Identification of SETD2-NF1 fusion gene in a pediatric spindle cell tumor with the chromosomal translocation t(3;17)(p21;q12).

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Identification of SETD2-NF1 fusion gene in a pediatric spindle cell tumor with the chromosomal translocation t(3;17)(p21;q12).

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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Identification of SETD2-NF1 fu ...... ranslocation t(3;17)(p21;q12).

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Identification of SETD2-NF1 fu ...... ranslocation t(3;17)(p21;q12).

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prefLabel

Identification of SETD2-NF1 fu ...... ranslocation t(3;17)(p21;q12).

@en

P1476

Identification of SETD2-NF1 fu ...... ranslocation t(3;17)(p21;q12).

@en

P2093

Bodil Bjerkehagen

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Ingvild Lobmaier

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Ludmila Gorunova

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P2860

The mRNA expression of SETD2 in human breast cancer: correlation with clinico-pathological parameters

Complex splicing pattern generates great diversity in human NF1 transcripts

Alternative splicing of the neurofibromatosis type I pre-mRNA

A RASopathy gene commonly mutated in cancer: the neurofibromatosis type 1 tumour suppressor

Adverse outcomes in clear cell renal cell carcinoma with mutations of 3p21 epigenetic regulators BAP1 and SETD2: a report by MSKCC and the KIRC TCGA research network

Huntingtin interacts with a family of WW domain proteins

High-density array-CGH with targeted NGS unmask multiple noncontiguous minute deletions on chromosome 3p21 in mesothelioma

Dynamic histone H3 methylation during gene induction: HYPB/Setd2 mediates all H3K36 trimethylation

Several fusion genes identified by whole transcriptome sequencing in a spindle cell sarcoma with rearrangements of chromosome arm 12q and MDM2 amplification

The "grep" command but not FusionMap, FusionFinder or ChimeraScan captures the CIC-DUX4 fusion gene from whole transcriptome sequencing data on a small round cell tumor with t(4;19)(q35;q13)

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3181-3188

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scholarly article

P356

10.3892/OR.2017.5628

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P433

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P478

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Sverre Heim

Ioannis Panagopoulos

P577

2017-05-04T00:00:00Z

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P698

28498454

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P932

5442398

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