ライフサイエンスコーパス: heparin-binding protein

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 lly related, extracellular matrix-associated heparin-binding proteins.

6 inity comparable to that of other identified heparin-binding proteins.

7 alpha-Chemokines are known heparin-binding proteins.

8 The Cyr61 protein is a secreted, heparin-binding protein (379 amino acids with 38 conserv

9 We aimed to evaluate and validate the heparin-binding protein, a neutrophil-derived mediator o

10 racellular matrix protein tenascin-R and two heparin-binding proteins, amphoterin and the heparin-bin

11 We have reported previously that Noggin is a heparin-binding protein and associates with the cell sur

12 recently showed that thyroglobulin (Tg) is a heparin-binding protein and that heparin inhibits bindin

13 vestigated, for example, as aptamers against heparin-binding proteins and as purine-motif triplex-for

14 bility-increasing protein, azurocidin (CAP37/heparin-binding protein), and neutrophil elastase were e

15 its target protease kallikrein 7 (KLK7) are heparin-binding proteins, and inhibition of KLK7 by vasp

16 sFRP-1 and Wnts are heparin-binding proteins, and their interaction can be s

17 heparin microarray with the highly specific heparin-binding protein antithrombin III (AT III).

18 Because circulating heparin-binding proteins are known to be rapidly sequest

19 eparin release, we demonstrated that Tg is a heparin-binding protein, as are several megalin ligands.

20 ple ionophores to model recognition sites of heparin-binding proteins at liquid/liquid interfaces.

21 peptide sequence analysis revealed that this heparin-binding protein corresponded to the extravesicul

22 Fibroblast growth factors (FGFs) are heparin-binding proteins crucial to embryogenesis, angio

23 phosphodiester oligonucleotides can bind to heparin-binding proteins (eg, basic fibroblast growth fa

24 CYR61 is a secreted, cysteine-rich, heparin-binding protein encoded by a growth factor-induc

25 ads, we demonstrated a high-molecular-weight heparin-binding protein expressed by H. somnus.

26 udies have shown that the neutrophil-derived heparin-binding protein (HBP), also known as CAP37 or az

27 Heparin-binding protein (HBP), also known as CAP37, is a

28 tivated polymorphonuclear leukocytes release heparin-binding protein (HBP; also known as CAP37 or azu

29 nding sites for a diverse array of mammalian heparin binding proteins, including adhesive glycoprotei

30 ents presenting at the emergency department, heparin-binding protein is an early indicator of infecti

31 sic fibroblast growth factor (bFGF), another heparin-binding protein is increased in Alzheimer's dise

32 Midkine (MK), a retinoic acid-inducible heparin-binding protein, is a mitogen which initiates a

33 o wounding was demonstrated by the fact that heparin-binding proteins isolated from wounded, but not

34 f the latter patients had an elevated plasma heparin-binding protein level (>30 ng/mL) prior to devel

35 n polarized myeloma cells are incubated with heparin-binding proteins, like hepatocyte growth factor

36 studies indicated that Tia, as a prokaryotic heparin binding protein, may also interact via sulfated

37 domains that have homology to somatomedin B, heparin-binding proteins, mucins and haemopexins.

38 OVAX is also the main heparin-binding protein of egg white.

39 BNP was tentatively identified as a heparin-binding protein on the basis of its cyclic struc

40 These data suggest that heparin-binding proteins on H. somnus could serve as ini

41 th Alzheimer disease is derived from a large heparin-binding protein precursor APP.

42 Plasma levels of heparin-binding protein, procalcitonin, C-reactive prote

43 The effect of heparin is neutralized by heparin-binding proteins, such as protamine sulfate, pla

44 atform is used to assess binding of specific heparin-binding protein targets at very high sensitivity

45 We demonstrate that this holds true for all heparin binding proteins tested but not for epidermal gr

46 way was able to interact with four different heparin-binding proteins tested, i.e., TSG-6, chemokines

47 early gene Cyr61, a secreted, cysteine-rich, heparin binding protein that promotes endothelial cell a

48 ed Cyr61 protein is a secreted, cystein-rich heparin-binding protein that associates with the cell su

49 rly gene, CYR61 is a secreted, cysteine-rich heparin-binding protein that associates with the extrace

50 Cyr61 is an extracellular matrix-associated heparin-binding protein that can mediate cell adhesion,

51 , and subsequent studies identified a second heparin-binding protein that co-purified with FGF-1.

52 mily, is an extracellular matrix-associated, heparin-binding protein that mediates cell adhesion, pro

53 ducible midkine gene encodes a highly basic, heparin-binding protein that possesses potential functio

54 f amphoterin and HB-GAM (Kd = 0.3-8 nM), two heparin-binding proteins that are developmentally regula

55 Because VEGF is a heparin-binding protein, the relation between VEGF and h

56 lthough they are traditionally classified as heparin-binding proteins, under normal physiological con

57 The performance of heparin-binding protein was confirmed in the validation

58 modimer, we sought to determine whether this heparin-binding protein was involved in the release of F

59 Compared with other biomarkers, heparin-binding protein was the best predictor of progre

60 or glypican-1 insofar as no other identified heparin-binding proteins were isolated using our affinit

61 Heparin-binding proteins were purified from kidney homog

62 The N-terminal domain mimics heparin, binding proteins with clustered basic amino aci

63 ere designed based on consensus sequences in heparin-binding proteins: XBBXBX and XBBBXXBX, where X a