ライフサイエンスコーパス: C4b-binding protein

1 inding of complement inhibitors factor H and C4b-binding protein.

2 classical and lectin pathways of complement, C4b-binding protein.

3 uid-phase complement regulators factor H and C4b-binding protein.

4 omologous positions in other CCP-bearing C3b/C4b-binding proteins.

5 ity of microprotein S was not neutralized by C4b-binding protein, a natural inhibitor of native prote

6 The complement inhibitors C4b-binding protein and factor H also interact with dyin

7 binding to the complement regulatory factors C4b-binding protein and factor H and confirmed that the

8 or outer membrane protein of NTHi, P5, binds C4b-binding protein and factor H to promote bacterial se

9 as also limited by the binding of inhibitors C4b-binding protein and factor H.

10 xidized LDL, IgG, amyloid beta peptide 1-42, C4b-binding protein, and factor H, in a CRP concentratio

11 rotein S cofactor function using recombinant C4b-binding protein beta chain significantly reduced the

12 istance, which was confirmed by factor H and C4b-binding protein binding studies, was more often asso

13 understanding of the need for both free and C4b-binding protein-bound protein S.

14 ontrast, binding of the complement regulator C4b-binding protein by the M. catarrhalis strains used i

15 an association between beta-chain containing C4b-binding protein (C4bBP-beta+) antigen levels and age

16 of Y. enterocolitica, presumably by binding C4b binding protein (C4BP) and factor H, which are both

17 We demonstrate that the alpha chain of human C4b binding protein (C4BP) binds directly to CD40 on hum

18 previously demonstrated that the binding of C4b binding protein (C4BP) is important for NTHi complem

19 binding of the complement regulatory protein C4b binding protein (C4BP) to the FA19 porin B (PorB), p

20 ontributes to serum resistance by binding to C4b binding protein (C4bp), a complement fluid phase reg

21 low fever virus NS1 directly associated with C4b binding protein (C4BP), a complement regulatory plas

22 issue of Immunity, Brodeur et al. show that C4b binding protein (C4BP), a regulator component of the

23 sides interacting with FH, FH related-1, and C4b binding protein (C4BP), also acquire FH like-1 from

24 urally related soluble complement inhibitors C4b-binding protein (C4BP) and factor H (FH) exert a tig

25 eumococci bind complement inhibitors such as C4b-binding protein (C4BP) and factor H via pneumococcal

26 interaction between the complement inhibitor C4b-binding protein (C4BP) and plasminogen of the fibrin

27 lement regulatory factors, such as factor H, C4b-binding protein (C4BP) and vitronectin (Vn).

28 t to facilitate this process by sequestering C4b-binding protein (C4BP) from host plasma.

29 the complement inhibitors factor H (FH) and C4b-binding protein (C4BP) in a human-specific manner, w

30 C4b-binding protein (C4BP) is a fluid-phase complement i

31 The classical pathway complement regulator C4b-binding protein (C4BP) is composed of two polypeptid

32 athway of complement down-regulatory protein C4b-binding protein (C4bp) to evade killing by human com

33 trep A) are responsible for recruiting human C4b-binding protein (C4BP) to the bacterial surface, whi

34 the classical complement pathway inhibitor, C4b-binding protein (C4BP), via their porin (Por) molecu

35 In stark contrast, human C4b-binding protein (C4BP), which is recruited to the GA

36 y protein H to bind the complement inhibitor C4b-binding protein (C4BP).

37 classical and lectin pathways of complement, C4b-binding protein (C4BP).

38 lso bound complement inhibitors factor H and C4b-binding protein (C4BP).

39 strains that bound the complement regulator, C4b-binding protein (C4bp).

40 ence patterns conserved for recruiting human C4b-binding protein (C4BP).

41 VRs that confers binding to human complement C4b-binding protein (C4BP).

42 ccus evades complement, including binding to C4b-binding protein (C4BP; classical pathway inhibitor)

43 em, factor H (FH) and the alpha chain of the C4b binding protein (C4bpalpha), and included in this st

44 ence of several cofactors, such as factor H, C4b-binding protein, complement receptor 1, and membrane

45 Despite the fact that C4b-binding protein, factor H, and C1q share some ligand

46 C4BP (C4b-binding protein) is a polymer of seven identical alp

47 cofactor protein (MCP; CD46), factor H, and C4b binding protein mediate this reaction, known as cofa

48 ieved to interfere with protein S binding to C4b-binding protein resulting in reduced free protein S

49 In addition, protein S bound to C4b binding protein showed greatly reduced enhancement o

50 otein S to the association of protein S with C4b-binding protein, thus establishing the importance of

51 oth a sublethal dose of Escherichia coli and C4b binding protein to assess the impact of inhibiting p

52 that PRELP competitively inhibits binding of C4b-binding protein to bacteria, which enhances membrane

53 /-) mice) or humanized complement system (FH/C4b-binding protein transgenic mice).

54 uiting to its surface a complement inhibitor C4b-binding protein, which is also a ligand for PRELP.

55 gh-affinity, calcium-stabilized complex with C4b-binding protein, which renders this fraction devoid

56 nd to interact with the complement inhibitor C4b-binding protein, which was suggested to locally down