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Acta Crystallographica. Section D, Biological Crystallography|August 16, 2008
Structures of the wild-type and activated catalytic domains of Brachydanio rerio Polo-like kinase 1 (Plk1): changes in the active-site conformation and interactions with ligandsRobert A Elling, Raymond V Fucini, Michael J RomanowskiMolecular Biology of the Cell|February 21, 2002
Golgi vesicle proteins are linked to the assembly of an actin complex defined by mAbp1Raymond V Fucini, Ji-Long Chen, Catherine Sharma, et al.Nucleic Acid Therapeutics|April 24, 2012
Adenosine modification may be preferred for reducing siRNA immune stimulationRaymond V Fucini, Henry J Haringsma, Patricia Deng, et al.The Journal of Cell Biology|May 4, 2005
Coatomer-bound Cdc42 regulates dynein recruitment to COPI vesiclesJi-Long Chen, Raymond V Fucini, Lynne Lacomis, et al.Molecular Cancer Therapeutics|April 18, 2009
The Aurora kinase inhibitor SNS-314 shows broad therapeutic potential with chemotherapeutics and synergy with microtubule-targeted agents in a colon carcinoma modelErica C VanderPorten, Pietro Taverna, Jennifer N Hogan, et al.Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|August 6, 2008
Structure of the Brachydanio rerio Polo-like kinase 1 (Plk1) catalytic domain in complex with an extended inhibitor targeting the adaptive pocket of the enzymeRobert A Elling, Raymond V Fucini, Emily J Hanan, et al.Bioorganic & Medicinal Chemistry Letters|September 16, 2008
Design and synthesis of 2-amino-isoxazolopyridines as Polo-like kinase inhibitorsEmily J Hanan, Raymond V Fucini, Michael J Romanowski, et al.Journal of the American Chemical Society|May 27, 2011
Nucleobase and ribose modifications control immunostimulation by a microRNA-122-mimetic RNAHayden Peacock, Raymond V Fucini, Prasanna Jayalath, et al.Journal of Medicinal Chemistry|February 3, 2006
Aminoethylenes: a tetrahedral intermediate isostere yielding potent inhibitors of the aspartyl protease BACE-1Wenjin Yang, Wanli Lu, Yafan Lu, et al.Bioorganic & Medicinal Chemistry Letters|September 17, 2008
Design and synthesis of 2-amino-pyrazolopyridines as Polo-like kinase 1 inhibitorsRaymond V Fucini, Emily J Hanan, Michael J Romanowski, et al.Pageof 2