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1 t does approach an only slightly more costly local minimum.

2 nses to near-threshold white noise exhibit a local minimum.

3 lity fine-tuned with phonon stability at the local minimum.

4 The former corresponds to a local minimum.

5 is is augmented by a grid search to identify local minimums.

6 here traveling-wave phase velocity attains a local minimum and a local maximum and where the onset la

7 between the TRS and random B-DNA revealed a local minimum at approximately 520 base pairs.

8 ell-defined alternating manner, displaying a local minimum at or very close to the critical sterol mo

9 amic global energy minimum (twist-boat) to a local minimum (chair), as the origin of this abnormal th

10 ffected by feedback loops appears to be at a local minimum compared with surrogate shuffled networks.

11 hat over 60% of the ligands do not bind in a local minimum conformation.

12 There is no local minimum for adsorption over the symmetric bridging

13 ation versus shock duration curve contains a local minimum for moderate shock durations, and it grows

14 One extreme, corresponding to the local minimum for Si-Si and Ge-Ge, is a diradicaloid mul

15 Another extreme, corresponding to a local minimum for Sn-Sn, is a relatively closed-shell si

16 This geometry is a higher energy local minimum for the pentadienyl anion and is not a sta

17 based on the local Fisher Information of one local minimum generates additional data that allows one

18 Therefore, the length corresponding to the local minimum in free energy of supercoiling correlates

19 tally that branches initiate at sites with a local minimum in the concentration of autocrine inhibito

20 le intermediate that represents a productive local minimum in the energy landscape that increases the

21 outward directions, and there is no similar local minimum in the two-dimensional free-energy landsca

22 tional theory methods identified (4)E as the local minimum in this hemisphere.

23 analytes are detected as gaps (regions with local minimums in intensity) in the fluorescent signals

24 When a local minimum is avoided and optimization is achieved, 2

25 We find that the number of local minimums is highly sequence dependent, with certai

26 ely flat free energy surfaces, with a small, local minimum observed for the flipped G base.

27 rocapsid represents a kinetically accessible local minimum of free energy.

28 The block state occurs in an unstable local minimum of the equilibrium unperturbed free-energy

29 r dynamics--every spanning tree is exactly a local minimum of total energy dissipation.

30 Each substate reflects a local minimum on the free-energy landscape with a distin

31 with known XeF5 (-) ion, is computed to be a local minimum on the potential energy surface of CsF5 ,

32 ly cause the intermediate to sit in a deeper local minimum on the potential energy surface.

33 eriodicity attributed to codons, which has a local minimum probability at approximately 10.5 bp.

34 To circumvent the local-minimum problem efficiently, this method performs

35 ed by the N,N'-disubstitutes, resulting in a local minimum state, i.e., the intermediate.

36 r tetra-, penta-, and hexacoordinate carbon (local-minimum) structures are obtained.

37 r 24 of the 30 oligomers, we find low-energy local minimums that match the experimental step paramete

38 The activity reaches a local minimum when the membrane cholesterol content is a

39 Each vertex of the BHG is a local minimum, which represents the corresponding basin

40 pentane lead to a metastable intermediate (a local minimum with relatively small barriers to escape t

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