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...
Hlavní autoři: | 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 |
---|---|
Médium: | Journal article |
Jazyk: | English |
Vydáno: |
2010
|
Podobné jednotky
-
Inactivating mutations of the histone methyltransferase EZH2 in myeloid disorders
Autor: Ernst, T, a další
Vydáno: (2010) -
INACTIVATING MUTATIONS OF THE HISTONE METHYLTRANSFERASE EZH2 ARE ASSOCIATED WITH CHROMOSOME 7 ABNORMALITIES IN MYELOID DISORDERS
Autor: Ernst, T, a další
Vydáno: (2010) -
Transcription factor mutations in myelodysplastic/myeloproliferative neoplasms
Autor: Thomas Ernst, a další
Vydáno: (2010-09-01) -
EZH2 in Myeloid Malignancies
Autor: Jenny Rinke, a další
Vydáno: (2020-07-01) -
Germinal center dysregulation by histone methyltransferase EZH2 promotes lymphomagenesis
Autor: Su, I-hsin, a další
Vydáno: (2013)