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1 ic properties similar to RENCA mitochondrial protein preparation.
2  sites of inoculations with different alphaS protein preparations.
3  proteins and peptides in simple and complex protein preparations.
4 ing a mass spectroscopic analysis of adaptor protein preparations.
5 ovo selection experiments with GFP and other protein preparations.
6  determine the immunogenic properties of the protein preparations.
7 allergens to assess the allergenicity of the protein preparations.
8                       Each of these purified protein preparations activated Akt, inhibited cytokine-i
9 its (p140, p40, p38, p37, and p36) yielded a protein preparation active in two assays characteristic
10 summarized and compared different methods of protein preparation and crystallization used by differen
11 resence of MchA1 and MchA2 in outer membrane protein preparations and concentrated culture supernatan
12 ure and oligomeric state using both purified protein preparations and in-cell NMR on E. coli overexpr
13           Glycosidase digestions of membrane protein preparations and metabolic treatments of KG1a ce
14 lial cells to gingipain-active extracellular protein preparations and/or purified gingipains from P.
15 a 160-kDa protein in trypomastigote membrane protein preparations as well as with native, purified CR
16  of reperfusion, either thaumatin, a control-protein preparation, at 2 mg/kg body weight, or rBPI21 a
17      HpuA was identified in a total-membrane-protein preparation by construction of a mutant lacking
18 ound antibodies confirmed recognition of the protein preparation by the antibodies.
19                                          The protein preparations contained 1 mol sulfide and 3-4 mol
20                          Using heterodimeric protein preparations containing both wild-type and catal
21 sect cells infected with four baculoviruses, protein preparations containing the four polypeptides of
22  have unwittingly used commercial C-reactive protein preparations contaminated by other bioactive com
23 ice with preexisting cancers with heat shock protein preparations derived from autologous cancer resu
24                    Treatment with heat shock protein preparations derived from cancers other than the
25               It is not found in standard SR protein preparations, does not precipitate in the presen
26          The procedure yielded a homogeneous protein preparation, evidenced by both SDS-polyacrylamid
27 esults demonstrate that the more homogeneous protein preparations exhibit more uniform affinities and
28 nd that CVAK104 co-fractionates with adaptor protein preparations extracted from clathrin-coated vesi
29                        CNBr digestion of the protein preparations followed by MALDI-TOF MS analysis o
30 ween 6 kDa and 15 kDa by electroelution of a protein preparation from an SDS-PAGE gel and analysis of
31 was achieved by affinity chromatography of a protein preparation from rat brain on immobilized C16-se
32                                 First, total protein preparations from atxA4+ and atxA isolates grown
33  used anti-AtxA(His) serum to detect AtxA in protein preparations from B. anthracis cells.
34 ctivated virus and recombinant hemagglutinin protein preparations from both lineages raised hemagglut
35 ere exposed to protease-active extracellular protein preparations from isogenic mutants of P. gingiva
36  appeared hyperflagellated, and sheared cell protein preparations from motN contained more flagellin
37  flagella altogether; moreover, sheared-cell protein preparations from the fliC mutant lacked a 30-kD
38 ifolia) increased the use value of egg white protein preparations, generated as byproducts in the ind
39 ulation consistently outperforms a denatured protein preparation in all of the metrics studied, which
40 , RNA preparation in approximately 1.5 h and protein preparation in approximately 1 h.
41  or by a fluorescence assay on mitochondrial protein preparations in the range of 0.4 to 5.0 micro g
42 phosphorylation of the PDGFRbeta in purified protein preparations, in intact cells expressing a tyros
43 e dissociation rates are robust for distinct protein preparations, in the presence of noncompetitive
44 tes is demonstrated on cardiac mitochondrial protein preparations, in which, for example, the ADP/ATP
45 eport the thermodynamic stability of several protein preparations, including chick egg-white lysozyme
46       PTX treatment of a CFTR-immunodepleted protein preparation incorporated into bilayer membranes
47             Analysis of a partially purified protein preparation indicates that Rad32 is likely to ac
48                 Because absolute purity of a protein preparation is a metaphysical concept, other app
49              The first part of the protocol, protein preparation, may take several weeks, whereas the
50 lagen and laminin, was detectable in surface protein preparations only after growth at 46 degrees C,
51 ult from contaminating nucleases in the H-NS protein preparation or non-specific effects of the nucle
52 hat neither Hop or Hsp40 were present in our protein preparations or in the stripped receptors.
53 C remains competent for stimulation by S-100 protein preparations or Mn2+/Triton X-100, indicating th
54                  Using three different islet protein preparations, PBMC responses of IDDM patients (n
55 g the detergent present in purified membrane protein preparations prior to conducting crystallization
56                 The detergent-based membrane protein preparation protocol not only extracts proteins
57 y GRK5 in smooth muscle cells or in purified protein preparations reduced PDGFRbeta-mediated peptide
58 xtracts and S100 extracts but absent from SR protein preparations, suggesting that it is not a classi
59 tative proteomic profiles of plasma membrane protein preparations under conditions of vegetative grow
60 their RNA-unwinding activity, which, for the protein preparations used here, was greatest for Mss116p
61 ana tabacum) plasmodesmal-enriched cell wall protein preparation using as bait the NCAP, pumpkin (Cuc
62                                         When protein preparation was carried out in a zinc containing
63  AP endonuclease activity from GST-PO fusion protein preparations, whereas the resin was ineffective
64  P. gingivalis protease active extracellular protein preparations with the cysteine protease inhibito

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