Jonathan A. Doorn, Ph.D.
Affiliations: | 2001 | University of Michigan, Ann Arbor, Ann Arbor, MI |
Area:
Toxicology, Public Health, Environmental SciencesGoogle:
"Jonathan Doorn"Mean distance: (not calculated yet)
Cross-listing: PHTree
Parents
Sign in to add mentor| Rudy J. Richardson | grad student | 2001 | University of Michigan | |
| (Stereoselective inactivation of serine hydrolases by isomalathion: Inhibitory reactions with (1R)- and (1S)-isomers proceed by different mechanisms.) | ||||
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Crawford RA, Bowman KR, Cagle BS, et al. (2021) In vitro inhibition of glutathione-S-transferase by dopamine and its metabolites, 3,4-dihydroxyphenylacetaldehyde and 3,4-dihydroxyphenylacetic acid. Neurotoxicology |
| Allen EM, Anderson DG, Florang VR, et al. (2010) Relative inhibitory potency of molinate and metabolites with aldehyde dehydrogenase 2: implications for the mechanism of enzyme inhibition. Chemical Research in Toxicology. 23: 1843-50 |
| Doorn JA, Hurley TD, Petersen DR. (2006) Inhibition of human mitochondrial aldehyde dehydrogenase by 4-hydroxynon-2-enal and 4-oxonon-2-enal. Chemical Research in Toxicology. 19: 102-10 |
| Doorn JA, Thompson CM, Christner RB, et al. (2003) Stereoselective inactivation of Torpedo californica acetylcholinesterase by isomalathion: inhibitory reactions with (1R)- and (1S)-isomers proceed by different mechanisms. Chemical Research in Toxicology. 16: 958-65 |
| Doorn JA, Schall M, Gage DA, et al. (2001) Identification of butyrylcholinesterase adducts after inhibition with isomalathion using mass spectrometry: difference in mechanism between (1R)- and (1S)-stereoisomers. Toxicology and Applied Pharmacology. 176: 73-80 |
| Doorn JA, Talley TT, Thompson CM, et al. (2001) Probing the active sites of butyrylcholinesterase and cholesterol esterase with isomalathion: conserved stereoselective inactivation of serine hydrolases structurally related to acetylcholinesterase. Chemical Research in Toxicology. 14: 807-13 |
| Doorn JA, Gage DA, Schall M, et al. (2000) Inhibition of acetylcholinesterase by (1S,3S)-isomalathion proceeds with loss of thiomethyl: kinetic and mass spectral evidence for an unexpected primary leaving group. Chemical Research in Toxicology. 13: 1313-20 |