Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10909564 | Leukemia Research | 2005 | 10 Pages |
Abstract
Fluorescent-labeled DNA probes were used to study 52 chronic lymphocytic leukemia (B-CLL) patients for (1) disease progression, (2) angiogenesis genes, (3) T-cell leukemia 1 gene (TCL1), (4) immunoglobulin heavy chain variable region (IGHv) and (5) chromosome 6q. Compared to stable disease, more patients with progressive disease had â¥2 anomalies and a high percentage of neoplastic nuclei. Anomalies of genes for basic fibroblast growth factor, interleukin 4, vascular endothelial growth factor or TCL1 were not detected. Deletions in IGHv occurred in 25% of patients and correlated with IGHv gene expression. Probes for 6q23 detected more deletions in 6q than probes for 6q21.
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Authors
Stephanie R. Fink, Sarah F. Paternoster, Stephanie A. Smoley, Heather C. Flynn, Susan M. Geyer, Tait D. Shanafelt, You Kyoung Lee, Diane F. Jelinek, Neil E. Kay, Gordon W. Dewald,