C
C. Shad Thaxton
Researcher at Northwestern University
Publications - 104
Citations - 10390
C. Shad Thaxton is an academic researcher from Northwestern University. The author has contributed to research in topics: Cancer & Colloidal gold. The author has an hindex of 36, co-authored 101 publications receiving 9704 citations. Previous affiliations of C. Shad Thaxton include International Institute of Minnesota.
Papers
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Journal ArticleDOI
Comparison of prostate specific antigen velocity in screened versus referred patients with prostate cancer.
Joshua J. Meeks,C. Shad Thaxton,Stacy Loeb,Kimberly A. Roehl,Brian T. Helfand,William J. Catalona +5 more
TL;DR: Prostate specific antigen velocity more than 2 ng/ml per year has been linked to a significantly greater risk of prostate cancer specific mortality, suggesting that screen detected prostate cancer may be more likely to be cured with definitive therapy.
Journal ArticleDOI
Knockdown of intraislet IKKβ by spherical nucleic acid conjugates prevents cytokine-induced injury and enhances graft survival.
Jonathan S. Rink,Kaylin M. McMahon,Xiaomin Zhang,Xiaojuan Chen,Chad A. Mirkin,C. Shad Thaxton,Dixon B. Kaufman +6 more
TL;DR: Results are consistent with the hypothesis that inhibition of intraislet NF-&kgr;B activation ameliorates the detrimental effects of host cytokines and demonstrates that preconditioning freshly isolated islets in culture with IKK&bgr; SNA-NCs may be a promising therapy to enhance islet graft function and survival after transplantation.
Posted ContentDOI
Induction of DISE in ovarian cancer cells in vivo
Andrea E. Murmann,Kaylin M. McMahon,Ashley Haluck-Kangas,Nandini Ravindran,Monal Patel,Calvin Law,Sonia Brockway,Jian-Jun Wei,C. Shad Thaxton,Marcus E. Peter +9 more
TL;DR: In this paper, a form of off-target effect DISE (for death induced by survival gene elimination) was proposed for cancer cells in the absence of the target by targeting the 3′UTRs of critical survival genes through canonical RNAi.
Journal ArticleDOI
Mosaic Interdigitated Structure in Nanoparticle-Templated Phospholipid Bilayer Supports Partial Lipidation of Apolipoprotein A-I.
TL;DR: The discontinuous lipid milieu supports partial lipidation of apolipoprotein A-I, different from an ordinary phospholipid bilayer, suggesting that synergy between nanoparticle templates and bound phospholIPid layers can modulate amphiphilic proteins for desired functions.
Patent
High density lipoprotein nanoparticles for inflammation
C. Shad Thaxton,Linda Foit +1 more
TL;DR: In this paper, the use of nanoparticles having a core and a lipid based shell with optimal lipids therein is described, which are used for treating sepsis using HDL-NP.