PON3 c.146-784T>C

Variant ID: 7-95020305-A-G

NM_000940.2(PON3):c.146-784T>C

This variant was identified in 9 publications

View GRCh38 version.




Publications:


Paraoxonase Role in Human Neurodegenerative Diseases.

Antioxidants (Basel, Switzerland)
Reichert, Cadiele Oliana CO; Levy, Debora D; Bydlowski, Sergio P SP
Publication Date: 2020-12-24

Variant appearance in text: rs10487132
PubMed Link: 33374313
Variant Present in the following documents:
  • Main text
  • antioxidants-10-00011.pdf
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Paraoxonase 3: Structure and Its Role in Pathophysiology of Coronary Artery Disease.

Biomolecules
Priyanka, Kumari K; Singh, Surjit S; Gill, Kirandip K
Publication Date: 2019-12-03

Variant appearance in text: rs10487132
PubMed Link: 31816846
Variant Present in the following documents:
  • Main text
  • biomolecules-09-00817.pdf
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Paraoxonases Activities and Polymorphisms in Elderly and Old-Age Diseases: An Overview.

Antioxidants (Basel, Switzerland)
Levy, Débora D; Reichert, Cadiele Oliana CO; Bydlowski, Sérgio Paulo SP
Publication Date: 2019-05-02

Variant appearance in text: rs10487132
PubMed Link: 31052559
Variant Present in the following documents:
  • Main text
  • antioxidants-08-00118.pdf
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Additional Common Polymorphisms in the PON Gene Cluster Predict PON1 Activity but Not Vascular Disease.

Journal Of Lipids
Kim, Daniel S DS; Burt, Amber A AA; Ranchalis, Jane E JE; Richter, Rebecca J RJ; Marshall, Julieann K JK; Eintracht, Jason F JF; Rosenthal, Elisabeth A EA; Furlong, Clement E CE; Jarvik, Gail P GP
Publication Date: 2012

Variant appearance in text: rs10487132
PubMed Link: 22685667
Variant Present in the following documents:
  • Main text
View BVdb publication page



Paraoxonase (PON1 and PON3) Polymorphisms: Impact on Liver Expression and Atorvastatin-Lactone Hydrolysis.

Frontiers In Pharmacology
Riedmaier, Stephan S; Klein, Kathrin K; Winter, Stefan S; Hofmann, Ute U; Schwab, Matthias M; Zanger, Ulrich M UM
Publication Date: 2011

Variant appearance in text: rs10487132
PubMed Link: 21852972
Variant Present in the following documents:
  • Main text
  • fphar-02-00041.pdf
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Serum paraoxonase activity is associated with variants in the PON gene cluster and risk of Alzheimer disease.

Neurobiology Of Aging
Erlich, Porat M PM; Lunetta, Kathryn L KL; Cupples, L Adrienne LA; Abraham, Carmela R CR; Green, Robert C RC; Baldwin, Clinton T CT; Farrer, Lindsay A LA
Publication Date: 2012-05

Variant appearance in text: rs10487132
PubMed Link: 20980077
Variant Present in the following documents:
  • Main text
View BVdb publication page



A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS.

Neurology
Wills, A-M AM; Cronin, S S; Slowik, A A; Kasperaviciute, D D; Van Es, M A MA; Morahan, J M JM; Valdmanis, P N PN; Meininger, V V; Melki, J J; Shaw, C E CE; Rouleau, G A GA; Fisher, E M C EM; Shaw, P J PJ; Morrison, K E KE; Pamphlett, R R; Van den Berg, L H LH; Figlewicz, D A DA; Andersen, P M PM; Al-Chalabi, A A; Hardiman, O O; Purcell, S S; Landers, J E JE; Brown, R H RH
Publication Date: 2009-07-07

Variant appearance in text: rs10487132
PubMed Link: 19321847
Variant Present in the following documents:
  • Main text
View BVdb publication page



A common haplotype within the PON1 promoter region is associated with sporadic ALS.

Amyotrophic Lateral Sclerosis : Official Publication Of The World Federation Of Neurology Research Group On Motor Neuron Diseases
Landers, John E JE; Shi, Lijia L; Cho, Ting-Jan TJ; Glass, Jonathan D JD; Shaw, Christopher E CE; Leigh, P Nigel PN; Diekstra, Frank F; Polak, Meraida M; Rodriguez-Leyva, Ildefonso I; Niemann, Stephan S; Traynor, Bryan J BJ; McKenna-Yasek, Diane D; Sapp, Peter C PC; Al-Chalabi, Ammar A; Wills, Anne-Marie A AM; Brown, Robert H RH
Publication Date: 2008-10

Variant appearance in text: rs10487132
PubMed Link: 18618303
Variant Present in the following documents:
  • Main text
  • iafd-9-306.pdf
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Paraoxonase promoter and intronic variants modify risk of sporadic amyotrophic lateral sclerosis.

Journal Of Neurology, Neurosurgery, And Psychiatry
Cronin, Simon S; Greenway, Matthew J MJ; Prehn, Jochen H M JH; Hardiman, Orla O
Publication Date: 2007-09

Variant appearance in text: rs10487132
PubMed Link: 17702780
Variant Present in the following documents:
  • Main text
View BVdb publication page