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Purification and properties of human hepatic aspartylglucosaminidaseMCGOVERN, M. M; AULA, P; DESNICK, R. J et al.The Journal of biological chemistry (Print). 1983, Vol 258, Num 17, pp 10743-10747, issn 0021-9258Article

Synthesis of silk sericin peptides-L-asparaginase bioconjugates and their characterizationZHANG, Yu-Qing; TAO, Mei-Lin; SHEN, Wei-De et al.Journal of chemical technology and biotechnology (1986). 2006, Vol 81, Num 2, pp 136-145, issn 0268-2575, 10 p.Article

Post-translational processing and Thr-206 are required for glycosylasparaginase activityFISHER, K. J; KLEIN, M; HYEJEONG PARK et al.FEBS letters. 1993, Vol 323, Num 3, pp 271-275, issn 0014-5793Article

Substrate specificity and reaction mechanism of human glycoasparaginase : the N-glycosidic likage of various glycoasparagines is cleaved through a reaction mechanism similar to L-asparaginaseKAARTINEN, V; MONONEN, T; LAATIKAINEN, R et al.The Journal of biological chemistry (Print). 1992, Vol 267, Num 10, pp 6855-6858, issn 0021-9258Article

Deletion of the 3'-untranslated region of aspartylglucosaminidase mRNA results in a lysosomal accumulation diseaseIKONEN, E; ULMANEN, I; PELTONEN, L et al.The Journal of biological chemistry (Print). 1992, Vol 267, Num 13, pp 8715-8718, issn 0021-9258Article

Human leucocyte glycosylasparaginase is an α/β-heterodimer of 19 kDa α-subunit and 17 and 18 kDa β-subunitTOLLERSRUD, O. K; HEISKANEN, T; PELTONEN, L et al.Biochemical journal (London. 1984). 1994, Vol 300, pp 541-544, issn 0264-6021, 2Article

Lysosomal aspartylglucosaminidase is processed to the active subunit complex in the endoplasmic reticulumIKONEN, E; JULKUNEN, I; TOLLERSRUD, O.-K et al.EMBO journal (Print). 1993, Vol 12, Num 1, pp 295-302, issn 0261-4189Article

Assignment of the aspartylglucosaminidase gene (AGA) to 4q33→q35 based on decreased activity in a girl with a 46,XX,del(4)(q33)karyotypeENGELEN, J; HAMERS, A; SCHRANDER-STUMPEL, C et al.Cytogenetics and cell genetics. 1992, Vol 60, Num 3-4, pp 208-209, issn 0301-0171Conference Paper

Effect of Vitreoscilla Hemoglobin and Culture Conditions on Production of Bacterial L-Asparaginase, an Oncolytic EnzymeERENLER, Sebnem O; GECKIL, Hikmet.Applied biochemistry and biotechnology. 2014, Vol 173, Num 8, pp 2140-2151, issn 0273-2289, 12 p.Article

Isolation of a human hepatic 60 kDa aspartylglucosaminidase consisting of three non-identical polypeptidesBAUMANN, M; PELTONEN, L; AULA, P et al.Biochemical journal (London. 1906). 1989, Vol 262, Num 1, pp 189-194, issn 0006-2936Article

Purification and structure of human liver aspartylglucosaminidaseRIP, J. W; COULTER-MACKIE, M. B; RUPAR, C. A et al.Biochemical journal (London. 1984). 1992, Vol 288, pp 1005-1010, issn 0264-6021, 3Article

The first demonstration of a procaryotic glycosylasparaginaseTARENTINO, A. L; PLUMMER, T. H.Biochemical and biophysical research communications (Print). 1993, Vol 197, Num 1, pp 179-186, issn 0006-291XArticle

Chromosomal localization of the human glycoasparaginase gene to 4q32-q33MORRIS, C; HEISTERKAMP, N; GROFFEN, J et al.Human genetics. 1992, Vol 88, Num 3, pp 295-297, issn 0340-6717Article

Glycoasparaginase in human urineKAARTINEN, V.Biochimica et biophysica acta. Molecular basis of disease. 1991, Vol 1097, Num 1, pp 28-30, 3 p.Article

Comparison of liver glycosylasparaginases from six vertebratesTOLLERSRUD, O. K; ARONSON, N. N.Biochemical journal (London. 1984). 1992, Vol 282, pp 891-897, issn 0264-6021, 3Article

The turnover of lysosomal glycosylasparaginase in rat liverTOLLERSRUD, O. K; HOFMANN, S. H; ARONSON, N. N. JR et al.Biochimica et biophysica acta. 1988, Vol 953, Num 3, pp 353-356, issn 0006-3002Article

Dissection of the molecular pathology of aspartylglucosaminuria provides the basis for DNA diagnosis and future therapeutic interventionsIKONEN, E; SYVÄNEN, A.-C; PELTONEN, L et al.Scandinavian journal of clinical & laboratory investigation. Supplement. 1993, Vol 53, Num 213, pp 19-27, issn 0085-591XArticle

Single base deletion in exon 7 of the glycosylasparaginase gene causes a mild form of aspartylglycosaminuria in a patient of Mauritian originPARK, H; ROSSITER, M; FENSOM, A. H et al.Journal of inherited metabolic disease. 1996, Vol 19, Num 1, pp 76-83, issn 0141-8955Article

Urinary proteins and enzymes as early indicators of renal dysfunction in chronic exposure to cadmiumJUNG, K; PERGANDE, M; GRAUBAUM, H.-J et al.Clinical chemistry (Baltimore, Md.). 1993, Vol 39, Num 5, pp 757-765, issn 0009-9147Article

Glycoasparaginase from human leukocytes : inactivation and covalent modification with diazo-oxonorvalineKAARTINEN, V; WILLIAMS, J. C; TOMICH, J et al.The Journal of biological chemistry (Print). 1991, Vol 266, Num 9, pp 5860-5869, issn 0021-9258, 10 p.Article

Deletion of exon 8 causes glycosylasparaginase deficiency in an African American aspartylglucosaminuria (AGU) patientFISHER, K. J; ARONSON, N. N.FEBS letters. 1991, Vol 288, Num 1-2, pp 173-178, issn 0014-5793Article

Human aspartylglucosaminidase : a biochemical and immunocytochemical characterization of the enzyme in normal and aspartylglucosaminuria fibroblastsENOMAA, N; HEISKANEN, T; HALILA, R et al.Biochemical journal (London. 1984). 1992, Vol 286, pp 613-618, issn 0264-6021, 2Article

A novel exonic mutation in the aspartylglucosaminidase gene causes exon skippingCOULTER-MACKIE, M. B.Journal of inherited metabolic disease. 1999, Vol 22, Num 5, pp 682-683, issn 0141-8955Article

Deletion of the C-terminal end of asparthylglucosaminidase resulting in a lysosomal accumulation disease : evidence for a unique genomic rearrangementJALANKO, A; MANNINEN, T; PELTONEN, L et al.Human molecular genetics (Print). 1995, Vol 4, Num 3, pp 435-441, issn 0964-6906Article

A fluorometric assay for glycosylasparaginase activity and detection of aspartylglycosaminuriaMONONEN, I. T; KAARTINEN, V. M; WILLIAMS, J. C et al.Analytical biochemistry. 1993, Vol 208, Num 2, pp 372-374, issn 0003-2697Article

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