Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
1983 | Structure of the mouse cytochrome P1-450 genomic gene | Nakamura, M.; Negishi, M.; Altieri, M.; Chen, Y. T.; Ikeda, T.; Tukey, R. H.; Nebert, D. W. | Eur J Biochem 134, 19-25 | | | |
2013 | Suppressed polarizaton polarization in single InGaN/GaN heterostructure nanowires | Tsai, W. C.; Chen, Y. T.; Lin, C. H.; Hsu, W. T.; Hsu, Y. S.; Chen, L. C.; Chen, K. H.; Chang, W. H. | PHYSICAL REVIEW B | | | |
2008 | Synthesis and biological activity of stable and potent antitumor agnets, aniline nitrogen mustards linked to 9-anilinoacridines via a urea linkage | Kapuriya, N.; Kapuriya, K.; Zhang, X.; Chou, T. C.; Kakadiya, R.; Wu, Y. T.; Tsai, T. H.; Chen, Y. T.; Lee, T. C.; Shah, A.; Naliapara, Y.; Su, T. L. | BIOORGANIC & MEDICINAL CHEMISTRY 16(10), 5413-5423 | | | |
1999 | Systemic correction of the muscle disorder glycogen storage disease type II after hepatic targeting of a modified adenovirus vector encoding human acid-alpha-glucosidase | Amalfitano, A.; McVie-Wylie, A. J.; Hu, H.; Dawson, T. L.; Raben, N.; Plotz, P.; Chen, Y. T. | Proc Natl Acad Sci U S A 96, 8861-8866 | | | |
2007 | The exchange-biasing in the Si(100)/Ta/Co/IrMn/Ta system | Chen, Y. T.; Jen, S. U.; Yao, Y. D.; Wu, J. M. | J. Magn. Magn. Mater.310, 2307 | | | |
2011 | The impact of antibodies on clinical outcomes in diseases treated with therapeutic protein: lessons learned from infantile Pompe disease. | Banugaria, S. G.; Prater, S. N.; Ng, Y. K.; Kobori, J. A.; Finkel, R. S.; Ladda, R. L.; Chen, Y. T.; Rosenberg, A. S.; Kishnani, P. S. | Genetics in Medicine 13(8), 729-736 | | | |
1993 | The loss of a polymorphic glycosylation site caused by Thr-927-->Ile is linked to a second polymorphic Val-816-->Ile substitution in lysosomal alpha-glucosidase of American blacks | Hermans, M. M.; Svetkey, L. P.; Oostra, B. A.; Chen, Y. T.; Reuser, A. J. | Genomics 16, 300-301 | | | |
1999 | The putative glucose 6-phosphate translocase gene is mutated in essentially all cases of glycogen storage disease type I non-a | Veiga-da-Cunha, M.; Gerin, I.; Chen, Y. T.; Lee, P. J.; Leonard, J. V.; Maire, I.; Wendel, U.; Vikkula, M.; Van Schaftingen, E. | Eur J Hum Genet 7, 717-723 | | | |
1986 | The role of raw starches in the treatment of type I glycogenosis | Sidbury, J. B.; Chen, Y. T.; Roe, C. R. | Arch Intern Med 146, 370-373 | | | |
1992 | The role of tandem mass spectrometry in the diagnosis of fatty acid oxidation disorders | Millington, D. S.; Terada, N.; Chace, D. H.; Chen, Y. T.; Ding, J. H.; Kodo, N.; Roe, C. R. | Prog Clin Biol Res 375, 339-354 | | | |
2003 | Tissue-specific inactivation of murine M6P/IGF2R | Wylie, A. A.; Pulford, D. J.; McVie-Wylie, A. J.; Waterland, R. A.; Evans, H. K.; Chen, Y. T.; Nolan, C. M.; Orton, T. C.; Jirtle, R. L. | Am J Pathol 162, 321-328 | | | |
2000 | Towards a molecular therapy for glycogen storage disease type II (Pompe disease) | Chen, Y. T.; Amalfitano, A. | Mol Med Today 6, 245-251 | | | |
1989 | Transfection of a human cytochrome P-450 gene into the human lymphoblastoid cell line, AHH-1, and use of the recombinant cell line in gene mutation assays | Crespi, C. L.; Langenbach, R.; Rudo, K.; Chen, Y. T.; Davies, R. L. | Carcinogenesis 10, 295-301 | | | |
1998 | Two new mutations in the 3' coding region of the glycogen debranching enzyme in a glycogen storage disease type IIIa Ashkenazi Jewish patient | Parvari, R.; Shen, J.; Hershkovitz, E.; Chen, Y. T.; Moses, S. W. | J Inherit Metab Dis 21, 141-148 | | | |
1991 | Type I glycogen storage disease: kidney involvement, pathogenesis and its treatment | Chen, Y. T. | Pediatr Nephrol 5, 71-76 | | | |
1993 | Type I glycogen storage disease: nine years of management with cornstarch | Chen, Y. T.; Bazzarre, C. H.; Lee, M. M.; Sidbury, J. B.; Coleman, R. A. | Eur J Pediatr 152, S56-S59 | | | |
2002 | Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex | Chou, J. Y.; Matern, D.; Mansfield, B. C.; Chen, Y. T. | Curr Mol Med 2, 121-143 | | | |
2005 | Type II collagen gene variants and inherited osteonecrosis of the femoral head | Liu, Y. F.; Chen, W. M.; Lin, Y. F.; Yang, R. C.; Lin, M. W.; Li, L. H.; Chang, Y. H.; Jou, Y. S.; Lin, P. Y.; Su, J. S.; Huang, S. F.; Hsiao, K. J.; Fann, C. S. J.; Hwang, H. W.; Chen, Y. T.; Tsai, S. F. | NEW ENGLAND JOURNAL OF MEDICINE 352, 2294-2301 | | | |
2005 | Type II collagen gene variants and inherited osteonecrosis of the frmoral head | Liu, Y. F.; Chen, W. M.; Lin, Y. F.; Yang, R. C.; Lin, M. W.; Li, L. H.; Chang, Y. H.; Jou, J. S.; Lin, P. Y.; Su, J. S.; Huang, S. F.; Hsiao, K. J.; Fann, C. S.; Hwang, H. W.; Chen, Y. T.; Tsai, S. F. | New England Journal of Medicine 352, 2294-2301 | | | |
1991 | Type III glycogen storage disease: an adult case with mild disease but complete absence of debrancher protein | Yang, B. Z.; Stewart, C.; Ding, J. H.; Chen, Y. T. | Neuromuscul Disord 1, 173-176 | | | |