ライフサイエンスコーパス: reconstitution system

1 by the lack of a functional nonhematopoietic reconstitution system.

2 CSN6, requiring coexpression in a bacterial reconstitution system.

3 induce Golgi membrane tubule formation in a reconstitution system.

4 ctivation based on the bifragment luciferase reconstitution system.

5 ficient in IKKbeta and IKKalpha and in yeast reconstitution system.

6 g was examined in an Sf9 cell membrane-based reconstitution system.

7 studied in a cell-free planar lipid bilayer reconstitution system.

8 inding and catalytic (TBC) channel in an RNP reconstitution system.

9 ane tubules from Golgi stacks in an in vitro reconstitution system.

10 carried out earlier using a natural protein reconstitution system.

11 tion-selective channels in the lipid bilayer reconstitution system.

12 s of full-length Bcl-xl in the lipid bilayer reconstitution system.

13 budding of SVs was addressed in a cell-free reconstitution system.

14 ulated prolactin promoter activity in a HeLa reconstitution system.

15 The reconstitution system allowed us to determine accurately

16 A reconstitution system allowed us to measure the ATPase a

17 roduction, PS1 FAD missense mutations in the reconstitution system alter the cleavage sites in the C9

18 These studies establish an in vitro RNAi reconstitution system and identify C3PO as a key activat

19 This report, using a full reconstitution system and natural chromatin substrates,

20 We employed an in vitro reconstitution system as well as cell cultures and an an

21 NADPH oxidase can be activated in cell-free reconstitution systems by several agonists, most notably

22 ximal activity of CYP3A4 is obtained using a reconstitution system consisting of NADPH-P450 reductase

23 rthermore, TIFA activates IKK in an in vitro reconstitution system consisting of purified proteins, i

24 These results suggested that this reconstitution system could be used to discern the catal

25 We have used a nuclear reconstitution system derived from Xenopus eggs to exami

26 rapid apoptosis in vitro using an apoptotic reconstitution system derived from Xenopus eggs.

27 The COS-7 reconstitution system described herein provides a valuab

28 s, and because excised organelle and bilayer reconstitution systems disrupt the Ca(2+)-induced Ca(2+)

29 It is anticipated that the reconstitution system established here will facilitate t

30 euronal cultures from rat hippocampus and in reconstitution systems expressing the cloned rat brain G

31 S; Rv3025c) and developed a native enzymatic reconstitution system for assembling Fe-S clusters in Mt

32 ting the validity of the recombinant protein reconstitution system for probing studies.

33 s study, we examined VX-770 activity using a reconstitution system for purified CFTR protein, a syste

34 eveloped and characterized a robust in vitro reconstitution system for Tetrahymena telomerase and tes

35 An in vitro reconstitution system for the analysis of replication-co

36 We have established a reconstitution system for the translocon SecYEG in prote

37 work establishes yeast as a powerful in vivo reconstitution system for the uniporter.

38 An inducible E2A reconstitution system further demonstrated that E2A-medi

39 The establishment of a defined in vitro reconstitution system has now paved the way for future b

40 Furthermore, this defined in vitro reconstitution system has now paved the way for future b

41 4 using purified Ubr2 and Rad6 proteins in a reconstitution system have been unsuccessful, suggesting

42 Here, we used a reconstitution system in IL-17RA-null fibroblasts to map

43 emonstrated in this study using a functional reconstitution system in NK cells.

44 Thus, through use of an in vitro nuclear reconstitution system, it has been possible to biochemic

45 cted U937 cells, and in vitro, using a novel reconstitution system of solubilized components.

46 We first confirmed that our reconstitution system produced UCP1 that exhibited known

47 Using an in vitro reconstitution system, purified nucleolin was likewise s

48 In an in vitro reconstitution system stable base pairing of the P6.1 st

49 Here we have developed a NHEJ reconstitution system that includes the nuclease, polyme

50 Using a functional in vitro reconstitution system, this study identified three HeLa

51 Here, we used a COS-7 cell reconstitution system to address this question.

52 ivery system also comprises a semi-automatic reconstitution system to facilitate its use and a specif

53 ished a nonhematopoietic BM microenvironment reconstitution system to functionally study specific cel

54 We developed an inducible reconstitution system to interrogate rhomboid proteolysi

55 ct on the value of mouse cardiomyocytes as a reconstitution system to investigate AR signaling in the

56 We used a MT-actin dynamics co-reconstitution system to observe CLIP-170-mDia1 complexe

57 We used this core reconstitution system to purify an RNAi regulator that w

58 The use of the cable-reconstitution system to test roles for the key actin-bi

59 variant bA2 proteins were also tested in two reconstitution systems to determine activity and affinit

60 Furthermore, in an in vitro reconstitution system, tyrosine-phosphorylated IkappaBal

61 ction of IDO in vivo should improve in vitro reconstitution systems used to identify potential IDO in

62 A newly developed 30 S subunit reconstitution system using a complete set of recombinan

63 We established a TACE-reconstitution system using TACE-deficient cells co-tran

64 have been extensively studied with in vitro reconstitution systems using purified components.

65 A whole-cell-based reconstitution system was developed to study the signali

66 Recently, an in vitro reconstitution system was developed using isolated OCP a

67 formation in a cell-free, cytosol-dependent reconstitution system was equally sensitive PLA(2) antag

68 By titrating PD-1 signaling in a biochemical reconstitution system, we demonstrate that the co-recept

69 Using the TACE-reconstitution system, we identified two additional subs

70 Using a chemically defined reconstitution system, we performed a systematic study o

71 Having established yeast as an in vivo reconstitution system, we then reconstituted the human u

72 Using an in vitro reconstitution system whereby the cellular heat shock pr

73 We report an in vitro chromatin reconstitution system, which uses arrays of 12 and 19 co

74 beta gamma-stimulated PLC-beta activity in a reconstitution system, while having no significant effec

75 Using a defined apoptosome reconstitution system with recombinant Apaf-1 and cytoch