Rachel E. Johns, Ph.D.
Affiliations: | University of Washington, Seattle, Seattle, WA |
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Parents
Sign in to add mentor| Allan S. Hoffman | grad student | 2007 | University of Washington | |
| (Delivery of anti -inflammatory nucleic acid therapeutics using smart polymeric carriers.) | ||||
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Publications
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| Seth S, Johns R, Templin MV. (2012) Delivery and biodistribution of siRNA for cancer therapy: challenges and future prospects. Therapeutic Delivery. 3: 245-61 |
| Liu Y, Chen Y, Fosnaugh K, et al. (2012) Abstract 281: Novel nucleic acid constructs and formulations for treatment of bladder cancer and malignant ascites Cancer Research. 72: 281-281 |
| Adami RC, Seth S, Harvie P, et al. (2011) An amino acid-based amphoteric liposomal delivery system for systemic administration of siRNA. Molecular Therapy : the Journal of the American Society of Gene Therapy. 19: 1141-51 |
| Seth S, Matsui Y, Fosnaugh K, et al. (2011) RNAi-based therapeutics targeting survivin and PLK1 for treatment of bladder cancer. Molecular Therapy : the Journal of the American Society of Gene Therapy. 19: 928-35 |
| Collie AM, Bota PC, Johns RE, et al. (2011) Differential monocyte/macrophage interleukin-1β production due to biomaterial topography requires the β2 integrin signaling pathway. Journal of Biomedical Materials Research. Part A. 96: 162-9 |
| Vaish N, Chen F, Seth S, et al. (2011) Improved specificity of gene silencing by siRNAs containing unlocked nucleobase analogs. Nucleic Acids Research. 39: 1823-32 |
| Fosnaugh KL, Seth S, Matsui Y, et al. (2010) Abstract 581: Development of RNA interference-based therapeutics for bladder cancer and hepatocellular carcinoma Cancer Research. 70: 581-581 |
| Johns RE, El-Sayed ME, Bulmus V, et al. (2008) Mechanistic analysis of macrophage response to IRAK-1 gene knockdown by a smart polymer-antisense oligonucleotide therapeutic. Journal of Biomaterials Science. Polymer Edition. 19: 1333-46 |
| Johns RE, Hoffman AS, Stayton PS. (2004) 639. Gene Expression Analysis of LPS Stimulated THP-1 Cells Treated with Antisense IRAK1 Delivered Using a pH-Sensitive, Membrane Disruptive Polymer Molecular Therapy. 9 |