Maire F. Osborn, Ph.D.

Affiliations: 
Chemistry and Biochemistry University of Oregon, Eugene, OR, United States 
Area:
Bioinorganic Chemistry, Biophysical Chemistry & Chemical Biology
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"Maire Osborn"
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Victoria J. DeRose grad student 2014 University of Oregon
 (Cellular RNA targeting by platinum (II) anticancer therapeutics.)
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Publications

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Biscans A, Coles A, Haraszti R, et al. (2019) Diverse lipid conjugates for functional extra-hepatic siRNA delivery in vivo. Nucleic Acids Research. 47: 1082-1096
Osborn MF, Coles AH, Biscans A, et al. (2018) Hydrophobicity drives the systemic distribution of lipid-conjugated siRNAs via lipid transport pathways. Nucleic Acids Research
Osborn MF, Khvorova A. (2018) Improving Small Interfering RNA Delivery In Vivo Through Lipid Conjugation. Nucleic Acid Therapeutics
Osborn MF, Coles AH, Golebiowski D, et al. (2018) Efficient gene silencing in brain tumors with hydrophobically modified siRNAs. Molecular Cancer Therapeutics
Hassler MR, Turanov AA, Alterman JF, et al. (2018) Comparison of partially and fully chemically-modified siRNA in conjugate-mediated delivery in vivo. Nucleic Acids Research
Nikan M, Osborn MF, Coles AH, et al. (2017) Synthesis and Evaluation of Parenchymal Retention and Efficacy of a Metabolically Stable, O-phosphocholine-N-docosahexaenoyl-L-serine siRNA Conjugate in Mouse Brain. Bioconjugate Chemistry
Nikan M, Osborn MF, Coles AH, et al. (2016) Docosahexaenoic Acid Conjugation Enhances Distribution and Safety of siRNA upon Local Administration in Mouse Brain. Molecular Therapy. Nucleic Acids. 5: e344
Coles AH, Osborn MF, Golebowski D, et al. (2016) Abstract PR12: Robust modulation of gene expression in aggressive glioblastoma mouse models: A new approach for in vivo target validation Cancer Research. 76
Alterman JF, Hall LM, Coles AH, et al. (2015) Hydrophobically Modified siRNAs Silence Huntingtin mRNA in Primary Neurons and Mouse Brain. Molecular Therapy. Nucleic Acids. 4: e266
Coles AH, Osborn MF, Alterman JF, et al. (2015) A High-Throughput Method for Direct Detection of Therapeutic Oligonucleotide-Induced Gene Silencing In Vivo. Nucleic Acid Therapeutics
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