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1 ng a rank order of A53T > A30P > wild-type > untransfected.
3 ypeptides did not suppress the growth of the untransfected 32D parental cell line in methylcellulose
5 used chromatin immunoprecipitation assays in untransfected A549 cells to infer the mechanism by which
6 Selected A9 transfectant clones (and control untransfected and 'irrelevant' alphoid YAC transfectant
7 t tumour suppression compared to the control untransfected and 'irrelevant' YAC transfected A9 cells.
8 alpha-syn in conditioned culture media from untransfected and alpha-syn-transfected human neuroblast
9 he absence of serum while differentiation of untransfected and alpha6-transfected myoblasts is insens
10 on factor of approximately 1.4 compared with untransfected and control vector-transfected cells at th
11 Because vitamin K is in excess in both the untransfected and vitamin K epoxide reductase (VKOR)-tra
12 duced dynamic mass redistribution changes in untransfected and, even more so, in FZD4 green fluoresce
13 se DCs were derived from monocytes that were untransfected (Arm A; n = 4), transfected with control s
18 ecific antibody, co-transfection assays, and untransfected bovine aortic endothelial cells we determi
19 l death compared to control CM obtained from untransfected C6 cells (CM-Mock) or CM obtained from cel
24 conditions where it caused no stimulation in untransfected cells and also stimulated an increase in [
25 tibodies to ubiquitin in the majority of the untransfected cells and cells expressing alpha-synuclein
26 otein dynein in immunoprecipitants from both untransfected cells and cells transfected with GFP-Rab5
27 this notion for physiological situations in untransfected cells and determine the significance of th
28 ed KS cells activated NF-kappaB signaling in untransfected cells and elicited the chemotaxis of monoc
30 mor growth against subsequent challenge with untransfected cells compared with mice immunized with em
34 nce of synuclein aggregation was observed in untransfected cells or cells expressing beta-synuclein.
35 AP effectively, could be recreated in either untransfected cells or cells expressing wild-type Arf6 b
37 urvival after EGFR blockade when compared to untransfected cells or HaCaT keratinocytes transfected w
38 G-kinase Ibeta expression vector but not in untransfected cells or in cells transfected with a catal
39 expression system, no responses were seen in untransfected cells or in cells transfected with alpha 1
40 in transfected VSMC exceeded that induced in untransfected cells treated for 24 h with a combination
42 higher specificity (ABCA1-transfected versus untransfected cells) than 37pA (5A, 9.7+/-0.77%, 18 h, 1
44 for cells expressing RhoA (T19N) vs 20 h for untransfected cells); (2) TRAMP cells expressing constit
45 ly in Muc4/SMC-transfected cells, but not in untransfected cells, and is co-localized with the apical
46 expressing either receptor subtype, but not untransfected cells, bound ligand and mobilized Ca2+ in
47 s and for endogenous PS-1 at the surfaces of untransfected cells, by immunofluorescence studies using
48 ansfected cells to produce NO, compared with untransfected cells, could not be ascribed to difference
49 in soft agar with more cells per colony than untransfected cells, or cells transfected with the Tax 1
50 catalytically inactive ribozyme control and untransfected cells, suggesting a role for SPF45 in intr
51 xpressing hBVR and PKC betaII, as well as in untransfected cells, upon treatment with phorbol myrista
76 for D1B DA receptor proteins was detected in untransfected CHO cells, or in D1A DA receptor-transfect
77 ibozyme expression vector compared with both untransfected clones and clones transfected with the emp
78 ot analyses performed on 3 transfected and 3 untransfected clones demonstrated markedly reduced TF mR
80 ected cells lost the round appearance of the untransfected control C6 cells, acquired a flat morpholo
81 viability (70 +/- 4% survival) compared with untransfected control cells (46 +/- 4% survival) when ch
83 well-organized collagen fibrillar matrix in untransfected, control chondrocyte cultures, while the m
84 deoxyinosine, mtDNA depletion that resembled untransfected controls was observed in both instances.
