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There are 1724153 results for: content related to: Studies of reduced folate carrier 1 ( RFC1 ) A80G and 5,10-methylenetetrahydrofolate reductase ( MTHFR ) C677T polymorphisms with neural tube and orofacial cleft defects

  1. You have free access to this content
    Candidate gene analysis in human neural tube defects

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 135C, Issue 1, 15 May 2005, Pages: 9–23, Abee L. Boyles, Preston Hammock and Marcy C. Speer

    Version of Record online : 6 APR 2005, DOI: 10.1002/ajmg.c.30048

  2. Association of aberrations in one-carbon metabolism with molecular phenotype and grade of breast cancer

    Molecular Carcinogenesis

    Volume 51, Issue S1, October 2012, Pages: E32–E41, Shaik Mohammad Naushad, Addepalli Pavani, Yedluri Rupasree, Shree Divyya, Sripurna Deepti, Raghunadha Rao Digumarti, Suryanarayana Raju Gottumukkala, Aruna Prayaga and Vijay Kumar Kutala

    Version of Record online : 15 NOV 2011, DOI: 10.1002/mc.21830

  3. Association between MTHFR C677T polymorphism and neural tube defect risks: A comprehensive evaluation in three groups of NTD patients, mothers, and fathers

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 103, Issue 6, June 2015, Pages: 488–500, Yi Yang, Jie Chen, Beiyu Wang, Chen Ding and Hao Liu

    Version of Record online : 24 MAR 2015, DOI: 10.1002/bdra.23361

  4. Association of reduced folate carrier gene polymorphism and maternal folic acid use with neural tube defects

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 150B, Issue 6, 5 September 2009, Pages: 874–878, Lijun Pei, Jianmeng Liu, Yewu Zhang, Huiping Zhu and Aiguo Ren

    Version of Record online : 22 DEC 2008, DOI: 10.1002/ajmg.b.30911

  5. Fetal and maternal MTHFR C677T genotype, maternal folate intake and the risk of nonsyndromic oral clefts

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 3, 1 February 2007, Pages: 248–257, Cécile Chevrier, Claire Perret, Michel Bahuau, Huiping Zhu, Agnès Nelva, Christine Herman, Christine Francannet, Elisabeth Robert-Gnansia, Richard H. Finnell and Sylvaine Cordier

    Version of Record online : 11 JAN 2007, DOI: 10.1002/ajmg.a.31462

  6. Association between MTHFR polymorphisms and orofacial clefts risk: A meta-analysis

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 94, Issue 4, April 2012, Pages: 237–244, Ya L. Luo, Yu L. Cheng, Ping Ye, Wei Wang, Xiao H. Gao and Qing Chen

    Version of Record online : 27 MAR 2012, DOI: 10.1002/bdra.23005

  7. Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A

    American Journal of Medical Genetics

    Volume 107, Issue 2, 15 January 2002, Pages: 162–168, Peter L. Rady, Sylvia Szucs, James Grady, S. David Hudnall, Leonard H. Kellner, Harold Nitowsky, Stephen K. Tyring and Reuben K. Matalon

    Version of Record online : 26 DEC 2001, DOI: 10.1002/ajmg.10122

  8. Maternal periconceptional vitamin use, genetic variation of infant reduced folate carrier (A80G), and risk of spina bifida

    American Journal of Medical Genetics

    Volume 108, Issue 1, 15 February 2002, Pages: 1–6, Gary M. Shaw, Edward J. Lammer, Huiping Zhu, Mei Wang Baker, Eric Neri and Richard H. Finnell

    Version of Record online : 14 JAN 2002, DOI: 10.1002/ajmg.10195

  9. Genetic Association Analyses of Nitric Oxide Synthase Genes and Neural Tube Defects Vary by Phenotype

    Birth Defects Research Part B: Developmental and Reproductive Toxicology

    Volume 98, Issue 5, October 2013, Pages: 365–373, Karen L. Soldano, Melanie E. Garrett, Heidi L. Cope, J. Michael Rusnak, Nathen J. Ellis, Kaitlyn L. Dunlap, Marcy C. Speer, Simon G. Gregory and Allison E. Ashley-Koch

    Version of Record online : 9 DEC 2013, DOI: 10.1002/bdrb.21079

  10. Methylenetetrahydrofolate reductase (MTHFR): The incidence of mutations C677T and A1298C in the Ashkenazi Jewish population

    American Journal of Medical Genetics

    Volume 86, Issue 4, 8 October 1999, Pages: 380–384, Peter L. Rady, Stephen K. Tyring, S. David Hudnall, Trini Vargas, Leonard H. Kellner, Harold Nitowsky and Reuben K. Matalon

