戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1  those antibodies were employed to isolate a heparin binding protein.
2 ment leads to degranulation and secretion of heparin-binding protein.
3 e serine proteinase inhibitor (serpin) and a heparin-binding protein.
4  (PF4) is an abundant platelet alpha-granule heparin-binding protein.
5 eins, including many previously unidentified heparin-binding proteins.
6 lly related, extracellular matrix-associated heparin-binding proteins.
7 inity comparable to that of other identified heparin-binding proteins.
8                   alpha-Chemokines are known heparin-binding proteins.
9             The Cyr61 protein is a secreted, heparin-binding protein (379 amino acids with 38 conserv
10        We aimed to evaluate and validate the heparin-binding protein, a neutrophil-derived mediator o
11 racellular matrix protein tenascin-R and two heparin-binding proteins, amphoterin and the heparin-bin
12 We have reported previously that Noggin is a heparin-binding protein and associates with the cell sur
13 recently showed that thyroglobulin (Tg) is a heparin-binding protein and that heparin inhibits bindin
14 vestigated, for example, as aptamers against heparin-binding proteins and as purine-motif triplex-for
15 bility-increasing protein, azurocidin (CAP37/heparin-binding protein), and neutrophil elastase were e
16  its target protease kallikrein 7 (KLK7) are heparin-binding proteins, and inhibition of KLK7 by vasp
17                          sFRP-1 and Wnts are heparin-binding proteins, and their interaction can be s
18  heparin microarray with the highly specific heparin-binding protein antithrombin III (AT III).
19                          Because circulating heparin-binding proteins are known to be rapidly sequest
20 eparin release, we demonstrated that Tg is a heparin-binding protein, as are several megalin ligands.
21 ple ionophores to model recognition sites of heparin-binding proteins at liquid/liquid interfaces.
22 we characterized one of the newly-discovered heparin-binding proteins, C-type lectin 14a (CLEC14A), a
23 peptide sequence analysis revealed that this heparin-binding protein corresponded to the extravesicul
24         Fibroblast growth factors (FGFs) are heparin-binding proteins crucial to embryogenesis, angio
25              Here, we showed that UNC-5 is a heparin-binding protein, determined its structure bound
26  phosphodiester oligonucleotides can bind to heparin-binding proteins (eg, basic fibroblast growth fa
27          CYR61 is a secreted, cysteine-rich, heparin-binding protein encoded by a growth factor-induc
28 ads, we demonstrated a high-molecular-weight heparin-binding protein expressed by H. somnus.
29                                              Heparin-binding protein (HBP) has been shown to be a rob
30 studies have demonstrated elevated levels of heparin-binding protein (HBP) in patients with sepsis an
31                               The neutrophil heparin-binding protein (HBP) is an inflammatory mediato
32 udies have shown that the neutrophil-derived heparin-binding protein (HBP), also known as CAP37 or az
33                                              Heparin-binding protein (HBP), also known as CAP37, is a
34 tivated polymorphonuclear leukocytes release heparin-binding protein (HBP; also known as CAP37 or azu
35 ction of cell surface HSPGs by serum-derived heparin-binding proteins (HBPs).
36 nding sites for a diverse array of mammalian heparin binding proteins, including adhesive glycoprotei
37 ents presenting at the emergency department, heparin-binding protein is an early indicator of infecti
38 sic fibroblast growth factor (bFGF), another heparin-binding protein is increased in Alzheimer's dise
39      Midkine (MK), a retinoic acid-inducible heparin-binding protein, is a mitogen which initiates a
40 o wounding was demonstrated by the fact that heparin-binding proteins isolated from wounded, but not
41 f the latter patients had an elevated plasma heparin-binding protein level (>30 ng/mL) prior to devel
42 n polarized myeloma cells are incubated with heparin-binding proteins, like hepatocyte growth factor
43 studies indicated that Tia, as a prokaryotic heparin binding protein, may also interact via sulfated
44 domains that have homology to somatomedin B, heparin-binding proteins, mucins and haemopexins.
45                        OVAX is also the main heparin-binding protein of egg white.
46          BNP was tentatively identified as a heparin-binding protein on the basis of its cyclic struc
47                      These data suggest that heparin-binding proteins on H. somnus could serve as ini
48 ivity (>300-fold) for HPSE compared to other heparin-binding proteins (platelet factor 4 and antithro
49 th Alzheimer disease is derived from a large heparin-binding protein precursor APP.
50                             Plasma levels of heparin-binding protein, procalcitonin, C-reactive prote
51 owth arrested G0/G1 RMCs in order to extract heparin-binding protein(s).
52      The effect of heparin is neutralized by heparin-binding proteins, such as protamine sulfate, pla
53 atform is used to assess binding of specific heparin-binding protein targets at very high sensitivity
54  We demonstrate that this holds true for all heparin binding proteins tested but not for epidermal gr
55 way was able to interact with four different heparin-binding proteins tested, i.e., TSG-6, chemokines
56              We further show that IL-37 is a heparin binding protein that modulates this self-associa
57 early gene Cyr61, a secreted, cysteine-rich, heparin binding protein that promotes endothelial cell a
58 ed Cyr61 protein is a secreted, cystein-rich heparin-binding protein that associates with the cell su
59 rly gene, CYR61 is a secreted, cysteine-rich heparin-binding protein that associates with the extrace
60  Cyr61 is an extracellular matrix-associated heparin-binding protein that can mediate cell adhesion,
61 , and subsequent studies identified a second heparin-binding protein that co-purified with FGF-1.
62 mily, is an extracellular matrix-associated, heparin-binding protein that mediates cell adhesion, pro
63 ducible midkine gene encodes a highly basic, heparin-binding protein that possesses potential functio
64 f amphoterin and HB-GAM (Kd = 0.3-8 nM), two heparin-binding proteins that are developmentally regula
65                            Because VEGF is a heparin-binding protein, the relation between VEGF and h
66 lthough they are traditionally classified as heparin-binding proteins, under normal physiological con
67                           The performance of heparin-binding protein was confirmed in the validation
68 modimer, we sought to determine whether this heparin-binding protein was involved in the release of F
69              Compared with other biomarkers, heparin-binding protein was the best predictor of progre
70 or glypican-1 insofar as no other identified heparin-binding proteins were isolated using our affinit
71                                              Heparin-binding proteins were purified from kidney homog
72                 The N-terminal domain mimics heparin, binding proteins with clustered basic amino aci
73 ere designed based on consensus sequences in heparin-binding proteins: XBBXBX and XBBBXXBX, where X a