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The American Journal of Surgical Pathology, ISSN 0147-5185, 02/2019, Volume 43, Issue 2, pp. 220 - 228
The evolving classification of round cell sarcomas is driven by molecular alterations. EWSR1-PATZ1 fusion positive spindle and round cell sarcoma is one such... 
EWS | SURGERY | DIAGNOSIS | sarcoma | polyphenotypic differentiation | MARKER | PATHOLOGY | SOFT-TISSUE | EWING SARCOMA | fusion | EWSR1 | TUMOR-SUPPRESSOR | PATZ1 | Usage | Phenotype | Nucleotide sequencing | Research | DNA sequencing
Journal Article
Journal of Cutaneous Pathology, ISSN 0303-6987, 06/2019, Volume 46, Issue 6, pp. 421 - 424
Cutaneous syncytial myoepithelioma (CSM) is a recently recognized, histopathological variant of myoepithelial (ME) tumors of the skin. It is characterized by a... 
PBX3 | skin | EWSR1 | syncytial | myoepithelioma | NEOPLASM | PATHOLOGY | EXPRESSION | DERMATOLOGY | Immunohistochemistry | RNA sequencing | Genetic research | Keratin | Genes | Cytokeratin | Actin | Gene rearrangement | Stroma | Skin | Bone tumors | EWSR1 gene | Hybridization | Ribonucleic acid--RNA | Gene fusion | FLI-1 protein
Journal Article
American Journal of Surgical Pathology, ISSN 0147-5185, 02/2019, Volume 43, Issue 2, pp. 220 - 228
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 05/2019, Volume 43, Issue 5, pp. 695 - 702
Primary intraosseous rhabdomyosarcomas (RMSs) are extremely rare. Recently 2 studies reported 4 cases of primary intraosseous RMS with EWSR1/FUS-TFCP2 gene... 
intraosseous | NCOA2 | MEIS1 | TFCP2 | EWSR1 | FUS | rhabdomyosarcoma | SURGERY | INVOLVEMENT | PATHOLOGY | SOFT-TISSUE | IDENTIFICATION | ONCOGENE | SMALL-MOLECULE INHIBITORS | EMBRYONAL RHABDOMYOSARCOMA | BONE | EXPRESSION | LSF
Journal Article
Brain Pathology, ISSN 1015-6305, 03/2018, Volume 28, Issue 2, pp. 183 - 191
Journal Article
Brain Pathology, ISSN 1015-6305, 01/2019, Volume 29, Issue 1, pp. 53 - 62
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 06/2014, Volume 38, Issue 6, pp. 801 - 808
Sclerosing epithelioid fibrosarcoma (SEF) and low-grade fibromyxoid sarcoma (LGFMS) are 2 distinct types of sarcoma, with a subset of cases showing overlapping... 
EWSR1 | FUS | CREB3L1 | CREB3L2 | Hybrid | Low-grade fibromyxoid sarcoma | Sclerosing epithelioid fibrosarcoma | Gene fusion | RNA-POLYMERASE-II | SURGERY | TRANSLOCATION | PROTEIN | B-LYMPHOCYTE DEVELOPMENT | GIANT ROSETTES | AMYOTROPHIC-LATERAL-SCLEROSIS | PATHOLOGY | sclerosing epithelioid fibrosarcoma | hybrid | gene fusion | SPINDLE-CELL TUMOR | low-grade fibromyxoid sarcoma | GRADE-FIBROMYXOID-SARCOMA | PROTEOMIC ANALYSIS | RNA-Binding Proteins - genetics | Fibrosarcoma - secondary | Humans | Middle Aged | RNA, Messenger - analysis | Male | Sclerosis | Young Adult | Neoplasm Grading | Soft Tissue Neoplasms - chemistry | Aged, 80 and over | Adult | Female | Mucin-4 - analysis | Soft Tissue Neoplasms - genetics | Epithelioid Cells - pathology | Calmodulin-Binding Proteins - genetics | Genetic Predisposition to Disease | Biomarkers, Tumor - analysis | Neoplasm Recurrence, Local | RNA-Binding Protein FUS - genetics | Gene Fusion | In Situ Hybridization, Fluorescence | Fibroma - genetics | Epithelioid Cells - chemistry | Reverse Transcriptase Polymerase Chain Reaction | Nerve Tissue Proteins - genetics | Fibroma - pathology | Cyclic AMP Response Element-Binding Protein - genetics | Fibrosarcoma - genetics | Phenotype | Sequence Analysis, RNA | Fibrosarcoma - chemistry | Gene Rearrangement | Soft Tissue Neoplasms - pathology | Aged | Biomarkers, Tumor - genetics | Fibroma - chemistry | RNA-Binding Protein EWS | Index Medicus | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Surgery | Kirurgi
Journal Article
Genes Chromosomes and Cancer, ISSN 1045-2257, 2009, Volume 49, Issue 12, pp. 1114 - 1124
The diagnosis of myoepithelial (ME) tumors outside salivary glands remains challenging, especially in unusual clinical presentations, such as bone or visceral... 
