Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2008-2-4
pubmed:abstractText
Polymorphisms in genes coding for chemokine receptors, CCR2 and CCR5 have been studied as genetic markers of coronary artery disease (CAD). V64Ile polymorphism in CCR2 has been implicated in the manifestation of myocardial infarction in different populations, but data on association of the CCR5 deletion variant in etiology of CAD are conflicting. In the present study we tested genetic association between CCR5 Delta32 polymorphism and CAD among North Indians (Uttar Pradesh).
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1874-1754
pubmed:author
pubmed:issnType
Electronic
pubmed:day
29
pubmed:volume
124
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
254-8
pubmed:meshHeading
pubmed-meshheading:17383752-Adolescent, pubmed-meshheading:17383752-Adult, pubmed-meshheading:17383752-Aged, pubmed-meshheading:17383752-Alleles, pubmed-meshheading:17383752-Case-Control Studies, pubmed-meshheading:17383752-Chi-Square Distribution, pubmed-meshheading:17383752-Confidence Intervals, pubmed-meshheading:17383752-Coronary Angiography, pubmed-meshheading:17383752-Coronary Disease, pubmed-meshheading:17383752-Female, pubmed-meshheading:17383752-Gene Deletion, pubmed-meshheading:17383752-Genetic Predisposition to Disease, pubmed-meshheading:17383752-Genotype, pubmed-meshheading:17383752-Humans, pubmed-meshheading:17383752-Incidence, pubmed-meshheading:17383752-India, pubmed-meshheading:17383752-Male, pubmed-meshheading:17383752-Middle Aged, pubmed-meshheading:17383752-Odds Ratio, pubmed-meshheading:17383752-Polymorphism, Genetic, pubmed-meshheading:17383752-Receptors, CCR5, pubmed-meshheading:17383752-Reference Values, pubmed-meshheading:17383752-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:17383752-Risk Assessment
pubmed:year
2008
pubmed:articleTitle
Chemokine receptor 5 (CCR5) deletion polymorphism in North Indian patients with coronary artery disease.
pubmed:publicationType
Letter