Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders.
Abnormalities of chromosome 7q are common in myeloid malignancies, but no specific target genes have yet been identified. Here, we describe the finding of homozygous EZH2 mutations in 9 of 12 individuals with 7q acquired uniparental disomy. Screening of a total of 614 individuals with myeloid disord...
المؤلفون الرئيسيون: | Ernst, T, Chase, A, Score, J, Hidalgo-Curtis, C, Bryant, C, Jones, A, Waghorn, K, Zoi, K, Ross, F, Reiter, A, Hochhaus, A, Drexler, H, Duncombe, A, Cervantes, F, Oscier, D, Boultwood, J, Grand, F, Cross, N |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2010
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مواد مشابهة
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Inactivating mutations of the histone methyltransferase EZH2 in myeloid disorders
حسب: Ernst, T, وآخرون
منشور في: (2010) -
INACTIVATING MUTATIONS OF THE HISTONE METHYLTRANSFERASE EZH2 ARE ASSOCIATED WITH CHROMOSOME 7 ABNORMALITIES IN MYELOID DISORDERS
حسب: Ernst, T, وآخرون
منشور في: (2010) -
Transcription factor mutations in myelodysplastic/myeloproliferative neoplasms
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EZH2 in Myeloid Malignancies
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منشور في: (2020-07-01) -
Germinal center dysregulation by histone methyltransferase EZH2 promotes lymphomagenesis
حسب: Su, I-hsin, وآخرون
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