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

Direct and selective pharmacological disruption of the YAP-TEAD interface by IAG933 inhibits Hippo-dependent and RAS-MAPK-altered cancers

IAG933通过直接和选择性地药理学手段破坏YAP-TEAD界面,从而抑制Hippo依赖性和RAS-MAPK改变的癌症。

Emilie A Chapeau ,Laurent Sansregret ,Giorgio G Galli ,Patrick Chène ,Markus Wartmann ,Thanos P Mourikis ,Patricia Jaaks ,Sabrina Baltschukat ,Ines A M Barbosa ,Daniel Bauer ,Saskia M Brachmann ,Clara Delaunay ,Claire Estadieu ,Jason E Faris ,Pascal Furet ,Stefanie Harlfinger ,Andreas Hueber ,Eloísa Jiménez Núñez ,David P Kodack ,Emeline Mandon ,Typhaine Martin ,Yannick Mesrouze ,Vincent Romanet ,Clemens Scheufler ,Holger Sellner ,Christelle Stamm ,Dario Sterker ,Luca Tordella ,Francesco Hofmann ,Nicolas Soldermann ,Tobias Schmelzle

p53 dynamics vary between tissues and are linked with radiation sensitivity

p53的动态变化因组织而异,并且与辐射敏感性相关。

Jacob Stewart-Ornstein ,Yoshiko Iwamoto ,Miles A Miller ,Mark A Prytyskach ,Stephane Ferretti ,Philipp Holzer ,Joerg Kallen ,Pascal Furet ,Ashwini Jambhekar ,William C Forrester ,Ralph Weissleder ,Galit Lahav

Identification of FAM181A and FAM181B as new interactors with the TEAD transcription factors

鉴定出 FAM181A 和 FAM181B 是与 TEAD 转录因子相互作用的新蛋白

Fedir Bokhovchuk, Yannick Mesrouze, Clara Delaunay, Typhaine Martin, Frédéric Villard, Marco Meyerhofer, Patrizia Fontana, Catherine Zimmermann, Dirk Erdmann, Pascal Furet, Clemens Scheufler, Tobias Schmelzle, Patrick Chène

Dose and Schedule Determine Distinct Molecular Mechanisms Underlying the Efficacy of the p53-MDM2 Inhibitor HDM201

剂量和给药方案决定了 p53-MDM2 抑制剂 HDM201 疗效背后的不同分子机制

Sébastien Jeay #, Stéphane Ferretti #, Philipp Holzer #, Jeanette Fuchs, Emilie A Chapeau, Markus Wartmann, Dario Sterker, Vincent Romanet, Masato Murakami, Grainne Kerr, Eric Y Durand, Swann Gaulis, Marta Cortes-Cros, Stephan Ruetz, Therese-Marie Stachyra, Joerg Kallen, Pascal Furet, Jens Würthner,

The vascular endothelial growth factor receptor inhibitor PTK787/ZK222584 inhibits aromatase

血管内皮生长因子受体抑制剂 PTK787/ZK222584 抑制芳香化酶

Susana Banerjee, Marketa Zvelebil, Pascal Furet, Ursula Mueller-Vieira, Dean B Evans, Mitch Dowsett, Lesley-Ann Martin

Catalytic inhibition of topoisomerase II by a novel rationally designed ATP-competitive purine analogue

一种新型合理设计的 ATP 竞争性嘌呤类似物对拓扑异构酶 II 的催化抑制

Patrick Chène #, Joëlle Rudloff #, Joseph Schoepfer, Pascal Furet, Peter Meier, Zhiyan Qian, Jean-Marc Schlaeppi, Rita Schmitz, Thomas Radimerski

Antileukemic effects of the novel, mutant FLT3 inhibitor NVP-AST487: effects on PKC412-sensitive and -resistant FLT3-expressing cells

新型突变型 FLT3 抑制剂 NVP-AST487 的抗白血病作用:对 PKC412 敏感和抗性的 FLT3 表达细胞的影响

Ellen Weisberg, Johannes Roesel, Guido Bold, Pascal Furet, Jingrui Jiang, Jan Cools, Renee D Wright, Erik Nelson, Rosemary Barrett, Arghya Ray, Daisy Moreno, Elizabeth Hall-Meyers, Richard Stone, Ilene Galinsky, Edward Fox, Gary Gilliland, John F Daley, Suzan Lazo-Kallanian, Andrew L Kung, James D G

Imidazo[4,5-c]quinolines as inhibitors of the PI3K/PKB-pathway

咪唑并[4,5-c]喹啉作为 PI3K/PKB 通路抑制剂

Frédéric Stauffer, Sauveur-Michel Maira, Pascal Furet, Carlos García-Echeverría

Biochemical and three-dimensional-structural study of the specific inhibition of protein kinase CK2 by [5-oxo-5,6-dihydroindolo-(1,2-a)quinazolin-7-yl]acetic acid (IQA)

[5-氧代-5,6-二氢吲哚-(1,2-a)喹唑啉-7-基]乙酸 (IQA) 对蛋白激酶 CK2 特异性抑制的生化和三维结构研究

Stefania Sarno, Erika de Moliner, Maria Ruzzene, Mario A Pagano, Roberto Battistutta, Jenny Bain, Doriano Fabbro, Joseph Schoepfer, Matthew Elliott, Pascal Furet, Flavio Meggio, Giuseppe Zanotti, Lorenzo A Pinna