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The results indicated that the proportion of mature DCs (CD80 + CD86 + ) in the TDLNs of mice treated with NP4 (82.8%) was approximately 1.46 times higher than that in the mice treated with NP2 (56.7%) (Fig

Mutations in glial cells and their contribution to PD Familial Parkinson's disease occurs as a result of mutations in six different genes, namely SCNA, Parkin, DJ-1, PINK1, LRRK2, and ATP13A2

Cardiomyocytespecific telomere shortening is a distinct signature of heart failure in humans

At MC4R, the hypothalamic Gs pathway combined with ERK1/2 pathways and modulation of ion channels (ATP-sensitive potassium channel Kir6.2) underpins satietogenic signaling