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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

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

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

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

Characterization of three alleles causing aspartylglycosaminuria : two from a British family and one from an American patientHYEJEONG PARK; VETTESE, M. B; FENSOM, A. H et al.Biochemical journal (London. 1984). 1993, Vol 290, pp 735-741, issn 0264-6021, 3Article

Characterization of the mutation responsible for aspartylglucosaminuria in three Finnish patients : amino acid substitution Cys163 → Ser abolishes the activity of lysosomal glycosylasparaginase and its conversion into subunitsFISHER, K. J; ARONSON, N. N.The Journal of biological chemistry (Print). 1991, Vol 266, Num 18, pp 12105-12113, issn 0021-9258Article

Interstitial tandem direct duplication of the long arm of chromosome 4 (q23-q27) and possible assignment of the structural gene encoding human aspartylglucosaminidase to this segmentHALAL, F; VEKEMANS, M; CHITAYAT, D et al.American journal of medical genetics. 1991, Vol 39, Num 4, pp 418-421, issn 0148-7299, 4 p.Article

Purification and characterization of rat liver glycosylasparaginaseTOLLERSRUD, O. K; ARONSON, N. N. JR.Biochemical journal (London. 1906). 1989, Vol 260, Num 1, pp 101-108, issn 0006-2936Article

Dissection of the molecular consequences of a double mutation causing a human lysosomal diseaseRIIKONEN, A; IKONEN, E; SORMUNEN, R et al.DNA and cell biology. 1994, Vol 13, Num 3, pp 257-264, issn 1044-5498Article

E. coli K-12 asparaginase-based asparagine biosensor for leukemiaVERMA, Neelam; KUMAR, Kuldeep; KAUR, Gurnoor et al.Artificial cells, blood substitutes, and biotechnology. 2007, Vol 35, Num 4, pp 449-456, 8 p.Article

Glycosylasparaginase as a marker enzyme in the detection of I-cell disease,YLIKANGAS, P. K; MONONEN, I. T.Clinical chemistry (Baltimore, Md.). 1998, Vol 44, Num 12, pp 2543-2544, issn 0009-9147Article

Aspartyglycosaminuria : protein chemistry and molecular biology of the most common lysosomal storage disorder of glycoprotein degradationMONONEN, I; FISHER, K. J; KAARTINEN, V et al.The FASEB journal. 1993, Vol 7, Num 13, pp 1247-1256, issn 0892-6638Article

L-Asparaginase release from Escherichia coli cells with aqueous two-phase micellar systemsMINJUN QIN; FENGSHENG ZHAO.Applied biochemistry and biotechnology. 2003, Vol 110, Num 1, pp 11-21, issn 0273-2289, 11 p.Article

Co-occurrence of both L-asparaginase subtypes in Arabidopsis : At3gl6150 encodes a K+-dependent L-asparaginaseBRUNEAU, Luanne; CHAPMAN, Ralph; MARSOLAIS, Frédéric et al.Planta. 2006, Vol 224, Num 3, pp 668-679, issn 0032-0935, 12 p.Article

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