The role of SMARCB1/INI1 in development of rhabdoid tumor.
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The Skin as an Early Expression of Malignancies in the Neonatal Age: A Review of the Literature and a Case SeriesChildren's Oncology Group's 2013 blueprint for research: renal tumorsAtypical teratoid/rhabdoid tumors: challenges and search for solutionsOncogenic roles of SMARCB1/INI1 and its deficient tumorsGermline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome.Reexpression of hSNF5 in malignant rhabdoid tumor cell lines causes cell cycle arrest through a p21(CIP1/WAF1)-dependent mechanismChromatin-regulating proteins as targets for cancer therapy.Epigenetic antagonism between polycomb and SWI/SNF complexes during oncogenic transformationThe chromatin remodelling component SMARCB1/INI1 influences the metastatic behavior of colorectal cancer through a gene signature mapping to chromosome 22.SNF5 is an essential executor of epigenetic regulation during differentiation.Congenital anomalies and rhabdoid tumor associated with 22q11 germline deletion and somatic inactivation of the SMARCB1 tumor suppressor.Characterization of DNA binding property of the HIV-1 host factor and tumor suppressor protein Integrase Interactor 1 (INI1/hSNF5).Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors.p16INK4A and p14ARF tumor suppressor pathways are deregulated in malignant rhabdoid tumors.Promiscuous partnerships in Ewing's sarcoma.Disrupting LIN28 in atypical teratoid rhabdoid tumors reveals the importance of the mitogen activated protein kinase pathway as a therapeutic target.A Rare Case of Undifferentiated Carcinoma of the Colon with Rhabdoid Features: A Case Report and Review of the Literature.Identification of a core member of the SWI/SNF complex, BAF155/SMARCC1, as a human tumor suppressor gene.The chromatin remodeling and mRNA splicing functions of the Brahma (SWI/SNF) complex are mediated by the SNR1/SNF5 regulatory subunit.A remarkably simple genome underlies highly malignant pediatric rhabdoid cancersMalignant rhabdoid tumor of the lung in the young adult: a case reportSequencing of local therapy affects the pattern of treatment failure and survival in children with atypical teratoid rhabdoid tumors of the central nervous system.Absence of oncogenic canonical pathway mutations in aggressive pediatric rhabdoid tumors.Establishment and characterization of MRT cell lines from genetically engineered mouse models and the influence of genetic background on their development.Right-sided rhabdoid colorectal tumors might be related to the serrated pathway.LIN28B is highly expressed in atypical teratoid/rhabdoid tumor (AT/RT) and suppressed through the restoration of SMARCB1.Durable tumor regression in genetically altered malignant rhabdoid tumors by inhibition of methyltransferase EZH2.Integrating diverse information to gain more insight into microarray analysis.The molecular pathogenesis of schwannomatosis, a paradigm for the co-involvement of multiple tumour suppressor genes in tumorigenesis.Hijacking the chromatin remodeling machinery: impact of SWI/SNF perturbations in cancer.Molecular diagnostics of CNS embryonal tumors.Rhabdoid tumors of the liver: rare, aggressive, and poorly responsive to standard cytotoxic chemotherapy.Combinatorial assembly and function of chromatin regulatory complexes.Current issues and controversies in the classification of pediatric hepatocellular tumors.Familial rhabdoid tumour 'avant la lettre'--from pathology review to exome sequencing and back again.Selected topics in the pathology of epithelioid soft tissue tumors.High dose alkylator therapy for extracranial malignant rhabdoid tumors in children.Coffin-Siris syndrome and related disorders involving components of the BAF (mSWI/SNF) complex: historical review and recent advances using next generation sequencing.Chromatin remodeler mutations in human cancers: epigenetic implications.High-resolution genomic analysis suggests the absence of recurrent genomic alterations other than SMARCB1 aberrations in atypical teratoid/rhabdoid tumors.
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The role of SMARCB1/INI1 in development of rhabdoid tumor.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 29 March 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
The role of SMARCB1/INI1 in development of rhabdoid tumor.
@en
The role of SMARCB1/INI1 in development of rhabdoid tumor.
@nl
type
label
The role of SMARCB1/INI1 in development of rhabdoid tumor.
@en
The role of SMARCB1/INI1 in development of rhabdoid tumor.
@nl
prefLabel
The role of SMARCB1/INI1 in development of rhabdoid tumor.
@en
The role of SMARCB1/INI1 in development of rhabdoid tumor.
@nl
P2860
P356
P1476
The role of SMARCB1/INI1 in development of rhabdoid tumor
@en
P2093
Jaclyn A Biegel
P2860
P304
P356
10.4161/CBT.8.5.8019
P577
2009-03-29T00:00:00Z