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iduronate 2-sulfate and Mucopolysaccharidosis II

iduronate 2-sulfate has been researched along with Mucopolysaccharidosis II in 3 studies

*Mucopolysaccharidosis II: Systemic lysosomal storage disease marked by progressive physical deterioration and caused by a deficiency of L-sulfoiduronate sulfatase. This disease differs from MUCOPOLYSACCHARIDOSIS I by slower progression, lack of corneal clouding, and X-linked rather than autosomal recessive inheritance. The mild form produces near-normal intelligence and life span. The severe form usually causes death by age 15. [MeSH]

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's1 (33.33)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ashbaugh, L; Basheeruddin, K; Braddock, SR; Burton, BK; Christensen, KM; Fleischer, J; Grange, DK; Groepper, D; Hickey, R; Hitchins, L; Hoganson, GE; Kirby, A; Moody, C; Shao, R; Shryock, H1
Battini, R; Bembi, B; Corsolini, F; Cotugno, G; Di Rocco, M; Filocamo, M; Gabriela Pittis, M; Lualdi, S; Spada, M; Stroppiano, M1
Daniele, A; Di Natale, P1

Other Studies

3 other study(ies) available for iduronate 2-sulfate and Mucopolysaccharidosis II

ArticleYear
Population-Based Newborn Screening for Mucopolysaccharidosis Type II in Illinois: The First Year Experience.
    The Journal of pediatrics, 2019, Volume: 214

    Topics: Biomarkers; Dried Blood Spot Testing; Follow-Up Studies; Humans; Iduronic Acid; Illinois; Incidence; Infant, Newborn; Mucopolysaccharidosis II; Neonatal Screening; Reproducibility of Results; Retrospective Studies; Tandem Mass Spectrometry; Time Factors

2019
Identification of nine new IDS alleles in mucopolysaccharidosis II. Quantitative evaluation by real-time RT-PCR of mRNAs sensitive to nonsense-mediated and nonstop decay mechanisms.
    Biochimica et biophysica acta, 2006, Volume: 1762, Issue:4

    Topics: Alleles; Cells, Cultured; Child; Child, Preschool; Codon, Nonsense; Codon, Terminator; Frameshift Mutation; Genotype; Humans; Iduronic Acid; Infant; Mucopolysaccharidosis II; Mutation, Missense; Phenotype; Reverse Transcriptase Polymerase Chain Reaction; RNA Stability; RNA, Messenger; Sequence Deletion

2006
Expression of the two iduronate-2-sulfatase cDNAs.
    Biochemistry and molecular biology international, 1995, Volume: 36, Issue:2

    Topics: Animals; Base Sequence; Cell Line, Transformed; DNA Primers; Gene Expression; Humans; Iduronate Sulfatase; Iduronic Acid; Mice; Molecular Sequence Data; Mucopolysaccharidosis II; Polymerase Chain Reaction; RNA, Messenger; Tumor Cells, Cultured

1995