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Showing results for "aboriginal respiratory"
The Kids Research Institute Australia researchers will have continued access to the latest equipment to support and enable their important research, thanks to Maia Financial.
Exposure to sunlight may limit cardiometabolic risk.
Dietary vitamin D3 increased the suppressive activity of regulatory T cells in the skin-draining lymph nodes, which are poised to suppress dermal inflammation
Perinatal characteristics, early childhood development and medical co-morbidities in MECP2 Duplication syndrome
Measures of allergic sensitization and therapeutic strategies could be optimized with knowledge of Der p 2 variants
Here we discuss how skin exposure to sunlight may suppress liver inflammation and the severity of NAFLD.
In this study, we aimed to uncover the molecular mechanisms contributing to altered lung structure and function.
In experimental models, both vitamin D3-dependent and vitamin D3-independent pathways have been implicated in the mechanisms of UVR-induced systemic...
The analysis of 25-hydroxyvitamin D3 (25(OH)D3) and related metabolites represents a considerable challenge for both clinical and research laboratories...
B cells are critical to the development of multiple sclerosis (MS), but the mechanisms by which they contribute to the disease are poorly defined. We hypothesised that the expression of CD32b (FcγRIIb), a receptor for the Fc region of IgG with inhibitory activities in B cells, is lower on B cell subsets from people with clinically isolated syndrome (CIS) or MS. CD32b expression was highest on post-naive IgM+ B cell subsets in healthy controls. For females with MS or CIS, significantly lower CD32b expression was identified on IgM+ B cell subsets, including naive and IgMhi MZ-like B cells, when compared with control females. Lower CD32b expression on these B cell subsets was associated with detectable anti-Epstein Barr Virus viral capsid antigen IgM antibodies, and higher serum levels of B cell activating factor. To investigate the effects of lower CD32b expression, B cells were polyclonally activated in the presence of IgG immune complexes, with or without a CD32b blocking antibody, and the expression of TNF and IL-10 in B cell subsets was assessed.