|
Aronson Jr, N N (1999) Aspartylglycosaminuria: biochemistry and molecular biology. Biochim Biophys Acta 1455:139-54
|
|
Liu, Y; Guan, C; Aronson Jr, N N (1998) Site-directed mutagenesis of essential residues involved in the mechanism of bacterial glycosylasparaginase. J Biol Chem 273:9688-94
|
|
Park, H; Rossiter, M; Fensom, A H et al. (1996) Single base deletion in exon 7 of the glycosylasparaginase gene causes a mild form of aspartylglycosaminuria in a patient of Mauritian origin. J Inherit Metab Dis 19:76-83
|
|
Aronson Jr, N N (1996) Lysosomal glycosylasparaginase: a member of a family of amidases that employ a processed N-terminal threonine, serine or cysteine as a combined base-nucleophile catalyst. Glycobiology 6:669-75
|
|
Liu, Y; Dunn, G S; Aronson Jr, N N (1996) Purification, biochemistry and molecular cloning of an insect glycosylasparaginase from Spodoptera frugiperda. Glycobiology 6:527-36
|
|
Ahmad, W; Li, S; Chen, H et al. (1995) Lysosomal chitobiase (CTB) and the G-protein gamma 5 subunit (GNG5) genes co-localize to human chromosome 1p22. Cytogenet Cell Genet 71:44-6
|
|
Fisher, K J; Klein, M; Park, H et al. (1993) Post-translational processing and Thr-206 are required for glycosylasparaginase activity. FEBS Lett 323:271-5
|
|
Mononen, I; Fisher, K J; Kaartinen, V et al. (1993) Aspartylglycosaminuria: protein chemistry and molecular biology of the most common lysosomal storage disorder of glycoprotein degradation. FASEB J 7:1247-56
|
|
Hancock, L W; Raab, L S; Aronson Jr, N N (1993) Synthesis and processing of rat sperm-associated alpha-L-fucosidase. Biol Reprod 48:1228-38
|
|
Park, H; Vettese, M B; Fensom, A H et al. (1993) Characterization of three alleles causing aspartylglycosaminuria: two from a British family and one from an American patient. Biochem J 290 ( Pt 3):735-41
|
Showing the most recent 10 out of 23 publications
