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Overall, these hyperspectral unmixing results support the uniqueness of the basis spectra extracted from small representative regions of epithelium, laminar propria, collagen and lymphatic tissue, demonstrating that they are consistently able to identify these tissue types throughout a range of samples, mice and GI tissue types.
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Each matrix has 40 samples (mice) (Genotype, 2 levels and Diet, 5 levels); K1 has 115 genes and K2 has 21 FA.
The lapses include missing pathogen samples, escaped mice, and tears in protective equipment being used by researchers studying deadly viruses such as Ebola and the H5N1 bird flu.
Serum samples from mice and concentrated conditioned medium were used as the source of S-SMase.
We used quantitative RT-PCR, gel mobility shift, and luciferase activity assays in human samples, live mice, and cell culture.
All the samples from mice and rats (pool of liver, spleen, and kidney) had negative results after 3 passages on both cell lines.
Analysis of lung DNA samples from mice and rats exposed to butadiene through inhalation showed that adenine N6 adducts were formed in vivo in a dose responsive manner.
L5 vertebrae were extracted from a random sample of mice and fixed in formalin.
After the last sample, mice were anaesthetized and tissues were collected.
Hippocampus and heart tissues samples from mouse and rat pups (3 different biological samples from 1 week old animals) were isolated and stored immediately at -80°C.
Viral infection was monitored by checking viral reads, and sample mice for which no viral reads could be detected were removed from further analysis.
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