ジホスホグリセリン酸ムターゼ欠損症。DPGムターゼ欠損症
WordNet
- the 4th letter of the Roman alphabet (同)d
PrepTutorEJDIC
- 〈U〉〈C〉(…の)(量・額などの)不足,欠乏《+『of』(『in』)+『名』》 / 〈C〉不足分,不足量,不足額 / 〈C〉(精神・肉体などの)欠陥
- deuteriumの化学記号
UpToDate Contents
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English Journal
- New procedures to measure synthase and phosphatase activities of bisphosphoglycerate mutase. Interest for development of therapeutic drugs.
- Ravel P1, Garel MC, Toullec D.
- Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie.C R Acad Sci III.1997 Jan;320(1):27-33.
- In red blood cells, a modulation of the level of the allosteric effector of hemoglobin, 2,3-diphosphoglycerate (2,3-DPG) would have implications in the treatment of ischemia and sickle cell anemia. Its concentration is determined by the relative activities of the synthase and phosphatase reactions o
- PMID 9099261
- Metabolic manipulation of key glycolytic enzymes: a novel proposal for the maintenance of red cell 2,3-DPG and ATP levels during storage.
- Vora S.
- Biomedica biochimica acta.Biomed Biochim Acta.1987;46(2-3):S285-9.
- Red cell 2,3-DPG and ATP levels decline rather rapidly during storage which result in poor oxygen offloading ability and post-transfusion viability respectively of such cells. Since the steady-state levels of these metabolites are determined by the relative activities of the key enzymes of glycolysi
- PMID 3593307
- [Diphosphoglyceromutase deficiency: new cases associated with erythrocytosis].
- Galacteros F, Rosa R, Prehu MO, Najean Y, Calvin MC.
- Nouvelle revue française d'hématologie.Nouv Rev Fr Hematol.1984;26(2):69-74.
- New cases of diphosphoglyceromutase (DPGM) have been detected, associated with erythrocytosis in two unrelated families. The deficiency appears to be inherited as an autosomal dominant trait. Diphosphoglycerate phosphatase activity paralleled DPGM activity in all the subjects. Three of the latter di
- PMID 6326048
Related Links
- 2,3-diphosphoglycerate (2,3-DPG) is a small molecule found at high concentrations in red blood cells where it binds to and decreases the oxygen affinity of hemoglobin. This gene encodes a multifunctional enzyme that ...
- Clinical Synopsis TEXT A number sign (#) is used with this entry because erythrocyte bisphosphoglycerate mutase deficiency can be caused by compound heterozygous mutation in the BPGM gene (), which encodes a ...
★リンクテーブル★
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- 英
- diphosphoglycerate mutase deficiency
- 同
- DPGムターゼ欠損症 DPG mutase deficiency、ジホスホグリセリン酸ホスファターゼ欠損症 diphosphoglycerate phosphatase deficiency
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- 不足、欠乏、欠失、欠如、欠損、不十分。栄養不足、栄養素欠乏、欠乏症。(遺伝子)(染色体内の)遺伝子欠失
- 欠けているもの、不足している物。不足分。不完全なもの、欠点のあるもの
- 関
- absence, agenesis, dearth, defect, defective, deficient, deficit, delete, deletion, deletional, depletion, deprivation, deprive, lack, miss, missing, morphological defect, paucity, scarce, scarcity, starve
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幽門側胃切除 distal partial gastrectomy
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ムターゼ
- 関
- intramolecular transferase