About: Spectrum of hSNF5/INI1 somatic mutations in human cancer and genotype-phenotype correlations

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About: Spectrum of hSNF5/INI1 somatic mutations in human cancer and genotype-phenotype correlations Goto Sponge NotDistinct Permalink

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scientific article published on 01 December 1999

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 1999 (uk) article scientifique publié en 1999 (fr) im Dezember 1999 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'avientu de 1999 (ast) scientific article published on 01 December 1999 (en)
publication date	wds:Q55670910-9B8C338D-B307-48C5-BEB8-504FFBB8649F
publication date	1999-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q55670910-7A492C8C-867A-481F-B1BE-9C3DDC898B9F
language of work or name	English
cites work	wds:Q55670910-0BDD89CB-B775-4AEC-9093-9C1F48651E99
cites work	Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer
author name string	wds:Q55670910-0E59212D-57AD-4657-80B9-69820CE5D743 wds:Q55670910-3F381CA9-4FDC-4691-9452-60F183B92FAF wds:Q55670910-5444E717-A60C-4ECF-94FA-7995075B93DD wds:Q55670910-6E9241E1-48D5-423F-B7CF-DAB644D7C71A wds:Q55670910-900399EA-988C-4EBD-9717-279F902CE117 wds:Q55670910-DE5C90BC-AA90-4DA7-8C05-EEAA9116F71E wds:Q55670910-FA936B60-F4FB-464E-A697-9BD542CCDBC4
author name string	D Birnbaum M Gessler N Sévenet K Hoang-Xuan A Jouvet A Lellouch-Tubiana D Schofield
rdfs:label	Spectrum of hSNF5/INI1 somatic mutations in human cancer and genotype-phenotype correlations (en) Spectrum of hSNF5/INI1 somatic mutations in human cancer and genotype-phenotype correlations (nl)
skos:prefLabel	Spectrum of hSNF5/INI1 somatic mutations in human cancer and genotype-phenotype correlations (en) Spectrum of hSNF5/INI1 somatic mutations in human cancer and genotype-phenotype correlations (nl)
name	Spectrum of hSNF5/INI1 somatic mutations in human cancer and genotype-phenotype correlations (en) Spectrum of hSNF5/INI1 somatic mutations in human cancer and genotype-phenotype correlations (nl)
author	wds:Q55670910-37710B20-0CC3-4A61-A070-DA43B14F4A8F wds:Q55670910-453220E9-EDE6-48D8-B3C7-D8FCEAD7C784
author	Cécile Jeanpierre Olivier Delattre
title	wds:Q55670910-F023F2E4-881A-4BA3-BC68-7E84757C7F3F
title	Spectrum of hSNF5/INI1 somatic mutations in human cancer and genotype-phenotype correlations (en)
page(s)	wds:Q55670910-5AB2DD09-1EE8-407D-B724-C71A0A611B6B
page(s)	2359-2368
instance of	wds:Q55670910-5D5DFA57-AF38-40C3-8F6C-B37F8786B216
instance of	scholarly article
main subject	wds:Q55670910-6A91EFE2-4DD0-46DE-942A-CDAB135A4EE3
main subject	phenotype
PubMed ID	wds:Q55670910-71C41C1E-055A-4DB8-ACDE-39C368912DA2
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10556283
PubMed ID	10556283
published in	wds:Q55670910-544D4FE7-ACC2-426E-9E10-D4EF4E199452
published in	Human Molecular Genetics
issue	wds:Q55670910-83E1531A-9E48-4CD9-9501-FA374D95676C
volume	wds:Q55670910-475FA4D3-44E6-434F-A459-523292CF60CD
issue	13
volume	8
DOI	wds:Q55670910-829ED91E-7BF3-4990-BB65-E38F89CF8467
DOI	http://dx.doi.org/10.1093/HMG/8.13.2359
DOI	10.1093/HMG/8.13.2359
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q55670910
is cites work of	Microarray analysis of pediatric ependymoma identifies a cluster of 112 candidate genes including four transcripts at 22q12.1-q13.3 Comparative genomic hybridization detects specific cytogenetic abnormalities in pediatric ependymomas and choroid plexus papillomas. Microarray analysis of pediatric ependymoma identifies a cluster of 112 candidate genes including four transcripts at 22q12.1-q13.3 Fine-needle aspiration of renal and extrarenal rhabdoid tumors: the experience of the Institut Curie regarding 20 tumors in 13 patients. Transcription activator interactions with multiple SWI/SNF subunits. Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors Lineage dependency and lineage-survival oncogenes in human cancer Proline oxidase functions as a mitochondrial tumor suppressor in human cancers Molecular analysis of the rhabdoid predisposition syndrome in a child: a novel germline hSNF5/INI1 mutation and absence of c-myc amplification Interferon-gamma-induced chromatin remodeling at the CIITA locus is BRG1 dependent When the SWI/SNF complex remodels...the cell cycle Nuclear transport and cancer: from mechanism to intervention A key role of the hSNF5/INI1 tumour suppressor in the control of the G1-S transition of the cell cycle Constitutional mutations of the hSNF5/INI1 gene predispose to a variety of cancers Cell cycle arrest and repression of cyclin D1 transcription by INI1/hSNF5. Disruption of Ini1 leads to peri-implantation lethality and tumorigenesis in mice The SWI/SNF complex and cancer Proline oxidase, a p53-induced gene, targets COX-2/PGE2 signaling to induce apoptosis and inhibit tumor growth in colorectal cancers. Aberrations of the hSNF5/INI1 gene are restricted to malignant rhabdoid tumors or atypical teratoid/rhabdoid tumors in pediatric solid tumors Complex chromosome 22 rearrangements in astrocytic tumors identified using microsatellite and chromosome 22 tile path array analysis Denaturing high-performance liquid chromatography: A review The SWI/SNF complex--chromatin and cancer. Chromatin remodeling enzymes: who's on first? Molecular pathogenesis of childhood brain tumors Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia. Genetic and epigenetic screening for gene alterations of the chromatin-remodeling factor, SMARCA4/BRG1, in lung tumors. The murine SNF5/INI1 chromatin remodeling factor is essential for embryonic development and tumor suppression Hijacking the chromatin remodeling machinery: impact of SWI/SNF perturbations in cancer Case report: long-term survival of an infant syndromic patient affected by atypical teratoid-rhabdoid tumor Clinicopathologic comparison of familial versus sporadic atypical teratoid/rhabdoid tumors (AT/RT) of the central nervous system Diverse roles and interactions of the SWI/SNF chromatin remodeling complex revealed using global approaches Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome Linking the epigenetic 'language' of covalent histone modifications to cancer The chromatin remodelling component SMARCB1/INI1 influences the metastatic behavior of colorectal cancer through a gene signature mapping to chromosome 22. BRG1 controls the activity of the retinoblastoma protein via regulation of p21CIP1/WAF1/SDI. Function of the c-Myc oncoprotein in chromatin remodeling and transcription. Real-time quantitative PCR analysis of pediatric ependymomas identifies novel candidate genes including TPR at 1q25 and CHIBBY at 22q12-q13. The role of SMARCB1/INI1 in development of rhabdoid tumor. Novel role for insulin as an autocrine growth factor for malignant brain tumour cells SNR1 is an essential subunit in a subset of Drosophila brm complexes, targeting specific functions during development. Imprinted CDKN1C is a tumor suppressor in rhabdoid tumor and activated by restoration of SMARCB1 and histone deacetylase inhibitors Loss of the INI1 tumor suppressor does not impair the expression of multiple BRG1-dependent genes or the assembly of SWI/SNF enzymes

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