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In contrast to primary GBMs, TP53 mutations associated with methylation of the MGMT promoter are observed in most secondary GBMs, along with partial loss of heterozygosity of 10q, 13q, 19q, and 22q (4)

Patients should be offered genetic testing if they have a personal or family history of intrahepatic cholestasis, such as PFIC, BRIC, ICP, and LPAC combined with drug at-cholestasis risk use [20] (Fig

Jill opens up about the identity loss, shame, and resilience that followed, and how that moment became a catalyst for deep personal growth

Impact of melatonin foliar treatment on physiological traits of tomato genotypes Data regarding photosynthetic rate (Fig