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Items: 3

1.

Early Relapse in ALL is identified by Time To Leukemia in NOD/SCID mice and is characterized by a gene signature involving survival pathways

(Submitter supplied) Gene expression analysis identified a specific signature of differentially expressed genes discriminating TTLshort and TTLlong phenotypes. Gene expression signatures of xenografted leukemia samples with different TTL phenotypes were analyzed on cohorts of pediatric BCP-ALL patients.
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS4206 GDS4779
Platform:
GPL570
209 Samples
Download data: CEL
Series
Accession:
GSE13576
ID:
200013576
2.
Full record GDS4779

NOD/SCID/huALL xenotransplant model of pediatric acute leukemia

Analysis of xenograft leukemia samples from NOD/SCID mice transplanted with leukemia cells from patients with pediatric BCP-ALL. The xenograft samples displayed short or long “Time To Leukemia” (TTL). Results provide insight into molecular mechanisms underlying the distinct TTL phenotypes.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 disease state sets
Platform:
GPL570
Series:
GSE13576
12 Samples
Download data: CEL
DataSet
Accession:
GDS4779
ID:
4779
3.
Full record GDS4206

Pediatric acute leukemia patients with early relapse: white blood cells

Analysis of WBCs from pediatric B cell precursor (BCP) acute lymphoblastic leukemia (ALL) patients with early, late, or no relapse. For patients with relapsed BCP-ALL, early relapses fare worse than later relapses. Results provide insight into the molecular basis of early relapses in BCP-ALL.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 3 disease state sets
Platform:
GPL570
Series:
GSE13576
197 Samples
Download data: CEL
DataSet
Accession:
GDS4206
ID:
4206
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