    Version of Record online : 22 SEP 1999, DOI: 10.1002/(SICI)1096-8628(19991008)86:4<380::AID-AJMG13>3.0.CO;2-9

  11. A functional polymorphism in the reduced folate carrier gene and DNA hypomethylation in mothers of children with autism

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 153B, Issue 6, September 2010, Pages: 1209–1220, S. Jill James, Stepan Melnyk, Stefanie Jernigan, Oleksandra Pavliv, Timothy Trusty, Sara Lehman, Lisa Seidel, David W. Gaylor and Mario A. Cleves

    Version of Record online : 12 MAY 2010, DOI: 10.1002/ajmg.b.31094

  12. Hyperhomocysteinemia and MTHFR polymorphisms in association with orofacial clefts and congenital heart defects: A meta-analysis

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 9, 1 May 2007, Pages: 952–960, Anna Verkleij-Hagoort, Johannes Bliek, Fakhredin Sayed-Tabatabaei, Nicolette Ursem, Eric Steegers and Régine Steegers-Theunissen

    Version of Record online : 12 APR 2007, DOI: 10.1002/ajmg.a.31684

  13. You have free access to this content
    Methylenetetrahydrofolate reductase C677T gene mutation and hyperhomocysteinemia in Budd–Chiari syndrome and portal vein thrombosis: A systematic review and meta-analysis of observational studies

    Hepatology Research

    Volume 44, Issue 14, December 2014, Pages: E480–E498, Xingshun Qi, Zhiping Yang, Valerio De Stefano and Daiming Fan

    Version of Record online : 20 MAY 2014, DOI: 10.1111/hepr.12348

  14. Importance of gene–environment interactions in the etiology of selected birth defects

    Clinical Genetics

    Volume 75, Issue 5, May 2009, Pages: 409–423, H Zhu, S Kartiko and RH Finnell

    Version of Record online : 28 APR 2009, DOI: 10.1111/j.1399-0004.2009.01174.x

  15. Methylenetetrahydrofolate reductase and spina bifida: Evaluation of level of defect and maternal genotypic risk in Hispanics

    American Journal of Medical Genetics

    Volume 95, Issue 1, 6 November 2000, Pages: 21–27, K.A. Volcik, S.H. Blanton, G.H. Tyerman, S.T. Jong, E.J. Rott, T.Z. Page, N.K. Romaine and H. Northrup

    Version of Record online : 7 NOV 2000, DOI: 10.1002/1096-8628(20001106)95:1<21::AID-AJMG6>3.0.CO;2-M

  16. Folate and one-carbon metabolism gene polymorphisms and their associations with oral facial clefts

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 4, 15 February 2008, Pages: 440–449, Abee L. Boyles, Allen J. Wilcox, Jack A. Taylor, Klaus Meyer, Åse Fredriksen, Per Magne Ueland, Christian A. Drevon, Stein Emil Vollset and Rolv Terje Lie

    Version of Record online : 17 JAN 2008, DOI: 10.1002/ajmg.a.32162

  17. Correlation of polymorphism of MTHFRs and RFC-1 genes with neural tube defects in China

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 82, Issue 1, January 2008, Pages: 3–7, Yali Shang, Hong Zhao, Bo Niu, Wan-I Li, Ran Zhou, Ting Zhang and Jun Xie

    Version of Record online : 16 NOV 2007, DOI: 10.1002/bdra.20416

  18. Folate

    Vitamins: Their Role in the Human Body

    G.F.M. Ball, Pages: 347–382, 2008

    Published Online : 25 FEB 2008, DOI: 10.1002/9780470774571.ch17

  19. Folate-mediated one-carbon metabolism and neural tube defects: Balancing genome synthesis and gene expression

    Birth Defects Research Part C: Embryo Today: Reviews

    Volume 81, Issue 3, September 2007, Pages: 183–203, Anna E. Beaudin and Patrick J. Stover

    Version of Record online : 26 OCT 2007, DOI: 10.1002/bdrc.20100

  20. Polymorphisms in folate pathway genes are not associated with somatic nondisjunction in turner syndrome

    American Journal of Medical Genetics Part A

    Volume 167, Issue 7, July 2015, Pages: 1510–1517, Adriana Valéria Sales Bispo, Luana Oliveira dos Santos, Juliana Vieira de Barros, Andrea Rezende Duarte, Jacqueline Araújo, Maria Tereza Cartaxo Muniz and Neide Santos

    Version of Record online : 9 APR 2015, DOI: 10.1002/ajmg.a.37055