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

BCL-xL as a therapeutic target in cetuximab-refractory colorectal cancer.

BCL-xL 作为西妥昔单抗耐药性结直肠癌的治疗靶点。

Asmanidou Stella, Thiel Julia, Ekstrom Thomas L, Schueler Julia, Oswald Eva, Metzger Patrick, Blaumeiser Andreas C, Boerries Melanie, Wiebl Lisa-Marie, Schiffler Ronja, Tamas Raluca, Essmann Frank, Dong Meng, Johnsen Steven A, Kontermann Roland E, Olayioye Monilola A

Spatial single-cell profiling and neighbourhood analysis reveal the determinants of immune architecture connected to checkpoint inhibitor therapy outcome in hepatocellular carcinoma

空间单细胞谱分析和邻域分析揭示了与肝细胞癌检查点抑制剂治疗结果相关的免疫结构决定因素

Salié, Henrike; Wischer, Lara; D'Alessio, Antonio; Godbole, Ira; Suo, Yuan; Otto-Mora, Patricia; Beck, Juergen; Neumann, Olaf; Stenzinger, Albrecht; Schirmacher, Peter; Fulgenzi, Claudia A M; Blaumeiser, Andreas; Boerries, Melanie; Roehlen, Natascha; Schultheiß, Michael; Hofmann, Maike; Thimme, Robert; Pinato, David J; Longerich, Thomas; Bengsch, Bertram

Comorbid Bronchial Asthma, Atopic Dermatitis and Hashimoto's Thyroiditis Are Risk Factors for Early-Onset, Severe and Prolonged Alopecia Areata

合并支气管哮喘、特应性皮炎和桥本甲状腺炎是早发性、严重和长期斑秃的危险因素

Friedrich, Annika; Schmitz, Marie-Therese; Gossmann, Yasmina; Redler, Silke; Blaumeiser, Bettina; Lutz, Gerhard; Blume-Peytavi, Ulrike; Nöthen, Markus M; Betz, Regina C; Basmanav, F Buket

Empowering personalized oncology: evolution of digital support and visualization tools for molecular tumor boards

赋能个性化肿瘤学:分子肿瘤委员会数字化支持和可视化工具的演进

Strantz, Cosima; Böhm, Dominik; Ganslandt, Thomas; Börries, Melanie; Metzger, Patrick; Pauli, Thomas; Blaumeiser, Andreas; Scheiter, Alexander; Jung, Ian-Christopher; Christoph, Jan; Manuilova, Iryna; Strauch, Konstantin; Ustjanzew, Arsenij; Reimer, Niklas; Busch, Hauke; Unberath, Philipp

Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles

15q11-q13重复的群体筛查:证实母系遗传和父系遗传等位基因影响的差异

Parijs, Ilse; Brison, Nathalie; Vancoillie, Leen; Baetens, Machteld; Blaumeiser, Bettina; Boulanger, Sébastien; Désir, Julie; Dimitrov, Boyan; Fieremans, Nathalie; Janssens, Katrien; Janssens, Sandra; Marichal, Axel; Menten, Björn; Meunier, Colombine; Van Berkel, Kim; Van Den Bogaert, Ann; Devriendt, Koenraad; Van Den Bogaert, Kris; Vermeesch, Joris Robert

Multicentric pilot study to standardize clinical whole exome sequencing (WES) for cancer patients

一项旨在规范癌症患者临床全外显子组测序 (WES) 的多中心试点研究

Menzel, Michael; Ossowski, Stephan; Kral, Sebastian; Metzger, Patrick; Horak, Peter; Marienfeld, Ralf; Boerries, Melanie; Wolter, Steffen; Ball, Markus; Neumann, Olaf; Armeanu-Ebinger, Sorin; Schroeder, Christopher; Matysiak, Uta; Goldschmid, Hannah; Schipperges, Vincent; Fürstberger, Axel; Allgäuer, Michael; Eberhardt, Timo; Niewöhner, Jakob; Blaumeiser, Andreas; Ploeger, Carolin; Haack, Tobias Bernd; Tay, Timothy Kwang Yong; Kelemen, Olga; Pauli, Thomas; Kirchner, Martina; Kluck, Klaus; Ott, Alexander; Renner, Marcus; Admard, Jakob; Gschwind, Axel; Lassmann, Silke; Kestler, Hans; Fend, Falko; Illert, Anna Lena; Werner, Martin; Möller, Peter; Seufferlein, Thomas Theodor Werner; Malek, Nisar; Schirmacher, Peter; Fröhling, Stefan; Kazdal, Daniel; Budczies, Jan; Stenzinger, Albrecht

Syntaxin 18 Defects in Human and Zebrafish Unravel Key Roles in Early Cartilage and Bone Development

人类和斑马鱼的突触融合蛋白 18 缺陷揭示了其在早期软骨和骨骼发育中的关键作用

Brecht Guillemyn, Hanna De Saffel, Jan Willem Bek, Piyanoot Tapaneeyaphan, Adelbert De Clercq, Tamara Jarayseh, Sophie Debaenst, Andy Willaert, Riet De Rycke, Peter H Byers, Toon Rosseel, Paul Coucke, Bettina Blaumeiser, Delfien Syx, Fransiska Malfait, Sofie Symoens

MIRACUM-Pipe: An Adaptable Pipeline for Next-Generation Sequencing Analysis, Reporting, and Visualization for Clinical Decision Making

MIRACUM-Pipe:用于临床决策的下一代测序分析、报告和可视化的可适应性流程

Metzger, Patrick; Hess, Maria Elena; Blaumeiser, Andreas; Pauli, Thomas; Schipperges, Vincent; Mertes, Ralf; Christoph, Jan; Unberath, Philipp; Reimer, Niklas; Scheible, Raphael; Illert, Anna L; Busch, Hauke; Andrieux, Geoffroy; Boerries, Melanie

Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance

先天性脑积水:新的孟德尔突变及寡基因遗传的证据

Jacquemin, Valerie; Versbraegen, Nassim; Duerinckx, Sarah; Massart, Annick; Soblet, Julie; Perazzolo, Camille; Deconinck, Nicolas; Brischoux-Boucher, Elise; De Leener, Anne; Revencu, Nicole; Janssens, Sandra; Moorgat, Stèphanie; Blaumeiser, Bettina; Avela, Kristiina; Touraine, Renaud; Abou Jaoude, Imad; Keymolen, Kathelijn; Saugier-Veber, Pascale; Lenaerts, Tom; Abramowicz, Marc; Pirson, Isabelle

Implementation of Exome Sequencing in Prenatal Diagnostics: Chances and Challenges

外显子组测序在产前诊断中的应用:机遇与挑战

Janicki, Ewa; De Rademaeker, Marjan; Meunier, Colombine; Boeckx, Nele; Blaumeiser, Bettina; Janssens, Katrien