-
1
-
-
0034792891
-
The effect of folic acid deficiency and MTHFR C677T polymorphism on chromosome damage in human lymphocytes in vitro
-
Crott J.W., Mashiyama S.T., Ames B.N., and Fenech M. The effect of folic acid deficiency and MTHFR C677T polymorphism on chromosome damage in human lymphocytes in vitro. Cancer Epidemiol. Biomarkers Prev. 10 (2001) 1089-1096
-
(2001)
Cancer Epidemiol. Biomarkers Prev.
, vol.10
, pp. 1089-1096
-
-
Crott, J.W.1
Mashiyama, S.T.2
Ames, B.N.3
Fenech, M.4
-
2
-
-
4444363632
-
Associations between two common variants C677T and A1298C in the methylenetetrahydrofolate reductase gene and measures of folate metabolism and DNA stability (strand breaks, misincorporated uracil, and DNA methylation status) in human lymphocytes in vivo
-
Narayanan S., McConnell J., Little J., Sharp L., Piyathilake C.J., Powers H., Basten G., and Duthie S.J. Associations between two common variants C677T and A1298C in the methylenetetrahydrofolate reductase gene and measures of folate metabolism and DNA stability (strand breaks, misincorporated uracil, and DNA methylation status) in human lymphocytes in vivo. Cancer Epidemiol. Biomarkers Prev. 13 (2004) 1436-1443
-
(2004)
Cancer Epidemiol. Biomarkers Prev.
, vol.13
, pp. 1436-1443
-
-
Narayanan, S.1
McConnell, J.2
Little, J.3
Sharp, L.4
Piyathilake, C.J.5
Powers, H.6
Basten, G.7
Duthie, S.J.8
-
3
-
-
34547973144
-
Genetic polymorphisms in folate-metabolizing enzymes and risk of gastroesophageal cancers: a potential nutrient-gene interaction in cancer development
-
Lin D., Li H., Tan W., Miao X., and Wang L. Genetic polymorphisms in folate-metabolizing enzymes and risk of gastroesophageal cancers: a potential nutrient-gene interaction in cancer development. Forum Nutr. 60 (2007) 140-145
-
(2007)
Forum Nutr.
, vol.60
, pp. 140-145
-
-
Lin, D.1
Li, H.2
Tan, W.3
Miao, X.4
Wang, L.5
-
4
-
-
34848887427
-
The role of folate in depression and dementia
-
Mischoulon D., and Raab M.F. The role of folate in depression and dementia. J. Clin. Psychiatry 10 (2007) 28-33
-
(2007)
J. Clin. Psychiatry
, vol.10
, pp. 28-33
-
-
Mischoulon, D.1
Raab, M.F.2
-
5
-
-
48249138116
-
Folate and vitamin B12 metabolism: overview and interaction with riboflavin, vitamin B6, and polymorphisms
-
Shane B. Folate and vitamin B12 metabolism: overview and interaction with riboflavin, vitamin B6, and polymorphisms. Food Nutr. Bull. 29 (2008) S6-S16
-
(2008)
Food Nutr. Bull.
, vol.29
-
-
Shane, B.1
-
6
-
-
39149145892
-
Genome health nutrigenomics and nutrigenetics-diagnosis and nutritional treatment of genome damage on an individual basis
-
Fenech M. Genome health nutrigenomics and nutrigenetics-diagnosis and nutritional treatment of genome damage on an individual basis. Food Chem. Toxicol. 46 (2008) 1365-1370
-
(2008)
Food Chem. Toxicol.
