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The EMBO Journal|November 17, 2011
Optimal functional levels of activation-induced deaminase specifically require the Hsp40 DnaJa1Alexandre Orthwein, Astrid Zahn, Stephen P Methot, et al.The Journal of Experimental Medicine|April 1, 2015
Consecutive interactions with HSP90 and eEF1A underlie a functional maturation and storage pathway of AID in the cytoplasmStephen P Methot, Ludivine C Litzler, Felipe Trajtenberg, et al.Journal of Molecular Biology|November 28, 2012
A combined nuclear and nucleolar localization motif in activation-induced cytidine deaminase (AID) controls immunoglobulin class switchingYi Hu, Ida Ericsson, Kathrin Torseth, et al.Seminars in Immunology|June 13, 2012
Activation induced deaminase: how much and where?Alexandre Orthwein, Javier M Di NoiaMicrobes and Infection|May 10, 2003
Trypanosoma cruzi clonal diversity and the epidemiology of Chagas' diseaseCarlos A Buscaglia, Javier M Di NoiaEuropean Journal of Immunology|February 10, 2004
Immunoglobulin gene conversion in chicken DT40 cells largely proceeds through an abasic site intermediate generated by excision of the uracil produced by AID-mediated deoxycytidine deaminationJavier M Di Noia, Michael S NeubergerAnnual Review of Biochemistry|March 3, 2007
Molecular mechanisms of antibody somatic hypermutationJavier M Di Noia, Michael S NeubergerNucleus (Austin, Tex.)|February 18, 2011
The mechanisms regulating the subcellular localization of AIDAnne-Marie Patenaude, Javier M Di NoiaProceedings of the National Academy of Sciences of the United States of America|March 5, 2014
Activation induced deaminase C-terminal domain links DNA breaks to end protection and repair during class switch recombinationAstrid Zahn, Anil K Eranki, Anne-Marie Patenaude, et al.The EMBO Journal|January 13, 2006
SMUG1 is able to excise uracil from immunoglobulin genes: insight into mutation versus repairJavier M Di Noia, Cristina Rada, Michael S NeubergerPageof 7