
词语导航
基本信息
词语:甲基叶酸
繁体:甲基葉酸
拼音:jiǎ jī yè suānWWW.WEntIYI.cOm
英语翻译
【化】 methopterin
分词翻译
甲基的英语翻译:
methyl
【化】 methyl; methylic
【医】 Me.; methyl; methyl group; methylium
叶酸的英语翻译:
【化】 folic acid; folic aicd; pteroylglutamic acid; vitamin Bc
【医】 Day"s factor; factors U; folacin; folic acid; folvite
Lactobacillus casei factor; liver Lactobacillus casei fsctors; P. G. A.
pteroylglutamic acid; R factors; SLR factors; vitamin Bc
vitamin Bc conjugate; vitamin M; yeast Lactobacillus casei factors
翻译例句
1. 这些物质加上叶酸,维生素b - 12和蛋氨酸都是甲基供体。
These substances plus Folic acid, Vitamin B-12 and SAMe are all methyl donors.
2. 结论亚甲基四氢叶酸还原酶基因C677T基因多态性可能是我国大肠癌的遗传易感因素。
Conclusion These findings demonstrated that the genetic variation of MTHFR C677T should be a genetic susceptibility factor for colorectal cancer in a Chinese population.
3. 亚甲基四氢叶酸还原酶基因突变导致的遗传多态现象可增加神经管缺陷(ntd)发生的危险性。
The genetic polymorphisms due to mutations in the methylene tetrahydrofolate reductase gene may increase the risk for NTDs.
4. 目的探讨北方乡村妇女亚甲基四氢叶酸还原酶(MTHFR)基因多态性与神经管畸形的关系。
Objective To explore relationship between methylenetetra hydrofolate reductase (MTHFR) polymorphism and neural tube defects (NTDs)of women in the northern countryside.
5. 期末血清叶酸、胎鼠血清叶酸及胎鼠脑组织DNA甲基化水平作相关分析。
Correlation analysis was processed among serum folate concentration of dam and fetus and DNA methylation level in fetal brain.
6. 目的:探讨叶酸缺乏对胎鼠宫内脑发育的影响,研究叶酸缺乏孕鼠子代脑组织基因组dna甲基化水平的改变,为叶酸缺乏造成脑发育障碍提供分子水平的依据。
Purpose: To verify the effect of folate deficiency on fetal rats intrauterine brain development, the change of DNA methylation in fetal rats brain with maternal folate deficiency was studied.
7. 该文就近年来亚甲基四氢叶酸还原酶基因多态性与高危妊娠和胎儿畸形关系做一简要综述。
In this review, we summarized researches on the correlation between methylenetetrahydroflate reductase gene polymorphism, high-risk pregnancy and congenital anomalies.
8. 目的建立一种简便、实用的检测亚甲基四氢叶酸还原酶(MTHFR)等位基因C677 T点突变的方法,并初步观察部分健康老人和老年血管性痴呆(VD)患者中mthfr等位基因C677 T点突变情况。
Objective to establish a simple and practical method for detecting the MTHFR gene C677T mutation so as to investigate MTHFR genotypes in the healthy elder and Vascular Dementia (VD).
9. 目的建立一种简便、实用的检测亚甲基四氢叶酸还原酶(MTHFR)等位基因C677 T点突变的方法,并初步观察部分健康老人和老年血管性痴呆(VD)患者中mthfr等位基因C677 T点突变情况。
Objective to establish a simple and practical method for detecting the MTHFR gene C677T mutation so as to investigate MTHFR genotypes in the healthy elder and Vascular Dementia (VD).
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