Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 118

1.

Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism.

James SJ, Melnyk S, Jernigan S, Cleves MA, Halsted CH, Wong DH, Cutler P, Bock K, Boris M, Bradstreet JJ, Baker SM, Gaylor DW.

Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 5;141B(8):947-56.

2.

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.

3.

Efficacy of methylcobalamin and folinic acid treatment on glutathione redox status in children with autism.

James SJ, Melnyk S, Fuchs G, Reid T, Jernigan S, Pavliv O, Hubanks A, Gaylor DW.

Am J Clin Nutr. 2009 Jan;89(1):425-30. doi: 10.3945/ajcn.2008.26615. Epub 2008 Dec 3.

4.

Association of COMT, MTHFR, and SLC19A1(RFC-1) polymorphisms with homocysteine blood levels and cognitive impairment in Parkinson's disease.

Białecka M, Kurzawski M, Roszmann A, Robowski P, Sitek EJ, Honczarenko K, Gorzkowska A, Budrewicz S, Mak M, Jarosz M, Gołąb-Janowska M, Koziorowska-Gawron E, Droździk M, Sławek J.

Pharmacogenet Genomics. 2012 Oct;22(10):716-24. doi: 10.1097/FPC.0b013e32835693f7.

PMID:
22890010
5.

Thymidylate synthase gene polymorphisms and markers of DNA methylation capacity.

Ho V, Massey TE, King WD.

Mol Genet Metab. 2011 Apr;102(4):481-7. doi: 10.1016/j.ymgme.2010.12.015. Epub 2010 Dec 31.

PMID:
21269855
6.

Association between decreased vitamin levels and MTHFR, MTR and MTRR gene polymorphisms as determinants for elevated total homocysteine concentrations in pregnant women.

Barbosa PR, Stabler SP, Machado AL, Braga RC, Hirata RD, Hirata MH, Sampaio-Neto LF, Allen RH, Guerra-Shinohara EM.

Eur J Clin Nutr. 2008 Aug;62(8):1010-21. Epub 2007 May 23.

PMID:
17522601
7.

Aberrations in folate metabolic pathway and altered susceptibility to autism.

Mohammad NS, Jain JM, Chintakindi KP, Singh RP, Naik U, Akella RR.

Psychiatr Genet. 2009 Aug;19(4):171-6. doi: 10.1097/YPG.0b013e32832cebd2.

PMID:
19440165
8.

Decreased glutathione and elevated hair mercury levels are associated with nutritional deficiency-based autism in Oman.

Hodgson NW, Waly MI, Al-Farsi YM, Al-Sharbati MM, Al-Farsi O, Ali A, Ouhtit A, Zang T, Zhou ZS, Deth RC.

Exp Biol Med (Maywood). 2014 Jun;239(6):697-706.

PMID:
24676906
9.

Association of the transcobalamin II gene 776C → G polymorphism with Alzheimer's type dementia: dependence on the 5, 10-methylenetetrahydrofolate reductase 1298A → C polymorphism genotype.

Cascalheira JF, Gonçalves M, Barroso M, Castro R, Palmeira M, Serpa A, Dias-Cabral AC, Domingues FC, Almeida S.

Ann Clin Biochem. 2015 Jul;52(Pt 4):448-55. doi: 10.1177/0004563214561770. Epub 2014 Nov 13.

PMID:
25395544
10.

Homocysteine metabolism in children with Down syndrome: in vitro modulation.

Pogribna M, Melnyk S, Pogribny I, Chango A, Yi P, James SJ.

Am J Hum Genet. 2001 Jul;69(1):88-95. Epub 2001 Jun 5.

11.

Methionine metabolism in an animal model of sepsis.

Semmler A, Smulders Y, Struys E, Smith D, Moskau S, Blom H, Linnebank M.

Clin Chem Lab Med. 2008;46(10):1398-402. doi: 10.1515/CCLM.2008.277.

PMID:
18844494
12.

Impaired synthesis and antioxidant defense of glutathione in the cerebellum of autistic subjects: alterations in the activities and protein expression of glutathione-related enzymes.

Gu F, Chauhan V, Chauhan A.

Free Radic Biol Med. 2013 Dec;65:488-96. doi: 10.1016/j.freeradbiomed.2013.07.021. Epub 2013 Jul 26.

13.

[Folate gene polymorphism and the risk of Down syndrome pregnancies in young Chinese women].

Liao YP, Bao MS, Liu CQ, Liu H, Zhang D.

Yi Chuan. 2010 May;32(5):461-6. Chinese.

PMID:
20466634
14.

Genetic variation throughout the folate metabolic pathway influences negative symptom severity in schizophrenia.

Roffman JL, Brohawn DG, Nitenson AZ, Macklin EA, Smoller JW, Goff DC.

Schizophr Bull. 2013 Mar;39(2):330-8. doi: 10.1093/schbul/sbr150. Epub 2011 Oct 20.

15.

Polymorphisms in genes related to folate and cobalamin metabolism and the associations with complex birth defects.

Brouns R, Ursem N, Lindemans J, Hop W, Pluijm S, Steegers E, Steegers-Theunissen R.

Prenat Diagn. 2008 Jun;28(6):485-93. doi: 10.1002/pd.2006.

PMID:
18435414
16.

Folate gene polymorphisms and the risk of Down syndrome pregnancies in young Italian women.

Coppedè F, Marini G, Bargagna S, Stuppia L, Minichilli F, Fontana I, Colognato R, Astrea G, Palka G, Migliore L.

Am J Med Genet A. 2006 May 15;140(10):1083-91.

PMID:
16596679
17.

Abnormal transmethylation/transsulfuration metabolism and DNA hypomethylation among parents of children with autism.

James SJ, Melnyk S, Jernigan S, Hubanks A, Rose S, Gaylor DW.

J Autism Dev Disord. 2008 Nov;38(10):1966-75. doi: 10.1007/s10803-008-0591-5. Epub 2008 May 30. Erratum in: J Autism Dev Disord. 2008 Nov;38(10):1976. Jill James, S [corrected to James, S Jill].

18.

Oxidative stress-induced regulation of the methionine metabolic pathway in human lung epithelial-like (A549) cells.

Panayiotidis MI, Stabler SP, Allen RH, Pappa A, White CW.

Mutat Res. 2009 Mar 31;674(1-2):23-30. doi: 10.1016/j.mrgentox.2008.10.006. Epub 2008 Oct 25.

PMID:
19010443
19.

Polymorphisms in folate-related genes and risk of pediatric acute lymphoblastic leukemia.

de Jonge R, Tissing WJ, Hooijberg JH, Jansen G, Kaspers GJ, Lindemans J, Peters GJ, Pieters R.

Blood. 2009 Mar 5;113(10):2284-9. doi: 10.1182/blood-2008-07-165928. Epub 2008 Nov 19.

20.

Variations in folate pathway genes are associated with unexplained female infertility.

Altmäe S, Stavreus-Evers A, Ruiz JR, Laanpere M, Syvänen T, Yngve A, Salumets A, Nilsson TK.

Fertil Steril. 2010 Jun;94(1):130-7. doi: 10.1016/j.fertnstert.2009.02.025. Epub 2009 Mar 26.

PMID:
19324355

Supplemental Content

Support Center