, vol.46
, pp. 1365-1370
-
-
Fenech, M.1
-
7
-
-
34047154552
-
An increased micronucleus frequency in peripheral blood lymphocytes predicts the risk of cancer in humans
-
Bonassi S., Znaor A., Ceppi M., Lando C., Chang W.P., Holland N., Kirsch-Volders M., Zeiger E., Ban S., Barale R., Bigatti M.P., Bolognesi C., Cebulska-Wasilewska A., Fabianova E., Fucic A., Hagmar L., Joksic G., Martelli A., Migliore L., Mirkova E., Scarfi M.R., Zijno A., Norppa H., and Fenech M. An increased micronucleus frequency in peripheral blood lymphocytes predicts the risk of cancer in humans. Carcinogenesis 28 (2007) 625-631
-
(2007)
Carcinogenesis
, vol.28
, pp. 625-631
-
-
Bonassi, S.1
Znaor, A.2
Ceppi, M.3
Lando, C.4
Chang, W.P.5
Holland, N.6
Kirsch-Volders, M.7
Zeiger, E.8
Ban, S.9
Barale, R.10
Bigatti, M.P.11
Bolognesi, C.12
Cebulska-Wasilewska, A.13
Fabianova, E.14
Fucic, A.15
Hagmar, L.16
Joksic, G.17
Martelli, A.18
Migliore, L.19
Mirkova, E.20
Scarfi, M.R.21
Zijno, A.22
Norppa, H.23
Fenech, M.24
more..
-
8
-
-
34447269629
-
Micronuclei, genetic polymorphisms and cardiovascular disease mortality in a nested case-control study in Italy
-
Murgia E., Maggini V., Barale R., and Rossi A.M. Micronuclei, genetic polymorphisms and cardiovascular disease mortality in a nested case-control study in Italy. Mutat. Res. 621 (2007) 113-118
-
(2007)
Mutat. Res.
, vol.621
, pp. 113-118
-
-
Murgia, E.1
Maggini, V.2
Barale, R.3
Rossi, A.M.4
-
10
-
-
34748912412
-
Folic acid metabolism in human subjects revisited: potential implications for proposed mandatory folic acid fortification in the UK
-
Wright A.J., Dainty J.R., and Finglas P.M. Folic acid metabolism in human subjects revisited: potential implications for proposed mandatory folic acid fortification in the UK. Brit. J. Nutr. 98 (2007) 667-675
-
(2007)
Brit. J. Nutr.
, vol.98
, pp. 667-675
-
-
Wright, A.J.1
Dainty, J.R.2
Finglas, P.M.3
-
11
-
-
0029089831
-
Assignment of the human folate transporter gene to chromosome 21q22.3 by somatic cell hybrid analysis and in situ hybridization
-
Yang-Feng T.L., Ma Y.-Y., Liang R., Prasad P.D., Leibach F.H., and Ganapathy V. Assignment of the human folate transporter gene to chromosome 21q22.3 by somatic cell hybrid analysis and in situ hybridization. Biochem. Biophys. Res. Commun. 210 (1995) 874-879
-
(1995)
Biochem. Biophys. Res. Commun.
, vol.210
, pp. 874-879
-
-
Yang-Feng, T.L.1
Ma, Y.-Y.2
Liang, R.3
Prasad, P.D.4
Leibach, F.H.5
Ganapathy, V.6
-
12
-
-
0028487161
-
Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification
-
Goyette P., Sumner J.S., Milos R., Duncan A.M., Rosenblatt D.S., Matthews R.G., and Rozen R. Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification. Nature Genet. 7 (1994) 195-200
-
(1994)
Nature Genet.
, vol.7
, pp. 195-200
-
-
Goyette, P.1
Sumner, J.S.2
Milos, R.3
Duncan, A.M.4
Rosenblatt, D.S.5
Matthews, R.G.6
Rozen, R.7
-
13
-
-
10544249877
-
Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders
-
Leclerc D., Campeau E., Goyette P., Adjalla C.E., Christensen B., Ross M., Eydoux P., Rosenblatt D.S., Rozen R., and Gravel R.A. Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders. Hum. Mol. Genet. 5 (1996) 1867-1874
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1867-1874
-
-
Leclerc, D.1
Campeau, E.2
Goyette, P.3
Adjalla, C.E.4
Christensen, B.5
Ross, M.6
Eydoux, P.7
Rosenblatt, D.S.8
Rozen, R.9
Gravel, R.A.10
-
14
-
-
0032856882
-
A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida
-
Wilson A., Platt R., Wu Q., Leclerc D., Christensen B., Yang H., Gravel R.A., and Rozen R. A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida. Mol. Genet. Metab. 67 (1999) 317-323
-
(1999)
Mol. Genet. Metab.
