ciliata decreased the levels of tumor markers: aspartate aminotransferase, alanine aminotransferase, lactate dehydrogenase, alpha-fetoprotein, gamma glutamyl transferase, 5' nucleotidase and glucose-6-phosphate
Severe hemolysis and renal failure in glucose-6-phosphate
dehydrogenase deficient patients with hepatitis E.
Severe neonatal hyperbilirubinemia: a potential complication of glucose-6-phosphate
dehydrogenase deficiency," The Lancet, vol.
dehydrogenase: a biomarker and potential therapeutic target for cancer," Anti-Cancer Agents in Medicinal Chemistry, vol.
Alpha Amylase and Glucose-6-phosphate
A typical optimized assay mixture contained 1.0 mM ethoxyresorufin, 100 mM Tris-HCl buffer (pH 7.8), NADPH generating system consisting of 0.25 mM NADP+, 2.5 mM MgC[l.sub.2], 2.5 mM glucose-6-phosphate
, 1.0 U glucose-6-phosphate
dehydrogenase, and 14.2 mM potassium phosphate buffer (pH 7.8) and 0.2 mg liver microsomal protein in a final volume of 1.0 mL.
The panel includes tests for total serum bilirubin, albumin, direct bilirubin, and glucose-6-phosphate
dehydrogenase (G6PD) on a single cartridge, making it the first comprehensive, rapid and near-patient testing solution for hyperbilirubinemia.
Total concentrations of glycogen, glucose, and glucose-6-phosphate
in muscle were determined using commercially available analysis kits (Sigma, USA) according to the manufacturers direction.
The presence or absence of some of these variants is associated with an increased risk for developing any one of the following 10 diseases or conditions: Parkinson's disease, late-onset Alzheimer's disease; celiac disease, alpha-1 antitrypsin deficiency; early-onset primary dystonia; factor XI deficiency; Gaucher disease type 1; glucose-6-phosphate
dehydrogenase deficiency; hereditary hemochromatosis; and hereditary thrombophilia.
The other diseases covered by the tests are celiac disease, alpha-1 antitrypsin deficiency, early onset primary dystonia, Factor XI deficiency, Gaucher disease type 1, glucose-6-Phosphate
Dehydrogenase deficiency (also known as G6PD), hereditary hemochromatosis, and hereditary thrombophilia.
Parts of the peaks were identified as 1, lactic acid; 2, alanine; 3, valine; 4, leucine; 5, proline; 6, glycine; 7, uracil; 8, fumaric acid; 9, serine; 10, threonine; 11, malic acid; 12, pyroglutamic acid; 13, asparagine; 14, hydroxyproline; 15, creatinine; 16, ornithine; 17, glutamic acid; 18, phenylalanine; 19, ribose; 20, glutamine; 21, hypoxanthine; 22, glucose; 23, hexadecanoic acid; 24, linoleic acid; 25, oleic acid; 26, tryptophan; 27, stearic acid; 28, glucose-6-phosphate
; 29, maltose; and 30, cholesterol.