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1  were used to identify the compounds in each purified fraction.
2 d mutant in either cell extracts or membrane-purified fractions.
3 as1p) are preferentially excluded from these purified fractions.
4 a point but could be separated in the highly purified fractions.
5 lecular weight of about 27,000, and the most purified fraction also gave a major band on SDS-PAGE cor
6 t assays, western blot analysis of partially purified fractions and UV-crosslinking studies.
7 ize of the largest polynucleotide present in purified fractions at an abundance of one molecule per i
8 at the largest polynucleotide present in our purified fractions at one molecule per ID50 unit is appr
9 s along culture growth, and their profile in purified fractions (bodies and faeces) and international
10                         Analysis of the most purified fraction by SDS-polyacrylamide gel electrophore
11                  Sequence information on the purified fraction, by automatic Edman degradation and ma
12          The CBE isolation produces a highly purified fraction (CD45-, CD33-, CD7-, CD235a-) of small
13                              The most highly purified fractions contain approximately 30 polypeptides
14 lso reduced adherence of strain 86-24, but a purified fraction containing antibodies to the N-termina
15 urification and protein sequencing of highly purified fractions containing potent bone forming activi
16                                         HPLC-purified fractions containing the individual radiolabele
17 purified core histones, ATP, and a partially purified fraction (containing at least one other assembl
18 lex size is approximately 1,600 kDa, and the purified fraction contains 20 major polypeptides.
19 the 48 kDa band seen in the final, partially purified fraction correlates with the ERE-BP activity.
20 e-polyacrylamide gel electrophoresis of this purified fraction demonstrated a predominant 65-kDa mole
21 sed to analyze a library of 36,000 partially purified fractions derived from plant materials.
22              Silver staining of the affinity-purified fraction detected a single prominent protein of
23  significant anticancer properties of a semi-purified fraction, DW-F5, from the dichloromethane extra
24 hy, we obtained from HCV-seronegative sera a purified fraction enriched in inhibitory factors.
25 ocytes, dead cells, and/or platelets) to the purified fractions exacerbated the aggregation response.
26  Upon PMA treatment, a mitochondria-enriched/purified fraction exhibited significant increases in C(1
27 induced [Ca2+]i oscillations, including FPLC-purified fractions, exhibited high in vitro PLC activity
28 pendent on PCNA, hMutSalpha, and a partially purified fraction from a HeLa nuclear extract.
29 brain extracts, microsomal preparations, and purified fractions from A117V patients and to determine
30 c nucleic acid, we analyzed nucleic acids in purified fractions from the brains of Syrian hamsters in
31 nrichment of torsinA in ATP-agarose affinity-purified fractions from tissue homogenates.
32                                              Purified fractions (granulocytes, CD2+, and CD- cells) o
33                                          The purified fraction had no effect on the activity of NR wh
34                                   The highly purified fraction hydrolyzed at the sn-1 position, imply
35    UV cross-linking reactions with partially purified fractions implicated a 29-kDa protein directly
36                     SDS/PAGE analysis of the purified fraction indicated that the pol delta complex c
37 on pattern with a wider spacing than in more purified fractions, indicating that the elongation compl
38 ting conditions, U insertion activity of the purified fraction is enhanced approximately 100-fold.
39 activity was restored upon the addition of a purified fraction isolated from HeLa cells by in vitro c
40 mol/mg of protein) starting from a partially purified fraction of 10-15% purity, further demonstratin
41  Similar results were obtained by exposing a purified fraction of LDL to fluid flow, suggesting that
42       After adding the recombinant O2 to the purified fraction of PBF-1, binding studies were perform
43 atase is stimulated >300-fold by a partially purified fraction of TFIIF.
44 atments comprising the DENV and DR4 affinity-purified fractions of anti-NS1 IgGs (anti-NS1-DR4 Ig), b
45                                       Highly purified fractions of bone extracts capable of inducing
46                                    Partially purified fractions of cytokinin oxidase from various spe
47                 In keeping with this, highly purified fractions of native T. brucei topoisomerase IB
48 s supported by fibrin generated from several purified fractions of plasma fibrinogen, purified proteo
49  in impure TIF-IB, TIF-IE is found in highly purified fractions of polymerase I, with which it associ
50  assayed in infected-cell lysates, partially purified fractions of soluble UL12.5 protein were genera
51  Investigations were carried out with highly purified fractions of VZV virions.
52                                              Purified fractions programmed transcription initiation f
53 he presence of four polypeptides in the most purified fraction, ranging in molecular masses between 3
54 e Brazilian scorpion Tityus serrulatus and a purified fraction selectively cleave essential SNARE pro
55                                    Partially purified fractions strongly stimulated both pancreatic s
56  resolve and characterize from ovine brain a purified fraction that contained both FGF-1 and p40 Syn-
57 tion of nucleoplasmin, RLF-M and a partially purified fraction that contains ORC, Cdc6 and RLF-B.
58 tivities and sequence data in an extensively purified fraction that will join ends by the repeat mech
59                                          The purified fraction was almost entirely CK19+ with no insu
60                                          The purified fraction was found to have 14.63+/-0.70% (w/w)
61                                          The purified fraction was homogeneously glycosylated.
62 ity of barley protein hydrolysates and their purified fractions was investigated and expressed as inc
63 ttering, the protein species present in each purified fraction were verified via sodium dodecyl sulfa
64 parated by size exclusion chromatography and purified fractions were analyzed for their antioxidant a
65  antigens on nitrocellulose strips; affinity-purified fractions were tested for anti-P by high-sensit
66 f NQO1-null mice liver cytosol and partially purified fractions with anti-GRP58 antibody led to a com
67                         Libraries consist of purified fractions with approximately one to five compou

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