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Plasma cell dyscrasias
PubMed Similar studies GEO Profiles Analyze DataSet
Plasma cell dyscrasias expression profiles associated with distinct IGH translocations in multiple myeloma
PubMed Similar studies Analyze with GEO2R
Molecular classification of multiple myeloma
Multiple myeloma molecular classification
Human myeloma cell lines gene expression profiling
Genome-wide analysis of primary plasma cell leukemia identifies recurrent imbalances associated with transcriptional Profile alterations
PubMed Full text in PMC Similar studies Analyze with GEO2R
Genome-wide analysis of primary plasma cell leukemia identifies recurrent imbalances associated with transcriptional Profile alterations (Expression)
Genome-wide analysis of primary plasma cell leukemia identifies recurrent imbalances associated with transcriptional Profile alterations (Copy number)
PubMed Full text in PMC Similar studies
Up-regulation of translational machinery and distinct genetic subgroups characterize hyperdiploidy in multiple myeloma
Transcriptional characterization of a prospective series of primary plasma cell leukemia revealed genes associated with tumor progression and poorest outcome
Expression data from brain tissue of Rattus norvegicus treated with D-Serine
D-serine effect on the brain: dose response
Downregulation of specific miRNAs in hyperdiploid multiple myeloma mimics the oncogenic effect of IgH translocations occurring in the non-hyperdiploid subtype
MicroRNAs in Myeloma
Global methylation patterns in Primary Plasma Cell leukemia
MicroRNA Expression in Multiple Myeloma is Associated with Genetic Subtype, Isotype and Prognostic Outcome
Transcriptome analysis reveals significant differences between primary plasma cell leukemia and multiple myeloma even when sharing a similar genetic background
Gene expression profiling of bone marrow endothelial cells in patients with multiple myeloma
Patterns of miRNA expression in primary plasma cell leukemias: implications for tumor progression in multiple myeloma
Assessment of MEK-ERK pathway targeting by BRAF, NRAS and KRAS gene mutations in plasma cell dyscrasias
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