This institutional DSA program has graduated a total of eight clinical scholars. In addition, four clinical scholars were trained on individual DSA/PSA awards. Four clinical scholars funded by other mechanisms have also graduated. Ten other graduates have been funded through other sources. Thus, our training history is a total of twenty-six graduates. Six of the present roster of ten active students are in combined programs, attesting to our commitment to combined certificate/Ph.D. training. All of our DSA clinical scholars have completed their certificate and Ph.D. programs and have entered productive careers; no one has defaulted either by leaving the program or by entering private practice. The clinical scholars who are positioned to obtain independent funding have done so; 89% are funded. The programs, both clinical and graduate, accommodate their schedules to ensure efficient and successful progress through the program. Because of the diversity and complexity of oral disease, training is focused on basic biological problems related to the oral cavity in health and disease rather than a single discipline- centered program. The organization of a faculty of basic scientists and dental and medical clinicians in this training program has permitted us to offer a range of opportunities for students of dental health and disease. In addition, research centers in chemosensory systems, dental and general clinical research and biomaterials have fostered the active participation of the Oral Biology Graduate Faculty (OBGF) in the clinical and scientific education of clinical scholars by serving as mentors for their research. Because the faculty are engaged in multidisciplinary collaborations, individually and through research centers and program projects, the OBGF is diverse, is drawn from all segments of the Health Center and represents a range of investigative expertise and interests. This mix of clinical programs and manifold research opportunities provides a dynamic and stimulating training environment. Consequently, the research projects devised for our students have had a similar breadth and scope. The objective of this program is to offer a program that produces highly qualified clinical scholars competent in their clinical disciplines and as independent scientists able to initiate and maintain funded research programs. In addition, the program will provide educational experiences that are tailored to each candidate, while maintaining a focus in the oral biological sciences through seminars, courses, clinical research centers and collaborative research activities.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Unknown (K16)
Project #
5K16DE000157-09
Application #
2896877
Study Section
Special Emphasis Panel (ZDE1-GH (26))
Project Start
1996-07-01
Project End
2001-06-30
Budget Start
1999-07-01
Budget End
2000-06-30
Support Year
9
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Connecticut
Department
Dentistry
Type
Schools of Dentistry
DUNS #
City
Farmington
State
CT
Country
United States
Zip Code
06030
Havens, Bruce A; Velonis, Dimitris; Kronenberg, Mark S et al. (2008) Roles of FGFR3 during morphogenesis of Meckel's cartilage and mandibular bones. Dev Biol 316:336-49
Mina, Mina; Havens, Bruce (2007) FGF signaling in mandibular skeletogenesis. Orthod Craniofac Res 10:59-66
Krebs, L J; Arnold, A (2002) Molecular basis of hyperparathyroidism and potential targets for drug development. Curr Drug Targets Immune Endocr Metabol Disord 2:167-79
Helms, J A; Della-Fera, M A; Mott, A E et al. (1995) Effects of chlorhexidine on human taste perception. Arch Oral Biol 40:913-20
Chandrasekaran, S; Tanzer, M L; Giniger, M S (1994) Characterization of oligomannoside binding to the surface of murine melanoma cells. Potential relationship to oligomannoside-initiated cell spreading. J Biol Chem 269:3367-73
Chandrasekaran, S; Tanzer, M L; Giniger, M S (1994) Oligomannosides initiate cell spreading of laminin-adherent murine melanoma cells. J Biol Chem 269:3356-66
Helms, J A; Kuratani, S; Maxwell, G D (1994) Cloning and analysis of a new developmentally regulated member of the basic helix-loop-helix family. Mech Dev 48:93-108
Tanzer, M L; Giniger, M S; Chandrasekaran, S (1993) Laminin oligosaccharides play a pivotal role in cell spreading. Symp Soc Exp Biol 47:147-54
Gronowicz, G; Hadjimichael, J; Richards, D et al. (1992) Correlation between tumor necrosis factor-alpha (TNF-alpha)-induced cytoskeletal changes and human collagenase gene induction. J Periodontal Res 27:562-8
Chandrasekaran, S; Dean 3rd, J W; Giniger, M S et al. (1991) Laminin carbohydrates are implicated in cell signaling. J Cell Biochem 46:115-24

Showing the most recent 10 out of 14 publications