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C-terminus of Sororin interacts with SA2 and regulates sister chromatid cohesion

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Pages 820-826 | Received 26 Sep 2014, Accepted 15 Dec 2014, Published online: 19 Mar 2015

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Wenya Hou, Yan Li, Jiaxin Zhang, Yisui Xia, Xueting Wang, Hongxiang Chen & Huiqiang Lou. (2022) Cohesin in DNA damage response and double-strand break repair. Critical Reviews in Biochemistry and Molecular Biology 57:3, pages 333-350.
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Laura A Díaz-Martínez & Duncan J Clarke. (2015) Sororin is tethered to Cohesin SA2. Cell Cycle 14:8, pages 1133-1133.
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锦博 范. (2023) Research Progress of the Function of CDCA5 and Its Role in Cancer Progression. Advances in Clinical Medicine 13:06, pages 10153-10162.
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Michaela Osadska, Tomas Selicky, Miroslava Kretova, Jan Jurcik, Barbara Sivakova, Ingrid Cipakova & Lubos Cipak. (2022) The Interplay of Cohesin and RNA Processing Factors: The Impact of Their Alterations on Genome Stability. International Journal of Molecular Sciences 23:7, pages 3939.
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Ming Yi, Tianye Li, Shuang Qin, Shengnan Yu, Qian Chu, Anping Li & Kongming Wu. (2020) Identifying Tumorigenesis and Prognosis-Related Genes of Lung Adenocarcinoma: Based on Weighted Gene Coexpression Network Analysis. BioMed Research International 2020, pages 1-15.
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Eva Kukolj, Tanja Kaufmann, Amalie E. Dick, Robert Zeillinger, Daniel W. Gerlich & Dea Slade. (2017) PARP inhibition causes premature loss of cohesion in cancer cells. Oncotarget 8:61, pages 103931-103951.
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Linli Zhou, Cai Liang, Qinfu Chen, Zhenlei Zhang, Bo Zhang, Haiyan Yan, Feifei Qi, Miao Zhang, Qi Yi, Youchen Guan, Xingfeng Xiang, Xiaoqing Zhang, Sheng Ye & Fangwei Wang. (2017) The N-Terminal Non-Kinase-Domain-Mediated Binding of Haspin to Pds5B Protects Centromeric Cohesion in Mitosis. Current Biology 27:7, pages 992-1004.
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Christopher Barrington, Ronald Finn & Suzana Hadjur. (2017) Cohesin biology meets the loop extrusion model. Chromosome Research 25:1, pages 51-60.
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Martine Isabel Boyle, Cathrine Jespersgaard, Lusine Nazaryan, Kirstine Ravn, Karen Brøndum-Nielsen, Anne-Marie Bisgaard & Zeynep Tümer. (2015) Deletion of 11q12.3–11q13.1 in a patient with intellectual disability and childhood facial features resembling Cornelia de Lange syndrome. Gene 572:1, pages 130-134.
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