mthfr

A case-control study of MTHFR polymorphism and neural tube defects

5,10-亚甲基四氢叶酸还原酶多态性和神经管畸形的病例对照研究

Polymorphisms of MTHFR among Han population in Henan area

河南汉族人群亚甲基四氢叶酸还原酶基因多态性检测

Study on Relationship between MTHFR Gene Polymorphism and Ischemic Cerebral Vascular Diseases

四氢叶酸还原酶基因多态性与缺血性脑卒中相关性的研究

Study of the correlation between cerebral apoplexy and MTHFR gene

甲烯四氢叶酸还原酶基因多态性与急性脑血管疾病关系的研究

Relationship between Patients with Cerebral Infarction and Plasma Homocysteine Levels Associated MTHFR Gene

脑梗死患者与其血浆同型半胱氨酸水平及MTHFR基因关系的研究

A Case-control Study of the Association between MTHFR Gene Mutation and Neural Tube Defects

MTHFR基因突变与神经管畸形关系的病例对照研究

Study on MTHFR gene polymorphism in atherosclerotic cerebral infarction

动脉粥样硬化性脑梗死的亚甲基四氢叶酸还原酶基因多态性研究

Levels of plasma homocysteine and MTHFR gene polymorphisms in different types of cerebral infarction

不同类型脑梗死Hcy水平及MTHFR基因多态性

Conclusion : MTHFR genotype is one of main factors which cause level of Hcy to rise .

结论：MTHFR基因突变是引起血浆Hcy水平升高的主要原因。

Relationship between plasma HCY , polymorphism in MTHFR and cerebral thrombosis

血浆同型半胱氨酸及MTHFR多态性与动脉粥样硬化性血栓性脑梗死

An Investigation on the Relationship Between the Polymorphism of MTHFR Gene and Type ⅱ Diabetic Cardiovascular Disease

糖尿病并心血管病患者与MTHFR基因多态性的关系

Study of gene polymorphism of CBS and MTHFR in miao of Guizhou

贵州苗族CBS基因与MTHFR基因多态性研究

MTHFR gene silencing affects mouse embryonic palatal mesenchymal cell proliferation and apoptosis

MTHFR基因沉默对小鼠胚胎腭突间充质细胞增殖和凋亡的影响

MTHFR polymorphisms and colorectal cancer susceptibility in Chongqing people

重庆地区人群亚甲基四氢叶酸还原酶基因多态性与结直肠癌易感性关系研究

Relationship of the Gene Polymorphism of MTHFR and Plasma Homocysteine with Recurrent Spontaneous Abortion

MTHFR基因多态性及血浆HCY水平与复发性流产的关系

Study on polymorphism of methylenetetrahydrofolate reductase ( MTHFR ) gene in patients with coronary heart disease

冠心病患者甲基四氢叶酸还原酶基因多态性的研究

Variants of MTHFR , for example , have been linked to increased risk of cardiovascular disease .

例如，MTHFR的变异体被认为能增加心血管病的风险。

Conclusions : MTHFR mutation is irrelevant to the occurrence of PIH .

结论：MTHFR基因突变与妊高征发生无关；

Determination of MTHFR / C677T polymorphism in deep venous thrombosis

深静脉血栓形成患者MTHFR/C677T基因多态性检测

Methods The expression of MTHFR is detected by RT-PCR in the MTX-Resistant mouse cell lines .

方法采用RT-PCR的方法，对小鼠氨甲蝶呤（MTX）抗性细胞系中MTHFR的表达进行分析。

Genetic polymorphisms of 5,10-methylenetetrahydrofolate reductase ( MTHFR ) in patients with cerebral infarction

脑梗死患者5,10-亚甲基四氢叶酸还原酶基因位点多态性的研究

Study on LDLR Gene 1972 T / C SNP and MTHFR Gene 677 C / T SNP

LDL受体基因1972T/CSNP及MTHFR基因677C/TSNP研究

Genetic epidemiology study on roles of α - adducin gene and MTHFR gene in the occurrence of hypertension

高血压与α-adducin基因及MTHFR基因关系的遗传流行病学研究

Analysis of ps-1 , ApoE , and MTHFR Polymorphisms or Mutations in Patients with Dementia

痴呆与PS-1、ApoE和MTHFR基因多态性或突变的相关性分析

OBJECTIVE : To study the correlation between polymorphism of gene MTHFR and CBS and heredity of cerebral infarction and hemorrhage .

目的：研究人体MTHFR和CBS基因多态性与脑梗死及脑出血的遗传相关性。

Conclusion The authors believe that MTHFR VV genotype is associated with the development of NTDs and preeclampsia .

结论MTHFR基因C677T多态与NTD及先兆子痫的发生有关。

Objective : To explore the relationship between methylenetetrahydrofolate reductase ( MTHFR ) polymorphism and risk of essential hypertension among Shanghai community based population .

目的：探讨上海社区人群亚甲基四氢叶酸还原酶（methylenetetrahydrofolatereductase，MTHFR）基因多态性与原发性高血压的关系。

Objective To investigate the effect of MTHFR thermolabile polymorphism on genetic susceptibility of NSCL / P in north China population .

目的探讨MTHFR基因热敏感性多态性在非综合征性唇腭裂（NSCL/P）发病以及遗传易感性中的作用。

Measurement of Homocysteine and Folic Acid in Chick Embryonic Microblood and Assay of MTHFR Genotype

鸡胚微量血中同型半胱氨酸、叶酸、HCY-2抗体水平和MTHFR基因型检测及其意义

Many studies have proved that MTHFR gene 677C → T mutation caused decreasing enzyme activity , which increased the blood levels of Hcy .

许多研究认为MTHFR基因的677C→T的突变引起了MTHFR活性的降低，从而升高了血中Hcy的水平。