LANZANO', LUCA
 Distribuzione geografica
Continente #
EU - Europa 1.843
Totale 1.843
Nazione #
IT - Italia 1.843
Totale 1.843
Città #
Genova 1.141
Rapallo 251
Genoa 230
Vado Ligure 220
Bordighera 1
Totale 1.843
Nome #
Advances in Gated CW STED Microscopy: Toward a Versatile Implementation 115
3 Color - 3 Dimensional STED Nanoscopy 101
Background-Free Super-Resolution Microscopy of Subcellular Structures by Lifetime Tuning and Photons Separation 100
Combining Expansion Microscopy and STED Nanoscopy for the Study of Cellular Organization 96
Measurement of nanoscale three-dimensional diffusion in the interior of living cells by STED-FCS 94
Comprehensive correlation analysis for super-resolution dynamic fingerprinting of cellular compartments using the Zeiss Airyscan detector 92
Chromatin Nanoscale Organization Investigated by FLIM-FRET and STED Superresolution Microscopy 90
A Novel Viewpoint to Analyze Structured Illumination Microscopy (Sim) Data 90
Chromatin Alterations in a Model of Oncogene Activation Studied by Advanced Fluorescence Microscopy 89
LIQUITOPY®: A Liquid Tunable Microscope to Study Chromatin Organization in the Cell Nucleus 87
Improving multiphoton STED nanoscopy with separation of photons by LIfetime Tuning (SPLIT) 86
Three-dimensional multiple-particle tracking with nanometric precision over tunable axial ranges 84
A robust and versatile platform for image scanning microscopy enabling super-resolution FLIM 82
Intensity Sorted Fluorescence Correlation Spectroscopy: A Novel Method to Probe Nuclear Dynamics and Chromatin Organization in Living Cells 79
Measuring expansion from macro- to nanoscale using NPC as intrinsic reporter 78
Measuring Mobility in Chromatin by Intensity-Sorted FCS 77
Airyscan Cca Provides Structural and Dynamics Fingerprinting of Subcellular Compartments in Living Cells 76
Photon-separation to enhance the spatial resolution of pulsed STED microscopy 76
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. 73
The Nucluear Pore Complex as Intrinsic Reporter for Isotropic Expansion Microscopy 73
The SPLIT approach for enhancing the spatial resolution in pulsed STED microscopy with FastFLIM and phasor plots 68
STED microscopy: Exploring fluorescence lifetime gradients for super-resolution at reduced illumination intensities 59
Totale 1.865
Categoria #
all - tutte 7.602
article - articoli 3.590
book - libri 0
conference - conferenze 3.753
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 259
Totale 15.204


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020495 0 0 0 0 0 89 119 63 56 96 58 14
2020/2021148 15 17 10 18 4 5 10 17 10 19 12 11
2021/2022268 22 2 6 42 2 40 7 53 39 25 3 27
2022/2023305 33 37 10 30 30 33 0 23 65 1 40 3
2023/2024164 6 21 1 26 13 32 8 6 11 13 12 15
2024/2025233 11 33 24 30 78 57 0 0 0 0 0 0
Totale 1.865