Education
M.S., McGill University
Current position
Research assistant, IRCM, Montreal, QC, Canada
Publications
-
Zahn, A., Eranki, A. K., Patenaude, A. M., Methot, S. P., Fifield, H., Cortizas, E. M., Foster, P., Imai, K., Durandy, A., Larijani, M., Verdun, R. E. and Di Noia, J. M. (2014). Activation induced deaminase C-terminal domain links DNA breaks to end protection and repair during class switch recombination. Proc Natl Acad Sci U S A 111(11): E988-997.
-
Cortizas, E. M., Zahn, A., Hajjar, M. E., Patenaude, A. M., Di Noia, J. M. and Verdun, R. E. (2013). Alternative end-joining and classical nonhomologous end-joining pathways repair different types of double-strand breaks during class-switch recombination. J Immunol 191(11): 5751-5763.
-
Campo, V. A., Patenaude, A. M., Kaden, S., Horb, L., Firka, D., Jiricny, J. and Di Noia, J. M. (2013). MSH6- or PMS2-deficiency causes re-replication in DT40 B cells, but it has little effect on immunoglobulin gene conversion or on repair of AID-generated uracils. Nucleic Acids Res 41(5): 3032-3046.
-
Orthwein, A., Patenaude, A. M., Affar el, B., Lamarre, A., Young, J. C. and Di Noia, J. M. (2010). Regulation of activation-induced deaminase stability and antibody gene diversification by Hsp90. J Exp Med 207(12): 2751-2765.
-
Patenaude, A. M. and Di Noia, J. M. (2010). The mechanisms regulating the subcellular localization of AID. Nucleus 1(4): 325-331.
-
Patenaude, A. M., Orthwein, A., Hu, Y., Campo, V. A., Kavli, B., Buschiazzo, A. and Di Noia, J. M. (2009). Active nuclear import and cytoplasmic retention of activation-induced deaminase. Nat Struct Mol Biol 16(5): 517-527.
-
Torban, E., Patenaude, A. M., Leclerc, S., Rakowiecki, S., Gauthier, S., Andelfinger, G., Epstein, D. J. and Gros, P. (2008). Genetic interaction between members of the Vangl family causes neural tube defects in mice. Proc Natl Acad Sci U S A 105(9): 3449-3454.
-
Iglesias, D. M., Hueber, P. A., Chu, L., Campbell, R., Patenaude, A. M., Dziarmaga, A. J., Quinlan, J., Mohamed, O., Dufort, D. and Goodyer, P. R. (2007). Canonical WNT signaling during kidney development. Am J Physiol Renal Physiol 293(2): F494-500.
-
Torban, E., Wang, H. J., Patenaude, A. M., Riccomagno, M., Daniels, E., Epstein, D. and Gros, P. (2007). Tissue, cellular and sub-cellular localization of the Vangl2 protein during embryonic development: effect of the Lp mutation. Gene Expr Patterns 7(3): 346-354.