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1 ter the substrate has been precipitated with trichloroacetic acid).
2 , commonly used alcohols, and mild acids (5% trichloroacetic acid).
3 oacetic acids (HAA): dichloroacetic acid and trichloroacetic acid.
4 ter clarifying the sample by the addition of trichloroacetic acid.
5 s are driven by aliquots of a chemical fuel, trichloroacetic acid.
6 f the deblocking reagent prepared from solid trichloroacetic acid.
7 er of silicone oil into a denser solution of trichloroacetic acid.
8 hrome P450Betamicro-3 was accomplished using trichloroacetic acid.
9  self-aggregating, acidic, and soluble in 5% trichloroacetic acid.
10 preparation was performed by extraction with trichloroacetic acid 5% and solid phase extraction clean
11                                              Trichloroacetic acid also demonstrated an increased numb
12           Antimicrobials were extracted with trichloroacetic acid and chromatographic separation was
13 Two other methods of precipitating proteins (trichloroacetic acid and phenol-ether) both exhibited va
14 d: 420 mum particle size, extraction with 5% trichloroacetic acid and three extractions.
15 methanol, acetonitrile, perchloric acid, and trichloroacetic acid and ultrafiltration approaches usin
16 cluding ultrafiltration, precipitation using trichloroacetic acid, and a direct in vivo measurement b
17   Prior to MSPE, the sample was treated with trichloroacetic acid, and the APs derivatized with aceti
18 mide, the protein was then precipitated with trichloroacetic acid, and the precipitate was separated
19  The metabolites released by extraction with trichloroacetic acid are recovered and quantitatively de
20                     During brief exposure to trichloroacetic acid at 0 degree C, significant amounts
21 AA5: chloroacetic acid, dichloroacetic acid, trichloroacetic acid, bromoacetic acid, and dibromoaceti
22 tively, azogelatin, which is precipitated by trichloroacetic acid, can be used.
23                           On the addition of trichloroacetic acid (CCl(3)CO(2)H)(19,31-33) fuel(19,34
24 ioxide laser resurfacing or Jessner solution/trichloroacetic acid chemical peel).
25 stereo- and regioselective epoxide formation/trichloroacetic acid cleavage to generate differentiated
26 with those obtained by use of directly added trichloroacetic acid (conventional synthesis).
27 ogenesis or mere carbon exchange between the trichloroacetic acid cycle and the gluconeogenic pathway
28 conclude that at least 2 HAAs (dichloro- and trichloroacetic acids, DCAA and TCAA) are always present
29 e pretreatments examined was provided by the trichloroacetic acid deproteinization procedure.
30                             In this work the trichloroacetic acid extracts of salmon backbones, heads
31            However, due to its solubility in trichloroacetic acid, gelatin is not suited to "in-solut
32                                      Urinary trichloroacetic acid has been the leading candidate expo
33 oxyl-[32P]CoA followed by precipitation with trichloroacetic acid indicates that inactivation correla
34                                              Trichloroacetic acid-insoluble radioactivity was measure
35  metal ion pulses with distinct periods when trichloroacetic acid is applied as chemical fuel.
36 raction of malonyl-CoA from tissue using 10% trichloroacetic acid, isolation using a reversed-phase s
37 e, chloromethane, hexachlorocyclohexane, and trichloroacetic acids methyl ester.
38  negated when thiamine was stored diluted in trichloroacetic acid or as thiochrome formed in situ, bo
39 gels can be rapidly visualized by soaking in trichloroacetic acid or chloroform followed by illuminat
40                                 In addition, trichloroacetic acid precipitable [(125)I] was detected
41 nd after a brief lag, a portion was bound to trichloroacetic acid precipitable macromolecules.
42                                  Most of the trichloroacetic acid-precipitable [3H]mannose label was
43 thesis using (3)H-proline incorporation into trichloroacetic acid-precipitable material and for glyco
44 by this digestion, but only about 10% of the trichloroacetic acid-precipitable material was released
45 ion of 14C-labeled NeuAc from CMP-NeuAc into trichloroacetic acid-precipitable material when the lst
46 oid gland and its appearance in the serum as trichloroacetic acid-precipitable radioactivity was grea
47                About 82% of the label in the trichloroacetic acid precipitate remained as spermidine,
48 asured by o-phthaldialdehyde derivatization, trichloroacetic acid precipitation and hydrochloric acid
49 H]UDP-GlcNAc from 3H-p62ST acceptor peptide (trichloroacetic acid precipitation and metal-chelation a
50 the medium remained intact, as determined by trichloroacetic acid precipitation and SDS/PAGE, and aft
51                                         When trichloroacetic acid precipitation is used to recover th
52         Collagen synthesis was determined by trichloroacetic acid precipitation of the radiolabeled s
53 e recovery of tritiated polyuridylic acid by trichloroacetic acid precipitation.
