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

Strain, procedures, and tools for reproducible genetic transformation and genome editing of the emerging plant model Spirodela polyrhiza

新兴植物模式植物多根紫菀(Spirodela polyrhiza)的可重复基因转化和基因组编辑的菌株、方法和工具

Barragán-Borrero, Verónica; de Santana Lopes, Amanda; Rodrigues Batista, Enrico Diniz; Höfer, Martin; Elias, Rana; Chakraborty, Abhisek; Ponce-Mañe, Arturo; Descombes, Clotilde; Diezma-Navas, Laura; Petraki, Lydia; Huber, Meret; Xu, Shuqing; Marí-Ordóñez, Arturo

Inhibition of Classical and Alternative Complement Pathway by Ravulizumab and Eculizumab

拉武利珠单抗和依库珠单抗对经典和替代补体途径的抑制作用

Gerischer, Lea; Stascheit, Frauke; Mönch, Maximilian; Doksani, Paolo; Dusemund, Carla; Herdick, Meret; Mergenthaler, Philipp; Stein, Maike; Suboh, Amani; Schröder-Braunstein, Jutta; Wabnitz, Guido; Lünemann, Jan D; Lehnerer, Sophie; Hoffmann, Sarah; Meisel, Andreas

Complement Inhibition Therapy in Myasthenic Crisis-A Multicentre Retrospective Analysis of 17 Cases From Germany

补体抑制疗法治疗重症肌无力危象——一项来自德国的17例病例多中心回顾性分析

Gerischer, Lea; Stein, Maike; Schneider, Alice; Tangen, Hanna; Loris, Johanna; Glaubitz, Stefanie; Zschüntzsch, Jana; Oy, Ulrich Hofstadt-van; Schubert, Charlotte; Heesen, Christoph; Schlag, Melina; Hagenacker, Tim; Oeztuerk, Menekse; Ruck, Tobias; Doksani, Paolo; Dusemund, Carla; Herdick, Meret; Herzig-Nichtweiß, Julia; Mergenthaler, Philipp; Stascheit, Frauke; Suboh, Amani; Schwarz, Lisa; Hoffmann, Sarah; Meisel, Andreas; Lehnerer, Sophie

Participatory co-creation of a smartphone application using Girl-Centred-Design to support adolescent girls' health: Barriers, enablers and lessons learned across six countries

运用以女孩为中心的设计理念,参与式共同开发一款智能手机应用程序,以支持青春期女孩的健康:六个国家面临的障碍、促进因素和经验教训

Benson, Jennifer; Lakeberg, Meret; Palmer, Tegan; Brand, Tilman; Zeeb, Hajo

Inhibition of RNA-binding proteins enhances immunotherapy in ovarian cancer

抑制RNA结合蛋白可增强卵巢癌的免疫疗法

Bley, Nadine; Rausch, Alexander; Müller, Simon; Simon, Theresa; Glaß, Markus; Misiak, Danny; Schian, Laura; Peters, Lara Meret; Dipto, Mohammad; Hmedat, Ali; Busch, Bianca; Schott, Annekatrin; Lederer, Marcell; Wedler, Alice; Rolnik, Robin Benedikt; Elrewany, Hend; Ghazy, Ehab; Sippl, Wolfgang; Vetter, Martina; Wallwiener, Markus; Hüttelmaier, Stefan

Reconstitution of SPO11-dependent double-strand break formation

SPO11依赖性双链断裂形成的重建

Zhi Zheng,Lyuqin Zheng #,Meret Arter #,Kaixian Liu #,Shintaro Yamada,David Ontoso,Soonjoung Kim,Scott Keeney

Gut microbiota-dependent increase in phenylacetic acid induces endothelial cell senescence during aging.

肠道菌群依赖性苯乙酸增加会诱导衰老过程中内皮细胞衰老

Saeedi Saravi Seyed Soheil, Pugin Benoit, Constancias Florentin, Shabanian Khatereh, Spalinger Marianne, Thomas Aurélien, Le Gludic Sylvain, Shabanian Taraneh, Karsai Gergely, Colucci Manuel, Menni Cristina, Attaye Ilias, Zhang Xinyuan, Allemann Meret Sarah, Lee Pratintip, Visconti Alessia, Falchi Mario, Alimonti Andrea, Ruschitzka Frank, Paneni Francesco, Beer Jürg H

