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kfwxz2022
Lv2
140 积分
2022-09-19 加入
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Discovery of Potent Isoindolinone Inhibitors That Target an Active Conformation of PARP1 Using DNA‐Encoded Libraries
11天前
已完结
Discovery of 3-hydroxymethyl-azetidine derivatives as potent polymerase theta inhibitors
12天前
已完结
Discovery of selective and potent ATR degrader for exploration its kinase-independent functions in acute myeloid leukemia cells
1个月前
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Discovery of novel poly(ADP-ribose) glycohydrolase inhibitors by a quantitative assay system using dot-blot with anti-poly(ADP-ribose)
2个月前
已完结
Roles of Poly(ADP-Ribose) Glycohydrolase in DNA Damage and Apoptosis
2个月前
已完结
Targeting poly(ADP-ribose) glycohydrolase to draw apoptosis codes in cancer
2个月前
已完结
DNA replication stress and emerging prospects for PARG inhibitors in ovarian cancer therapy
2个月前
已完结
Structural insights into the active site of poly(ADP-ribose) glycohydrolase using docking modes of 6-hydroxy-3H-xanthen-3-one derivative inhibitors
2个月前
已完结
Design and Preclinical Evaluation of a Novel B7-H4–Directed Antibody–Drug Conjugate, AZD8205, Alone and in Combination with the PARP1-Selective Inhibitor AZD5305
2个月前
已完结
Myt1 kinase inhibitors - Insight into structural features, offering potential frameworks
2个月前
已完结
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