, vol.67
, pp. 317-323
-
-
Wilson, A.1
Platt, R.2
Wu, Q.3
Leclerc, D.4
Christensen, B.5
Yang, H.6
Gravel, R.A.7
Rozen, R.8
-
15
-
-
0141590217
-
Genetic polymorphisms in folate and homocysteine metabolism as risk factors for DNA damage
-
Botto N., Andreassi M.G., Manfredi S., Masetti S., Cocci F., Colombo M.G., Storti S., Rizza A., and Biagini A. Genetic polymorphisms in folate and homocysteine metabolism as risk factors for DNA damage. Eur. J. Hum. Genet. 11 (2003) 671-678
-
(2003)
Eur. J. Hum. Genet.
, vol.11
, pp. 671-678
-
-
Botto, N.1
Andreassi, M.G.2
Manfredi, S.3
Masetti, S.4
Cocci, F.5
Colombo, M.G.6
Storti, S.7
Rizza, A.8
Biagini, A.9
-
16
-
-
0038687702
-
Folate status, metabolic genotype, and biomarkers of genotoxicity in healthy subjects
-
Zijno A., Andreoli C., Leopardi P., Marcon F., Rossi S., Caiola S., Verdina A., Galati R., Cafolla A., and Crebelli R. Folate status, metabolic genotype, and biomarkers of genotoxicity in healthy subjects. Carcinogenesis 24 (2003) 1097-1103
-
(2003)
Carcinogenesis
, vol.24
, pp. 1097-1103
-
-
Zijno, A.1
Andreoli, C.2
Leopardi, P.3
Marcon, F.4
Rossi, S.5
Caiola, S.6
Verdina, A.7
Galati, R.8
Cafolla, A.9
Crebelli, R.10
-
17
-
-
0037316039
-
Methylenetetrahydrofolate reductase gene C677T polymorphism, homocysteine, vitamin B12, and DNA damage in coronary artery disease
-
Andreassi M.G., Botto N., Cocci F., Battaglia D., Antonioli E., Masetti S., Manfredi S., Colombo M.G., Biagini A., and Clerico A. Methylenetetrahydrofolate reductase gene C677T polymorphism, homocysteine, vitamin B12, and DNA damage in coronary artery disease. Hum. Genet. 112 (2003) 171-177
-
(2003)
Hum. Genet.
, vol.112
, pp. 171-177
-
-
Andreassi, M.G.1
Botto, N.2
Cocci, F.3
Battaglia, D.4
Antonioli, E.5
Masetti, S.6
Manfredi, S.7
Colombo, M.G.8
Biagini, A.9
Clerico, A.10
-
18
-
-
33745893808
-
A polymorphism of the methionine synthase reductase gene increases chromosomal damage in peripheral lymphocytes in smokers
-
Ishikawa H., Ishikawa T., Miyatsu Y., Kurihara K., Fukao A., and Yokoyama K. A polymorphism of the methionine synthase reductase gene increases chromosomal damage in peripheral lymphocytes in smokers. Mutat. Res. 599 (2006) 135-143
-
(2006)
Mutat. Res.
, vol.599
, pp. 135-143
-
-
Ishikawa, H.1
Ishikawa, T.2
Miyatsu, Y.3
Kurihara, K.4
Fukao, A.5
Yokoyama, K.6
-
19
-
-
0031903189
-
Folate, vitamin B12, homocysteine status and DNA damage in young Australian adults
-
Fenech M., Aitken C., and Rinaldi J. Folate, vitamin B12, homocysteine status and DNA damage in young Australian adults. Carcinogenesis 19 (1998) 1163-1171
-
(1998)
Carcinogenesis
, vol.19
, pp. 1163-1171
-
-
Fenech, M.1
Aitken, C.2
Rinaldi, J.3
-
20
-
-
0032713815
-
Methionine synthase D919G polymorphism is a significant but modest determinant of circulating homocysteine concentrations
-
Harmon D.L., Shields D.C., Woodside J.V., McMaster D., Yarnell J.W., Young I.S., Peng K., Shane B., Evans A.E., and Whitehead A.S. Methionine synthase D919G polymorphism is a significant but modest determinant of circulating homocysteine concentrations. Genet. Epidemiol. 17 (1999) 298-309
-
(1999)
Genet. Epidemiol.
