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Paraoxonase gene mutations in amyotrophic lateral sclerosis.
Ticozzi N, LeClerc AL, Keagle PJ, Glass JD, Wills AM, van Blitterswijk M, Bosco DA, Rodriguez-Leyva I, Gellera C, Ratti A, Taroni F, McKenna-Yasek D, Sapp PC, Silani V, Furlong CE, Brown RH Jr, Landers JE. Ticozzi N, et al. Among authors: furlong ce. Ann Neurol. 2010 Jul;68(1):102-7. doi: 10.1002/ana.21993. Ann Neurol. 2010. PMID: 20582942 Free PMC article.
Paraoxonase 1 (PON1) organophosphate hydrolysis is not reduced in ALS.
Wills AM, Landers JE, Zhang H, Richter RJ, Caraganis AJ, Cudkowicz ME, Furlong CE, Brown RH Jr. Wills AM, et al. Among authors: furlong ce. Neurology. 2008 Mar 18;70(12):929-34. doi: 10.1212/01.wnl.0000305956.37931.dd. Neurology. 2008. PMID: 18347314
Paraoxonase 1 promoter and coding region polymorphisms in Parkinson's disease.
Kelada SN, Costa-Mallen P, Checkoway H, Viernes HA, Farin FM, Smith-Weller T, Franklin GM, Costa LG, Longstreth WT Jr, Furlong CE, Jarvik GP, Swanson PD. Kelada SN, et al. Among authors: furlong ce. J Neurol Neurosurg Psychiatry. 2003 Apr;74(4):546-7. doi: 10.1136/jnnp.74.4.546. J Neurol Neurosurg Psychiatry. 2003. PMID: 12640090 Free PMC article. No abstract available.
Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing Project.
Kim DS, Crosslin DR, Auer PL, Suzuki SM, Marsillach J, Burt AA, Gordon AS, Meschia JF, Nalls MA, Worrall BB, Longstreth WT Jr, Gottesman RF, Furlong CE, Peters U, Rich SS, Nickerson DA, Jarvik GP; NHLBI Exome Sequencing Project. Kim DS, et al. Among authors: furlong ce. J Lipid Res. 2014 Jun;55(6):1173-8. doi: 10.1194/jlr.P049247. Epub 2014 Apr 7. J Lipid Res. 2014. PMID: 24711634 Free PMC article. Clinical Trial.
Polymorphisms in the human paraoxonase (PON1) promoter.
Brophy VH, Hastings MD, Clendenning JB, Richter RJ, Jarvik GP, Furlong CE. Brophy VH, et al. Among authors: furlong ce. Pharmacogenetics. 2001 Feb;11(1):77-84. doi: 10.1097/00008571-200102000-00009. Pharmacogenetics. 2001. PMID: 11207034
171 results