Investigating the neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies

研究蛋白酶体ATPase亚基基因PSMC5在神经发育性蛋白酶体病中的神经元作用

Küry, Sébastien; Stanton, Janelle E; van Woerden, Geeske M; Bosc-Rosati, Amélie; Hsieh, Tzung-Chien; Bray, Lise; Oloudé, Marielle; Rosenfelt, Cory; Scott-Boyer, Marie Pier; Most, Victoria; Wang, Tianyun; Papendorf, Jonas J; de Konink, Charlotte; Deb, Wallid; Vignard, Virginie; Studencka-Turski, Maja; Besnard, Thomas; Hajdukowicz, Anna M; Thiel, Franziska G; Wolfgramm, Sophie; Florenceau, Laëtitia; Cuinat, Silvestre; Marsac, Sylvain; Verrès, Yann; Dangoumau, Audrey; Poirier, Léa; Wentzensen, Ingrid M; Tuttle, Annabelle; Forster, Cara; Striesow, Johanna; Golnik, Richard; Ortiz, Damara; Jenkins, Laura; Rosenfeld, Jill A; Ziegler, Alban; Houdayer, Clara; Bonneau, Dominique; Torti, Erin; Begtrup, Amber; Monaghan, Kristin G; Mullegama, Sureni V; Volker-Touw, Catharina M L Nienke; van Gassen, Koen L I; Oegema, Renske; de Pagter, Mirjam S; Steindl, Katharina; Rauch, Anita; Ivanovski, Ivan; McDonald, Kimberly; Boothe, Emily; Dauber, Andrew; Baker, Janice; Fabie, Noelle Andrea V; Bernier, Raphael A; Turner, Tychele N; Srivastava, Siddharth; Dies, Kira A; Swanson, Lindsay C; Costin, Carrie; Abdulrazak, Alali; Jobling, Rebekah K; Pappas, John; Rabin, Rachel; Niyazov, Dmitriy; Chun-Hui Tsai, Anne; Kovak, Karen; Beck, David B; Malicdan, May Christine V; Adams, David R; Wolfe, Lynne; Ganetzky, Rebecca D; Muraresku, Colleen C; Babikyan, Davit; Sedláček, Zdeněk; Hančárová, Miroslava; Timberlake, Andrew T; Saif, Hind Al; Nestler, Berkley; King, Kayla; Hajianpour, M J; Costain, Gregory; Prendergast, D'Arcy; Li, Chumei; Geneviève, David; Vitobello, Antonio; Sorlin, Arthur; Philippe, Christophe; Harel, Tamar; Toker, Ori; Sabir, Ataf; Lim, Derek; Hamilton, Mark J; Bryson, Lisa J; Cleary, Elaine; Weber, Sacha; Hoffman, Trevor L; Cueto-González, Anna M; Tizzano, Eduardo F; Gómez-Andrés, David; Codina-Solà, Marta; Ververi, Athina; Pavlidou, Efterpi; Lambropoulos, Alexandros; Garganis, Kyriakos; Rio, Marlène; Levy, Jonathan; Langas, Sarah J; McRae, Anne M; Lessard, Mathieu K; D'Agostino, Maria Daniela; De Bie, Isabelle; Wegler, Meret; Abou Jamra, Rami; Kamphausen, Susanne B; Bothe, Viktoria; Potocki, Lorraine; Olinger, Eric; Sznajer, Yves; Wiame, Elsa; Thompson, Michelle L; Schroeder, Molly C; Gooch, Catherine; Smith, Raphael A; Pandya, Arti; Busch, Larissa M; Völker, Uwe; Hammer, Elke; Wende, Kristian; Cogné, Benjamin; Isidor, Bertrand; Meiler, Jens; Ripoll, Clémentine; Bigou, Stéphanie; Laumonnier, Frédéric; Hildebrand, Peter W; Eichler, Evan E; McWalter, Kirsty; Krawitz, Peter M; Roux-Dalvai, Florence; Elgersma, Ype; Marcoux, Julien; Bousquet, Marie-Pierre; Droit, Arnaud; Poschmann, Jeremie; Grabrucker, Andreas M; Bolduc, Francois V; Bézieau, Stéphane; Ebstein, Frédéric; Krüger, Elke

Mitochondrial genomes of Middle Pleistocene horses from the open-air site complex of Schöningen

来自舍宁根露天遗址群的中更新世马的线粒体基因组

Weingarten, Arianna; Häusler, Meret; Serangeli, Jordi; Verheijen, Ivo; Reiter, Ella; Radzevičiūtė, Rita; Stoessel, Alexander; Krause, Johannes; Spyrou, Maria A; Conard, Nicholas J; Nieselt, Kay; Posth, Cosimo

Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability

UBR5基因杂合变异会导致一种神经发育综合征,表现为发育迟缓、自闭症和智力障碍。

Sabeh, Pascale; Dumas, Samantha A; Maios, Claudia; Daghar, Hiba; Korzeniowski, Marek; Rousseau, Justine; Lines, Matthew; Guerin, Andrea; Millichap, John J; Landsverk, Megan; Grebe, Theresa; Lindstrom, Kristin; Strober, Jonathan; Ait Mouhoub, Tarik; Zweier, Christiane; Steinraths, Michelle; Hebebrand, Moritz; Callewaert, Bert; Abou Jamra, Rami; Kautza-Lucht, Monika; Wegler, Meret; Kruszka, Paul; Kumps, Candy; Banne, Ehud; Waberski, Marta Biderman; Dieux, Anne; Raible, Sarah; Krantz, Ian; Medne, Livija; Pechter, Kieran; Villard, Laurent; Guerrini, Renzo; Bianchini, Claudia; Barba, Carmen; Mei, Davide; Blanc, Xavier; Kallay, Christine; Ranza, Emmanuelle; Yang, Xiao-Ru; O'Heir, Emily; Donald, Kirsten A; Murugasen, Serini; Bruwer, Zandre; Calikoglu, Muge; Mathews, Jennifer M; Lesieur-Sebellin, Marion; Baujat, Geneviève; Derive, Nicolas; Pierson, Tyler Mark; Murrell, Jill R; Shillington, Amelle; Ormieres, Clothilde; Rondeau, Sophie; Reis, André; Fernandez-Jaen, Alberto; Au, Ping Yee Billie; Sweetser, David A; Briere, Lauren C; Couque, Nathalie; Perrin, Laurence; Schymick, Jennifer; Gueguen, Paul; Lefebvre, Mathilde; Van Andel, Michael; Juusola, Jane; Antonarakis, Stylianos E; Parker, J Alex; Burnett, Barrington G; Campeau, Philippe M