Genomic profiling of Sézary Syndrome identifies alterations of key T-cell signaling and differentiation genes

Sézary Syndrome is a rare leukemic form of cutaneous T-cell lymphoma defined as erythroderma, adenopathy, and circulating atypical T-lymphocytes. It is rarely curable with poor prognosis. Here we present a multi-platform genomic analysis of 37 Sézary Syndrome patients that implicates dysregulation o...

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Publicat a:Nat Genet
Autors principals: Wang, Linghua, Ni, Xiao, Covington, Kyle R., Yang, Betty Y., Shiu, Jessica, Zhang, Xiang, Xi, Liu, Meng, Qingchang, Langridge, Timothy, Drummond, Jennifer, Donehower, Lawrence A., Doddapaneni, Harshavardhan, Muzny, Donna M., Gibbs, Richard A., Wheeler, David A., Duvic, Madeleine
Format: Artigo
Idioma:Inglês
Publicat: 2015
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4829974/
https://ncbi.nlm.nih.gov/pubmed/26551670
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.3444
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