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To be a true Alzheimer's model, the mice should go on to produce amyloid and develop plaques--and they show no biochemical evidence of either.
Because the ICE approach involves a series of univariate models rather than a single large model, the MICE approach imputes data on a variable by variable basis by specifying an imputation model per variable.
In our previous report comparing CD3/CD28 Dynabead T cells with OKT3/IL-2 T cells in the Nalm6 leukemia mouse model, the mice were treated with CD19 CAR RNA-electroporated T cells, and we found that OKT3/IL-2 T cells were inferior to the CD3/CD28 Dynabead T cells in controlling leukemia.
In our model the mice develop high levels of Hgb.
In this model, the mice express a TCR specific for LCMV gp33 41 peptide and the LCMV gp protein expressed in β-pancreatic cells.
When Xbp1S was expressed under the control of the immunoglobulin VH promoter/ Eμ enhancer in a transgenic mouse model, the mice developed multiple myeloma.
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The most extensively used animal model, the mouse, is not a natural host of M. tuberculosis.
Like all disease model systems, the mouse model of cerebral malaria is imperfect.
Cognition tests and memory assessment were done based on a water maze model where the mice had to find their way to a platform using given cues.
Compared to mice in the model group, the mice treated with 1,25(OhadD3 had a reduced DSS-induced histologic colitis.
In contrast to the rat models, the mouse PGIA model is a chronic and progressive model of RA [27].
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