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

GeneBits: ultra-sensitive tumour-informed ctDNA monitoring of treatment response and relapse in cancer patients

GeneBits:利用超灵敏的肿瘤信息ctDNA监测癌症患者的治疗反应和复发情况

Julian Broche # ,Olga Kelemen # ,Aishwarya Sekar ,Leon Schütz ,Francesc Muyas ,Andrea Forschner ,Christopher Schroeder ,Stephan Ossowski

Single-cell RNA-sequencing highlights a curtailed NK cell function in convalescent COVID-19 pregnant women

单细胞RNA测序揭示新冠肺炎康复孕妇NK细胞功能受损

Madhuri S Salker # ,Nor Haslinda Abd Aziz # ,Natalia Carman Prodan ,Zhiqi Yang ,Aditya Kumar Lankapalli ,Katrin Lazar ,Mohamad Nasir Shafiee ,Ersoy Kocak ,Harivignesh Ganesan ,Surya Sekhar Pal ,Omer Khalid ,Norhana Mohd Kasim ,Aida Kalok ,Norashikin Abdul Fuad ,Alfred Lennart Bissinger ,Tina Ganzenmueller ,Thomas Iftner ,Karl Oliver Kagan ,Stephan Ossowski ,Nicolas Casadei ,Sara Y Brucker ,Olaf Riess ,Yogesh Singh

Case Report: FGFR2 inhibitor resistance via PIK3CA and CDKN2A/B in an intrahepatic cholangiocarcinoma patient with FGFR2-SH3GLB1 fusion

病例报告:FGFR2-SH3GLB1融合基因肝内胆管癌患者通过PIK3CA和CDKN2A/B途径产生FGFR2抑制剂耐药性

Ballin, Nadja; Ott, Alexander; Seibel-Kelemen, Olga; Bonzheim, Irina; Nann, Dominik; Beha, Janina; Spahn, Stephan; Singer, Stephan; Ossowski, Stephan; Roggia, Cristiana; Schroeder, Christopher; Bitzer, Michael; Armeanu-Ebinger, Sorin

Biallelic MAD2L1BP (p31comet) mutation is associated with mosaic aneuploidy and juvenile granulosa cell tumors

双等位基因 MAD2L1BP (p31comet) 突变与嵌合性非整倍体和幼年颗粒细胞肿瘤相关

Ghada M H Abdel-Salam, Susanne Hellmuth, Elise Gradhand, Stephan Käseberg, Jennifer Winter, Ann-Sophie Pabst, Maha M Eid, Holger Thiele, Peter Nürnberg, Birgit S Budde, Mohammad Reza Toliat, Ines B Brecht, Christopher Schroeder, Axel Gschwind, Stephan Ossowski, Friederike Häuser, Heidi Rossmann, Moh

Absence of Non-Canonical, Inhibitory MYD88 Splice Variants in B Cell Lymphomas Correlates With Sustained NF-κB Signaling

细胞淋巴瘤中非典型抑制性 MYD88 剪接变体的缺失与持续的 NF-κB 信号传导相关

Yamel Cardona Gloria, Stephan H Bernhart, Sven Fillinger, Olaf-Oliver Wolz, Sabine Dickhöfer, Jakob Admard, Stephan Ossowski, Sven Nahnsen, Reiner Siebert, Alexander N R Weber

Detection of mobile elements insertions for routine clinical diagnostics in targeted sequencing data

利用靶向测序数据检测移动元件插入,以进行常规临床诊断

German Demidov ,Joohyun Park ,Sorin Armeanu-Ebinger ,Cristiana Roggia ,Ulrike Faust ,Isabell Cordts ,Maria Blandfort ,Tobias B Haack ,Christopher Schroeder ,Stephan Ossowski

Nuclear gene proximity and protein interactions shape transcript covariations in mammalian single cells

核基因邻近性和蛋白质相互作用塑造哺乳动物单细胞中的转录本共变

Marcel Tarbier,Sebastian D Mackowiak,João Frade,Silvina Catuara-Solarz,Inna Biryukova,Eleni Gelali,Diego Bárcena Menéndez,Luis Zapata,Stephan Ossowski,Magda Bienko,Caroline J Gallant,Marc R Friedländer

Comparative Transcriptional Profiling of Motor Neuron Disorder-Associated Genes in Various Human Cell Culture Models

不同人类细胞培养模型中运动神经元疾病相关基因的比较转录分析

Stefan Hauser, Stefanie Schuster, Elena Heuten, Philip Höflinger, Jakob Admard, Yvonne Schelling, Ana Velic, Boris Macek, Stephan Ossowski, Ludger Schöls

A genomic-scale artificial microRNA library as a tool to investigate the functionally redundant gene space in Arabidopsis

基因组规模的人工 microRNA 文库作为研究拟南芥功能冗余基因空间的工具

Felix Hauser, Wenxiao Chen, Ulrich Deinlein, Kenneth Chang, Stephan Ossowski, Joffrey Fitz, Gregory J Hannon, Julian I Schroeder