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Volumn 119, Issue 5, 2012, Pages 1318-1319
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Genetic defects in PRC2 components other than EZH2 are not common in myeloid malignancies
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Author keywords
[No Author keywords available]
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Indexed keywords
HISTONE H3;
HISTONE METHYLTRANSFERASE;
TRANSCRIPTION FACTOR EZH2;
BONE MARROW;
CHRONIC MYELOMONOCYTIC LEUKEMIA;
EMBRYONIC STEM CELL;
ENZYME ACTIVITY;
EPIGENETICS;
FRAMESHIFT MUTATION;
GENE DELETION;
GENE MUTATION;
GENE SILENCING;
GENETIC DISORDER;
GENETIC VARIABILITY;
HEMATOPOIESIS;
HUMAN;
INFORMED CONSENT;
LETHALITY;
LETTER;
MYELODYSPLASTIC SYNDROME;
MYELOPROLIFERATIVE DISORDER;
NONHUMAN;
PHENOTYPE;
PRIORITY JOURNAL;
SINGLE NUCLEOTIDE POLYMORPHISM;
T LYMPHOCYTE;
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EID: 84856623134
PISSN: 00064971
EISSN: 15280020
Source Type: Journal
DOI: 10.1182/blood-2011-07-365213 Document Type: Letter |
Times cited : (14)
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References (7)
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