The tumour suppressor p53 is frequently nonfunctional in Sézary syndrome.
about
Methotrexate and PralatrexateGenetic rearrangements result in altered gene expression and novel fusion transcripts in Sézary syndromeIdentification of p38β as a therapeutic target for the treatment of Sézary syndrome.TP53 alterations in primary and secondary Sézary syndrome: A diagnostic tool for the assessment of malignancy in patients with erythrodermaGenomic profiling of Sézary syndrome identifies alterations of key T cell signaling and differentiation genesCD1d-restricted peripheral T cell lymphoma in mice and humans.Mature T-cell leukemias: Molecular and Clinical Aspects.SIRT1 is upregulated in cutaneous T-cell lymphoma, and its inhibition induces growth arrest and apoptosis.T-cell Receptor Signaling Activates an ITK/NF-κB/GATA-3 axis in T-cell Lymphomas Facilitating Resistance to Chemotherapy.Role of dysregulated cytokine signaling and bacterial triggers in the pathogenesis of Cutaneous T Cell Lymphoma.
P2860
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P2860
The tumour suppressor p53 is frequently nonfunctional in Sézary syndrome.
description
2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年學術文章
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2012年學術文章
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2012年學術文章
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name
The tumour suppressor p53 is frequently nonfunctional in Sézary syndrome.
@en
The tumour suppressor p53 is frequently nonfunctional in Sézary syndrome.
@nl
type
label
The tumour suppressor p53 is frequently nonfunctional in Sézary syndrome.
@en
The tumour suppressor p53 is frequently nonfunctional in Sézary syndrome.
@nl
prefLabel
The tumour suppressor p53 is frequently nonfunctional in Sézary syndrome.
@en
The tumour suppressor p53 is frequently nonfunctional in Sézary syndrome.
@nl
P2093
P2860
P1476
The tumour suppressor p53 is frequently nonfunctional in Sézary syndrome
@en
P2093
B Lamprecht
P2860
P304
P356
10.1111/J.1365-2133.2012.10918.X
P407
P50
P577
2012-06-06T00:00:00Z