| Title | Date | PubMed ID |
|---|
| Structural basis of a point mutation that causes the genetic disease aspartylglucosaminuria. | 2014 Dec 2 | 25456816 |
| Crystallographic snapshot of glycosylasparaginase precursor poised for autoprocessing. | 2010 Oct 15 | 20800597 |
| Early initiation of enzyme replacement therapy improves metabolic correction in the brain tissue of aspartylglycosaminuria mice. | 2010 Oct | 20607610 |
| Molecular and biochemical analysis of an aspartylglucosaminidase from the venom of the parasitoid wasp Asobara tabida (Hymenoptera: Braconidae). | 2010 Jan | 20036741 |
| Depletion of L-asparagine supply and apoptosis of leukemia cells induced by human glycosylasparaginase. | 2009 Jun | 19158835 |
| Crystallographic snapshot of a productive glycosylasparaginase-substrate complex. | 2007 Feb 9 | 17157318 |
| Diagnosis of congenital disorders of glycosylation type-I using protein chip technology. | 2006 Apr | 16552784 |
| Elevation of plasma aspartylglucosaminidase is a useful marker for the congenital disorders of glycosylation type I (CDG I). | 2005 | 16435229 |
| A novel aspartylglucosaminuria mutation affects translocation of aspartylglucosaminidase. | 2004 Oct | 15365992 |
| Autoproteolytic activation of human aspartylglucosaminidase. | 2004 Mar 1 | 14616088 |