日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

ALC1 links chromatin accessibility to PARP inhibitor response in homologous recombination-deficient cells

ALC1 将染色质可及性与同源重组缺陷细胞中的 PARP 抑制剂反应联系起来

Priyanka Verma ,Yeqiao Zhou ,Zhendong Cao ,Peter V Deraska ,Moniher Deb ,Eri Arai ,Weihua Li ,Yue Shao ,Laura Puentes ,Yiwen Li ,Sonali Patankar ,Robert H Mach ,Robert B Faryabi ,Junwei Shi ,Roger A Greenberg

Detection of SARS-CoV-2 RNA using RT-LAMP and molecular beacons

利用RT-LAMP和分子信标检测SARS-CoV-2 RNA

Sherrill-Mix, Scott; Hwang, Young; Roche, Aoife M; Glascock, Abigail; Weiss, Susan R; Li, Yize; Haddad, Leila; Deraska, Peter; Monahan, Caitlin; Kromer, Andrew; Graham-Wooten, Jevon; Taylor, Louis J; Abella, Benjamin S; Ganguly, Arupa; Collman, Ronald G; Van Duyne, Gregory D; Bushman, Frederic D

MMB-FOXM1-driven premature mitosis is required for CHK1 inhibitor sensitivity

MMB-FOXM1驱动的过早有丝分裂是CHK1抑制剂敏感性的必要条件。

Timothy B Branigan ,David Kozono ,Amy E Schade ,Peter Deraska ,Hembly G Rivas ,Larissa Sambel ,Hunter D Reavis ,Geoffrey I Shapiro ,Alan D D'Andrea ,James A DeCaprio

CHK1 Inhibitor Blocks Phosphorylation of FAM122A and Promotes Replication Stress

CHK1抑制剂阻断FAM122A的磷酸化并促进复制应激

Feng Li, David Kozono, Peter Deraska, Timothy Branigan, Connor Dunn, Xiao-Feng Zheng, Kalindi Parmar, Huy Nguyen, James DeCaprio, Geoffrey I Shapiro, Dipanjan Chowdhury, Alan D D'Andrea

NF-κB inhibition by dimethylaminoparthenolide radiosensitizes non-small-cell lung carcinoma by blocking DNA double-strand break repair

二甲氨基小白菊内酯抑制 NF-κB,通过阻断 DNA 双链断裂修复增强非小细胞肺癌的放射敏感性

Peter V Deraska #, Colin O'Leary #, Hunter D Reavis, Shelby Labe, Tru-Khang Dinh, Jean-Bernard Lazaro, Christopher Sweeney, Alan D D'Andrea, David Kozono

USP9X inhibition promotes radiation-induced apoptosis in non-small cell lung cancer cells expressing mid-to-high MCL1

USP9X 抑制可促进表达中高 MCL1 的非小细胞肺癌细胞发生放射诱导的细胞凋亡

Deepa Kushwaha, Colin O'Leary, Kyle R Cron, Peter Deraska, Kaya Zhu, Alan D D'Andrea, David Kozono

Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity

LRP5基因突变通过降低Wnt信号通路活性,导致原发性骨质疏松症,但不伴有成骨不全症的特征。

Korvala, Johanna; Jüppner, Harald; Mäkitie, Outi; Sochett, Etienne; Schnabel, Dirk; Mora, Stefano; Bartels, Cynthia F; Warman, Matthew L; Deraska, Donald; Cole, William G; Hartikka, Heini; Ala-Kokko, Leena; Männikkö, Minna