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 unty-level income distributions, we estimate the fit of 17 previously proposed models and find that m

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

4 e using a linear term significantly improves the fit of a computational model of mood.

5 dependent grazing deepens the DCM, improving the fit of a global model with observational data.

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

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

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

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

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

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

12 Based on the fit of a reaction model to the geochemical data and

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

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

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

16 ixture spectrum and simultaneously optimizes the fit of all individual compound spectra in a given li

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

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

19 ting subsets of time series data, then ranks the fit of break point combinations using model selectio

20 The fits of cell spectra to individual biochemical compo

21 pillover effect, spontaneous improvement, or the fit of collaborative care for clinically complex pat

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

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

24 The fit of corrected paramagnetic susceptibility chi(T)

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

26 rid search over Ig1 orientations to optimize the fit of data to a single conformer for both forms pro

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

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

29 -making by attention weights did not improve the fit of data, providing little evidence for direct at

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

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

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

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

34 The fits of EXAFS spectra of the model ferric complexes

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

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

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

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

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

40 A second outcome measure included the fit of glasses designed by the 3DSI method as report

41 examine differences in growth; and to assess the fit of growth charts.

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

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

44 p learning emphysema classification improved the fit of linear mixed models in the prediction of thes

45 cies of corvoid passerines, and assessed (a) the fit of models of continuous trait evolution with dif

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

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

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

49 al pool prior to ART initiation and analyzed the fit of our experimentally derived data to these mode

50 The fit of our model's predictions demonstrates that mal

51 and applied automated methods for assessing the fit of participants' genomic findings to existing cl

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

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

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

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

56 ifferences in lattice confinement also limit the fit of RDCs to X-ray coordinates.

57 s-of-fit (GOF) tests were proposed to assess the fit of RE model.

58 We examined the fits of several pRF models based on the fMRI blood-o

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

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

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

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

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

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

65 identified a single LFI cutoff by evaluating the fit of the competing risk models, searching for the

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

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

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

69 The indicator improved the fit of the disease-mapping model (deviance informati

70 between the FRET efficiency calculated from the fit of the eGFP15eGFP fluorescence anisotropy decays

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

72 The fit of the final model was measured by R(2).

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

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

75 ctor analysis (CFA) was conducted to examine the fit of the hypothesized seven-factor model, and the

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

77 trieved from ChemSpider were scored based on the fit of the in silico fragments to the experimental t

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

79 The fit of the latent variable to comparison standards i

80 rved, finding that it significantly improved the fit of the model (P = .003).

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

82 of the IBD GRM did not significantly improve the fit of the model for the monogenic traits, it improv

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

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

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

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

87 is inferred, while simultaneously improving the fit of the model to the data.

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

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

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

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

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

93 nt theory (RMT) analysis was used to examine the fit of the observed data to the Rasch model for each

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

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

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

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

98 anded and asymmetric conformations improving the fit of the SANS data.

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

100 The fit of the statistical model for the prognostic scor

101 The fit of the stiffer material silicone hydrogel lens w

102 The fit of the thermally activated region above approxim

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

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

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

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

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

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

109 No significant difference was found between the fits of the models and with respect to parameters D(

110 the expressed model estimated, according to the fits of the models to each subject.

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

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

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

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

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

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

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

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

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

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

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