, vol.17
, pp. 298-309
-
-
Harmon, D.L.1
Shields, D.C.2
Woodside, J.V.3
McMaster, D.4
Yarnell, J.W.5
Young, I.S.6
Peng, K.7
Shane, B.8
Evans, A.E.9
Whitehead, A.S.10
-
21
-
-
0034904708
-
The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations
-
Gaughan D.J., Kluijtmans L.A.J., Barbaux S., McMaster D., Young I.S., Yarnell J.W.G., Evans A., and Whitehead A.S. The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations. Atherosclerosis 157 (2001) 451-456
-
(2001)
Atherosclerosis
, vol.157
, pp. 451-456
-
-
Gaughan, D.J.1
Kluijtmans, L.A.J.2
Barbaux, S.3
McMaster, D.4
Young, I.S.5
Yarnell, J.W.G.6
Evans, A.7
Whitehead, A.S.8
-
22
-
-
3042769514
-
Polymorphisms in the methylenetetrahydrofolate reductase and methionine synthase reductase genes and homocysteine levels in Brazilian children
-
Alessio A.C., Annichino-Bizzacchi J.M., Bydlowski S.P., Eberlin M.N., Vellasco A.P., and Hoehr N.F. Polymorphisms in the methylenetetrahydrofolate reductase and methionine synthase reductase genes and homocysteine levels in Brazilian children. Am. J. Med. Genet. 128 (2004) 256-260
-
(2004)
Am. J. Med. Genet.
, vol.128
, pp. 256-260
-
-
Alessio, A.C.1
Annichino-Bizzacchi, J.M.2
Bydlowski, S.P.3
Eberlin, M.N.4
Vellasco, A.P.5
Hoehr, N.F.6
-
23
-
-
0242577783
-
Age and gender affect the relation between methylenetetrahydrofolate reductase C677T genotype and fasting plasma homocysteine concentrations in the Framigham Offspring Study Cohort
-
Russo G.T., Friso S., Jacques P.F., Rogers G., Cucinotta D., Wilson P.W., Ordovas J.M., Rosenberg I.H., and Selhub J. Age and gender affect the relation between methylenetetrahydrofolate reductase C677T genotype and fasting plasma homocysteine concentrations in the Framigham Offspring Study Cohort. J. Nutr. 133 (2003) 3416-3421
-
(2003)
J. Nutr.
, vol.133
, pp. 3416-3421
-
-
Russo, G.T.1
Friso, S.2
Jacques, P.F.3
Rogers, G.4
Cucinotta, D.5
Wilson, P.W.6
Ordovas, J.M.7
Rosenberg, I.H.8
Selhub, J.9
-
24
-
-
0842281432
-
Methylenetetrahydrofolate reductase (MTHFR) c677t gene variant modulates the homocysteine folate correlation in a mild folate-deficient population
-
Pereira A.C., Schettert I.S., Morandini Filho A.A., Guerra-Shinohara E.M., and Krieger J.E. Methylenetetrahydrofolate reductase (MTHFR) c677t gene variant modulates the homocysteine folate correlation in a mild folate-deficient population. Clin. Chim. Acta. 340 (2004) 99-105
-
(2004)
Clin. Chim. Acta.
, vol.340
, pp. 99-105
-
-
Pereira, A.C.1
Schettert, I.S.2
Morandini Filho, A.A.3
Guerra-Shinohara, E.M.4
Krieger, J.E.5
-
25
-
-
34250187067
-
Cytokinesis-block micronucleus cytome assay
-
Fenech M. Cytokinesis-block micronucleus cytome assay. Nat. Protoc. 2 (2007) 1084-1104
-
(2007)
Nat. Protoc.
, vol.2
, pp. 1084-1104
-
-
Fenech, M.1
-
26
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase
-
Frosst P., Bloom H.J., Milos R., Goyette P., Sheppard C.A., Matthews R.G., Boers G.J., den Heijer M., Kluijtmans L.A., and van den Heuvel L.P. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat. Genet. 10 (1995) 111-113
-
(1995)
Nat. Genet.
