The proposed NICHD Population Research Core Grant will operate within the Laboratories for Reproductive Biology to promote interdisciplinary research leading to better methods for the control of fertility and the treatment of reproductive disorders. Major emphasis has been placed on the male. A broad range of research centering on molecular mechanisms regulating male reproductive functions has been brought together in The Laboratories for Reproductive Biology. On- going work includes: Steroid and neuropeptide regulation of pituitary gonadotropin secretion and sexual behavior, cholesterol utilization in steroidogenesis, the identification and regulation of Sertoli cell factors that control spermatogenesis, regulation of gene expression in the sperm maturing regions of epididymis, post-testicular modifications of the sperm plasma membrane influencing fertilization, and growth factor requirements of early embryo growth and implantation. The shared Core Facilities included in the P-30 population center will provide histochemistry-microscopy, radioimmunoassay, tissue culture, recombinant DNA and administrative services. In addition to enhancing the productivity, quality and cost effectiveness of research, these cores will serve to nurture interdisciplinary collaboration among clinical and basic scientists within The Laboratories for Reproductive Biology. Eligibility for core use is requested for 34 funded research projects which will be active at the proposed start date of this application.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Center Core Grants (P30)
Project #
5P30HD018968-08
Application #
3102986
Study Section
Population Research Committee (HDPR)
Project Start
1984-08-01
Project End
1992-07-31
Budget Start
1991-08-01
Budget End
1992-07-31
Support Year
8
Fiscal Year
1991
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
Schools of Medicine
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
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Kim, D; Gregory, C W; Smith, G J et al. (1999) Immunohistochemical quantitation of androgen receptor expression using color video image analysis. Cytometry 35:2-10
Fenstermacher, D A; Joseph, D R (1998) Analysis of promoter and androgen regulatory sequences required for optimal transcription of the rat androgen-binding protein gene. J Androl 19:81-91
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Halpern, C T; Udry, J R; Suchindran, C (1998) Monthly measures of salivary testosterone predict sexual activity in adolescent males. Arch Sex Behav 27:445-65
Eddy, E M; O'Brien, D A (1998) Gene expression during mammalian meiosis. Curr Top Dev Biol 37:141-200
Gregory, C W; Hamil, K G; Kim, D et al. (1998) Androgen receptor expression in androgen-independent prostate cancer is associated with increased expression of androgen-regulated genes. Cancer Res 58:5718-24
Langley, E; Kemppainen, J A; Wilson, E M (1998) Intermolecular NH2-/carboxyl-terminal interactions in androgen receptor dimerization revealed by mutations that cause androgen insensitivity. J Biol Chem 273:92-101

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