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Jens Meiler

Showing results (251-260 of 432) with videos related to

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Angewandte Chemie (International Ed. in English)|December 6, 2024
Hederagenin is a Highly Selective Antagonist of the Neuropeptide FF Receptor 1 that Reveals Mechanisms for Subtype SelectivityHannah Lentschat, Fabian Liessmann, Claiborne Tydings, et al.
Scientific Reports|November 13, 2020
Characterization of the ExoU activation mechanism using EPR and integrative modelingMaxx H Tessmer, Samuel A DeCero, Diego Del Alamo, et al.
Retrovirology|April 21, 2012
Second-site suppressors of HIV-1 capsid mutations: restoration of intracellular activities without correction of intrinsic capsid stability defectsRuifeng Yang, Jiong Shi, In-Ja L Byeon, et al.
Journal of the Endocrine Society|August 18, 2020
Phenotypic Profiling in Subjects Heterozygous for 1 of 2 Rare Variants in the Hypophosphatasia Gene (<i>ALPL</i>)Daniel R Tilden, Jonathan H Sheehan, John H Newman, et al.
ACS Chemical Neuroscience|June 7, 2024
Computer-Aided Design and Biological Evaluation of Diazaspirocyclic D<sub>4</sub>R AntagonistsCaleb A H Jones, Benjamin P Brown, Daniel C Schultz, et al.
Biochemistry|January 10, 2023
Rosetta's Predictive Ability for Low-Affinity Ligand Binding in Fragment-Based Drug DiscoveryElleansar Okwei, Shannon T Smith, Brian J Bender, et al.
Structure (London, England : 1993)|April 29, 2023
Computational modeling and prediction of deletion mutantsHope Woods, Dominic L Schiano, Jonathan I Aguirre, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 25, 2011
Interaction of a G protein with an activated receptor opens the interdomain interface in the alpha subunitNed Van Eps, Anita M Preininger, Nathan Alexander, et al.
Cellular and Molecular Life Sciences : CMLS|July 9, 2021
Ligand-binding and -scavenging of the chemerin receptor GPR1Tobias F Fischer, Anne S Czerniak, Tina Weiß, et al.
Cellular and Molecular Life Sciences : CMLS|January 13, 2026
The pathway-independent positive allosteric modulator C1 allows for the identification of active Y<sub>4</sub> receptor relevant positionsCorinna Schüß, Oanh Vu, Tim Pelczyk, et al.
Pageof 44

Showing results (251-260 of 432) with videos related to

Sort By:
Pageof 44
Angewandte Chemie (International Ed. in English)|December 6, 2024
Hederagenin is a Highly Selective Antagonist of the Neuropeptide FF Receptor 1 that Reveals Mechanisms for Subtype SelectivityHannah Lentschat, Fabian Liessmann, Claiborne Tydings, et al.
Scientific Reports|November 13, 2020
Characterization of the ExoU activation mechanism using EPR and integrative modelingMaxx H Tessmer, Samuel A DeCero, Diego Del Alamo, et al.
Retrovirology|April 21, 2012
Second-site suppressors of HIV-1 capsid mutations: restoration of intracellular activities without correction of intrinsic capsid stability defectsRuifeng Yang, Jiong Shi, In-Ja L Byeon, et al.
Journal of the Endocrine Society|August 18, 2020
Phenotypic Profiling in Subjects Heterozygous for 1 of 2 Rare Variants in the Hypophosphatasia Gene (<i>ALPL</i>)Daniel R Tilden, Jonathan H Sheehan, John H Newman, et al.
ACS Chemical Neuroscience|June 7, 2024
Computer-Aided Design and Biological Evaluation of Diazaspirocyclic D<sub>4</sub>R AntagonistsCaleb A H Jones, Benjamin P Brown, Daniel C Schultz, et al.
Biochemistry|January 10, 2023
Rosetta's Predictive Ability for Low-Affinity Ligand Binding in Fragment-Based Drug DiscoveryElleansar Okwei, Shannon T Smith, Brian J Bender, et al.
Structure (London, England : 1993)|April 29, 2023
Computational modeling and prediction of deletion mutantsHope Woods, Dominic L Schiano, Jonathan I Aguirre, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 25, 2011
Interaction of a G protein with an activated receptor opens the interdomain interface in the alpha subunitNed Van Eps, Anita M Preininger, Nathan Alexander, et al.
Cellular and Molecular Life Sciences : CMLS|July 9, 2021
Ligand-binding and -scavenging of the chemerin receptor GPR1Tobias F Fischer, Anne S Czerniak, Tina Weiß, et al.
Cellular and Molecular Life Sciences : CMLS|January 13, 2026
The pathway-independent positive allosteric modulator C1 allows for the identification of active Y<sub>4</sub> receptor relevant positionsCorinna Schüß, Oanh Vu, Tim Pelczyk, et al.
Pageof 44