The methylenetetrahydrofolate reductase 677 C→T polymorphism and preeclampsia in two populations

Obstetrics and Gynecology

Volumn 99, Issue 6, 2002, Pages 1085-1092

  Prasmusinto, D ^a,b   Skrablin, S ^a,b   Hofstaetter, C ^a,b   Fimmers, R ^a,b   Vander Ven, K ^a,b  

^a UNIVERSITY OF BONN   (Germany)

^b UNIVERSITY OF ZAGREB   (Croatia)

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); HOMOCYSTEINE; POLYACRYLAMIDE GEL;

ADULT; ALLELE; ARTICLE; BLOOD ANALYSIS; CONTROLLED STUDY; DISEASE PREDISPOSITION; ETHNOLOGY; FEMALE; GENE ACTIVITY; GENE AMPLIFICATION; GENE FREQUENCY; GENETIC POLYMORPHISM; GENOTYPE; GESTATIONAL AGE; HOMOZYGOSITY; HUMAN; INHERITANCE; MAJOR CLINICAL STUDY; NEWBORN; POLYMERASE CHAIN REACTION; PREECLAMPSIA; PREVALENCE; PRIORITY JOURNAL;

ADULT; AMINO ACID SUBSTITUTION; ASIAN CONTINENTAL ANCESTRY GROUP; CASE-CONTROL STUDIES; CROATIA; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; FETAL BLOOD; GENE EXPRESSION REGULATION, ENZYMOLOGIC; GENOTYPE; GERMANY; HUMANS; INDONESIA; INFANT, NEWBORN; MALE; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); OXIDOREDUCTASES ACTING ON CH-NH GROUP DONORS; POLYMORPHISM, GENETIC; PRE-ECLAMPSIA; PREGNANCY; PREVALENCE;

EID: 0036271250     PISSN: 00297844     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0029-7844(02)01997-X     Document Type: Article

References (41)

1. History and epidemiology of preeclampsia-eclampsia
2. Causes of maternal mortality in the United States
3. Epidemiology of preeclampsia and eclampsia in the United States 1979-1986
4. Maternal pathophysiology in pre-eclampsia
5. HELLP syndrome
6. Medical disorders in pregnancy including hypertensive diseases
7. Preeclampsia: An endothelial cell disorder
8. Pathogenesis and genetics of pre-eclampsia
9. National High Blood Pressure on Education Program Working Group report on high blood pressure in pregnancy. Consensus report
10. Inherited hypercoagulable states
11. Thrombophilia-associated pregnancy wastage
12. Heritable coagulopathies in pregnancy
13. Thrombophilia in pregnancy
14. Methylenetetrahydrofolate reductase polymorphism and pre-eclampsia
15. Methylenetetrahydrofolate reductase polymorphism folate and susceptibility to preeclampsia
16. Molecular biology of 5, 10-methylenetetrahydrofolate reductase
17. Thermolabile methylenetetrahydrofolate reductase in coronary artery disease
18. Hyperhomocysteinemia and thrombosis
19. Increased frequency of genetic thrombophilia in women with complications of pregnancy
20. Factor V Leiden C > T MTHFR polymorphism and genetic susceptibility to preeclampsia
21. Factor V Leiden and thermolabile methylenetetrahydrofolate reductase gene variants in an East Anglian preeclampsia cohort
22. Prospective evaluation of the risk conferred by factor V Leiden and thermolabile methylenetetrahydrofolate reductase polymorphisms in pregnancy
23. Maternal and neonatal outcome of preeclamptic pregnancies: The potential roles of factor V Leiden mutation and 5, 10 methylenetetrahydrofolate reductase
24. Absence of association between a common mutation in the methylenetetrahydrofolate reductase gene and preeclampsia in Japanese women
25. 677 C → T polymorphism of the methylenetetrahydrofolate reductase gene and preeclampsia
26. Methylenetetrahydrofolate reductase 677 C → T polymorphism plasma folate vitamin B(12) concentrations and risk of preeclampsia among black African women from Zimbabwe
27. Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease: The result of a meta-analysis
28. Empfehlungen für diagnostik und therapie bei Bluthochdruck in der Schwangerschaft
29. A simple salting out procedure for extracting DNA from human nucleated cells
30. A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
31. Methylenetetrahydrofolate reductase polymorphisms in preeclampsia and the HELLP syndrome
32. Severe preeclampsia and high frequency of genetic thrombophilic mutations
33. C677T methylenetetrahydrofolate reductase polymorphism is not a risk factor for pre-eclampsia/eclampsia among Australian women
34. Does the polymorphism 677C-T of the 5, 10-methylenetetrahydrofolate reductase gene contribute to homocysteine-related vascular disease?
35. Relation between folate status a common mutation in methylenetetrahydrofolate reductase and plasma homocysteine concentrations
36. Polymorphisms of methylenetetrahydrofolate reductase and other enzymes: Metabolic significance risks and impact on folate requirement
37. Evaluation of the MTHFR C677T allele and the MTHFR gene locus in a German spina bifida population
38. The 677T genotype of the common MTHFR thermolabile variant and fasting homocysteine in childhood venous thrombosis
39. The C677T mutation of the methylenetetrahydrofolate reductase gene is not associated with the risk of coronary artery disease or venous thrombosis among Chinese in Taiwan
40. Prevalence of the C677T methylenetetra-hydrofolate reductase mutation in Thai patients with deep vein thrombosis
41. C677T mutation of the methylenetetrahydrofolate reductase gene among the Korean infants in Seoul city