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Journal Abstract Search

349 related items for PubMed ID: 16207219

  • 21. Disturbed copper transport in humans. Part 2: mutations of the ATP7B gene lead to Wilson disease (WD).
    Seidel J, Caca K, Schwab SG, Berr F, Wildenauer DB, Mentzel HJ, Horn N, Kauf E.
    Cell Mol Biol (Noisy-le-grand); 2001; 47 Online Pub():OL149-57. PubMed ID: 11936861
    [Abstract] [Full Text] [Related]

  • 22. Identification of three novel insertion/deletion mutations in Wilson disease's gene.
    Fan Y, Yu L, Han Y, Ren M, Yang R, Zhao S.
    Biochem Genet; 2004 Oct; 42(9-10):377-84. PubMed ID: 15524314
    [No Abstract] [Full Text] [Related]

  • 23. Carrier frequency of the R778L, A874V, and N1270S mutations in the ATP7B gene in a Korean population.
    Park HD, Ki CS, Lee SY, Kim JW.
    Clin Genet; 2009 Apr; 75(4):405-7. PubMed ID: 19419418
    [No Abstract] [Full Text] [Related]

  • 24. Genotype-phenotype correlation of the Wilson disease ATP7B gene.
    Leggio L, Addolorato G, Loudianos G, Abenavoli L, Gasbarrini G.
    Am J Med Genet A; 2006 Apr 15; 140(8):933. PubMed ID: 16532467
    [No Abstract] [Full Text] [Related]

  • 25. Functional characterization of new mutations in Wilson disease gene (ATP7B) using the yeast model.
    Papur OS, Terzioglu O, Koc A.
    J Trace Elem Med Biol; 2015 Apr 15; 31():33-6. PubMed ID: 26004889
    [Abstract] [Full Text] [Related]

  • 26. Gene symbol: ATP7B. Disease: Wilson's disease.
    Yang J, Chan P.
    Hum Genet; 2005 Dec 15; 118(3-4):540. PubMed ID: 16521264
    [No Abstract] [Full Text] [Related]

  • 27. Gene symbol: ATP7B.
    Balakrishnan P, Kabra M, Arora NK, Kalra V.
    Hum Genet; 2007 Feb 15; 120(6):909. PubMed ID: 17438598
    [No Abstract] [Full Text] [Related]

  • 28.
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  • 29. Gene symbol: ATP7B. Disease: Wilson's disease.
    Chan P, Yang J.
    Hum Genet; 2005 Dec 15; 118(3-4):540. PubMed ID: 16521265
    [No Abstract] [Full Text] [Related]

  • 30. Gene symbol: ATP7B. Disease: Wilson's disease.
    Yang J, Chan P.
    Hum Genet; 2005 Dec 15; 118(3-4):539. PubMed ID: 16402213
    [No Abstract] [Full Text] [Related]

  • 31. Gene symbol: ATP7B. Disease: Wilson disease.
    Ray K, Gupta A.
    Hum Genet; 2008 Oct 15; 124(3):297. PubMed ID: 18846616
    [No Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
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  • 33. Gene symbol: ATP7B. Disease: Wilson's disease.
    Yang J, Chan P.
    Hum Genet; 2005 Dec 15; 118(3-4):544. PubMed ID: 16521292
    [No Abstract] [Full Text] [Related]

  • 34. Gene symbol: ATP7B. Disease: Wilson's disease.
    Yang J, Chan P.
    Hum Genet; 2005 Dec 15; 118(3-4):544. PubMed ID: 16521293
    [No Abstract] [Full Text] [Related]

  • 35. Gene symbol: ATP7B. Disease: Wilson's disease.
    Yang J, Chan P.
    Hum Genet; 2005 Dec 15; 118(3-4):544. PubMed ID: 16521291
    [No Abstract] [Full Text] [Related]

  • 36. Clinical and genetic analysis of pediatric patients with Wilson disease.
    Şimşek Papur Ö, Aşık Akman S, Terzioğlu O.
    Turk J Gastroenterol; 2015 Sep 15; 26(5):397-403. PubMed ID: 26215059
    [Abstract] [Full Text] [Related]

  • 37. Spectrum of mutations in the ATP binding domain of ATP7B gene of Wilson Disease in a regional Indian cohort.
    Guggilla SR, Senagari JR, Rao PN, Madireddi S.
    Gene; 2015 Sep 10; 569(1):83-7. PubMed ID: 25982861
    [Abstract] [Full Text] [Related]

  • 38. Gene symbol: ATP7B.
    Balakrishnan P, Kabra M, Arora NK, Kalra V.
    Hum Genet; 2007 Feb 10; 120(6):908. PubMed ID: 17438596
    [No Abstract] [Full Text] [Related]

  • 39. 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 10; 21(2):245-8. PubMed ID: 16211609
    [Abstract] [Full Text] [Related]

  • 40. Functional characterization of missense mutations in ATP7B: Wilson disease mutation or normal variant?
    Forbes JR, Cox DW.
    Am J Hum Genet; 1998 Dec 10; 63(6):1663-74. PubMed ID: 9837819
    [Abstract] [Full Text] [Related]

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