發表文獻

Ke C. C., Liu R. S., Suetsugu A., Kimura H., Ho J. H., Lee O. K., and Hoffman R. M. In vivo fluorescence imaging reveals the promotion of mammary tumorigenesis by mesenchymal stromal cells. PLoS ONE 2013; 8(7): e69658. doi:10.1371/journal.pone.0069658.acess

Yeh H .H., Lin C. F., Kong F. L., Wang H. E., Hsieh Y. J., Gelovani J., and Liu R. S. Molecular Imaging of Non-small Cell Lung Carcinomas Expressing Active Mutant EGFR Kinase using PET with [124I]-morpholino-IPQA. BioMed Research International 2013; 2013, Article ID 549359 .acess

Chen C. C. and Wong C. W. Neurosensory mechanotransduction through acid-sensing ion channels. J. Cell. Mol. Med. 2013;17(3): 337-349.acess

Chiang Y. J., Ho K. C., Sun C. T., Chiu J. J., Lee F. J., Liao F., Yang-Yen H. F., and Yen J. J. Y. CBAP Functions as a Novel Component in Chemokine-Induced ZAP70-Mediated T-Cell Adhesion and Migration. Plos One 2013; 8(4):e61761 acess

Krebs P., Fan W., Chen Y. H., Tobita K., Downes M. R., Wood M. R., Suna L., Li X., Xiaa Y., Ding N., Spaeth J. M., Moresco E. M. Y., Boyer T. G., Lo C. W. Y., Yen J.J.Y, Evans R. M., and Beutler B. Lethal mitochondrial cardiomyopathy in a hypomorphic Med30 mouse mutant is ameliorated by ketogenic diet. PNAS December 6, 2011; 108 (49), 19678-19682.acess

Weng S. Y., Yang C. Y., Li C. C., Sun T. P., Tung S. Y., Yen J. J.Y., Tsai T. F., Chen C. M., Chen S. H., Hsiao M., Huang P. S., Yang-Yen H. F. Synergism between p53 and Mcl-1 in protecting from hepatic injury, fibrosis and cancer. Journal of Hepatology 2011; 54(4), 685-694. acess

Akgül B., Lin K. W., Yang H. M. O., Chen Y. H., Lu T. H., Chen C. H., Kikuchi T., Chen Y. T. and Tu C. P. D. Garlic accelerates red blood cell turnover and splenic erythropoietic gene expression in mice: evidence for erythropoietin-independent erythropoiesis. PLoS One 2010; 5(12):e15358.acess

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