Cancer Drug Delivery Systems Using Bacterial Toxin Translocation Mechanisms
Author:
Affiliation:
1. Department of Urology, Boston Children’s Hospital, Boston, MA 02115, USA
2. Department of Surgery, Harvard Medical School, Boston, MA 02115, USA
3. Department of Microbiology, Harvard Medical School, Boston, MA 02115, USA
Abstract
Funder
National Institute of Health
Office of Faculty Development at Harvard Medical School
NIH-funded Harvard Digestive Disease Center
Boston Children’s Hospital Intellectual and Developmental Disabilities Research Center
Harvard Center for Glycoscience
Publisher
MDPI AG
Subject
Bioengineering
Link
https://www.mdpi.com/2306-5354/10/7/813/pdf
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3. Emerging enterococcus pore-forming toxins with MHC/HLA-I as receptors;Xiong;Cell,2022
4. Botulinum and Tetanus Neurotoxins;Dong;Annu. Rev. Biochem.,2019
5. Yin, L., Masuyer, G., Zhang, S., Zhang, J., Miyashita, S.I., Burgin, D., Lovelock, L., Coker, S.F., Fu, T.M., and Stenmark, P. (2020). Characterization of a membrane binding loop leads to engineering botulinum neurotoxin B with improved therapeutic efficacy. PLoS Biol., 18.
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