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Nature|January 5, 2018
Structure of the complement C5a receptor bound to the extra-helical antagonist NDT9513727Nathan Robertson, Mathieu Rappas, Andrew S Doré, et al.
Mabs|May 6, 2017
Antibodies targeting G protein-coupled receptors: Recent advances and therapeutic challengesMohammed Akli Ayoub, Pascale Crépieux, Markus Koglin, et al.
Neurobiology of Disease|November 9, 2021
Tau-tubulin kinase 1 phosphorylates TDP-43 at disease-relevant sites and exacerbates TDP-43 pathologyYuan Tian, Yi Wang, Angela M Jablonski, et al.
Mabs|November 21, 2013
Monoclonal anti-β1-adrenergic receptor antibodies activate G protein signaling in the absence of β-arrestin recruitmentCatherine J Hutchings, Gabriella Cseke, Greg Osborne, et al.
Journal of Medicinal Chemistry|March 23, 2013
Biophysical fragment screening of the β1-adrenergic receptor: identification of high affinity arylpiperazine leads using structure-based drug designJohn A Christopher, Jason Brown, Andrew S Doré, et al.
Journal of the American Chemical Society|July 12, 2024
High-Throughput Covalent Modifier Screening with Acoustic Ejection Mass SpectrometryXiujuan Wen, Chang Liu, Kiersten Tovar, et al.
Nature|April 26, 2016
Extra-helical binding site of a glucagon receptor antagonistAli Jazayeri, Andrew S Doré, Daniel Lamb, et al.
SLAS Discovery : Advancing Life Sciences R & D|August 27, 2025
High-throughput evaluation of novel WRN inhibitorsHaiyan Xu, Rachel L Palte, Meredith M Rickard, et al.
Nature Communications|January 3, 2026
WRN structural flexibility showcased through fragment-based lead discovery of inhibitorsRachel L Palte, Mihir Mandal, Justyna Sikorska, et al.
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