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Journal Abstract Search

269 related items for PubMed ID: 8244397

  • 1. Sequence of the human iduronate 2-sulfatase (IDS) gene.
    Wilson PJ, Meaney CA, Hopwood JJ, Morris CP.
    Genomics; 1993 Sep; 17(3):773-5. PubMed ID: 8244397
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  • 2. Morquio A syndrome: cloning, sequence, and structure of the human N-acetylgalactosamine 6-sulfatase (GALNS) gene.
    Morris CP, Guo XH, Apostolou S, Hopwood JJ, Scott HS.
    Genomics; 1994 Aug; 22(3):652-4. PubMed ID: 8001980
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  • 3. Identification of an alternative transcript from the human iduronate-2-sulfatase (IDS) gene.
    Malmgren H, Carlberg BM, Pettersson U, Bondeson ML.
    Genomics; 1995 Sep 01; 29(1):291-3. PubMed ID: 8530090
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  • 4. Cloning and characterization of the cDNA for the murine iduronate sulfatase gene.
    Daniele A, Faust CJ, Herman GE, Di Natale P, Ballabio A.
    Genomics; 1993 Jun 01; 16(3):755-7. PubMed ID: 8325651
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  • 5. DNA deletion confined to the iduronate-2-sulfatase promoter abolishes IDS gene expression.
    Timms KM, Huckett LE, Belmont JW, Shapira SK, Gibbs RA.
    Hum Mutat; 1998 Jun 01; 11(2):121-6. PubMed ID: 9482575
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  • 6. Extension of the molecular analysis to the promoter region of the iduronate 2-sulfatase gene reveals genomic alterations in mucopolysaccharidosis type II patients with normal coding sequence.
    Brusius-Facchin AC, Abrahão L, Schwartz IV, Lourenço CM, Santos ES, Zanetti A, Tomanin R, Scarpa M, Giugliani R, Leistner-Segal S.
    Gene; 2013 Sep 10; 526(2):150-4. PubMed ID: 23707223
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  • 7. Molecular basis of iduronate-2-sulphatase gene mutations in patients with mucopolysaccharidosis type II (Hunter syndrome).
    Li P, Bellows AB, Thompson JN.
    J Med Genet; 1999 Jan 10; 36(1):21-7. PubMed ID: 9950361
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  • 9. Novel type of genetic rearrangement in the iduronate-2-sulfatase (IDS) gene involving deletion, duplications, and inversions.
    Karsten S, Voskoboeva E, Krasnopolskaja X, Bondeson ML.
    Hum Mutat; 1999 Jan 10; 14(6):471-6. PubMed ID: 10571944
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  • 12. Two distinct deletions in the IDS gene and the gene W: a novel type of mutation associated with the Hunter syndrome.
    Karsten SL, Lagerstedt K, Carlberg BM, Kleijer WJ, Zaremba J, Van Diggelen OP, Czartoryska B, Pettersson U, Bondeson ML.
    Genomics; 1997 Jul 15; 43(2):123-9. PubMed ID: 9244428
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  • 13. Mucopolysaccharidosis IV A: molecular cloning of the human N-acetylgalactosamine-6-sulfatase gene (GALNS) and analysis of the 5'-flanking region.
    Nakashima Y, Tomatsu S, Hori T, Fukuda S, Sukegawa K, Kondo N, Suzuki Y, Shimozawa N, Orii T.
    Genomics; 1994 Mar 01; 20(1):99-104. PubMed ID: 8020961
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  • 14. Genomic organization of the JEM-1 (BLZF1) gene on human chromosome 1q24: molecular cloning and analysis of its promoter region.
    Tong JH, Fant X, Benoit G, Chen SJ, Chen Z, Lanotte M.
    Genomics; 2000 Nov 01; 69(3):380-90. PubMed ID: 11056056
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  • 15. Hunter syndrome: isolation of an iduronate-2-sulfatase cDNA clone and analysis of patient DNA.
    Wilson PJ, Morris CP, Anson DS, Occhiodoro T, Bielicki J, Clements PR, Hopwood JJ.
    Proc Natl Acad Sci U S A; 1990 Nov 01; 87(21):8531-5. PubMed ID: 2122463
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  • 16. Homologous nonallelic recombinations between the iduronate-sulfatase gene and pseudogene cause various intragenic deletions and inversions in patients with mucopolysaccharidosis type II.
    Bunge S, Rathmann M, Steglich C, Bondeson ML, Tylki-Szymanska A, Popowska E, Gal A.
    Eur J Hum Genet; 1998 Nov 01; 6(5):492-500. PubMed ID: 9801874
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  • 17. Presence of an IDS-related locus (IDS2) in Xq28 complicates the mutational analysis of Hunter syndrome.
    Bondeson ML, Malmgren H, Dahl N, Carlberg BM, Pettersson U.
    Eur J Hum Genet; 1995 Nov 01; 3(4):219-27. PubMed ID: 8528670
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  • 19. IDS gene-pseudogene exchange responsible for an intragenic deletion in a Hunter patient.
    Birot AM, Bouton O, Froissart R, Maire I, Bozon D.
    Hum Mutat; 1996 Nov 01; 8(1):44-50. PubMed ID: 8807335
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  • 20. [A new mutation of iduronate-2-sulfatase gene from the patient with Hunter syndrome].
    Guo YB, Lin QD, Du CS.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Feb 01; 23(1):67-9. PubMed ID: 16456790
    [Abstract] [Full Text] [Related]

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