ライフサイエンスコーパス: the fit(|s) of

1 on 32 terrestrial carnivore species to test the fit of 12 probability distributions.

2 eractions at the molecular level, we modeled the fit of 4-MEC and 4-MePPP into the binding pockets fo

3 related template structure while optimizing the fit of a model into the corresponding density map.

4 A local measure of the fit of a model to the density is used to directly gu

5 Additional data are presented supporting the fit of a porphyrin and monooleins.

6 use a predetermined critical value to assess the fit of a quantal model after parameter estimation ma

7 ond, a MC test enables a valid assessment of the fit of a quantal model after parameter estimation.

8 To find the best segmentation, we optimize the fit of a random-walk movement model to each motion t

9 among those lost as the value that maximizes the fit of a regression of the natural log of mortality

10 e removal of the extra tissue may compromise the fit of a subsequent prosthetic restoration.

11 xperimental values in order to determine how the fit of a substrate amino acid in one subsite influen

12 bstrate amino acid in one subsite influences the fit of amino acids in adjacent subsites.

13 The fit of blood level and response to a linear model wa

14 The fits of cell spectra to individual biochemical compo

15 parasites in migratory birds by contrasting the fit of competing models formulated in an occupancy m

16 Interestingly, the fit of computed versus observed gel mobilities using

17 The fit of corrected paramagnetic susceptibility chi(T)

18 An algorithm to improve the fit of cytogenetic bands sequence location reduces t

19 n that the most general test does not reject the fit of data to model (P approximately 0.5), but the

20 item bias or differential item functioning, the fit of data to model expectations, and whether or no

21 We test the fit of different MgSiO(3)-ppv deformation mechanisms

22 ry of the populations and formally comparing the fit of different models of language evolution.

23 Using this method we examine the fit of Erdos-Renyi (ER), ER with fixed degree distri

24 ion and a method is presented for evaluating the fit of estimated allele frequencies to the neutral i

25 The fits of EXAFS spectra of the model ferric complexes

26 From the fit of experimental data we estimate that the pK(a)

27 heir heavy-atom frames considerably improves the fit of experimental residual dipolar couplings to st

28 We used rigorous methods to evaluate the fits of expression readouts of 37 enhancers regulati

29 ent modifications including wing folding and the fit of folded wings.

30 tance is consistent with proposed models for the fit of Gb3 within the "cleft site" of the VT1 B-subu

31 The structures are discussed in terms of the fit of large metal ions to DPP with minimal steric s

32 e predictions of firing rates, based only on the fit of LFP data, correlated with the multiunit spike

33 is should be taken into account when testing the fit of models.

34 ormation of each fragment is scored based on the fit of multiple phi-psi angles of the fragment to a

35 Network properties are used to assess the fit of network models to the data.

36 dothelial TSPO in the kinetic model improved the fit of PET data.

37 e plasticity and local adaptation increasing the fit of phenotypes to local conditions and gene flow

38 We show that measuring the fit of predicted structural models to the allowed co

39 h how well the probability model "works": 6) the fit of probabilities calculated from the model to th

40 Explaining such variation across taxa in the fit of sex ratio theory remains a major challenge.

41 We compare the fit of simple random-walk models of trait evolution

42 The fit of sinusoids with the 3.6 residues per turn peri

43 An approximate halving of alpha improved the fit of the above equation to ERG a-wave and A(t)/Amo

44 The fit of the cellular 2-compartment model to the (18)F

45 ke information criterion was used to compare the fit of the competing models.

46 These thermodynamic parameters were used in the fit of the data from the coupled unfolding/ligand di

47 We also examined the fit of the data to possible alternative models.

48 Thermodynamic parameters obtained from the fit of the data to this model indicate that the inte

49 protein did not always significantly improve the fit of the evolutionary models to the data sets that

50 We compared the fit of the following 2 biometric models: the 2-facto

51 by maximum-likelihood methods revealed that the fit of the general reversible (REV) model was signif

52 The fit of the implemented models was assessed by mean o

53 The fit of the index was tested by applying it to anothe

54 The fit of the latent variable to comparison standards i

55 DSM risk score did not significantly improve the fit of the model (P = .75).

56 including additional CYP2A6 alleles improves the fit of the model in an independent data set and prov

57 CHA2DS2-VASc, CHA2DS2-VASc-R score improved the fit of the model significantly as measured by the lo

58 nonequilibrium model significantly increased the fit of the model to the breakthrough curves.

59 The fit of the model to the data yields an estimate of 5

60 ntrary to expectations, this did not improve the fit of the model to the experimental data, but resul

61 ified eight SNPs that consistently maximized the fit of the model to the phenotype.

62 ndividual rating scales that did not improve the fit of the model were systematically deleted, and a

63 Goodness-of-fit tests strongly supported the fit of the model, even though the detailed etiology

64 OA could be dropped without deterioration in the fit of the model.

65 The fit of the preferred models was better than that of

66 The P values for the fit of the preliminary and validation models are .93

67 d Bayesian uncertainty estimates, as well as the fit of the remainder of the spectrum using wavelets.

68 during the first year significantly improved the fit of the respective models and confirmed that ther

69 odel; the model-fit from BPSC is better than the fit of the standard gamma-Poisson model in > 80% of

70 The fit of the stiffer material silicone hydrogel lens w

71 The fit of the thermally activated region above approxim

72 As follows from the fit of the titration curve of Asp-85, deprotonation

73 From the fit of the VP8* core into the virion spikes, we prop

74 ble effects of anisotropic ligand motions on the fits of the calculated to the experimental XAFS spec

75 Interpreting the fits of the data at different [Mg] is consistent wit

76 The fits of the data to the model were constrained by in

77 t populated intermediate states as judged by the fits of the denaturation isotherms to a two-state mo

78 ore, which estimates the differences between the fits of the query structures and random coil structu

79 The performance of models based on the fit of their stationary distributions to the empiric

80 The FITs of these functions are exact inverses, and so t

81 The affinity recovered from the fits of these intensity profiles at 100 mM KCl was o

82 onfirmatory factor analysis was used to test the fit of this factor structure in the Bosnia and Era c

83 The fit of this model to early diverging eukaryotes, suc

84 ed in glucose-limited soft agar, we evaluate the fit of this model to experimental data.

85 We examined the fit of this model using likelihood-ratio tests by an

86 ed with its "protector" protein, Sigma3, and the fit of this Mu1(3)Sigma3(3) heterohexameric complex

87 The fit of transient dwell occurrence to the sum of thre

88 We compared the fit of two types of models to lung-function measurem