UneComperéhensionApprofondie de la Biologie Sruiturelle Cellulaire

低温显微镜Optique.雷霆成像er em cryo克莱姆

高级冷冻断层扫描工作流程开发 - 相关显微镜，铣削自动化和冷冻灯
J. Kuba，J. Mitchels，M. Hovorka，P. Erdmann，L.Berka，R.Kirmse，J.König，J. de Bock，B. Goetze，A. Rigort
https://doi.org/10.1111/jmi.12939
相关器：用于高精度低温相关光和电子显微镜的交互式和灵活的工具包
Jie E. Yang，Matthew R. Larson，Bryan S. Sibert，Samantha Shrum，伊丽莎白R. Wright
https://pubmed.ncbi.nlm.nih.gov/33610654/
前微生物。2017年4月11日; 8：596;莱姆病病原体Borrelia Burgdorferi暴露于生理胁迫条件的材料和活力：一种相关的低温荧光和冷冻扫描电子显微镜研究;Vancovám，Rudenko N，VanžčekJ，Golovchenko M，Strnad M，Rego Rom，TicháL，Grubhoffer L，NebesářováJ.
https://www.ncbi.nlm.nih.gov/pmc/articles/pmc5387694/
NAT PROTOC。2017年1月12日（1）：150-167;病毒感染或转染哺乳动物细胞的相关荧光显微镜和冷冻电子断层扫描;Hampton Cm，施特劳斯JD，Ke Z，Dillard Rs，Hammonds Je，Alonas E，Desai TM，Marin M，Storms Re，Leon F，Melikyan GB，Santangelo PJ，Spearman PW，Wright ER。
https://www.nature.com/articles/nprot.2016.168
Cell biology . 2017;140:321-333;Matrix maps -一个直观的软件，用于获取、分析和注释光学显微镜数据的CLEM;Schorb M, Sieckmann F。
http://www.sciencedirect.com/science/article/pii/s0091679x17300560
方法细胞Biol。2017; 140：303-320;TRICLEM：将高精度，室温克莱姆结合起来，用冷冻荧光显微镜检查识别非常罕见的事件;Ader NR，Kukulski W.
http://www.sciencedirect.com/science/article/pii/s0091679x17300535
方法细胞Biol。2017; 140：85-103;一种使用相关工作流程的冷冻切片细胞单层的新方法;Kolovou A，Schorb M，TaraMder A，Sachse C，Schwab Y，Santarella-Mellwig R.
http://www.sciencedirect.com/science/article/pii/s0091679x17300559.
新的硬件和工作流程用于半自动相关联荧光和冷冻电子显微镜断层扫描，Martin Schorba，B，Leander Gaechterc，Ori Avinoama，Frank Sieckmannd，Mairi Clarkea，Cecilia Bebeacuaa，E，Younty S. Bykova，Andreas F.-P.Sonnena, f, Reinhard Lihlg, John A.G. Briggsa, e, f,, a Structural and Computational Biology Unit, European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg, Germany, b Electron Microscopy Core Facility, European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg, Germany, c Leica Microsystems (Schweiz) AG, Max Schmidheiny-Strasse 201, 9435 Heerbrugg, Switzerland, d Leica Microsystems GmbH, Am Friedensplatz 3, 68165 Mannheim, Germany, e Cell Biology and Biophysics Unit, European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg, Germany, f Molecular Medicine Partnership Unit, EMBL/Universitätsklinikum Heidelberg, Heidelberg, Germany, g Leica Mikrosysteme GmbH, Hernalser Hauptstraße 219, 1170 Vienna, Austria,http://www.sciencedirect.com/science/article/pii/s1047847716301356
Correlative cryo-fluorescence and cryo-scanning electron microscopy as a straightforward tool to study host-pathogen interactions, Martin Strnad1,2, Jana Elsterová1,2,3, Jana Schrenková1,2, Marie Vancová1,2, Ryan O. M. Rego1,Libor Grubhoffer1,2 & Jana Nebesářová1,2,4, 1Institute of Parasitology, Biology Centre of the Czech Academy of Sciences, Branišovská 31, České Budějovice CZ- 37005, Czech Republic. 2Faculty of Science, University of South Bohemia in České Budějovice, Branišovská 1760, České Budějovice CZ-37005, Czech Republic. 3Department of Virology, Veterinary Research Institute, Brno CZ-62100, Czech Republic. 4Faculty of Science, Charles University in Prague, Viničná 1594/7, Praha CZ-12800, Czech Republic. Correspondence and requests for materials should be addressed to M.S. (email: martin.strnad.cze(at)gmail.com),
https://www.nature.com/articles/srep18029
Metskas La，Briggs Jag
基于荧光基于Cryo-EM网格上的膜融合状态的检测使用相关的冷冻荧光和冷冻电子显微镜
显微镜和微分分析。2019年8月;25（4）：942-949。
https://www.cambridge.org/core/journals/microscopy-and-microanalysis/article/fluorescebased-dettions-of-mebrane-fusion-state-o -a-cryoem-grid-using-correlated-cryofluorence-and-Cryoelectron-Microscopy / 4933BFD9777A1E735075BFE5A60DFC90＃FNDTN-Information