Effect of genetic variants of chemokine receptors on the development of myocardial infarction in Turkish population

Molecular Biology Reports

Volumn 37, Issue 7, 2010, Pages 3615-3619

  Karaali, Zeynep Ermis ^a   Sozen, Seyma ^b   Yurdum, Melis ^b   Cacina, Canan ^b   Toptas, Bahar ^b   Gok, Ozlem ^b   Agachan, Bedia ^b  

^a HASEKI EDUCATION AND RESEARCH HOSPITAL   (Turkey)

^b ISTANBUL UNIVERSITY   (Turkey)

Author keywords

CCR2 V64I; CCR5 delta32; Myocardial infarction; Polymorphisms

Indexed keywords

CHEMOKINE RECEPTOR; CHEMOKINE RECEPTOR CCR2; CHEMOKINE RECEPTOR CCR5; GENOMIC DNA;

ADULT; ARTICLE; CONTROLLED STUDY; CORONARY CARE UNIT; FEMALE; GENE DELETION; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HEART INFARCTION; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; PATHOGENESIS; POLYMERASE CHAIN REACTION; POPULATION GENETICS;

AMINO ACID SUBSTITUTION; CASE-CONTROL STUDIES; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOTYPE; HUMANS; MALE; MIDDLE AGED; MYOCARDIAL INFARCTION; RECEPTORS, CCR2; RECEPTORS, CCR5; TURKEY;

EID: 77956958244     PISSN: 03014851     EISSN: 15734978     Source Type: Journal    
DOI: 10.1007/s11033-010-0011-8     Document Type: Article

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