-
1
-
-
0035940757
-
The C677T methylenetetrahydrofolate reductase mutation is not associated with Alzheimer's disease
-
Brunellia T., Bagnolib S., Giustia B., Nacmiasb B., Pepea G., Sorbib S., and Abbate R. The C677T methylenetetrahydrofolate reductase mutation is not associated with Alzheimer's disease. Neurosci. Lett. 315 (2001) 103-105
-
(2001)
Neurosci. Lett.
, vol.315
, pp. 103-105
-
-
Brunellia, T.1
Bagnolib, S.2
Giustia, B.3
Nacmiasb, B.4
Pepea, G.5
Sorbib, S.6
Abbate, R.7
-
2
-
-
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
-
3
-
-
0031836810
-
ACE, MTHFR, factor V Leiden, and APOE polymorphisms in patients with vascular and Alzheimer's dementia
-
Chapman J., Wang N.S., Treves T.A., Korczyn A.D., and Bornstein N.M. ACE, MTHFR, factor V Leiden, and APOE polymorphisms in patients with vascular and Alzheimer's dementia. Stroke 29 (1998) 1401-1404
-
(1998)
Stroke
, vol.29
, pp. 1401-1404
-
-
Chapman, J.1
Wang, N.S.2
Treves, T.A.3
Korczyn, A.D.4
Bornstein, N.M.5
-
4
-
-
0031597388
-
12, and serum total homocysteine levels in confirmed Alzheimer disease
-
12, and serum total homocysteine levels in confirmed Alzheimer disease. Arch. Neurol. 55 (1998) 1449-1455
-
(1998)
Arch. Neurol.
, vol.55
, pp. 1449-1455
-
-
Clarke, R.1
Smith, A.D.2
Jobst, K.A.3
Refsum, H.4
Sutton, L.5
Ueland, P.M.6
-
5
-
-
33645635701
-
Interactions among polymorphisms in folate-metabolizing genes and serum total homocysteine concentrations in a healthy elderly population
-
Devlin A.M., Clarke R., Birks J., Evans J.G., and Halsted C.H. Interactions among polymorphisms in folate-metabolizing genes and serum total homocysteine concentrations in a healthy elderly population. Am. J. Clin. Nutr. 83 (2006) 708-713
-
(2006)
Am. J. Clin. Nutr.
, vol.83
, pp. 708-713
-
-
Devlin, A.M.1
Clarke, R.2
Birks, J.3
Evans, J.G.4
Halsted, C.H.5
-
6
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase
-
Frosst P., Blom H.J., Milos R., Goyette P., Sheppard C.A., Matthews R.G., Boers G.J.H., den Heijer M., Kluijtmans L.A., van den Heuve L.P., and Rozen R. 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
Blom, H.J.2
Milos, R.3
Goyette, P.4
Sheppard, C.A.5
Matthews, R.G.6
Boers, G.J.H.7
den Heijer, M.8
Kluijtmans, L.A.9
van den Heuve, L.P.10
Rozen, R.11
-
7
-
-
34247326565
-
Associations of common polymorphisms in the thymidylate synthase, reduced folate carrier and 5-aminoimidazole-4-carboxamide ribonucleotide transformylase/inosine monophosphate cyclohydrolase genes with folate and homocysteine levels and venous thrombosis risk
-
Gellekink H., Blom H.J., and den Heijer M. Associations of common polymorphisms in the thymidylate synthase, reduced folate carrier and 5-aminoimidazole-4-carboxamide ribonucleotide transformylase/inosine monophosphate cyclohydrolase genes with folate and homocysteine levels and venous thrombosis risk. Clin. Chem. Lab. Med. 45 (2007) 471-476
-
(2007)
Clin. Chem. Lab. Med.
, vol.45
, pp. 471-476
-
-
Gellekink, H.1
Blom, H.J.2
den Heijer, M.3
-
8
-
-
0025257612
-
Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with Hha I
-
Hixson J.E., and Vernier D.T. Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with Hha I. J. Lipid Res. 31 (1990) 545-548
-
(1990)
J. Lipid Res.
, vol.31
, pp. 545-548
-
-
Hixson, J.E.1
Vernier, D.T.2
-
9
-
-
0023696435
-
Intermediate homocysteinemia: a thermolabile variant of methylenete trahydrofolate reductase
-
Kang S.S., Zhou J., Wong P.W.K., Kowalisyn J., and Strokosch G. Intermediate homocysteinemia: a thermolabile variant of methylenete trahydrofolate reductase. Am. J. Hum. Genet. 43 (1988) 414-421
-
(1988)
Am. J. Hum. Genet.