85 e permissive for SB virus replication, while untransfected controls were essentially nonpermissive.
86 ent injection and visual stimuli compared to untransfected controls, with spiking occurring during a
95 n addition, some branchial arch explants and untransfected COS7 cells repelled geniculate but not tri
97 , SD = 9.39) compared with mice treated with untransfected D2SC/1 cells (mean = 12 days, median = 11
99 l lymph nodes, and (b) cross-presentation by untransfected DC of antigen released from or associated
100 imilar results were obtained by treatment of untransfected endothelial cells with the ligands transfo
101 including GATA4, alpha-MHC, and beta-MHC in untransfected ES cells in a developmentally controlled m
109 inant cell lines over that observed with the untransfected HEK cells, whereas kainate produced a 2-3-
111 blocked the increased immunoreactivity, and untransfected HEK293 cells did not increase MOR-Tyr166p-
115 o receptors can be coimmunoprecipitated from untransfected Hs27 fibroblasts and from COS-7 cells.
117 ng for D4 DA receptor protein was visible in untransfected, K1 CHO cells, and in D2 or D3 DA receptor
123 pecific values measured using either control untransfected ldlA-7 cells or by inhibiting SR-BI-mediat
124 mitogen-activated protein kinases 1 and 2 in untransfected LNCaP cells, as did bryostatin 1 in PKCalp
132 0-containing particles in HepG2 and parental untransfected McA-RH7777 cells were inhibited by 86-94%.
142 ibited the same survival and growth rates as untransfected NIH3T3 cells or cells transfected with pla
143 ctrin alphaI SigmaI/betaI SigmaI antibody in untransfected NIH3T3 cells; in addition, the anti-alphaI
145 10(7) cells from 9 to 11 nmol/10(7) WT(t) or untransfected normal fibroblasts) did not adversely affe
149 active oxygen species exposure compared with untransfected or control plasmid-transfected cells.
152 nude mice were injected subcutaneously with untransfected or Huh7 cells transfected with empty or MA
154 ned significantly less ANK 220 compared with untransfected or N-fragment cells, indicating a higher a
155 lls in anti-asialo-GM(1)-treated mice, while untransfected or ss(2)M-transfected RMAS cells were rapi
158 normally express fast embryonic myosin were untransfected, or stably transfected with a plasmid expr
164 y transfected clones were less invasive than untransfected parental cells and did not form tumors in
165 toxic effects of sodium arsenite than either untransfected parental cells or parental cells transfect
166 -2, the mouse homologue of FPRL1, but not by untransfected parental human embryonic kidney 293 cells,
168 detectable TIS for the alpha-CaMKII gene in untransfected PC12 cells was located near the ATG transl
169 C12 cells transfected with trk alone, and in untransfected PC12 cells, showing that overexpressed and
170 controls, which received chambers containing untransfected plasmacytoma cells, secreted primarily IL-
171 ity of several GL183+ NK clones, which lysed untransfected porcine cells effectively, was substantial
176 fectants were killed at levels comparable to untransfected RMA-S cells whereas protection from lysis
177 ic tumor targets tested, RNK.Ly-49D, but not untransfected RNK-16, preferentially lysed tumor cells d
180 tonic-level (1 mum) GABA-evoked currents in untransfected striatal neurons that could be recapitulat
181 d T cell proliferation more effectively than untransfected T51 cells in MLR cultures and increased th
182 Stimulation of attachment by incubation of untransfected target cells with neuraminidase-treated HN
184 solid tumor and resisted rejection, whereas untransfected tumors and interleukin-4 receptor transfec
185 human NK-1R (NCM460-NK-1R cells) as well as untransfected U373 MG cells expressing high levels of en
191 lysed YB2/0.Dd targets more efficiently than untransfected YB2/0 or YB2/0 transfected with Db, Kk, or
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