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 *

174 related articles for article (PubMed ID: 34893157)

  • 41. Molecular analysis of the iduronate-2-sulfatase gene in Thai patients with Hunter syndrome.
    Keeratichamroen S; Cairns JR; Wattanasirichaigoon D; Wasant P; Ngiwsara L; Suwannarat P; Pangkanon S; Kuptanon J; Tanpaiboon P; Rujirawat T; Liammongkolkul S; Svasti J
    J Inherit Metab Dis; 2008 Dec; 31 Suppl 2():S303-11. PubMed ID: 18500569
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Iduronate-2-sulfatase fused with anti-hTfR antibody, pabinafusp alfa, for MPS-II: A phase 2 trial in Brazil.
    Giugliani R; Martins AM; So S; Yamamoto T; Yamaoka M; Ikeda T; Tanizawa K; Sonoda H; Schmidt M; Sato Y
    Mol Ther; 2021 Jul; 29(7):2378-2386. PubMed ID: 33781915
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Chaperone effect of sulfated disaccharide from heparin on mutant iduronate-2-sulfatase in mucopolysaccharidosis type II.
    Hoshina H; Shimada Y; Higuchi T; Kobayashi H; Ida H; Ohashi T
    Mol Genet Metab; 2018 Feb; 123(2):118-122. PubMed ID: 29289480
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Generation of an induced pluripotent stem cells line, CSSi014-A 9407, carrying the variant c.479C>T in the human iduronate 2-sulfatase (hIDS) gene.
    Casamassa A; Zanetti A; Ferrari D; Lombardi I; Galluzzi G; D'Avanzo F; Cipressa G; Bertozzi A; Torrente I; Vescovi AL; Tomanin R; Rosati J
    Stem Cell Res; 2022 Aug; 63():102846. PubMed ID: 35759972
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Mucopolysaccharidosis type II in a female patient with a reciprocal X;9 translocation and skewed X chromosome inactivation.
    Lonardo F; Di Natale P; Lualdi S; Acquaviva F; Cuoco C; Scarano F; Maioli M; Pavone LM; Di Gregorio G; Filocamo M; Scarano G
    Am J Med Genet A; 2014 Oct; 164A(10):2627-32. PubMed ID: 25044788
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Development of idursulfase therapy for mucopolysaccharidosis type II (Hunter syndrome): the past, the present and the future.
    Whiteman DA; Kimura A
    Drug Des Devel Ther; 2017; 11():2467-2480. PubMed ID: 28860717
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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]  

  • 48. Enzyme replacement therapy in mucopolysaccharidosis type II (Hunter syndrome): a preliminary report.
    Muenzer J; Lamsa JC; Garcia A; Dacosta J; Garcia J; Treco DA
    Acta Paediatr Suppl; 2002; 91(439):98-9. PubMed ID: 12572850
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Status of newborn screening and follow up investigations for Mucopolysaccharidoses I and II in Taiwan.
    Chuang CK; Lin HY; Wang TJ; Huang YH; Chan MJ; Liao HC; Lo YT; Wang LY; Tu RY; Fang YY; Chen TL; Ho HC; Chiang CC; Lin SP
    Orphanet J Rare Dis; 2018 May; 13(1):84. PubMed ID: 29801497
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Hematopoietic Stem Cell Gene Therapy Corrects Neuropathic Phenotype in Murine Model of Mucopolysaccharidosis Type II.
    Wakabayashi T; Shimada Y; Akiyama K; Higuchi T; Fukuda T; Kobayashi H; Eto Y; Ida H; Ohashi T
    Hum Gene Ther; 2015 Jun; 26(6):357-66. PubMed ID: 25761450
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Neural cells generated from human induced pluripotent stem cells as a model of CNS involvement in mucopolysaccharidosis type II.
    Rybová J; Ledvinová J; Sikora J; Kuchař L; Dobrovolný R
    J Inherit Metab Dis; 2018 Mar; 41(2):221-229. PubMed ID: 29168031
    [TBL] [Abstract][Full Text] [Related]  

  • 52. 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]  

  • 53. Severe phenotype in MPS II patients associated with a large deletion including contiguous genes.
    Brusius-Facchin AC; De Souza CF; Schwartz IV; Riegel M; Melaragno MI; Correia P; Moraes LM; Llerena J; Giugliani R; Leistner-Segal S
    Am J Med Genet A; 2012 May; 158A(5):1055-9. PubMed ID: 22492741
    [TBL] [Abstract][Full Text] [Related]  

  • 54. 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]  

  • 55. Therapeutic Options for Mucopolysaccharidosis II (Hunter Disease).
    Kubaski F; Vairo F; Baldo G; de Oliveira Poswar F; Corte AD; Giugliani R
    Curr Pharm Des; 2020; 26(40):5100-5109. PubMed ID: 33138761
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Case report: a rare case of Hunter syndrome (type II mucopolysaccharidosis) in a girl.
    Semyachkina AN; Voskoboeva EY; Zakharova EY; Nikolaeva EA; Kanivets IV; Kolotii AD; Baydakova GV; Kharabadze MN; Kuramagomedova RG; Melnikova NV
    BMC Med Genet; 2019 May; 20(1):66. PubMed ID: 31046699
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Genotype-phenotype findings in patients with mucopolysaccharidosis II from the Hunter Outcome Survey.
    Muenzer J; Amartino H; Burton BK; Scarpa M; Tylki-Szymańska A; Audi J; Botha J; Fertek D; Merberg D; Natarajan M; Whiteman DAH; Giugliani R
    Mol Genet Metab; 2024; 143(1-2):108576. PubMed ID: 39303318
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Genotype-phenotype spectrum of 130 unrelated Indian families with Mucopolysaccharidosis type II.
    Agrawal N; Verma G; Saxena D; Kabra M; Gupta N; Mandal K; Moirangthem A; Sheth J; Puri RD; Bijarnia-Mahay S; Kapoor S; Danda S; H SV; Datar CA; Ranganath P; Shukla A; Dalal A; Srivastava P; Devi RR; Phadke SR
    Eur J Med Genet; 2022 Mar; 65(3):104447. PubMed ID: 35144014
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Shutdown of ER-associated degradation pathway rescues functions of mutant iduronate 2-sulfatase linked to mucopolysaccharidosis type II.
    Osaki Y; Saito A; Kanemoto S; Kaneko M; Matsuhisa K; Asada R; Masaki T; Orii K; Fukao T; Tomatsu S; Imaizumi K
    Cell Death Dis; 2018 Jul; 9(8):808. PubMed ID: 30042467
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Mutational spectrum of the iduronate-2-sulfatase (IDS) gene in 36 unrelated Russian MPS II patients.
    Karsten S; Voskoboeva E; Tishkanina S; Pettersson U; Krasnopolskaja X; Bondeson ML
    Hum Genet; 1998 Dec; 103(6):732-5. PubMed ID: 9921913
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.