1) methylenetetrahydrofolate reductase deficiency
亚甲基四氢叶酸还原酶缺乏症
2) dihydrofolate reductase deficiency
二氢叶酸还原酶缺乏症
3) methylenetetrahydrofolate reductase
亚甲基四氢叶酸还原酶
1.
Relationships between the polymorphism of methylenetetrahydrofolate reductase gene C677T and hypertension,cardiac structure and function;
亚甲基四氢叶酸还原酶基因C677T多态性与高血压及心脏结构功能的相关性
2.
Detection of polymorphisms of methylenetetrahydrofolate reductase C677T in patients with coronary heart disease in Henan Han population;
河南汉族冠心病患者N5,N10-亚甲基四氢叶酸还原酶基因C677T多态性检测
3.
Expression of Folate Receptor alpha and its Correlation with Folate, Methylenetetrahydrofolate Reductase Gene Polymorphisms and Biological Behaviour of Gastric Cancerous Tissue;
叶酸受体α在胃癌组织中的表达及其与叶酸、亚甲基四氢叶酸还原酶基因多态性以及胃癌生物学行为的关系
4) MTHFR
亚甲基四氢叶酸还原酶
1.
Study on the polymorphysm of MTHFR gene in coronary heart disease in Guizhou;
冠心病患者亚甲基四氢叶酸还原酶基因多态性87例研究
2.
Meta Analysis on Relationship Between MTHFR C677T Polymorphism and Susceptibility of Cerebral Infarction in Chinese Population;
中国人亚甲基四氢叶酸还原酶基因C677T多态性与脑梗死关系的Meta分析
3.
A Rapid Detection System for C677T Polymorphism of MTHFR Gene;
亚甲基四氢叶酸还原酶基因C677T多肽性快速检测系统的建立
5) methylene tetrahydrofolate reductase
亚甲基四氢叶酸还原酶
1.
Relationship between homocysteine methylene tetrahydrofolate reductase polymorphism and coronary heart disease in Chinese type 2 diabetes mellitus;
同型半胱氨酸及亚甲基四氢叶酸还原酶C677T基因多态性与2型糖尿病合并冠心病的关系
2.
Objective: To investigate the relationship between methylene tetrahydrofolate reductase(MTHFR) gene C677T polymorphism,angiotensin converting enzyme (ACE) gene I/D polymorphism and lowerextremity deep venous thrombosis(LEDVT) respectively and jointly.
目的:探讨亚甲基四氢叶酸还原酶(Methylene tetrahydrofolate reductase,MTHFR)基因C677T多态性、血管紧张素转换酶(Angiotensin converting enzyme,ACE)基因I/D多态性及不同基因型组合与下肢深静脉血栓形成(Lowerextremity deep venous thrombosis,LEDVT)的关系。
6) Methylenetetrahydrofolate reductase(MTHFR)
亚甲基四氢叶酸还原酶
1.
Objective To study the relationship among polymorphism of 28bp tandem repeat sequence in 5’-UTR and 6-bp variation at bp1494 in the 3’-UTR of thymidylate synthase(TS), a mutation at nucleotide 677 in methylenetetrahydrofolate reductase(MTHFR) , plasma homocysteine (Hcy) levels and coronary heart disease.
目的 研究胸腺苷合成酶(thymidylate synthase, TS)5’-非翻译区(untranslated regeion,UTR)28bp串联重复序列多态性、3’-UTR1494bp位6bp插入或缺失多态性、亚甲基四氢叶酸还原酶(methylenetetrahydrofolate reductase,MTHFR)677位多态性(C-T)与血浆同型半胱氨酸(homocysteine, Hcy)水平及冠心病之间的关系。
补充资料：17酮类固醇还原酶缺乏症
17酮类固醇还原酶缺乏症
病名。系男性假两性畸形中睾丸激素合成缺陷的一种类型。因睾酮生成障碍，外生殖器可完全女性化，可有一浅的阴道，但无子宫。患者被当作女孩抚养，一般至青春期误认为有原发性闭经等症状来妇科检查时始被发现。可能是常染色体显性遗传病。一般进行睾丸切除术，同时用雌激素替代疗法。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条