Dr. Chen, Yuan-Tsong 陳垣崇 博士
| 91. | Li, S.C., Chen, C.M., Goldstein, J.L., Wu, J.Y., Lemyre, E., Burrow, T.A., Kang, P.B., Chen, Y.T. and Bali, D.S. Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder JOURNAL OF INHERITED METABOLIC DISEASE 33(S3), S83-S90 (2010) [JCR] [WOS] |
| 92. | Chang, C.F., Li, L.H., Wang, C.H., Tsai, F.J., Chen, T.C., Wu, J.Y., Chen, Y.T., Tsai, A.C.H. Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2-13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high-density oligonucleotide array-a recognizable syndrome American J of Medical Genetics Part A 152A(9), 2365-2371 (2010) [JCR] [WOS] |
| 93. | Saleem, A.N., Chen. Y.H., Baek, H.J., Hsiao, Y.W., Huang, H.W., Kao, H.J., Liu, K.M., Shen, L.F., Song, I.W., Tu, C.P.D., Wu, J.Y., Kikuchi, T., Justice, M.J., Yen, J.J.Y., Chen, Y.T. Mice with alopecia, osteoporosis and systemic amyloidosis due to mutation in Zdhhc13, a gene coding for palmitoyl acyltransferase PLoS Genetics 6(6), e1000985 (2010) [JCR] [WOS] |
| 94. | Lee, Y.C., Huang, H.Y., Chang, C.J., Cheng, C.H. and Chen, Y.T. Mitochondrial GLUT 10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: mechanistic insights into arterial tortuosity syndrome HUMAN MOLECULAR GENETICS 19(19), 3721-3733 (2010) [JCR] [WOS] |
| 95. | Lin, Y.M., Wu, S.J., Chang, T.W., Wang, C.F., Suen, C.S., Hwang, M.J., Chang, M.D.T., Chen, Y.T., Liao, Y.D. Outer membrane protein I of Pseudomonas aeruginosa is a target of cationic antimicrobial peptide/protein Journal of Biological Chemistry 285(12), 8985-8994 (2010) [JCR] [WOS] |
| 96. | Chen, C.F., Hsu, E.C., Lin, K.Y., Tu, P.H., Chang, H.W., Lin, C.H., Chen, Y.J., Gu, D.L., Lin, C.H., Wu, J.Y., Chen, Y.T., Hsu, M.Y., Jou, Y.S. Overlapping high-resolution copy number alterations in cancer genomes identified putative cancer genes in hepatocellular carcinoma HEPATOLOGY 52(5), 1690-1701 (2010) [JCR] [WOS] |
| 97. | Lee, M.T.M., Hung, S.I., Wei, C.Y., Chen, Y.T. Pharmacogenetics of toxic epidermal necrolysis EXPERT OPINION ON PHARMACOTHERAPY 13, 2153-2162 (2010) [JCR] [WOS] |
| 98. | Chen, Y.-T. and Bali, Deeksha Prenatal diagnosis of Disorders of Carbohydrate Metabolism Genetic Disorders of the Fetus, 6th edition 554-576 (2010) [JCR] [WOS] |
| 99. | Jiang, Y.D., Chang, Y.C., Chiu, Y.F., Chang, T.J., Li, H.Y., Lin, W.H., Yuan, H.Y., Chen, Y.T., Chuang, L.M. SLC2A10 genetic polymorphism predicts development of peripheral arterial disease in patients with type 2 diabetes. SLC2A10 and PAD in type 2 diabetes BMC MEDICAL GENETICS 11, 126 (2010) [JCR] [WOS] |
| 100. | Nicolino, M., Byrne, B., Wraith, J.E., Leslie, N., Mandel, H., Freyer, D.R., Arnold, G.L., Pivbick, E.K., Ottinger, C.J., Robinson, P.H., Loo, J.C.A., von der Hagen, M., Smitka, M., Jardine, P., Tato, L., Chabrol, B., McCandless, S., Kimura, S., Mehta, L., Levine, J., Spencer, C., Bali, D., Skrinar, A., Morgan, C., Rangachari, L., Chen, Y.T., Corzo, D., Kishnani, P.S. Clinical outcomes after long-term treatment with algucosidase alfa in infants and children with advanced pompe disease GENETICS IN MEDICINE 11(3), 210-219 (2009-03) [JCR] [WOS] |
| Record 91 to 100, total of 306 records |