Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction-Reference-Cited by-同舟云学术

Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction

Published:2008-07-01 Issue:10 Volume:86 Page:1163-1170
ISSN:0946-2716
Container-title:Journal of Molecular Medicine
language:en
Short-container-title:J Mol Med

Author:

Lieb Wolfgang,Zeller Tanja,Mangino Massimo,Götz Anika,Braund Peter,Wenzel Juergen J.,Horn Christian,Proust Carole,Linsel-Nitschke Patrick,Amouyel Philippe,Bruse Petra,Arveiler Dominique,König Inke R.,Ferrières Jean,Ziegler Andreas,Balmforth Anthony J.,Evans Alun,Ducimetière Pierre,Cambien Francois,Hengstenberg Christian,Stark Klaus,Hall Alistair S.,Schunkert Heribert,Blankenberg Stefan,Samani Nilesh J.,Erdmann Jeanette,Tiret Laurence

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Drug Discovery,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00109-008-0376-5.pdf

Reference15 articles.

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5. McPherson R, Pertsemlidis A, Kavaslar N, Stewart A, Roberts R, Cox DR, Hinds DA, Pennacchio LA, Tybjaerg-Hansen A, Folsom AR, Boerwinkle E, Hobbs HH, Cohen JC (2007) A common allele on chromosome 9 associated with coronary heart disease. Science 316(5830):1488–1491

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1. miR-1322 protects against the myocardial ischemia via LRP8/PI3K/AKT pathway;Biochemical and Biophysical Research Communications;2023-01

2. Identification of Genetic Variants Associated With Myocardial Infarction in Saudi Arabia;The Heart Surgery Forum;2020-07-23

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4. Genetic variants of ApoE and ApoER2 differentially modulate endothelial function;Proceedings of the National Academy of Sciences;2014-09-02

5. A Novel Molecular Diagnostic Marker for Familial and Early-Onset Coronary Artery Disease and Myocardial Infarction in the LRP8 Gene;Circulation: Cardiovascular Genetics;2014-08