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Journal Abstract Search

177 related items for PubMed ID: 9352100

  • 1. Altered cell proliferation in the spinal cord of mouse neural tube mutants curly tail and Pax3 splotch-delayed.
    Keller-Peck CR, Mullen RJ.
    Brain Res Dev Brain Res; 1997 Sep 20; 102(2):177-88. PubMed ID: 9352100
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  • 2. Patterns of neuronal differentiation in neural tube mutant mice: curly tail and Pax3 splotch-delayed.
    Keller-Peck CR, Mullen RJ.
    J Comp Neurol; 1996 May 13; 368(4):516-26. PubMed ID: 8744440
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  • 4. Interaction between splotch (Sp) and curly tail (ct) mouse mutants in the embryonic development of neural tube defects.
    Estibeiro JP, Brook FA, Copp AJ.
    Development; 1993 Sep 13; 119(1):113-21. PubMed ID: 8275849
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  • 6. Mini-review: toward understanding mechanisms of genetic neural tube defects in mice.
    Harris MJ, Juriloff DM.
    Teratology; 1999 Nov 13; 60(5):292-305. PubMed ID: 10525207
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  • 8. Role of differential cell proliferation in the tail bud in aberrant mouse neurulation.
    Peeters MC, Schutte B, Lenders MH, Hekking JW, Drukker J, Van Straaten HW.
    Dev Dyn; 1998 Apr 13; 211(4):382-9. PubMed ID: 9566957
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  • 9. Neural tube development in mutant (curly tail) and normal mouse embryos: the timing of posterior neuropore closure in vivo and in vitro.
    Copp AJ, Seller MJ, Polani PE.
    J Embryol Exp Morphol; 1982 Jun 13; 69():151-67. PubMed ID: 7119666
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  • 10. Relationship between altered axial curvature and neural tube closure in normal and mutant (curly tail) mouse embryos.
    Peeters MC, Shum AS, Hekking JW, Copp AJ, van Straaten HW.
    Anat Embryol (Berl); 1996 Feb 13; 193(2):123-30. PubMed ID: 8742053
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  • 11. Quantification and localization of expression of the retinoic acid receptor-beta and -gamma mRNA isoforms during neurulation in mouse embryos with or without spina bifida.
    Mao GE, Collins MD.
    Teratology; 2002 Dec 13; 66(6):331-43. PubMed ID: 12486767
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  • 12. Neurulation abnormalities secondary to altered gene expression in neural tube defect susceptible Splotch embryos.
    Bennett GD, An J, Craig JC, Gefrides LA, Calvin JA, Finnell RH.
    Teratology; 1998 Jan 13; 57(1):17-29. PubMed ID: 9516748
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  • 13. Genetic patterning of the posterior neuropore region of curly tail mouse embryos: deficiency of Wnt5a expression.
    Gofflot F, Hall M, Morriss-Kay GM.
    Int J Dev Biol; 1998 Jul 13; 42(5):637-44. PubMed ID: 9712518
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  • 14. Immunohistochemical localization of chondroitin and heparan sulfate proteoglycans in pre-spina bifida splotch mouse embryos.
    Trasler DG, Morriss-Kay G.
    Teratology; 1991 Nov 13; 44(5):571-9. PubMed ID: 1771598
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  • 16. 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
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  • 17. Studies of the effect of retinoic acid on anterior neural tube closure in mice genetically liable to exencephaly.
    Tom C, Juriloff DM, Harris MJ.
    Teratology; 1991 Jan 01; 43(1):27-40. PubMed ID: 2006470
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  • 18. 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
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  • 19. 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
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  • 20. Developmental basis of severe neural tube defects in the loop-tail (Lp) mutant mouse: use of microsatellite DNA markers to identify embryonic genotype.
    Copp AJ, Checiu I, Henson JN.
    Dev Biol; 1994 Sep 01; 165(1):20-9. PubMed ID: 8088438
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