메뉴 건너뛰기




Volumn 17, Issue 3, 2011, Pages 126-131

Neural tube defects between folate metabolism and genetics

Author keywords

Folic acid; MTHFR; MTR; MTRR; NTDs

Indexed keywords

CYANOCOBALAMIN; FOLIC ACID; HOMOCYSTEINE; METHIONINE; METHIONINE SYNTHASE;

EID: 84856373202     PISSN: 09716866     EISSN: 1998362X     Source Type: Journal    
DOI: 10.4103/0971-6866.92082     Document Type: Review
Times cited : (15)

References (40)
  • 2
    • 0035191481 scopus 로고    scopus 로고
    • Neural tube defects in the Asir region of Saudi Arabia
    • Asindi A, Al-Shehri A. Neural tube defects in the Asir region of Saudi Arabia. Ann Saudi Med 2001;21:26-9. (Pubitemid 33094717)
    • (2001) Annals of Saudi Medicine , vol.21 , Issue.1-2 , pp. 26-29
    • Asindi, A.1    Al-Shehri, A.2
  • 3
    • 1942469552 scopus 로고    scopus 로고
    • Gene-gene interaction in folate related genes and risk of neural tube defects in a UK population
    • Relton CL, Wilding CS, Pearce MS, Laffling AJ, Jonas PA, Lynch SA, et al. Gene-gene interaction in folate related genes and risk of neural tube defects in a UK population. J Med Genet 2003;41:256-60.
    • (2003) J Med Genet , vol.41 , pp. 256-260
    • Relton, C.L.1    Wilding, C.S.2    Pearce, M.S.3    Laffling, A.J.4    Jonas, P.A.5    Lynch, S.A.6
  • 5
    • 84875851447 scopus 로고    scopus 로고
    • Available from:. [Retrieved on 2008 Aug 30]
    • World Health Organization, 2006. Prevention of neural tube defects. Available from: http://www.who.int/makingpregnancy-safer/publications/en/. [Retrieved on 2008 Aug 30].
    • (2006) Prevention of Neural Tube Defects
  • 8
    • 33646185584 scopus 로고    scopus 로고
    • Incidence of Neural tube defects among neonates at King Hussein medical center, Jordan
    • Aqrabawi H. Incidence of Neural tube defects among neonates at King Hussein Medical Center, Jordan. Eastern Mediterranean Health J 2005;11:819-23.
    • (2005) Eastern Mediterranean Health J , vol.11 , pp. 819-823
    • Aqrabawi, H.1
  • 9
    • 33845529187 scopus 로고    scopus 로고
    • Neural tube defects in Jordan: A hospital based study
    • Masri A. Neural tube defects in Jordan: A hospital based study. J Pediatr Neurol 2006;4:245-9. (Pubitemid 44920934)
    • (2006) Journal of Pediatric Neurology , vol.4 , Issue.4 , pp. 245-249
    • Masri, A.T.1
  • 10
    • 33646749888 scopus 로고    scopus 로고
    • Etiology, pathogenesis and prevention of neural tube defects
    • Padmanabhan R. Etiology, pathogenesis and prevention of neural tube defects. Congenital Anomalies 2006;46: 55-67.
    • (2006) Congenital Anomalies , vol.46 , pp. 55-67
    • Padmanabhan, R.1
  • 12
    • 0036043697 scopus 로고    scopus 로고
    • Genetic basis of neural tube defects. I. Regulatory genes for the neurulation process
    • Gos M, Szpecht-Potocka A. Genetic basis of neural tube defects: Irregulatory genes for the neurulation process. J Appl Genet 2002;43:343-50. (Pubitemid 135705671)
    • (2002) Journal of Applied Genetics , vol.43 , Issue.3 , pp. 343-350
    • Gos, M.1    Szpecht-Potocka, A.2
  • 13
    • 0036488107 scopus 로고    scopus 로고
    • Genetic control of caudal development
    • Catala M. Genetic control of caudal development. Clin Genet 2002;61:86-96.
    • (2002) Clin Genet , vol.61 , pp. 86-96
    • Catala, M.1
  • 15
    • 0033808685 scopus 로고    scopus 로고
    • Folic acid: Nutritional biochemistry, molecular biology, and role in disease processes
