INTERACTION OF A COMMON MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE (MTHFR) WITH LOW FOLATE STATUS IN HYPERHOMOCYSTEINEMIA

被引：0
|
作者：
ROZEN, R
JACQUES, P
BOSTOM, A
ELLISON, C
WILLIAMS, R
ROSENBERG, I
SELHUB, J
机构：
[1] MCGILL UNIV,MONTREAL,PQ,CANADA
[2] TUFTS UNIV,BOSTON,MA
[3] BOSTON UNIV,BOSTON,MA
[4] UNIV UTAH,SALT LAKE CITY,UT
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1995年 / 57卷 / 04期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：1449 / 1449
页数：1
相关论文
共 50 条
  • [1] A common mutation in methylenetetrahydrofolate reductase is an important determinant of hyperhomocysteinemia
    McQuillan, BM
    Hung, J
    Hunt, C
    Chin, C
    Beilby, JP
    [J]. CIRCULATION, 1997, 96 (08) : 3669 - 3669
  • [2] Hyperhomocysteinemia and genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) in patients with renal failure supplemented with folate
    Domenici, Fernanda A.
    Vannucchi, Maria Terezinha I.
    Lataro, Renata C.
    Meirelles, Monica S. S.
    Vannucchi, Helio
    [J]. NEPHROLOGY DIALYSIS TRANSPLANTATION, 2006, 21 : 433 - 433
  • [3] Is hyperhomocysteinemia in hemodialysis (HD) patients associated with a mutation of the methylenetetrahydrofolate reductase (MTHFR) gene?
    Fodinger, M
    Mannhalter, C
    PabingerFasching, I
    Horl, WH
    SunderPlassmann, G
    [J]. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 1996, 7 (09): : A1817 - A1817
  • [4] Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations
    Jacques, PF
    Bostom, AG
    Williams, RR
    Ellison, RC
    Eckfeldt, JH
    Rosenberg, IH
    Selhub, J
    Rozen, R
    [J]. CIRCULATION, 1996, 93 (01) : 7 - 9
  • [5] Association of a common polymorphism in the methylenetetrahydrofolate reductase (MTHFR) gene with bone phenotypes depends on plasma folate status
    McLean, RR
    Karasik, D
    Selhub, J
    Tucker, KL
    Ordovas, JM
    Russo, GT
    Cupples, LA
    Jacques, PF
    Kiel, DP
    [J]. JOURNAL OF BONE AND MINERAL RESEARCH, 2004, 19 (03) : 410 - 418
  • [6] Genetic predisposition to hyperhomocysteinemia: Deficiency of methylenetetrahydrofolate reductase (MTHFR)
    Rozen, R
    [J]. THROMBOSIS AND HAEMOSTASIS, 1997, 78 (01) : 523 - 526
  • [7] A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status
    Friso, S
    Choi, SW
    Girelli, D
    Mason, JB
    Dolnikowski, GG
    Bagley, PJ
    Olivieri, O
    Jacques, PF
    Rosenberg, IH
    Corrocher, R
    Selhub, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (08) : 5606 - 5611
  • [8] A common polymorphism, in the methylenetetrahydrofolate reductase (MTHFR) gene is associated with quantitative ultrasound in those with low plasma folate.
    McLean, RR
    Karasik, D
    Selhub, J
    Tucker, KL
    Ordovas, J
    Friso, S
    Cupples, LA
    Jacques, PF
    Kiel, DP
    [J]. JOURNAL OF BONE AND MINERAL RESEARCH, 2002, 17 : S325 - S325
  • [9] Increased risk of mortality associated with a common mutation in the methylenetetrahydrofolate reductase gene (MTHFR)
    Heijmans, BT
    Gussekloo, J
    Kluft, C
    Droog, S
    Lagaay, AM
    Knook, DL
    Westendorp, RGJ
    Slagboom, PE
    [J]. ATHEROSCLEROSIS, 1999, 144 : 19 - 19
  • [10] Mortality risk in men is associated with a common mutation in the methylenetetrahydrofolate reductase gene (MTHFR)
    Bastiaan T Heijmans
    Jacobijn Gussekloo
    Cornelis Kluft
    Simone Droog
    A Margot Lagaay
    Dick L Knook
    Rudi GJ Westendorp
    Eline P Slagboom
    [J]. European Journal of Human Genetics, 1999, 7 : 197 - 204
12345