Sebastian Wesselborg相关文献与解析，生知库

Laura Schmitt ,Karina S Krings ,Andre Wolsing ,Xabier Buque ,Marcel Zimmermann ,Hector Flores-Romero ,Thomas Lenz ,Ilka Lechtenberg ,Christoph Peter ,Björn Stork ,Nicole Teusch ,Peter Proksch ,Kai Stühler ,Ana J García-Sáez ,Andreas S Reichert ,Patricia Aspichueta ,Sanil Bhatia ,Sebastian Wesselborg

代谢

淋巴瘤

细胞生物学

Novel meriolin derivatives potently inhibit cell cycle progression and transcription in leukemia and lymphoma cells via inhibition of cyclin-dependent kinases (CDKs)

新型美利康衍生物通过抑制细胞周期依赖性蛋白激酶 (CDK) 有效抑制白血病和淋巴瘤细胞中的细胞周期进程和转录

期刊:Cell Death Discovery

影响因子:6.1

doi:10.1038/s41420-024-02056-6

Laura Schmitt, Julia Hoppe, Pablo Cea-Medina, Peter-Martin Bruch, Karina S Krings, Ilka Lechtenberg, Daniel Drießen, Christoph Peter, Sanil Bhatia, Sascha Dietrich, Björn Stork, Gerhard Fritz, Holger Gohlke, Thomas J J Müller, Sebastian Wesselborg

Novel 4-alkoxy Meriolin Congeners Potently Induce Apoptosis in Leukemia and Lymphoma Cells

新型 4-烷氧基美利奴林同类物可有效诱导白血病和淋巴瘤细胞凋亡

期刊:Molecules

影响因子:4.2

doi:10.3390/molecules29246050

Karina S Krings, Tobias R Wassenberg, Pablo Cea-Medina, Laura Schmitt, Ilka Lechtenberg, Tanya R Llewellyn, Nan Qin, Holger Gohlke, Sebastian Wesselborg, Thomas J J Müller

Phosphorylation of pICln by the autophagy activating kinase ULK1 regulates snRNP biogenesis and splice activity of the cell

自噬激活激酶 ULK1 对 pICln 的磷酸化调节细胞的 snRNP 生物合成和剪接活性

期刊:Computational and Structural Biotechnology Journal

影响因子:4.4

doi:10.1016/j.csbj.2023.03.015

Lea Marie Esser, Katharina Schmitz, Frank Hillebrand, Steffen Erkelenz, Heiner Schaal, Björn Stork, Matthias Grimmler, Sebastian Wesselborg, Christoph Peter

The Impact of p70S6 Kinase-Dependent Phosphorylation of Gemin2 in UsnRNP Biogenesis

p70S6激酶依赖性Gemin2磷酸化对UsnRNP生物合成的影响

期刊:International Journal of Molecular Sciences

影响因子:0.7

doi:10.3390/ijms242115552

Lea Marie Esser ,Qiaoping Li ,Maximilian Jüdt ,Thilo Kähne ,Björn Stork ,Matthias Grimmler ,Sebastian Wesselborg ,Christoph Peter

Fin56-induced ferroptosis is supported by autophagy-mediated GPX4 degradation and functions synergistically with mTOR inhibition to kill bladder cancer cells

Fin56诱导的铁死亡依赖于自噬介导的GPX4降解，并与mTOR抑制剂协同作用杀死膀胱癌细胞。

期刊:Cell Death & Disease

影响因子:8.1

doi:10.1038/s41419-021-04306-2

Yadong Sun,Niklas Berleth,Wenxian Wu,David Schlütermann,Jana Deitersen,Fabian Stuhldreier,Lena Berning,Annabelle Friedrich,Seda Akgün,María José Mendiburo,Sebastian Wesselborg,Marcus Conrad,Carsten Berndt,Björn Stork

40 Years of Research on Polybrominated Diphenyl Ethers (PBDEs)-A Historical Overview and Newest Data of a Promising Anticancer Drug

多溴二苯醚 (PBDEs) 研究 40 年 - 一种有前景的抗癌药物的历史回顾和最新数据

期刊:Molecules

影响因子:4.2

doi:10.3390/molecules26040995

Laura Schmitt, Ilka Hinxlage, Pablo A Cea, Holger Gohlke, Sebastian Wesselborg

肿瘤

发表日期：2021

文献求助收藏

Carbamoyl-Phosphate Synthase 1 as a Novel Target of Phomoxanthone A, a Bioactive Fungal Metabolite

氨基甲酰磷酸合酶 1 是生物活性真菌代谢物 Phomoxanthone A 的新靶点

期刊:Biomolecules

影响因子:4.8

doi:10.3390/biom10060846

Sara Ceccacci, Jana Deitersen, Matteo Mozzicafreddo, Elva Morretta, Peter Proksch, Sebastian Wesselborg, Björn Stork, Maria Chiara Monti

