|1.||Nascu, Ioana: 1 article (01/2013)|
|2.||Grigorescu-Sido, Paula: 1 article (01/2013)|
|3.||Denes, Carmencita: 1 article (01/2013)|
|4.||Bucerzan, Simona: 1 article (01/2013)|
|5.||Al-Khzouz, Camelia: 1 article (01/2013)|
|6.||Lazea, Cecilia: 1 article (01/2013)|
|7.||Beck, Michael: 1 article (09/2011)|
|8.||Schulze-Frenking, Gudrun: 1 article (09/2011)|
|9.||Hoffmann, Björn: 1 article (09/2011)|
|10.||Al-Sawaf, Sulaiman: 1 article (09/2011)|
|1.||Mucopolysaccharidosis II (Hunter Syndrome)
05/01/2000 - "Hunter syndrome is an X-linked metabolic storage disorder arising from deficiency of iduronate sulfatase enzyme activity. "
03/01/1998 - "We describe 12 Hunter's syndrome patients and seven carriers, with precise analysis of glycosaminoglycan content in urine and iduronate sulfatase activity in cultured fibroblasts and plasma. "
01/01/1995 - "Evidence for an iduronate-sulfatase pseudogene near the functional Hunter syndrome gene in Xq27.3-q28."
01/01/1994 - "Hunter syndrome (mucopolysaccharidosis II) is an X-linked lysosomal storage disorder caused by the deficiency of iduronate sulfatase (IDS), the gene of which is located at Xq28. "
01/01/1992 - "The iduronate sulfatase gene: isolation of a 1.2-Mb YAC contig spanning the entire gene and identification of heterogeneous deletions in patients with Hunter syndrome."
05/01/2001 - "Type II mucopolysaccharidosis (Hunter's disease) is a hereditary condition due to a deficit of a lysosome specific hydrolase (iduronate sulfatase) inducing an accumulation of dermatane-sulphate and heparane-sulphate in certain organs. "
09/01/1998 - "About 20% of patients with mucopolysaccharidosis type II (MPS II) have gross structural rearrangements involving the iduronate-sulfatase (IDS) gene in Xq27.3-q28. "
09/01/1998 - "Homologous nonallelic recombinations between the iduronate-sulfatase gene and pseudogene cause various intragenic deletions and inversions in patients with mucopolysaccharidosis type II."
05/01/1995 - "Hunter disease, Mucopolysaccharidosis type II, is an X-linked recessive lysosomal storage disorder caused by a deficiency in iduronate sulfatase activity. "
03/16/1992 - "Intermediate form of mucopolysaccharidosis type II (Hunter disease): a C1327 to T substitution in the iduronate sulfatase gene."
|3.||Multiple Sulfatase Deficiency Disease (Mucosulfatidosis)
|4.||Lysosomal Storage Diseases (Lysosomal Storage Disease)
08/01/1976 - "The iduronate sulfatase activity of sera from patients with mucolipidoses II and III was elevated 20-fold, but their parents had a normal level of the enzyme. "
08/01/1976 - "In fibroblasts of patients with mucolipidoses II and III, both iduronate sulfatase and iduronidase activities were markedly decreased. "
|1.||Complementary DNA (cDNA)
|3.||Sulfates (Sulfates, Inorganic)
|4.||Staphylococcal Protein A (A, Protein)
|5.||Heparitin Sulfate (Heparan Sulfate)
|6.||DNA (Deoxyribonucleic Acid)
|2.||Transplantation (Transplant Recipients)