DNA repair XRCC1 Arg399Gln polymorphism is associated with the risk of development of end-stage renal disease

Molecular Biology Reports

Volumn 39, Issue 6, 2012, Pages 6995-7001

  Trabulus, Sinan ^a   Guven, Gulgun S ^a   Altiparmak, Mehmet R ^a   Batar, Bahadir ^a   Tun, Ozlem ^a   Yalin, Ayse S ^a   Tunckale, Aydin ^a   Guven, Mehmet ^a  

^a ISTANBUL UNIVERSITY   (Turkey)

Author keywords

Dialysis; Polymorphism; XPD; XRCC1

Indexed keywords

XERODERMA PIGMENTOSUM GROUP D PROTEIN;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CONTROLLED STUDY; DNA REPAIR; FEMALE; GENE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; HEMODIALYSIS; HUMAN; KIDNEY FAILURE; MAJOR CLINICAL STUDY; MALE; PERITONEAL DIALYSIS; POLYMERASE CHAIN REACTION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SINGLE NUCLEOTIDE POLYMORPHISM; XPD GENE; XRCC1 GENE;

ADULT; AGED; AMINO ACID SUBSTITUTION; AMPLIFIED FRAGMENT LENGTH POLYMORPHISM ANALYSIS; CASE-CONTROL STUDIES; DNA REPAIR; DNA-BINDING PROTEINS; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; KIDNEY FAILURE, CHRONIC; MALE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; RENAL DIALYSIS; RISK FACTORS; SEQUENCE ANALYSIS, DNA;

EID: 84864277275     PISSN: 03014851     EISSN: 15734978     Source Type: Journal    
DOI: 10.1007/s11033-012-1529-8     Document Type: Article

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