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Items: 1 to 20 of 81

1.
2.

Association of MTRRA66G polymorphism (but not of MTHFR C677T and A1298C, MTRA2756G, TCN C776G) with homocysteine and coronary artery disease in the French population.

Guéant-Rodriguez RM, Juilliére Y, Candito M, Adjalla CE, Gibelin P, Herbeth B, Van Obberghen E, Gueánt JL.

Thromb Haemost. 2005 Sep;94(3):510-5.

PMID:
16268464
3.

Cerebrospinal fluid and serum markers of inflammation in autism.

Zimmerman AW, Jyonouchi H, Comi AM, Connors SL, Milstien S, Varsou A, Heyes MP.

Pediatr Neurol. 2005 Sep;33(3):195-201.

PMID:
16139734
5.

Transcobalamin 776C->G polymorphism negatively affects vitamin B-12 metabolism.

von Castel-Dunwoody KM, Kauwell GP, Shelnutt KP, Vaughn JD, Griffin ER, Maneval DR, Theriaque DW, Bailey LB.

Am J Clin Nutr. 2005 Jun;81(6):1436-41.

6.

Effect of catechol-O-methyltransferase val158met genotype on attentional control.

Blasi G, Mattay VS, Bertolino A, Elvevåg B, Callicott JH, Das S, Kolachana BS, Egan MF, Goldberg TE, Weinberger DR.

J Neurosci. 2005 May 18;25(20):5038-45.

7.
8.

Congenital heart defects and abnormal maternal biomarkers of methionine and homocysteine metabolism.

Hobbs CA, Cleves MA, Melnyk S, Zhao W, James SJ.

Am J Clin Nutr. 2005 Jan;81(1):147-53.

9.

Metabolic biomarkers of increased oxidative stress and impaired methylation capacity in children with autism.

James SJ, Cutler P, Melnyk S, Jernigan S, Janak L, Gaylor DW, Neubrander JA.

Am J Clin Nutr. 2004 Dec;80(6):1611-7.

10.

Redox regulation and reaction mechanism of human cystathionine-beta-synthase: a PLP-dependent hemesensor protein.

Banerjee R, Zou CG.

Arch Biochem Biophys. 2005 Jan 1;433(1):144-56. Review.

PMID:
15581573
11.

Methionine metabolism in mammals.

Finkelstein JD.

J Nutr Biochem. 1990 May;1(5):228-37. No abstract available.

PMID:
15539209
12.

Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain.

Chen J, Lipska BK, Halim N, Ma QD, Matsumoto M, Melhem S, Kolachana BS, Hyde TM, Herman MM, Apud J, Egan MF, Kleinman JE, Weinberger DR.

Am J Hum Genet. 2004 Nov;75(5):807-21. Epub 2004 Sep 27. Erratum in: Am J Hum Genet. 2005 Jun;76(6):1089.

13.
14.

Physiology of folate and vitamin B12 in health and disease.

Stover PJ.

Nutr Rev. 2004 Jun;62(6 Pt 2):S3-12; discussion S13. Review.

PMID:
15298442
15.

Increased oxidative stress and altered activities of erythrocyte free radical scavenging enzymes in autism.

Zoroglu SS, Armutcu F, Ozen S, Gurel A, Sivasli E, Yetkin O, Meram I.

Eur Arch Psychiatry Clin Neurosci. 2004 Jun;254(3):143-7.

PMID:
15205966
16.

Polymorphisms and haplotypes in folate-metabolizing genes and risk of non-Hodgkin lymphoma.

Skibola CF, Forrest MS, Coppedé F, Agana L, Hubbard A, Smith MT, Bracci PM, Holly EA.

Blood. 2004 Oct 1;104(7):2155-62. Epub 2004 Jun 15.

17.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
18.

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, Tawn EJ, Burn J.

J Med Genet. 2004 Apr;41(4):256-60.

19.

Genetic and neurochemical modulation of prefrontal cognitive functions in children.

Diamond A, Briand L, Fossella J, Gehlbach L.

Am J Psychiatry. 2004 Jan;161(1):125-32.

PMID:
14702260
20.

Genetic determinants of folate and vitamin B12 metabolism: a common pathway in neural tube defect and Down syndrome?

Guéant JL, Guéant-Rodriguez RM, Anello G, Bosco P, Brunaud L, Romano C, Ferri R, Romano A, Candito M, Namour B.

Clin Chem Lab Med. 2003 Nov;41(11):1473-7. Review.

PMID:
14656028

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