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1 ns that include C-reactive protein and serum amyloid P component.
3 attached pyruvate acetal, a ligand for human amyloid P component, and conjugation to poly[acrylamide-
4 ng serum glycoproteins, ceruloplasmin, serum amyloid P-component, and amyloid precursor protein, were
5 pondin-1 and 5, alpha-1B-glycoprotein, serum amyloid P-component, and tenascin-X, were selected as pr
10 postulated that C-reactive protein and serum amyloid P component are products of a gene duplication e
11 haperones such as apolipoprotein E and serum amyloid P-component (arrows) as well as the identity of
13 nd mice with targeted deletions of the serum amyloid P component gene (Sap) develop a lupus-like illn
14 popolysaccharide-induced mouse CRP and serum amyloid P component gene expression in the liver, wherea
15 Although sequence homology with human serum amyloid P component is relatively low, structural homolo
19 on amino-acid residues 27-38 of human serum amyloid P component represent a novel type of heparin bi
22 idin, concanavalin A (conA), and human serum amyloid P component (SAP) at elevated temperatures prior
24 giform encephalopathies always contain serum amyloid P component (SAP) bound to the amyloid fibrils.
25 IgG1 monoclonal antibody that binds to serum amyloid P component (SAP) for potential treatment of sys
26 oclinic (P2(1)) crystal forms of human serum amyloid P component (SAP) in complex with the 4,6-pyruva
31 for changes in plasma concentration of serum amyloid P component (SAP), a protein that is up-regulate
32 constitutive plasma pentraxin protein, serum amyloid P component (SAP), in serum samples obtained fro
34 ic fibroblast growth factor (bFGF) and serum amyloid P component (SAP), we investigated a novel route
36 ivating FcgammaRs are also involved in serum amyloid P component (SAP)-mediated clearance of apoptoti
44 te transcription of the genes encoding serum amyloid P-component (SAP) and C-reactive protein (CRP).
47 phages secrete cathepsin B (CATB), and serum amyloid p component (SAPC), inducing neuronal apoptosis
52 of the previously undiscovered Limulus serum amyloid P component, the first invertebrate lectin struc
55 se exclusion and failure to bind human serum amyloid P component, which acts as a lectin for terminal
56 in-1, fibronectin, vitronectin, laminin, and amyloid P-component, which are well-known extracellular