cameron dodd

*  Reorganized older files by date for greater departmental efficiency *  Reorganized key and locking system for greater departmental efficiency *  Created cabinet space organizational system for the department *  Improved imaging cover sheets for greater departmental efficiency *  Reconciled, created, converted, and quality controlled invoices *  Created, filed, scanned, updated, checked, processed, executed, and notarized loan modifications *  Recorded, coded, processed, scanned, and filed Rejections *  Managed, organized, coded, imaged, processed, and distributed mail *  Trained new hires

* Supervised by Dr. Michael Roner *  Reviewed latest literature pertaining to Natural Killer Cells *  Designed an experiment to examine how activation of Natural Killer Cells activated by exercise impact cancer rates. * Supervised by Dr. Robert Gatchel *  Examined treatment efficacy for Tempomandibular Joint and Muscle Disorder (TMJMD) *  Entered patient data for the Beck’s Depression Inventory and Structured Clinical Interview for Diagnostics *  Consolidated multiple patient entries into one concise folder for each patient *  Created initial filing organization for consolidated patient folders *  Checked large databases for accuracy of content *  Literature searches for musculoskeletal and neurological pain in reference to TMJMD *  Developed poster and presentation for research *  Assisted in the meta-analysis of treatment success for chronic back pain *  Rated articles for level of evidence according to the Journal of Bone and Joint Surgery levels *  Denoted bias using Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) methods

* Supervised by Dr. Michael Roner *  Tested inhibition of Rotavirus through co-infection with Reovirus and stained to make the results more visible *  Aided in animal trial to test the ability of saponin extracts to inhibit Rotavirus *  Maintained epithelial cell cultures for infection *  Cultured virus stock through multi-passage lysate *  Performed HPLC to fractionate the saponin, in an attempt to identify the active component *  Determined effectiveness of saponins to inhibit Rotavirus through Plaque Inhibition Assays *  Examined in vitro viability using Cytotoxicity Assays. *  Volunteered at adjacent lab and performed site-directed mutagenesis PCR, cloning PCR, common PCR, ELISA, and blotting techniques in an attempt to increase targeted protein synthesis in E. coli. *  Mixed media, alcohol, buffer, and trypsin solutions. *  Maintained lab through inventory, autoclaving glassware and waste, and general maintenance

In progress, expected graduation date: August 2015