, vol.43
, pp. 414-421
-
-
Kang, S.S.1
Zhou, J.2
Wong, P.W.K.3
Kowalisyn, J.4
Strokosch, G.5
-
10
-
-
0038446637
-
Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults
-
Kluijtmans L.J., Young I.S., Boreham C.A., Murray L., McMaster D., McNulty H., Strain J.J., McPartlin J., Scott J.M., and Whitehead A.S. Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults. Blood 101 (2003) 2483-2488
-
(2003)
Blood
, vol.101
, pp. 2483-2488
-
-
Kluijtmans, L.J.1
Young, I.S.2
Boreham, C.A.3
Murray, L.4
McMaster, D.5
McNulty, H.6
Strain, J.J.7
McPartlin, J.8
Scott, J.M.9
Whitehead, A.S.10
-
11
-
-
7244229777
-
Lack of genetic dispositions to hyperhomocysteinemia in Alzheimer disease
-
Linnebank M., Linnebank A., Jeub M., Klockgether T., Wullner U., Kolsch H., Heun R., Koch H.G., Suormala T., and Fowler B. Lack of genetic dispositions to hyperhomocysteinemia in Alzheimer disease. Am. J. Med. Genet. 131 (2004) 101-102
-
(2004)
Am. J. Med. Genet.
, vol.131
, pp. 101-102
-
-
Linnebank, M.1
Linnebank, A.2
Jeub, M.3
Klockgether, T.4
Wullner, U.5
Kolsch, H.6
Heun, R.7
Koch, H.G.8
Suormala, T.9
Fowler, B.10
-
12
-
-
0029806746
-
Methelenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine and risk of myocardial infarction in US physicians
-
Ma J., Stampfer M.J., Hennekens C.H., Frosst P., Selhub J., and Horsford J. Methelenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine and risk of myocardial infarction in US physicians. Circulation 94 (1996) 2410-2416
-
(1996)
Circulation
, vol.94
, pp. 2410-2416
-
-
Ma, J.1
Stampfer, M.J.2
Hennekens, C.H.3
Frosst, P.4
Selhub, J.5
Horsford, J.6
-
13
-
-
33845608177
-
Dietary factors and biomarkers involved in the methyenetetrahydrofolate reductase genotype-colrectal adenoma pathway
-
Martinez M.E., Thompson P., Jacobs E.T., Giovannucci E., Jiang R., Klimecki W., and Alberts D.S. Dietary factors and biomarkers involved in the methyenetetrahydrofolate reductase genotype-colrectal adenoma pathway. Gastroenterology 131 (2006) 1706-1716
-
(2006)
Gastroenterology
, vol.131
, pp. 1706-1716
-
-
Martinez, M.E.1
Thompson, P.2
Jacobs, E.T.3
Giovannucci, E.4
Jiang, R.5
Klimecki, W.6
Alberts, D.S.7
-
14
-
-
0036792804
-
Moderately elevated plasma homocysteine methylenetetrahydrofolate reductase genotype, and risk for stroke, vascular dementia, and Alzheimer disease in northern Ireland
-
McIlroy S.P., Dynan K.B., Lawson J.T., Patterson C.C., and Passmore A.P. Moderately elevated plasma homocysteine methylenetetrahydrofolate reductase genotype, and risk for stroke, vascular dementia, and Alzheimer disease in northern Ireland. Stroke 33 (2002) 2351-2356
-
(2002)
Stroke
, vol.33
, pp. 2351-2356
-
-
McIlroy, S.P.1
Dynan, K.B.2
Lawson, J.T.3
Patterson, C.C.4
Passmore, A.P.5
-
15
-
-
0030744634
-
Microbiological assay for serum, plasma, and red cell folate using cryopreserved, microtiter plate method
-
Molloy A.M., and Scott J.M. Microbiological assay for serum, plasma, and red cell folate using cryopreserved, microtiter plate method. Method Enzymol. 281 (1997) 43-53
-
(1997)
Method Enzymol.
, vol.281
, pp. 43-53
-
-
Molloy, A.M.1
Scott, J.M.2
-
16
-
-
0037677623
-
Evaluation of genetic variants in the reduced folate carrier and in glutamate carboxypeptidase II for spina bifida risk
-
Morin I., Devlin A.M., Leclerc D., Sabbaghian N., Halsted C.H., Finnell R., and Rozen R. Evaluation of genetic variants in the reduced folate carrier and in glutamate carboxypeptidase II for spina bifida risk. Mol. Genet. Metab. 79 (2003) 197-200
-
(2003)
Mol. Genet. Metab.
