about
Multi-photon excitation microscopyHuman SIR2 deacetylates p53 and antagonizes PML/p53-induced cellular senescence.Mad2 binding to Mad1 and Cdc20, rather than oligomerization, is required for the spindle checkpoint.Sgt1 is required for human kinetochore assemblyPML is required for telomere stability in non-neoplastic human cellsMethyltransferase recruitment and DNA hypermethylation of target promoters by an oncogenic transcription factorThe Mad1/Mad2 complex as a template for Mad2 activation in the spindle assembly checkpointCellular heterogeneity during embryonic stem cell differentiation to epiblast stem cells is revealed by the ShcD/RaLP adaptor proteinMechanisms through which Sos-1 coordinates the activation of Ras and Rac.A repertoire library that allows the selection of synthetic SH2s with altered binding specificities.Photoactivation of pa-GFP in 3D: optical tools for spatial confinement.Live-cell 3D super-resolution imaging in thick biological samples.Effects of the acute myeloid leukemia--associated fusion proteins on nuclear architecture.DNA damage in stem cells activates p21, inhibits p53, and induces symmetric self-renewing divisions.Two-photon activation and excitation properties of PA-GFP in the 720-920-nm regionA computational platform for robotized fluorescence microscopy (I): high-content image-based cell-cycle analysis.Molecular investigation of coexistent chronic myeloid leukaemia and peripheral T-cell lymphoma - a case reportExtracellular vesicle-mediated transfer of CLIC1 protein is a novel mechanism for the regulation of glioblastoma growth.Mode of action of thiocoraline, a natural marine compound with anti-tumour activity.High-resolution cytometry for high-content cell cycle analysis.Confocal microscopy for high-resolution and high-content analysis of the cell cycle.The Combination of the PARP Inhibitor Rucaparib and 5FU Is an Effective Strategy for Treating Acute Leukemias.Light-sheet confined super-resolution using two-photon photoactivation.A computational platform for robotized fluorescence microscopy (II): DNA damage, replication, checkpoint activation, and cell cycle progression by high-content high-resolution multiparameter image-cytometry.Endocytic trafficking of Rac is required for the spatial restriction of signaling in cell migration.Spatial control of pa-GFP photoactivation in living cells.New method to detect histone acetylation levels by flow cytometry.From cells to tissues: fluorescence confocal microscopy in the study of histological samples.Kinetic heterogeneity of an experimental tumour revealed by BrdUrd incorporation and mathematical modelling.Cell cycle perturbations and apoptosis induced by isohomohalichondrin B (IHB), a natural marine compound.Cell cycle effects of gemcitabine.Understanding biological dynamics: following cells and molecules to track functions and mechanisms.Bacteria-induced gap junctions in tumors favor antigen cross-presentation and antitumor immunity.Dose estimate of exposure to radioisotopes in molecular and cellular biology.Retroviral microarray-based platform on nanostructured TiO2 for functional genomics and drug discovery.In vitro FRAP identifies the minimal requirements for Mad2 kinetochore dynamics.The tumor suppressor p53 regulates polarity of self-renewing divisions in mammary stem cells.Assessment of histone acetylation levels in relation to cell cycle phase.Blue-light (488nm)-irradiation-induced photoactivation of the photoactivatable green fluorescent proteinErratum: PML is required for telomere stability in non-neoplastic human cells
P50
Q21245877-C6CAB9AF-530B-4190-AB51-23AD8C712AF3Q24297146-63CCC8AC-2B45-49B4-A69C-21BEC6BBAE7AQ24534571-2284E108-CC98-482E-A440-EC4BE900E5E2Q24537151-D5718E5B-A5B3-4FD4-B29F-26A40561E8A9Q27309962-21288615-6A48-4F4C-98AC-D84B72C6AAAFQ28217975-59FCB33B-7235-4DDB-BDD5-8B74E8BFDE39Q28305958-CFE54BD4-ED31-43BC-94E2-5E5505045C26Q28507649-F685EF26-D456-42DB-A38C-EC3E383F83B7Q30167694-C6249D91-0C9F-480A-9707-8D093C4763C5Q31004980-A226AAC0-5294-41B8-82FA-E8349CCFB1F0Q33326437-AB0F5DA2-A04F-4A7C-A680-E30E3FAEE62CQ34028867-4C856C09-7BE2-41E3-A780-D372E3546A9BQ34137335-34B1051E-A01B-40B3-9047-65885F519256Q34328242-1A99AAA8-02A8-47E2-B09C-2D5BDBBA4859Q34350817-DF882129-4713-4D64-A2BE-3AD1819D4853Q34609567-2155E4DA-9785-48BE-99F5-B0D512AEDDE3Q36123511-4E76DB15-609B-4F6E-AF97-1BBFB4C0DD0CQ36544592-EF98BF54-AF30-491B-9C96-A93BA04C59A5Q36620274-6A740A91-0EDE-496E-BDCF-EBADA14AE501Q38255845-1D91139C-9819-4DCA-AA4A-EEF2CCBD2E8EQ38255846-E0145F23-D46B-4957-BB03-2A6EB155F8B3Q38911196-9B6FABB6-6347-41ED-A9F3-7179F1798735Q39127477-31B62FDA-963D-4E50-9A6F-12E30EFD0E6EQ39184921-93749C56-A519-4BD9-8462-1ADB2F51E979Q39963386-421B20A6-1EE7-47D3-A670-7730D6D5607EQ39995259-A39B0CFA-A2C3-4B23-822D-3A134FE75BFEQ40417508-C94ACAA7-35CE-4766-8B62-325005BAD6C4Q40518345-660A4273-4F04-459B-886D-778122B912BDQ40741078-833C9BC2-9B1D-4723-84BB-9435C57AFD6BQ42130780-D75281B7-5C12-4161-880C-874602D9DD5DQ43658876-C802430A-1841-439D-B7E8-7FA2ABC096E6Q48851417-5A8DCCA4-0543-4F52-8D72-3780130CB7FCQ50047000-C9772BA8-978B-4413-9A8F-B689DD514D8AQ50649370-55A6DA7C-F5F0-445F-9977-0CE9BD127D59Q50698780-746CBE2B-F9D2-40F6-882C-62172965FDE6Q51220895-4C06AB11-6C9D-49D5-91B9-3B6D6FB9DF29Q53370119-A6BB76AC-E285-4F0F-98FF-4687256DB036Q53443166-78F9DAB4-3BF5-4ECD-9143-114D0D7C932AQ57985549-5D2AD250-5820-4AE6-809E-B0B92CAA20BDQ58195821-6A46E0E0-73FA-4684-A497-C372F466316E
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Mario Faretta
@ast
Mario Faretta
@en
Mario Faretta
@es
Mario Faretta
@fr
Mario Faretta
@nl
Mario Faretta
@sl
type
label
Mario Faretta
@ast
Mario Faretta
@en
Mario Faretta
@es
Mario Faretta
@fr
Mario Faretta
@nl
Mario Faretta
@sl
prefLabel
Mario Faretta
@ast
Mario Faretta
@en
Mario Faretta
@es
Mario Faretta
@fr
Mario Faretta
@nl
Mario Faretta
@sl
P1053
H-8946-2012
P106
P21
P31
P3829
P496
0000-0003-1678-5781