英: 2-oxoglutarate dehydrogenase

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1. ヘキソースリン酸側路およびグルタチオン代謝疾患（グルコース-6-リン酸脱水素酵素欠損症を除く）disorders of the hexose monophosphate shunt and glutathione metabolism other than glucose 6 phosphate dehydrogenase deficiency [show details]
…following. All are extremely rare with the exception of glucose-6-phosphate dehydrogenase deficiency. Glucose-6-phosphate dehydrogenase (G6PD) deficiency – The most common abnormality in this system is G6PD …
2. 乳酸脱水素酵素欠損症lactate dehydrogenase deficiency [show details]
…gluconeogenesis by the liver. The M isoform is a product of the lactate dehydrogenase A (LDHA) gene, located at 11p15 . The lactate dehydrogenase B (LDHB) gene that encodes the H isoform has been mapped to chromosome …
3. 原発性高シュウ酸尿症primary hyperoxaluria [show details]
… encodes the mitochondrial 4-hydroxy-2-oxoglutarate aldolase enzyme, which catalyzes the cleavage of 4-hydroxy-2-oxoglutarate (HOG) to pyruvate and glyoxylate.… which are converted by lactate dehydrogenase to oxalate and L-glycerate These metabolites are excreted in excessive amounts in the urine,…
4. グルコース-6-リン酸脱水素酵素（G6PD）欠損症の遺伝学的特徴および病態生理genetics and pathophysiology of glucose 6 phosphate dehydrogenase g6pd deficiency [show details]
… Glucose-6-phosphate dehydrogenase (G6PD) deficiency, an X-linked disorder, is the most common enzymatic disorder of red blood cells in humans, affecting more than 400 million people worldwide . The clinical …
5. グルコース-6-リン酸脱水素酵素（G6PD）欠損症の診断とマネージメントdiagnosis and management of glucose 6 phosphate dehydrogenase g6pd deficiency [show details]
… Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an inherited disorder caused by a genetic defect in the red blood cell (RBC) enzyme G6PD, which generates NADPH and protects RBCs from oxidative …