    • Lucock M. Folic acid: Nutritional biochemistry, molecular biology, and role in disease processes. Mol Genet Metab 2000;71:121-38.
    • (2000) Mol Genet Metab , vol.71 , pp. 121-138
    • Lucock, M.1
  • 16
    • 0035122292 scopus 로고    scopus 로고
    • The folate cycle and disease in humans
    • Fowler B. The folate cycle and disease in humans. Kidney Int 2001;59:S221-9. (Pubitemid 32144102)
    • (2001) Kidney International, Supplement , vol.59 , Issue.78
    • Fowler, B.1
  • 17
  • 18
    • 0034703084 scopus 로고    scopus 로고
    • Increase in plasma homocysteine associated with parallel increases in plasma S-adenosylhomocysteine and lymphocyte DNA hypomethylation
    • DOI 10.1074/jbc.M002725200
    • Yi P, Melnyk S, Pogribna M, Pogribny IP, Hine RJ, James SJ. Increase in plasma homocysteine associated with parallel increases in plasma S-adenosylhomocysteine and lymphocyte DNA hypomethylation. J Biol Chem 2000;275:29,318-29,323. (Pubitemid 32043802)
    • (2000) Journal of Biological Chemistry , vol.275 , Issue.38 , pp. 29318-29323
    • Yi, P.1    Melnyk, S.2    Pogribna, M.3    Pogribny, I.P.4    Hine, R.J.5    James, S.J.6
  • 19
    • 0022842769 scopus 로고
    • Role of vitamin B12 and folate in carcinogenesis
    • Poirier LA, Newberne PM, Pariza MW, editors. New York: Academic Press
    • Eto I, Krumdieck CL. Role of vitamin B12 and folate in carcinogenesis. In Essential Nutrients in Carcinogenesis. In: Poirier LA, Newberne PM, Pariza MW, editors. New York: Academic Press; 1986. p. 313-30.
    • (1986) Essential Nutrients in Carcinogenesis , pp. 313-330
    • Eto, I.1    Krumdieck, C.L.2
  • 21
    • 0030979178 scopus 로고    scopus 로고
    • Folate deficiency causes uracil mis incorporation into human DNA and chromosome breakage: Implications for cancer and neuronal damage
    • Blount BC, Mack MM, Wehr CM, MacGregor JT, Hiatt RA, Wang G, et al. Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: Implications for cancer and neuronal damage. Proc Natl Acad Sci USA 1997;94:3290-5.
    • (1997) Proc Natl Acad Sci USA , vol.94 , pp. 3290-3295
    • Blount, B.C.1    MacK, M.M.2    Wehr, C.M.3    MacGregor, J.T.4    Hiatt, R.A.5    Wang, G.6
  • 22
    • 0031416750 scopus 로고    scopus 로고
    • Genetic and epigenetic aspects of DNA methylation on genome expression, evolution, mutation and carcinogenesis
    • DOI 10.1093/carcin/18.5.869
    • Zingg JM, Jones PA. Genetic and epigenetic aspects of DNA methylation on genome expression, evolution, mutation and carcinogenesis. Carcinogenesis 1997;18:869-82. (Pubitemid 28132329)
    • (1997) Carcinogenesis , vol.18 , Issue.5 , pp. 869-882
    • Zingg, J.-M.1    Jones, P.A.2
  • 23
    • 0033520969 scopus 로고    scopus 로고
    • Quality control by DNA repair
    • Lindahl T, Wood RD. Quality control by DNA repair. Science 1999;286:1897-905. (Pubitemid 129515891)
    • (1999) Science , vol.286 , Issue.5446 , pp. 1897-1905
    • Lindahl, T.1    Wood, R.D.2
  • 25
    • 50549208782 scopus 로고
    • Folic acid metabolism and human embryopathy
    • Hibbard BM, Smithells RW. Folic acid metabolism and human embryopathy. Lancet 1965;1:1254.
    • (1965) Lancet , vol.1 , pp. 1254
    • Hibbard, B.M.1    Smithells, R.W.2
  • 26
    • 84981812991 scopus 로고
    • The role of folic acid in pregnancy with particular reference to anaemia, abruption, and abortion
    • Hibbard BM. The role of folic acid in pregnancy with particular reference to anaemia, abruption, and abortion. J Obstet Gynaecol Br Commonwlth 1964;71:529-42.
