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Institution

Bowling Green State University

EducationBowling Green, Ohio, United States
About: Bowling Green State University is a education organization based out in Bowling Green, Ohio, United States. It is known for research contribution in the topics: Population & Poison control. The organization has 8315 authors who have published 16042 publications receiving 482564 citations. The organization is also known as: BGSU.


Papers
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Book
01 Jan 1988
TL;DR: In this article, the authors present an evaluation and crime prevention section I: Primary Prevention Section II: Secondary Prevention Section III: Tertiary Prevention 15. Specific Deterrence and Incapacitation 16. Rehabilitation 17.
Abstract: 1. Crime and the Fear of Crime 2. Crime Prevention 3. Evaluation and Crime Prevention Section I: Primary Prevention 4. The Physical Environment and Crime 5. Neighborhood Crime Prevention 6. Displacement and Diffusion 7. The Mass Media and Crime Prevention 8. Developmental Prevention 9. General Deterrence Section II: Secondary Prevention 10. Prediction for Secondary Prevention 11. Situational Crime Prevention 12. Partnerships for Crime Prevention 13. Drugs, Crime, and Crime Prevention 14. The School and Crime Prevention Section III: Tertiary Prevention 15. Specific Deterrence and Incapacitation 16. Rehabilitation 17. Some Closing Thoughts on Crime Prevention and the Future

196 citations

Journal ArticleDOI
TL;DR: In this article, the authors use two waves of the National Longitudinal Study of Adolescent Health to analyze adolescents' reports of non-romantic sexual intercourse, and whether key protective and risk factors as well as normative orientations distinguish the context within which sexual activity occurs.

195 citations

Journal ArticleDOI
TL;DR: The results obtained indicate that besides the overall lipophilicity, the presence and position of the alkyl groups in a molecule play an important role in tumor uptake, tumor selectivity, and in vivo PDT efficacy.
Abstract: Starting from methylpheophorbide-a, a homologous series of purpurinimides containing alkyl substituents at two different positions [as 3-(1(1)-O-alkyl) and 13(2)-N-alkyl] were synthesized. These compounds with variable lipophilicity (log P 5.32-16.44) exhibit long wavelength absorption near lambda(max)700 nm (epsilon: 45 000 in dichloromethane) with singlet oxygen ((1)O2) production in the range of 57-60%. The shifts in in vivo absorptions and tumor/skin uptake of these compounds were determined in C3H mice bearing RIF tumors by in vivo reflectance spectroscopy. The results obtained from a set of photosensitizers with similar lipophilicity (log P 10.68-10.88) indicate that besides the overall lipophilicity, the presence and position of the alkyl groups (O-alkyl vs N-alkyl) in a molecule play an important role in tumor uptake, tumor selectivity, and in vivo PDT efficacy. At present, all purpurinimide analogues are being evaluated at various doses, and experiments are underway to establish a quantitative structure-activity relationship on a limited set of compounds. The 1D and 2D NMR and mass spectrometry analyses confirmed the structures of the desired purpurinimides and the byproducts formed during various reaction conditions. The mechanisms of the formation of the unexpected 12-formyl- and 12-(hydroxymethyl)purpurinimides under certain reaction conditions are also discussed.

195 citations


Authors

Showing all 8365 results

NameH-indexPapersCitations
Eduardo Salas12971162259
Russell A. Barkley11935560109
Hong Liu100190557561
Jaak Panksepp9944640748
Kenneth I. Pargament9637241752
Robert C. Green9152640414
Robert W. Motl8571227961
Evert Jan Baerends8531852440
Hugh Garavan8441928773
Janet Shibley Hyde8322738440
Michael L. Gross8270127140
Jerry Silver7820125837
Michael E. Robinson7436619990
Abraham Clearfield7451319006
Kirk S. Schanze7351219118
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20241
202321
202274
2021485
2020511
2019497