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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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| Vydáno v: | Nat Genet |
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| Hlavní autoři: | , , , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2015
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| Témata: | |
| On-line přístup: | 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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