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New Biotechnology|September 17, 2014
Transthyretin complexes with curcumin and bromo-estradiol: evaluation of solubilizing multicomponent mixturesLidia Ciccone, Livia Tepshi, Susanna Nencetti, et al.
Biotechnology Reports (Amsterdam, Netherlands)|June 20, 2017
Multicomponent mixtures for cryoprotection and ligand solubilizationLidia Ciccone, Laura Vera, Livia Tepshi, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|August 4, 2015
X-ray crystal structure and activity of fluorenyl-based compounds as transthyretin fibrillogenesis inhibitorsLidia Ciccone, Susanna Nencetti, Armando Rossello, et al.
Scientific Reports|June 5, 2017
Ancestral protein resurrection and engineering opportunities of the mamba aminergic toxinsGuillaume Blanchet, Doria Alili, Adèle Protte, et al.
The Journal of Biological Chemistry|December 19, 2015
Mambalgin-1 Pain-relieving Peptide, Stepwise Solid-phase Synthesis, Crystal Structure, and Functional Domain for Acid-sensing Ion Channel 1a InhibitionGilles Mourier, Miguel Salinas, Pascal Kessler, et al.
Chemmedchem|July 1, 2016
Sugar-Based Arylsulfonamide Carboxylates as Selective and Water-Soluble Matrix Metalloproteinase-12 InhibitorsElisa Nuti, Doretta Cuffaro, Felicia D'Andrea, et al.
Nature Chemical Biology|February 12, 2019
PH-domain-binding inhibitors of nucleotide exchange factor BRAG2 disrupt Arf GTPase signalingAgata Nawrotek, Sarah Benabdi, Supaporn Niyomchon, et al.
Nature Chemical Biology|March 6, 2019
Publisher Correction: PH-domain-binding inhibitors of nucleotide exchange factor BRAG2 disrupt Arf GTPase signalingAgata Nawrotek, Sarah Benabdi, Supaporn Niyomchon, et al.
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