Human uracil–DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination
By K. Imai, G. Slupphaug, Wen-I. Lee, P. Revy, S. Nonoyama, Nadia Catalan, L. Yel, M. Forveille, B. Kavli, H. Krokan and 3 more. Nature Immunology, 2003
621 citations recorded by the source corpus.
Subfields: Epidemiology, Immunology
View Paper: https://www.semanticscholar.org/paper/56aac6f9ed959756739a1bb4f62a24e0cd287b0d
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
- J. Stavnezer
- D. Barnes
- J. Guikema
- C. E. Schrader
- Tomas Lindahl
- D. Hanahan
Citations in the corpus
- Repair and genetic consequences of endogenous DNA base damage in mammalian cells. (2004, background): “Mutations in the human UNG gene have been correlated with impaired class switch recombination in a subgroup of hyper-IgM syndrome patients (66); it has yet to be established if UNG-deficiency is associated with human B cell malignancies.”
- Mechanism and regulation of class switch recombination. (2008, background): “Some of the dU residues are excised by UNG, and some of the abasic sites are nicked by APE.”