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2 tanding derived from studies of patients with MS and animal models of how specific cytokines produced by autoreactive CD4
3 inhibits mast cells and that has shown potential in animal models as a treatment for eosinophilic gastritis and duodenit
4 R PBM improves functional and structural outcomes in animal models of retinal injury and retinal degenerative disease.
5 We further present advances in animal models that are important for understanding the pathogenesis
7 ent and unique CCL17-driven inflammatory pain and arthritis models, the latter permitting a radiation chimera approach to
8 onventional structural-biology approaches, to obtain atomic models of multiple protein complexes implicated in intraeryth
9 a machine learning approach, we built gene expression-based models to predict drug sensitivity for 265 common anticancer
11 eed for methods facilitating the expansion of computational models to incorporate these newly-discovered components.
13 ts, which enable modeling of kinematic loops (e.g., cycling models) and complex anatomy (e.g., patellar motion).
15 long-range looping interactions change across developmental models, genetic perturbations, drug treatments, and disease s
16 pigenetic alterations in schizophrenia and relevant disease models and discuss their putative origin.
18 As we used an ensemble of state-of-the-art fire models, including effects of land use and the ensemble median
19 The largest quantities of products were formed in food models at pH 6.4, which is close to the pH optimum of LOX.
22 results suggest the need to refine PSB and crack-initiation models in metals to account for gradual and heterogeneous evo
24 The training performance of all machine learning models, including six other algorithms, was evaluated by inte
25 , accurate prediction of relative permeability using legacy models (e.g. Brooks-Corey (B-C), van Genuchten, etc.) that we
29 Multivariable generalized linear mixed models for binary outcomes were used to examine the relations
30 rolled by diverse NUP98-fusion proteins, we developed mouse models for regulatable expression of NUP98/NSD1, NUP98/JARID1
31 In vivo, m-RCT was evaluated in mouse models of hypercholesterolemia that were naturally deficient
34 Harnessing the rich information contained in multistate models, we investigate cell-to-cell variability of chromatin
36 The imaging readouts can be obtained in both preclinical models of diabetes mellitus and patients with diabetes mellit
40 our models improves fitness by 70% and 77% over the random models for a discoidal or an ellipsoidal stem cell confinemen
43 A lack of cost-effective, reproducible models for the study of M. haemolytica pathogenesis has hampe