172 related articles for article (PubMed ID: 1733863)
21. 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]
22. Gene diagnosis and carrier detection in Hunter syndrome by the iduronate-2-sulphatase cDNA probe.
Gal A; Beck M; Sewell AC; Morris CP; Schwinger E; Hopwood JJ
J Inherit Metab Dis; 1992; 15(3):342-6. PubMed ID: 1357230
[No Abstract] [Full Text] [Related]
23. 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]
24. Carrier detection of deletions of the Hunter gene by in situ hybridization.
Stone S; Adinolfi M
Ann Hum Genet; 1992 May; 56(2):93-7. PubMed ID: 1503397
[TBL] [Abstract][Full Text] [Related]
25. 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; 3(4):219-27. PubMed ID: 8528670
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Mucopolysaccharidosis type II (Hunter syndrome): mutation "hot spots" in the iduronate-2-sulfatase gene.
Rathmann M; Bunge S; Beck M; Kresse H; Tylki-Szymanska A; Gal A
Am J Hum Genet; 1996 Dec; 59(6):1202-9. PubMed ID: 8940265
[TBL] [Abstract][Full Text] [Related]
28. 130 kb of DNA sequence reveals two new genes and a regional duplication distal to the human iduronate-2-sulfate sulfatase locus.
Timms KM; Lu F; Shen Y; Pierson CA; Muzny DM; Gu Y; Nelson DL; Gibbs RA
Genome Res; 1995 Aug; 5(1):71-8. PubMed ID: 8717057
[TBL] [Abstract][Full Text] [Related]
29. Genetic analysis of 17 children with Hunter syndrome: identification and functional characterization of four novel mutations in the iduronate-2-sulfatase gene.
Chistiakov DA; Kuzenkova LM; Savost'anov KV; Gevorkyan AK; Pushkov AA; Nikitin AG; Vashakmadze ND; Zhurkova NV; Podkletnova TV; Namazova-Baranova LS; Baranov AA
J Genet Genomics; 2014 Apr; 41(4):197-203. PubMed ID: 24780617
[TBL] [Abstract][Full Text] [Related]
30. A deletion involving exons 2-4 in the iduronate-2-sulfatase gene of a patient with intermediate Hunter syndrome.
Bonuccelli G; Regis S; Filocamo M; Corsolini F; Caroli F; Gatti R
Clin Genet; 1998 Jun; 53(6):474-7. PubMed ID: 9712538
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Identification of 9 novel IDS gene mutations in 19 unrelated Hunter syndrome (mucopolysaccharidosis Type II) patients. Mutations in brief no. 202. Online.
Karsten SL; Voskoboeva E; Carlberg BM; Kleijer WJ; Tsnnesen T; Pettersson U; Bondeson ML
Hum Mutat; 1998; 12(6):433. PubMed ID: 10671065
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. A yeast artificial chromosome (YAC) contig encompassing the critical region of the X-linked lymphoproliferative disease (XLP) locus.
Lanyi A; Li B; Li S; Talmadge CB; Brichacek B; Davis JR; Kozel BA; Trask B; van den Engh G; Uzvolgyi E; Stanbridge EJ; Nelson DL; Chinault C; Heslop H; Gross TG; Seemayer TA; Klein G; Purtilo DT; Sumegi J
Genomics; 1997 Jan; 39(1):55-65. PubMed ID: 9027486
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. 1.5-Mb YAC contig in Xq28 formatted with sequence-tagged sites and including a region unstable in the clones.
Palmieri G; Romano G; Casamassimi A; D'Urso M; Little RD; Abidi FE; Schlessinger D; Lagerström M; Malmgren H; Steen-Bondeson ML
Genomics; 1993 Jun; 16(3):586-92. PubMed ID: 8325630
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. 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]
39. Metabolic correction and cross-correction of mucopolysaccharidosis type II (Hunter syndrome) by retroviral-mediated gene transfer and expression of human iduronate-2-sulfatase.
Braun SE; Aronovich EL; Anderson RA; Crotty PL; McIvor RS; Whitley CB
Proc Natl Acad Sci U S A; 1993 Dec; 90(24):11830-4. PubMed ID: 8265633
[TBL] [Abstract][Full Text] [Related]
40. Inversion of the IDS gene resulting from recombination with IDS-related sequences is a common cause of the Hunter syndrome.
Bondeson ML; Dahl N; Malmgren H; Kleijer WJ; Tönnesen T; Carlberg BM; Pettersson U
Hum Mol Genet; 1995 Apr; 4(4):615-21. PubMed ID: 7633410
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
