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107 related items for PubMed ID: 8453768

  • 1. Characterization of the neural crest defect in Splotch (Sp1H) mutant mice using a lacZ transgene.
    Franz T, Kothary R.
    Brain Res Dev Brain Res; 1993 Mar 19; 72(1):99-105. PubMed ID: 8453768
    [Abstract] [Full Text] [Related]

  • 2. The Splotch (Sp1H) and Splotch-delayed (Spd) alleles: differential phenotypic effects on neural crest and limb musculature.
    Franz T.
    Anat Embryol (Berl); 1993 Apr 19; 187(4):371-7. PubMed ID: 8512089
    [Abstract] [Full Text] [Related]

  • 3. Analysis of neural crest cell migration in Splotch mice using a neural crest-specific LacZ reporter.
    Serbedzija GN, McMahon AP.
    Dev Biol; 1997 May 15; 185(2):139-47. PubMed ID: 9187079
    [Abstract] [Full Text] [Related]

  • 4. 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 15; 171(2):317-29. PubMed ID: 7556916
    [Abstract] [Full Text] [Related]

  • 5. The Splotch mutation interferes with muscle development in the limbs.
    Franz T, Kothary R, Surani MA, Halata Z, Grim M.
    Anat Embryol (Berl); 1993 Feb 15; 187(2):153-60. PubMed ID: 8238963
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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]

  • 8. Over-expression of the chondroitin sulphate proteoglycan versican is associated with defective neural crest migration in the Pax3 mutant mouse (splotch).
    Henderson DJ, Ybot-Gonzalez P, Copp AJ.
    Mech Dev; 1997 Dec 15; 69(1-2):39-51. PubMed ID: 9486530
    [Abstract] [Full Text] [Related]

  • 9. Spinal ganglia reduction in the splotch-delayed mouse neural tube defect mutant.
    Moase CE, Trasler DG.
    Teratology; 1989 Jul 15; 40(1):67-75. PubMed ID: 2763211
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Cardiac neural crest of the mouse embryo: axial level of origin, migratory pathway and cell autonomy of the splotch (Sp2H) mutant effect.
    Chan WY, Cheung CS, Yung KM, Copp AJ.
    Development; 2004 Jul 01; 131(14):3367-79. PubMed ID: 15226254
    [Abstract] [Full Text] [Related]

  • 12. Neural tube defects without neural crest defects in splotch mice.
    Franz T.
    Teratology; 1992 Dec 01; 46(6):599-604. PubMed ID: 1290160
    [Abstract] [Full Text] [Related]

  • 13. Insertion of Cre into the Pax3 locus creates a new allele of Splotch and identifies unexpected Pax3 derivatives.
    Engleka KA, Gitler AD, Zhang M, Zhou DD, High FA, Epstein JA.
    Dev Biol; 2005 Apr 15; 280(2):396-406. PubMed ID: 15882581
    [Abstract] [Full Text] [Related]

  • 14. Migration of cardiac neural crest cells in Splotch embryos.
    Epstein JA, Li J, Lang D, Chen F, Brown CB, Jin F, Lu MM, Thomas M, Liu E, Wessels A, Lo CW.
    Development; 2000 May 15; 127(9):1869-78. PubMed ID: 10751175
    [Abstract] [Full Text] [Related]

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  • 16. 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]

  • 17. Pax3 is required for cardiac neural crest migration in the mouse: evidence from the splotch (Sp2H) mutant.
    Conway SJ, Henderson DJ, Copp AJ.
    Development; 1997 Jan 15; 124(2):505-14. PubMed ID: 9053326
    [Abstract] [Full Text] [Related]

  • 18. Abnormal skeletogenesis occurs coincident with increased apoptosis in the Splotch (Sp2H) mutant: putative roles for Pax3 and PDGFRalpha in rib patterning.
    Dickman ED, Rogers R, Conway SJ.
    Anat Rec; 1999 Jul 01; 255(3):353-61. PubMed ID: 10411402
    [Abstract] [Full Text] [Related]

  • 19. Transgenic mice expressing PAX3-FKHR have multiple defects in muscle development, including ectopic skeletal myogenesis in the developing neural tube.
    Finckenstein FG, Davicioni E, Osborn KG, Cavenee WK, Arden KC, Anderson MJ.
    Transgenic Res; 2006 Oct 01; 15(5):595-614. PubMed ID: 16952014
    [Abstract] [Full Text] [Related]

  • 20. Changes in sialylation in homozygous Sp2H mouse mutant embryos.
    Glogarová K, Buckiová D.
    Birth Defects Res A Clin Mol Teratol; 2004 Mar 01; 70(3):142-52. PubMed ID: 15039928
    [Abstract] [Full Text] [Related]

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