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Journal of Interpersonal Violence|February 13, 2020
Expanding Our View: Demographic, Behavioral, and Contextual Factors in College Sexual VictimizationSarah A Rogers, Baker A Rogers
Journal of Immunology (Baltimore, Md. : 1950)|March 1, 1992
Cleavage of the cell-surface O-sialoglycoproteins CD34, CD43, CD44, and CD45 by a novel glycoprotease from Pasteurella haemolyticaD R Sutherland, K M Abdullah, P Cyopick, et al.
Tropenmedizin Und Parasitologie|March 1, 1978
The generation of phospholipase A and hemolytic fatty acids by autolysing suspensions of Trypanosoma congolenseI R Tizard, A Mellors, W L Holmes, et al.
FEMS Microbiology Letters|February 15, 1994
Preparation of recombinant glycoprotease of Pasteurella haemolytica A1 utilizing the Escherichia coli alpha-hemolysin secretion systemR Y Lo, M A Watt, S Gyroffy, et al.
Life Sciences|August 9, 1982
Halogenated biphenyls as AHH inducers: effects of different halogen substituentsS Bandiera, T Sawyer, M A Campbell, et al.
Molecular Pharmacology|December 1, 1991
Effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin on 17 beta-estradiol-induced glucose metabolism in MCF-7 human breast cancer cells: 13C nuclear magnetic resonance spectroscopy studiesT R Narasimhan, S Safe, H J Williams, et al.
Cancer Research|August 15, 1989
Structure-dependent induction of aryl hydrocarbon hydroxylase in human breast cancer cell lines and characterization of the Ah receptorM Harris, J Piskorska-Pliszczynska, T Zacharewski, et al.
Toxicology|March 1, 1983
Hepta-, hexa-, tetra- and dichloronaphthalene congeners as inducers of hepatic microsomal drug-metabolizing enzymesM A Campbell, S Bandiera, L Robertson, et al.
Cancer Research|October 1, 1987
Quantitative structure-activity relationships: analysis of interactions of 2,3,7,8-tetrachlorodibenzo-p-dioxin and 2-substituted analogues with rat, mouse, guinea pig, and hamster cytosolic receptorM Romkes, J Piskorska-Pliszczynska, B Keys, et al.
Toxicology|June 1, 1987
Polybrominated dibenzo-p-dioxins and related compounds: quantitative in vivo and in vitro structure-activity relationshipsG Mason, T Zacharewski, M A Denomme, et al.
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