Neutrophil extracellular traps target senescent vasculature for tissue remodeling in retinopathy von Binet, François, Cagnone, Gael, Crespo-Garcia, Sergio, Hata, Masayuki, Neault, Mathieu, Dejda, Agnieszka, Wilson, Ariel M., Buscarlet, Manuel, Mawambo, Gaelle Tagne, Howard, Joel P., Diaz-Marin, Roberto, Parinot, Celia, Guber, Vera, Pilon, Frédérique, Juneau, Rachel, Laflamme, Rémi, Sawchyn, Christina, Boulay, Karine, Leclerc, Severine, Abu-Thuraia, Afnan, Côté, Jean-François, Andelfinger, Gregor, Rezende, Flavio A., Sennlaub, Florian, Joyal, Jean-Sébastien, Mallette, Frédérick A., Sapieha, Przemyslaw

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A genome-wide screen identifies SCAI as a modulator of the UV-induced replicative stress response von Lemay, Jean-François, St-Hilaire, Edlie, Ronato, Daryl A, Gao, Yuandi, Bélanger, François, Gezzar-Dandashi, Sari, Kimenyi Ishimwe, Aimé Boris, Sawchyn, Christina, Lévesque, Dominique, McQuaid, Mary, Boisvert, François-Michel, Mallette, Frédérick A, Masson, Jean-Yves, Drobetsky, Elliot A, Wurtele, Hugo

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HIF1α-dependent hypoxia response in myeloid cells requires IRE1α von Mawambo, Gaëlle, Oubaha, Malika, Ichiyama, Yusuke, Blot, Guillaume, Crespo-Garcia, Sergio, Dejda, Agnieszka, Binet, François, Diaz-Marin, Roberto, Sawchyn, Christina, Sergeev, Mikhail, Juneau, Rachel, Kaufman, Randal J, Affar, El Bachir, Mallette, Frédérick A, Wilson, Ariel M, Sapieha, Przemyslaw

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A genome-wide screen reveals that Dyrk1A kinase promotes nucleotide excision repair by preventing aberrant overexpression of cyclin D1 and p21 von Bélanger, François, Roussel, Cassandra, Sawchyn, Christina, St-Hilaire, Edlie, Gezzar-Dandashi, Sari, Kimenyi Ishimwe, Aimé Boris, Mallette, Frédérick Antoine, Wurtele, Hugo, Drobetsky, Elliot

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Non‐canonical ATM/MRN activities temporally define the senescence secretory program von Malaquin, Nicolas, Olivier, Marc‐Alexandre, Martinez, Aurélie, Nadeau, Stéphanie, Sawchyn, Christina, Coppé, Jean‐Philippe, Cardin, Guillaume, Mallette, Frédérick A, Campisi, Judith, Rodier, Francis

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HIF1[alpha]-dependent hypoxia response in myeloid cells requires IRE1[alpha] von Mawambo, Gaëlle, Oubaha, Malika, Ichiyama, Yusuke, Blot, Guillaume, Crespo-Garcia, Sergio, Dejda, Agnieszka, Binet, François, Diaz-Marin, Roberto, Sawchyn, Christina, Sergeev, Mikhail, Juneau, Rachel, Kaufman, Randal J, Affar, El Bachir, Mallette, Frédérick A, Wilson, Ariel M, Sapieha, Przemyslaw

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A MOUSE MODEL OF ACUTE MEGAKARYOBLASTIC LEUKEMIA TO REVEAL NOVEL THERAPEUTIC VULNERABILITIES von Neault, Mathieu, Lebert-Ghali, Charles-Étienne, Fournier, Marilaine, Sawchyn, Christina, Boulay, Karine, Delisle, Jean-Sébastien, Drobetsky, Elliot, Zuber, Johannes, Melichar, Heather, Mallette, Frédérick Antoine

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3168 – INVESTIGATING THE ROLE OF THE KDM4A LYSINE DEMETHYLASE IN PEDIATRIC ACUTE MYELOID LEUKEMIA von Mallette, Frederick A., Sawchyn, Christina, Couteau, Florence, Lalonde, Marie-Eve, Boulay, Karine, Glatz, Dagmar, Fernandez-Diaz, Erlinda, Zuber, Johannes, Cellot, Sonia, Mercier, Francois

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CBFA2T3-GLIS2-dependent pediatric acute megakaryoblastic leukemia is driven by GLIS2 and sensitive to navitoclax von Neault, Mathieu, Lebert-Ghali, Charles-Étienne, Fournier, Marilaine, Capdevielle, Caroline, Garfinkle, Elizabeth A.R., Obermayer, Alyssa, Cotton, Anitria, Boulay, Karine, Sawchyn, Christina, St-Amand, Sarah, Nguyen, Kamy H., Assaf, Béatrice, Mercier, François E., Delisle, Jean-Sébastien, Drobetsky, Elliot A., Hulea, Laura, Shaw, Timothy I., Zuber, Johannes, Gruber, Tanja A., Melichar, Heather J., Mallette, Frédérick A.

