Identification of Gene Mutations and Fusion Genes in Patients with Sézary Syndrome.
about
TP53 alterations in primary and secondary Sézary syndrome: A diagnostic tool for the assessment of malignancy in patients with erythrodermaFacultative CTCF sites moderate mammary super-enhancer activity and regulate juxtaposed gene in non-mammary cells.Interactions between RASA2, CADM1, HIF1AN gene polymorphisms and body fatness with breast cancer: a population-based case-control study in China.Genomic analysis of 220 CTCLs identifies a novel recurrent gain-of-function alteration in RLTPR (p.Q575E).Knockdown of TBRG4 affects tumorigenesis in human H1299 lung cancer cells by regulating DDIT3, CAV1 and RRM2.
P2860
Identification of Gene Mutations and Fusion Genes in Patients with Sézary Syndrome.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Identification of Gene Mutations and Fusion Genes in Patients with Sézary Syndrome.
@en
type
label
Identification of Gene Mutations and Fusion Genes in Patients with Sézary Syndrome.
@en
prefLabel
Identification of Gene Mutations and Fusion Genes in Patients with Sézary Syndrome.
@en
P2093
P50
P1476
Identification of Gene Mutations and Fusion Genes in Patients with Sézary Syndrome.
@en
P2093
Carme Melero
Fernando Gallardo
Ingrid Lopez-Lerma
Maria P Garcia-Muret
Octavio Servitje
Teresa Estrach
Yaris Sarria-Trujillo
P304
P356
10.1016/J.JID.2016.03.024
P407
P50
P577
2016-03-30T00:00:00Z