Simple method for detection of MYH11 DNA rearrangements in patients with inv(16)(p13q22) and acute myeloid leukemia.
Data(s) |
01/09/1996
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Resumo |
The pericentric inversion on chromosome 16 [inv(16)(p13q22)] and related t(16;16)(p13;q22) are recurrent aberrations associated with acute myeloid leukemia (AML) M4 Eo. Both abberations result in a fusion of the core binding factor beta (CBFB) and smooth muscle myosin heavy chain gene (MYH11). A selected genomic 6.9-kb BamHl probe detects MYH11 DNA rearrangements in 18 of 19 inv(16)/t(16;16) patients tested using HindIII digested DNA. The rearranged fragments were not detectable after remission in two cases tested, while they were present after relapse in one of these two cases tested. |
Identificador |
https://serval.unil.ch/notice/serval:BIB_7898ADC0B96B info:pmid:8751463 pmid:8751463 isiid:A1996VF59800007 |
Idioma(s) |
eng |
Fonte |
Leukemia1091459-1462 |
Palavras-Chave | #Chromosome Inversion; Chromosomes, Human, Pair 16; DNA, Neoplasm/genetics; Gene Rearrangement; Humans; Leukemia, Myelomonocytic, Acute/genetics; Myosin Heavy Chains/biosynthesis; Myosin Heavy Chains/genetics; Oncogene Proteins, Fusion/biosynthesis; Oncogene Proteins, Fusion/genetics; Translocation, Genetic |
Tipo |
info:eu-repo/semantics/article article |