iduronate 2-sulfatase ; Homo sapiens






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1 106967 alpha-L-iduronidase, beta-D-glucuronidase, and 2-sulfo-L-iduronate 2-sulfatase: preparation and characterization of radioactive substrates from heparin. Carbohydr Res 1979 Mar 2
2 203648 Regulatory substances produced by lymphocytes. VI. Cell cycle specificity of inhibitor of DNA synthesis action in L cells. J Exp Med 1978 Jan 1 4
3 1670748 Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA). Am J Hum Genet 1991 Jan 1
4 2122463 Hunter syndrome: isolation of an iduronate-2-sulfatase cDNA clone and analysis of patient DNA. Proc Natl Acad Sci U S A 1990 Nov 4
5 2428915 Idiotypic network connectivity and a possible cause of myasthenia gravis. J Exp Med 1986 Oct 1 1
6 2713547 Mass spectrometric analysis of cardiac glycosides by the desorption/ionization technique potassium ion ionization of desorbed species. Biomed Environ Mass Spectrom 1989 Mar 10
7 3043316 [Experiences with the preventive use of aminophylline (Euphylline) in apnea and periodic respiration in infants]. Padiatr Padol 1988 1
8 3214676 Potassium ion ionization of desorbed species (K+IDS): a rapid method for the screening of urine for organic acidemias. Biomed Environ Mass Spectrom 1988 Sep 2
9 7626005 Processing of iduronate 2-sulphatase in human fibroblasts. Biochem J 1995 Jul 15 4
10 7663435 Expression of the two iduronate-2-sulfatase cDNAs. Biochem Mol Biol Int 1995 Jun 5
11 8168940 Variable region sequences and idiotypic expression of a protective human immunoglobulin M antibody to capsular polysaccharides of Neisseria meningitidis group B and Escherichia coli K1. Infect Immun 1994 May 2
12 8193474 Nicotine and cotinine levels in pericardial fluid in victims of SIDS. Acta Paediatr 1994 Jan 4
13 8244397 Sequence of the human iduronate 2-sulfatase (IDS) gene. Genomics 1993 Sep 6
14 8265633 Metabolic correction and cross-correction of mucopolysaccharidosis type II (Hunter syndrome) by retroviral-mediated gene transfer and expression of human iduronate-2-sulfatase. Proc Natl Acad Sci U S A 1993 Dec 15 1
15 8387617 Psychometric evaluation of a short form of the inventory of drinking situations. J Stud Alcohol 1993 May 1
16 8518808 Dinucleotide repeat polymorphism close to IDS gene in Xq27.3-q28 (DXS1113). Hum Mol Genet 1993 May 1
17 8530090 Identification of an alternative transcript from the human iduronate-2-sulfatase (IDS) gene. Genomics 1995 Sep 1 4
18 8556564 Human auto-anti-idiotypic antibodies to mite-specific IgE can degranulate human basophils in vitro. Clin Exp Allergy 1995 Oct 2
19 9337875 Characterization of iduronate sulphatase mutants affecting N-glycosylation sites and the cysteine-84 residue. Biochem J 1997 Aug 15 6
20 9370236 Decreased kainate receptor binding in the arcuate nucleus of the sudden infant death syndrome. J Neuropathol Exp Neurol 1997 Nov 1
21 10388343 Inborn defects of fatty acid oxidation: a preventable cause of SIDS. S D J Med 1999 Jun 1
22 10447264 Mutation analysis of iduronate-2-sulphatase gene in 24 patients with Hunter syndrome: characterisation of 6 novel mutations. Mutation in brief no. 249. Online. Hum Mutat 1999 2
23 10500241 The 2.1-, 5.4- and 5.7-kb transcripts of the IDS gene are generated by different polyadenylation signals. Biochim Biophys Acta 1999 Oct 6 1
24 10584926 Combined ultrafiltration-transduction in a hollow-fiber bioreactor facilitates retrovirus-mediated gene transfer into peripheral blood lymphocytes from patients with mucopolysaccharidosis type II. Hum Gene Ther 1999 Nov 20 1
