Possible pathophysiological roles of mitogen-activated protein kinases (MAPKs) in endometriosis
Other causes of carnitine deficiency besides mutations in the SLC22A5 gene are classified as secondary carnitine deficiency and include other hereditary metabolic diseases (e.g., fatty acid oxidation defects), medication (valproic acid, cyclosporine, and pivampicillin), malnutrition, hemodialysis and renal tubular dysfunction (Fanconi nephropathy), and prematurity (lower placentary transfer)
Los estudios sugieren que la suplementacin con L-carnitina puede reducir la grasa del hgado
Negative feedback between prostaglandin and - and -chemokine synthesis in human microglial cells and astrocytes
It is yet unclear whether central and peripheral symptoms are linked or develop independently of each other, hence a better understanding of their connections is important
Fish gonadal functions, gametogenesis, and steroidogenesis are all governed by the kisspeptin-gonadotropin-releasing hormone (GnRH)-gonadotropins (follicle-stimulating hormone (FSH) and luteinizing hormone LH) axis, just like in other vertebrates
