Human formyl peptide receptor 1 C32T SNP interacts with age and is associated with blood pressure levels-Reference-Cited by-同舟云学术

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Human formyl peptide receptor 1 C32T SNP interacts with age and is associated with blood pressure levels

Published:2012-01 Issue:1-2 Volume:413 Page:34-38
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

El Shamieh Said,Herbeth Bernard,Azimi-Nezhad Mohsen,Benachour Hamanou,Masson Christine,Visvikis-Siest Sophie

Funder

Institut National de Santé et de Recherche Médicale (INSERM)

“Région Lorraine, the communauté Urbaine”

Université Henri Poincaré

Publisher

Elsevier BV

Subject

Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine

Reference32 articles.

1. Relationship between the regulatory region polymorphism of human tissue kallikrein gene and essential hypertension;Hua;J Hum Hypertens,2005

2. Global burden of hypertension: analysis of worldwide data;Kearney;Lancet,2005

3. Genetic determinants of blood pressure regulation;Marteau;J Hypertens,2005

4. Genome-wide association study identifies eight loci associated with blood pressure;Newton-Cheh;Nat Genet,2009

5. Linkage of angiotensinogen gene polymorphisms with hypertension in a sibling study of Hong Kong Chinese;Fang;J Hypertens,2010

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Regulation of Inflammation and Oxidative Stress by Formyl Peptide Receptors in Cardiovascular Disease Progression;Life;2021-03-15

2. The Role of Formyl Peptide Receptor 1 Gene Polymorphisms in Human Colorectal Cancer;Journal of Cancer;2020

3. rs2569190A>G in CD14 is Independently Associated with Hypercholesterolemia: A Brief Report;Journal of Cardiovascular Development and Disease;2019-10-30

4. Formyl peptide receptor 1 up-regulation and formyl peptide receptor 2/3 down-regulation of blood immune cells along with defective lipoxin A4/resolvin D1 production in obstructive sleep apnea patients;PLOS ONE;2019-05-22

5. The mitochondrial tRNAAla 5587T>C and tRNALeu(CUN) 12280A>G mutations may be associated with hypertension in a Chinese family;Experimental and Therapeutic Medicine;2018-12-28

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