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Bloom, H.J.2
Milos, R.3
Goyette, P.4
Sheppard, C.A.5
Matthews, R.G.6
Boers, G.J.7
den Heijer, M.8
Kluijtmans, L.A.9
van den Heuvel, L.P.10
-
27
-
-
0031971515
-
A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?
-
van der Put N.M., Gabreels F., Stevens E.M., Smeitink J.A., Trijbels F.J., Eskes T.K., van den Heuvel L.P., and Bloom H.J. A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?. Am. J. Hum. Genet. 62 (1998) 1044-1051
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 1044-1051
-
-
van der Put, N.M.1
Gabreels, F.2
Stevens, E.M.3
Smeitink, J.A.4
Trijbels, F.J.5
Eskes, T.K.6
van den Heuvel, L.P.7
Bloom, H.J.8
-
28
-
-
0034703861
-
Glutamate carboxypeptidase II: a polymorphism associated with lower levels of serum folate and hyperhomocysteinemia
-
Devlin A.M., Ling E., Peerson J.M., Fernando S., Clarke R., Smith A.D., and Halsted C.H. Glutamate carboxypeptidase II: a polymorphism associated with lower levels of serum folate and hyperhomocysteinemia. Hum. Mol. Genet. 9 (2000) 2837-2844
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2837-2844
-
-
Devlin, A.M.1
Ling, E.2
Peerson, J.M.3
Fernando, S.4
Clarke, R.5
Smith, A.D.6
Halsted, C.H.7
-
29
-
-
0033805360
-
A polymorphism (80G->A) in the reduced folate carrier gene and its associations with folate status and homocysteinemia
-
Chango A., Emery-Fillon N., de Courcy G.P., Lambert D., Pfister M., Rosenblatt D.S., and Nicolas J.P. A polymorphism (80G->A) in the reduced folate carrier gene and its associations with folate status and homocysteinemia. Mol. Genet. Metab. 70 (2000) 310-315
-
(2000)
Mol. Genet. Metab.
, vol.70
, pp. 310-315
-
-
Chango, A.1
Emery-Fillon, N.2
de Courcy, G.P.3
Lambert, D.4
Pfister, M.5
Rosenblatt, D.S.6
Nicolas, J.P.7
-
30
-
-
0037212592
-
Effects of polymorphisms of methionine synthase and methionine synthase reductase on total plasma homocysteine in the NHLBI Family Heart Study
-
Jacques P.F., Bostom A.G., Selhub J., Rich S., Ellison R.C., Eckfeldt J.H., Gravel R.A., and Rozen R. Effects of polymorphisms of methionine synthase and methionine synthase reductase on total plasma homocysteine in the NHLBI Family Heart Study. Atherosclerosis 166 (2003) 49-55
-
(2003)
Atherosclerosis
, vol.166
, pp. 49-55
-
-
Jacques, P.F.1
Bostom, A.G.2
Selhub, J.3
Rich, S.4
Ellison, R.C.5
Eckfeldt, J.H.6
Gravel, R.A.7
Rozen, R.8
-
31
-
-
0036795697
-
Essential hypertension in adolescents: association with insulin resistance and with metabolism of homocysteine and vitamins
-
Kahleova R., Palyzova D., Zvara K., Zvarova J., Hrach K., Novakova I., Hyanek J., Bendlova B., and Kozich V. Essential hypertension in adolescents: association with insulin resistance and with metabolism of homocysteine and vitamins. Am. J. Hyper. 15 (2002) 857-864
-
(2002)
Am. J. Hyper.
, vol.15
, pp. 857-864
-
-
Kahleova, R.1
Palyzova, D.2
Zvara, K.3
Zvarova, J.4
Hrach, K.5
Novakova, I.6
Hyanek, J.7
Bendlova, B.8
Kozich, V.9
-
32
-
-
0029122937
-
Functional analysis and DNA polymorphism of the tandemly repeated sequences in the 5′-terminal regulatory region of the human gene for thymidylate synthase
-
Horie N., Aiba H., Oguro K., and Takeishi K. Functional analysis and DNA polymorphism of the tandemly repeated sequences in the 5′-terminal regulatory region of the human gene for thymidylate synthase. Cell Struct. Funct. 20 (1995) 191-197
-
(1995)
Cell Struct. Funct.
