Taken together, the beneficial effects of n-3 PUFA on metabolic derangements are mediated in part by alleviation of AT inflammation, especially resulting from decreased secretion of proinflammatory adipokines, increased secretion of adiponectin, and induced synthesis of proresolving lipid mediators.

These cells that result from genome transplantation are phenotypically identical to the M. mycoides LC donor strain as judged by several criteria.

There are many such mysteria: milk is a mysterium of cheese and butter, and cheese in turn a mysterium of maggots, which were thought to form spontaneously in rotting food.

Desmin (DES) mutations have been recognized as a cause of desmin-related myopathy (OMIM 601419), or desminopathy, a disease characterized by progressive limb muscle weakness and accumulation of desmin-reactive granular aggregates in the myofibers. We have studied three families with skeletal or cardioskeletal myopathy caused by small in-frame deletions in the desmin gene.