These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

246 related items for PubMed ID: 12854658

  • 1. 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; 67(4):231-9. PubMed ID: 12854658
    [Abstract] [Full Text] [Related]

  • 2. Teratogenic response to arsenite during neurulation: relative sensitivities of C57BL/6J and SWV/Fnn mice and impact of the splotch allele.
    Machado AF, Hovland DN, Pilafas S, Collins MD.
    Toxicol Sci; 1999 Sep; 51(1):98-107. PubMed ID: 10496681
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Diabetic embryopathy in C57BL/6J mice. Altered fetal sex ratio and impact of the splotch allele.
    Machado AF, Zimmerman EF, Hovland DN, Weiss R, Collins MD.
    Diabetes; 2001 May 01; 50(5):1193-9. PubMed ID: 11334426
    [Abstract] [Full Text] [Related]

  • 5. Effects of folate supplementation on the risk of spontaneous and induced neural tube defects in Splotch mice.
    Gefrides LA, Bennett GD, Finnell RH.
    Teratology; 2002 Feb 01; 65(2):63-9. PubMed ID: 11857507
    [Abstract] [Full Text] [Related]

  • 6. 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 01; 36(2):163-73. PubMed ID: 9463628
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. The Sp4H deletion may contain a new locus essential for postimplantation development.
    Fleming J, Pearce A, Brown SD, Steel KP.
    Genomics; 1996 Jun 01; 34(2):205-12. PubMed ID: 8661050
    [Abstract] [Full Text] [Related]

  • 9. Contributions of dam and conceptus to differences in sensitivity to valproic acid among C57 black and SWV mice.
    Beck SL.
    Reprod Toxicol; 1999 Jun 01; 13(5):353-60. PubMed ID: 10560583
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Reduction in the frequency of neural tube defects in splotch mice by retinoic acid.
    Kapron-Brás CM, Trasler DG.
    Teratology; 1985 Aug 15; 32(1):87-92. PubMed ID: 3898457
    [Abstract] [Full Text] [Related]

  • 12. Early morphological abnormalities in splotch mouse embryos and predisposition to gene- and retinoic acid-induced neural tube defects.
    Dempsey EE, Trasler DG.
    Teratology; 1983 Dec 15; 28(3):461-72. PubMed ID: 6665745
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Transgenic rescue of congenital heart disease and spina bifida in Splotch mice.
    Li J, Liu KC, Jin F, Lu MM, Epstein JA.
    Development; 1999 Jun 15; 126(11):2495-503. PubMed ID: 10226008
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Fetal neural tube stem cells from Pax3 mutant mice proliferate, differentiate, and form synaptic connections when stimulated with folic acid.
    Ichi S, Nakazaki H, Boshnjaku V, Singh RM, Mania-Farnell B, Xi G, McLone DG, Tomita T, Mayanil CS.
    Stem Cells Dev; 2012 Jan 20; 21(2):321-30. PubMed ID: 21521032
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. A transgenic neuroanatomical marker identifies cranial neural crest deficiencies associated with the Pax3 mutant Splotch.
    Tremblay P, Kessel M, Gruss P.
    Dev Biol; 1995 Oct 20; 171(2):317-29. PubMed ID: 7556916
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.