Functional Studies of a Novel Mutation in HARS, the Gene Encoding histidyl-tRNA Synthetase, Associated With Usher IIIB Syndrome
Achilly, Nathan P.
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Characterization of congenital vascular and intracardiac defects in the Ts65Dn murine model for Down syndrome Williams, Austin D. (2007)The Ts65Dn mouse is the most-studied murine model for Down syndrome (DS) or trisomy 21. Homology between triplicated murine genes and genes on human chromosome 21 (Hsa21) correlates with the shared anomalies of Ts65Dn ...
Branchial arch artery formation and apoptosis during cardiogenesis in the Ts65Dn mouse model for Down syndrome Hakkinen, Lauren A. (2007)Ts65Dn is the mouse model most widely used in Down syndrome (DS) research. In this model, triplication of the distal portion of mouse chromosome 16 (MMU16), which contains orthologs to genes on human chromosome 21, results ...
Quantification and analysis of apoptosis in embryonic atrioventricular endocardial cushions of the Ts65Dn mouse model for Down syndrome Gotlieb, Naomi R. (2009)The Ts65Dn mouse model for Down syndrome (DS) has triplication of more than half of the mouse genes orthologous to those on human chromosome 21, and exhibits many phenotypes characteristic of human DS. Previous gross ...