These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

49 related articles for article (PubMed ID: 20960629)

  • 1. Gene symbol: IDS. Disease: Hunter syndrome.
    Oller Ramirez AM; Coll MJ; Chabás A; Azar NB; Ghio AV; Kremer RD
    Hum Genet; 2008 Jun; 123(5):546. PubMed ID: 20960629
    [No Abstract]   [Full Text] [Related]  

  • 2. Gene symbol: IDS. Disease: mucopolysaccharidosis type II (Hunter syndrome).
    Villani GR; Pontarelli G; Kotroni G; Parenti G; Sibilio M; Andria G; Di Natale P
    Hum Genet; 2006 Jul; 119(6):682. PubMed ID: 16738950
    [No Abstract]   [Full Text] [Related]  

  • 3. Gene symbol: IDS. Disease: Mucopolysaccharidosis II.
    Oller Ramirez AM; Coll MJ; Chabás A; Azar NB; Ghio AV; Kremer RD
    Hum Genet; 2008 Jun; 123(5):545. PubMed ID: 20960627
    [No Abstract]   [Full Text] [Related]  

  • 4. Detection of Hunter syndrome (mucopolysaccharidosis type II) in Taiwanese: biochemical and linkage studies of the iduronate-2-sulfatase gene defects in MPS II patients and carriers.
    Lin SP; Chang JH; Lee-Chen GJ; Lin DS; Lin HY; Chuang CK
    Clin Chim Acta; 2006 Jul; 369(1):29-34. PubMed ID: 16480701
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Hunter syndrome: gene deletions and rearrangements.
    Froissart R; Blond JL; Maire I; Guibaud P; Hopwood JJ; Mathieu M; Bozon D
    Hum Mutat; 1993; 2(2):138-40. PubMed ID: 8318991
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Novel Mutation in the IDS Gene in Hunter Syndrome Associated with Severe Cardiac Lesions.
    Satekge TM; Honey EM; Pitso B; Dercksen M; Pillay TS
    Clin Chem; 2021 Mar; 67(3):564-566. PubMed ID: 33674846
    [No Abstract]   [Full Text] [Related]  

  • 13. [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]  

  • 14. 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]  

  • 15. Mucopolysaccharidosis type II in females: case report and review of literature.
    Tuschl K; Gal A; Paschke E; Kircher S; Bodamer OA
    Pediatr Neurol; 2005 Apr; 32(4):270-2. PubMed ID: 15797184
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Mucopolysaccharidosis II (Hunter syndrome): identification of the carrier state of the disease by means of mutation analysis].
    Balzano N; Villani GR; Coppa G; Di Natale P
    Pediatr Med Chir; 1996; 18(1):91-3. PubMed ID: 8685031
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. Two new nonsense mutations (Q80X; Q389X) in patients with severe Hunter syndrome (mucopolysaccharidosis type II.).
    Carrozzo R; Tonlorenzi R; Corsolini F; Gatti R
    Hum Mutat; 1996; 7(2):184-5. PubMed ID: 8829647
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 3.