Conjugation of arginine oligomers to cyclosporin A facilitates topical delivery and inhibition of inflammation
By J. Rothbard, Sarah B. Garlington, Q. Lin, T. Kirschberg, Erik Kreider, P. Mcgrane, P. Wender, P. Khavari. Nature Medicine, 2000
622 citations recorded by the source corpus.
Subfields: Epidemiology, Immunology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/af9265398d923497e6c15f2594bd4679d732f4b8
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In Epidemiology
In Molecular Biology
- A. Letai
- S. Korsmeyer
- Michael C. Bassik
- Douglas R. Green
- Jerry M. Adams
- J. Chipuk
- Suzanne Cory
- A. Strasser
Citations in the corpus
- Distinct BH3 domains either sensitize or activate mitochondrial apoptosis, serving as prototype cancer therapeutics. (2002, background): “This finding suggests that a conformational peptides across the plasma membrane (Rothbard et al., 2000). change takes place in either BCL-2 and/or a BH3 peptide upon r8BIDBH3 was capable of killing Jurkat leukemic cells, whereas binding.”
- Cell-Penetrating Peptides: From Basic Research to Clinics. (2017, background): “However, this problem was overcome by conjugating CsA to a polyarginine [114].”