Disulfide Bond Replacement with Non-Reducible Side Chain to Tail Macrolactamization for the Development of Potent and Selective Cxcr4 Peptide Antagonists Endowed with Flanking Binding Sites-Reference-Cited by-同舟云学术

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Disulfide Bond Replacement with Non-Reducible Side Chain to Tail Macrolactamization for the Development of Potent and Selective Cxcr4 Peptide Antagonists Endowed with Flanking Binding Sites

Published:2024 Issue: Volume: Page:
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Author:

Trotta Anna Maria,Tomassi Stefano,Di Maiolo Gaetana,Ieranò Caterina,Vetrei Cinzia,Merlino Francesco,Messere Anna,D’Aniello Antonia,Natale Benito,Del Bene Alessandra,Mazzarella Vincenzo,Roggia Michele,Cutolo Roberto,Campagna Erica,Mottola Salvatore,Russo Rosita,Chambery Angela,Altucci Lucia,Benedetti Rosaria,Cosconati Sandro,Scala Stefania,Di Maro Salvatore

Publisher

Elsevier BV

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2. CXCR4 expression in the bone marrow microenvironment is required for hematopoietic stem and progenitor cell maintenance and early hematopoietic regeneration after myeloablation;P Singh;Stem Cells,2020

3. Vascular endothelial growth factor and basic fibroblast growth factor induce expression of CXCR4 on human endothelial cells: In vivo neovascularization induced by stromal-derived factor-1alpha;R Salcedo;Am. J. Pathol,1999

4. CXCR4 regulates interneuron migration in the developing neocortex;R K Stumm;J. Neurosci,2003

5. HIV-1 entry cofactor: functional cDNA cloning of a seven-transmembrane, G protein-coupled receptor;Y Feng;Science,1996

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