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141 related items for PubMed ID: 8512089
1. The Splotch (Sp1H) and Splotch-delayed (Spd) alleles: differential phenotypic effects on neural crest and limb musculature. Franz T. Anat Embryol (Berl); 1993 Apr; 187(4):371-7. PubMed ID: 8512089 [Abstract] [Full Text] [Related]
2. Neural tube defects without neural crest defects in splotch mice. Franz T. Teratology; 1992 Dec; 46(6):599-604. PubMed ID: 1290160 [Abstract] [Full Text] [Related]
3. 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; 187(2):153-60. PubMed ID: 8238963 [Abstract] [Full Text] [Related]
4. 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]
5. Persistent truncus arteriosus in the Splotch mutant mouse. Franz T. Anat Embryol (Berl); 1989 Mar 19; 180(5):457-64. PubMed ID: 2619088 [Abstract] [Full Text] [Related]
9. Abnormalities of neural tube formation in pre-spina bifida splotch-delayed mouse embryos. Yang XM, Trasler DG. Teratology; 1991 Jun 19; 43(6):643-57. PubMed ID: 1882355 [Abstract] [Full Text] [Related]
10. Immunohistochemical localization of chondroitin and heparan sulfate proteoglycans in pre-spina bifida splotch mouse embryos. Trasler DG, Morriss-Kay G. Teratology; 1991 Nov 19; 44(5):571-9. PubMed ID: 1771598 [Abstract] [Full Text] [Related]
11. 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 19; 36(2):163-73. PubMed ID: 9463628 [Abstract] [Full Text] [Related]
12. 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 19; 119(1):113-21. PubMed ID: 8275849 [Abstract] [Full Text] [Related]
13. The splotch-delayed (Spd) mouse mutant carries a point mutation within the paired box of the Pax-3 gene. Vogan KJ, Epstein DJ, Trasler DG, Gros P. Genomics; 1993 Aug 19; 17(2):364-9. PubMed ID: 8406487 [Abstract] [Full Text] [Related]
14. 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]
15. 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]
16. 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 01; 69(1-2):39-51. PubMed ID: 9486530 [Abstract] [Full Text] [Related]
17. Schwann cells are not required for guidance of motor nerves in the hindlimb in Splotch mutant mouse embryos. Grim M, Halata Z, Franz T. Anat Embryol (Berl); 1992 Sep 01; 186(4):311-8. PubMed ID: 1416080 [Abstract] [Full Text] [Related]
18. 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 01; 57(1):17-29. PubMed ID: 9516748 [Abstract] [Full Text] [Related]
19. 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 01; 126(11):2495-503. PubMed ID: 10226008 [Abstract] [Full Text] [Related]
20. Defective ensheathment of motoric nerves in the Splotch mutant mouse. Franz T. Acta Anat (Basel); 1990 Jun 01; 138(3):246-53. PubMed ID: 2389670 [Abstract] [Full Text] [Related] Page: [Next] [New Search]