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Pluripotent stem cells, created from human skin or mouse ear tissue, are shown here developing into neurons.
Details of lipid identification in mouse ear tissue.
b Result of lipid profiling in a mouse ear tissue.
The lipid molecules from HEK cells, HeLa cells, mouse liver tissue, and mouse ear tissue are depicted in green, red, black, and blue, respectively.
The common parameters in both positive and negative ion mode were collision energy, 45 V; collision energy spread, 15 V; mass range, m/z 70 1250; curtain gas, 30; ion source gas 1, 50; ion source gas 2, 50; temperature, 500 °C for mouse ear tissue and 300 °C for the other samples; declustering potential, 80 V; RF transmission, default.
To explore if nanoparticles are as effective as microparticles, we biolistically transfected mouse ear tissue and then examined sections of tissue to determine the location of the particles.
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Histological analysis was further performed to check whether LERD inhibited mast cell degranulation in mouse ear tissues.
The mouse ear tissues presented in Figure 1A C were prepared for transmission electron microscopy (TEM) 24 hr after sub-cutaneous injection of saline or 1 × 10 PFU of a clinical isolate of DENV.
MYH7B was found to be concordantly expressed in embryonic mouse inner ear tissue but not in non-inner ear tissue, with atonal homolog 1a, ATOH1, a gene required for hair cell differentiation [ 22].
However, there is indirect support for MYH7B involvement in hearing including expression in embryonic mouse inner ear tissue [ 22], expression in the primary auditory complex in humans, and the control of dendritic spine morphology, excitatory synaptic strength, and the actin cytoskeleton in rat neurons [ 23].
For ex vivo mouse ear imaging, the ear tissue was acquired via ear punch (Φ = 3 mm).
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