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The discovery of high-affinity peptides to many intracellular targets has become feasible through the development of diverse macrocyclic peptide libraries. But lack of cell permeability is a key feature hampering the use of these peptides as therapeu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aad090e547e0b7cd0e6537bbdf4ce531
https://doi.org/10.26434/chemrxiv.12445226
https://doi.org/10.26434/chemrxiv.12445226