PARP-2, A Novel Mammalian DNA Damage-dependent Poly(ADP-ribose) Polymerase
Jean-Christophe Amé,V. Rolli,Valérie Schreiber,Claude Niedergang,Françoise Apiou,Patrice Decker,Sylviane Muller,Thomas Höger,Josiane Ménissier-de Murcia,Gilbert de Murcia +9 more
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TL;DR: A cDNA encoding a 62-kDa protein that shares considerable homology with the catalytic domain of PARP-1 and also contains a basic DNA-binding domain is described, which is proposed to call this enzyme poly(ADP-ribose) polymerase 2 (PARP-2).
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About: This article is published in Journal of Biological Chemistry. The article was published on 18 Jun 1999. and is currently open access. The article focuses on the topics: Poly [ADP-Ribose] Polymerase 2 & Poly ADP ribose polymerase.
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Inhibiteurs de la PARP : des avancées significatives dans le traitement des cancers
TL;DR: These properties highlight the innovative potency of PARP inhibitor to target cancer cells in their repair capacity and open the way to promising therapeutic strategies aimed to combine PARP inhibitors with DNA-damaging chimio- or radiotherapy and as single agents for the treatment of BRCA mutation-associated tumors.
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The interaction of CtIP with DNA damage response proteins
Iga Agnieszka Abramowicz
- 01 Jul 2010
TL;DR: It was found that CtIP associates in vivo with DNA damage sensor proteins such as the MRN complex (Mre11, Rad50 and NBS1) and RPA70, signal transducer proteinssuch as the PIKK kinases ATM, ATR and SMG1 and the mediator proteins 53BP1 and MDC1.
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Tolerability, safety, and preliminary antitumor activity of fuzuloparib in combination with SHR-1316 in patients with relapsed small cell lung cancer: a multicenter, open-label, two-stage, phase Ib trial
Yanjun Xu,Zhiyu Huang,Jian Fang,Anwen Liu,Hongyang Lu,Xinmin Yu,Kaiyan Chen,Xiaoling Xu,Wei Shi,Young Hak Kim,Taiki Hakozaki,Alfredo Addeo,Yuang-Kuang Shen,Shaorong Li,Yun Fan +14 more
TL;DR: Fuzuloparib combined with SHR-1316 failed to improve the outcomes in unselected patients with relapsed SCLC and a recommended phase II dose (RP2D) was introduced in the stage 2 expansion phase.
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Synthesis of 2,3-dihydrobenzo[b][1,4]dioxine-5-carboxamide and 3-oxo-3,4-dihydrobenzo[b][1,4]oxazine-8-carboxamide derivatives as PARP1 inhibitors.
Xuwei Shao,Steven Pak,Uday Kiran Velagapudi,Shruthi Gobbooru,Sai Shilpa Kommaraju,Woon-Kai Low,Gopal Subramaniam,Sanjai K. Pathak,Tanaji T. Talele +8 more
TL;DR: High-throughput virtual screening of a Maybridge small molecule library using the PARP1-benzimidazole-4-carboxamide co-crystal structure and pharmacophore model led to the identification of eleven compounds, including (Z)-2-(4-hydroxybenzylidene)-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-8- carboxamide
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