ライフサイエンスコーパス: nonhomogeneous

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1 f individual patients shows this group to be nonhomogeneous.

2 es although granulation tissue formation was nonhomogeneous and there seemed to be greater inflammati

3 n of binding affinity is mainly derived from nonhomogeneous-based methods such as surface plasmon res

4 in basement membrane nephropathy (TBMN); one nonhomogeneous basement membrane abnormalities; one IgA

5 method to account for the nonstationary and nonhomogeneous characteristics of ambient air pollution

6 ectors derived from content-free word usage, nonhomogeneous decay rates of stylistic influence, and a

7 Single-molecule analysis revealed nonhomogeneous diffusion of Munc18-1 and syntaxin-1A in

8 Digital autoradiography images revealed a nonhomogeneous distribution of (99m)Tc-SPIONs within the

9 The nonhomogeneous distribution of information across brain

10 The nonhomogeneous distribution of signal transduction prote

11 e use of molar fraction ratios overcomes the nonhomogeneous distribution of the tagging element withi

12 This nonhomogeneous distribution of variation suggests that m

13 psule was honeycomb-like networks containing nonhomogeneous distributions of HBEO.

14 -density DNA-Cy3 located in spot centers and nonhomogeneous DNA distribution within printed spots.

15 tly of short compositionally homogeneous and nonhomogeneous domains and a few long ones.

16 s a tapestry of mostly short homogeneous and nonhomogeneous domains and few long ones thus providing

17 of the genome is composed of compositionally nonhomogeneous domains and the remaining is a mixture of

18 a mixture of compositionally homogeneous and nonhomogeneous domains of varying lengths and nucleotide

19 We postulate that this nonhomogeneous electrostatic effect of cholesterol has a

20 1b-specific antisera indicated a predominant nonhomogeneous, extranuclear distribution within the cel

21 ing scales, resulting in a nonstationary and nonhomogeneous formulation of the inference problem.

22 lla, while alphaB-crystallin labeling became nonhomogeneous in outer medulla, and increased in Bowman

23 es, VA/VL projections terminate in a patchy, nonhomogeneous manner, indicating another level of compl

24 Nonhomogeneous Markov models of nucleotide substitution

25 Here we explore the possibility of using nonhomogeneous models to identify host shift nodes along

26 istress syndrome (RDS) may be limited by the nonhomogeneous nature of ventilation in the preterm lung

27 g the discrete gamma distribution, and using nonhomogeneous nonstationary representations of the subs

28 A nonhomogeneous Poisson model with a piecewise log-consta

29 We propose a cascading nonhomogeneous Poisson process that explicitly integrate

30 We use nonhomogeneous Poisson processes to model the acquisitio

31 re is a significant ratio of defects in this nonhomogeneous sample that contains regions with differe

32 This nonhomogeneous solvation shell has been ignored in studi

33 s or bovine serum albumin (BSA) results in a nonhomogeneous solvation shell that is reflected by nons

34 an explain the observed La III emissions and nonhomogeneous spatial distribution of exited species.

35 valuable tool for the assessment of regional nonhomogeneous strains in various depths and locations o

36 NM categories within 7th TNM stages revealed nonhomogeneous survival rates in stages IIB, IIIB, and I

37 how to assign dielectric constants in mixed, nonhomogeneous systems.

38 l with now classic analyses and is generally nonhomogeneous though axisymmetric down to the submicron

39 t genes differentially expressed between two nonhomogeneous time-series data sets.

40 Because of the nonhomogeneous, traveling wave (TW) field utilized in th

41 endothelial cells were used to calculate the nonhomogeneous two-dimensional strain field over the ima

42 time, especially for pollutants with strong nonhomogeneous variances across space.

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