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Differences in methylenetetrahydrofolate reductase genotype frequencies, between Whites and Blacks.白人和黑人之间亚甲基四氢叶酸还原酶基因型频率的差异。
Am J Hum Genet. 1997 Jan;60(1):229-30.
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The prevalence of two genetic traits related to venous thrombosis in whites and African-Americans.
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Methylenetetrahydrofolate reductase mutation and neural tube defects.亚甲基四氢叶酸还原酶突变与神经管缺陷
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COVID-19 spreading across world correlates with C677T allele of the methylenetetrahydrofolate reductase (MTHFR) gene prevalence.新冠病毒在全球的传播与亚甲基四氢叶酸还原酶(MTHFR)基因 C677T 等位基因的流行有关。
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Plausible relationship between homocysteine and obesity risk via gene: a meta-analysis of 38,317 individuals implementing Mendelian randomization.通过基因分析同型半胱氨酸与肥胖风险之间可能存在的关系:对38317名个体进行孟德尔随机化的荟萃分析
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MTHFR 677C>T polymorphism increases the male infertility risk: a meta-analysis involving 26 studies.亚甲基四氢叶酸还原酶(MTHFR)677C>T基因多态性增加男性不育风险:一项纳入26项研究的荟萃分析
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Polymorphism (C677T) in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene: A preliminary study on north Indian men.5,10-亚甲基四氢叶酸还原酶(MTHFR)基因多态性(C677T):对印度北部男性的初步研究。
Indian J Clin Biochem. 2002 Jan;17(1):99-107. doi: 10.1007/BF02867949.
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A comprehensive review on host genetic susceptibility to human papillomavirus infection and progression to cervical cancer.关于宿主对人乳头瘤病毒感染及进展为宫颈癌的遗传易感性的综合综述。
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Metabolic correction in the management of diabetic peripheral neuropathy: improving clinical results beyond symptom control.糖尿病周围神经病变管理中的代谢纠正:超越症状控制改善临床效果。
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本文引用的文献

1
5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects.5,10-亚甲基四氢叶酸还原酶基因多态性作为神经管缺陷的一个风险因素。
Am J Med Genet. 1996 Jun 28;63(4):610-4. doi: 10.1002/(SICI)1096-8628(19960628)63:4<610::AID-AJMG15>3.0.CO;2-L.
2
Nutritional ecogenetics: homocysteine-related arteriosclerotic vascular disease, neural tube defects, and folic acid.营养生态遗传学:同型半胱氨酸相关的动脉硬化性血管疾病、神经管缺陷与叶酸
Am J Hum Genet. 1996 Jan;58(1):17-20.
3
Spina bifida, 677T-->C mutation, and role of folate.脊柱裂、677T→C突变与叶酸的作用
Lancet. 1995;346(8991-8992):1703. doi: 10.1016/s0140-6736(95)92865-0.
4
A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects.神经管缺陷中5,10-亚甲基四氢叶酸还原酶的基因缺陷。
QJM. 1995 Nov;88(11):763-6.
5
A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase.一种血管疾病的潜在遗传风险因素:亚甲基四氢叶酸还原酶的常见突变
Nat Genet. 1995 May;10(1):111-3. doi: 10.1038/ng0595-111.
6
Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida.突变的亚甲基四氢叶酸还原酶作为脊柱裂的一个风险因素。
Lancet. 1995 Oct 21;346(8982):1070-1. doi: 10.1016/s0140-6736(95)91743-8.

Differences in methylenetetrahydrofolate reductase genotype frequencies, between Whites and Blacks.

作者信息

Stevenson R E, Schwartz C E, Du Y Z, Adams M J

出版信息

Am J Hum Genet. 1997 Jan;60(1):229-30.

PMID:8981967
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1712549/
Abstract
摘要