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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

280 related items for PubMed ID: 25089800

  • 1. Mutational characterization of ATP7B gene in 103 Wilson's disease patients from Southern China: identification of three novel mutations.
    Wei Z, Huang Y, Liu A, Diao S, Yu Q, Peng Z, Hong M.
    Neuroreport; 2014 Oct 01; 25(14):1075-80. PubMed ID: 25089800
    [Abstract] [Full Text] [Related]

  • 2. Genetic and Clinical Analysis in a Cohort of Patients with Wilson's Disease in Southwestern China.
    Liu Y, Zhou H, Guo H, Bai Y.
    Arch Med Res; 2015 Feb 01; 46(2):164-9. PubMed ID: 25704634
    [Abstract] [Full Text] [Related]

  • 3. Mutation analysis of the ATP7B gene and genotype-phenotype correlation in Chinese patients with Wilson disease.
    Li M, Ma J, Wang W, Yang X, Luo K.
    BMC Gastroenterol; 2021 Sep 01; 21(1):339. PubMed ID: 34470610
    [Abstract] [Full Text] [Related]

  • 4. Novel ATPase Cu(2+) transporting beta polypeptide mutations in Chinese families with Wilson's disease.
    Gu S, Yang H, Qi Y, Deng X, Zhang L, Guo Y, Huang Q, Li J, Shi X, Song Z, Deng H.
    PLoS One; 2013 Sep 01; 8(7):e66526. PubMed ID: 23843956
    [Abstract] [Full Text] [Related]

  • 5. Mutation analysis of 73 southern Chinese Wilson's disease patients: identification of 10 novel mutations and its clinical correlation.
    Wang LH, Huang YQ, Shang X, Su QX, Xiong F, Yu QY, Lin HP, Wei ZS, Hong MF, Xu XM.
    J Hum Genet; 2011 Sep 01; 56(9):660-5. PubMed ID: 21796144
    [Abstract] [Full Text] [Related]

  • 6. p.H1069Q mutation in ATP7B and biochemical parameters of copper metabolism and clinical manifestation of Wilson's disease.
    Gromadzka G, Schmidt HH, Genschel J, Bochow B, Rodo M, Tarnacka B, Litwin T, Chabik G, Członkowska A.
    Mov Disord; 2006 Feb 01; 21(2):245-8. PubMed ID: 16211609
    [Abstract] [Full Text] [Related]

  • 7. Mutation spectrum and polymorphisms in ATP7B identified on direct sequencing of all exons in Chinese Han and Hui ethnic patients with Wilson's disease.
    Gu YH, Kodama H, Du SL, Gu QJ, Sun HJ, Ushijima H.
    Clin Genet; 2003 Dec 01; 64(6):479-84. PubMed ID: 14986826
    [Abstract] [Full Text] [Related]

  • 8. Clinical and molecular characterization of Wilson's disease in China: identification of 14 novel mutations.
    Li XH, Lu Y, Ling Y, Fu QC, Xu J, Zang GQ, Zhou F, De-Min Y, Han Y, Zhang DH, Gong QM, Lu ZM, Kong XF, Wang JS, Zhang XX.
    BMC Med Genet; 2011 Jan 11; 12():6. PubMed ID: 21219664
    [Abstract] [Full Text] [Related]

  • 9. [Direct sequencing and analysis of exons of Wilson' disease gene with the most mutations: a study in Hunan Han patients].
    Luo KZ, Yang X, Tong DJ, He G, Yi LX.
    Zhonghua Gan Zang Bing Za Zhi; 2006 Dec 11; 14(12):920-3. PubMed ID: 17196137
    [Abstract] [Full Text] [Related]

  • 10. Direct sequencing of mutations in the copper-transporting P-type adenosine triphosphate (ATP7B) gene for diagnosis and pathogenesis of Wilson's disease.
    Zhang DF, Teng JF.
    Genet Mol Res; 2016 Sep 23; 15(3):. PubMed ID: 27706781
    [Abstract] [Full Text] [Related]

