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

Multivariate Brain-Blood Signatures in Early-Stage Depression and Psychosis

早期抑郁症和精神病的多变量脑血特征

Popovic, David; Weyer, Clara; Dwyer, Dominic B; Griffiths, Sian Lowri; Lalousis, Paris Alexandros; Barnes, Nicholas M; Vetter, Clara; Neuner, Lisa-Maria; Buciuman, Madalina-Octavia; Sarisik, Elif; Paolini, Marco; Lichtenstein, Theresa; Kambeitz-Ilankovic, Lana; Kambeitz, Joseph; Ruhrmann, Stephan; Chisholm, Katharine; Schultze-Lutter, Frauke; Falkai, Peter; Schiltz, Kolja; Steiner, Johann; Ziller, Michael; Pergola, Giulio; Blasi, Giuseppe; Bertolino, Alessandro; Romer, Georg; Lencer, Rebekka; Dannlowski, Udo; Salokangas, Raimo K R; Pantelis, Christos; Brambilla, Paolo; Borgwardt, Stefan; Wood, Stephen J; Meisenzahl, Eva; Koutsouleris, Nikolaos; Upthegrove, Rachel

Thyrotropin-releasing hormone neurons of different hypothalamic nuclei increase energy expenditure

不同下丘脑核团的促甲状腺激素释放激素神经元会增加能量消耗。

Constantinescu, Andreea; Chandrasekar, Akila; Kleindienst, Lena; Höhne, Luca; Da Silva Lima, Natalia; Richter, Marius; Neve, Vanessa; Spiecker, Frauke; Stölting, Ines; Brandt, Wiebke; Matschl, Urte; Wenzel, Jan; Oelkrug, Rebecca; Prevot, Vincent; Heuer, Heike; Mittag, Jens; Nogueiras, Ruben; Schwaninger, Markus; Müller-Fielitz, Helge

KIMMDY: a biomolecular reaction emulator

KIMMDY:一种生物分子反应模拟器

Hartmann, Eric; Buhr, Jannik; Riedmiller, Kai; Ulanov, Evgeni; Schüpp, Boris N; Kiesewetter, Denis; Sucerquia, Daniel; Aponte-Santamaría, Camilo; Gräter, Frauke

Advanced Human Immune Cell-Organoid Co-Cultures for Functional Testing of Cancer Nanovaccines

用于癌症纳米疫苗功能测试的高级人类免疫细胞-类器官共培养

Ferreira, Nathalia; Agorku, David; Rosa, Andre; Roosz, Julia; Christ, Lena; Anderle, Nicole; Kulkarni, Ajinkya; Hussein, Abir; Sayedipour, Sana S; Luna, Omar F; Legler, Tobias; Ströbel, Philipp; Albericio, Fernando; Cruz, Luis; Beckhove, Phillipp; Loskill, Peter; Alves, Frauke; Markus, M Andrea; Ramos-Gomes, Fernanda

Optogenetic BlueGENEs engineered into a human safe harbor locus.

将光遗传学 BlueGENEs 基因工程改造到人类安全港基因位点。

Geidies Alexander, Nieke Marius, Witte Nils, McLean Benjamin J, Evangelopoulou Maria, Koh Cha San, Kuschel Stefanie, Stölting Frauke, Zurbriggen Matias D, Beyer Hannes M

Parasutterella excrementihominis is associated with attenuated metabolic improvements during obesity therapy in humans

人类肥胖治疗期间代谢改善减弱与排泄副梭菌(Parasutterella excrementihominis)有关

Liu, Shuo; Schlicht, Kristina; Beckmann, Alexia; Hartmann, Katharina; Wang, Weixiao; Kruse, Lucy; Wietzke-Braun, Perdita; Hollstein, Tim; Becker, Ulla; Ziegenbruch, Ursula; Baumgartner, Frauke; Diederich, Wiebke; Laudes, Amelie; Muchaier, Janne; Stobbe, Mareike; Homeister, Lea; Remy, Sophia; Dornstauder, Nele; Vogel, Maja; Schindler, Carl; Türk, Kathrin; Geisler, Corinna; Rohmann, Nathalie; Laudes, Matthias

Genetic dissection of serum pro-neurotensin suggests potential causal impact on brain structure

对血清前神经降压素的基因分析表明其可能对大脑结构产生因果影响

Breitfeld, Jana; Horn, Katrin; Velluva, Akhil; Beyer, Frauke; Pott, Janne; Baber, Ronny; Stumvoll, Michael; Le Duc, Diana; Witte, Veronica; Giontella, Alice; Melander, Olle; Kovacs, Peter; Scholz, Markus; Tönjes, Anke

Exploring endometriosis through 3D in vitro models: A narrative review

利用三维体外模型探索子宫内膜异位症:一篇叙述性综述

Juli, Cara; Nyang'au, Edward Mairura; Götte, Martin; Versen-Höynck, Frauke von

GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy

GRIN2A基因的无义突变会增加早发性精神分裂症和其他精神障碍的风险,并有可能实现精准治疗。

Lemke, Johannes R; Eoli, Andrea; Krey, Ilona; Popp, Bernt; Strehlow, Vincent; Wittekind, Dirk A; Vuorinen, Anna-Leena; Aldhalaan, Hesham M; Baer, Sarah; de Saint Martin, Anne; Hammer, Trine B; Herman, Isabella; Hornemann, Frauke; Ingebrigtsen, Trine; Lederer, Damien; Lesca, Gaetan; Marafie, Dana; Mathot, Mikael; Rosenfeld, Jill A; Møller, Rikke S; Schelhaas, Helenius J; Stillman, Chelsey; Orsini, Alessandro; Patel, Anup D; Piard, Juliette; Veggiotti, Pierangelo; Vlaskamp, Danique R M; Weckhuysen, Sarah; Traynelis, Stephen F; Benke, Tim A; Heyne, Henrike O; Syrbe, Steffen

Correction: GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy

更正:GRIN2A 基因缺失变异会增加早发性精神分裂症和其他精神障碍的风险,并可能使精准治疗成为可能。

Lemke, Johannes R; Eoli, Andrea; Krey, Ilona; Popp, Bernt; Strehlow, Vincent; Wittekind, Dirk A; Vuorinen, Anna-Leena; Aldhalaan, Hesham M; Baer, Sarah; de Saint Martin, Anne; Hammer, Trine B; Herman, Isabella; Hornemann, Frauke; Ingebrigtsen, Trine; Lederer, Damien; Lesca, Gaetan; Marafie, Dana; Mathot, Mikael; Rosenfeld, Jill A; Møller, Rikke S; Schelhaas, Helenius J; Stillman, Chelsey; Orsini, Alessandro; Patel, Anup D; Piard, Juliette; Veggiotti, Pierangelo; Vlaskamp, Danique R M; Weckhuysen, Sarah; Traynelis, Stephen F; Benke, Tim A; Heyne, Henrike O; Syrbe, Steffen