Population research at Johns Hopkins benefits greatly from the facilities provided by the Hopkins Population Center. The list of publications and working papers submitted with this application document a sustained high level of research output in demography and reproductive biology. The Population Center provides a variety of services and facilities which stimulate and advance research activity, bringing together investigators interested in population by providing a first class library and documents center, by supporting computer facilities and software development, by making available a central group for consultation on research design and analysis. Inter-departmental collaboration in reproductive biology is encouraged through support of the Reproductive Biology Council and the Core EM laboratory. A comparable development relative to demographic and social science research is the responsibility of the Demography Council which also oversees the Data Processing Unit and the Mathematical and Statistical Services Unit. Funds are requested for the continuation of support for a Directorate which has responsibility for overall coordination; an Information Unit with capacity for sophisticated information retrieval; a Data Processing Unit which provides remote entry terminals, data management services, software development and guidance in operating in the University's complex computational environment; an EM Laboratory, and a Mathematical and Statistical Services Unit. The Hopkins Center is unique in that it contains two parallel structures: a demographic division and a reproductive biology division. There is frequent interaction between these divisions but essentially each one is self-contained with its own network of investigators. All of the core facilities except the EM laboratory are utilized by both divisions.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Center Core Grants (P30)
Project #
5P30HD006268-13
Application #
3102837
Study Section
Population Research and Training Committee (HDPR)
Project Start
1978-03-01
Project End
1987-02-28
Budget Start
1986-03-01
Budget End
1987-02-28
Support Year
13
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
Schools of Public Health
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Becker, Stan; Hossain, Mian B; Thomson, Elizabeth (2006) Disagreement in spousal reports of current contraceptive use in sub-Saharan Africa. J Biosoc Sci 38:779-96
Misra, Dawn P; Astone, Nan; Lynch, Courtney D (2005) Maternal smoking and birth weight: interaction with parity and mother's own in utero exposure to smoking. Epidemiology 16:288-93
Choi, Yoonjoung; Bishai, David; Hill, Kenneth (2005) Socioeconomic differentials in supplementation of vitamin A: evidence from the Philippines. J Health Popul Nutr 23:156-64
Kagaayi, Joseph; Dreyfuss, Michele L; Kigozi, Godfrey et al. (2005) Maternal self-medication and provision of nevirapine to newborns by women in Rakai, Uganda. J Acquir Immune Defic Syndr 39:121-4
Hinson, Ella R; Shone, Scott M; Zink, M Christine et al. (2004) Wounding: the primary mode of Seoul virus transmission among male Norway rats. Am J Trop Med Hyg 70:310-7
Beenhakker, Britta; Becker, Stan; Hires, Stephanie et al. (2004) Are partners available for post-abortion contraceptive counseling? A pilot study in a Baltimore City clinic. Contraception 69:419-23
Hanna, William F; Kerr, Candace L; Shaper, Joel H et al. (2004) Lewis X-containing neoglycoproteins mimic the intrinsic ability of zona pellucida glycoprotein ZP3 to induce the acrosome reaction in capacitated mouse sperm. Biol Reprod 71:778-89
Wisniewski, Amy B; Klein, Sabra L; Lakshmanan, Yegappen et al. (2003) Exposure to genistein during gestation and lactation demasculinizes the reproductive system in rats. J Urol 169:1582-6
Charron, Martin; DeCerbo, Joshua N; Wright, William W (2003) A GC-box within the proximal promoter region of the rat cathepsin L gene activates transcription in Sertoli cells of sexually mature rats. Biol Reprod 68:1649-56
Charron, Martin; Folmer, Janet S; Wright, William W (2003) A 3-kilobase region derived from the rat cathepsin L gene directs in vivo expression of a reporter gene in sertoli cells in a manner comparable to that of the endogenous gene. Biol Reprod 68:1641-8

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