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1       In this study, we conjugated GALA with lauryl and palmitoyl fatty acid tails as model hydrophob
2                                            N-Lauryl- and N-myristoyl-GCAP1 activated RetGC in a simil
3 aterial, folic acid-conjugated carboxymethyl lauryl chitosan (FA-CLC), and superparamagnetic iron oxi
4 ecular dynamics simulations performed on the lauryl derivative, bound to a short strand of DNA in aqu
5                   Inclusion of the detergent lauryl dimethylamine oxide (LDAO) improves protease and
6 f CF1 respond differently in the presence of lauryl dimethylamine oxide (LDAO) in the assay medium.
7 of Mg2+ during assay, and less stimulated by lauryl dimethylamine oxide (LDAO).
8 hondria displays a far-UV CD spectrum (in 1% lauryl dimethylamine oxide at pH 6-8) similar to that of
9 ylamine oxide, whereas this concentration of lauryl dimethylamine oxide inhibits the mutant complex b
10 n the presence of the zwitterionic detergent lauryl dimethylamine oxide, increasing concentrations of
11 ld-type complex is stimulated 4-fold by 0.1% lauryl dimethylamine oxide, whereas this concentration o
12    The nonionic detergent polyoxyethylene 10 lauryl ether (C12E10) proved to be unique in its ability
13 lized from the membrane by polyoxyethylene-9-lauryl ether and purified by DEAE-Sepharose CL-6B column
14  C-100, Triton X-100, and polyoxyethylene-10-lauryl ether did not interfere with any of the four beta
15                                   At pH 5.5, lauryl-GALA was shown to form transmembrane pores with a
16                                              Lauryl-GALA was tolerated well by SJSA-1 osteocarcinoma
17 resence of l-ascorbic acid, was inhibited by lauryl gallate, propyl gallate, protocatechuic acid ethy
18  the presence of cyclododecanone accumulated lauryl lactone, 12-hydroxylauric acid, and/or DDDA depen
19 domains of mouse TMEM16A in nanodiscs and in lauryl maltose neopentyl glycol as determined by single-
20                             The structure in lauryl maltose neopentyl glycol has one Ca(2+) ion resol
21 branes upon light activation, solubilized in lauryl maltose neopentyl glycol, and purified with a com
22 complex I using the branched-chain detergent lauryl maltose neopentyl glycol.
23        Suspensions of bovine rhodopsin in 2% lauryl maltoside detergent were treated with Cu(phen)(3)
24 uch as C(12)EO(8), octyl glucoside, SDS, and lauryl maltoside initiate membrane lysis after reaching
25 orbance changes produced after excitation of lauryl maltoside pigment suspensions with 7 ns laser pul
26 ure photoexcitation of bovine rhodopsin in a lauryl maltoside suspension.
27 om 30 ns to milliseconds after photolysis of lauryl maltoside suspensions of artificial visual pigmen
28 mes from 1 to 128 micros after photolysis of lauryl maltoside suspensions of rhodopsin prepared from
29 5, octyl glucoside, octyl thioglucoside, and lauryl maltoside, with high recovery of proteins and pep
30               To test this idea, we purified lauryl maltoside-solubilized Aer protein by His-tag affi
31  fabricated in fused-silica capillaries from lauryl methacrylate (LMA) and ethylene glycol dimethacry
32 hemistry and were further copolymerized with lauryl methacrylate via a simple one-step free radical p
33                A series of oil-miscible poly(lauryl methacrylate) brush-grafted silica and titania NP
34 hacrylate (BzMA) is polymerized using a poly(lauryl methacrylate) macromolecular chain transfer agent
35 2-x quantum dots into photo-polymerized poly(lauryl methacrylate), we obtain freestanding, colourless
36 e nanoLC separation of peptides using a poly(lauryl methacrylate-co-ethylene dimethacrylate) monolith
37 th an IC50 of 0.05 muM, followed by dodecyl (lauryl) protocatechuate with an IC50 of 0.06 muM.
38 mogeneity by extraction with the detergent N-lauryl sarcosinate.
39 ulfide bonds for their maintenance in sodium lauryl sarcosine- and sodium dodecyl sulfate-insoluble c
40    0.025% all-trans retinoic acid, 5% sodium lauryl sulfate (irritant control), or vehicle were appli
41 ippings and (iii) skin pre-exposed to sodium lauryl sulfate (SLS) were used to assess the penetration
42              HaCaT cells treated with sodium lauryl sulfate (SLS), a model irritant, were used to exa
43 terials included slight irritants: 5% sodium lauryl sulfate (SLS), polyoxyethylene glycol monoalkyl e
44 rushiol and by the irritant chemicals sodium lauryl sulfate and PMA.
45 tch tested with the specific allergen sodium lauryl sulfate as an irritant, and appropriate controls.
46 ard water had significantly increased sodium lauryl sulfate deposits.
47 bination of photomechanical waves and sodium lauryl sulfate enhances the efficiency of transdermal de
48 n of each participant was washed with sodium lauryl sulfate in water of varying hardness levels and c
49  exposed to photomechanical waves and sodium lauryl sulfate showed that the lacunar spaces expanded s
50 following all-trans retinoic acid and sodium lauryl sulfate treatments, with all-trans retinoic acid
51 r dimensions was observed when 1% w/v sodium lauryl sulfate was added to the coupling medium.
52 amphiphilic CPEs (octyl glucoside and sodium lauryl sulfate, respectively), by measuring the flux of
53 ound (US) and/or a chemical enhancer (sodium lauryl sulfate--SLS) relative to untreated skin (the con
54 lammonium chloride/pentanol/D(2)O and sodium lauryl sulfate/octanol/brine lamellar systems.

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