메뉴 건너뛰기




Volumn 34, Issue 3, 2008, Pages 301-306

ACE and MTHFR gene polymorphisms in unexplained recurrent pregnancy loss

Author keywords

ACE; MTHFR; Polymorphism; Recurrent pregnancy loss

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); DIPEPTIDYL CARBOXYPEPTIDASE;

EID: 45149131378     PISSN: 13418076     EISSN: 14470756     Source Type: Journal    
DOI: 10.1111/j.1447-0756.2008.00792.x     Document Type: Article
Times cited : (42)

References (23)
  • 1
    • 0029951573 scopus 로고    scopus 로고
    • Frequency of factors associated with habitual abortion in 197 couples
    • Stephenson MD. Frequency of factors associated with habitual abortion in 197 couples. Fertil Steril 1996 66 : 24 29.
    • (1996) Fertil Steril , vol.66 , pp. 24-29
    • Stephenson, M.D.1
  • 2
    • 16044369784 scopus 로고    scopus 로고
    • Increased fetal loss in women with heritable thrombophilia
    • Preston FE, Rosendaal FR, Walker ID. Increased fetal loss in women with heritable thrombophilia. Lancet 1996 348 : 913 916.
    • (1996) Lancet , vol.348 , pp. 913-916
    • Preston, F.E.1    Rosendaal, F.R.2    Walker, I.D.3
  • 3
    • 0037484301 scopus 로고    scopus 로고
    • Inherited thrombophilia: Impact on human reproduction
    • Buchholz T, Thaler CJ. Inherited thrombophilia: impact on human reproduction. Am J Reprod Immunol 2003 49 : 1 13.
    • (2003) Am J Reprod Immunol , vol.49 , pp. 1-13
    • Buchholz, T.1    Thaler, C.J.2
  • 4
    • 0034495761 scopus 로고    scopus 로고
    • Clinical implications of disturbances of uterine vascular morphology and function
    • Hickey M, Fraser IS. Clinical implications of disturbances of uterine vascular morphology and function. Clin Obstet Gynecol 2000 14 : 937 951.
    • (2000) Clin Obstet Gynecol , vol.14 , pp. 937-951
    • Hickey, M.1    Fraser, I.S.2
  • 5
  • 6
    • 0031854738 scopus 로고    scopus 로고
    • Fibrinolytic balance, the renin-angiotensin system and atherosclerotic disease
    • Vaughan DE. Fibrinolytic balance, the renin-angiotensin system and atherosclerotic disease. Eur Heart J 1998 19 : 9 12.
    • (1998) Eur Heart J , vol.19 , pp. 9-12
    • Vaughan, D.E.1
  • 7
    • 0025165779 scopus 로고
    • An insertion-deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels
    • Rigat B, Hubert C, Alhenc-Gelas F, Cambien F, Corvol P, Soubrier F. An insertion-deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels. J Clin Invest 1990 86 : 1343 1346.
    • (1990) J Clin Invest , vol.86 , pp. 1343-1346
    • Rigat, B.1    Hubert, C.2    Alhenc-Gelas, F.3    Cambien, F.4    Corvol, P.5    Soubrier, F.6
  • 8
    • 0037390270 scopus 로고    scopus 로고
    • Maternal-fetal flow, negative events, and preecalmpsia. Role of ACE I/D polymorphism
    • Mello G, Parretti E, Gensini F et al. Maternal-fetal flow, negative events, and preecalmpsia. Role of ACE I/D polymorphism. Hypertension 2003 41 : 932 937.
    • (2003) Hypertension , vol.41 , pp. 932-937
    • Mello, G.1    Parretti, E.2    Gensini, F.3
  • 9
    • 0032832989 scopus 로고    scopus 로고
    • Angiotensin II stimulates intercellular adhesion molecole-1 (ICAM-1) expression by human vascular endothelial cells and increases solubile ICAM-1 release in vivo
    • Pastore L, Tessitore A, Martinetti S et al. Angiotensin II stimulates intercellular adhesion molecole-1 (ICAM-1) expression by human vascular endothelial cells and increases solubile ICAM-1 release in vivo. Circulation 1999 100 : 1646 1652.
    • (1999) Circulation , vol.100 , pp. 1646-1652
    • Pastore, L.1    Tessitore, A.2    Martinetti, S.3
  • 11
    • 0042666940 scopus 로고    scopus 로고
    • ACE DD genotype: An independent predisposition factor to venous thromboembolism
    • Fatini C, Gensini F, Sticchi E et al. ACE DD genotype: an independent predisposition factor to venous thromboembolism. Eur J Clin Invest 2003 33 : 642 647.
    • (2003) Eur J Clin Invest , vol.33 , pp. 642-647
    • Fatini, C.1    Gensini, F.2    Sticchi, E.3
  • 12
    • 0030610090 scopus 로고    scopus 로고
    • The mutation Ala6774Val in the methylene tetrahydrofolate reductase gene: A risk factor for arterial disease and venous thrombosis
    • Arruda VR, von Zuben PM, Chiaparini LC, Annichino-Bizzacchi JM, Costa FF. The mutation Ala6774Val in the methylene tetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis. Thromb Haemost 1997 77 : 818 821.
