PESCE, LUCA
 Distribuzione geografica
Continente #
EU - Europa 1.323
Totale 1.323
Nazione #
IT - Italia 1.323
Totale 1.323
Città #
Genova 907
Rapallo 235
Genoa 176
Bordighera 5
Totale 1.323
Nome #
The nucleus under the microscope. A biophysical approach. 169
Apomyoglobin is an efficient carrier for zinc phthalocyanine in photodynamic therapy of tumors 91
A Liquid Tunable Microscope as a New Paradigm in Optical Microscopy to Paint 4D Chromatin Organisation in the Cell Nucleus 90
Combining Expansion Microscopy and STED Nanoscopy for the Study of Cellular Organization 88
Circular intensity differential scattering (CIDS) scanning microscopy to image chromatin-DNA nuclear organization 87
SPLIT-STED Imaging of Nuclear Structures 84
Expansion Microscopy: A Tool to Investigate Hutchinson-Gilford Progeria Syndrome at Molecular Level 82
Monitoring cell substrate interactions in exopolysaccharide-based films reinforced with chitin whiskers and starch nanoparticles used as cell substrates 79
Study of Tumor Cellular Damage Induced by Photosensitizing Molecules 76
LIQUITOPY®: A Liquid Tunable Microscope to Study Chromatin Organization in the Cell Nucleus 74
Measuring expansion from macro- to nanoscale using NPC as intrinsic reporter 68
A robust and versatile platform for image scanning microscopy enabling super-resolution FLIM 68
The Nucluear Pore Complex as Intrinsic Reporter for Isotropic Expansion Microscopy 64
Hypericin-Apomyoglobin: An Enhanced Photosensitizer Complex for the Treatment of Tumor Cells 62
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. 62
[Laparoscopic cholecystocholangiography in the differential diagnosis of jaundice] 44
Fluorescence microscopy 43
Expansion microscopy 22
Totale 1.353
Categoria #
all - tutte 4.927
article - articoli 3.323
book - libri 0
conference - conferenze 810
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 415
Totale 9.475


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201970 0 0 0 0 0 0 0 0 0 19 30 21
2019/2020495 19 26 20 37 42 60 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
2023/2024131 8 22 2 27 12 18 16 11 6 9 0 0
Totale 1.353