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Volumn 320, Issue 1-2, 2002, Pages 135-138
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The mutagenically separated polymerase chain reaction is a rapid and reliable method for genotyping of the tumour necrosis factor-α promoter polymorphism (-308 G/A)
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Author keywords
Analysis; Gene polymorphism; Polymerase chain reaction; Tumour necrosis factor
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Indexed keywords
TUMOR NECROSIS FACTOR ALPHA;
AGAR GEL ELECTROPHORESIS;
ALLELE;
ARTICLE;
CALCULATION;
CAUCASIAN;
CHEMICAL REACTION;
CONTROLLED STUDY;
COST EFFECTIVENESS ANALYSIS;
CROSS REACTION;
GENE AMPLIFICATION;
GENE FREQUENCY;
GENE SEQUENCE;
GENETIC ANALYSIS;
GENETIC POLYMORPHISM;
GENOTYPE;
GERMANY;
HUMAN;
MASS SPECTROMETRY;
METHODOLOGY;
MUTAGENESIS;
POLYMERASE CHAIN REACTION;
PRIORITY JOURNAL;
PROMOTER REGION;
PUBLISHING;
RACE;
REDUCTION;
REGULATORY MECHANISM;
RELIABILITY;
RESTRICTION FRAGMENT LENGTH POLYMORPHISM;
ADULT;
FEMALE;
GENE FREQUENCY;
GENETIC PREDISPOSITION TO DISEASE;
GENOTYPE;
HUMANS;
MALE;
POLYMERASE CHAIN REACTION;
POLYMORPHISM, GENETIC;
POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;
PROMOTER REGIONS (GENETICS);
SENSITIVITY AND SPECIFICITY;
TIME FACTORS;
TUMOR NECROSIS FACTOR-ALPHA;
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EID: 0036240173
PISSN: 00098981
EISSN: None
Source Type: Journal
DOI: 10.1016/S0009-8981(02)00054-2 Document Type: Article |
Times cited : (17)
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References (11)
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