Michael J. Santostefano

Author

Also Known As

M SANTOSTEFANO, M Santostefano, M. Santostefano, MICHAEL J. SANTOSTEFANO, MICHAEL SANTOSTEFANO, Michael J Santostefano, Michael J. Santostefano, Michael Santostefano

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

Texas A&M University Research Triangle Park Foundation University of North Carolina at Chapel Hill Environmental Protection Agency GlaxoSmithKline (United States)

About

Michael J. Santostefano is an author at Texas A&M University specializing in medicine, pharmacology, and biochemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	23	955
2	Natural Sciences	7	7	224
3	Health Sciences	3	3	139
4	Engineering	1	1	12
5	Public Health	1	1	14

Michael J. Santostefano

Publications

1.5K

Citations

H-Index

Page 1

	Year	Citations
Molecular Mechanism of Inhibition of Estrogen-Induced Cathepsin D Gene Expression by 2,3,7,8-Tetrachlorodibenzo- <i>p</i> -Dioxin (TCDD) in MCF-7 Cells Venkatesh Krishnan, Weston W. Porter, Michael J. Santostefano, Molecular and Cellular Biology	1995	202
Identification of 3′-Methoxy-4′-nitroflavone as a Pure Aryl Hydrocarbon (Ah) Receptor Antagonist and Evidence for More Than One Form of the Nuclear Ah Receptor in MCF-7 Human Breast Cancer Cells Yu-Fang Lu, Michael J. Santostefano, Bernadette Cunningham, Archives of Biochemistry and Biophysics Molecular PharmacologyBreast OncologyBiochemistryPure Aryl HydrocarbonMedicine	1995	108
alpha-Naphthoflavone-induced CYP1A1 gene expression and cytosolic aryl hydrocarbon receptor transformation. Michael J. Santostefano, Mark Merchant, Luis Armando De la Peña Arellano, Molecular Pharmacology	1993	89
Substituted flavones as aryl hydrocarbon (Ah) receptor agonists and antagonists Yu-Fang Lu, Michael J. Santostefano, Bernadette D.M. Cunningham, Biochemical Pharmacology Molecular PharmacologyAryl HydrocarbonBiochemistryFunctional SelectivityMedicine	1996	73
Determination of Parameters Responsible for Pharmacokinetic Behavior of TCDD in Female Sprague–Dawley Rats Xiaofeng Wang, Michael J. Santostefano, Marina V. Evans, Toxicology and Applied Pharmacology Pharmacokinetic ModelingPharmacological StudyFemale Sprague–dawley RatsPhysiologyPharmacology	1997	71
Fibrates induce hepatic peroxisome and mitochondrial proliferation without overt evidence of cellular proliferation and oxidative stress in cynomolgus monkeys Debie J. Hoivik, Charles W. Qualls, Rosanna C. Mirabile, Carcinogenesis Lipid PeroxidationPathologyCell ProliferationPharmacotherapyMitochondrial Proliferation	2004	71
Mechanism of action of aryl hydrocarbon receptor antagonists: Inhibition of 2,3,7,8-tetrachlorodibenzo-p-dioxin-induced CYP1A1 gene expression Mark Merchant, V. Morrison, Michael J. Santostefano, Archives of Biochemistry and Biophysics BiochemistryFunctional SelectivityMedicineMechanism Of ActionReceptor (Biochemistry)	1992	68
Synergistic activity of polynuclear aromatic hydrocarbon mixtures as aryl hydrocarbon (Ah) receptor agonists K. Chaloupka, N. Harper, Venkatesh Krishnan, Chemico-Biological Interactions Synergistic ActivityAryl HydrocarbonBiochemistryFunctional SelectivityMedicine	1993	66
Daily Cycle of bHLH-PAS Proteins, Ah Receptor and Arnt, in Multiple Tissues of Female Sprague–Dawley Rats Vicki M. Richardson, Michael J. Santostefano, Linda S. Birnbaum Biochemical and Biophysical Research Communications Bhlh-pas ProteinsSignal TransductionMolecular PhysiologyDevelopmental BiologyEndocrine Mechanism	1998	64
Induction of Cyp1a-1 and Cyp1a-2 gene expression by a reconstituted mixture of polynuclear aromatic hydrocarbons in B6C3F1 mice K. Chaloupka, Michael A. Steinberg, Michael J. Santostefano, Chemico-Biological Interactions Cyp1a-2 Gene ExpressionBiochemistryNatural SciencesReconstituted MixtureMolecular Biology	1995	59

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