12
results
for uniprot:Q64191
in citationmapping
| 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 15:79-85(2005) GeneRIF 11593 MGI 104873 · Mapped (3) |
| 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. 27:1467-1474(1999) MGI 104873 · Mapped (1) |
| Enzyme replacement therapy in a mouse model of aspartylglycosaminuria. Dunder U., Kaartinen V., Valtonen P., Vaananen E., Kosma V.M., Heisterkamp N., Groffen J., Mononen I. FASEB J. 14:361-367(2000) MGI 104873 · Mapped (1) |
| Functional annotation of a full-length mouse cDNA collection. Kawai J., Shinagawa A., Shibata K., Yoshino M., Itoh M., Ishii Y., Arakawa T., Hara A., Fukunishi Y., Konno H. et al. Nature 409:685-690(2001) MGI 104873 · UniProtKB (17,855) · Mapped (8,931) |
| Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Okazaki Y., Furuno M., Kasukawa T., Adachi J., Bono H., Kondo S., Nikaido I., Osato N., Saito R., Suzuki H. et al. Nature 420:563-573(2002) MGI 104873 · UniProtKB (17,858) · Mapped (12,469) |
| Enzymatic cleavage of glycopeptides. Makino M., Kojima T., Yamashina I. Biochem. Biophys. Res. Commun. 24:961-966(1966) MGI 104873 · Mapped (1) |
| A mouse model for the human lysosomal disease aspartylglycosaminuria. Kaartinen V., Mononen I., Voncken J.W., Noronkoski T., Gonzalez-Gomez I., Heisterkamp N., Groffen J. Nat. Med. 2:1375-1378(1996) MGI 104873 · Mapped (1) |
| Expression and regulation of the human and mouse aspartylglucosaminidase gene. Uusitalo A., Tenhunen K., Tenhunen J., Matikainen S., Peltonen L., Jalanko A. J. Biol. Chem. 272:9524-9530(1997) MGI 104873 · Mapped (1) |
| Mice with an aspartylglucosaminuria mutation similar to humans replicate the pathophysiology in patients. Jalanko A., Tenhunen K., McKinney C.E., LaMarca M.E., Rapola J., Autti T., Joensuu R., Manninen T., Sipila I., Ikonen S. et al. Hum. Mol. Genet. 7:265-272(1998) MGI 104873 · Mapped (1) |
| Phenotypic characterization of mice with targeted disruption of glycosylasparaginase gene: a mouse model for aspartylglycosaminuria. Kaartinen V., Mononen I., Gonzalez-Gomez I., Noronkoski T., Heisterkamp N., Groffen J. J. Inherit. Metab. Dis. 21:207-209(1998) MGI 104873 · Mapped (1) |
| Progressive neurodegeneration in aspartylglycosaminuria mice. Gonzalez-Gomez I., Mononen I., Heisterkamp N., Groffen J., Kaartinen V. Am. J. Pathol. 153:1293-1300(1998) MGI 104873 · Mapped (1) |
| Monitoring the CNS pathology in aspartylglucosaminuria mice. Tenhunen K., Uusitalo A., Autti T., Joensuu R., Kettunen M., Kauppinen R.A., Ikonen S., LaMarca M.E., Haltia M., Ginns E.I. et al. J. Neuropathol. Exp. Neurol. 57:1154-1163(1998) MGI 104873 · Mapped (1) |
