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

Drug and single-cell gene expression integration identifies sensitive and resistant glioblastoma cell populations

药物和单细胞基因表达整合可识别对药物敏感和耐药的胶质母细胞瘤细胞群

Suter, Robert K; Jermakowicz, Anna M; Veeramachaneni, Rithvik; D'Antuono, Matthew; Zhang, Longwei; Chowdary, Rishika; Kaeppeli, Simon; Sharp, Madison; Palwai, Pravallika; Stathias, Vasileios; Baker, Grace; Ruiz, Luz; Walters, Winston; Cepero, Maria; Burgenske, Danielle; Reilly, Edward B; Oleksijew, Anatol; Anderson, Mark G; Williams, Sion Ll; Ivan, Michael E; Komotar, Ricardo J; De La Fuente, Macarena I; Stein, Gregory; Wojcinski, Alexandre; Kesari, Santosh; Sarkaria, Jann N; Schürer, Stephan C; Ayad, Nagi G

Pathogenic variants in the cohesin loader subunit MAU2 underlie a distinct Cornelia de Lange Syndrome subtype.

黏连蛋白装载亚基 MAU2 的致病变异是 Cornelia de Lange 综合征的一个独特亚型的根本原因。

Parenti Ilaria, Hesters Alina, Gil-Salvador Marta, Duffy Laura, Kanber Deniz, Beygo Jasmin, Kerkhof Jennifer, Steenpaß Laura, Leitão Elsa, Woestefeld Julia, Boone Philip M, Kao Emeline M, Alabdi Lama, Aldhalaan Hesham M, Alkuraya Fowzan S, Alshammari Muneera J, Antonarakis Stylianos E, Basel Donald, Cassinari Kevin, de Polli Cellin Laurana, Clause Amanda R, de Lima Jorge Alexander Augusto, de Castro Leal Andréa, Collins Stephan C, Durand Benjamin, Eckhold Juliane, Hashem Mais O, Jayakar Parul, Khan Arif O, Kato Kohji, Kubica Regina, Lyon Gholson J, Marchi Elaine, McCarrier Julie, Kimmig Lara K, Mizuno Seiji, Nicolas Gael, Nishio Yosuke, Ogi Tomoo, Pié Juan, Prell Jordyn, Puisac Beatriz, Ramos Feliciano J, Ranza Emmanuelle, Redin Claire, Rush Eric, Saitoh Shinji, Shamseldin Hanan E, Starling Susan, Astiazaran-Symonds Esteban, Eltahir Sara H, Kuechler Alma, Sadikovic Bekim, Yalcin Binnaz, Wendt Kerstin S, Kaiser Frank J

Editor's Note: The Genetic Landscape of Ocular Adnexa MALT Lymphoma Reveals Frequent Aberrations in NFAT and MEF2B Signaling Pathways

编者按:眼附属器MALT淋巴瘤的遗传图谱揭示了NFAT和MEF2B信号通路中常见的异常

Magistri, Marco; Happ, Lanie E; Ramdial, Jeremy; Lu, XiaoQing; Stathias, Vasileios; Kunkalla, Kranthi; Agarwal, Nitin; Jiang, Xiaoyu; Schürer, Stephan C; Dubovy, Sander R; Chapman, Jennifer R; Vega, Francisco; Dave, Sandeep; Lossos, Izidore S

Advancing the bioassay ontology through integrated PK/PD and safety pharmacology representation

通过整合药代动力学/药效动力学和安全性药理学表征来推进生物测定本体论的发展

Glenny-Pescov, Joan; Chung, Caty; Ross, Nicolette; Hu, Jiaming; Sinclair, Michael; Khurshid, Rabia; Karlsson, Anneli; Schürer, Stephan C

Dermatophagoides pteronyssinus in ambient air bioaerosols

环境空气生物气溶胶中的屋尘螨

Gusareva, Elena S; Vettath, Vineeth Kodengil; Gaultier, Nicolas E; Sadovoy, Anton V; Dacanay, Justine G A; Schuster, Stephan C

Ultrasound-driven programmable artificial muscles

超声波驱动的可编程人工肌肉

Shi, Zhan; Zhang, Zhiyuan; Schnermann, Justus; Neuhauss, Stephan C F; Nama, Nitesh; Wittkowski, Raphael; Ahmed, Daniel

MorPhiC Consortium: towards functional characterization of all human genes

MorPhiC联盟:迈向所有人类基因的功能表征

Adli, Mazhar; Przybyla, Laralynne; Burdett, Tony; Burridge, Paul W; Cacheiro, Pilar; Chang, Howard Y; Engreitz, Jesse M; Gilbert, Luke A; Greenleaf, William J; Hsu, Li; Huangfu, Danwei; Hung, Ling-Hong; Kundaje, Anshul; Li, Sheng; Parkinson, Helen; Qiu, Xiaojie; Robson, Paul; Schürer, Stephan C; Shojaie, Ali; Skarnes, William C; Smedley, Damian; Studer, Lorenz; Sun, Wei; Vidović, Dušica; Vierbuchen, Thomas; White, Brian S; Yeung, Ka Yee; Yue, Feng; Zhou, Ting

Biocatalytic Alkylation of Ambident Nucleophiles Enables Selective N-Functionalization of Heterocycles and Late-Stage Modifications

双齿亲核试剂的生物催化烷基化可实现杂环化合物的选择性N-官能化和后期修饰

Ospina, Felipe; Schülke, Kai H; Schnutenhaus, Marius; Klein, Alina; Desai, Om; Jain, Shubhanshu; Krofta, Christine; Stratmann, Lukas; Yang, Jianing; Gröger, Harald; Hammer, Stephan C

Inhibition mediated by group III metabotropic glutamate receptors regulates habenula activity and defensive behaviors

III型代谢型谷氨酸受体介导的抑制作用调节缰核活动和防御行为。

Ostenrath, Anna Maria; Faturos, Nicholas; Çiftci Çobanoğlu, Yağnur Işık; Serneels, Bram; Jeong, Inyoung; Dongel Dayanc, Ekin; Enz, Anja; Hinrichsen, Francisca; Mutlu, Aytac Kadir; Bardenhewer, Ricarda; Jetti, Suresh Kumar; Neuhauss, Stephan C F; Jurisch-Yaksi, Nathalie; Yaksi, Emre

Bi-allelic variants in WDR47 cause a complex neurodevelopmental syndrome

WDR47 中的双等位基因变异会导致复杂的神经发育综合征

Efil Bayam, Peggy Tilly, Stephan C Collins, José Rivera Alvarez, Meghna Kannan, Lucile Tonneau, Elena Brivio, Bruno Rinaldi, Romain Lecat, Noémie Schwaller, Ludovica Cotellessa, Sateesh Maddirevula, Fabiola Monteiro, Carlos M Guardia, João Paulo Kitajima, Fernando Kok, Mitsuhiro Kato, Ahlam A A Hame