ライフサイエンスコーパス: association state

1 nd 3 without significantly altering its self-association state.

2 s responsible for the observed difference in association state.

3 roenvironments in response to changes in its association state.

4 ntermembrane junctions and find two distinct association states.

5 Association states above this are known, as are antipara

6 al studies have been performed regarding its association state and biological/structural stability.

7 iologic mechanisms may alter the native self-association state and contribute to apoA-I dysfunction.

8 ype enzyme in secondary structure or subunit association state, as shown by circular dichroism spectr

9 rations of denaturants show no change in the association state before the unfolding transition and ar

10 ittin, corresponding to two melittin-bilayer association states, could be used to interpret the exper

11 otides and related the binding properties to association states determined from sedimentation propert

12 ociating proteins, can reveal a time-average association state for rapidly reversible self-associatio

13 Representatives from state hospital associations, state health departments, and other partic

14 oth the amphiphilic environment and the self-association state of CcO affect its kinetic stability.

15 SAXS and SEC-HPLC results indicate that the association state of DnaK is very sensitive to the buffe

16 The association state of FliN in solution was studied by ana

17 These findings about the association state of free L chains are independent of th

18 s of hDlg interactions, we examined the self-association state of full-length hDlg as well as defined

19 Further evaluation of the self-association state of hDlg using sedimentation equilibriu

20 tions may lead to substantial changes in the association state of the adsorbed proteins, the biologic

21 44' and His 55 and Thr 67' do not change the association state of the dimer.

22 l content and by consolidating the monomeric association state of the full-length protein.

23 owever, EGF stimulation had no effect on the association state of the Grb2-SOS or the Nck-SOS complex

24 ny of the uncertainty sources (the solvation/association state of the guest in solution, deviations i

25 enables unique insight into the aggregation/association state of the ions and the nucleophilicity of

26 This is not related to a change in association state of the polypeptide.

27 surements have not discriminated between the association state of the receptor.

28 In this study, we characterized the self-association states of ExsC, ExsD, and ExsE and the bindi

29 anges in dynamics, high-order structure, and association states of macromolecules in fully formulated

30 Characterizing the association states of proteins during folding is critica

31 re, SiMPull can distinguish between multiple association states of the same protein.

32 erived neurotrophic factor, and the solution association states of these molecules.

33 To study the association states of unfolded, folded, and intermediate

34 this experiment can be used to determine the association states of unfolded, folded, and kinetic inte

35 within adherens cell-cell junctions, but its association state outside these clusters is unknown.

36 merization at the replication origin but the association state remains unclear.

37 concentrations of urea on the conformation, association state, stability, and kinetics of fibrillati

38 The new Guidelines of the American Heart Association state that lay rescuers can no longer rely o

39 In 2016, the American Statistical Association stated that the use of statistical significa

40 us subtilis NOS loose dimer shows an altered association state with severely destabilized subdomains.

41 tion of insulin involves both changes in the association state (with rate-limiting hexamer dissociati