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Bioorganic Chemistry|November 4, 2018
Synthesis and evaluation of an AZD2461 [18F]PET probe in non-human primates reveals the PARP-1 inhibitor to be non-blood-brain barrier penetrantSean W Reilly, Laura N Puentes, Alexander Schmitz, et al.Journal of Medicinal Chemistry|April 26, 2019
Leveraging a Low-Affinity Diazaspiro Orthosteric Fragment to Reduce Dopamine D3 Receptor (D3R) Ligand Promiscuity across Highly Conserved Aminergic G-Protein-Coupled Receptors (GPCRs)Sean W Reilly, Aladdin A Riad, Chia-Ju Hsieh, et al.Nuclear Medicine and Biology|October 3, 2019
Improved production of 76Br, 77Br and 80mBr via CoSe cyclotron targets and vertical dry distillationPaul A Ellison, Aeli P Olson, Todd E Barnhart, et al.Ecology|April 22, 2025
Linking functional responses and effects with stoichiometric traitsEric K Moody, Katie Anania, Kate S Boersma, et al.Molecular Cancer Therapeutics|May 11, 2019
Targeting PARP-1 with Alpha-Particles Is Potently Cytotoxic to Human Neuroblastoma in Preclinical ModelsMehran Makvandi, Hwan Lee, Laura N Puentes, et al.Pageof 10