代谢

发表日期：2020

文献求助收藏

Didymellanosine, a new decahydrofluorene analogue, and ascolactone C from Didymella sp. IEA-3B.1, an endophyte of Terminalia catappa

Didymellanosine（一种新的十氢芴类似物）和来自榄仁树内生菌 Didymella sp. IEA-3B.1 的 ascolactone C

期刊:RSC Advances

影响因子:3.9

doi:10.1039/c9ra10685e

Ni P Ariantari, Elena Ancheeva, Marian Frank, Fabian Stuhldreier, Dieter Meier, Yvonne Gröner, Irene Reimche, Nicole Teusch, Sebastian Wesselborg, Werner E G Müller, Rainer Kalscheuer, Zhen Liu, Peter Proksch

微生物学

发表日期：2020

文献求助收藏

First Results from a Screening of 300 Naturally Occurring Compounds: 4,6-dibromo-2-(2',4'-dibromophenoxy)phenol, 4,5,6-tribromo-2-(2',4'-dibromophenoxy)phenol, and 5-epi-nakijinone Q as Substances with the Potential for Anticancer Therapy

筛选 300 种天然化合物的初步结果：4,6-二溴-2-(2',4'-二溴苯氧基)苯酚、4,5,6-三溴-2-(2',4'-二溴苯氧基)苯酚和 5-表-nakijinone Q 作为具有抗癌治疗潜力的物质

期刊:Marine Drugs

影响因子:4.9

doi:10.3390/md17090521

Saskia Mayer, Marie Prechtl, Pia Liebfried, Ron-Patrick Cadeddu, Fabian Stuhldreier, Matthias Kohl, Folker Wenzel, Björn Stork, Sebastian Wesselborg, Peter Proksch, Ulrich Germing, Rainer Haas, Paul Jäger

肿瘤

发表日期：2019

文献求助收藏

Targeting mitochondrial metabolism by the mitotoxin bromoxib in leukemia and lymphoma cells

利用线粒体毒素溴昔布靶向白血病和淋巴瘤细胞中的线粒体代谢

Novel meriolin derivatives potently inhibit cell cycle progression and transcription in leukemia and lymphoma cells via inhibition of cyclin-dependent kinases (CDKs)

新型美利康衍生物通过抑制细胞周期依赖性蛋白激酶 (CDK) 有效抑制白血病和淋巴瘤细胞中的细胞周期进程和转录

Novel 4-alkoxy Meriolin Congeners Potently Induce Apoptosis in Leukemia and Lymphoma Cells

新型 4-烷氧基美利奴林同类物可有效诱导白血病和淋巴瘤细胞凋亡

Phosphorylation of pICln by the autophagy activating kinase ULK1 regulates snRNP biogenesis and splice activity of the cell

自噬激活激酶 ULK1 对 pICln 的磷酸化调节细胞的 snRNP 生物合成和剪接活性

The Impact of p70S6 Kinase-Dependent Phosphorylation of Gemin2 in UsnRNP Biogenesis

p70S6激酶依赖性Gemin2磷酸化对UsnRNP生物合成的影响

Fin56-induced ferroptosis is supported by autophagy-mediated GPX4 degradation and functions synergistically with mTOR inhibition to kill bladder cancer cells

Fin56诱导的铁死亡依赖于自噬介导的GPX4降解，并与mTOR抑制剂协同作用杀死膀胱癌细胞。

40 Years of Research on Polybrominated Diphenyl Ethers (PBDEs)-A Historical Overview and Newest Data of a Promising Anticancer Drug

多溴二苯醚 (PBDEs) 研究 40 年 - 一种有前景的抗癌药物的历史回顾和最新数据

Carbamoyl-Phosphate Synthase 1 as a Novel Target of Phomoxanthone A, a Bioactive Fungal Metabolite

氨基甲酰磷酸合酶 1 是生物活性真菌代谢物 Phomoxanthone A 的新靶点

Didymellanosine, a new decahydrofluorene analogue, and ascolactone C from Didymella sp. IEA-3B.1, an endophyte of Terminalia catappa

Didymellanosine（一种新的十氢芴类似物）和来自榄仁树内生菌 Didymella sp. IEA-3B.1 的 ascolactone C

First Results from a Screening of 300 Naturally Occurring Compounds: 4,6-dibromo-2-(2',4'-dibromophenoxy)phenol, 4,5,6-tribromo-2-(2',4'-dibromophenoxy)phenol, and 5-epi-nakijinone Q as Substances with the Potential for Anticancer Therapy

筛选 300 种天然化合物的初步结果：4,6-二溴-2-(2',4'-二溴苯氧基)苯酚、4,5,6-三溴-2-(2',4'-二溴苯氧基)苯酚和 5-表-nakijinone Q 作为具有抗癌治疗潜力的物质