ライフサイエンスコーパス: reassociate

1 zation and cause completely monomeric CcO to reassociate.

2 her, DNA both ahead of and behind the enzyme reassociates.

3 tol, but dithiothreitol failed to completely reassociate 3,4-dichloroisocoumarin- or H2O2 treated MCP

4 in the absence of PP1 activity, but rapidly reassociates after its reactivation.

5 during mitosis at the beginning of prophase, reassociating again at the end of telophase and cytokine

6 insect tissues are exhausted, whereupon they reassociate and leave the cadaver in search of new prey.

7 s with two, three, six, nine or 27 arms were reassociated as complementary pairs in solution or with

8 tubules at the beginning of mitosis and then reassociates at cytokinesis.

9 Reassociating double-stranded DNA from single-stranded c

10 resent a method that is equally suitable for reassociating either simple or complex DNA mixtures.

11 of thin sections of naturally colonized and reassociated flies.

12 ric complex dissociated, and it subsequently reassociated following more prolonged agonist stimulatio

13 dissociation, but differ in their ability to reassociate in darkness, setting the stage for bioengine

14 Dissociated rat cortical neurons reassociate in vitro to form synaptically connected netw

15 pdDronpa, that dissociates in cyan light and reassociates in violet light.

16 mer can dissociate, change conformation, and reassociate into a different oligomer.

17 rtantly, the oxygenase domain monomers could reassociate into a dimeric form even in the absence of t

18 rea-generated monomers of the mutant fail to reassociate into dimers when incubated with l-Arg and te

19 This implies that the nervous system quickly reassociates new relationships between vestibular sensor

20 kinetics and the dissociated monomers do not reassociate readily back to the oligomer.

21 Unlike GroEL, GroES monomers do reassociate readily.

22 by deacylation of initiator caspases cannot reassociate to active heterotetramer, thus resulting in

23 ns in the monomer are able to dissociate and reassociate to form a dimer, or diabody, but in which sy

24 When cultured, murine islet cells reassociate to form pseudoislets, which recover normal g

25 cleoprotein (hnRNP) complexes quantitatively reassociated to form regular helical filaments ranging i

26 emoved, the resulting monomeric CcO will not reassociate upon the addition of sodium cholate.

27 protein heterotrimer rapidly dissociated and reassociated upon addition and removal of chemoattractan

28 chloromercuri) benzenesulfonic acid could be reassociated upon treatment with the reducing agent dith

29 Both triple-site mutants reassociated well with RTA.

30 These receptors reassociate when cells return to a spherical morphology.

31 The polypeptides reassociated when shifted back to pH 8.0.

32 16 (M16) is followed by G1, and MCMs do not reassociate with chromatin at the end of M16.

33 hin nuclei or nuclear extracts allows MCM to reassociate with chromatin during S phase and induces re

34 hyperphosphorylated mitotic chromosomes, but reassociate with chromatin late in M-phase.

35 nic cell cycles, which lack a G1 phase, MCMs reassociate with condensed chromosomes toward the end of

36 Removal of cadmium allows PML to reassociate with eIF4E nuclear bodies, leading to decrea

37 e show that Ply released by autolysis cannot reassociate with intact cells, suggesting that there is

38 ins in close proximity to that fragment, can reassociate with it, and diffuse back to the recognition

39 Once transcription is halted, cohesin can reassociate with its original sites, independent of DNA

40 cell binding, immunoreactivites, ability to reassociate with RTA, and recombinant heterodimer cell c

41 ylmethionylleucylphenylalanine, FAK and TrxR reassociate with sF-actin and cause SNO-actin removal.

42 e end of the cell cycle, Epac is observed to reassociate with the nuclear envelope and concentrate ar

43 In one, RT was allowed to reassociate with the primer-template after falling off,

44 some markers near the centromere transiently reassociate with their sisters and oscillate from one sp

45 that Gbeta gamma dimers dissociate from and reassociate with these Ca channels at very similar rates

46 h as exchangeable apolipoproteins, appear to reassociate with TRLs in the vascular compartment.

47 er salt removal, sigmaK, but not pro-sigmaK, reassociated with exogenous core RNA polymerase to form

48 arriage by antibiotic treatment and could be reassociated with laboratory strains.

49 Instead, FAs reassociated with LDs and fluxed into neighboring cells.

50 aseins and denatured whey proteins partially reassociated with the caseins, although a complex behavi

51 m these structures back to the ER where they reassociated with the chaperone.

52 anes, but after Ca2+ chelation, they rapidly reassociated with the Golgi, the intracellular vesicles

53 In RyRs reassociated with triadin 1 and junctin, adding luminal

54 g cortical granule exocytosis, however, rab3 reassociates with a different population of vesicles, at

55 contrast, purified EcapZ stoichiometrically reassociates with all the actin filament barbed ends in

56 .e., it microscopically dissociates from and reassociates with DNA as it diffuses rather than remaini

57 ed by galactose depletion, preexisting Gal80 reassociates with Gal4, indicating that sequestration of

58 t the prophase I/metaphase I transition, and reassociates with rDNA before anaphase I onset.

59 due to a rapid IkappaBalpha resynthesis that reassociates with Rel A and completely inhibits its DNA

60 Upon relief of stress, HBO1 reassociates with replication origins.

61 release of unencumbered Gt beta gamma, which reassociates with the membrane and Gt alpha to form a si

62 bleaching (FRAP) showed that fibrillarin-GFP reassociates with the NDF and PNBs at rapid and similar

63 After actin assembly, CP reassociates with the new actin cytoskeleton.

64 In one, only the DNA ahead of the polymerase reassociates with the octamer.

65 ociates from p130/DREAM, binds to B-Myb, and reassociates with the promoters of late genes during S p

66 dk2-cyclin E within nuclei prevents MCM from reassociating with chromatin after replication.

67 iates from salivary mucin-linked HBGA before reassociating with HBGAs linked to intestinal epithelial