J. Teiber

发表

Role of the alanine at position 363 of cytochrome P450 2B2 in influencing the NADPH- and hydroperoxide-supported activities.

P. Hollenberg, I. H. Hanna, J. Teiber, 1998, Archives of biochemistry and biophysics.

Novel Paraoxonase 2-Dependent Mechanism Mediating the Biological Effects of the Pseudomonas aeruginosa Quorum-Sensing Molecule N-(3-Oxo-Dodecanoyl)-l-Homoserine Lactone

P. Wilgenbus, Junhui Xiao, G. Kramer, 2015, Infection and Immunity.

Maintenance of Paraoxonase 2 Activity as a Strategy to Attenuate P. Aeruginosa Virulence

J. Teiber, 2014 .

PONs’ Natural Substrates – The Key for their Physiological Roles

D. Draganov, J. Teiber, 2008 .

One Enzyme, Two Functions

U. Förstermann, P. Wilgenbus, A. Daiber, 2010, The Journal of Biological Chemistry.

Paraoxonases-2 and -3 Are Important Defense Enzymes against Pseudomonas aeruginosa Virulence Factors due to Their Anti-Oxidative and Anti-Inflammatory Properties

U. Förstermann, P. Wilgenbus, S. Horke, 2012, Journal of lipids.

Mouse serum paraoxonase-1 lactonase activity is specific for medium-chain length fatty acid lactones.

P. Potter, P. Connelly, D. Ng, 2011, Biochimica et Biophysica Acta.

Development of an immunoblot assay with infrared fluorescence to quantify paraoxonase 1 in serum and plasma Published, JLR Papers in Press, September 28, 2007.

P. Connelly, G. Maguire, D. Draganov, 2008, Journal of Lipid Research.

Paraoxonase 2 is down-regulated by the Pseudomonas aeruginosa quorumsensing signal N-(3-oxododecanoyl)-L-homoserine lactone and attenuates oxidative stress induced by pyocyanin.

R. Haley, U. Förstermann, P. Wilgenbus, 2010, The Biochemical journal.

Association of the serum myeloperoxidase/high-density lipoprotein particle ratio and incident cardiovascular events in a multi-ethnic population: Observations from the Dallas Heart Study.

A. Khera, C. Ayers, Anand Rohatgi, 2017, Atherosclerosis.

Lactonase and lactonizing activities of human serum paraoxonase (PON1) and rabbit serum PON3.

B. La Du, D. Draganov, J. Teiber, 2003, Biochemical pharmacology.

Methods for measuring serum activity levels of the 192 Q and R isoenzymes of paraoxonase 1 in QR heterozygous individuals.

R. Haley, G. Kramer, J. Teiber, 2013, Clinical chemistry.

Paraoxonase-2 regulates coagulation activation through endothelial tissue factor.

P. Wilgenbus, K. Jurk, W. Ruf, 2018, Blood.

Paraoxonase 2 deficiency alters mitochondrial function and exacerbates the development of atherosclerosis.

S. Reddy, K. Reue, M. Navab, 2009, Antioxidants & redox signaling.

Estrogen esters as substrates for human paraoxonases.

B. La Du, D. Draganov, J. Teiber, 2007, Archives of biochemistry and biophysics.

Evaluation of a Gene–Environment Interaction of PON1 and Low-Level Nerve Agent Exposure with Gulf War Illness: A Prevalence Case–Control Study Drawn from the U.S. Military Health Survey’s National Population Sample

R. Haley, J. Teiber, Jill A Dever, 2022, Environmental health perspectives.

Identification of biologically active δ-lactone eicosanoids as paraoxonase substrates.

E. Carreira, R. Haley, D. Shih, 2018, Biochemical and biophysical research communications.

Human paraoxonases (PON1, PON2, and PON3) are lactonases with overlapping and distinct substrate specificitiess⃞s⃞ The online version of this article (available at http://www.jlr.org) contains additional text, figures, and references. Published, JLR Papers in Press, March 16, 2005. DOI 10.1194/jlr.M

R. Sunahara, B. La Du, Dragomir I Draganov, 2005, Journal of Lipid Research.

The human serum paraoxonase/arylesterase gene (PON1) is one member of a multigene family.

B. La Du, J. Teiber, R. Sorenson, 1996, Genomics.

Metabolism of the β-oxidized intermediates of N-nitrosodi-n-propylamine: N-nitroso-β-hydroxypropylpropylamine and N-nitroso-β-oxopropylpropylamine

P. Hollenberg, K. Macé, J. Teiber, 2001 .

Dominant Role of Paraoxonases in Inactivation of the Pseudomonas aeruginosa Quorum-Sensing Signal N-(3-Oxododecanoyl)-l-Homoserine Lactone

R. Haley, Junhui Xiao, G. Kramer, 2008, Infection and Immunity.

Identification of the human liver microsomal cytochrome P450s involved in the metabolism of N-nitrosodi-n-propylamine.

P. Hollenberg, J. Teiber, 2000, Carcinogenesis.

PON3 is upregulated in cancer tissues and protects against mitochondrial superoxide-mediated cell death

D. Shih, U. Förstermann, S. Reddy, 2012, Cell Death and Differentiation.

PON1 and oxidative stress in human sepsis and an animal model of sepsis.

T. Standiford, D. Remick, J. Nemzek, 2010, Advances in experimental medicine and biology.

Pitfalls in the assessment of PON1 status in clinical populations.

J. Teiber, S. Billecke, 2011, Fertility and sterility.

The neuroprotective effect of lovastatin on MPP(+)-induced neurotoxicity is not mediated by PON2.

C. Ríos, L. Tristán-López, S. Montes, 2015, Neurotoxicology.

Response to “Comment on ‘Evaluation of a Gene–Environment Interaction of PON1 and Low-Level Nerve Agent Exposure with Gulf War Illness: A Prevalence Case–Control Study Drawn from the U.S. Military Health Survey’s National Population Sample’”

R. Haley, J. Teiber, Jill A Dever, 2022, Environmental health perspectives.

Paraoxonase 2 is down-regulated by the Pseudomonas aeruginosa quorumsensing signal N-(3-oxododecanoyl)-L-homoserine lactone and attenuates oxidative stress induced by pyocyanin.

R. Haley, U. Förstermann, P. Wilgenbus, 2010, The Biochemical journal.

One Enzyme, Two Functions

U. Förstermann, P. Wilgenbus, A. Daiber, 2010, The Journal of Biological Chemistry.

Mouse serum paraoxonase-1 lactonase activity is specific for medium-chain length fatty acid lactones.

P. Potter, P. Connelly, D. Ng, 2011, Biochimica et biophysica acta.

High-performance liquid chromatography analysis of N-acyl homoserine lactone hydrolysis by paraoxonases.

D. Draganov, J. Teiber, 2011, Methods in molecular biology.

The effect of disease misclassification on the ability to detect a gene-environment interaction: implications of the specificity of case definitions for research on Gulf War illness

J. Teiber, Gerald Kramer, Robert W. Haley, 2023, BMC Medical Research Methodology.