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UnknownLarge scale screening for known fusion genes in cancer cell lines
Not available
ORGANISM(S): Homo sapiens 
S-ECPF-GEOD-24737 | biostudies-other
UnknownTranscriptional profiling demonstrates altered characteristics of CD8+ cytotoxic T-cells and regulatory T-cells in TP53-mutated acute myeloid leukemia.
Not available
S-EPMC9359873 | biostudies-literature
TranscriptomicsAffymetrix SNP-array data for 2 ETV6/RUNX1-positive Acute Lymphoblastic Leukemia samples and corresponding normal samples
Acute lymphoblastic leukemia (ALL), the most common malignant disorder in childhood, is typically associated with numerical chromosomal aberrations, fusion genes or small focal deletions, thought to represent important pathogenetic events in the development of the leukemia. Mutations, such as single...
ORGANISM(S): Homo sapiens 
2012-07-02 | E-GEOD-25116 | biostudies-arrayexpress
TranscriptomicsIllumina SNP-array data for 2 ETV6/RUNX1-positive Acute Lymphoblastic Leukemia samples and corresponding normal samples
Acute lymphoblastic leukemia (ALL), the most common malignant disorder in childhood, is typically associated with numerical chromosomal aberrations, fusion genes or small focal deletions, thought to represent important pathogenetic events in the development of the leukemia. Mutations, such as single...
ORGANISM(S): Homo sapiens 
2012-07-02 | E-GEOD-25102 | biostudies-arrayexpress
UnknownGene expression signatures in childhood acute leukemias are largely unique and distinct from those of normal tissues and other malignancies.
Not available
S-EPMC2845086 | biostudies-literature
UnknownClonal conversion of B lymphoid leukemia reveals cross-lineage transfer of malignant states.
Not available
S-EPMC5159664 | biostudies-literature
TranscriptomicsAffy SNP-array data for 23 ETV6/RUNX1-positive ALL patient samples and one cell line
The ETV6/RUNX1 fusion gene, present in 25% of B-lineage childhood acute lymphoblastic leukemia (ALL), is thought to represent an initiating event, which requires additional genetic changes for leukemia development. To identify additional genetic alterations, 24 ETV6/RUNX1-positive ALLs were analyzed...
ORGANISM(S): Homo sapiens 
2010-07-07 | E-GEOD-19996 | biostudies-arrayexpress
UnknownWhy B(-)other? About the gap of unknowns in ALL.
Not available
S-EPMC9203700 | biostudies-literature
UnknownActivating mutations remodel the chromatin accessibility landscape to drive distinct regulatory networks in KMT2A-rearranged acute leukemia.
Not available
S-EPMC11426354 | biostudies-literature
UnknownTransgenic expression of human cytokines in immunodeficient mice does not facilitate myeloid expansion of BCR-ABL1 transduced human cord blood cells.
Not available
S-EPMC5638313 | biostudies-literature
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