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There are 35323 results for: content related to: The MTHFD1 Gene is not Involved in Cleft Lip with or Without Palate Onset Among the Italian Population

  1. Maternal MTR genotype contributes to the risk of non-syndromic cleft lip and palate in the Polish population

    Clinical Genetics

    Volume 69, Issue 6, June 2006, Pages: 512–517, A Mostowska, KK Hozyasz and PP Jagodzinski

    Version of Record online : 24 APR 2006, DOI: 10.1111/j.1399-0004.2006.00618.x

  2. Murine MTHFD1-synthetase deficiency, a model for the human MTHFD1 R653Q polymorphism, decreases growth of colorectal tumors

    Molecular Carcinogenesis

    Volume 56, Issue 3, March 2017, Pages: 1030–1040, Nancy Lévesque, Karen E. Christensen, Lauren Van Der Kraak, Ana F. Best, Liyuan Deng, Don Caldwell, Amanda J. MacFarlane, Nicole Beauchemin and Rima Rozen

    Version of Record online : 1 NOV 2016, DOI: 10.1002/mc.22568

  3. Evidence of gene–gene interactions between MTHFD1 and MTHFR in relation to anterior encephalocele susceptibility in Northeast India

    Birth Defects Research

    Volume 109, Issue 6, April 3, 2017, Pages: 432–444, Hemonta Kr Dutta, Debasish Borbora, Mauchumi Baruah and Kanwar Narain

    Version of Record online : 20 FEB 2017, DOI: 10.1002/bdra.23607

  4. MTHFD1 formyltetrahydrofolate synthetase deficiency, a model for the MTHFD1 R653Q variant, leads to congenital heart defects in mice

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 103, Issue 12, December 2015, Pages: 1031–1038, Karen E. Christensen, Liyuan Deng, Renata H. Bahous, Loydie A. Jerome-Majewska and Rima Rozen

    Version of Record online : 26 SEP 2015, DOI: 10.1002/bdra.23451

  5. An NTD-Associated Polymorphism in the 3′ UTR of MTHFD1L can Affect Disease Risk by Altering miRNA Binding

    Human Mutation

    Volume 35, Issue 1, January 2014, Pages: 96–104, Stefano Minguzzi, S. Duygu Selcuklu, Charles Spillane and Anne Parle-McDermott

    Version of Record online : 18 DEC 2013, DOI: 10.1002/humu.22459

  6. Association Study of MTHFD1 Coding Polymorphisms R134K and R653Q With Migraine Susceptibility

    Headache: The Journal of Head and Face Pain

    Volume 54, Issue 9, October 2014, Pages: 1506–1514, Heidi G. Sutherland, Heloise Hermile, Rebecca Sanche, Saras Menon, Rod A. Lea, Larisa M. Haupt and Lyn R. Griffiths

    Version of Record online : 18 JUL 2014, DOI: 10.1111/head.12428

  7. 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

  8. Gene variants in the folate-mediated one-carbon metabolism (FOCM) pathway as risk factors for conotruncal heart defects

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 5, May 2012, Pages: 1124–1134, Huiping Zhu, Wei Yang, Wei Lu, Analee J. Etheredge, Edward J. Lammer, Richard H. Finnell, Suzan L. Carmichael and Gary M. Shaw

    Version of Record online : 11 APR 2012, DOI: 10.1002/ajmg.a.35313

  9. Folate pathway and nonsyndromic cleft lip and palate

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 91, Issue 1, January 2011, Pages: 50–60, Susan H. Blanton, Robin R. Henry, Quiping Yuan, John B. Mulliken, Samuel Stal, Richard H. Finnell and Jacqueline T. Hecht

    Version of Record online : 1 DEC 2010, DOI: 10.1002/bdra.20740

  10. The methylenetetrahydrofolate dehydrogenase (MTHFD1) 1958G>A variant is not associated with spina bifida risk in the Dutch population

    Clinical Genetics

    Volume 72, Issue 6, December 2007, Pages: 599–600, IJM van der Linden, SG Heil, IC Kouwenberg, M den Heijer and HJ Blom

    Version of Record online : 25 SEP 2007, DOI: 10.1111/j.1399-0004.2007.00904.x

  11. Maternal polymorphisms in folic acid metabolic genes are associated with nonsyndromic cleft lip and/or palate in the Brazilian population

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 88, Issue 11, November 2010, Pages: 980–986, Andreia Bufalino, Lívia Máris Ribeiro Paranaíba, Sibele Nascimento de Aquino, Hercílio Martelli-Júnior, Mario Sergio Oliveira Swerts and Ricardo D. Coletta