, vol.20
, pp. 191-197
-
-
Horie, N.1
Aiba, H.2
Oguro, K.3
Takeishi, K.4
-
33
-
-
0034518362
-
Searching expressed sequence tag databases: discovery and confirmation of a common polymorphism in the thymidylate synthase gene
-
Ulrich C., Bigler J., Velicer C., Greene E., Farin F., and Potter J.D. Searching expressed sequence tag databases: discovery and confirmation of a common polymorphism in the thymidylate synthase gene. Cancer Epidemiol. Biomarkers Prev. 9 (2000) 1381-1385
-
(2000)
Cancer Epidemiol. Biomarkers Prev.
, vol.9
, pp. 1381-1385
-
-
Ulrich, C.1
Bigler, J.2
Velicer, C.3
Greene, E.4
Farin, F.5
Potter, J.D.6
-
34
-
-
0022589981
-
Cytokinesis-block micronucleus method in human lymphocytes: effect of in vivo ageing and low dose X-irradiation
-
Fenech M., and Morley A.A. Cytokinesis-block micronucleus method in human lymphocytes: effect of in vivo ageing and low dose X-irradiation. Mutat. Res. 161 (1986) 193-198
-
(1986)
Mutat. Res.
, vol.161
, pp. 193-198
-
-
Fenech, M.1
Morley, A.A.2
-
35
-
-
10744219719
-
Cancer risks attributable to low doses of ionizing radiation: assessing what we really know
-
Brenner D.J., Doll R., Goodhead D.T., Hall E.J., Land C.E., Little J.B., Lubin J.H., Preston D.L., Preston R.J., Puskin J.S., Ron E., Sachs R.K., Samet J.M., Setlow R.B., and Zaider M. Cancer risks attributable to low doses of ionizing radiation: assessing what we really know. Proc. Natl. Acad. Sci. U.S.A. 100 (2003) 13761-13766
-
(2003)
Proc. Natl. Acad. Sci. U.S.A.
, vol.100
, pp. 13761-13766
-
-
Brenner, D.J.1
Doll, R.2
Goodhead, D.T.3
Hall, E.J.4
Land, C.E.5
Little, J.B.6
Lubin, J.H.7
Preston, D.L.8
Preston, R.J.9
Puskin, J.S.10
Ron, E.11
Sachs, R.K.12
Samet, J.M.13
Setlow, R.B.14
Zaider, M.15
-
36
-
-
33644688027
-
The methionine synthase polymorphism c.2756Aright curved arrow G (D919G) is relevant for disease-free longevity
-
Linnebank M., Fliessbach K., Kolsch H., Rietschel M., and Wullner U. The methionine synthase polymorphism c.2756Aright curved arrow G (D919G) is relevant for disease-free longevity. Int. Mol. Med. 16 (2005) 759-761
-
(2005)
Int. Mol. Med.
, vol.16
, pp. 759-761
-
-
Linnebank, M.1
Fliessbach, K.2
Kolsch, H.3
Rietschel, M.4
Wullner, U.5
-
37
-
-
0032439244
-
Chromosomal damage rate, aging, and diet
-
Fenech M. Chromosomal damage rate, aging, and diet. Ann. N.Y. Acad. Sci. 854 (1998) 23-36
-
(1998)
Ann. N.Y. Acad. Sci.
, vol.854
, pp. 23-36
-
-
Fenech, M.1
-
38
-
-
0035140477
-
Genomic instability in Down syndrome and Fanconi anemia assessed by micronucleus analysis and single-cell gel electrophoresis
-
Maluf S.W., and Erdtmann B. Genomic instability in Down syndrome and Fanconi anemia assessed by micronucleus analysis and single-cell gel electrophoresis. Cancer Genet. Cytogenet. 124 (2001) 71-75
-
(2001)
Cancer Genet. Cytogenet.
