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Thomas Durek

Showing results (51-60 of 89) with videos related to

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Nature Chemistry|May 24, 2024
Repurposing a plant peptide cyclase for targeted lysine acylationFabian B H Rehm, Tristan J Tyler, Yan Zhou, et al.
Journal of Medicinal Chemistry|December 7, 2018
Highly Potent and Selective Plasmin Inhibitors Based on the Sunflower Trypsin Inhibitor-1 Scaffold Attenuate Fibrinolysis in PlasmaJoakim E Swedberg, Guojie Wu, Tunjung Mahatmanto, et al.
ACS Chemical Biology|September 25, 2018
Targeted Delivery of Cyclotides via Conjugation to a NanobodySoohyun Kwon, Joao N Duarte, Zeyang Li, et al.
Chemical Communications (Cambridge, England)|February 15, 2013
Efficient chemical synthesis of human complement protein C3aArtin Ghassemian, Ching-I Anderson Wang, Mei-Kwan Yau, et al.
Biochemical Pharmacology|February 25, 2014
Isolation, synthesis and characterization of ω-TRTX-Cc1a, a novel tarantula venom peptide that selectively targets L-type Cav channelsJulie K Klint, Géza Berecki, Thomas Durek, et al.
RSC Chemical Biology|June 7, 2024
Chemical synthesis of grafted cyclotides using a "plug and play" approachJohannes Koehbach, Edin Muratspahić, Zakaria M Ahmed, et al.
Biomedicines|June 18, 2020
Characterization of Synthetic Tf2 as a Na<sub>V</sub>1.3 Selective Pharmacological ProbeMathilde R Israel, Thomas S Dash, Stefanie N Bothe, et al.
ACS Pharmacology & Translational Science|October 19, 2023
Development of Melanocortin 4 Receptor Agonists by Exploiting Animal-Derived Macrocyclic, Disulfide-Rich Peptide ScaffoldsEdin Muratspahić, Despoina Aslanoglou, Andrew M White, et al.
Bioorganic & Medicinal Chemistry Letters|November 3, 2015
Potent complement C3a receptor agonists derived from oxazole amino acids: Structure-activity relationshipsRanee Singh, Anthony N Reed, Peifei Chu, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 17, 2017
Mapping of voltage sensor positions in resting and inactivated mammalian sodium channels by LRETTomoya Kubota, Thomas Durek, Bobo Dang, et al.
Pageof 9

Showing results (51-60 of 89) with videos related to

Sort By:
Pageof 9
Nature Chemistry|May 24, 2024
Repurposing a plant peptide cyclase for targeted lysine acylationFabian B H Rehm, Tristan J Tyler, Yan Zhou, et al.
Journal of Medicinal Chemistry|December 7, 2018
Highly Potent and Selective Plasmin Inhibitors Based on the Sunflower Trypsin Inhibitor-1 Scaffold Attenuate Fibrinolysis in PlasmaJoakim E Swedberg, Guojie Wu, Tunjung Mahatmanto, et al.
ACS Chemical Biology|September 25, 2018
Targeted Delivery of Cyclotides via Conjugation to a NanobodySoohyun Kwon, Joao N Duarte, Zeyang Li, et al.
Chemical Communications (Cambridge, England)|February 15, 2013
Efficient chemical synthesis of human complement protein C3aArtin Ghassemian, Ching-I Anderson Wang, Mei-Kwan Yau, et al.
Biochemical Pharmacology|February 25, 2014
Isolation, synthesis and characterization of ω-TRTX-Cc1a, a novel tarantula venom peptide that selectively targets L-type Cav channelsJulie K Klint, Géza Berecki, Thomas Durek, et al.
RSC Chemical Biology|June 7, 2024
Chemical synthesis of grafted cyclotides using a "plug and play" approachJohannes Koehbach, Edin Muratspahić, Zakaria M Ahmed, et al.
Biomedicines|June 18, 2020
Characterization of Synthetic Tf2 as a Na<sub>V</sub>1.3 Selective Pharmacological ProbeMathilde R Israel, Thomas S Dash, Stefanie N Bothe, et al.
ACS Pharmacology & Translational Science|October 19, 2023
Development of Melanocortin 4 Receptor Agonists by Exploiting Animal-Derived Macrocyclic, Disulfide-Rich Peptide ScaffoldsEdin Muratspahić, Despoina Aslanoglou, Andrew M White, et al.
Bioorganic & Medicinal Chemistry Letters|November 3, 2015
Potent complement C3a receptor agonists derived from oxazole amino acids: Structure-activity relationshipsRanee Singh, Anthony N Reed, Peifei Chu, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 17, 2017
Mapping of voltage sensor positions in resting and inactivated mammalian sodium channels by LRETTomoya Kubota, Thomas Durek, Bobo Dang, et al.
Pageof 9