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- databases for immunodeficiency-causing variations

   UNGbase
   Variation registry for  UNG deficiency


UNGbase mutation publications

[2006] [2005] [2003]

Search PubMed latest citations for UNG mutations

    2006

  • Evaluation of NTHL1, NEIL1, NEIL2, MPG, TDG, UNG and SMUG1 genes in familial colorectal cancer predisposition.
    Broderick P, Bagratuni T, Vijayakrishnan J, Lubbe S, Chandler I, Houlston RS
    BMC Cancer 2006(): 243 [PubMed abstract].

    2005

  • Molecular analysis of a large cohort of patients with the hyper immunoglobulin M (IgM) syndrome.
    Lee WI, Torgerson TR, Schumacher MJ, Yel L, Zhu Q, Ochs HD
    Blood 2005(5): 1881-90 [PubMed abstract].

    2003

  • Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination.
    Imai K, Slupphaug G, Lee WI, Revy P, Nonoyama S, Catalan N, Yel L, Forveille M, Kavli B, Krokan HE, Ochs HD, Fischer A, Durandy A
    Nat Immunol 2003(10): 1023-8 [PubMed abstract].