INI1-deficient tumors: diagnostic features and molecular genetics.
about
High expression of CD109 antigen regulates the phenotype of cancer stem-like cells/cancer-initiating cells in the novel epithelioid sarcoma cell line ESX and is related to poor prognosis of soft tissue sarcomaGene of the month: SMARCB1Immunohistochemical Markers of Soft Tissue Tumors: Pathologic Diagnosis, Genetic Contributions, and Therapeutic OptionsNovel uses of immunohistochemistry in the diagnosis and classification of soft tissue tumorsSMARCB1 (INI-1)-deficient Sinonasal Carcinoma: A Series of 39 Cases Expanding the Morphologic and Clinicopathologic Spectrum of a Recently Described Entity.Histopathological, immunohistochemical and molecular spectrum of myoepithelial tumours of soft tissues.Secondary EWSR1 gene abnormalities in SMARCB1-deficient tumors with 22q11-12 regional deletions: Potential pitfalls in interpreting EWSR1 FISH resultsOncogenic roles of SMARCB1/INI1 and its deficient tumorsEmbryonic signature distinguishes pediatric and adult rhabdoid tumors from other SMARCB1-deficient cancers.Primary atypical teratoid/rhabdoid tumor of central nervous system in children: a clinicopathological analysis and review of literature in China.SMARCB1 (INI-1)-deficient carcinomas of the sinonasal tract.SMARCB1(INI1)-deficient sinonasal basaloid carcinoma: a novel member of the expanding family of SMARCB1-deficient neoplasms.Cribriform neuroepithelial tumor in the third ventricle: a case report and literature review.Glomerular sparing pattern in primary kidney neoplasms: clinical, morphological and immunohistochemical study.The chromatin remodelling component SMARCB1/INI1 influences the metastatic behavior of colorectal cancer through a gene signature mapping to chromosome 22.Consistent SMARCB1 homozygous deletions in epithelioid sarcoma and in a subset of myoepithelial carcinomas can be reliably detected by FISH in archival material.SMARCB1 protein and mRNA loss is not caused by promoter and histone hypermethylation in epithelioid sarcoma.Case report: long-term survival of an infant syndromic patient affected by atypical teratoid-rhabdoid tumor.Extremely rare case of vulvar myxoid epithelioid sarcoma.Beware of immunohistochemistry--report of a cytokeratin-, desmin- and INI-1-negative pelvic desmoplastic small round cell tumor in a 51 year old woman.VCL-ALK renal cell carcinoma in children with sickle-cell trait: the eighth sickle-cell nephropathy?Atypical ossifying fibromyxoid tumor unusually located in the mediastinum: report of a case showing mosaic loss of INI-1 expression.Malignant rhabdoid tumor of the floor of mouth: first reported case in the oral cavity of an adult.Rhabdoid Variant of Myoepithelial Carcinoma, with EWSR1 Rearrangement: Expanding the Spectrum of EWSR1-Rearranged Myoepithelial Tumors.A SMARCB1-deficient vulvar neoplasm with prominent myxoid stroma: report of a case showing ERG and FLI1 expression.Absence of oncogenic canonical pathway mutations in aggressive pediatric rhabdoid tumors.Genomic and phenotypic profiles of two Brazilian breast cancer cell lines derived from primary human tumors.Cutaneous syncytial myoepithelioma: clinicopathologic characterization in a series of 38 casesRight-sided rhabdoid colorectal tumors might be related to the serrated pathway.Molecular inversion probe analysis detects novel copy number alterations in Ewing sarcomaClinical Neuropathology practice guide 6-2013: morphology and an appropriate immunohistochemical screening panel aid in the identification of synovial sarcoma by neuropathologistsRhabdoid carcinoma of the rectum.The molecular pathogenesis of schwannomatosis, a paradigm for the co-involvement of multiple tumour suppressor genes in tumorigenesis.Pathology of peripheral nerve sheath tumors: diagnostic overview and update on selected diagnostic problemsThe utility of immunohistochemistry for providing genetic information on tumors.Syndrome-associated soft tissue tumours.Selected topics in the pathology of epithelioid soft tissue tumors.Recently characterized soft tissue tumors that bring biologic insight.Differential microRNA expression profiles between malignant rhabdoid tumor and epithelioid sarcoma: miR193a-5p is suggested to downregulate SMARCB1 mRNA expression.Molecular diagnostics in soft tissue sarcomas and gastrointestinal stromal tumors.
P2860
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P2860
INI1-deficient tumors: diagnostic features and molecular genetics.
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
INI1-deficient tumors: diagnostic features and molecular genetics.
@en
INI1-deficient tumors: diagnostic features and molecular genetics.
@nl
type
label
INI1-deficient tumors: diagnostic features and molecular genetics.
@en
INI1-deficient tumors: diagnostic features and molecular genetics.
@nl
prefLabel
INI1-deficient tumors: diagnostic features and molecular genetics.
@en
INI1-deficient tumors: diagnostic features and molecular genetics.
@nl
P1476
INI1-deficient tumors: diagnostic features and molecular genetics.
@en
P2093
Travis J Hollmann
P304
P356
10.1097/PAS.0B013E31822B325B
P407
P577
2011-10-01T00:00:00Z