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J., Cao, Y., Li, C
[DOI] [PubMed] [Google Scholar] 3.Ilic S, Drmic D, Zarkovic K, Kolenc D, Brcic L, Radic B, et al
doi: 10.3390/ijms25021276 174 YumnamSKangMCOhSHKwonHCKimJCJungESet al
Identification of N-terminally diversified GLP-1R agonists using saturation mutagenesis and chemical design
IGF-1 decreases GH levels by growth hormone releasing hormone (GHRH)-dependent feedback mechanisms
Pharmacokinetic limitations, such as rapid metabolism and short half-lives, further complicate achieving therapeutic concentrations within brain tumors while minimizing systemic toxicity
