Publications by authors named "M R De Niese"

Article Synopsis
  • Van der Waals heterostructures allow for the customization of electronic properties by combining two-dimensional materials, particularly bilayer graphene and transition metal dichalcogenides (TMDs).
  • The study confirms two types of spin-orbit coupling (SOC) in bilayer graphene when in contact with molybdenum disulfide: Ising and Rashba coupling, with respective energy values of 1.55 meV and 2.5 meV.
  • Observations include a unique pattern in conductivity as the electric displacement field changes, attributed to Ising SOC-induced gaps, and noticeable spikes in magnetoconductivity that challenge current theoretical understandings.
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Atopic dermatitis results in diminished barrier function and altered production of antimicrobial peptides. Dendritic epidermal T cells (DETCs) play an important role in the wound repair and inflammation process. Our previous work identified an IL-4-dependent loss of DETCs in Stat6VT mice and in the MC903-induced skin inflammation mouse model.

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Multi-cytokine-producing Th9 cells secrete IL-9 and type 2 cytokines and mediate mouse and human allergic inflammation. However, the cytokines that promote a multi-cytokine secreting phenotype have not been defined. Tumor necrosis factor superfamily member TL1A signals through its receptor DR3 to increase IL-9.

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The polarization of naive Th cells into differentiated subsets in vitro was a powerful approach to define the development and function of Th cells in vivo. Th cell cultures identified cytokines that promote polarization and defined the phenotype and stability of differentiated cells. One of the limitations of this approach is the heterogeneity of the differentiated culture, essentially with regard to what proportion of the culture is secreting the hallmark cytokine of interest.

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The multifunctional serine protease thrombin has been shown to be a specific agonist for a variety of functional responses of cells including osteoblasts. The current study was conducted to determine if thrombin was capable of inhibiting apoptosis in osteoblasts, and if so, to examine the mechanism by which this occurred. Thrombin (20-100 nM) significantly inhibited apoptosis in serum-starved cultures of the human osteoblast-like Saos-2 cell line and cultures of primary osteoblasts isolated from mouse calvariae, as well as dexamethasone-treated primary mouse osteoblasts.

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