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

Smooth trends in fermium charge radii and the impact of shell effects

镄电荷半径的平滑变化趋势及壳层效应的影响

Warbinek, Jessica; Rickert, Elisabeth; Raeder, Sebastian; Albrecht-Schönzart, Thomas; Andelic, Brankica; Auler, Julian; Bally, Benjamin; Bender, Michael; Berndt, Sebastian; Block, Michael; Brizard, Alexandre; Chauveau, Pierre; Cheal, Bradley; Chhetri, Premaditya; Claessens, Arno; de Roubin, Antoine; Devlin, Charlie; Dorrer, Holger; Düllmann, Christoph E; Ezold, Julie; Ferrer, Rafael; Gadelshin, Vadim; Gaiser, Alyssa; Giacoppo, Francesca; Goriely, Stephane; Gutiérrez, Manuel J; Harvey, Ashley; Hasse, Raphael; Heinke, Reinhard; Heßberger, Fritz-Peter; Hilaire, Stephane; Kaja, Magdalena; Kaleja, Oliver; Kieck, Tom; Kim, EunKang; Kneip, Nina; Köster, Ulli; Kraemer, Sandro; Laatiaoui, Mustapha; Lantis, Jeremy; Lecesne, Nathalie; Loria Basto, Andrea Tzeitel; Mistry, Andrew Kishor; Mokry, Christoph; Moore, Iain; Murböck, Tobias; Münzberg, Danny; Nazarewicz, Witold; Niemeyer, Thorben; Nothhelfer, Steven; Péru, Sophie; Raggio, Andrea; Reinhard, Paul-Gerhard; Renisch, Dennis; Rey-Herme, Emmanuel; Romans, Jekabs; Romero Romero, Elisa; Runke, Jörg; Ryssens, Wouter; Savajols, Hervé; Schneider, Fabian; Sperling, Joseph; Stemmler, Matou; Studer, Dominik; Thörle-Pospiech, Petra; Trautmann, Norbert; Urquiza-González, Mitzi; van Beek, Kenneth; Van Cleve, Shelley; Van Duppen, Piet; Vandebrouck, Marine; Verstraelen, Elise; Walther, Thomas; Weber, Felix; Wendt, Klaus

Novel variants in CSF1R associated with adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP)

CSF1R 中的新变异与成人发病的轴突球体和色素胶质细胞白质脑病 (ALSP) 有关

Anne S Schmitz, Janani Raju, Wolfgang Köhler, Stephan Klebe, Khaled Cheheb, Franziska Reschke, Saskia Biskup, Tobias B Haack, Benjamin Roeben, Melanie Kellner, Nils Rahner, Thomas Bloch, Johannes Lemke, Benjamin Bender, Ludger Schöls, Holger Hengel, Stefanie N Hayer

AL amyloidosis clonal plasma cells are regulated by microRNAs and dependent on anti-apoptotic BCL2 family members

AL 淀粉样变性克隆浆细胞受 microRNA 调控,并依赖于抗凋亡 BCL2 家族成员

Hila Fishov, Eli Muchtar, Mali Salmon-Divon, Angela Dispenzieri, Tal Zvida, Claudio Schneider, Benjamin Bender, Adrian Duek, Merav Leiba, Ofer Shpilberg, Oshrat Hershkovitz-Rokah