ONCOLOGY | CHORDOMA | GENETICS & HEREDITY | IN-SITU HYBRIDIZATION | DEFINES | SALIVARY-GLANDS | MUCOEPIDERMOID CARCINOMA | EXPRESSION | ADENOMAS | POU5F1 | RNA-Binding Proteins - genetics | Salivary Gland Neoplasms - genetics | Soft Tissue Neoplasms - diagnosis | Humans | Middle Aged | Biomarkers, Tumor | Octamer Transcription Factor-3 - genetics | Young Adult | Molecular Diagnostic Techniques | Oncogene Fusion | Skin Neoplasms - diagnosis | Adult | Bone Neoplasms - genetics | Cytogenetic Analysis | Pre-B-Cell Leukemia Transcription Factor 1 | Child | Soft Tissue Neoplasms - genetics | Calmodulin-Binding Proteins - genetics | Myoepithelioma - diagnosis | Gene Expression | Zinc Fingers | Bone Neoplasms - diagnosis | RNA-Binding Protein FUS - genetics | Immunophenotyping | In Situ Hybridization, Fluorescence | Proto-Oncogene Proteins - genetics | DNA-Binding Proteins - genetics | Myoepithelioma - genetics | Salivary Gland Neoplasms - diagnosis | Oncogene Proteins, Fusion - genetics | Gene Rearrangement | Skin Neoplasms - genetics | Adolescent | Aged | RNA-Binding Protein EWS | Pediatrics | Lung | Benign | Cytology | FUS gene | Salivary gland | Bone tumors | EWSR1 gene | FLI-1 protein | Soft tissues | Clear cells | FUS protein | Fluorescence in situ hybridization | Skin | Children | gene rearrangement | Differentiation | Tumors | Index Medicus
Journal Article
Histopathology, ISSN 0309-0167, 12/2014, Volume 65, Issue 6, pp. 917 - 922
Journal Article
Human Pathology, ISSN 0046-8177, 11/2018, Volume 81, pp. 281 - 290
Mesenchymal round cell tumors are a diverse group of neoplasms defined by primitive, often high-grade cytomorphology. The most common molecular alterations... 
NFATC2 | Ewing sarcoma | Myoepithelial | Soft tissue | Bone | EWSR1 | TRANSLOCATION | READ ALIGNMENT | PATHOLOGY | VARIANT | CHROMOSOME | MYOEPITHELIAL TUMORS | GENERATION | EWSR1 REARRANGEMENT | PAIRED-END | Antigens | Keratin | Sarcoma | Genes | Stem cells | Cancer | Polymerase chain reaction | Chemotherapy | Laboratories | Morphology | Tumors
Journal Article
Journal Article
Human Pathology, ISSN 0046-8177, 01/2019, Volume 83, pp. 204 - 211
Ovarian ependymomas are rare glial neoplasms that typically occur in women on their third to fourth decades of life. They are histologically similar to... 
Ovarian | Next-generation sequencing | NF2 | EWSR1 | Ependymoma | ATRX | CLASSIFICATION | PATHOLOGY | RECEPTORS | TUMORS | Keratin | Chemotherapy | Laboratories | Surgery | Nervous system | Mesentery | Metastasis | Mutation | Tumors
Journal Article