WordNet

any of several complex proteins that are produced by cells and act as catalysts in specific biochemical reactions

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1. 貧血を有する成人患者に対するアプローチ approach to the adult patient with anemia
2. アデノシンデアミナーゼ欠損症：治療 adenosine deaminase deficiency treatment
3. 小児における溶血性貧血の概要 overview of hemolytic anemias in children
4. 赤血球水分量の制御 control of red blood cell hydration
5. 成人における赤血球輸血：保管、専門的調整、および輸血パラメータ red blood cell transfusion in adults storage specialized modifications and infusion parameters

Congenital Recessive Methemoglobinemia Revealed in Adulthood: Description of a New Mutation in Cytochrome b5 Reductase Gene.

Forestier A1, Pissard S2,3, Cretet J2, Mambie A1, Pascal L1,4, Cliquennois M1,4, Cambier N1,4, Rose C1,4.
Hemoglobin.Hemoglobin.2015 Dec;39(6):438-441. Epub 2015 Jul 31.
Methemoglobinemia can be acquired (oxidizing drugs or chemicals products) or inherited either by mutations affecting globin chains [M hemoglobins (M Hbs)] or by defects in the enzymatic system involved in the reduction of spontaneous Hb oxidation: nicotinamide adenine dinucleotide (NADH)-cytochrome
PMID 26291966

Intravenous infusion of haptoglobin for the prevention of adverse clinical outcome in Sickle Cell Disease.

Quimby KR1, Hambleton IR2, Landis RC2.
Medical hypotheses.Med Hypotheses.2015 Oct;85(4):424-32. doi: 10.1016/j.mehy.2015.06.023. Epub 2015 Jun 29.
Sickle Cell Disease (SCD) is a genetic condition which manifests as altered hemoglobin (Hb) protein that can aggregate under hypoxic conditions. The resultant sickled erythrocytes experience premature hemolysis, releasing an estimated 10g of free Hb (fHb) into the intravascular space. FHb participat
PMID 26141635

Zhou SS1, Li D1, Chen NN1, Zhou Y1.
World journal of diabetes.World J Diabetes.2015 Aug 25;6(10):1158-67. doi: 10.4239/wjd.v6.i10.1158.
Since synthetic vitamins were used to fortify food and as supplements in the late 1930s, vitamin intake has significantly increased. This has been accompanied by an increased prevalence of obesity, a condition associated with diabetes, hypertension, cardiovascular disease, asthma and cancer. Paradox
PMID 26322161

Parallel Reductions in Stomatin and Na,K-ATPase through the Exosomal Pathway during Reticulocyte Maturation in Dogs: Stomatin as a Genotypic and Phenotypic Marker of High K+ and Low K+ Red Cells

Komatsu Tomohiko,Sato Kota,Otsuka Yayoi [他],ARASHIKI Nobuto,TANAKA Kohei,TAMAHARA Satoshi,ONO Ken-ichiro,INABA Mutsumi
Journal of Veterinary Medical Science 72(7), 893-901, 2010
… Dogs can be divided into two genetic groups (a minor HK phenotype and a major LK phenotype) based on erythrocyte monovalent cation concentrations, which are controlled by the putative hk and lk allelic genes. … HK dogs retain Na,K-ATPase in their erythrocytes due to the high activity of the enzyme in their precursor cells, whereas total loss of reticulocyte Na,K-ATPase occurs in LK dogs. … similar to the deficiency seen in human red cells with overhydrated stomatocytosis. …
NAID 130000264273

E-CELLシステムによる赤血球細胞シミュレーション(<小特集>ポストゲノムにおけるバイオシステムシミュレーション : 生命システム現象の包括的な理解に向かって)

中山洋一,冨田勝
シミュレーション 20(2), 123-128, 2001-06-15
… We constructed a computer model of the human erythrocyte using E-CELL simulation system. … (ii) The simulation of the hereditary enzyme deficiency of glucose-6-phosphate dehydrogenase (G6PD), including the pathways for glutathione (GSH) de novo synthesis and export system of glutathione disulfide (GSSG). …
NAID 110003890955