Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 32 checked references that resolve
resolves10.1039/C3CC46317FRecent advances in amino acid N-carboxyanhydrides and synthetic polypeptides: chemistry, self-assembly and biological applications
resolves10.1016/j.progpolymsci.2013.10.008Functional polypeptide and hybrid materials: Precision synthesis via α-amino acid N-carboxyanhydride polymerization and emerging biomedical applications
resolves10.1039/C4CS00271GBiodegradable stimuli-responsive polypeptide materials prepared by ring opening polymerization
resolves10.1021/ja3007484Glycopolypeptides with a Redox-Triggered Helix-to-Coil Transition
resolves10.1021/ja993637vMethylated Mono- and Diethyleneglycol Functionalized Polylysines: Nonionic, α-Helical, Water-Soluble Polypeptides
resolves10.1021/ma400678wThermoresponsive Oligo(ethylene glycol) Functionalized Poly-<scp>l</scp>-cysteine
resolves10.1021/ja500372uMultimodal Switching of Conformation and Solubility in Homocysteine Derived Polypeptides
resolves10.1039/C6CC01253AChemoselective synthesis of functional homocysteine residues in polypeptides and peptides
resolves10.1039/C4PY01560FNon-ionic water-soluble “clickable” α-helical polypeptides: synthesis, characterization and side chain modification
resolves10.1021/ja107425fGlycopolypeptides via Living Polymerization of Glycosylated-<scp>l</scp>-lysine <i>N</i>-Carboxyanhydrides
resolves10.1021/bm201813sControlled Synthesis of <i>O</i>-Glycopolypeptide Polymers and Their Molecular Recognition by Lectins
resolves10.1039/c0py00412jSynthesis of glycopolypeptides by the ring opening polymerization of O-glycosylated-α-amino acid N-carboxyanhydride (NCA)
resolves10.1038/nmat1093Stimuli-responsive polypeptide vesicles by conformation-specific assembly
resolves10.1002/mabi.201400348Blending of Diblock and Triblock Copolypeptide Amphiphiles Yields Cell Penetrating Vesicles with Low Toxicity
resolves10.1021/jo100448qCarbohydrate-Based Synthetic Approach to Control Toxicity Profiles of Folate−Drug Conjugates
resolves10.1021/bc2005522Engineering Folate–Drug Conjugates to Target Cancer: From Chemistry to Clinic
resolves10.1021/jo00035a044The use of triphosgene in preparation of N-carboxy .alpha.-amino acid anhydrides
resolves10.1021/ja803304x<i>N</i>-Trimethylsilyl Amines for Controlled Ring-Opening Polymerization of Amino Acid <i>N</i>-Carboxyanhydrides and Facile End Group Functionalization of Polypeptides
resolves10.1021/bi000099mDifferences in Stability among the Human Apolipoprotein E Isoforms Determined by the Amino-Terminal Domain
resolves10.1021/ma00081a040Glycopeptide Synthesis by an .alpha.-Amino Acid N-Carboxyanhydride (NCA) Method: Ring-Opening Polymerization of a Sugar-Substituted NCA
resolves10.1021/cr900049tSynthesis of Well-Defined Polypeptide-Based Materials via the Ring-Opening Polymerization of α-Amino Acid <i>N</i>-Carboxyanhydrides
resolves10.1021/ja074961qHexamethyldisilazane-Mediated Controlled Polymerization of α-Amino Acid<i>N</i>-Carboxyanhydrides
resolves10.1110/ps.4210102Natively unfolded proteins: A point where biology waits for physics
resolves10.1038/srep05224Transient α-helices in the disordered RPEL motifs of the serum response factor coactivator MKL1
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