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Multiple polymorphisms within the α-L-iduronidase gene (IDUA): implications for a role in modification of MPS-I disease phenotypeSCOTT, H. S; NELSON, P. V; LITJENS, T et al.Human molecular genetics (Print). 1993, Vol 2, Num 9, pp 1471-1473, issn 0964-6906Article

Human α-L-iduronidase : cDNA isolation and expressionSCOTT, H. S; ANSON, D. S; ORSBORN, A. M et al.Proceedings of the National Academy of Sciences of the United States of America. 1991, Vol 88, Num 21, pp 9695-9699, issn 0027-8424Article

Structure and sequence of the human α-L-iduronidase geneSCOTT, H. S; XIAO-HUI GUO; HOPWOOD, J. J et al.Genomics (San Diego, Calif.). 1992, Vol 13, Num 4, pp 1311-1313, issn 0888-7543Article

Human α-L-iduronidase. I: Purification and properties of the high uptake (higher molecular weight) and the low uptake (processed) formsSCHUCHMAN, E. H; GUZMAN, N. A; DESNICK, R. J et al.The Journal of biological chemistry (Print). 1984, Vol 259, Num 5, pp 3132-3140, issn 0021-9258Article

Post-transcriptional factors are important for high-level expression of the human α-L-iduronidase gene in Arabidopsis cgl (complex -glycan -deficient) seedsDOWNING, Willa L; XIAOKE HU; KERMODE, Allison R et al.Plant science (Limerick). 2007, Vol 172, Num 2, pp 327-334, issn 0168-9452, 8 p.Article

Purification, characterization and subcellular localization of pig liver α-L-iduronidaseOHSHITA, T; SAKUDA, H; NAKASONE, S et al.European journal of biochemistry (Print). 1989, Vol 179, Num 1, pp 201-207, issn 0014-2956Article

Human α-L-iduronidase. II: Catalytic propertiesCLEMENTS, P. R; MULLER, V; HOPWOOD, J. J et al.European journal of biochemistry (Print). 1985, Vol 152, Num 1, pp 29-34, issn 0014-2956Article

The clinical spectrum of α-L-iduronidase deficiencyROUBICEK, M; GEHLER, J; SPRANGER, J et al.American journal of medical genetics. 1985, Vol 20, Num 3, pp 471-481, issn 0148-7299Article

Hurler syndrome : a patient with abnormally high levels of α-L-iduronidase proteinBROOKS, D. A; HARPER, G. S; GIBSON, G. J et al.Biochemical medicine and metabolic biology. 1992, Vol 47, Num 3, pp 211-220, issn 0885-4505Article

Immunoquantification and enzyme kinetics of α-L-iduronidase in cultured fibroblasts from normal controls and mucopolysaccharidosis type I patientsASHTON, L. J; BROOKS, D. A; MCCOURT, P. A. G et al.American journal of human genetics. 1992, Vol 50, Num 4, pp 787-794, issn 0002-9297Article

Characteristics of leukocyte and plasma methylumbelliferyl-α-L-iduronide iduronidaseDEN TANDT, W. R; SCHARPE, S.Biochemical medicine and metabolic biology. 1989, Vol 41, Num 1, pp 18-24, issn 0885-4505, 7 p.Article

Biochemical characterization of fluorescent-labeled recombinant human alpha-L-iduronidase in vitroTIPPIN, Brigette L; TROITSKAYA, Larisa; KAN, Shih-Hsin et al.Biotechnology and applied biochemistry. 2011, Vol 58, pp 391-396, issn 0885-4513, 6 p., 6Article

PRENATAL EXCLUSION OF HURLER'S DISEASE BY LEUCOCYTE ALPHA -L-IDURONIDASE ASSAYRODECK CH; TANSLEY RL; BENSON PF et al.1983; PRENATAL DIAGNOSIS; ISSN 0197-3851; GBR; DA. 1983; VOL. 3; NO 1; PP. 61-63; BIBL. 8 REF.Article