54 el electrophoresis (SDS-PAGE) but only after trichloroacetic acid precipitation; heating to 95 degree
55 oxidative metabolites, median predictions of trichloroacetic acid production were less variable (2-fo
56 acids and related compounds by perchloric or trichloroacetic acid results in the formation of methylg
57                       Chloroquine treatment, trichloroacetic acid solubility, and sodium dodecyl sulp
58  rate of ATP-dependent conversion of CFTR to trichloroacetic acid soluble fragments by only 40%.
59 ulin was degraded and released from cells in trichloroacetic acid-soluble form after 4 h.
60 ted CFTR could be subsequently degraded into trichloroacetic acid-soluble fragments upon incubation i
61 her by the degradation of 125I-labeled OS to trichloroacetic acid-soluble label or by the cleavage of
62                              The increase in trichloroacetic acid-soluble peptides over the hydrolysi
63                               The release of trichloroacetic acid-soluble peptides over the hydrolysi
64 a series of large fragments as well as small trichloroacetic acid-soluble peptides.
65 otein degradation was examined by release of trichloroacetic acid-soluble radioactivity from cells pr
66 d subsequently released increased amounts of trichloroacetic acid-soluble radioactivity.
67 imultaneously carried out by the addition of trichloroacetic acid (TCA) and subsequent centrifugation
68                      Incomplete oxidation of trichloroacetic acid (TCA) and trifluoroacetic acid (TFA
69 formats (macro-, micro-, and nanoassay) with trichloroacetic acid (TCA) as protein precipitating agen
70 s obtained for dichloroacetic acid (DCA) and trichloroacetic acid (TCA) in methylene chloride were fo
71 ived from rHag B-immunized rats reacted with trichloroacetic acid (TCA) precipitates of P. gingivalis
72                                              Trichloroacetic acid (TCA) precipitation revealed that t
73 te precipitation, and the second is based on trichloroacetic acid (TCA) precipitation.
74      This method is based on extraction with trichloroacetic acid (TCA), reaction with 2-thiobarbitur
75 ing materials through iterative additions of trichloroacetic acid (TCA).
76 -urea, thiourea/urea, phenol, and a modified trichloroacetic acid (TCA)/acetone-to determine their ef
77  and by measuring maternal urinary levels of trichloroacetic acid (TCAA) during early pregnancy in a
78                                The levels of trichloroacetic acid (TCAA) in the heated water were sim
79                      Among the HAAs, urinary trichloroacetic acid (TCAA) is a potential valid biomark
80 tic acid (MBAA), dichloroacetic acid (DCAA), trichloroacetic acid (TCAA), and summary DBP measures (H
81 ribromoacetaldehyde (TBAL), bromate (BrO3-), trichloroacetic acid (TCAA), and trichloroacetaldehyde (
82 studied in drinking water exposure included: trichloroacetic acid (TCAA), monochloroacetic acid (MCAA
83 n kinetics of dichloroacetic acid (DCAA) and trichloroacetic acid (TCAA), the two predominant HAA spe
84 is data: monobromoacetic acid [MBAA] = 1.00, trichloroacetic acid [TCAA] = 0.0011, and dichloroacetic
85 nly the analysis of PLP requires mixing with trichloroacetic acid to release the protein-bound vitami
86 ic c-subunits that are released from them by trichloroacetic acid treatment.
87        Apoflavodoxin forms were generated by trichloroacetic acid treatment.
88                        Isopropanol with 1.0% trichloroacetic acid was found to be the most effective
89 tic, tribromoacetic, chlorodibromoacetic and trichloroacetic acid were the major HAAs components.
90  active states by pulses of a chemical fuel (trichloroacetic acid), which is itself decomposed by the
91 pha-chloro-substituted acetic acids, such as trichloroacetic acid, which are widely and successfully