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References in periodicals archive ?
Conclusion: We confirmed a strong association between high monocyte counts and past VTE.
Now, Tokyo Medical and Dental University (TMDU) has identified equivalent monocyte progenitors in humans.
According to the company, the method of use claims granted for this patent will provide protection for the treatment of cancer where a plurality of doses of IMP321 is used to generate a monocyte mediated response.
Monocyte chemoattractant protein-1 (MCP-1) facilitates the migration of inflammatory cells by chemotaxis and is the trigger signal of inflammation in atherosclerosis.
Besides, we also examined the effects of asiatic acid on U937 monocyte adhesion and monocyte migration in HAECs using fluorescent-based assays.
Therefore, it is important to be careful and take these differences into consideration when extending experimental murine monocyte studies to human disease.
Mesoblast's bone marrow-derived MPCs are potent modulators of monocyte inflammation, and have been shown in preclinical studies to reduce monocyte infiltration in diabetic kidneys and to reverse endothelial dysfunction.
Prior to currently acknowledged division of monocyte population into classical CD14++CD16-, non-classical CD14+CD16++ and intermediate CD14++CD16+ cells, monocytes have been divided to CD16-negative (referred to as CD14+CD16- or CD14highCD16low) and CD16-positive (referred to as CD14lowCD16+ or CD14lowCD16high) monocytes [5-7].
TLC and eosinophil count was higher while monocyte count was lower in smokers (insignificantly low in light smokers).
The expression of immunomodulatory membrane molecules such as inter-cellular adhesion molecule-1 (ICAM-1) by Western blot analysis, and the release of chemokines such as monocyte chemoattractant protein-1 (MCP-1) and interleukin-8 (IL-8) through ELISA kits, were determined.
The objective of this work was to study the expression of TLR7, TLR8 and TLR9 intracellular receptors, and the activation of its signaling pathway in the monocyte population starting with peripheral blood mononuclear cells (PBMC) of HIV patients to contribute to the knowledge of involvement by innate immune mechanisms in the pathogenesis of the disease, supporting the search for possible therapeutic alternatives that involve these structural components.
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