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Items: 2

1.

Whole-exome sequencing identifies mutations of BCOR in acute myeloid leukemia with normal karyotype

(Submitter supplied) Among acute myeloid leukemias (AML) with normal karyotype (CN-AML), NPM1 and CEBPA mutations define WHO provisional entities accounting for ~60% of cases, but the remaining ~40% remains poorly characterized. By whole exome-sequencing (WES) of one CN-AML patient lacking mutations in NPM1, CEBPA, FLT3, MLL-PTD and IDH1, we newly identified a clonal somatic mutation in BCOR (BCL6 co-repressor), a gene located in chromosome X. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4280
Platform:
GPL570
24 Samples
Download data: CEL
Series
Accession:
GSE30442
ID:
200030442
2.
Full record GDS4280

BCL6 corepressor somatic mutation in acute myeloid leukemia with normal karyotype: Ficoll-enriched mononuclear cells

Analysis of mononuclear cells from normal karyotype, acute myeloid leukemia (CN-AML) patients with BCL6 corepressor (BCOR) mutation. CN-AML BCOR mutations are associated with oculo-facio-cardiodental genetic syndrome and poor outcome. Results provide insight into role of BCOR in CN-AML pathogenesis.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL570
Series:
GSE30442
24 Samples
Download data: CEL
DataSet
Accession:
GDS4280
ID:
4280

Supplemental Content

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