, vol.79
, pp. 197-200
-
-
Morin, I.1
Devlin, A.M.2
Leclerc, D.3
Sabbaghian, N.4
Halsted, C.H.5
Finnell, R.6
Rozen, R.7
-
17
-
-
0031058560
-
Human intestinal folate transport: cloning, expression, and distribution of complementary RNA
-
Nguyen T.T., Dyer D.L., Dunning D.D., Rubin S.A., Grant K.E., and Said H.M. Human intestinal folate transport: cloning, expression, and distribution of complementary RNA. Gastroenterology 112 (1997) 783-791
-
(1997)
Gastroenterology
, vol.112
, pp. 783-791
-
-
Nguyen, T.T.1
Dyer, D.L.2
Dunning, D.D.3
Rubin, S.A.4
Grant, K.E.5
Said, H.M.6
-
18
-
-
0034971263
-
Lack of replication of association findings in complex disease: an analysis of 15 polymorphisms in prior candidate genes for sporadic Alzheimer's disease
-
Prince J.A., Feuk L., Sawyer S.L., Gottfries J., Ricksten A., NaÈgga K., Bogdanovic N., Kaj Blennow K., and Brookes A.J. Lack of replication of association findings in complex disease: an analysis of 15 polymorphisms in prior candidate genes for sporadic Alzheimer's disease. Eur. J. Hum. Genet. 9 (2001) 437-444
-
(2001)
Eur. J. Hum. Genet.
, vol.9
, pp. 437-444
-
-
Prince, J.A.1
Feuk, L.2
Sawyer, S.L.3
Gottfries, J.4
Ricksten, A.5
NaÈgga, K.6
Bogdanovic, N.7
Kaj Blennow, K.8
Brookes, A.J.9
-
19
-
-
3042784367
-
Homocysteine, folate, and vitamin B-12 in mild cognitive impairment, Alzheimer disease, and vascular dementia
-
Quadri P., Fragiacomo C., Pezzati R., Zanda E., Forloni G., Tettamanti M., and Lucca U. Homocysteine, folate, and vitamin B-12 in mild cognitive impairment, Alzheimer disease, and vascular dementia. Am. J. Clin. Nutr. 80 (2004) 114-122
-
(2004)
Am. J. Clin. Nutr.
, vol.80
, pp. 114-122
-
-
Quadri, P.1
Fragiacomo, C.2
Pezzati, R.3
Zanda, E.4
Forloni, G.5
Tettamanti, M.6
Lucca, U.7
-
20
-
-
27244445944
-
Homocysteine and folate as risk factors for dementia and Alzheimer disease
-
Ravaglia G., Forti P., Maioli F., Martelli M., Servadei L., Brunetti N., Porcellini E., and Licastro F. Homocysteine and folate as risk factors for dementia and Alzheimer disease. Am. J. Clin. Nutr. 82 (2005) 636-643
-
(2005)
Am. J. Clin. Nutr.
, vol.82
, pp. 636-643
-
-
Ravaglia, G.1
Forti, P.2
Maioli, F.3
Martelli, M.4
Servadei, L.5
Brunetti, N.6
Porcellini, E.7
Licastro, F.8
-
21
-
-
0042090361
-
Methylenetetrahydrofolate reductase and angiotensin converting enzyme gene polymorphisms in two genetically and diagnostically distinct cohort of Alzheimer patients
-
Seripa D., Forno G.D., Matera M.G., Gravina C., Margaglione M., Palermo M.T., Wekstein D.R., Antuono P., Davis D.G., Daniele A., Masullo C., Bizzarro A., Gennarelli M., and Fazio V.M. Methylenetetrahydrofolate reductase and angiotensin converting enzyme gene polymorphisms in two genetically and diagnostically distinct cohort of Alzheimer patients. Neurobiol. Aging 24 (2003) 933-939
-
(2003)
Neurobiol. Aging
, vol.24
, pp. 933-939
-
-
Seripa, D.1
Forno, G.D.2
Matera, M.G.3
Gravina, C.4
Margaglione, M.5
Palermo, M.T.6
Wekstein, D.R.7
Antuono, P.8
Davis, D.G.9
Daniele, A.10
Masullo, C.11
Bizzarro, A.12
Gennarelli, M.13
Fazio, V.M.14
-
22
-
-
0037075257
-
Plasma homocysteine as a risk factor for dementia and Alzheimer's disease
-
Seshadri S., Beiser A., Selhub J., Jacques P.F., Rosenberg I.H., D'agostino P.B., Wilson W.F., and Wolf P.A. Plasma homocysteine as a risk factor for dementia and Alzheimer's disease. N. Eng. J. Med. 346 (2002) 476-483
-
(2002)
N. Eng. J. Med.
, vol.346
, pp. 476-483
-
-
Seshadri, S.1
Beiser, A.2
Selhub, J.3
Jacques, P.F.4
Rosenberg, I.H.5
D'agostino, P.B.6
Wilson, W.F.7
Wolf, P.A.8
-
23
-
-
0034068273
-
Serum folate and the severity of atrophy of the neocortex in Alzheimer disease: findings from the Nun Study
-
Snowdon D.A., Tully C.L., Smith C.D., Riley K.P., and Markesbery W.R. Serum folate and the severity of atrophy of the neocortex in Alzheimer disease: findings from the Nun Study. Am. J. Clin. Nutr. 71 (2000) 993-998
-
(2000)
Am. J. Clin. Nutr.
