Single nucleotide polymorphisms in base-excision repair genes hOGG1, APE1 and XRCC1 do not alter risk of Alzheimer's disease

Neuroscience Letters

Volumn 442, Issue 3, 2008, Pages 287-291

  Parildar Karpuzoǧlu, Hande ^a   Doǧru Abbasoǧlu, Semra ^a   Hanagasi, Hasmet A ^a   Karadaǧ, Berrin ^b   Gürvit, Hakan ^a   Emre, Murat ^a   Uysal, Müjdat ^a  

^a ISTANBUL UNIVERSITY   (Turkey)

^b ISTANBUL UNIVERSITY   (Turkey)

Author keywords

Alzheimer's disease; APE1; Base excision repair; hOGG1; Polymorphism; XRCC1

Indexed keywords

AGED; ALZHEIMER DISEASE; APE1 GENE; ARTICLE; CONTROLLED STUDY; EXCISION REPAIR; FEMALE; GENE; GENE FREQUENCY; GENETIC RISK; GENETIC VARIABILITY; HOGG1 GENE; HUMAN; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; XRCC1 GENE;

AGED; AGED, 80 AND OVER; ALZHEIMER DISEASE; CASE-CONTROL STUDIES; DNA GLYCOSYLASES; DNA-(APURINIC OR APYRIMIDINIC SITE) LYASE; DNA-BINDING PROTEINS; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; MALE; MIDDLE AGED; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 48749130340     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2008.07.047     Document Type: Article

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