Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor. - Wikidata - awgldk - TriplyDB

Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor.

Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor.

http://www.wikidata.org/entity/Q33408326

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Mesenchymal tumours of the mediastinum--part I Massive malignant solitary fibrous tumor arising from the bladder serosa: a case report Novel uses of immunohistochemistry in the diagnosis and classification of soft tissue tumors Role of Immunohistochemistry in the Diagnosis of Solitary Fibrous Tumor, a Review GRIA2 is a novel diagnostic marker for solitary fibrous tumour identified through gene expression profiling 'Papillary' solitary fibrous tumor/hemangiopericytoma with nuclear STAT6 expression and NAB2-STAT6 fusion.Nuclear expression of STAT6 distinguishes solitary fibrous tumor from histologic mimics.A case of dedifferentiated solitary fibrous tumor of the thoracic cavity.Nuclear relocation of STAT6 reliably predicts NAB2-STAT6 fusion for the diagnosis of solitary fibrous tumour.Phenotypical and molecular distinctness of sinonasal haemangiopericytoma compared to solitary fibrous tumour of the sinonasal tract.A case of dedifferentiated solitary fibrous tumor in the pelvis with TP53 mutation.Adaptive immune contexture at the tumour site and downmodulation of circulating myeloid-derived suppressor cells in the response of solitary fibrous tumour patients to anti-angiogenic therapy Solitary fibrous tumor - clinicopathologic, immunohistochemical and molecular analysis of 28 cases.Extensive survey of STAT6 expression in a large series of mesenchymal tumors.Clinicopathological and genetic heterogeneity of the head and neck solitary fibrous tumours: a comparative histological, immunohistochemical and molecular study of 36 cases.NAB2-STAT6 fusion types account for clinicopathological variations in solitary fibrous tumors.Retroperitoneal solitary fibrous tumor: surgery as first line therapy.The clinicopathological significance of NAB2-STAT6 gene fusions in 52 cases of intrathoracic solitary fibrous tumors Immunohistochemical detection of STAT6, CD34, CD99 and BCL-2 for diagnosing solitary fibrous tumors/hemangiopericytomas.NAB2-STAT6 Gene Fusion in Meningeal Hemangiopericytoma and Solitary Fibrous Tumor.Endobronchial solitary fibrous tumor.STAT6 Reliably Distinguishes Solitary Fibrous Tumors from Myofibromas.Fluorescence in situ hybridization in surgical pathology: principles and applications.The Current Status of Solitary Fibrous Tumor: Diagnostic Features, Variants, and Genetics.GRM1 is upregulated through gene fusion and promoter swapping in chondromyxoid fibroma.Sarcoma classification: an update based on the 2013 World Health Organization Classification of Tumors of Soft Tissue and Bone.Clinical Characteristics and Outcomes for Solitary Fibrous Tumor (SFT): A Single Center Experience.A GRIA2 and PAX8-positive renal solitary fibrous tumor with NAB2-STAT6 gene fusion.Immunohistochemical evaluation of stem cell markers and signal transducer and activator of transcription 6 (STAT6) in solitary fibrous tumors Update on Select Benign Mesenchymal and Meningothelial Sinonasal Tract Lesions Gene fusions in soft tissue tumors: Recurrent and overlapping pathogenetic themes Solitary Fibrous Tumor of the Sigmoid Colon Masquerading as an Adnexal Neoplasm.Rarely metastasizing soft tissue tumours.Evolving techniques for gene fusion detection in soft tissue tumours.The role of cytogenetics and molecular diagnostics in the diagnosis of soft-tissue tumors.Molecular diagnosis of soft tissue neoplasia: clinical applications and recent advances.Genital soft tissue tumors.The emerging complexity of gene fusions in cancer.Identification of SETD2-NF1 fusion gene in a pediatric spindle cell tumor with the chromosomal translocation t(3;17)(p21;q12).Doing more with less: New markers for sarcoma diagnosis and their applicability to cytology specimens.

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P2860

Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor.

http://www.wikidata.org/entity/Q33408326

description

2013 nî lūn-bûn

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2013 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2013 թվականի հունիսին հրատարակված գիտական հոդված

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2013年の論文

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Comprehensive genetic analysis ...... ile in solitary fibrous tumor.

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Comprehensive genetic analysis ...... ile in solitary fibrous tumor.

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type

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Comprehensive genetic analysis ...... ile in solitary fibrous tumor.

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Comprehensive genetic analysis ...... ile in solitary fibrous tumor.

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Comprehensive genetic analysis ...... ile in solitary fibrous tumor.

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Comprehensive genetic analysis ...... ile in solitary fibrous tumor.

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Genes, Chromosomes and Cancer

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Comprehensive genetic analysis ...... ile in solitary fibrous tumor.

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P2093

Anna Collin

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Arezoo Mohajeri

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Fredrik Vult von Steyern

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Henryk A Domanski

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Otte Brosjö

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P2860

NAB2, a corepressor of NGFI-A (Egr-1) and Krox20, is induced by proliferative and differentiative stimuli

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Fast and accurate short read alignment with Burrows-Wheeler transform

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873-886

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10.1002/GCC.22083

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10

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52

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Jason L. Hornick

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Maria Debiec-Rychter

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237200006

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