  • 11. Mutational analysis of exon 8 and exon 14 of ATP7B gene in Bangladeshi children with Wilson disease.
    Tasmeen R, Karim ASMB, Banu LA, Hossain E, Rokunuzzaman M, Majumder W, Alam ST, Rasid R, Benzamin M, Hasan MS.
    Indian J Gastroenterol; 2022 Oct 23; 41(5):456-464. PubMed ID: 36308701
    [Abstract] [Full Text] [Related]

  • 12. Novel mutations of the ATP7B gene in Han Chinese families with pre-symptomatic Wilson's disease.
    Yuan ZF, Wu W, Yu YL, Shen J, Mao SS, Gao F, Xia ZZ.
    World J Pediatr; 2015 Aug 23; 11(3):255-60. PubMed ID: 26253413
    [Abstract] [Full Text] [Related]

  • 13. ATP7B mutations in families in a predominantly Southern Indian cohort of Wilson's disease patients.
    Santhosh S, Shaji RV, Eapen CE, Jayanthi V, Malathi S, Chandy M, Stanley M, Selvi S, Kurian G, Chandy GM.
    Indian J Gastroenterol; 2006 Aug 23; 25(6):277-82. PubMed ID: 17264425
    [Abstract] [Full Text] [Related]

  • 14. [Genotype-phenotype relationship and genetics study of 115 cases with Wilson's disease].
    Xia JK, Ning HF, Luo X, Zeng Y, Chen YB, Kong XD.
    Zhonghua Gan Zang Bing Za Zhi; 2024 Jun 20; 32(6):558-562. PubMed ID: 38964899
    [Abstract] [Full Text] [Related]

  • 15. Mutation Analysis of the ATP7B Gene in Seven Chinese Families with Wilson's Disease.
    Xiao H, Deng S, Deng X, Gu S, Yang Z, Yin H, Deng H.
    Digestion; 2019 Jun 20; 99(4):319-326. PubMed ID: 30384382
    [Abstract] [Full Text] [Related]

  • 16. Mutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilson's disease in Serbia.
    Tomić A, Dobricić V, Novaković I, Svetel M, Pekmezović T, Kresojević N, Potrebić A, Kostić VS.
    Vojnosanit Pregl; 2013 May 20; 70(5):457-62. PubMed ID: 23789284
    [Abstract] [Full Text] [Related]

  • 17. High frequency of the c.3207C>A (p.H1069Q) mutation in ATP7B gene of Lithuanian patients with hepatic presentation of Wilson's disease.
    Kucinskas L, Jeroch J, Vitkauskiene A, Sakalauskas R, Petrenkiene V, Kucinskas V, Naginiene R, Schmidt H, Kupcinskas L.
    World J Gastroenterol; 2008 Oct 14; 14(38):5876-9. PubMed ID: 18855987
    [Abstract] [Full Text] [Related]

  • 18. New mutations and polymorphisms of the ATP7B gene in sporadic Wilson disease.
    Lu CX, Qing Lin, Huang WQ, Tzeng CM.
    Eur J Med Genet; 2014 Sep 14; 57(9):498-502. PubMed ID: 24878384
    [Abstract] [Full Text] [Related]

  • 19. Analysis of exon 8 of ATP7B gene in Thai patients with Wilson disease.
    Keandaungjuntr J, Busabaratana M, Kositchaiwat C, Sura T, Pulkes T.
    J Med Assoc Thai; 2011 Oct 14; 94(10):1184-8. PubMed ID: 22145502
    [Abstract] [Full Text] [Related]

  • 20. The His1069Gln mutation in the ATP7B gene in Romanian patients with Wilson's disease referred to a tertiary gastroenterology center.
    Iacob R, Iacob S, Nastase A, Vagu C, Ene AM, Constantinescu A, Anghel D, Banica C, Paslaru L, Coriu D, Dima S, Gheorghe C, Ionica E, Gheorghe L.
    J Gastrointestin Liver Dis; 2012 Jun 14; 21(2):181-5. PubMed ID: 22720308
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.