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.


Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 27512952)

  • 21. Quantitative in vivo brain magnetic resonance spectroscopic monitoring of neurological involvement in mucopolysaccharidosis type II (Hunter Syndrome).
    Davison JE; Hendriksz CJ; Sun Y; Davies NP; Gissen P; Peet AC
    J Inherit Metab Dis; 2010 Dec; 33 Suppl 3():S395-9. PubMed ID: 20886296
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Auditory characteristics and therapeutic effects of enzyme replacement in mouse model of the mucopolysaccharidosis (MPS) II.
    Hong SH; Chu H; Kim KR; Ko MH; Kwon SY; Moon IJ; Chung WH; Cho YS; Kim CH; Suh MW; Choi EW; Sohn YB; Park SW; Kim SH; Cho SY; Ko AR; Jin DK
    Am J Med Genet A; 2012 Sep; 158A(9):2131-8. PubMed ID: 22847837
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Enzyme replacement therapy (ERT) procedure for mucopolysaccharidosis type II (MPS II) by intraventricular administration (IVA) in murine MPS II.
    Higuchi T; Shimizu H; Fukuda T; Kawagoe S; Matsumoto J; Shimada Y; Kobayashi H; Ida H; Ohashi T; Morimoto H; Hirato T; Nishino K; Eto Y
    Mol Genet Metab; 2012 Sep; 107(1-2):122-8. PubMed ID: 22704483
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Prenatal diagnosis of mucopolysaccharidosis type II].
    Zhang XS; Zhang HW; Gu XF
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Oct; 28(5):536-8. PubMed ID: 21983729
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. NK and B cell deficiency in a MPS type II family with novel mutation in the IDS gene.
    Torres LC; Soares DC; Kulikowski LD; Franco JF; Kim CA
    Clin Immunol; 2014 Oct; 154(2):100-4. PubMed ID: 25038527
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Mucopolysaccharidosis type II zebrafish model exhibits early impaired proteasomal-mediated degradation of the axon guidance receptor Dcc.
    Manzoli R; Badenetti L; Bruzzone M; Macario MC; Rubin M; Dal Maschio M; Roveri A; Moro E
    Cell Death Dis; 2024 Apr; 15(4):269. PubMed ID: 38627369
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [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]  

  • 29. 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]  

  • 30. 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]  

  • 31. [Postnatal and prenatal diagnosis of mucopolysaccharidosis type II (Hunter syndrome)].
    Zhang WM; Shi HP; Li BT; Zhao SM; Qi QW; Sun NH; Huang SZ
    Zhonghua Er Ke Za Zhi; 2006 Sep; 44(9):644-7. PubMed ID: 17217652
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Human iPSC-based models highlight defective glial and neuronal differentiation from neural progenitor cells in metachromatic leukodystrophy.
    Frati G; Luciani M; Meneghini V; De Cicco S; Ståhlman M; Blomqvist M; Grossi S; Filocamo M; Morena F; Menegon A; Martino S; Gritti A
    Cell Death Dis; 2018 Jun; 9(6):698. PubMed ID: 29899471
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Wide allelic heterogeneity with predominance of large IDS gene complex rearrangements in a sample of Mexican patients with Hunter syndrome.
    Alcántara-Ortigoza MA; García-de Teresa B; González-Del Angel A; Berumen J; Guardado-Estrada M; Fernández-Hernández L; Navarrete-Martínez JI; Maza-Morales M; Rius-Domínguez R
    Clin Genet; 2016 May; 89(5):574-83. PubMed ID: 26762690
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Aluminum-induced degeneration of astrocytes occurs via apoptosis and results in neuronal death.
    Suárez-Fernández MB; Soldado AB; Sanz-Medel A; Vega JA; Novelli A; Fernández-Sánchez MT
    Brain Res; 1999 Jul; 835(2):125-36. PubMed ID: 10415367
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Neural Stem Cells from Shank3-ko Mouse Model Autism Spectrum Disorders.
    Grasselli C; Carbone A; Panelli P; Giambra V; Bossi M; Mazzoccoli G; De Filippis L
    Mol Neurobiol; 2020 Mar; 57(3):1502-1515. PubMed ID: 31773410
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Effect of genistein and coenzyme Q10 in oxidative damage and mitochondrial membrane potential in an attenuated type II mucopolysaccharidosis cellular model.
    Delgado CA; Poletto E; Vera LNP; Jacques CED; Vianna P; Reinhardt LS; Baldo G; Vargas CR
    Cell Biochem Funct; 2024 Mar; 42(2):e3932. PubMed ID: 38332678
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Autophagy in the Central Nervous System and Effects of Chloroquine in Mucopolysaccharidosis Type II Mice.
    Maeda M; Seto T; Kadono C; Morimoto H; Kida S; Suga M; Nakamura M; Kataoka Y; Hamazaki T; Shintaku H
    Int J Mol Sci; 2019 Nov; 20(23):. PubMed ID: 31757021
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Molecular investigations of a novel iduronate-2-sulfatase mutant in a Chinese patient.
    Lau KC; Lam CW
    Clin Chim Acta; 2008 Jun; 392(1-2):8-10. PubMed ID: 18331837
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Characterization of heart disease in mucopolysaccharidosis type II mice.
    Tavares AMV; Gonzalez EA; Viana IS; Visioli F; Vera LNP; Baldo G
    Cardiovasc Pathol; 2023; 67():107575. PubMed ID: 37730078
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.