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3124 - Identification of Novel Therapeutic Targets in Acute Megakaryoblastic Leukemia von Neault, Mathieu, Lebert-Ghali, Charles-Étienne, Fournier, Marilaine, Sawchyn, Christina, Boulay, Karine, Samavarchi-Tehrani, Payman, Gingras, Anne-Claude, Delisle, Jean-Sébastien, Drobetsky, Elliot, Zuber, Johannes, Melichar, Heather, Mallette, Frédérick

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Identification of Novel Therapeutic Targets in Acute Megakaryoblastic Leukemia von Neault, Mathieu, Lebert-Ghali, Charles-Étienne, Fournier, Marilaine, Sawchyn, Christina, Boulay, Karine, Samavarchi-Tehrani, Payman, Gingras, Anne-Claude, Delisle, Jean-Sébastien, Drobetsky, Elliot, Zuber, Johannes, Melichar, Heather, Mallette, Frédérick

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Additional file 2 of HIF1α-dependent hypoxia response in myeloid cells requires IRE1α von Mawambo, Gaëlle, Oubaha, Malika, Ichiyama, Yusuke, Blot, Guillaume, Crespo-Garcia, Sergio, Dejda, Agnieszka, Binet, François, Diaz-Marin, Roberto, Sawchyn, Christina, Sergeev, Mikhail, Juneau, Rachel, Kaufman, Randal J., Affar, El Bachir, Mallette, Frédérick A., Wilson, Ariel M., Sapieha, Przemyslaw

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Additional file 3 of HIF1α-dependent hypoxia response in myeloid cells requires IRE1α von Mawambo, Gaëlle, Oubaha, Malika, Ichiyama, Yusuke, Blot, Guillaume, Crespo-Garcia, Sergio, Dejda, Agnieszka, Binet, François, Diaz-Marin, Roberto, Sawchyn, Christina, Sergeev, Mikhail, Juneau, Rachel, Kaufman, Randal J., Affar, El Bachir, Mallette, Frédérick A., Wilson, Ariel M., Sapieha, Przemyslaw

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Additional file 4 of HIF1α-dependent hypoxia response in myeloid cells requires IRE1α von Mawambo, Gaëlle, Oubaha, Malika, Ichiyama, Yusuke, Blot, Guillaume, Crespo-Garcia, Sergio, Dejda, Agnieszka, Binet, François, Diaz-Marin, Roberto, Sawchyn, Christina, Sergeev, Mikhail, Juneau, Rachel, Kaufman, Randal J., Affar, El Bachir, Mallette, Frédérick A., Wilson, Ariel M., Sapieha, Przemyslaw

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HIF1[alpha]-dependent hypoxia response in myeloid cells requires IRE1[alpha] von Mawambo, Gaëlle, Oubaha, Malika, Ichiyama, Yusuke, Blot, Guillaume, Crespo-Garcia, Sergio, Dejda, Agnieszka, Binet, François, Diaz-Marin, Roberto, Sawchyn, Christina, Sergeev, Mikhail, Juneau, Rachel, Kaufman, Randal J, Affar, El Bachir, Mallette, Frédérick A, Wilson, Ariel M, Sapieha, Przemyslaw

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A genome-wide screen identifies SCAI as a modulator of the UV-induced replicative stress response von Lemay, Jean-François, St-Hilaire, Edlie, Ronato, Daryl A, Gao, Yuandi, Bélanger, François, Gezzar-Dandashi, Sari, Kimenyi Ishimwe, Aimé Boris, Sawchyn, Christina, Lévesque, Dominique, McQuaid, Mary, Boisvert, François-Michel, Mallette, Frédérick A, Masson, Jean-Yves, Drobetsky, Elliot A, Wurtele, Hugo

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A genome-wide screen identifies SCAI as a modulator of the UV-induced replicative stress response von Lemay, Jean-François, St-Hilaire, Edlie, Ronato, Daryl A, Gao, Yuandi, Bélanger, François, Gezzar-Dandashi, Sari, Kimenyi Ishimwe, Aimé Boris, Sawchyn, Christina, Lévesque, Dominique, McQuaid, Mary, Boisvert, François-Michel, Mallette, Frédérick A, Masson, Jean-Yves, Drobetsky, Elliot A, Wurtele, Hugo

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A genome-wide screen identifies SCAI as a modulator of the UV-induced replicative stress response von Lemay, Jean-François, St-Hilaire, Edlie, Ronato, Daryl A, Gao, Yuandi, Bélanger, François, Gezzar-Dandashi, Sari, Kimenyi Ishimwe, Aimé Boris, Sawchyn, Christina, Lévesque, Dominique, McQuaid, Mary, Boisvert, François-Michel, Mallette, Frédérick A, Masson, Jean-Yves, Drobetsky, Elliot A, Wurtele, Hugo

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A genome-wide screen identifies SCAI as a modulator of the UV-induced replicative stress response von Lemay, Jean-François, St-Hilaire, Edlie, Ronato, Daryl A, Gao, Yuandi, Bélanger, François, Gezzar-Dandashi, Sari, Kimenyi Ishimwe, Aimé Boris, Sawchyn, Christina, Lévesque, Dominique, McQuaid, Mary, Boisvert, François-Michel, Mallette, Frédérick A, Masson, Jean-Yves, Drobetsky, Elliot A, Wurtele, Hugo

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