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Items: 1 to 20 of 96

1.

Novel single nucleotide polymorphisms in the superoxide dismutase 1 and 2 genes among children with myelomeningocele.

Kase BA, Northrup H, Au KS.

Am J Obstet Gynecol. 2013 Oct;209(4):388.e1-7. doi: 10.1016/j.ajog.2013.06.004. Epub 2013 Jun 20.

2.

Genetic studies of the cystathionine beta-synthase gene and myelomeningocele.

Tilley MM, Northrup H, Au KS.

Birth Defects Res A Clin Mol Teratol. 2012 Jan;94(1):52-6. doi: 10.1002/bdra.22855. Epub 2011 Sep 28.

3.

Association of copper-zinc superoxide dismutase (SOD1) and manganese superoxide dismutase (SOD2) genes with nonsyndromic myelomeningocele.

Kase BA, Northrup H, Morrison AC, Davidson CM, Goiffon AM, Fletcher JM, Ostermaier KK, Tyerman GH, Au KS.

Birth Defects Res A Clin Mol Teratol. 2012 Oct;94(10):762-9. doi: 10.1002/bdra.23065. Epub 2012 Sep 13. Erratum in: Birth Defects Res A Clin Mol Teratol. 2013 Jan;97(1):68.

4.

Deep sequencing study of the MTHFR gene to identify variants associated with myelomeningocele.

Aneji CN, Northrup H, Au KS.

Birth Defects Res A Clin Mol Teratol. 2012 Feb;94(2):84-90. doi: 10.1002/bdra.22884. Epub 2012 Jan 12.

5.

Association of facilitated glucose transporter 2 gene variants with the myelomeningocele phenotype.

Ruggiero JE, Northrup H, Au KS.

Birth Defects Res A Clin Mol Teratol. 2015 Jun;103(6):479-87. doi: 10.1002/bdra.23358. Epub 2015 Mar 17.

6.

Genetic variations in the GLUT3 gene associated with myelomeningocele.

Connealy BD, Northrup H, Au KS.

Am J Obstet Gynecol. 2014 Sep;211(3):305.e1-8. doi: 10.1016/j.ajog.2014.05.013. Epub 2014 May 9. Erratum in: Am J Obstet Gynecol. 2015 Sep;213(3):397.

7.

Genetic polymorphisms of superoxide dismutases, catalase, and glutathione peroxidase in age-related cataract.

Zhang Y, Zhang L, Sun D, Li Z, Wang L, Liu P.

Mol Vis. 2011;17:2325-32. Epub 2011 Aug 30.

8.

Involvement of superoxide dismutase isoenzymes and their genetic variants in progression of and higher susceptibility to vitiligo.

Laddha NC, Dwivedi M, Gani AR, Shajil EM, Begum R.

Free Radic Biol Med. 2013 Dec;65:1110-25. doi: 10.1016/j.freeradbiomed.2013.08.189. Epub 2013 Sep 12.

PMID:
24036105
9.

Human heart rate: heritability of resting and stress values in twin pairs, and influence of genetic variation in the adrenergic pathway at a microribonucleic acid (microrna) motif in the 3'-UTR of cytochrome b561 [corrected].

Zhang K, Deacon DC, Rao F, Schork AJ, Fung MM, Waalen J, Schork NJ, Nievergelt CM, Chi NC, O'Connor DT.

J Am Coll Cardiol. 2014 Feb 4;63(4):358-68. doi: 10.1016/j.jacc.2013.09.025. Epub 2013 Oct 16. Erratum in: J Am Coll Cardiol. 2014 Mar 25;63(11):1122.

10.

A 10 bp deletion polymorphism and 2 new variations in the GLUT1 gene associated with meningomyelocele.

Cormier CM, Au KS, Northrup H.

Reprod Sci. 2011 May;18(5):463-8. doi: 10.1177/1933719110388293. Epub 2010 Dec 6.

11.

Functional variant of manganese superoxide dismutase (SOD2 V16A) polymorphism is associated with prostate cancer risk in the prostate, lung, colorectal, and ovarian cancer study.

Kang D, Lee KM, Park SK, Berndt SI, Peters U, Reding D, Chatterjee N, Welch R, Chanock S, Huang WY, Hayes RB.

Cancer Epidemiol Biomarkers Prev. 2007 Aug;16(8):1581-6. Epub 2007 Jul 23.

12.

Folate metabolism gene 5,10-methylenetetrahydrofolate reductase (MTHFR) is associated with ADHD in myelomeningocele patients.

Spellicy CJ, Northrup H, Fletcher JM, Cirino PT, Dennis M, Morrison AC, Martinez CA, Au KS.

PLoS One. 2012;7(12):e51330. doi: 10.1371/journal.pone.0051330. Epub 2012 Dec 5.

13.
14.

Rare single nucleotide polymorphisms in the regulatory regions of the superoxide dismutase genes in autism spectrum disorder.

Kovač J, Macedoni Lukšič M, Trebušak Podkrajšek K, Klančar G, Battelino T.

Autism Res. 2014 Feb;7(1):138-44. doi: 10.1002/aur.1345. Epub 2013 Oct 23.

15.

Association of SOD1 and SOD2 single nucleotide polymorphisms with susceptibility to gastric cancer in a Korean population.

Han L, Lee SW, Yoon JH, Park YG, Choi YJ, Nam SW, Lee JY, Wang YP, Park WS.

APMIS. 2013 Mar;121(3):246-56. doi: 10.1111/j.1600-0463.2012.02963.x. Epub 2012 Aug 8.

PMID:
23030347
16.

Multiplex single base extension method for simultaneous genotyping of non-synonymous SNP in the three human SOD genes.

Iida R, Tsubota E, Takeshita H, Yasuda T.

Electrophoresis. 2008 Dec;29(23):4788-94. doi: 10.1002/elps.200800332.

PMID:
19016244
17.

Genetic polymorphisms of superoxide dismutase in Parkinson's disease.

Farin FM, Hitosis Y, Hallagan SE, Kushleika J, Woods JS, Janssen PS, Smith-Weller T, Franklin GM, Swanson PD, Checkoway H.

Mov Disord. 2001 Jul;16(4):705-7.

PMID:
11481695
18.

Association of Superoxide dismutases (SOD1 and SOD2) and Glutathione peroxidase 1 (GPx1) gene polymorphisms with type 2 diabetes mellitus.

Vats P, Sagar N, Singh TP, Banerjee M.

Free Radic Res. 2015 Jan;49(1):17-24. doi: 10.3109/10715762.2014.971782. Epub 2014 Oct 31.

PMID:
25283363
19.

Superoxide Dismutase and Catalase Genotypes in Pediatric Migraine Patients.

Saygi S, Erol İ, Alehan F, Yalçın YY, Kubat G, Ataç FB.

J Child Neurol. 2015 Oct;30(12):1586-90. doi: 10.1177/0883073815575366. Epub 2015 Mar 27.

PMID:
25818327
20.

Association of retinoic acid receptor genes with meningomyelocele.

Tran PX, Au KS, Morrison AC, Fletcher JM, Ostermaier KK, Tyerman GH, Northrup H.

Birth Defects Res A Clin Mol Teratol. 2011 Jan;91(1):39-43. doi: 10.1002/bdra.20744. Epub 2010 Dec 1.

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