    Version of Record online : 1 OCT 2010, DOI: 10.1002/bdra.20732

  12. Mitochondrial one-carbon metabolism and neural tube defects

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 100, Issue 8, August 2014, Pages: 576–583, Jessica Momb and Dean R. Appling

    Version of Record online : 1 JUL 2014, DOI: 10.1002/bdra.23268

  13. You have free access to this content
    Paternal transmission of MTHFD1 G1958A variant predisposes to neural tube defects in the offspring

    Developmental Medicine & Child Neurology

    Volume 58, Issue 6, June 2016, Pages: 625–631, Kattekola R Prasoona, Tella Sunitha, Buragadda Srinadh, Madireddy L N Deepika, Tiruvatturu M Kumari and Akka Jyothy

    Version of Record online : 22 SEP 2015, DOI: 10.1111/dmcn.12929

  14. Folate-genetics and colorectal neoplasia: What we know and need to know next

    Molecular Nutrition & Food Research

    Volume 57, Issue 4, April 2013, Pages: 607–627, Jane C. Figueiredo, A. Joan Levine, Jimmy W. Crott, James Baurley and Robert W. Haile

    Version of Record online : 8 FEB 2013, DOI: 10.1002/mnfr.201200278

  15. Polymorphisms in maternal folate pathway genes interact with arsenic in drinking water to influence risk of myelomeningocele

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 103, Issue 9, September 2015, Pages: 754–762, Maitreyi Mazumdar, Linda Valeri, Ema G. Rodrigues, Md Omar Sharif Ibne Hasan, Rezina Hamid, Ligi Paul, Jacob Selhub, Fareesa Silva, Md Golam Mostofa, Quazi Quamruzzaman, Mahmuder Rahman and David C. Christiani

    Version of Record online : 6 AUG 2015, DOI: 10.1002/bdra.23399

  16. You have free access to this content
    Genotype frequencies and linkage disequilibrium in the CEPH human diversity panel for variants in folate pathway genes MTHFR, MTHFD, MTRR, RFC1, and GCP2

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 67, Issue 8, August 2003, Pages: 545–549, Min Shi, Diana Caprau, Paul Romitti, Kaare Christensen and Jeffrey C. Murray

    Version of Record online : 31 JUL 2003, DOI: 10.1002/bdra.10076

  17. You have free access to this content
    Polymorphisms in the one-carbon metabolic pathway, plasma folate levels and colorectal cancer in a prospective study

    International Journal of Cancer

    Volume 110, Issue 4, 1 July 2004, Pages: 617–620, Jia Chen, Charles Kyte, Martin Valcin, Wendy Chan, James G. Wetmur, Jacob Selhub, David J. Hunter and Jing Ma

    Version of Record online : 15 MAR 2004, DOI: 10.1002/ijc.20148

  18. Association of dietary and supplemental folate intake and polymorphisms in three FOCM pathway genes with colorectal cancer in a population-based case-control study

    Genes, Chromosomes and Cancer

    Volume 52, Issue 10, October 2013, Pages: 945–953, Joseph H. Ashmore, Samuel M. Lesko, Joshua E. Muscat, Carla J. Gallagher, Arthur S. Berg, Paige E. Miller, Terryl J. Hartman and Philip Lazarus

    Version of Record online : 26 JUL 2013, DOI: 10.1002/gcc.22089

  19. Xenobiotic and folate pathway gene polymorphisms and risk of childhood acute lymphoblastic leukaemia in Javanese children

    Hematological Oncology

    Volume 29, Issue 3, September 2011, Pages: 116–123, Jason Yong-Sheng Chan, Dewa G Ugrasena, Danny Wai-Kiong Lum, Yi Lu and Allen Eng-Juh Yeoh

    Version of Record online : 7 SEP 2010, DOI: 10.1002/hon.965

  20. MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae

    American Journal of Medical Genetics Part A

    Volume 132A, Issue 4, 1 February 2005, Pages: 365–368, Anne Parle-McDermott, James L. Mills, Peadar N. Kirke, Christopher Cox, Caroline C. Signore, Sandra Kirke, Anne M. Molloy, Valerie B. O'Leary, Faith J. Pangilinan, Colm O'Herlihy, Lawrence C. Brody and John M. Scott

    Version of Record online : 4 JAN 2005, DOI: 10.1002/ajmg.a.30354