, vol.124
, pp. 71-75
-
-
Maluf, S.W.1
Erdtmann, B.2
-
39
-
-
0037179510
-
Chromosomal instability in B-lymphoblasotoid cell lines from Werner and Bloom syndrome patients
-
Honma M., Tadokoro S., Sakamoto H., Tanabe H., Sugimoto M., Furuichi Y., Satoh T., Sofuni T., Goto M., and Hayashi M. Chromosomal instability in B-lymphoblasotoid cell lines from Werner and Bloom syndrome patients. Mutat. Res. 520 (2002) 15-24
-
(2002)
Mutat. Res.
, vol.520
, pp. 15-24
-
-
Honma, M.1
Tadokoro, S.2
Sakamoto, H.3
Tanabe, H.4
Sugimoto, M.5
Furuichi, Y.6
Satoh, T.7
Sofuni, T.8
Goto, M.9
Hayashi, M.10
-
40
-
-
0034919492
-
Spontaneous and induced chromosome damage in somatic cells of sporadic and familial Alzheimer's disease patients
-
Trippi F., Botto N., Scarpato R., Petrozzi L., Bonuccelli U., Latorraca S., Sorbi S., and Migliore L. Spontaneous and induced chromosome damage in somatic cells of sporadic and familial Alzheimer's disease patients. Mutagenesis 16 (2001) 323-327
-
(2001)
Mutagenesis
, vol.16
, pp. 323-327
-
-
Trippi, F.1
Botto, N.2
Scarpato, R.3
Petrozzi, L.4
Bonuccelli, U.5
Latorraca, S.6
Sorbi, S.7
Migliore, L.8
-
41
-
-
0041699719
-
Methionine synthase polymorphism is a risk factor for Alzheimer disease
-
Beyer K., Lao J.I., Latorre P., Riutort N., Matute B., Fernández-Figueras M.T., Mate J.L., and Ariza A. Methionine synthase polymorphism is a risk factor for Alzheimer disease. Neuroreport 14 (2003) 1391-1394
-
(2003)
Neuroreport
, vol.14
, pp. 1391-1394
-
-
Beyer, K.1
Lao, J.I.2
Latorre, P.3
Riutort, N.4
Matute, B.5
Fernández-Figueras, M.T.6
Mate, J.L.7
Ariza, A.8
-
42
-
-
41549104565
-
Association analysis of methionine synthase gene 2756 A > G polymorphism and Alzheimer disease in a Chinese population
-
Zhao H.L., Li X.Q., Zhang Z.X., Bi X.H., Wang B., and Zhang J.W. Association analysis of methionine synthase gene 2756 A > G polymorphism and Alzheimer disease in a Chinese population. Brain Res. 1204 (2008) 118-122
-
(2008)
Brain Res.
, vol.1204
, pp. 118-122
-
-
Zhao, H.L.1
Li, X.Q.2
Zhang, Z.X.3
Bi, X.H.4
Wang, B.5
Zhang, J.W.6
-
43
-
-
34548312384
-
Polymorphisms in folate and homocysteine metabolizing genes and chromosome damage in mothers of Down syndrome children
-
Coppede F., Colognato R., Bonelli A., Astrea G., Bargagna S., Siciliano G., and Migliore L. Polymorphisms in folate and homocysteine metabolizing genes and chromosome damage in mothers of Down syndrome children. Am. J. Med. Genet. 143 (2007) 2006-2015
-
(2007)
Am. J. Med. Genet.
, vol.143
, pp. 2006-2015
-
-
Coppede, F.1
Colognato, R.2
Bonelli, A.3
Astrea, G.4
Bargagna, S.5
Siciliano, G.6
Migliore, L.7
-
44
-
-
0346726185
-
Methylenetetrahydrofolate reductase C677T polymorphism, folic acid and riboflavin are important determinants of genome stability in cultured human lymphocytes
-
Kimura M., Umegaki K., Higuchi M., Thomas P., and Fenech M. Methylenetetrahydrofolate reductase C677T polymorphism, folic acid and riboflavin are important determinants of genome stability in cultured human lymphocytes. J. Nutr. 134 (2004) 48-56
-
(2004)
