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4. Early initiation of enzyme replacement therapy improves metabolic correction in the brain tissue of aspartylglycosaminuria mice. Dunder U; Valtonen P; Kelo E; Mononen I J Inherit Metab Dis; 2010 Oct; 33(5):611-7. PubMed ID: 20607610 [TBL] [Abstract][Full Text] [Related]
5. Progressive neurodegeneration in aspartylglycosaminuria mice. Gonzalez-Gomez I; Mononen I; Heisterkamp N; Groffen J; Kaartinen V Am J Pathol; 1998 Oct; 153(4):1293-300. PubMed ID: 9777961 [TBL] [Abstract][Full Text] [Related]
6. Massive accumulation of Man2GlcNAc2-Asn in nonneuronal tissues of glycosylasparaginase-deficient mice and its removal by enzyme replacement therapy. Kelo E; Dunder U; Mononen I Glycobiology; 2005 Jan; 15(1):79-85. PubMed ID: 15342551 [TBL] [Abstract][Full Text] [Related]
7. A mouse model for the human lysosomal disease aspartylglycosaminuria. Kaartinen V; Mononen I; Voncken JW; Noronkoski T; Gonzalez-Gomez I; Heisterkamp N; Groffen J Nat Med; 1996 Dec; 2(12):1375-8. PubMed ID: 8946839 [TBL] [Abstract][Full Text] [Related]
8. Correction of peripheral lysosomal accumulation in mice with aspartylglucosaminuria by bone marrow transplantation. Laine M; Richter J; Fahlman C; Rapola J; Renlund M; Peltonen L; Karlsson S; Jalanko A Exp Hematol; 1999 Sep; 27(9):1467-74. PubMed ID: 10480438 [TBL] [Abstract][Full Text] [Related]
9. Mice with an aspartylglucosaminuria mutation similar to humans replicate the pathophysiology in patients. Jalanko A; Tenhunen K; McKinney CE; LaMarca ME; Rapola J; Autti T; Joensuu R; Manninen T; Sipilä I; Ikonen S; Riekkinen P; Ginns EI; Peltonen L Hum Mol Genet; 1998 Feb; 7(2):265-72. PubMed ID: 9425233 [TBL] [Abstract][Full Text] [Related]
11. Adenovirus-mediated gene transfer results in decreased lysosomal storage in brain and total correction in liver of aspartylglucosaminuria (AGU) mouse. Peltola M; Kyttälä A; Heinonen O; Rapola J; Paunio T; Revah F; Peltonen L; Jalanko A Gene Ther; 1998 Oct; 5(10):1314-21. PubMed ID: 9930336 [TBL] [Abstract][Full Text] [Related]
12. Aspartylglycosaminuria: protein chemistry and molecular biology of the most common lysosomal storage disorder of glycoprotein degradation. Mononen I; Fisher KJ; Kaartinen V; Aronson NN FASEB J; 1993 Oct; 7(13):1247-56. PubMed ID: 8405810 [TBL] [Abstract][Full Text] [Related]
13. Human leukocyte glycosylasparaginase: cell-to-cell transfer and properties in correction of aspartylglycosaminuria. Dunder U; Mononen I FEBS Lett; 2001 Jun; 499(1-2):77-81. PubMed ID: 11418116 [TBL] [Abstract][Full Text] [Related]
14. Characterization of three alleles causing aspartylglycosaminuria: two from a British family and one from an American patient. Park H; Vettese MB; Fensom AH; Fisher KJ; Aronson NN Biochem J; 1993 Mar; 290 ( Pt 3)(Pt 3):735-41. PubMed ID: 8457202 [TBL] [Abstract][Full Text] [Related]
15. Dissection of the molecular pathology of aspartylglucosaminuria provides the basis for DNA diagnostics and future therapeutic interventions. Ikonen E; Syvänen AC; Peltonen L Scand J Clin Lab Invest Suppl; 1993; 213():19-27. PubMed ID: 8322015 [TBL] [Abstract][Full Text] [Related]
16. Single base deletion in exon 7 of the glycosylasparaginase gene causes a mild form of aspartylglycosaminuria in a patient of Mauritian origin. Park H; Rossiter M; Fensom AH; Winchester B; Aronson NN J Inherit Metab Dis; 1996; 19(1):76-83. PubMed ID: 8830180 [TBL] [Abstract][Full Text] [Related]
17. Enzymatic diagnosis of aspartylglycosaminuria by fluorometric assay of glycosylasparaginase in serum, plasma, or lymphocytes. Mononen I; Mononen T; Ylikangas P; Kaartinen V; Savolainen K Clin Chem; 1994 Mar; 40(3):385-8. PubMed ID: 8131272 [TBL] [Abstract][Full Text] [Related]
18. Use of nonviral promoters in adenovirus-mediated gene therapy: reduction of lysosomal storage in the aspartylglucosaminuria mouse. Virta S; Rapola J; Jalanko A; Laine M J Gene Med; 2006 Jun; 8(6):699-706. PubMed ID: 16518877 [TBL] [Abstract][Full Text] [Related]