Associated Papers
Insights on SNPs of Human Activation-Induced Cytidine Deaminase AID.
Koveshnikova EA et al.
International Journal of Molecular Sciences, 2025
Clinical implications of experimental analyses of AID function on predictive computational tools: Challenge of missense variants.
Abolhassani H et al.
Clinical Genetics, 2020
AID and Apobec3G haphazard deamination and mutational diversity.
Jaszczur M et al.
Cellular and Molecular Life Sciences : Cmls, 2013
A structural basis for the biochemical behavior of activation-induced deoxycytidine deaminase class-switch recombination-defective hyper-IgM-2 mutants.
Mu Y et al.
The Journal of Biological Chemistry, 2012
Novel mutation of the activation-induced cytidine deaminase gene in a Tajik family: special review on hyper-immunoglobulin M syndrome.
Mahdaviani SA et al.
Expert Review of Clinical Immunology, 2012
Stochastic properties of processive cytidine DNA deaminases AID and APOBEC3G.
Chelico L et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences, 2009
Hypermutation at A/T sites during G.U mismatch repair in vitro by human B-cell lysates.
Pham P et al.
The Journal of Biological Chemistry, 2008
Interaction between antibody-diversification enzyme AID and spliceosome-associated factor CTNNBL1.
Conticello SG et al.
Molecular Cell, 2008
Impact of phosphorylation and phosphorylation-null mutants on the activity and deamination specificity of activation-induced cytidine deaminase.
Pham P et al.
The Journal of Biological Chemistry, 2008
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