Daniel Durocher

Affiliations: 
Molecular and Medical Genetics University of Toronto, Toronto, ON, Canada 
Area:
Genetics, Cell Biology, Molecular Biology, Oncology, Immunology
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"Daniel Durocher"

Parents

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Stephen P. Jackson post-doc (Neurotree)
Michael B. Yaffe post-doc MIT (Chemistry Tree)
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Publications

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Fradet-Turcotte A, Canny MD, Escribano-Díaz C, et al. (2025) Editorial Expression of Concern: 53BP1 is a reader of the DNA-damage-induced H2A Lys 15 ubiquitin mark. Nature
Nakada S, Chen GI, Gingras AC, et al. (2025) Author Correction: PP4 is a γH2AX phosphatase required for recovery from the DNA damage checkpoint. Embo Reports
Feng S, Liu K, Shang J, et al. (2024) Profound synthetic lethality between SMARCAL1 and FANCM. Molecular Cell
Cho T, Hoeg L, Setiaputra D, et al. (2024) NFATC2IP is a mediator of SUMO-dependent genome integrity. Genes & Development
Zhao Y, Tabet D, Rubio Contreras D, et al. (2023) Genome-scale mapping of DNA damage suppressors through phenotypic CRISPR-Cas9 screens. Molecular Cell
Sifri C, Hoeg L, Durocher D, et al. (2023) An AlphaFold2 map of the 53BP1 pathway identifies a direct SHLD3-RIF1 interaction critical for shieldin activity. Embo Reports. e56834
De Marco Zompit M, Esteban MT, Mooser C, et al. (2022) The CIP2A-TOPBP1 complex safeguards chromosomal stability during mitosis. Nature Communications. 13: 4143
Setiaputra D, Escribano-Díaz C, Reinert JK, et al. (2022) RIF1 acts in DNA repair through phosphopeptide recognition of 53BP1. Molecular Cell
Adam S, Rossi SE, Moatti N, et al. (2021) The CIP2A-TOPBP1 axis safeguards chromosome stability and is a synthetic lethal target for BRCA-mutated cancer. Nature Cancer. 2: 1357-1371
Feng Y, Li C, Stewart JA, et al. (2021) FAM72A antagonizes UNG2 to promote mutagenic repair during antibody maturation. Nature
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