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

LMP7-Specific Inhibitor M3258 Modulates the Tumor Microenvironment of Triple-Negative Breast Cancer and Inflammatory Breast Cancer.

LMP7 特异性抑制剂 M3258 调节三阴性乳腺癌和炎性乳腺癌的肿瘤微环境

Xie Xuemei, Lee Jangsoon, Manyam Ganiraju C, Pearson Troy, Walter-Bausch Gina, Friese-Hamim Manja, Zhao Sheng, Jabs Julia, Manginelli Angela A, Piske Nadine, Mrowiec Thomas, Wolf Corinna M, Kuntal Bharat S, Tripathy Debu, Wang Jing, Sanderson Michael P, Ueno Naoto T

Novel Methionine Aminopeptidase 2 Inhibitor M8891 Synergizes with VEGF Receptor Inhibitors to Inhibit Tumor Growth of Renal Cell Carcinoma Models

新型甲硫氨酸氨肽酶2抑制剂M8891与VEGF受体抑制剂协同作用抑制肾细胞癌模型的肿瘤生长

Manja Friese-Hamim ,Maria J Ortiz Ruiz # ,Olga Bogatyrova # ,Marina Keil # ,Felix Rohdich ,Beatrix Blume ,Birgitta Leuthner ,Frank Czauderna ,Diane Hahn ,Julia Jabs ,Frank Jaehrling ,Timo Heinrich ,Roland Kellner ,Katherine Chan ,Amy H Y Tong ,Dirk Wienke ,Jason Moffat ,Andree Blaukat ,Frank T Zenke

E2F1-Associated Purine Synthesis Pathway Is a Major Component of the MET-DNA Damage Response Network

E2F1相关嘌呤合成途径是MET-DNA损伤反应网络的主要组成部分

Michaela Poliaková Turan, Rahel Riedo, Matúš Medo, Chiara Pozzato, Manja Friese-Hamim, Jonas P Koch, Si'Ana A Coggins, Qun Li, Baek Kim, Joachim Albers, Daniel M Aebersold, Nicola Zamboni, Yitzhak Zimmer, Michaela Medová

The Preclinical Pharmacology of Tepotinib-A Highly Selective MET Inhibitor with Activity in Tumors Harboring MET Alterations

Tepotinib 的临床前药理学研究——一种对携带 MET 改变的肿瘤具有活性的高选择性 MET 抑制剂

Albers, Joachim; Friese-Hamim, Manja; Clark, Anderson; Schadt, Oliver; Walter-Bausch, Gina; Stroh, Christopher; Johne, Andreas; Karachaliou, Niki; Blaukat, Andree

Preclinical Pharmacokinetics and Translational Pharmacokinetic/Pharmacodynamic Modeling of M8891, a Potent and Reversible Inhibitor of Methionine Aminopeptidase 2

M8891(一种强效且可逆的蛋氨酸氨基肽酶 2 抑制剂)的临床前药代动力学和转化药代动力学/药效学建模

Floriane Lignet, Manja Friese-Hamim, Frank Jaehrling, Samer El Bawab, Felix Rohdich

M3258 Is a Selective Inhibitor of the Immunoproteasome Subunit LMP7 (β5i) Delivering Efficacy in Multiple Myeloma Models

M3258 是免疫蛋白酶体亚基 LMP7 (β5i) 的选择性抑制剂,在多发性骨髓瘤模型中有效

Michael P Sanderson #, Manja Friese-Hamim #, Gina Walter-Bausch #, Michael Busch, Stefanie Gaus, Djordje Musil, Felix Rohdich, Ugo Zanelli, Sondra L Downey-Kopyscinski, Constantine S Mitsiades, Oliver Schadt, Markus Klein, Christina Esdar #

Translational pharmacokinetic-pharmacodynamic modeling of preclinical and clinical data of the oral MET inhibitor tepotinib to determine the recommended phase II dose

利用口服MET抑制剂tepotinib的临床前和临床数据进行转化药代动力学-药效学建模,以确定推荐的II期剂量。

Xiong, Wenyuan; Friese-Hamim, Manja; Johne, Andreas; Stroh, Christopher; Klevesath, Manfred; Falchook, Gerald S; Hong, David S; Girard, Pascal; El Bawab, Samer

The c-Met Inhibitor MSC2156119J Effectively Inhibits Tumor Growth in Liver Cancer Models

c-Met 抑制剂 MSC2156119J 可有效抑制肝癌模型中的肿瘤生长

Friedhelm Bladt, Manja Friese-Hamim, Christian Ihling, Claudia Wilm, Andree Blaukat