J. Nutr.
, vol.134
, pp. 48-56
-
-
Kimura, M.1
Umegaki, K.2
Higuchi, M.3
Thomas, P.4
Fenech, M.5
-
45
-
-
0035144198
-
HUman MicroNucleus project: international database comparison for results with the cytokinesis-block micronucleus assay in human lymphocytes: I. Effect of laboratory protocol, scoring criteria, and host factors on the frequency of micronuclei
-
Bonassi S., Fenech M., Lando C., Lin Y.P., Ceppi M., Chang W.P., Holland N., Kirsch-Volders M., Zeiger E., Ban S., Barale R., Bigatti M.P., Bolognesi C., Jia C., Di Giorgio M., Ferguson L.R., Fucic A., Lima O.G., Hrelia P., Krishnaja A.P., Lee T.K., Migliore L., Mikhalevich L., Mirkova E., Mosesso P., Müller W.U., Odagiri Y., Scarffi M.R., Szabova E., Vorobtsova I., Vral A., and Zijno A. HUman MicroNucleus project: international database comparison for results with the cytokinesis-block micronucleus assay in human lymphocytes: I. Effect of laboratory protocol, scoring criteria, and host factors on the frequency of micronuclei. Environ. Mol. Mutagen. 37 (2001) 31-45
-
(2001)
Environ. Mol. Mutagen.
, vol.37
, pp. 31-45
-
-
Bonassi, S.1
Fenech, M.2
Lando, C.3
Lin, Y.P.4
Ceppi, M.5
Chang, W.P.6
Holland, N.7
Kirsch-Volders, M.8
Zeiger, E.9
Ban, S.10
Barale, R.11
Bigatti, M.P.12
Bolognesi, C.13
Jia, C.14
Di Giorgio, M.15
Ferguson, L.R.16
Fucic, A.17
Lima, O.G.18
Hrelia, P.19
Krishnaja, A.P.20
Lee, T.K.21
Migliore, L.22
Mikhalevich, L.23
Mirkova, E.24
Mosesso, P.25
Müller, W.U.26
Odagiri, Y.27
Scarffi, M.R.28
Szabova, E.29
Vorobtsova, I.30
Vral, A.31
Zijno, A.32
more..
-
46
-
-
43149090300
-
Genetic polymorphisms and micronucleus frequency-a review of the literature
-
Iarmarcovai G., Bonassi S., Botta A., Baan R.A., and Orsiere T. Genetic polymorphisms and micronucleus frequency-a review of the literature. Mutat. Res. 658 (2008) 215-233
-
(2008)
Mutat. Res.
, vol.658
, pp. 215-233
-
-
Iarmarcovai, G.1
Bonassi, S.2
Botta, A.3
Baan, R.A.4
Orsiere, T.5
-
47
-
-
0037224868
-
The H475Y polymorphism in the glutamate carboxypeptidase II gene increases plasma folate without affecting the risk for neural tube defects in humans
-
Afman L.A., Trijbels F.J., and Blom H.J. The H475Y polymorphism in the glutamate carboxypeptidase II gene increases plasma folate without affecting the risk for neural tube defects in humans. J. Nutr. 133 (2003) 75-77
-
(2003)
J. Nutr.
, vol.133
, pp. 75-77
-
-
Afman, L.A.1
Trijbels, F.J.2
Blom, H.J.3
-
48
-
-
33745551531
-
The MTHFR 1298CC and 677TT genotypes have opposite associations with red cell folate levels
-
Parle-McDermott A., Mills J.L., Molloy A.M., Carroll N., Kirke P.N., Cox C., Conley M.R., Pangilinan F.J., Brody L.C., and Scott J.M. The MTHFR 1298CC and 677TT genotypes have opposite associations with red cell folate levels. Mol. Genet. Metab. 88 (2006) 290-294
-
(2006)
Mol. Genet. Metab.
, vol.88
, pp. 290-294
-
-
Parle-McDermott, A.1
Mills, J.L.2
Molloy, A.M.3
Carroll, N.4
Kirke, P.N.5
Cox, C.6
Conley, M.R.7
Pangilinan, F.J.8
Brody, L.C.9
Scott, J.M.10
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