25 11768586 A fluorimetric enzyme assay for the diagnosis of MPS II (Hunter disease). J Inherit Metab Dis 2001 Nov 4
26 12393174 Uptake of recombinant iduronate-2-sulfatase into neuronal and glial cells in vitro. Biochim Biophys Acta 2002 Dec 12 1
27 12572850 Enzyme replacement therapy in mucopolysaccharidosis type II (Hunter syndrome): a preliminary report. Acta Paediatr Suppl 2002 5
28 15500445 Analysis of normal and mutant iduronate-2-sulphatase conformation. Biochem J 2005 Mar 1 4
29 16377754 A defect in exodegradative pathways provides insight into endodegradation of heparan and dermatan sulfates. Glycobiology 2006 Apr 2
30 16497940 Detection of mucopolysaccharidosis type II by measurement of iduronate-2-sulfatase in dried blood spots and plasma samples. Clin Chem 2006 Apr 1
31 17185020 A phase I/II clinical trial of enzyme replacement therapy in mucopolysaccharidosis II (Hunter syndrome). Mol Genet Metab 2007 Mar 1
32 17345556 [Clinical study of enzyme replacement therapy with idursulfase]. Rev Neurol 2007 Feb 19 2
33 17459751 Preclinical dose ranging studies for enzyme replacement therapy with idursulfase in a knock-out mouse model of MPS II. Mol Genet Metab 2007 Jun 4
34 17616540 Molecular analysis in two siblings African patients with severe form of Hunter Syndrome: identification of a novel (p.Y54X) nonsense mutation. J Trop Pediatr 2007 Dec 4
35 17876721 The characterization of a murine model of mucopolysaccharidosis II (Hunter syndrome). J Inherit Metab Dis 2007 Nov 3
36 18174963 Idursulfase in Hunter syndrome treatment. Drugs Today (Barc) 2007 Nov 6
37 18245410 Recognition and diagnosis of mucopolysaccharidosis II (Hunter syndrome). Pediatrics 2008 Feb 1
38 18331837 Molecular investigations of a novel iduronate-2-sulfatase mutant in a Chinese patient. Clin Chim Acta 2008 Jun 3
39 18367670 The lack of anti-idiotypic antibodies, not the presence of the corresponding autoantibodies to glutamate decarboxylase, defines type 1 diabetes. Proc Natl Acad Sci U S A 2008 Apr 8 1
40 18396123 Early response to idursulfase treatment in a 3 year-old boy affected of Hunter syndrome. Eur J Med Genet 2008 May-Jun 2
41 18580692 Initial report from the Hunter Outcome Survey. Genet Med 2008 Jul 1
42 19602578 Role of iduronate-2-sulfatase in glucose-stimulated insulin secretion by activation of exocytosis. Am J Physiol Endocrinol Metab 2009 Sep 4
43 19707363 Review of the use of idursulfase in the treatment of mucopolysaccharidosis II. Biologics 2008 Jun 3
44 19933090 [Identification of a novel mutation of IDS gene from a Chinese pedigree with MPS II]. Yi Chuan 2009 Nov 4
45 20000684 Genetic engineering of a bifunctional IgG fusion protein with iduronate-2-sulfatase. Bioconjug Chem 2010 Jan 2
46 20038812 Human voltage-gated sodium channel mutations that cause inherited neuronal and muscle channelopathies increase resurgent sodium currents. J Clin Invest 2010 Jan 4
47 20361748 Measurement of urinary total desmosine and isodesmosine using isotope-dilution liquid chromatography-tandem mass spectrometry. Anal Chem 2010 May 1 4
48 20652491 Characterization of a novel mucopolysaccharidosis type II mouse model and recombinant AAV2/8 vector-mediated gene therapy. Mol Cells 2010 Jul 8
49 20658560 Overestimation of the 25(OH)D serum concentration with the automated IDS EIA kit. J Bone Miner Res 2011 Feb 2
50 21192662 Tandem mass spectrometry for the direct assay of lysosomal enzymes in dried blood spots: application to screening newborns for mucopolysaccharidosis II (Hunter Syndrome). Anal Chem 2011 Feb 1 8