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Arnab Rudra, Ph.D.

Affiliations: 
2006-2013 Chemistry University of Utah, Salt Lake City, UT 
 2013-2015 Chemistry Johns Hopkins University, Baltimore, MD 
Area:
Organic synthesis, Nucleic acid chemistry
Website:
http://www.ncbi.nlm.nih.gov/myncbi/browse/collection/42803414/?sort=date&direction=descending
Google:
"https://scholar.google.com/citations?user=WUtSYXYAAAAJ&hl=en (remove quotes)"
Mean distance: 7.83
 
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Publications

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Gupta A, Rudra A, Reed K, et al. (2024) Advanced technologies for the development of infectious disease vaccines. Nature Reviews. Drug Discovery
Momin N, Pabel S, Rudra A, et al. (2024) Therapeutic silencing in TREM2 cardiac macrophages suppresses atrial fibrillation. Biorxiv : the Preprint Server For Biology
Rudra A, Li J, Shakur R, et al. (2020) Addition to "Trends in Therapeutic Conjugates: Bench to Clinic". Bioconjugate Chemistry
Rudra A, Li J, Shakur R, et al. (2020) Trends in Therapeutic Conjugates: Bench to Clinic. Bioconjugate Chemistry
Kowalski PS, Rudra A, Miao L, et al. (2019) Delivering the Messenger: Advances in Technologies for Therapeutic mRNA Delivery. Molecular Therapy : the Journal of the American Society of Gene Therapy
Kowalski PS, Capasso Palmiero U, Huang Y, et al. (2018) Ionizable Amino-Polyesters Synthesized via Ring Opening Polymerization of Tertiary Amino-Alcohols for Tissue Selective mRNA Delivery. Advanced Materials (Deerfield Beach, Fla.). e1801151
Rudra A, Hou D, Zhang Y, et al. (2015) Bromopyridone Nucleotide Analogues, Anoxic Selective Radiosensitizing Agents That Are Incorporated in DNA by Polymerases. The Journal of Organic Chemistry. 80: 10675-85
Kedei N, Lewin NE, Géczy T, et al. (2013) Biological profile of the less lipophilic and synthetically more accessible bryostatin 7 closely resembles that of bryostatin 1. Acs Chemical Biology. 8: 767-77
Kedei N, Telek A, Michalowski AM, et al. (2013) Comparison of transcriptional response to phorbol ester, bryostatin 1, and bryostatin analogs in LNCaP and U937 cancer cell lines provides insight into their differential mechanism of action. Biochemical Pharmacology. 85: 313-24
Keck GE, Poudel YB, Rudra A, et al. (2012) Role of the C8 gem-dimethyl group of bryostatin 1 on its unique pattern of biological activity. Bioorganic & Medicinal Chemistry Letters. 22: 4084-8
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