Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
1990 | Definitive prenatal diagnosis for type III glycogen storage disease | Yang, B. Z.; Ding, J. H.; Brown, B. I.; Chen, Y. T. | Am J Hum Genet 47, 735-739 | | | |
1986 | Expression and chromosomal localization of the cytochrome P1-450 gene in human mitogen-stimulated lymphocytes | Amsbaugh, S. C.; Ding, J. H.; Swan, D. C.; Popescu, N. C.; Chen, Y. T. | Cancer Res 46, 2423-2428 | | | |
1987 | Glycogen debranching enzyme: purification, antibody characterization, and immunoblot analyses of type III glycogen storage disease | Chen, Y. T.; He, J. K.; Ding, J. H.; Brown, B. I. | Am J Hum Genet 41, 1002-1015 | | | |
1985 | Identification and quantification of a messenger ribonucleic acid induced by polynuclear aromatic hydrocarbons--using a cloned human cytochrome P-450 gene | Kato, T.; Ding, J. H.; Chen, Y. T. | Eur J Biochem 151, 489-495 | | | |
1992 | Identification of a new mutation in medium-chain acyl-CoA dehydrogenase (MCAD) deficiency | Ding, J. H.; Yang, B. Z.; Bao, Y.; Roe, C. R.; Chen, Y. T. | Am J Hum Genet 50, 229-233 | | | |
1990 | Immunoblot analyses of glycogen debranching enzyme in different subtypes of glycogen storage disease type III | Ding, J. H.; de Barsy, T.; Brown, B. I.; Coleman, R. A.; Chen, Y. T. | J Pediatr 116, 95-100 | | | |
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 | | | |
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 | | | |
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 | | | |
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 | | | |
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 | | | |
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 | | | |
1987 | Vitamins E and K induce aryl hydrocarbon hydroxylase activity in human cell cultures | Chen, Y. T.; Ding, J. H. | Biochem Biophys Res Commun 143, 863-871 | | | |