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Cancer Cells Employ Nuclear Caspase-8 to Overcome the p53-Dependent G2/M Checkpoint through Cleavage of USP28.

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第一作者: Ines,Müller
第一单位: Experimental Dermatology, Department of Dermatology, TU-Dresden, Dresden 01307, Germany; Center for Regenerative Therapies Dresden, TU-Dresden, Dresden 01307, Germany.
作者单位: Experimental Dermatology, Department of Dermatology, TU-Dresden, Dresden 01307, Germany; Center for Regenerative Therapies Dresden, TU-Dresden, Dresden 01307, Germany. [1] Experimental Dermatology, Department of Dermatology, TU-Dresden, Dresden 01307, Germany. [2] Department of Urologic Sciences, Faculty of Medicine, University of British Columbia, Vancouver, BC V5Z 1M9, Canada; Vancouver Prostate Centre, Vancouver, BC V6H 3Z6, Canada. [3] Systems Biology, Life Science Research Unit, University of Luxembourg, 1511 Luxembourg, Luxembourg. [4] Institute of Cell Biology and Immunology and Stuttgart Research Centre Systems Biology, University of Stuttgart, Stuttgart 70569, Germany. [5] Institute of Pharmacology, University of Bern, Bern 3010, Switzerland. [6] Centre for Cell Death, Cancer and Inflammation, UCL Cancer Institute, University College London, London WC1E 6DD, UK. [7] Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA. [8] Danish Cancer Society Research Center, Copenhagen 2100, Denmark; Division of Genome Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm 171 77, Sweden. [9] Experimental Dermatology, Department of Dermatology, TU-Dresden, Dresden 01307, Germany; Center for Regenerative Therapies Dresden, TU-Dresden, Dresden 01307, Germany. Electronic address: dagmar.kulms@uniklinikum-dresden.de. [10]
DOI 10.1016/j.molcel.2019.12.023
PMID 31982308
发布时间 2023-11-13
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