Sentence examples for mouse brain tumor from inspiring English sources

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Primary mouse brain tumor cultures were established from GL26 tumor removed at time of euthanasia after acquisition of terminal neurological symptoms.

Ten days later, the mouse brain tumor site was injected with 5 µL of lentiviral vector (pCDH-CMV-MCS-EF1-copGFP) with or without miR-101.

More recent work with an orthotopic mouse brain tumor McCann, et al. successfully applied fluorescent molecular tomographic imaging to monitor protease activity in tumor by using protease activatable fluorescence, ProSense680 (peak light emission at 680 nm).

It is also important to mention that our recently developed highly invasive VM3 mouse brain tumor cells are of myeloid origin and are highly positive for AIF1/Iba1 by gene and protein expression [97].

In addition, recent IVM and MRI studies in a U87 mouse brain tumor model demonstrated that cediranib significantly prolongs survival despite persistent tumor growth, where the survival benefit was primarily attributed to decreased vascular permeability and reduction of edema [20].

The fact that the VCI and ADC were not sensitive to cediranib therapy in our mouse brain tumor model, in contrast to the clinical cediranib study [7], suggests that the sensitivity of a particular MRI biomarker varies depending on which physiological factors are being altered most by a given therapy for a particular tumor.

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Magnetic resonance imaging of patched heterozygous and xenografted mouse brain tumors.

Tumor triggers: Evidence is growing for the existence of cancer stem cells, a population of tumor cells with stem-cell like properties, such as the cells that glow green in these two images of mouse brain tumors.

In the B6C3F1 mouse, brain tumors are exceedingly rare.

These mtDNA mutations in the mouse brain tumors are similar to those found previously in hypervariable regions of the D-loop in human brain tumors.

However, none of the mouse mutations were pathogenic suggesting that mtDNA changes do not contribute to the carcinogenic progression of these chemically induced and spontaneous mouse brain tumors.

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