Macromolecular modeling and design in Rosetta: recent methods and frameworks

Rosetta中的大分子建模与设计:最新方法和框架

Leman, Julia Koehler; Weitzner, Brian D; Lewis, Steven M; Adolf-Bryfogle, Jared; Alam, Nawsad; Alford, Rebecca F; Aprahamian, Melanie; Baker, David; Barlow, Kyle A; Barth, Patrick; Basanta, Benjamin; Bender, Brian J; Blacklock, Kristin; Bonet, Jaume; Boyken, Scott E; Bradley, Phil; Bystroff, Chris; Conway, Patrick; Cooper, Seth; Correia, Bruno E; Coventry, Brian; Das, Rhiju; De Jong, René M; DiMaio, Frank; Dsilva, Lorna; Dunbrack, Roland; Ford, Alexander S; Frenz, Brandon; Fu, Darwin Y; Geniesse, Caleb; Goldschmidt, Lukasz; Gowthaman, Ragul; Gray, Jeffrey J; Gront, Dominik; Guffy, Sharon; Horowitz, Scott; Huang, Po-Ssu; Huber, Thomas; Jacobs, Tim M; Jeliazkov, Jeliazko R; Johnson, David K; Kappel, Kalli; Karanicolas, John; Khakzad, Hamed; Khar, Karen R; Khare, Sagar D; Khatib, Firas; Khramushin, Alisa; King, Indigo C; Kleffner, Robert; Koepnick, Brian; Kortemme, Tanja; Kuenze, Georg; Kuhlman, Brian; Kuroda, Daisuke; Labonte, Jason W; Lai, Jason K; Lapidoth, Gideon; Leaver-Fay, Andrew; Lindert, Steffen; Linsky, Thomas; London, Nir; Lubin, Joseph H; Lyskov, Sergey; Maguire, Jack; Malmström, Lars; Marcos, Enrique; Marcu, Orly; Marze, Nicholas A; Meiler, Jens; Moretti, Rocco; Mulligan, Vikram Khipple; Nerli, Santrupti; Norn, Christoffer; Ó'Conchúir, Shane; Ollikainen, Noah; Ovchinnikov, Sergey; Pacella, Michael S; Pan, Xingjie; Park, Hahnbeom; Pavlovicz, Ryan E; Pethe, Manasi; Pierce, Brian G; Pilla, Kala Bharath; Raveh, Barak; Renfrew, P Douglas; Burman, Shourya S Roy; Rubenstein, Aliza; Sauer, Marion F; Scheck, Andreas; Schief, William; Schueler-Furman, Ora; Sedan, Yuval; Sevy, Alexander M; Sgourakis, Nikolaos G; Shi, Lei; Siegel, Justin B; Silva, Daniel-Adriano; Smith, Shannon; Song, Yifan; Stein, Amelie; Szegedy, Maria; Teets, Frank D; Thyme, Summer B; Wang, Ray Yu-Ruei; Watkins, Andrew; Zimmerman, Lior; Bonneau, Richard

Confirmation of TACO1 as a Leigh Syndrome Disease Gene in Two Additional Families

在另外两个家族中证实TACO1是莱氏综合征的致病基因

Oktay, Yavuz; Güngör, Serdal; Zeltner, Lena; Wiethoff, Sarah; Schöls, Ludger; Sonmezler, Ece; Yilmaz, Elmasnur; Munro, Benjamin; Bender, Benjamin; Kernstock, Christoph; Kaemereit, Sofie; Liepelt, Inga; Töpf, Ana; Yis, Uluc; Laurie, Steven; Yaramis, Ahmet; Zuchner, Stephan; Hiz, Semra; Lochmüller, Hanns; Schüle, Rebecca; Horvath, Rita

STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutations

STUB1/CHIP 突变导致 Gordon Holmes 综合征,这是一种广泛的多系统神经退行性疾病的一部分:来自四种新突变的证据

Stefanie Nicole Hayer, Tine Deconinck, Benjamin Bender, Katrien Smets, Stephan Züchner, Selina Reich, Ludger Schöls, Rebecca Schüle, Peter De Jonghe, Jonathan Baets, Matthis Synofzik0

PI3K Pathway Inhibition Achieves Potent Antitumor Activity in Melanoma Brain Metastases In Vitro and In Vivo

PI3K 通路抑制在体内和体外对黑色素瘤脑转移瘤发挥强效抗肿瘤活性

Heike Niessner, Jennifer Schmitz, Ghazaleh Tabatabai, Andreas M Schmid, Carsten Calaminus, Tobias Sinnberg, Benjamin Weide, Thomas K Eigentler, Claus Garbe, Birgit Schittek, Leticia Quintanilla-Fend, Benjamin Bender, Marion Mai, Christian Praetorius, Stefan Beissert, Gabriele Schackert, Michael H Mu

Motor protein mutations cause a new form of hereditary spastic paraplegia

运动蛋白突变导致一种新型遗传性痉挛性截瘫

Andrés Caballero Oteyza, Esra Battaloğlu, Levent Ocek, Tobias Lindig, Jennifer Reichbauer, Adriana P Rebelo, Michael A Gonzalez, Yasar Zorlu, Burcak Ozes, Dagmar Timmann, Benjamin Bender, Günther Woehlke, Stephan Züchner, Ludger Schöls, Rebecca Schüle