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Previously, we established a process of in vivo guided tracheal regeneration using vascular allografts as a biological scaffold.
Previously we established the hypotensive action of nitric oxide donors, dinitrosyl-iron complexes (DNIC) with thiol-containing ligands, stored in frozen solution at 77 K.
Previously, we established a collagen coating method for fabricating a micrometer-sized collagen matrix on cell surfaces to control cell distance or cell densities inside tissues.
Previously, we established the echo model of target with micro-motion, and time-frequency transformation of the echoed signal is applied to gain the time-varying micro-Doppler frequency features of target.
Previously, we established a Drosophila FraX model and showed that dFMRP acts as a negative translational regulator of Futsch/MAP1B and negatively regulates synaptic branching and structural elaboration in the peripheral neuromuscular junction (NMJ) [8].
Previously, we established the feasibility of using solid phase capturable (SPC) dideoxynucleotides to generate single base extension (SBE) products which were detected by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) for multiplex genotyping, an approach that we refer to as SPC SBE.
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As previously mentioned, we established endogenous DRAM knockdown cell lines in wild-type p53.
Previously, we have established that one factor that affects energy output is initialization with natural convection.
Previously, we have established an organotypic culture system of skin to induce epidermal differentiation in adult stem cells.
Previously, we have established a novel mice model of FM, using intermittent cold stress (ICS) exposure.
We measured loss of intravascular fluorescence activity using an eye assay that we established previously [18].
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CEO of Professional Science Editing for Scientists @ prosciediting.com