The Laboratories for Reproductive Biology (LRB) proposes to continue a multidisciplinary postdoctoral training program for scientists interested in pursuing careers in reproductive biology. The program is designed to produce reproductive scientists for research in academic, industrial or government laboratories. It is intended that the training program will produce well trained investigators needed to further our understanding of molecular mechanisms regulating reproductive functions. The program provides training in four interrelated areas: 1) Molecular Mechanisms Controlling Gonadal Functions; 2) Reproductive Steroid Hormone Action; 3) Regulation of Sperm Maturation; 4) Fertilization and Implantation. The training faculty consists of 6 members at the University of North Carolina at Chapel Hill (UNCCH). In addition there are collaborating members of the training faculty at UNC-CH, at the National Institute of Environmental Health Sciences (NIEHS) in North Carolina's Research Triangle Park, and at Duke University and North Carolina State University. Although collaborating members do not serve as primary preceptors, they enrich the depth of training experience through research interactions with trainees and training preceptors. Research training is centered in the laboratories of the primary sponsors and includes: 1) courses in basic reproductive biology; 2) a seminar series at which trainees present their research results to other trainees and the training faculty; 3) basic and clinical reproductive science seminars at UNC-CH, Duke University, NC State University, the Environmental Protection Agency and the NIEHS; 4) a one-day symposium held each year by the Triangle Consortium for Reproductive Biology in which trainees have an opportunity to present their-research and participate in discussions with other reproductive scientists in the Triangle area; 5) Carolina Workshops at UNC-CH, sponsored by the Program in Molecular Biology and Biotechnology, which offer intensive 1-to-2-week courses on advances in new molecular technology; 6) individual counselling of trainees in training activities to fit their particular needs, which may include taking graduate courses, attending workshops or visiting other laboratories to learn techniques. Most importantly, guidance and stimulation are provided for trainees to complete a significant piece of scientific investigation in reproductive biology.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Institutional National Research Service Award (T32)
Project #
5T32HD007315-14
Application #
2838677
Study Section
Population Research Committee (HDPR)
Program Officer
Vogel, Donna L
Project Start
1986-01-01
Project End
2001-04-30
Budget Start
1999-05-01
Budget End
2000-04-30
Support Year
14
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Pediatrics
Type
Schools of Medicine
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Tan, J; Hall, S H; Hamil, K G et al. (2000) Protein inhibitor of activated STAT-1 (signal transducer and activator of transcription-1) is a nuclear receptor coregulator expressed in human testis. Mol Endocrinol 14:14-26
Tan, J A; Hall, S H; Petrusz, P et al. (2000) Thyroid receptor activator molecule, TRAM-1, is an androgen receptor coactivator. Endocrinology 141:3440-50
Ghosh, B R; Wu, J C; Strahl, B D et al. (1996) Inhibin and estradiol alter gonadotropes differentially in ovine pituitary cultures: changing gonadotrope numbers and calcium responses to gonadotropin-releasing hormone. Endocrinology 137:5144-54
Hughes Jr, F M; Cidlowski, J A (1994) Regulation of apoptosis in S49 cells. J Steroid Biochem Mol Biol 49:303-10
Ho, K C; Marschke, K B; Tan, J et al. (1993) A complex response element in intron 1 of the androgen-regulated 20-kDa protein gene displays cell type-dependent androgen receptor specificity. J Biol Chem 268:27226-35
Tsuruta, J K; O'Brien, D A; Griswold, M D (1993) Sertoli cell and germ cell cystatin C: stage-dependent expression of two distinct messenger ribonucleic acid transcripts in rat testes. Biol Reprod 49:1045-54
Mulheron, G W; Mulheron, J G; Danielpour, D et al. (1992) Porcine granulosa cells do not express transforming growth factor-beta 2 (TGF-beta 2) messenger ribonucleic acid: molecular basis for their inability to produce TGF-beta activity comparable to that of rat granulosa cells. Endocrinology 131:2609-14
Mulheron, G W; Schomberg, D W (1992) Effects of diethylstilbestrol on rat granulosa cell and thecal/interstitial cell transforming growth factor-beta 2 mRNA expression in vivo: analysis by reverse transcription-polymerase chain reaction. Biol Reprod 46:546-50
Mulheron, G W; Bossert, N L; Lapp, J A et al. (1992) Human granulosa-luteal and cumulus cells express transforming growth factors-beta type 1 and type 2 mRNA. J Clin Endocrinol Metab 74:458-60
Gaido, M L; Cidlowski, J A (1991) Identification, purification, and characterization of a calcium-dependent endonuclease (NUC18) from apoptotic rat thymocytes. NUC18 is not histone H2B. J Biol Chem 266:18580-5

Showing the most recent 10 out of 15 publications