Publications:

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Proteomic Exploration of Paraoxonase 1 Function in Health and Disease.

International Journal Of Molecular Sciences

Jakubowski, Hieronim H

Publication Date: 2023-04-24

Variant appearance in text: rs854565

PubMed Link: 37175471

Variant Present in the following documents:

• Main text
• ijms-24-07764.pdf

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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: rs854565

PubMed Link: 33374313

Variant Present in the following documents:

• Main text
• antioxidants-10-00011.pdf

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Non-syndromic Cleft Palate: An Overview on Human Genetic and Environmental Risk Factors.

Frontiers In Cell And Developmental Biology

Martinelli, Marcella M; Palmieri, Annalisa A; Carinci, Francesco F; Scapoli, Luca L

Publication Date: 2020

Variant appearance in text: rs854565

PubMed Link: 33195260

Variant Present in the following documents:

• Main text

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Candidate Gene Analysis Reveals Strong Association of CETP Variants With High Density Lipoprotein Cholesterol and PCSK9 Variants With Low Density Lipoprotein Cholesterol in Ghanaian Adults: An AWI-Gen Sub-Study.

Frontiers In Genetics

Agongo, Godfred G; Amenga-Etego, Lucas L; Nonterah, Engelbert A EA; Debpuur, Cornelius C; Choudhury, Ananyo A; Bentley, Amy R AR; Oduro, Abraham R AR; Rotimi, Charles N CN; Crowther, Nigel J NJ; Ramsay, Michèle M; , ; H Africa,

Publication Date: 2020

Variant appearance in text: rs854565

PubMed Link: 33193594

Variant Present in the following documents:

• Main text
• fgene-11-456661.pdf

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Interactions between paraoxonase 1 genetic polymorphisms and smoking and their effects on oxidative stress and lung cancer risk in a Korean population.

Plos One

Eom, Sang-Yong SY; Yim, Dong-Hyuk DH; Lee, Chul-Ho CH; Choe, Kang-Hyeon KH; An, Jin Young JY; Lee, Kye Young KY; Kim, Yong-Dae YD; Kim, Heon H

Publication Date: 2015

Variant appearance in text: rs854565

PubMed Link: 25741997

Variant Present in the following documents:

• Main text
• pone.0119100.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: rs854565

PubMed Link: 22685667

Variant Present in the following documents:

• Main text
• JL2012-476316.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: rs854565

PubMed Link: 20980077

Variant Present in the following documents:

• Main text

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Effects of PON polymorphisms and haplotypes on molecular phenotype in Mexican-American mothers and children.

Environmental And Molecular Mutagenesis

Huen, Karen K; Barcellos, Lisa L; Beckman, Kenneth K; Rose, Sherri S; Eskenazi, Brenda B; Holland, Nina N

Publication Date: 2011-03

Variant appearance in text: rs854565

PubMed Link: 20839225

Variant Present in the following documents:

• Main text

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A loss-of-function polymorphism in the propeptide domain of the LOX gene and breast cancer.

Cancer Research

Min, Chengyin C; Yu, Ziyang Z; Kirsch, Kathrin H KH; Zhao, Yingshe Y; Vora, Siddharth R SR; Trackman, Philip C PC; Spicer, Douglas B DB; Rosenberg, Lynn L; Palmer, Julie R JR; Sonenshein, Gail E GE

Publication Date: 2009-08-15

Variant appearance in text: rs854565

PubMed Link: 19654310

Variant Present in the following documents:

• Main text

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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: rs854565

PubMed Link: 18618303

Variant Present in the following documents:

• Main text
• iafd-9-306.pdf

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