    • (1997) Thromb Haemost , vol.77 , pp. 818-821
    • Arruda, V.R.1    Von Zuben, P.M.2    Chiaparini, L.C.3    Annichino-Bizzacchi, J.M.4    Costa, F.F.5
  • 13
    • 0030797307 scopus 로고    scopus 로고
    • Hyperhomocysteinemia as a risk factor for arterial and venous disease: A review of evidence and relevance
    • Boers GH. Hyperhomocysteinemia as a risk factor for arterial and venous disease: a review of evidence and relevance. Thromb Haemost 1997 78 : 520 522.
    • (1997) Thromb Haemost , vol.78 , pp. 520-522
    • Boers, G.H.1
  • 14
    • 0031004309 scopus 로고    scopus 로고
    • Activated protein C resistance can be associated with recurrent fetal loss
    • Brenner B, Mandel H, Lanir N et al. Activated protein C resistance can be associated with recurrent fetal loss. Br J Haematol 1997 97 : 551 554.
    • (1997) Br J Haematol , vol.97 , pp. 551-554
    • Brenner, B.1    Mandel, H.2    Lanir, N.3
  • 15
    • 0030963627 scopus 로고    scopus 로고
    • Fetal carriers of the factor V Leiden mutation are prone to miscarriage and placental infarction
    • Dizon-Townson DS, Meline L, Nelson LM, Varner M, Ward K. Fetal carriers of the factor V Leiden mutation are prone to miscarriage and placental infarction. Am J Obstet Gynecol 1997 177 : 402 405.
    • (1997) Am J Obstet Gynecol , vol.177 , pp. 402-405
    • Dizon-Townson, D.S.1    Meline, L.2    Nelson, L.M.3    Varner, M.4    Ward, K.5
  • 16
    • 0029557183 scopus 로고
    • DNA methylation and polyamines in embryonic development and cancer
    • Heby O. DNA methylation and polyamines in embryonic development and cancer. Int J Dev Biol 1995 39 : 737 757.
    • (1995) Int J Dev Biol , vol.39 , pp. 737-757
    • Heby, O.1
  • 17
    • 0024284028 scopus 로고
    • A simple salting out procedure for extracting DNA from human nucleated cells
    • Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988 16 : 121 122.
    • (1988) Nucleic Acids Res , vol.16 , pp. 121-122
    • Miller, S.A.1    Dykes, D.D.2    Polesky, H.F.3
  • 18
    • 0029049553 scopus 로고
    • A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
    • Frosst P, Blom HJ, Milos R et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 1995 10 : 111 113.
    • (1995) Nat Genet , vol.10 , pp. 111-113
    • Frosst, P.1    Blom, H.J.2    Milos, R.3
  • 19
    • 0033766424 scopus 로고    scopus 로고
    • Angiotensin-converting enzyme DD genotype, angiotensin type 1 receptor CC genotype, and hyperhomocysteinemia increase first-trimester fetal-loss susceptibility
    • Fatini C, Gensini F, Battaglini B et al. Angiotensin-converting enzyme DD genotype, angiotensin type 1 receptor CC genotype, and hyperhomocysteinemia increase first-trimester fetal-loss susceptibility. Blood Coagul Fibrinolysis 2000 11 : 657 662.
    • (2000) Blood Coagul Fibrinolysis , vol.11 , pp. 657-662
    • Fatini, C.1    Gensini, F.2    Battaglini, B.3
  • 20
    • 0343471524 scopus 로고    scopus 로고
    • Genetic risk factor for unexplained recurrent early pregnancy loss
    • Nelen WL, Steegers EA, Eskes TK, Blom HJ. Genetic risk factor for unexplained recurrent early pregnancy loss. Lancet 1997 350 : 861 863.
    • (1997) Lancet , vol.350 , pp. 861-863
    • Nelen, W.L.1    Steegers, E.A.2    Eskes, T.K.3    Blom, H.J.4
  • 21
    • 0031883045 scopus 로고    scopus 로고
    • A woman with five consecutive fetal deaths: Case report and retrospective analysis of hyperhomocysteinemia prevalence in 100 consecutive women with recurrent miscarriages
    • Quere I, Bellet H, Hoffet M, Janbon C, Mares P, Gris JC. A woman with five consecutive fetal deaths: case report and retrospective analysis of hyperhomocysteinemia prevalence in 100 consecutive women with recurrent miscarriages. Fertil Steril 1998 69 : 152 154.
    • (1998) Fertil Steril , vol.69 , pp. 152-154
    • Quere, I.1    Bellet, H.2    Hoffet, M.3    Janbon, C.4    Mares, P.5    Gris, J.C.6
  • 22
    • 0031978235 scopus 로고    scopus 로고
    • Methylene tetrahydrofolate reductase (MTHFR) 677T C mutation and unexplained early pregnancy loss [letter]
    • Grandone E, Margaglione M, Colaizzo D et al. Methylene tetrahydrofolate reductase (MTHFR) 677T C mutation and unexplained early pregnancy loss [letter]. Thromb Haemost 1998 79 : 1056 1057.
    • (1998) Thromb Haemost , vol.79 , pp. 1056-1057
    • Grandone, E.1    Margaglione, M.2    Colaizzo, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.