+), Ba(2+),
36 ted only through L- and R-type channels, and tetramethylammonium currents were observed only in L-typ
39 erent agonists (acetylcholine, nicotine, and tetramethylammonium) does not discriminate between these
41 f phenols with sulfuryl fluoride (SO2F2) and tetramethylammonium fluoride (NMe4F) via aryl fluorosulf
45 ion of either N-methyl-D-glucamine- Cl(-) or tetramethylammonium for Na(+) and by lumen addition of 5
47 t of sodium in the perfusate with choline or tetramethylammonium greatly attenuated ERK activation by
48 methylformamide dimethylacetal (DMF-DMA) and tetramethylammonium hydroxide (TMAH) as methylating agen
50 NO3, KNO3, tetrasodium pyrophosphate (TSPP), tetramethylammonium hydroxide (TMAH)), soil-to-reagent r
52 e replace conventional ammonium hydroxide by tetramethylammonium hydroxide (TMAH, a much stronger bas
53 centrations of the small cationic surfactant tetramethylammonium hydroxide (TMH), when present alone,
55 n of hafnium-peroxo-sulfate films in aqueous tetramethylammonium hydroxide enables extreme UV lithogr
57 In situ thermal hydrolysis/methylation with tetramethylammonium hydroxide was necessary for the diff
58 d to improve separation through the use of a tetramethylammonium hydroxide-sodium hydroxide gradient.
60 ) head group analogs, dimethyl phosphate and tetramethylammonium ions, shows that the ion hydrodynami
62 ECS volume fraction (alpha) in vivo has been tetramethylammonium iontophoresis, a technically challen
65 tion, Shaker IR becomes permeable to Na+ and tetramethylammonium-positive (TMA+), signaling deformati
68 has been synthesized by a rapid reaction of tetramethylammonium superoxide and LiClO4 in solution, a
70 ia postsynthetic cation exchange with either tetramethylammonium, tetraethylammonium, or tetrabutylam
74 ablished real-time iontophoresis method with tetramethylammonium (TMA(+)) to measure three diffusion
75 vorable desolvation free energy reported for tetramethylammonium (TMA(+)), a frequently utilized surr
76 chain lengths ranging from 1 to 16 carbons: tetramethylammonium (TMA) clay; decyltrimethylammonium (
77 (6)O(15)(6-) in relation with the ability of tetramethylammonium (TMA) to form an adsorption layer ar
78 from the behaviour of the monovalent cation tetramethylammonium (TMA), a commonly used diffusion pro
82 centration of the extracellular space marker tetramethylammonium (TMA+) in the intact cat eye using d
83 ceptors activated by acetylcholine (ACh+) or tetramethylammonium (TMA+) were examined at the single-c
85 a mass range of 60-146 amu (trimethylamine, tetramethylammonium, trimethylethylammonium, N,N-dimethy
86 nophoretically induced diffusion profiles of tetramethylammonium, using ion-selective microelectrodes
87 e cell surface because the impermeant ligand tetramethylammonium was as efficacious as nicotine in el
88 y, secondary, and tertiary amines as well as tetramethylammonium with 19-21 water molecules were inve
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