Influence of genomic variation in FTO at 16q12.2, MC4R at 18q22 and NRXN3 at 14q31 genes on breast cancer risk

Molecular Biology Reports

Volumn 39, Issue 3, 2012, Pages 2915-2919

  Kusinska, Renata ^a   Goírniak, Patryk ^a   Pastorczak, Agata ^a   Fendler, Wojciech ^a   Potemski, Piotr ^a   Mlynarski, Wojciech ^a   Kordek, Radzislaw ^a  

^a MEDICAL UNIVERSITY OF LODZ   (Poland)

Author keywords

Breast cancer risk; FTO; MC4R; NRXN3

Indexed keywords

ADULT; AGE; ALLELE; ARTICLE; BREAST CANCER; BREAST CARCINOGENESIS; CANCER RISK; CANCER SUSCEPTIBILITY; CHROMOSOME 14Q; CHROMOSOME 16Q; CHROMOSOME 18Q; CONTROLLED STUDY; FEMALE; FTO GENE; GENE; GENE FREQUENCY; GENE FUNCTION; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; MC4R GENE; NRXN3 GENE; OBESITY; POLYMORPHIC LOCUS; SINGLE NUCLEOTIDE POLYMORPHISM;

AGE FACTORS; BREAST NEOPLASMS; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; NERVE TISSUE PROTEINS; ODDS RATIO; POLAND; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEINS; RECEPTOR, MELANOCORTIN, TYPE 4; RISK FACTORS;

EID: 84863812319     PISSN: 03014851     EISSN: 15734978     Source Type: Journal    
DOI: 10.1007/s11033-011-1053-2     Document Type: Article

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