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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Myocardial Infarction and OLR1[original query]
Oxidized LDL receptor gene (OLR1) is associated with the risk of myocardial infarction.
Biochemical and biophysical research communications 2003 Mar 303 (1): 247-50.
Tatsuguchi Mariko, Furutani Michiko, Hinagata Jun-ichi, Tanaka Takeshi, Furutani Yoshiyuki, Imamura Shin-ichiro, Kawana Masatoshi, Masaki Tomoh, Kasanuki Hiroshi, Sawamura Tatsuya, Matsuoka Rumi
On the association of the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction or coronary artery disease.
European journal of human genetics : EJHG 2006 Jan 14 (1): 127-30.
Trabetti Elisabetta, Biscuola Michele, Cavallari Ugo, Malerba Giovanni, Girelli Domenico, Olivieri Oliviero, Martinelli Nicola, Corrocher Roberto, Pignatti Pier Fran
The 3'-UTR C>T polymorphism of the oxidized LDL-receptor 1 (OLR1) gene does not associate with coronary artery disease in Italian CAD patients or with the severity of coronary disease.
Nutrition, metabolism, and cardiovascular diseases : NMCD 2006 Jul 16 (5): 345-52.
Sentinelli Federica, Filippi Emanuela, Fallarino Mara, Romeo Stefano, Fanelli Marzia, Buzzetti Raffaella, Berni Andrea, Baroni Marco
Failure to replicate an association of SNPs in the oxidized LDL receptor gene (OLR1) with CAD.
BMC medical genetics 2008 9 23.
Knowles Joshua W, Assimes Themistocles L, Boerwinkle Eric, Fortmann Stephen P, Go Alan, Grove Megan L, Hlatky Mark, Iribarren Carlos, Li Jun, Myers Richard, Risch Neil, Sidney Stephen, Southwick Audrey, Volcik Kelly A, Quertermous Thom
Population differences in allele frequencies at the OLR1 locus may suggest geographic disparities in cardiovascular risk events.
Annals of human biology 2010 Apr 37 (2): 136-48.
Predazzi Irene M, Martínez-Labarga Cristina, Vecchione Lucia, Mango Ruggiero, Ciccacci Cinzia, Amati Francesca, Ottoni Claudio, Crawford Michael H, Rickards Olga, Romeo Francesco, Novelli Giusep
IVS4-14 A/G and IVS4-73 C/T polymorphisms in OLR1 gene in patients with ischemic cerebrovascular diseases.
Genetic testing and molecular biomarkers 2010 Feb 14 (1): 9-11.
Vietri Maria Teresa, Molinari Anna Maria, Boggia Maria, Parisi Mariarita, Cioffi Miche
Discovering Genotype Variants in an Infant with VACTERL through Clinical Exome Sequencing: A Support for Personalized Risk Assessment and Disease Prevention.
Pediatric reports 2021 1 13 (1): 45-56.
Pelizzo Gloria, Chiricosta Luigi, Mazzon Emanuela, Zuccotti Gian Vincenzo, Avanzini Maria Antonietta, Croce Stefania, Lima Mario, Bramanti Placido, Calcaterra Valer
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