Heparitin Sulfate

N-acetyl-alpha-glucosaminidase ; Homo sapiens







30 Article(s)
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1 34806811 Sanfilippo syndrome type B: Analysis of patients diagnosed by the MPS Brazil Network. 2022 Mar 2
2 33839004 Biochemical evaluation of intracerebroventricular rhNAGLU-IGF2 enzyme replacement therapy in neonatal mice with Sanfilippo B syndrome. 2021 Jun 1
3 34106504 Iminosugar C-Glycosides Work as Pharmacological Chaperones of NAGLU, a Glycosidase Involved in MPS IIIB Rare Disease*. 2021 Aug 5 2
4 34165649 A GH89 human α-N-acetylglucosaminidase (hNAGLU) homologue from gut microbe Bacteroides thetaiotaomicron capable of hydrolyzing heparosan oligosaccharides. 2021 Jun 24 3
5 34411609 Disease modeling for Mucopolysaccharidosis type IIIB using patient derived induced pluripotent stem cells. 2021 Oct 1 5
6 35155448 Downregulation of NAGLU in VEC Increases Abnormal Accumulation of Lysosomes and Represents a Predictive Biomarker in Early Atherosclerosis. 2021 2
7 31965290 Cerebellar tumour-like aggregate of glycosaminoglycans in a MPS IIIB patient: a case report. 2020 Sep 1
8 30635159 Final results of the phase 1/2, open-label clinical study of intravenous recombinant human N-acetyl-α-d-glucosaminidase (SBC-103) in children with mucopolysaccharidosis IIIB. 2019 Feb 2
9 31309128 Differential Uptake of NAGLU-IGF2 and Unmodified NAGLU in Cellular Models of Sanfilippo Syndrome Type B. 2019 Sep 13 8
10 28836185 High-Throughput Screen Fails to Identify Compounds That Enhance Residual Enzyme Activity of Mutant N-Acetyl-α-Glucosaminidase in Mucopolysaccharidosis Type IIIB. 2018 1
11 28751108 Processing of mutant N-acetyl-α-glucosaminidase in mucopolysaccharidosis type IIIB fibroblasts cultured at low temperature. 2017 Sep 2
12 26907177 Residual N-acetyl-α-glucosaminidase activity in fibroblasts correlates with disease severity in patients with mucopolysaccharidosis type IIIB. 2016 May 6
13 25256447 Early Umbilical Cord Blood-Derived Stem Cell Transplantation Does Not Prevent Neurological Deterioration in Mucopolysaccharidosis Type III. 2015 1
14 23667853 A novel mutation (c.200T>C) in the NAGLU gene of a Korean patient with mucopolysaccharidosis IIIB. 2013 May 2
15 22156940 GM130 gain-of-function induces cell pathology in a model of lysosomal storage disease. 2012 Apr 1 2
16 21685203 Modeling neuronal defects associated with a lysosomal disorder using patient-derived induced pluripotent stem cells. 2011 Sep 15 2
17 21910976 Molecular characterization of MPS IIIA, MPS IIIB and MPS IIIC in Tunisian patients. 2011 Nov 20 1
18 19399896 Intravenous administration of human umbilical cord blood cells in an animal model of MPS III B. 2009 Jul 1 2
19 19416848 Sanfilippo syndrome type B, a lysosomal storage disease, is also a tauopathy. 2009 May 19 1
20 17640047 Is Sanfilippo type B in your mind when you see adults with mental retardation and behavioral problems? 2007 Aug 15 1
21 16137227 Transplantation of human umbilical cord blood cells benefits an animal model of Sanfilippo syndrome type B. 2005 Aug 1
22 11793481 Sanfilippo syndrome in Turkey: Identification of novel mutations in subtypes A and B. 2002 Feb 1
23 11068184 Mucopolysaccharidosis type IIIB: characterisation and expression of wild-type and mutant recombinant alpha-N-acetylglucosaminidase and relationship with sanfilippo phenotype in an attenuated patient. 2000 Nov 15 1
24 11153910 Molecular defects in the alpha-N-acetylglucosaminidase gene in Italian Sanfilippo type B patients. 2000 Dec 1
25 10094189 Sanfilippo type B syndrome (mucopolysaccharidosis III B): allelic heterogeneity corresponds to the wide spectrum of clinical phenotypes. 1999 Jan 2
26 9443878 NAGLU mutations underlying Sanfilippo syndrome type B. 1998 Jan 2
27 9832037 Identification of 12 novel mutations in the alpha-N-acetylglucosaminidase gene in 14 patients with Sanfilippo syndrome type B (mucopolysaccharidosis type IIIB). 1998 Nov 2
28 8776591 Cloning and expression of the gene involved in Sanfilippo B syndrome (mucopolysaccharidosis III B). 1996 Jun 1
29 8973472 Differences in the nonreducing ends of heparan sulfates excreted by patients with mucopolysaccharidoses revealed by bacterial heparitinases: a new tool for structural studies and differential diagnosis of Sanfilippo's and Hunter's syndromes. 1996 Dec 1
30 6402508 Utilization of exogenously added acetyl coenzyme A by intact isolated lysosomes. 1983 Mar 10 2