Contribution

Saleem A. N., Chen Y. H., Baek H. J., Hsiao Y. W., Huang H. W., Kao H. J., Liu K. M., Shen L. F. , Tu C. P. D., Wu J. Y., Kikuchi T., Justice M. J., Yen J. J.Y., and Chen Y. T. Mice with alopecia, osteoporosis and systemic amyloidosis due to mutation in Zdhhc13, a gene coding for palmitoyl acyltransferase. PLoS Genet. 2010; 6(6):e1000985.acess

Chen C. M., Wang H. Y., You L. R., Shang R. L., and Liu F. C. Expression analysis of an evolutionary conserved metallophosphodiesterase gene, Mpped1, in the normal and β-catenin-deficient malformed dorsal telencephalon. Developmental Dynamics 2010; 239:1797-1806.acess

Cheng C. H., Kikuchi T., Chen Y. H., Sabbagha N. G. A.-A.-A., Lee Y. C., Pan H. J., Chang C., and Chen Y. T. Mutations in the SLC2A10 gene cause arterial abnormalities in mice. Cardiovasc Res. 2009; 81(2):381-388.acess