No abstract available
Keywords:
ASXL1; Clonal dynamics; Myelodysplastic syndrome; Paroxysmal nocturnal hemoglobinuria.
MeSH terms
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Abnormal Karyotype
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Aged
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Anemia / etiology
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Antibodies, Monoclonal, Humanized / therapeutic use
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Chromosome Deletion
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Chromosomes, Human, Pair 13
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Clone Cells / pathology
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Combined Modality Therapy
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DNA (Cytosine-5-)-Methyltransferases / genetics
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DNA Methyltransferase 3A
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Erythrocyte Transfusion
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Hemoglobinuria, Paroxysmal / complications
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Hemoglobinuria, Paroxysmal / drug therapy
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Hemoglobinuria, Paroxysmal / genetics
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Hemoglobinuria, Paroxysmal / pathology*
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Humans
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Male
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Myelodysplastic Syndromes / complications
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Myelodysplastic Syndromes / genetics
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Myelodysplastic Syndromes / pathology*
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Neutrophils / pathology
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Remission Induction
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Repressor Proteins / genetics
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Splicing Factor U2AF / genetics
Substances
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ASXL1 protein, human
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Antibodies, Monoclonal, Humanized
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DNMT3A protein, human
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Repressor Proteins
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Splicing Factor U2AF
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U2AF1 protein, human
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eculizumab
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DNA (Cytosine-5-)-Methyltransferases
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DNA Methyltransferase 3A