New PDF release: Mouse Models of Developmental Genetic Disease

By Robert S. Krauss (Eds.)

ISBN-10: 0123744547

ISBN-13: 9780123744548

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Birth Defects Res. A Clin. Mol. Teratol. 79, 187–210. Haycraft, C. , et al. (2005). Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function. PLoS Genet. 1, e53. , et al. (1995). Interaction between undulated and Patch leads to an extreme form of spina bifida in double-mutant mice. Nat. Genet. 11, 60–63. Hol, F. , et al. (1995). A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mild signs of Waardenburg syndrome.

Epstein, D. , et al. (1991b). Splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3. Cell 67, 767–774. Modeling NTDs in the Mouse 29 Epstein, D. , et al. (1993). A mutation within intron 3 of the Pax-3 gene produces aberrantly spliced mRNA transcripts in the splotch (Sp) mouse mutant. Proc. Natl Acad. Sci. USA 90, 532–536. Estibeiro, J. , et al. (1993). Interaction between splotch (Sp) and curly tail (ct) mouse mutants in the embryonic development of neural tube defects.

Med. 9, 1513–1519. Ting, S. , et al. (2005). A homolog of Drosophila grainy head is essential for epidermal integrity in mice. Science 308, 411–413. , et al. (2004). Independent mutations in mouse Vangl2 that cause neural tube defects in looptail mice impair interaction with members of the Dishevelled family. J. Biol. Chem. 279, 52703–52713. , et al. (2008). Genetic interaction between members of the Vangl family causes neural tube defects in mice. Proc. Natl Acad. Sci. USA 105, 3449–3454. , and Briscoe, J.

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Mouse Models of Developmental Genetic Disease by Robert S. Krauss (Eds.)


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