Facts : X linked recessive disorder, MC in AA men G6PD enzyme involved in creating NADPH (cofactor required to create glutathione and prevent oxidation of hemoglobin) Without G6PD, hemoglobin becomes oxidized and denatures into Heinz bodies Variants are G6PD A- (moderate enzyme deficiency) and G6PD Mediterranean (severe enzyme deficiency History / PE : Fever Jaundice Abdominal pain Hematuria Diagnosis : Heinz bodies (denatured hemoglobin) and bite cells Positive Prussian blue staining (detects hemosiderin) G6PD levels are usually paradoxically normal during hemolytic episode Notes : Patients are less susceptible to malaria Associated With : Episodic hemolysis from fava beans , oxidant drugs (esp
Partial AsGGT1 , AsGGT2 , and AsGGT3 , fused with the sequence encoding hexa-Gly residues, were cut out as Sal I- Nco I fragments and were inserted between the Sal I and Nco I sites in pTH2 ( PHYLOGENETIC ANALYSIS Phylogenetic analysis was performed using MEGA version 6 software (Tamura et al., 2013) based on the ClustalW multiple alignment
Milk Scent : I love the scent it smells like milk and butter
The first relates to L-carnitine's role in supporting cellular ATP production (Ori, Freo, Pizzolato, & Dam, 2002), which may help support cellular energy efficiency in neural tissue
LIP: labile iron pool
