Jeffrey Parker Henderson, MD, PhD
Current Position
Instructor, Medicine
Division of Infectious Diseases
Specialty Areas
Infectious Diseases
Mailing Address
|
Washington University School of Medicine Division of Infectious Diseases
660 South Euclid Avenue Campus Box 8051
St. Louis,
MO
63110
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Areas of Clinical Interest
Infectious diseases
Areas of Research Interest
Pathophysiology of enteric gram negative infections
Board Certification
Internal Medicine
--
Certified
Medical Education
B.S.: University of Wisconsin, Madison, Wisconsin
, 1994
Ph.D.: Molecular Biophysics, Washington University School of Medicine, St. Louis, Missouri
, 2002
Medical Degree: Washington University School of Medicine, St. Louis, Missouri
, 2002
Residency: Barnes-Jewish Hospital at Washington University School of Medicine, St. Louis, Missouri
, 2004
Fellowship: Infectious Diseases, Washington University School of Medicine, St. Louis, Missouri
, 2006
Hospital Affiliations
Barnes-Jewish Hospital
Major or Recent Publications/Awards
Honors and Awards
Washington University Internal Medicine Club Research Award, 2002
The Walter Nicolai Award for Meritorious Research In Biomedical Gerontology, First Place, American
Federation for Aging Research Grantee Conference "Halogenation of DNA by the Myeloperoxidase System of Activated Phagocytes: Implications for Carcinogenesis at Sites of Inflammation", 2001
Books and Book Chapters
Henderson JP, Heinecke JW.
“Myeloperoxidase and Eosinophil Peroxidase: Phagocyte Enzymes for Halogenation in Humans”, The Handbook of Environmental Chemistry: The Natural Production of Halogenated Compounds. 2003; Vol. 3, pp 201-214
Selected Publications
Yeh GC, Henderson JP, Byun J, d'Avignon D, Heinecke JW. 8-Nitroxanthine, a Product of Myeloperoxidase, Peroxynitrite, and Activated Human Neutrophils, Enhances Generation of Superoxide by Xanthine Oxidase. Archives of Biochemistry and Biophysics 2003; 418(1):1-12
Byun J, Henderson JP, Heinecke JW. Identification and Quantification of Mutagenic Halogenated Cytosines by Gas Chromatography, Fast Atom Bombardment, and Electrospray Ionization Tandem Mass Spectrometry. Analytical Biochemistry 2003; 317(2): 201-209
Henderson JP, Byun J, Takeshita J, Heinecke JW. Phagocytes Produce 5-Chlorouracil and 5-Bromouracil, Two Mutagenic Products of Myeloperoxidase in Human Inflammatory Tissue. Journal of Biological Chemistry 2003; 278(26):23522-23528
Gaut JP, Yeh GC, Tran HD, Byun J, Henderson JP, Richter GM, Belaaouaj A, Hotchkiss RS and Heinecke JW. Neutrophils generate antimicrobial brominating and chlorinating oxidants during sepsis, Proceedings of the National Academy of Sciences, USA 2001; 98(21):11961-11966
Henderson JP, Byun J, Williams MV, McCormick ML, Parks WC, Ridnour LA, Heinecke JW. Bromination of deoxycytidine by eosinophil peroxidase: A Mechanism for Mutagenesis by Oxidative Damage of Nucleotide Precursors, Proceedings of the National Academy of Sciences, USA 2001; 98(4):1631-1636
Henderson JP, Byun J, Williams MV, Mueller DM, McCormick ML, Heinecke JW. Production of brominating intermediates by myeloperoxidase: A Transhalogenation Pathway for Generating Mutagenic Nucleobases during Inflammation, Journal of Biological Chemistry 2001; 276(11):7867-7875
Henderson JP, Byun J, Mueller DM, Heinecke JW. The Eosinophil peroxidase-hydrogen peroxide-bromide system of human eosinophils generates 5-Bromouracil, a Mutagenic Thymine Analog, Biochemistry 40(7):2052-2059, 2001.
For more articles and abstracts, take this off-site link to the National Library of Medicine Pub Med page for Dr. Jeffrey Henderson