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1 n isolated axonemes in the presence of cAMP, co-purified with 22 S dynein and not with inner arm dyne
2 entially tagged DAT molecules, HA-tagged DAT co-purified with 6His-tagged DAT demonstrating a physica
3 class IA PI3K enzymes, PI3K-C2alpha could be co-purified with a population of clathrin-coated vesicle
4 ) which reacted with specific antibodies and co-purified with a reverse transcriptase activity not pr
5                                Proteins that co-purified with ABCA1 on an antibody affinity column we
6 he PDGF type-beta receptor, and consistently co-purified with activated p21 ras, with Syp/PTP-2, and
7 rgazin/TARP family of transmembrane proteins co-purified with AMPA-Rs and contributed to the density
8 immunoprecipitated by anti-AflR antibody and co-purified with an AflR-maltose-binding protein fusion
9 between NFT and mitotic kinase, NFT proteins co-purified with and became phosphorylated by the p13suc
10 lasmic l-asparaginase II, AnsB (EC 3.5.1.1), co-purified with AphA and was also necessary for PRA for
11 igrated as a dimer during gel filtration and co-purified with ATPase activity.
12                      In observing that GRP94 co-purified with bacterial beta-galactosidase through mu
13 aperone, which consistently and specifically co-purified with Bax.
14 AF47 and were found to be identical to those co-purified with BRG1, strongly indicating that this gro
15 munoprecipitate with CCR4 and CAF1, and NOT1 co-purified with CCR4 and CAF1 through three chromatogra
16 adenosine triphosphate synthase complex, was co-purified with cholesterol in crystals formed from a c
17 t the components of the CSN complex could be co-purified with CSN3-TAPa.
18                      Two polypeptides, which co-purified with DGAT activity, were isolated from the l
19                            Moreover, the APC co-purified with epitope-tagged Mnd2 and Swm1.
20  low abundance protein in bovine uterus that co-purified with estrogen receptor (ER) in a ligand-inde
21 tified a second heparin-binding protein that co-purified with FGF-1.
22                Upon co-expression, FtsQp was co-purified with FtsBp and FtsLp from E. coli extracts a
23 -43 fragments formed in translation mixtures co-purified with full-length GAP-43.
24                   Fourth, HSC70 and CSP were co-purified with GAD by specific anti-GAD immunoaffinity
25 0, as identified from amino acid sequencing, co-purified with GAD.
26        A GMPPNP-stimulated PTPase (PTPase-G) co-purified with Galphai/o subunits during Superose 6 an
27                Molecular chaperone GroEL was co-purified with Gap3 only when Gap1 was absent and also
28 ubunit of virion RNA polymerase specifically co-purified with GST-NPH I, consistent with a physical i
29                                   MASP-2 was co-purified with H-ficolin, and the purified H-ficolin.M
30 eine/histidine substitutions (of CXXCH) were co-purified with HCCS.
31                A single protein of Mr 45,000 co-purified with hepatoma cell-derived Vn, which was imm
32 from a strain also expressing PrgX, PrgX was co-purified with His-PrgX.
33            Surprisingly, both PNPase and Hfq co-purified with His-tagged PAP I under native condition
34             A 16-kDa cytosolic protein (p16) co-purified with Hsc70 obtained from a fish hepatocyte c
35                    Amylin-degrading activity co-purified with IDE from rat muscle through several chr
36 us nuclear ribonucleoproteins A2/B1 and RBM3 co-purified with in vitro late transcription stimulation
37                       However, SicA could be co-purified with InvF, suggesting that InvF and SicA int
38 24 nt was tightly bound to RecBCD enzyme and co-purified with it.
39 itional data showing RybB and MicF sRNAs are co-purified with ITS(metZ-metW) and ITS(metW-metV) stron
40     Both the small and large isoforms of Sp3 co-purified with KCS protein binding activity (KBP) by u
41      In pull-down experiments, LapA and LapB co-purified with LPS, Lpt proteins, FtsH (protease), Dna
42                   PP2C alpha and PP2C beta 2 co-purified with Mg(2+)-dependent Cdk2/Cdk6 phosphatase
43                The majority of this activity co-purified with microsomes.
44                          This protein kinase co-purified with microtubules and co-immunoprecipitated
45                            Furthermore, Arl3 co-purified with microtubules from bovine brain.
46 es and biochemical analyses showed that MAPK co-purified with microtubules.
