By Robert S. Krauss (Eds.)
ISBN-10: 0123744547
ISBN-13: 9780123744548
Read or Download Mouse Models of Developmental Genetic Disease PDF
Similar developmental biology books
Bradley Yoder's Ciliary Function in Mammalian Development PDF
Cilia-the tiny hair-like constructions at the floor of cells-have lately been pointed out as taking part in a job in a number of affliction and developmental issues. Absent or faulty cilia in yes cells may cause infertility, blindness, kidney sickness, and lung sickness. This quantity provides fresh findings in cilia examine and present proposal at the position of cilia in sickness and developmental abnormalities.
New PDF release: Environment, Development, and Evolution: Toward a Synthesis
Evolutionary developmental biology, often referred to as evo-devo or EDB, seeks to discover hyperlinks among improvement and evolution by means of establishing the "black field" of development's function in evolution and within the evolution of developmental mechanisms. In specific, this quantity emphasizes the jobs of our surroundings and of hormonal signaling in evo-devo.
Homology. The Hierarchial Basis of Comparative Biology by Brian K. Hall PDF
Homology, the similarity among organisms that's because of universal ancestry, is the important thought of all comparative biology. despite the fact that, the appliance of this idea varies counting on the knowledge being tested. This quantity represents a cutting-edge therapy of different functions of this unifying thought.
The Zebrafish: mobile and Developmental Biology, half A mobile Biology, is the newest variation within the equipment in mobile Biology sequence that appears at tools for examining mobile and developmental biology of zebrafish. Chapters hide such issues as mobile biology and developmental and neural biology.
Extra info for Mouse Models of Developmental Genetic Disease
Sample text
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.
Mouse Models of Developmental Genetic Disease by Robert S. Krauss (Eds.)
by James
4.1