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1 o the assembly of Sindbis virus particles in baby hamster kidney cells.
2 s synthesized in vitro were transfected into baby hamster kidney cells.
3 fection in both C6/36 (Aedes albopictus) and baby hamster kidney cells.
4 otein in the plasma membranes of transfected baby hamster kidney cells.
5 se, from vesicular stomatitis virus-infected baby hamster kidney cells.
6 nked immunosorbent assay-based cGMP assay in baby hamster kidney cells.
7 NAs replicate when transfected into cultured baby hamster kidney cells.
8 eta and θ and various mutant forms in baby hamster kidney cells.
9 omains of Madin-Darby canine kidney cells or baby hamster kidney cells.
10 mammalian expression vector and expressed in baby hamster kidney cells.
11 to vesicles mediating export from the ER in baby hamster kidney cells.
12 m of this I domain (I-GPI) on the surface of baby hamster kidney cells.
13 suppresses the surface expression of CFTR on baby hamster kidney cells.
15 that full-length Tax was secreted from both baby hamster kidney cells and a human kidney tumor cell
16 eavage site has been expressed (>30 mg/L) in baby hamster kidney cells and purified from the tissue c
18 n different expression systems, COS-7 cells, baby hamster kidney cells, and in VWF-deficient mice thr
19 rain implants were compared with those of wt baby hamster kidney cells (BHK) and adenosine releasing
21 ttle effect on a full-length fos promoter in baby hamster kidney cells, but it synergistically enhanc
24 s work we have engineered stably transfected baby hamster kidney cells containing gamma-carboxylase a
25 1/A3C1C2 dimer purified from wild type (WT), baby hamster kidney cell-expressed factor VIII, factor I
27 rodimers were examined in stably transfected baby hamster kidney cells expressing combinations of nor
28 nd identified several host cell factors from baby hamster kidney cell extracts that bind with high sp
29 re we show that human ABCG1 overexpressed in baby hamster kidney cells in the absence of lipoproteins
30 of CD40 with CD40 ligand (CD40L)-transfected baby hamster kidney cells induces NF-kappaB, as demonstr
31 eavage fragment of Bcl-2 is transfected into baby hamster kidney cells, it localizes to mitochondria
32 tes or to ectopically expressed receptors on baby hamster kidney cells leads to activation of the sig
33 P binding cassette transporter A1-expressing baby hamster kidney cells leads to formation of two popu
35 anges we generated a stably transfected BHK (baby hamster kidney) cell line that expresses a moderate
36 fusion experiments using stably transfected baby hamster kidney cell lines expressing one or combina
38 d in murine macrophages or ABCA1-transfected baby hamster kidney cells, PLTP gained the ability to pr
40 with mGluRs expressed in stably transfected baby hamster kidney cells suggests that each of the anti
42 2 were cotranscribed by T7 RNA polymerase in baby hamster kidney cells that expressed T7 RNA polymera
43 pressed by transfection in human, monkey, or baby hamster kidney cells, the E1B protein colocalized i
44 t to the interaction observed in primate and baby hamster kidney cells, the E4 protein failed to dire
45 We recently showed that when expressed in baby hamster kidney cells, the human beta1-but not the b
46 on of von Willebrand factor was expressed in baby hamster kidney cells, the propeptide and D'D3 forme
47 on of p38 results in the hypersensitivity of baby hamster kidney cells to aerolysin, a pore-forming t
48 nt from negligible in some cell lines (e.g., baby hamster kidney cells) to severe in others (e.g., hu
49 cardiac L-type) channels stably expressed in baby hamster kidney cells together with beta1a and alpha
50 -Cys-583 in EGF-4) and transfected them into baby hamster kidney cells together with normal alphav or
54 ith the activation of IKK, CD40L-transfected baby hamster kidney cell treatment strongly activates c-
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