47 by immunofluorescence assay, but it was also co-purified with Myb1 in certain vesicle fractions from
48 tagged Ste14p also co-immunoprecipitated and co-purified with N-terminal-tagged His(10)-myc(3)-Ste14p
49                                        ParD2 co-purified with ParE2 and interacted with it directly.
50 tified an essential light chain (PfELC) that co-purified with PfMyoA isolated from parasite lysates.
51                       The fusion protein was co-purified with plasma membrane markers 1,3 beta-glucan
52                                      AKAP220 co-purified with PP1c by affinity chromatography on micr
53 aled promoter-specific binding activity that co-purified with promoter-dependent transcription activi
54 n, fibronectin, and factor XIII, whereas Coa co-purified with prothrombin and fibrinogen.
55 ase, signal peptide peptidase, predominantly co-purified with PS2-containing gamma-secretase complexe
56 RCC3 formed stable complexes with Rad51C and co-purified with Rad51C, whereas the K113R mutant did no
57               Methyltransferase activity was co-purified with Rb.
58                   The cross-reacting protein co-purified with ribosomes, and a monoclonal antibody ra
59                                          PP1 co-purified with RNAPII by gel filtration and associated
60 f bovine retinas, the 44-kDa Gbeta5L protein co-purified with rod outer segment membranes.
61                 Several plasma proteins that co-purified with serpin-protease complexes, most notably
62          Our approach reduced 1,099 proteins co-purified with spermatogenic chromatin, currently the
63          The cytosolic Hsp70 chaperone Ssa1p co-purified with TAP-Pdr3p.
64           A preliminary analysis of proteins co-purified with tau in secreted exosomes identified sev
65   A novel Ig superfamily protein, EWI-2, was co-purified with tetraspanin protein CD81 under relative
66         A minor protein of about 24 kDa that co-purified with the above subunits was identified by ma
67  g pellet fraction from bovine liver, and it co-purified with the activity and immunoreactivity of a
68 1 cell extracts showed that the beta subunit co-purified with the alpha(2) subunit.
69                       In addition, EF-1alpha co-purified with the archaeal multi-synthetase complex (
70                 The third subunit (BchB) was co-purified with the BchN protein indicating that BchN a
71                           [14C]beta-Carotene co-purified with the binding protein throughout the puri
72 and CAF1/POP2, a CCR4-associated factor, and co-purified with the CCR4 complex.
73 expressed in E. coli as a GST fusion protein co-purified with the E. coli Hsp70 protein DnaK in the a
74                     The NAD+ cofactor, which co-purified with the enzyme, is bound to the Rossmann do
75 and contains four TPRs binds to hsp90 and is co-purified with the glucocorticoid receptor (GR).
76 odies; the endonucleolytic cleavage activity co-purified with the immunoreactive 70 kDa peptide.
77 BCL-2 from ER membranes and found that BCL-2 co-purified with the main two subunits of the serine/thr
78 d acetylated tetrapeptide (AcMMXX) that have co-purified with the protein.
79 d G-protein, as: 1) its alpha-subunit can be co-purified with the receptor protein using both ligand
80 combinant C4orf14 isolated from human cells, co-purified with the small, 28S subunit of the mitochond
81                          eIF5, eIF1 and HCR1 co-purified with this subcomplex, but not with distinct
82 ded the ovalbumin-derived epitope, SIINFEKL, co-purified with TOP.
83                                       Parkin co-purified with tubulin and was found in highly purifie
84 yltransferase activity when co-expressed and co-purified with untagged wild-type Ste14p.
85                    Membrane-associated Vta1p co-purified with Vps60p, suggesting that Vta1p is a clas

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