Frequency of close positioning of chromosomal loci detected by FRET correlates with their participation in carcinogenic rearrangements in human cells

Genes Chromosomes and Cancer

Volumn 51, Issue 11, 2012, Pages 1037-1044

  Gandhi, Manoj ^a   Evdokimova, Viktoria ^a   Nikiforov, Yuri E ^a  

^a UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; CARCINOGENESIS; CHROMOSOME POSITIONING; CHROMOSOME REARRANGEMENT; FLUORESCENCE IN SITU HYBRIDIZATION; FLUORESCENCE RESONANCE ENERGY TRANSFER; GENE FUSION; GENE LOCUS; GENE REARRANGEMENT; HUMAN; HUMAN CELL; HUMAN TISSUE; ONCOGENE RET; PRIORITY JOURNAL; THYROID CANCER; VALIDATION PROCESS;

ANALYSIS OF VARIANCE; CHROMOSOME ABERRATIONS; DNA; FLUORESCENCE RESONANCE ENERGY TRANSFER; FLUORESCENT DYES; GENE ORDER; GENETIC LOCI; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; ONCOGENE PROTEINS, FUSION; REPRODUCIBILITY OF RESULTS; THYROID GLAND; THYROID NEOPLASMS;

EID: 84865987218     PISSN: 10452257     EISSN: 10982264     Source Type: Journal    
DOI: 10.1002/gcc.21988     Document Type: Article

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