BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

286 related articles for article (PubMed ID: 9482575)

  • 1. 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; 11(2):121-6. PubMed ID: 9482575
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Analysis of a 43.6 kb deletion in a patient with Hunter syndrome (MPSII): identification of a fusion transcript including sequences from the gene W and the IDS gene.
    Lagerstedt K; Carlberg BM; Karimi-Nejad R; Kleijer WJ; Bondeson ML
    Hum Mutat; 2000; 15(4):324-31. PubMed ID: 10737977
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 43(2):123-9. PubMed ID: 9244428
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 36(1):21-7. PubMed ID: 9950361
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 14(6):471-6. PubMed ID: 10571944
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 526(2):150-4. PubMed ID: 23707223
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations of the iduronate-2-sulfatase (IDS) gene in patients with Hunter syndrome (mucopolysaccharidosis II).
    Schröder W; Wulff K; Wehnert M; Seidlitz G; Herrmann FH
    Hum Mutat; 1994; 4(2):128-31. PubMed ID: 7981716
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Deletion of the Hunter gene and both DXS466 and DXS304 in a patient with mucopolysaccharidosis type II.
    Beck M; Steglich C; Zabel B; Dahl N; Schwinger E; Hopwood JJ; Gal A
    Am J Med Genet; 1992 Sep; 44(1):100-3. PubMed ID: 1355630
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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; 23(1):67-9. PubMed ID: 16456790
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Differences in methylation patterns in the methylation boundary region of IDS gene in Hunter syndrome patients: implications for CpG hot spot mutations.
    Tomatsu S; Sukegawa K; Trandafirescu GG; Gutierrez MA; Nishioka T; Yamaguchi S; Orii T; Froissart R; Maire I; Chabas A; Cooper A; Di Natale P; Gal A; Noguchi A; Sly WS
    Eur J Hum Genet; 2006 Jul; 14(7):838-45. PubMed ID: 16617305
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A 38.8 kb deletion mutation of the iduronate-2-sulfatase gene in a patient with Hunter syndrome.
    Chou YY; Chao SC; Kuo PL; Lin SJ
    J Formos Med Assoc; 2005 Apr; 104(4):273-5. PubMed ID: 15909065
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Detection of a new mutation (G1253T) of iduronate-2-sulfatase gene for the patient with mucopolysaccharidosis type II].
    Zhang CY; Li LY; Liu SF; Fu JJ; Lu GX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Jun; 21(3):269-71. PubMed ID: 15192834
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of an alternative transcript from the human iduronate-2-sulfatase (IDS) gene.
    Malmgren H; Carlberg BM; Pettersson U; Bondeson ML
    Genomics; 1995 Sep; 29(1):291-3. PubMed ID: 8530090
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutational spectrum of the iduronate 2 sulfatase gene in 25 unrelated Korean Hunter syndrome patients: identification of 13 novel mutations.
    Kim CH; Hwang HZ; Song SM; Paik KH; Kwon EK; Moon KB; Yoon JH; Han CK; Jin DK
    Hum Mutat; 2003 Apr; 21(4):449-50. PubMed ID: 12655569
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [The detection of the frequent mutations of iduronate-2-sulphatase gene in mucopolysaccharidosis type II patients in Chinese].
    Liu S; Li L; Fu J; Zhong C; Lu G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Jun; 19(3):243-5. PubMed ID: 12048688
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular analysis of 40 Italian patients with mucopolysaccharidosis type II: New mutations in the iduronate-2-sulfatase (IDS) gene.
    Filocamo M; Bonuccelli G; Corsolini F; Mazzotti R; Cusano R; Gatti R
    Hum Mutat; 2001 Aug; 18(2):164-5. PubMed ID: 11462244
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations of the iduronate-2-sulfatase gene on a T146T background in three patients with Hunter syndrome.
    Li P; Huffman P; Thompson JN
    Hum Mutat; 1995; 5(3):272-4. PubMed ID: 7599640
    [No Abstract]   [Full Text] [Related]  

  • 19. Mutation analysis of iduronate-2-sulphatase gene in 24 patients with Hunter syndrome: characterisation of 6 novel mutations. Mutation in brief no. 249. Online.
    Hartog C; Fryer A; Upadhyaya M
    Hum Mutat; 1999; 14(1):87. PubMed ID: 10447264
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 6(5):492-500. PubMed ID: 9801874
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.