G6P

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AcronymDefinition
G6PGlucose-6-Phosphate
References in periodicals archive ?
ciliata decreased the levels of tumor markers: aspartate aminotransferase, alanine aminotransferase, lactate dehydrogenase, alpha-fetoprotein, gamma glutamyl transferase, 5' nucleotidase and glucose-6-phosphate dehydrogenase.
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.
Fiorelli, "Glucose-6-phosphate dehydrogenase deficiency," The Lancet, vol.
Qin, "Glucose-6-phosphate dehydrogenase: a biomarker and potential therapeutic target for cancer," Anti-Cancer Agents in Medicinal Chemistry, vol.
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.
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