Genomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive analysis of INI1/SMARCB1 in malignant rhabdoid tumors
about
ARID2: a new tumor suppressor gene in hepatocellular carcinomaCancer epigenetics drug discovery and development: the challenge of hitting the markSynovial sarcoma: recent discoveries as a roadmap to new avenues for therapySecondary EWSR1 gene abnormalities in SMARCB1-deficient tumors with 22q11-12 regional deletions: Potential pitfalls in interpreting EWSR1 FISH resultsGermline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome.Integrated (epi)-Genomic Analyses Identify Subgroup-Specific Therapeutic Targets in CNS Rhabdoid TumorsTemporal lobe pleomorphic xanthoastrocytoma and acquired BRAF mutation in an adolescent with the constitutional 22q11.2 deletion syndrome.Consistent SMARCB1 homozygous deletions in epithelioid sarcoma and in a subset of myoepithelial carcinomas can be reliably detected by FISH in archival material.Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors.Fibroblast growth factor receptors as novel therapeutic targets in SNF5-deleted malignant rhabdoid tumorsGenome-wide approach to identify second gene targets for malignant rhabdoid tumors using high-density oligonucleotide microarrays.p16INK4A and p14ARF tumor suppressor pathways are deregulated in malignant rhabdoid tumors.Clinicopathologic comparison of familial versus sporadic atypical teratoid/rhabdoid tumors (AT/RT) of the central nervous systemDisrupting 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.Epithelioid malignant peripheral nerve sheath tumor arising in a schwannoma, in a patient with "neuroblastoma-like" schwannomatosis and a novel germline SMARCB1 mutationIntegrated genomics has identified a new AT/RT-like yet INI1-positive brain tumor subtype among primary pediatric embryonal tumors.Alisertib is active as single agent in recurrent atypical teratoid rhabdoid tumors in 4 children.Molecularly confirmed primary malignant rhabdoid tumor of the urinary bladder: implications of accurate diagnosis.Oncolytic measles virus efficacy in murine xenograft models of atypical teratoid rhabdoid tumorsThe chromatin-modifying protein HMGA2 promotes atypical teratoid/rhabdoid cell tumorigenicityAbsence of oncogenic canonical pathway mutations in aggressive pediatric rhabdoid tumors.Epithelioid sarcoma is associated with a high percentage of SMARCB1 deletions.Whole Exome- and mRNA-Sequencing of an AT/RT Case Reveals Few Somatic Mutations and Several Deregulated Signalling Pathways in the Context of SMARCB1 Deficiency.Genetics of Bladder Malignant Tumors in ChildhoodMarkers of survival and metastatic potential in childhood CNS primitive neuro-ectodermal brain tumours: an integrative genomic analysis.Targeting EZH2-mediated methylation of H3K27 inhibits proliferation and migration of Synovial Sarcoma in vitroAtypical teratoid/rhabdoid tumors-current concepts, advances in biology, and potential future therapies.MYC interaction with the tumor suppressive SWI/SNF complex member INI1 regulates transcription and cellular transformation.BAF180 regulates cellular senescence and hematopoietic stem cell homeostasis through p21Proximal-type Epithelioid Sarcoma of the Head and Neck (HN): A Study with Immunohistochemical and Molecular Analysis of SMARCB1.Genome-Wide Profiles of Extra-cranial Malignant Rhabdoid Tumors Reveal Heterogeneity and Dysregulated Developmental Pathways.The role of SMARCB1/INI1 in development of rhabdoid tumor.Implementation of next generation sequencing into pediatric hematology-oncology practice: moving beyond actionable alterations.Genetic variant in SWI/SNF complexes influences hepatocellular carcinoma risk: a new clue for the contribution of chromatin remodeling in carcinogenesis.The molecular pathogenesis of schwannomatosis, a paradigm for the co-involvement of multiple tumour suppressor genes in tumorigenesis.Molecular diagnostics of CNS embryonal tumors.A complex karyotype in an atypical teratoid/rhabdoid tumor: case report and review of the literature.Diverse functions of ATP-dependent chromatin remodeling complexes in development and cancer.Loss of INI1 protein expression defines a subgroup of aggressive central nervous system primitive neuroectodermal tumors.
P2860
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P2860
Genomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive analysis of INI1/SMARCB1 in malignant rhabdoid tumors
description
2009 nî lūn-bûn
@nan
2009 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի մարտին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Genomic analysis using high-de ...... 1 in malignant rhabdoid tumors
@ast
Genomic analysis using high-de ...... 1 in malignant rhabdoid tumors
@en
Genomic analysis using high-de ...... 1 in malignant rhabdoid tumors
@nl
type
label
Genomic analysis using high-de ...... 1 in malignant rhabdoid tumors
@ast
Genomic analysis using high-de ...... 1 in malignant rhabdoid tumors
@en
Genomic analysis using high-de ...... 1 in malignant rhabdoid tumors
@nl
prefLabel
Genomic analysis using high-de ...... 1 in malignant rhabdoid tumors
@ast
Genomic analysis using high-de ...... 1 in malignant rhabdoid tumors
@en
Genomic analysis using high-de ...... 1 in malignant rhabdoid tumors
@nl
P2093
P2860
P3181
P1476
Genomic analysis using high-de ...... 1 in malignant rhabdoid tumors
@en
P2093
Alexander R Judkins
Angela J Sievert
Eric M Jackson
Hongbo Xie
Jaclyn A Biegel
Juan Carlos Perin
Laura Tooke
Tamim H Shaikh
Xiaowu Gai
P2860
P304
P3181
P356
10.1158/1078-0432.CCR-08-2091
P407
P577
2009-03-15T00:00:00Z