Succinate
dehydrogenase (SDH)-deficient renal carcinoma: a morphologically distinct entity: a clinicopathologic series of 36 tumors from 27 patients.
LDH--lactate
dehydrogenase (U/L), Bili T--total bilirubin, Retic--reticulocyte percentage
To study the diagnostic significance of estimating lactate
dehydrogenase in ascitic and pleural fluid.
According to World Health Organization (WHO), every year around 20 million people get infected with hepatitis E virus.1 Of these 3.3 million people have the disease.1 Hepatitis E infection in 2015 resulted in around 44000 deaths worldwide.1,2 The highest prevalence of Hepatitis E is in East Asia and South Asia due to inadequate sanitation.3-5 It is a mild and self-limiting disease, which requires conservative management with no aggressive mode of treatment.6,7 Glucose - 6 - phosphate
dehydrogenase (G6PD) deficiency is one of the most common type of enzyme deficiencies.
Hydrops fetalis and stillbirth in a male glucose-6-phosphate
dehydrogenase deficient fetus possibly due to maternal ingestion of sulfisoxazole; a case report.
Motulsky, "Negro variant of glucose-6-phosphate
dehydrogenase deficiency (A-) in man" Science, vol.
Holzhutter, "Kinetic modeling of the mitochondrial energy metabolism of neuronal cells: the impact of reduced [alpha]-Ketoglutarate
dehydrogenase activities on ATP production and generation of reactive oxygen species," International Journal of Cell Biology, vol.
Stroud, "Structure of a bacterial enzyme regulated by phosphorylation, isocitrate
dehydrogenase," Proceedings of the National Academy of Sciences of the United States of America, vol.
To date, an alternative type-2 NADH
dehydrogenase (NADH2), a mitochondrial glycerol-3-phosphate
dehydrogenase (mtGPDH), and an AOX are the three enzymes reported as part of the mitochondrial branched respiratory chains of mammals, yeast, and marine invertebrates (Abele et al.
Congenital adrenal hyperplasia secondary to 3-beta hydroxysteroid
dehydrogenase deficiency
Four maize hybrids and their parental lines were used to find genetic purity through testing with four isoenzymes such as alcohol
dehydrogenase (ADH), esterase (EST), acid phosphatase (ACP) and malate
dehydrogenase (MDH) and evaluated with thirty pairs of simple sequence repeat (SSR) markers.