    • (1964) J Obstet Gynaecol Br Commonwlth , vol.71 , pp. 529-542
    • Hibbard, B.M.1
  • 31
    • 0031969348 scopus 로고    scopus 로고
    • Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD (methylenetetrahydrofolate-dehydrogenase, methenyltetrahydrofolate- cyclohydrolase, formyltetrahydrofolate synthetase) in patients with neural tube defect
    • Hol FA, van der Put NM, Geurds MP, Heil SG, Trijbels FJ, Hamel BC, et al. Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD1 (mthylenetetrahydrofolatecyclohdrolase, formyltetrahydrofolate synthase) in patients with neural tube defects. Clin Genet 1998;53:119-25. (Pubitemid 28188213)
    • (1998) Clinical Genetics , vol.53 , Issue.2 , pp. 119-125
    • Hol, F.A.1    Van Der Put, N.M.J.2    Geurds, M.P.A.3    Heil, S.G.4    Trijbels, F.J.M.5    Hamel, B.C.J.6    Mariman, E.C.M.7    Blom, H.J.8
  • 32
    • 18644379774 scopus 로고    scopus 로고
    • A polymorphism, R653Q, in the trifunctional enzyme methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase/formyltetrahydrofolate synthetase is a maternal genetic risk factor for neural tube defects: Report of the birth defects research group
    • DOI 10.1086/344213
    • Brody LC, Conley M, Cox C, Kirke PN, McKeever MP, Mills JL, et al. A polymorphism, R653Q, in the trifunctional enzyme methylenetetrahydrofolate -dehydrogenase methenyltetrahydrofolate cyclohydrolase/ formyltetrahydrofolate synthetase is a maternal genetic risk factor for neural tube defects. Am Soc Hum Genet 2002;71:1207-15. (Pubitemid 35305240)
    • (2002) American Journal of Human Genetics , vol.71 , Issue.5 , pp. 1207-1215
    • Brody, L.C.1    Conley, M.2    Cox, C.3    Kirke, P.N.4    McKeever, M.P.5    Mills, J.L.6    Molloy, A.M.7    O'Leary, V.B.8    Parle-McDermott, A.9    Scott, J.M.10    Swanson, D.A.11
  • 33
    • 0036096526 scopus 로고    scopus 로고
    • Changes in frequencies of heterozygous thermolabile 5, 10-methylenetetrahydrofolate reductase gene in fetuses with neural tube defects [8]
    • Johanning GL, Wenstrom KD, Tamura T. Changes in frequencies of heterozygous thermolabile 5, 10-methylenetetrahydrofolate reductase gene in fetuses with neural tube defects. J Med Genet 2002;39:366-7. (Pubitemid 34526359)
    • (2002) Journal of Medical Genetics , vol.39 , Issue.5 , pp. 366-367
    • Johanning, G.L.1    Wenstrom, K.D.2    Tamura, T.3
  • 38
    • 78650165958 scopus 로고    scopus 로고
    • Methionine synthase polymorphisms (MTR 2756 A>G and MTR 2758 C>G) frequencies and distribution in the Jordanian population and their correlation with neural tube defects in the population of the northern part of Jordan
    • Al Farra HY. Methionine synthase polymorphisms (MTR 2756 A>G and MTR 2758 C>G) frequencies and distribution in the Jordanian population and their correlation with neural tube defects in the population of the northern part of Jordan. Indian J Hum Genet 2010;16:72-7.
    • (2010) Indian J Hum Genet , vol.16 , pp. 72-77
    • Al Farra, H.Y.1
  • 39
    • 34247570440 scopus 로고    scopus 로고
    • Toward understanding the genetic basis of neural tube defects
    • DOI 10.1111/j.1399-0004.2007.00793.x
    • Kibar Z, Capra V, Gros P. Toward understanding the genetic basis of neural tube defects. Clin Genet 2007;71:295-310. (Pubitemid 46680796)
    • (2007) Clinical Genetics , vol.71 , Issue.4 , pp. 295-310
    • Kibar, Z.1    Capra, V.2    Gros, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.