Human α-L-iduronidase : catalytic properties and an integrated role in the lysosomal degradation of heparan sulphateFREEMAN, C; HOPWOOD, J. J.Biochemical journal (London. 1984). 1992, Vol 282, pp 899-908, issn 0264-6021, 3Article

Tissue and cellular distribution of α-L-Iduronidase in the pigSAKUDA, H; KUSABA, A; OHSHITA, T et al.The Journal of histochemistry and cytochemistry. 1990, Vol 38, Num 6, pp 785-792, issn 0022-1554Article

Alterations in neuron morphology in mucopolysaccharidosis type I: a Golgi studyWALKLEY, S. U; HASKINS, M. E; SHULL, R. M et al.Acta neuropathologica. 1988, Vol 75, Num 6, pp 611-620, issn 0001-6322Article

Detection of mucopolysaccharidosis type I heterozygotes on the basis of the biochemical properties of plasma α-L-iduronidaseMANDELLI, Jovana; WAJNER, Alessandro; PIRES, Ricardo et al.Clinica chimica acta. 2001, Vol 312, Num 1-2, pp 81-86, issn 0009-8981Article

An 86-bp VNTR within IDUA is the basis of the D4S111 polymorphic locusSCOTT, H. S; NELSON, P. V; MACDONALD, M. E et al.Genomics (San Diego, Calif.). 1992, Vol 14, Num 4, pp 1118-1120, issn 0888-7543Article

THE USE OF ALPHA -L-IDURONIDASE ACTIVITY DETERMINATIONS IN LEUCOCYTES FOR THE DETECTION OF HURLER AND SCHEIE SYNDROMES = UTILISATION DU DOSAGE DE L'ACTIVITE ALPHA -L-IDURONIDASIQUE DES LEUCOCYTES POUR LA DETECTION DES SYNDROMES DE HURLER ET DE SCHEIELIEM KO; HOOGHWINKEL GJM.1975; CLIN. CHIM. ACTA; U.S.A.; DA. 1975; VOL. 60; NO 2; PP. 259-262; BIBL. 12REF.Article

Regional assignment of the structural gene for human α-L-iduronidaseSCHUCHMAN, E. H; ASTRIN, K. H; AULA, P et al.Proceedings of the National Academy of Sciences of the United States of America. Biological sciences. 1984, Vol 81, Num 4, pp 1169-1173, issn 0273-1134Article

Selective depolymerisation of dermatan sulfate: production of radiolabelled substrates for α-L-iduronidase, sulfoiduronate sulfatase, and β-D-glucuronidaseHOPWOOD, J. J; MULLER, V. J.Carbohydrate research. 1983, Vol 122, Num 2, pp 227-239, issn 0008-6215Article

Huntington disease-linked locus D4S111 exposed as the α-L-iduronidase geneMACDONALD, M. E; SCOTT, H. S; WHALEY, W. L et al.Somatic cell and molecular genetics. 1991, Vol 17, Num 4, pp 421-425, issn 0740-7750Article

Immunopurification and characterization of human α-L-iduronidase with the use of monoclonal antibodiesCLEMENTS, P. R; BROOKS, D. A; MCCOURT, P. A. G et al.Biochemical journal (London. 1906). 1989, Vol 259, Num 1, pp 199-208, issn 0006-2936Article

Hurler-Scheie phenotype associated with consanguinityDAVIES, D. L; DUTTON, G. N; FARQUHARSON, J et al.Journal of inherited metabolic disease. 1989, Vol 12, pp 365-368, issn 0141-8955, suppl. 2Article

Mucopolysaccharidosis Type I in 21 Czech and Slovak Patients : Mutation Analysis Suggests a Functional Importance of C-Terminus of the IDUA ProteinVAZNA, Alzbeta; BEESLEY, Clare; HLAVATA, Anna et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 5, pp 965-974, issn 1552-4825, 10 p.Article

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