ライフサイエンスコーパス: models

1 e force of infection (FOI) between districts, we compared 6 models of population movement (adjacency, gravity, radiation,

2 In fully adjusted models, only death-censored graft loss remained significant (

3 simulated biomass and in k (severe underestimations by all models except JeDi and VISIT compared to observation-based av

4 Animal models have begun to elucidate how skin barrier defects can l

5 arenaviruses, as well as a discussion of the current animal models of infection.

6 ummarize the conceptual foundations of genetic group animal models and provide extensive, step-by-step tutorials that dem

7 Cell or animal models that accurately reflect the pathology of LAM have been

8 Both models found that antibodies to 5 proteins of the Merozoite S

9 Both models remained effective after inclusion of older patients i

10 PCR) genotyping technology to create scarless isogenic cell models of cancer variants in 1 month.

11 Here, we studied causes of uncertainty among 16 crop models in predicting rice yield in response to elevated [CO2]

12 nd nucleator deficiency, consistent with microscopy-derived models proposing PMS as specialized cortical actin.

13 We study in three different models of this system how these two seemingly conflicting cri

14 ics of a broad class of resource-limited community dynamics models, regardless of parameterization and model assumptions.

15 ion hemodynamic trends derived from nonlinear mixed-effects models showed small early favorable changes in the first few

16 We have extended the framework of Nested Effects Models (NEMs), a type of graphical model specifically tailore

17 Experimentally validated FE models are combined for that purpose in one joint simulation.

18 urveillance data provide opportunity to develop forecasting models.

19 nnotation with a substantially increased resolution of gene models will not only further our understanding of the biologi

20 To address the issue that deep probabilistic graphical models requires large number of labeled training samples, we

21 Cox proportional hazards models were fitted to assess associations of asthma history w

22 IDREAM models contain many fewer interactions than PROM and yet prod

23 Using three mouse infection models, we show that the SIP signaling pathway is active duri

24 Our results suggest that in these inflammatory models, acute administration of peripherally restricted NaV1.

25 equence capacity has been extensively studied using lattice models and theory, numerical estimates for real protein struc

26 Log-linear models were used to estimate prevalence ratios (PRs) of feedi

27 We advanced LUR models for benzene, toluene, ethylbenzene, p-xylene, m-xylene

28 We have developed mathematic models of brain activity that allow for accurate prediction o

29 Most conceptual and mathematical models of soil vapor intrusion assume that the transport of v

30 Here we develop mathematical models of Tfh cells in germinal centers to explicitly define

31 Continuum mechanics models suggest that buckled cofilactin filaments localize ela

32 Bayesian mixed models estimated the plausible range of effects for televisio

33 We review current molecular models to explain ribosomopathies and attempt to reconcile th

34 Mouse models of T. cruzi infection have been used to study heart da

35 rp3 is expressed in reactive cholangiocytes, in both murine models and patients with PSC.

36 Two murine models of synucleinopathy (a Gaucher-related synucleinopathy

37 e engineering approach to infer data-driven dynamic network models of multi-organ gene regulatory influences.

38 effects of cortistatin in two well-established preclinical models of atherosclerosis, and the molecular and cellular mec

39 nological tools to study anti-ZIKV responses in preclinical models, particularly T cell responses, remain sparse.

40 However, the ictal characteristics of these rat models, including SWDs and associated immobility, are also pr

41 Multivariable binomial regression models were used to evaluate the effects of oral health, gene

42 rd ratios (HR) and 95% CIs with multivariate Cox regression models fitting stromal TILs as a continuous variable (per 10%

43 We used Cox proportional hazards regression models to assess the association between later-generation flu

44 SNPs to all phenotypes using logistic and linear regression models.

45 rall, larger and deeper perforations were found in the skin models with increasing water content.

46 ly dissect this data requires the development of stochastic models that can both deconvolve the stages of polymerase acti

47 ve, step-by-step tutorials that demonstrate how to fit such models in a variety of software programs.

48 riggering neuroprotective Treg responses in synucleinopathy models, and the combined vaccine is more effective than the h

49 esults in T-cell activation and antitumor activity in tumor models.

50 ster than wild-type clones in s.c. and orthotopic xenograft models.