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Journal Abstract Search

241 related items for PubMed ID: 17623803

  • 1. Modifier locus for exencephaly in Cecr2 mutant mice is syntenic to the 10q25.3 region associated with neural tube defects in humans.
    Davidson CE, Li Q, Churchill GA, Osborne LR, McDermid HE.
    Physiol Genomics; 2007 Oct 22; 31(2):244-51. PubMed ID: 17623803
    [Abstract] [Full Text] [Related]

  • 2. Strain-specific modifier genes of Cecr2-associated exencephaly in mice: genetic analysis and identification of differentially expressed candidate genes.
    Kooistra MK, Leduc RY, Dawe CE, Fairbridge NA, Rasmussen J, Man JH, Bujold M, Juriloff D, King-Jones K, McDermid HE.
    Physiol Genomics; 2012 Jan 18; 44(1):35-46. PubMed ID: 22045912
    [Abstract] [Full Text] [Related]

  • 3. Genetic backgrounds and modifier genes of NTD mouse models: An opportunity for greater understanding of the multifactorial etiology of neural tube defects.
    Leduc RY, Singh P, McDermid HE.
    Birth Defects Res; 2017 Jan 30; 109(2):140-152. PubMed ID: 27768235
    [Abstract] [Full Text] [Related]

  • 4. Neurofibromin deficiency in mice causes exencephaly and is a modifier for Splotch neural tube defects.
    Lakkis MM, Golden JA, O'Shea KS, Epstein JA.
    Dev Biol; 1999 Aug 01; 212(1):80-92. PubMed ID: 10419687
    [Abstract] [Full Text] [Related]

  • 5. Effect of arsenite, maternal age, and embryonic sex on spina bifida, exencephaly, and resorption rates in the splotch mouse.
    Martin LJ, Machado AF, Loza MA, Mao GE, Lee GS, Hovland DN, Cantor RM, Collins MD.
    Birth Defects Res A Clin Mol Teratol; 2003 Apr 01; 67(4):231-9. PubMed ID: 12854658
    [Abstract] [Full Text] [Related]

  • 6. Mouse mutants with neural tube closure defects and their role in understanding human neural tube defects.
    Harris MJ, Juriloff DM.
    Birth Defects Res A Clin Mol Teratol; 2007 Mar 01; 79(3):187-210. PubMed ID: 17177317
    [Abstract] [Full Text] [Related]

  • 7. Genetic landmarks for defects in mouse neural tube closure.
    Harris MJ, Juriloff DM.
    Teratology; 1997 Sep 01; 56(3):177-87. PubMed ID: 9358605
    [Abstract] [Full Text] [Related]

  • 8. A genetic risk factor for mouse neural tube defects: defining the embryonic basis.
    Fleming A, Copp AJ.
    Hum Mol Genet; 2000 Mar 01; 9(4):575-81. PubMed ID: 10699180
    [Abstract] [Full Text] [Related]

  • 9. Mini-review: toward understanding mechanisms of genetic neural tube defects in mice.
    Harris MJ, Juriloff DM.
    Teratology; 1999 Nov 01; 60(5):292-305. PubMed ID: 10525207
    [Abstract] [Full Text] [Related]

  • 10. Understanding the causes and prevention of neural tube defects: Insights from the splotch mouse model.
    Greene ND, Massa V, Copp AJ.
    Birth Defects Res A Clin Mol Teratol; 2009 Apr 01; 85(4):322-30. PubMed ID: 19180568
    [Abstract] [Full Text] [Related]

  • 11. Spontaneous neural tube defects in splotch mice supplemented with selected micronutrients.
    Wlodarczyk BJ, Tang LS, Triplett A, Aleman F, Finnell RH.
    Toxicol Appl Pharmacol; 2006 May 15; 213(1):55-63. PubMed ID: 16226775
    [Abstract] [Full Text] [Related]

  • 12. Impact of methylenetetrahydrofolate reductase deficiency and low dietary folate on the development of neural tube defects in splotch mice.
    Li D, Pickell L, Liu Y, Rozen R.
    Birth Defects Res A Clin Mol Teratol; 2006 Jan 15; 76(1):55-9. PubMed ID: 16397891
    [Abstract] [Full Text] [Related]

  • 13. Multifactorial inheritance of neural tube defects: localization of the major gene and recognition of modifiers in ct mutant mice.
    Neumann PE, Frankel WN, Letts VA, Coffin JM, Copp AJ, Bernfield M.
    Nat Genet; 1994 Apr 15; 6(4):357-62. PubMed ID: 8054974
    [Abstract] [Full Text] [Related]

  • 14. Cecr2 mutations causing exencephaly trigger misregulation of mesenchymal/ectodermal transcription factors.
    Fairbridge NA, Dawe CE, Niri FH, Kooistra MK, King-Jones K, McDermid HE.
    Birth Defects Res A Clin Mol Teratol; 2010 Aug 15; 88(8):619-25. PubMed ID: 20589882
    [Abstract] [Full Text] [Related]

  • 15. An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closure.
    Harris MJ, Juriloff DM.
    Birth Defects Res A Clin Mol Teratol; 2010 Aug 15; 88(8):653-69. PubMed ID: 20740593
    [Abstract] [Full Text] [Related]

  • 16. Development of a lethal congenital heart defect in the splotch (Pax3) mutant mouse.
    Conway SJ, Henderson DJ, Kirby ML, Anderson RH, Copp AJ.
    Cardiovasc Res; 1997 Nov 15; 36(2):163-73. PubMed ID: 9463628
    [Abstract] [Full Text] [Related]

  • 17. Analysis of select folate pathway genes, PAX3, and human T in a Midwestern neural tube defect population.
    Trembath D, Sherbondy AL, Vandyke DC, Shaw GM, Todoroff K, Lammer EJ, Finnell RH, Marker S, Lerner G, Murray JC.
    Teratology; 1999 May 15; 59(5):331-41. PubMed ID: 10332959
    [Abstract] [Full Text] [Related]

  • 18. Multifactorial genetics of exencephaly in SELH/Bc mice.
    Juriloff DM, Gunn TM, Harris MJ, Mah DG, Wu MK, Dewell SL.
    Teratology; 2001 Oct 15; 64(4):189-200. PubMed ID: 11598925
    [Abstract] [Full Text] [Related]

  • 19. Insights into prevention of human neural tube defects by folic acid arising from consideration of mouse mutants.
    Harris MJ.
    Birth Defects Res A Clin Mol Teratol; 2009 Apr 15; 85(4):331-9. PubMed ID: 19117321
    [Abstract] [Full Text] [Related]

  • 20. Characterization of a novel missense mutation on murine Pax3 through ENU mutagenesis.
    Xiao Y, Zhang L, He K, Gao X, Yang L, He L, Ma G, Guo X.
    J Genet Genomics; 2011 Aug 20; 38(8):333-9. PubMed ID: 21867959
    [Abstract] [Full Text] [Related]

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