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1 RNA oligonucleotide abolished the effect of kallistatin.
2 llikrein is a specific target proteinase for kallistatin.
3 nhibitor, affected vasorelaxation induced by kallistatin.
5 Here, we report that circulation levels of kallistatin, a member of the serine proteinase inhibitor
8 d region between the H helix and C2 sheet of kallistatin acquired heparin-suppressed inhibitory activ
11 PTBN1 express much less of the Wnt inhibitor kallistatin and exhibit decreased beta-catenin phosphory
12 inhibition of Wnt/beta-catenin signaling by kallistatin and rescued the wound-healing deficiency in
13 Conversely, adenovirus-mediated transfer of kallistatin antisense cDNA into cultured VSMCs inhibited
14 rmore, local delivery of adenovirus carrying kallistatin antisense cDNA significantly downregulated k
15 stimulated A549 human lung epithelial cells, kallistatin attenuated apoptosis, down-regulated Fas/Fas
21 ular modeling of the reactive center loop of kallistatin bound to the reactive crevice of tissue kall
22 that an intravenous bolus injection of human kallistatin caused a rapid, potent, and transient reduct
23 s, we prepared adenovirus carrying the human kallistatin cDNA (Ad.HKBP) and evaluated the effect of k
24 esponse markers (HR6 model), including SYWC, kallistatin, complement C9, gelsolin, testican-2, and al
26 e region between the H helix and C2 sheet of kallistatin, comprise a major heparin-binding site respo
27 The loop between the H helix and C2 sheet of kallistatin containing clusters of basic amino acid resi
28 hibitory characteristics similar to those of kallistatin demonstrates that the loop between the H hel
29 h regions were substituted to generate three kallistatin double mutants K187A/K188A (mutations in the
30 listatin in lung by gene transfer with human kallistatin-encoding plasmid ameliorated acute lung inju
35 n cDNA (Ad.HKBP) and evaluated the effect of kallistatin gene delivery on spontaneous angiogenesis in
37 kallistatin levels, and decreased SPTBN1 and kallistatin gene expression is associated with decreased
40 in the SERPINA4 gene, whose protein product, kallistatin, has been linked to apoptosis in the kidney.
44 3-P2-P1 residues (residues 386-388) of human kallistatin in determining inhibitory specificity toward
45 udy introduces the potential significance of kallistatin in directly regulating blood pressure to red
46 ride (LPS)-treated mice, expression of human kallistatin in lung by gene transfer with human kallista
47 These results demonstrate a novel role of kallistatin in the inhibition of angiogenesis and tumor
61 the loop between the H helix and C2 sheet of kallistatin is crucial in tissue kallikrein inhibition,
63 eet of kallistatin was shown to suppress the kallistatin-kallikrein interaction through competition f
66 is positively correlated with E-cadherin and kallistatin levels, and decreased SPTBN1 and kallistatin
67 ells of human blood vessels, suggesting that kallistatin may be involved in the regulation of vascula
70 n antisense cDNA significantly downregulated kallistatin mRNA levels and attenuated neointima formati
74 S inhibitor abolished the blocking effect of kallistatin on vascular cell adhesion molecule-1 and mon
78 t of the other chimera, which contained only kallistatin's P3-P2' sequence, and 2300-fold higher than
84 d a decreased number of blood vessels in the kallistatin-treated group as compared to the control.
86 empted to locate the heparin-binding site of kallistatin using synthetic peptides derived from its su
87 n mediating the anti-inflammatory actions of kallistatin via increasing eNOS expression in endothelia
89 sequence between the H helix and C2 sheet of kallistatin was shown to suppress the kallistatin-kallik
90 rotein that mediates the vascular actions of kallistatin, we screened and identified a positive clone
91 ion encompassing the H helix and C2 sheet of kallistatin, were used to assess their heparin binding a
92 , had no effect on the hypotensive effect of kallistatin yet it abolished the blood pressure-lowering
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