Molecular genetics of AML

Best Practice and Research: Clinical Haematology

Volumn 25, Issue 4, 2012, Pages 409-414

  Link, Daniel C ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

acute myeloid leukemia; AML; clone; coding mutation; driver mutation; genetics; genome; sequencing; subclone

Indexed keywords

DNA METHYLTRANSFERASE 3A; MICRORNA; TRANSCRIPTOME; UNTRANSLATED RNA;

ACUTE GRANULOCYTIC LEUKEMIA; ALTERNATIVE RNA SPLICING; CANCER CELL; CELL DIVISION; CHROMATIN STRUCTURE; CHROMOSOME TRANSLOCATION; DISOMY; DNA METHYLATION; DNA SEQUENCE; EXOME; GENE EXPRESSION; GENE FREQUENCY; GENE SEQUENCE; GENOMIC INSTABILITY; HEMATOPOIETIC STEM CELL; HUMAN; LEUKEMIA RELAPSE; LEUKEMOGENESIS; MOLECULAR GENETICS; MULTIGENE FAMILY; NONSENSE MEDIATED MRNA DECAY; PRIORITY JOURNAL; REVIEW; RNA SEQUENCE; SISTER CHROMATID; SOMATIC MUTATION;

CELL AGING; DNA MUTATIONAL ANALYSIS; FEMALE; GENOME, HUMAN; GENOME-WIDE ASSOCIATION STUDY; HEMATOPOIETIC STEM CELLS; HUMANS; LEUKEMIA, MYELOID, ACUTE; MALE; MUTATION;

EID: 84870694948     PISSN: 15216926     EISSN: 15321924     Source Type: Journal    
DOI: 10.1016/j.beha.2012.10.002     Document Type: Review

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