Breakages at common fragile sites set boundaries of amplified regions in two leukemia cell lines K562 - Molecular characterization of FRA2H and localization of a new CFS FRA2S

Cancer Letters

Volumn 299, Issue 1, 2010, Pages 37-44

  Pelliccia, Franca ^a   Bosco, Nazario ^a   Rocchi, Angela ^a  

^a SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

Cancer lines; Fragile sites; Genome amplification; K562

Indexed keywords

ARTICLE; BACTERIAL ARTIFICIAL CHROMOSOME; CANCER CELL CULTURE; CELL STRAIN K 562; CHROMOSOME 2Q; CHROMOSOME BREAKAGE; CHROMOSOME FRAGILE SITE; CHROMOSOME FRAGILITY; CONTROLLED STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; GENE DOSAGE; GENE DUPLICATION; GENE IDENTIFICATION; GENE LOCATION; GENE REARRANGEMENT; GENE SEQUENCE; HUMAN; HUMAN CELL; INVERTED REPEAT; KARYOTYPE; LEUKEMIA; MOLECULAR MECHANICS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; CHROMOSOMAL MAPPING; CHROMOSOME 2; GENETICS; K562 CELL LINE; NEOPLASM; TELOMERE;

CHROMOSOME FRAGILE SITES; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 2; GENE AMPLIFICATION; HUMANS; K562 CELLS; NEOPLASMS; TELOMERE;

EID: 77957904128     PISSN: 03043835     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.canlet.2010.08.001     Document Type: Article

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