, vol.71
, pp. 993-998
-
-
Snowdon, D.A.1
Tully, C.L.2
Smith, C.D.3
Riley, K.P.4
Markesbery, W.R.5
-
24
-
-
21844441674
-
Genetic determinants of folate status in central bohemia
-
Veselá K., Pavlíková M., Janošíková B., Anděl M., Zvárová J., Hyánek J., and Kožich V. Genetic determinants of folate status in central bohemia. Physiol. Res. 54 (2005) 295-303
-
(2005)
Physiol. Res.
, vol.54
, pp. 295-303
-
-
Veselá, K.1
Pavlíková, M.2
Janošíková, B.3
Anděl, M.4
Zvárová, J.5
Hyánek, J.6
Kožich, V.7
-
25
-
-
10744220005
-
A haplotype of the methylenetetrahydrofolate reductase gene is protective against late-onset Alzheimer's disease
-
Wakutani Y., Kowa H., Kusumi M., Nakaso K., Yasui K., Isoe-Wada K., Yano H., Urakami K., Takeshima T., and Nakashima K. A haplotype of the methylenetetrahydrofolate reductase gene is protective against late-onset Alzheimer's disease. Neurobiol. Aging 25 (2004) 291-294
-
(2004)
Neurobiol. Aging
, vol.25
, pp. 291-294
-
-
Wakutani, Y.1
Kowa, H.2
Kusumi, M.3
Nakaso, K.4
Yasui, K.5
Isoe-Wada, K.6
Yano, H.7
Urakami, K.8
Takeshima, T.9
Nakashima, K.10
-
26
-
-
23444441621
-
Association of MTHFR gene polymorphism C677T with susceptibility to late-onset Alzheimer's disease
-
Wang B., Jin F., Kan R., Ji S., Zhang C.F., Lu Z.P., Zheng C.G., Yang Z., and Wang L. Association of MTHFR gene polymorphism C677T with susceptibility to late-onset Alzheimer's disease. J. Mol. Neurosci. 27 (2005) 23-27
-
(2005)
J. Mol. Neurosci.
, vol.27
, pp. 23-27
-
-
Wang, B.1
Jin, F.2
Kan, R.3
Ji, S.4
Zhang, C.F.5
Lu, Z.P.6
Zheng, C.G.7
Yang, Z.8
Wang, L.9
-
27
-
-
0041326346
-
Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas worldwide
-
Wilcken B., Bamforth F., Li Z., Zhu H., Ritvanen A., Redlund M., Stoll C., Alembik Y., Dott B., Czeizel A.E., Gelman-Kohan A., Scarano G., Bianca S., Ettore G., Tenconi R., Bellato S., Scala I., Mutchinick O.M., López M.A., de Walle H., Hofstra R., Joutchenko L., Kavteladze L., Bermejo E., Maartínez-Fías M.L., Gallagher M., Erickson J.D., Vollset S.E., Mastroiacovo P., Andria G., and Botto L.D. Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas worldwide. J. Med. Genet. 40 (2003) 619-625
-
(2003)
J. Med. Genet.
, vol.40
, pp. 619-625
-
-
Wilcken, B.1
Bamforth, F.2
Li, Z.3
Zhu, H.4
Ritvanen, A.5
Redlund, M.6
Stoll, C.7
Alembik, Y.8
Dott, B.9
Czeizel, A.E.10
Gelman-Kohan, A.11
Scarano, G.12
Bianca, S.13
Ettore, G.14
Tenconi, R.15
Bellato, S.16
Scala, I.17
Mutchinick, O.M.18
López, M.A.19
de Walle, H.20
Hofstra, R.21
Joutchenko, L.22
Kavteladze, L.23
Bermejo, E.24
Maartínez-Fías, M.L.25
Gallagher, M.26
Erickson, J.D.27
Vollset, S.E.28
Mastroiacovo, P.29
Andria, G.30
Botto, L.D.31
more..
-
28
-
-
0029089831
-
Assignment of the human folate transporter gene to chromosome 21q22.3 by somatic cell hybrid analysis and in situ hybridisation
-
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 hybridisation. 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
-
29
-
-
0347416835
-
Liquid chromatographic determination of total homocysteine in blood plasma with photometric detection
-
Zhloba A.A., and Blashko E.L. Liquid chromatographic determination of total homocysteine in blood plasma with photometric detection. J. Chromatogr. B 800 (2004) 275-280
-
(2004)
J. Chromatogr. B
, vol.800
, pp. 275-280
-
-
Zhloba, A.A.1
Blashko, E.L.2
|