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1. グルコース-6-リン酸脱水素酵素欠損症の診断および治療 diagnosis and treatment of glucose 6 phosphate dehydrogenase deficiency
2. 乳酸脱水素酵素欠損症 lactate dehydrogenase deficiency
3. グルコース-6-リン酸脱水素酵素欠損症の臨床症状 clinical manifestations of glucose 6 phosphate dehydrogenase deficiency
4. 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
5. 脂質およびプリン代謝障害による代謝性ミオパチー metabolic myopathies caused by disorders of lipid and purine metabolism

English Journal

DMSO induced myocardial infarction during allogeneic cryopreserved bone marrow transplant.

Khawandanah M1, Hopps S, Nabeel S, Ahmad B, Weiss S, Holter Charkrabarty J, Yuen C, Selby G.
Annals of hematology.Ann Hematol.2015 Mar;94(3):511-3. doi: 10.1007/s00277-014-2181-2. Epub 2014 Aug 20.
PMID 25135449

Kim J1, Devalaraja-Narashimha K2, Padanilam BJ3.
American journal of physiology. Renal physiology.Am J Physiol Renal Physiol.2015 Feb 15;308(4):F298-308. doi: 10.1152/ajprenal.00459.2014. Epub 2014 Dec 10.
Tp53-induced glycolysis and apoptosis regulator (TIGAR) activation blocks glycolytic ATP synthesis by inhibiting phosphofructokinase-1 activity. Our data indicate that TIGAR is selectively induced and activated in renal outermedullary proximal straight tubules (PSTs) after ischemia-reperfusion injur
PMID 25503731

Hypoxia-induced glucose-6-phosphate dehydrogenase overexpression and -activation in pulmonary artery smooth muscle cells: implication in pulmonary hypertension.

Chettimada S1, Gupte R1, Rawat D1, Gebb SA2, McMurtry IF3, Gupte SA4.
American journal of physiology. Lung cellular and molecular physiology.Am J Physiol Lung Cell Mol Physiol.2015 Feb 1;308(3):L287-300. doi: 10.1152/ajplung.00229.2014. Epub 2014 Dec 5.
Severe pulmonary hypertension is a debilitating disease with an alarmingly low 5-yr life expectancy. Hypoxia, one of the causes of pulmonary hypertension, elicits constriction and remodeling of the pulmonary arteries. We now know that pulmonary arterial remodeling is a consequence of hyperplasia and
PMID 25480333

Comparative Analysis of Glucosephosphate Isomerase, Lactate Dehydrogenase and Malate Dehydrogenase Isozymes in 9 Cyprinid Species from Italy

Manaresi Sonia,Mantovani Barbara,Zaccanti Francesco
Zoological science 15(4), 461-467, 1998-08
… The developmental and the tissue-specific expression of glucosephosphate isomerase(GPI), lactate dehydrogenase(LDH)and malate dehydrogenase(MDH)multilocus isozymes were analyzed in samples of Leuciscus cephalus and the adult patterns compared with those of 8 additional Italian cyprinid species : Alburnus alburnus alborella, Chondrostoma genei, L. …
NAID 110003323577

芝田猛 [他],阿部恒夫,川上和夫,大西彰,武田久美子,秋田富士,落合厳,小坂昭三,大山真二,梶雄次,勝俣昌也
日本畜産学会報 65(6), 563-570, 1994
… On the other hand, prediction of the halothane genotypes by means of marker loci (glucosephosphate isomerase, 6-phosphogluconate dehydrogenase and a1 B-glycoprotein) closely linked to the halothane locus (Hal) was done in these populations. …
NAID 130000750075

四方崇文,Kheyyali Driss,示野貞夫
日本水産学会誌 59(5), 835-839, 1993
… With a decrease in the feeding rates, the activities of hepatopancreatic glucose-6-phosphate dehydrogenase, phosphogluconate dehydrogenase, NADP-isocitrate dehydrogenase, NADP-malate dehydrogenase, glucosephosphate isomerase, and pyruvate kinase were significantly depressed, while those of alanine aminotransferase and glucose-6-phosphatase were not markedly changed. …
NAID 130001545889

リンク元	「グルコースリン酸脱水素酵素」「グルコースリン酸デヒドロゲナーゼ」
拡張検索	「glucosephosphate dehydrogenase deficiency」
関連記事	「dehydrogenase」「dehydrogenases」