about
Iterative Nonproteinogenic Residue Incorporation Yields α/β-Peptides with a Helix-Loop-Helix Tertiary Structure and High Affinity for VEGF.Differential Effects of β - versus β -Amino Acid Residues on the Helicity and Recognition Properties of Bim BH3-Derived α/β-PeptidesFoldamer-templated catalysis of macrocycle formationGq/11-dependent regulation of endosomal cAMP generation by parathyroid hormone class B GPCRA Hendecad Motif Is Preferred for Heterochiral Coiled-Coil FormationRetention of Coiled-Coil Dimer Formation in the Absence of Ion Pairing at Positions Flanking the Hydrophobic CoreDual Inhibition of Human Parainfluenza Type 3 and Respiratory Syncytial Virus Infectivity with a Single AgentUse of a Stereochemical Strategy To Probe the Mechanism of Phenol-Soluble Modulin α3 ToxicityKetones from Nickel-Catalyzed Decarboxylative, Non-Symmetric Cross-Electrophile Coupling of Carboxylic Acid EstersRetention of Native Quaternary Structure in Racemic Melittin CrystalsRecognition of Class II MHC Peptide Ligands That Contain β-Amino AcidsPreparation of β2-Homologous Amino Acids Bearing Polar Side Chains via a Collective Synthesis StrategyImpact of Substitution Registry on the Receptor-Activation Profiles of Backbone-Modified Glucagon-like Peptide-1 AnaloguesStructure-Guided Improvement of a Dual HPIV3/RSV Fusion InhibitorReceptor selectivity from minimal backbone modification of a polypeptide agonistUse of Backbone Modification To Enlarge the Spatiotemporal Diversity of Parathyroid Hormone Receptor-1 Signaling via Biased AgonismCatalytic Intramolecular Conjugate Additions of Aldehyde-Derived Enamines to α,β-Unsaturated Esters
P50
Q39145905-3B934E59-30C8-4357-80A6-81122631E3FDQ57461225-4167EFA2-4D96-45D8-A6D1-A59CA2DA4EDFQ85544065-DA959F86-7AD2-4F47-AABB-8DF3B3A5A1F0Q90407605-02940F95-7535-49FF-8D8E-CE2CF4E1828BQ91052837-C1017994-A1E3-4187-98D7-F3BF5BAEA661Q91322426-6E9A97D2-9B4F-4785-B861-DF6F10D000D3Q91579410-DBFDFF12-DCBD-4466-BD7F-0E0760DDE544Q91689640-1109BD10-1619-4D49-A441-E68078748F79Q91743621-6B962175-4C77-4A6E-B158-9589C8375916Q91787146-14E9BD76-06FD-4ADE-8B53-139DE7EE1CDFQ92481860-09BA322C-DB8F-4DF8-904F-0D45278FF232Q92531870-63992CD0-DEE7-494C-B50C-CB8D93668E5EQ92577837-7FE2003E-4C66-4307-BA64-9AD212B90C2EQ92728251-36E8198E-A1C6-4D4D-AA62-B9B8119259DEQ93159389-E9764E91-F365-4CFB-A044-ABDC48E2FCABQ93182302-8DDB0EB3-5B32-4593-9960-58F27C8524F8Q95926255-08619A33-DD00-4075-8E34-F4265E17619D
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Samuel H. Gellman
@en
Samuel H. Gellman
@nl
type
label
Samuel H. Gellman
@en
Samuel H. Gellman
@nl
prefLabel
Samuel H. Gellman
@en
Samuel H. Gellman
@nl
P31
P496
0000-0001-5617-0058