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

Genotype-specific neoplastic risk profiles in patients with VHL disease

VHL病患者的基因型特异性肿瘤风险特征

Ganner, Athina; Ferrara, Alfonso Massimiliano; Sekula, Peggy; Schiavi, Francesca; Joo, Julia H; Sanso, Gabriela; Almeida, Madson Q; Knoblauch, Anna Laura; Gizaw, Christine Julia; Krzystolik, Karol; Astheimer, Sophie Charlotte; Achatz, Maria Isabel; Vieites, Ana; Donegan, Diane; Hundsberger, Thomas; Lubinski, Jan; Yildirim Simsir, Ilgin; Bandgar, Tushar; Hasse-Lazar, Kornelia; Pawlaczek, Agnieszka; Zandee, Wouter; Yu, Kai; Kater, Claudio E; Rostomyan, Liliya; Qi, Xiao-Ping; Deutschbein, Timo; Remde, Hanna; Dallagnol, Tabatha Nakakogue; Yukina, Marina; Baudrand, Rene; Andreescu, Corina E; Kunavisarut, Tada; Ishak, Nur Diana; Le Guillou Horn, Xavier; Shutler, Gemma; Jovanovic, Milan; Pęczkowska, Mariola; Calissendorff, Jan; Circosta, Francesco; Bugalho, Maria João; Corssmit, Eleonora P M; Gimm, Oliver; Quinkler, Marcus; Goldmann, Andrea; Watutantrige Fernando, Sara; Zovato, Stefania; Santana, Lucas S; Freitas-Castro, Felipe; Rothermundt, Christian; Zimmermann, Josa; Durmaz, Asude; Aykut, Ayca; Vroonen, Laurent; Krauss, Tobias; Taschner, Christian; Ruf, Juri; Klingler, Jan-Helge; Gläsker, Sven; Lang, Stefan; Bucher, Felicitas; Agostini, Hansjürgen; Jilg, Cordula; Schultze-Seemann, Wolfgang; Bausch, Birke; Bergfeld, Antonia; Rhein, Kilian; Uslar, Thomas; Concistrè, Antonio; Juhlin, C Christofer; Casali-da-Rocha, José Cláudio; Petramala, Luigi; Tsoy, Uliana; Grineva, Elena; Fang, Xu-Dong; Kotsis, Fruzsina; Schaefer, Tobias; Links, Thera P; Makay, Özer; Fagundes, Gustavo F C; Ngeow, Joanne; Shah, Nalini; Opocher, Giuseppe; Barontini, Marta; Larsson, Catharina; Januszewicz, Andrzej; Viana Lima, José; Wohllk, Nelson; Letizia, Claudio; Donatini, Gianluca; Maher, Eamonn R; Beltsevich, Dmitry; Bancos, Irina; Cybulski, Cezary; Walz, Martin K; Köttgen, Anna; Eng, Charis; Neumann, Hartmut P H; Neumann-Haefelin, Elke

Integrative genetic, epigenetic and pathological analysis of paraganglioma reveals complex dysregulation of NOTCH signaling

副神经节瘤的综合遗传、表观遗传和病理分析揭示了 NOTCH 信号的复杂失调

Alessandro Cama, Fabio Verginelli, Lavinia Vittoria Lotti, Francesco Napolitano, Annalisa Morgano, Andria D'Orazio, Michele Vacca, Silvia Perconti, Felice Pepe, Federico Romani, Francesca Vitullo, Filippo di Lella, Rosa Visone, Massimo Mannelli, Hartmut P H Neumann, Giancarlo Raiconi, Carlo Paties, 

Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome

因子 H 突变会降低溶血性尿毒症综合征中对 C3b 和肝素的结合亲和力以及对内皮细胞的表面附着力

Tamara Manuelian, Jens Hellwage, Seppo Meri, Jessica Caprioli, Marina Noris, Stefan Heinen, Mihaly Jozsi, Hartmut P H Neumann, Giuseppe Remuzzi, Peter F Zipfel