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TranscriptomicsSNP data from Down syndrome and non-Down syndrome pediatric acute lymphoblastic leukemia cases and controls
SNP profiling can reveal copy number abnormalities and loss of heterozygosity associated with distinct biologic subtypes of acute lymphoblastic leukemia (ALL). We performed SNP profiling of Down syndrome ALL cases and controls to identify unique biologic features of this ALL subgroup. Ficoll-enriche...
ORGANISM(S): Homo sapiens 
2011-07-12 | E-GEOD-21091 | biostudies-arrayexpress
TranscriptomicsExpression data from Down syndrome and non-Down syndrome pediatric acute lymphoblastic leukemia cases
Gene expression profiling (GEP) can reveal characteristic signatures associated with distinct biologic subtypes of acute lymphoblastic leukemia (ALL). We performed GEP on Down syndrome (DS) and comparison non-Down syndrome (NDS) ALL cases to identify biologic differences between these groups. Ficoll...
ORGANISM(S): Homo sapiens 
2011-07-12 | E-GEOD-20910 | biostudies-arrayexpress
UnknownIntegrated genomic analysis of relapsed childhood acute lymphoblastic leukemia reveals therapeutic strategies.
Not available
S-EPMC3217405 | biostudies-literature
UnknownGenomic profiling in Down syndrome acute lymphoblastic leukemia identifies histone gene deletions associated with altered methylation profiles.
Not available
S-EPMC4107887 | biostudies-literature
UnknownEndogenous knockdown of survivin improves chemotherapeutic response in ALL models.
Not available
S-EPMC3833621 | biostudies-literature
TranscriptomicsExpression data from ALL diagnosis and relapse pediatric acute lymphoblastic leukemia cases
There is a distinct signature of differentially expressed probes from diagnosis to relapse Gene expression profiles of pediatric patients with B-precursor ALL were compared to at 2 time points, diagnosis and relapse. The overall design was a comparison of gene expression at diagnosis and relapse wit...
ORGANISM(S): Homo sapiens 
2011-09-23 | E-GEOD-28460 | biostudies-arrayexpress
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