The Hollings Cancer Center (HCC) Administration provides key services to facilitate and enhance scientific productivity and collaboration among its 122 faculty research members who are organized into four research programs and who utilize HCC-supported shared resources. Administrative services include: ? Coordination of and participation in Center-wide strategic planning and evaluation efforts. ? Stimulation and support of inter-, intra-programmatic, and multi-center interactions;services include targeted grant development support and consultation, meeting organization and documentation, and retreat/seminar/symposia coordination. ? Administrative oversight and support for HCC-supported shared resources including the establishment of user fees, billing, auditing, coordination of and participation in oversight committees, and evaluations. ? Coordination and oversight of all Center-related development/fundraising activities. ? Fiscal management and oversight of all HCC resources and university and MUSC Foundation accounts related to the Center. ? Facilities management of all assigned HCC space and equipment. ? Coordination of new faculty recruitment in collaboration with other university departments. ? Human resource management of Center staff. ? Management of HCC membership including new application processes and annual reviews. ? Administration of pilot projects and other internal research award processes. ? Computer networking and design of research management databases. ? Coordination of internal communications and public relations for all Center activities.
The HCC Administration is an essential component of the overall Center's efforts in that it provides key services - fiscal management, meeting/project/program coordination, facilities management, and communications - to ensure that the Center is able to meet its mission, vision, and strategic goals.
|Link, Laura A; Howley, Breege V; Hussey, George S et al. (2016) PCBP1/HNRNP E1 Protects Chromosomal Integrity by Translational Regulation of CDC27. Mol Cancer Res 14:634-46|
|Nelson, Michelle H; Bowers, Jacob S; Bailey, Stefanie R et al. (2016) Toll-like receptor agonist therapy can profoundly augment the antitumor activity of adoptively transferred CD8(+) T cells without host preconditioning. J Immunother Cancer 4:6|
|Podbielska, Maria; Szulc, ZdzisÅ‚aw M; Kurowska, Ewa et al. (2016) Cytokine-induced release of ceramide-enriched exosomes as a mediator of cell death signaling in an oligodendroglioma cell line. J Lipid Res 57:2028-2039|
|Sambandam, Yuvaraj; Sakamuri, Sashank; Balasubramanian, Sundaravadivel et al. (2016) RANK Ligand Modulation of Autophagy in Oral Squamous Cell Carcinoma Tumor Cells. J Cell Biochem 117:118-25|
|Miller, Kayla; Dixit, Suraj; Bredlau, Amy-Lee et al. (2016) Delivery of a drug cache to glioma cells overexpressing platelet-derived growth factor receptor using lipid nanocarriers. Nanomedicine (Lond) 11:581-95|
|Basher, Fahmin; Jeng, Emily K; Wong, Hing et al. (2016) Cooperative therapeutic anti-tumor effect of IL-15 agonist ALT-803 and co-targeting soluble NKG2D ligand sMIC. Oncotarget 7:814-30|
|Small, James; Flanagan, Catherine; Armeson, Kent et al. (2016) Family history of cutaneous and noncutaneous malignancies in relation to the risk of keratinocyte carcinoma coupled with another type of cancer: A case-control study. J Am Acad Dermatol 75:1066-1068.e7|
|Maldonado, Eduardo N; DeHart, David N; Patnaik, Jyoti et al. (2016) ATP/ADP Turnover and Import of Glycolytic ATP into Mitochondria in Cancer Cells Is Independent of the Adenine Nucleotide Translocator. J Biol Chem 291:19642-50|
|Hendriks, Giel; Derr, Remco S; Misovic, Branislav et al. (2016) The Extended ToxTracker Assay Discriminates Between Induction of DNA Damage, Oxidative Stress, and Protein Misfolding. Toxicol Sci 150:190-203|
|Paul, Matt R; Levitt, Nicholas P; Moore, David E et al. (2016) Multivariate models from RNA-Seq SNVs yield candidate molecular targets for biomarker discovery: SNV-DA. BMC Genomics 17:263|
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