Kelly DP - Search Results

1

Molecular basis of inherited medium-chain acyl-CoA dehydrogenase deficiency causing sudden child death.

Kelly DP, Hale DE, Rutledge SL, Ogden ML, Whelan AJ, Zhang Z, Strauss AW. Kelly DP, et al. J Inherit Metab Dis. 1992;15(2):171-80. doi: 10.1007/BF01799626. J Inherit Metab Dis. 1992. PMID: 1356169

2

Identification of a novel retinoid-responsive element in the promoter region of the medium chain acyl-coenzyme A dehydrogenase gene.

Raisher BD, Gulick T, Zhang Z, Strauss AW, Moore DD, Kelly DP. Raisher BD, et al. Among authors: kelly dp. J Biol Chem. 1992 Oct 5;267(28):20264-9. J Biol Chem. 1992. PMID: 1328196 Free article.

3

Mutations in the medium chain acyl-CoA dehydrogenase (MCAD) gene.

Tanaka K, Yokota I, Coates PM, Strauss AW, Kelly DP, Zhang Z, Gregersen N, Andresen BS, Matsubara Y, Curtis D, et al. Tanaka K, et al. Among authors: kelly dp. Hum Mutat. 1992;1(4):271-9. doi: 10.1002/humu.1380010402. Hum Mutat. 1992. PMID: 1363805 Review.

4

Identification and characterization of the 5' regulatory region of the human medium-chain acyl-CoA dehydrogenase (MCAD) gene.

Kelly DP, Zhang Z, Raisher BD, Ogden ML, Strauss AW. Kelly DP, et al. Prog Clin Biol Res. 1992;375:143-9. Prog Clin Biol Res. 1992. PMID: 1438357 No abstract available.

5

Molecular characterization of medium-chain acyl-CoA dehydrogenase deficiency causing sudden death.

Kelly DP, Whelan AJ, Hale DE, Rinaldo P, Rutledge SL, Zhang Z, Strauss AW. Kelly DP, et al. Prog Clin Biol Res. 1992;375:463-72. Prog Clin Biol Res. 1992. PMID: 1438388 No abstract available.

6

Structural organization and regulatory regions of the human medium-chain acyl-CoA dehydrogenase gene.

Zhang ZF, Kelly DP, Kim JJ, Zhou YQ, Ogden ML, Whelan AJ, Strauss AW. Zhang ZF, et al. Among authors: kelly dp. Biochemistry. 1992 Jan 14;31(1):81-9. doi: 10.1021/bi00116a013. Biochemistry. 1992. PMID: 1731887

7

Characterization of a disease-causing Lys329 to Glu mutation in 16 patients with medium-chain acyl-CoA dehydrogenase deficiency.

Gregersen N, Andresen BS, Bross P, Winter V, Rüdiger N, Engst S, Ghisla S, Christensen E, Kelly D, Strauss AW, et al. Gregersen N, et al. J Inherit Metab Dis. 1991;14(3):314-6. doi: 10.1007/BF01811691. J Inherit Metab Dis. 1991. PMID: 1770781 No abstract available.

8

Molecular characterization of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: identification of a lys329 to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein in E. coli.

Gregersen N, Andresen BS, Bross P, Winter V, Rüdiger N, Engst S, Christensen E, Kelly D, Strauss AW, Kølvraa S, et al. Gregersen N, et al. Hum Genet. 1991 Apr;86(6):545-51. doi: 10.1007/BF00201539. Hum Genet. 1991. PMID: 1902818

9

Characterization of wild-type and an active site mutant of human medium chain acyl-CoA dehydrogenase after expression in Escherichia coli.

Bross P, Engst S, Strauss AW, Kelly DP, Rasched I, Ghisla S. Bross P, et al. Among authors: kelly dp. J Biol Chem. 1990 May 5;265(13):7116-9. J Biol Chem. 1990. PMID: 1970566 Free article.

10

Molecular characterization of inherited medium-chain acyl-CoA dehydrogenase deficiency.

Kelly DP, Whelan AJ, Ogden ML, Alpers R, Zhang ZF, Bellus G, Gregersen N, Dorland L, Strauss AW. Kelly DP, et al. Proc Natl Acad Sci U S A. 1990 Dec;87(23):9236-40. doi: 10.1073/pnas.87.23.9236. Proc Natl Acad Sci U S A. 1990. PMID: 2251268 Free PMC article.

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