Galactosemia is a rare genetic, metabolic disorder caused by a deficiency in the galactose-1-phosphate uridyltransferase (GALT). This means patients cannot break down galactose, causing a buildup of ...

Galactosaemia is a disorder of galactose metabolism in which raised levels of galactose and galactose-1-phosphate damage various organs. Although galactosaemia is a common metabolic liver disease in ...

[1] The purpose of this review paper is to analyze the role of the kidney in glucose homeostasis, emphasizing in SGLT2 inhibition as a new therapeutic target for diabetes management. placebo ...

Copious expression of protein arginine methyltransferase 1 (PRMT1) is associated with poor survival in many types of cancers, including acute myeloid leukemia. We observed that a specific acute ...

The equilibrium solubilities of carvedilol and nifedipine at pH 6.5 and 37 °C in 100 mM phosphate buffer were determined to be 55.3 ± 2.1 and 9.93 ± 1.3 μg/mL, respectively. The addition of mucin did ...

FIGURE 1. Representation of the histological structure of the vascular wall of arteries and veins. Arteries present a relatively thick tunica media and more VSMCs, whereas veins show a larger tunica ...