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Genome-wide R-loop analysis defines unique roles for DDX5, XRN2, and PRMT5 in DNA/RNA hybrid resolution
View ORCID ProfileOscar D Villarreal, Sofiane Y Mersaoui, Zhenbao Yu, Jean-Yves Masson, View ORCID ProfileStéphane Richard Correspondence email
Oscar D Villarreal
1Segal Cancer Center, Lady Davis Institute for Medical Research and Gerald Bronfman Department of Oncology and Departments of Biochemistry, Human Genetics and Medicine, McGill University, Montréal, Canada
Sofiane Y Mersaoui
1Segal Cancer Center, Lady Davis Institute for Medical Research and Gerald Bronfman Department of Oncology and Departments of Biochemistry, Human Genetics and Medicine, McGill University, Montréal, Canada
2Genome Stability Laboratory, Centre Hospitalier Universitaire de Québec Research Center, Oncology Axis; Department of Molecular Biology, Medical Biochemistry and Pathology; Laval University Cancer Research Center, Québec City, Canada
Zhenbao Yu
1Segal Cancer Center, Lady Davis Institute for Medical Research and Gerald Bronfman Department of Oncology and Departments of Biochemistry, Human Genetics and Medicine, McGill University, Montréal, Canada
Jean-Yves Masson
2Genome Stability Laboratory, Centre Hospitalier Universitaire de Québec Research Center, Oncology Axis; Department of Molecular Biology, Medical Biochemistry and Pathology; Laval University Cancer Research Center, Québec City, Canada
Stéphane Richard
1Segal Cancer Center, Lady Davis Institute for Medical Research and Gerald Bronfman Department of Oncology and Departments of Biochemistry, Human Genetics and Medicine, McGill University, Montréal, Canada
Published 3 August 2020. DOI: 10.26508/lsa.202000762
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DRIP-seq analysis of siDDX5, siXRN2 and siPRMT5 U2OS cells
Oscar D Villarreal, Sofiane Y Mersaoui, Zhenbao Yu, Jean-Yves Masson, Stéphane Richard
Life Science Alliance Aug 2020, 3 (10) e202000762; DOI: 10.26508/lsa.202000762
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Volume 3, No. 10
October 2020
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