About: Bruno Amati

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher (ORCID 0000-0002-2958-1799)

Attributes	Values
rdf:type	Item
description	forskare (sv) 연구원 (ko) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) wetenschapper (nl) дослідник (uk) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) researcher (ORCID 0000-0002-2958-1799) (en)
rdfs:label	Bruno Amati (en) Bruno Amati (nl) Bruno Amati (es) Bruno Amati (it) Bruno Amati (sl) Bruno Amati (ast)
skos:prefLabel	Bruno Amati (en) Bruno Amati (nl) Bruno Amati (es) Bruno Amati (it) Bruno Amati (sl) Bruno Amati (ast)
name	Bruno Amati (en) Bruno Amati (nl) Bruno Amati (es) Bruno Amati (it) Bruno Amati (sl) Bruno Amati (ast)
Scopus author ID	wds:Q43817846-9162087B-0DA9-46CB-A848-620234923B69
EMBO member ID	wds:Q43817846-9EF5222A-8C7D-4AB6-8940-0852F0E8AA03
Scopus author ID	7003826331
EMBO member ID	bruno-amati
given name	wds:Q43817846-ED153D02-16C6-4940-B6DE-6449AAFFB1F7
given name	Bruno
instance of	wds:Q43817846-399EA126-5B01-46AA-8B65-8088F8BD135B
instance of	Homo sapiens
curriculum vitae URL	wds:Q43817846-8a239b45-468e-97b7-3fe0-fcba67470d60
curriculum vitae URL	https://www.research.ieo.it/media/1221/bruno-amati-biosketch.pdf
occupation	wds:Q43817846-61C177B7-0979-49C5-8C1D-226B16E03217
employer	wds:q43817846-d362bb89-44de-7630-f90d-9719906e0bd4
sex or gender	wds:Q43817846-18884AF2-0F6F-4E47-AD45-A445563D3427
educated at	wds:q43817846-018698e1-442b-5a53-c5b2-5408d2052e1c wds:q43817846-3c6fa1e3-4145-08e7-84d7-1491eca35e75
family name	wds:Q43817846-31686DA3-8D6B-4BB5-A7A1-FBBC607F3D2A
official website	wds:Q43817846-F37CCEAE-BA1B-441B-BA46-756BAA5FD862
occupation	researcher
employer	European Institute of Oncology
sex or gender	male
educated at	University of Geneva Institut suisse de recherche expérimentale sur le cancer
family name	Amati
official website	http://www.ieo.it/en/RESEARCH/People/Researchers/Amati-Bruno/
ORCID iD	wds:Q43817846-499F3440-D3F6-416A-86C4-12625D07B9D6
Dimensions author ID	wds:Q43817846-34C0BA7B-F685-4A3D-ACA0-3CC598504F9B
ORCID iD	https://orcid.org/0000-0002-2958-1799
ORCID iD	0000-0002-2958-1799
Dimensions author ID	01331074631.05
SNSF person ID	wds:Q43817846-C967CC4B-908A-412F-A934-DF812B5B68C8
SNSF person ID	53417
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q43817846
is author of	Methylation of histone H3R2 by PRMT6 and H3K4 by an MLL complex are mutually exclusive Recruitment of TRRAP required for oncogenic transformation by E1A. SUMOylation of Myc-family proteins Myc-binding-site recognition in the human genome is determined by chromatin context Integrating Myc and TGF-beta signalling in cell-cycle control Myc degradation: dancing with ubiquitin ligases. MYC recruits the TIP60 histone acetyltransferase complex to chromatin Nucleophosmin and its AML-associated mutant regulate c-Myc turnover through Fbw7 gamma Werner syndrome protein limits MYC-induced cellular senescence Tip60 in DNA damage response and growth control: many tricks in one HAT. Deacetylase activity is required for recruitment of the basal transcription machinery and transactivation by STAT5. Tip60 is a haplo-insufficient tumour suppressor required for an oncogene-induced DNA damage response Genomic targets of the human c-Myc protein Binding of c-Myc to chromatin mediates mitogen-induced acetylation of histone H4 and gene activation. Symmetric dimethylation of H3R2 is a newly identified histone mark that supports euchromatin maintenance Oncogenic activity of the c-Myc protein requires dimerization with Max. Analysis of Myc-induced histone modifications on target chromatin Immortalization of human neural stem cells with the c-myc mutant T58A. Myc-Max-Mad: a transcription factor network controlling cell cycle progression, differentiation and death Exploiting oncogene-induced replicative stress for the selective killing of Myc-driven tumors Two sides of the Myc-induced DNA damage response: from tumor suppression to tumor maintenance A positive role for Myc in TGFbeta-induced Snail transcription and epithelial-to-mesenchymal transition Genome recognition by MYC. MYC regulates the core pre-mRNA splicing machinery as an essential step in lymphomagenesis Pin1 is required for sustained B cell proliferation upon oncogenic activation of Myc MYC degradation: deubiquitinating enzymes enter the dance Epigenome microarray platform for proteome-wide dissection of chromatin-signaling networks Myc represses transcription through recruitment of DNA methyltransferase corepressor Function of the c-Myc oncoprotein in chromatin remodeling and transcription. Cyclin E and c-Myc promote cell proliferation in the presence of p16INK4a and of hypophosphorylated retinoblastoma family proteins. Chromosomal ARS and CEN elements bind specifically to the yeast nuclear scaffold Cdk2 suppresses cellular senescence induced by the c-myc oncogene. Impairment of cytoplasmic eIF6 activity restricts lymphomagenesis and tumor progression without affecting normal growth Distinct DNA binding preferences for the c-Myc/Max and Max/Max dimers. Chromatin association and regulation of rDNA transcription by the Ras-family protein RasL11a Selective transcriptional regulation by Myc: Experimental design and computational analysis of high-throughput sequencing data methylPipe and compEpiTools: a suite of R packages for the integrative analysis of epigenomics data

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