IRIS
PESCE, LUCA
 Distribuzione geografica
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Continente #
EU - Europa 1.560
Totale 1.560
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Nazione #
IT - Italia 1.560
Totale 1.560
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Città #
Genova 907
Rapallo 235
Genoa 226
Vado Ligure 187
Bordighera 5
Totale 1.560
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Nome #
The nucleus under the microscope. A biophysical approach. 223
A Liquid Tunable Microscope as a New Paradigm in Optical Microscopy to Paint 4D Chromatin Organisation in the Cell Nucleus 104
Apomyoglobin is an efficient carrier for zinc phthalocyanine in photodynamic therapy of tumors 101
SPLIT-STED Imaging of Nuclear Structures 98
Circular intensity differential scattering (CIDS) scanning microscopy to image chromatin-DNA nuclear organization 97
Combining Expansion Microscopy and STED Nanoscopy for the Study of Cellular Organization 96
Expansion Microscopy: A Tool to Investigate Hutchinson-Gilford Progeria Syndrome at Molecular Level 92
Monitoring cell substrate interactions in exopolysaccharide-based films reinforced with chitin whiskers and starch nanoparticles used as cell substrates 88
LIQUITOPY®: A Liquid Tunable Microscope to Study Chromatin Organization in the Cell Nucleus 87
Study of Tumor Cellular Damage Induced by Photosensitizing Molecules 84
A robust and versatile platform for image scanning microscopy enabling super-resolution FLIM 82
Measuring expansion from macro- to nanoscale using NPC as intrinsic reporter 78
Imaging of nuclear structures within intact eukaryotic nuclei is imperative to understand the effect of chromatin folding on genome function. Recent developments of super-resolution fluorescence microscopy techniques combine high specificity, sensitivity, and less-invasive sample preparation procedures with the sub-diffraction spatial resolution required to image chromatin at the nanoscale. Here, we present a method to enhance the spatial resolution of a stimulated-emission depletion (STED) microscope based only on the modulation of the STED intensity during the acquisition of a STED image. This modulation induces spatially encoded variations of the fluorescence emission that can be visualized in the phasor plot and used to improve and quantify the effective spatial resolution of the STED image. We show that the method can be used to remove direct excitation by the STED beam and perform dual color imaging. We apply this method to the visualization of transcription and replication foci within intact nuclei of eukaryotic cells. 74
The Nucluear Pore Complex as Intrinsic Reporter for Isotropic Expansion Microscopy 73
Hypericin-Apomyoglobin: An Enhanced Photosensitizer Complex for the Treatment of Tumor Cells 72
[Laparoscopic cholecystocholangiography in the differential diagnosis of jaundice] 58
Fluorescence microscopy 51
Expansion microscopy 32
Totale 1.590
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Categoria #
all - tutte 6.519
article - articoli 4.345
book - libri 0
conference - conferenze 1.066
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 576
Totale 12.506
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020291 0 0 0 0 0 0 84 44 40 70 42 11
2020/2021142 10 11 17 16 6 5 14 14 9 15 14 11
2021/2022200 11 4 3 21 6 32 6 40 29 24 3 21
2022/2023284 25 23 4 24 29 41 1 18 61 6 48 4
2023/2024160 8 22 2 27 12 18 16 11 6 14 14 10
2024/2025208 24 29 31 27 54 40 3 0 0 0 0 0
Totale 1.590