Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2004-1-26
pubmed:abstractText
The common polymorphism at codon 311 (C311S) of paraoxonase 2 gene (PON2) was investigated in 165 patients with sporadic late-onset Alzheimer's disease (LOAD) and 174 controls in Chinese. The PON2*C allele frequency was significantly increased in the patients as compared with controls. However, no significant difference was observed after stratification of apolipoprotein E (ApoE) epsilon4 allele. These results suggested that the PON2 polymorphism might be a risk factor for LOAD independent of ApoE epsilon4 status in Chinese.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0169-328X
pubmed:author
pubmed:issnType
Print
pubmed:day
5
pubmed:volume
120
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
201-4
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:14741412-Aged, pubmed-meshheading:14741412-Aged, 80 and over, pubmed-meshheading:14741412-Alleles, pubmed-meshheading:14741412-Alzheimer Disease, pubmed-meshheading:14741412-Apolipoproteins E, pubmed-meshheading:14741412-Aryldialkylphosphatase, pubmed-meshheading:14741412-Asian Continental Ancestry Group, pubmed-meshheading:14741412-Chi-Square Distribution, pubmed-meshheading:14741412-Cysteine, pubmed-meshheading:14741412-Female, pubmed-meshheading:14741412-Gene Frequency, pubmed-meshheading:14741412-Genetic Predisposition to Disease, pubmed-meshheading:14741412-Genotype, pubmed-meshheading:14741412-Humans, pubmed-meshheading:14741412-Male, pubmed-meshheading:14741412-Polymerase Chain Reaction, pubmed-meshheading:14741412-Polymorphism, Genetic, pubmed-meshheading:14741412-Serine
pubmed:year
2004
pubmed:articleTitle
Possible association between Cys311Ser polymorphism of paraoxonase 2 gene and late-onset Alzheimer's disease in Chinese.
pubmed:affiliation
Key Laboratory of Biotherapy of Human Diseases, Department of Medical Genetics, West China Hospital and Division of Human Morbid Genomics, Ministry of Education, Sichuan University, Chengdu, 610041, China. szzhang@mcwcums.com
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't