Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
2004 | Medical genetics: a marker for Stevens-Johnson syndrome | Chung, W. H.; Hung, S. I.; Hong, H. S.; Hsih, M. S.; Yang, L. C.; Ho, H. C.; Wu, J. W.; Chen, Y. T. | Nature 428, 486 | | | |
1993 | Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in blood | Van Hove, J. L.; Zhang, W.; Kahler, S. G.; Roe, C. R.; Chen, Y. T.; Terada, N.; Chace, D. H.; Iafolla, A. K.; Ding, J. H.; Millington, D. S. | Am J Hum Genet 52, 958-966 | | | |
1993 | Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: the prevalent mutation G985 (K304E) is subject to a strong founder effect from northwestern Europe | Gregersen, N.; Winter, V.; Curtis, D.; Deufel, T.; Mack, M.; Willems, P.; Ponzone, A.; Parrella, T.; Ponzone, K.; Ding, J. H.; Zhang, W.; Chen, Y. T.; Kahler, S.; Roe, C. R.; Kolvraa, S.; Schneiderman, K.; Andresen, B. S.; Bross, P.; Bolund, L. | Hum Hered 43, 342-350 | | | |
1991 | Medium-chain acyl-coenzyme A dehydrogenase deficiency and sudden infant death | Ding, J. H.; Roe, C. R.; Iafolla, A. K.; Chen, Y. T. | N Engl J Med 325, 61-62 | | | |
2011 | Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians | Kato, N.; Takeuchi, F.; Tabara, Y.; Kelly, T. N.; Go, M. J.; Sim, X.; Tay, W. T.; Chen, C. H.; Zhang, Y.; Yamamoto, K.; Katsuya, T.; Yokota, M.; Kim, Y. J.; Ong, R. T. H; Nabika, T.; Gu, DF; Chang, L. C; Kokubo, Y.; Huang, W.; Ohnaka, K.; Yamori, Y.; Nakashima, E.; Jaquish, C. E.; Lee, J. Y.; Seielstad, M.; Isono, M.; Hixson, J. E.; Chen, Y. T.; Miki, T.; Zhou, X.; Sugiyama, T.; Jeon, J. P.; Liu, J. J.; Takayanagi, R.; Kim, S. S.; Aung, T.; Sung, Y. J.; Zhang, X.; Wong, T. Y.; Han, B. G.; Kobayashi, S.; Ogihara, T.; Zhu, DL; Iwai, N.; Wu, J. Y.; Teo, Y. Y.; Tai, E. S.; Cho, Y. S.; He, J. | Nature Genetics 43, 531-538 | | | |
2010 | Mice with alopecia, osteoporosis and systemic amyloidosis due to mutation in Zdhhc13, a gene coding for palmitoyl acyltransferase | 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. | PLoS Genetics 6(6), e1000985 | | | |
1989 | Mild cystic fibrosis linked to chromosome 7q22 markers with an uncommon haplotype | McConkie-Rosell, A.; Chen, Y. T.; Harris, D.; Speer, M. C.; Pericak-Vance, M. A.; Ding, J. H.; Highsmith, W. E.; Knowles, M.; Kahler, S. G. | Ann Intern Med 111, 797-801 | | | |
2010 | Mitochondrial GLUT 10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: mechanistic insights into arterial tortuosity syndrome | Lee, Y. C.; Huang, H. Y.; Chang, C. J.; Cheng, C. H.; Chen, Y. T. | HUMAN MOLECULAR GENETICS 19(19), 3721-3733 | | | |
2002 | Molecular characterization of glycogen storage disease type III | Shen, J. J.; Chen, Y. T. | Curr Mol Med 2, 167-175 | | | |
1992 | Molecular cloning and nucleotide sequence of cDNA encoding human muscle glycogen debranching enzyme | Yang, B. Z.; Ding, J. H.; Enghild, J. J.; Bao, Y.; Chen, Y. T. | J Biol Chem 267, 9294-9299 | | | |
2001 | Molecular cloning of a novel member of the GLUT family of transporters, SLC2a10 (GLUT10), localized on chromosome 20q13.1: a candidate gene for NIDDM susceptibility | McVie-Wylie, A. J.; Lamson, D. R.; Chen, Y. T. | Genomics 72, 113-117 | | | |
1997 | Molecular cloning of acid alpha-glucosidase cDNA of Japanese quail (Coturnix coturnix japonica) and the lack of its mRNA in acid maltase deficient quails | Kunita, R.; Nakabayashi, O.; Wu, J. Y.; Hagiwara, Y.; Mizutani, M.; Pennybacker, M.; Chen, Y. T.; Kikuchi, T. | Biochim Biophys Acta 1362, 269-278 | | | |
2001 | Molecular genetic basis and prevalence of glycogen storage disease type IIIA in the Faroe Islands | Santer, R.; Kinner, M.; Steuerwald, U.; Kjaergaard, S.; Skovby, F.; Simonsen, H.; Shaiu, W. L.; Chen, Y. T.; Schneppenheim, R.; Schaub, J. | Eur J Hum Genet 9, 388-391 | | | |
2011 | Molecular profile and copy number analysis of sporadic colorectal cancer in Taiwan | Lin, C. H.; Lin, J. K.; Chang, S. C.; Chang, Y. H.; Chang, H. M.; Liu, J. H.; Li, L. H.; Chen, Y. T.; Tsai, S. F.; Chen, W. S | Journal of Biomedical Science 18, 36 | | | |
2012 | Monitoring extracellular K+ flux with a valinomycin-coated silicon nanowire field-effect transistor | Chang, K. S.; Sun, C. J.; Chiang, P. L.; Chou, A. C.; Lin, M. C.; Liang, C.; Hung, H. H.; Yeh, Y. H.; Chen, C. D.; Pan, C. Y.; Chen, Y. T. | BIOSENSORS & BIOELECTRONICS31, 137–143 | | | |
2008 | MPDA: microarray pooled DNA analyzer | Yang, H. C.; Huang, M. C.; Li, L. H.; Lin, C. H.; Yu, A. L.; Diccianni, M. B.; Wu, J. Y.; Chen, Y. T.; Fann, C. S. J. | BMC Bioinformatics 9, 196 | | | |
2003 | Multiple muscles in the AMD quail can be ""cross-corrected"" of pathologic glycogen accumulation after intravenous injection of an [E1-, polymerase-] adenovirus vector encoding human acid-alpha-glucosidase | McVie-Wylie, A. J.; Ding, E. Y.; Lawson, T.; Serra, D.; Migone, F. K.; Pressley, D.; Mizutani, M.; Kikuchi, T.; Chen, Y. T.; Amalfitano, A. | J Gene Med 5, 399-406 | | | |
1996 | Mutations in exon 3 of the glycogen debranching enzyme gene are associated with glycogen storage disease type III that is differentially expressed in liver and muscle | Shen, J.; Bao, Y.; Liu, H. M.; Lee, P.; Leonard, J. V.; Chen, Y. T. | J Clin Invest 98, 352-357 | | | |
1990 | Mutations in medium chain acyl-CoA dehydrogenase deficiency | Ding, J. H.; Roe, C. R.; Chen, Y. T.; Matsubara, Y.; Narisawa, K. | Lancet 336, 748-749 | | | |
1995 | Mutations in the glucose-6-phosphatase gene are associated with glycogen storage disease types 1a and 1aSP but not 1b and 1c | Lei, K. J.; Shelly, L. L.; Lin, B.; Sidbury, J. B.; Chen, Y. T.; Nordlie, R. C.; Chou, J. Y. | J Clin Invest 95, 234-240 | | | |