<p>Observation of the same microscopy field by phase contrast (left), autofluorescence (middle) and DAPI staining (right). The same section of each panel is enlarged. The arrows in the enlarged sections point to a doublet of cells, still partially attached and deriving from the same mother cell, in which only one cell (grey arrows) is autofluorescent.</p
Segmentation of transparent cells in brightfield microscopy images could facilitate the quantitative...
Label-free quantitative measurement of morphological features of cells (e.g., size of nucleus, thick...
<p>a–b: Cell morphology on a glass slide (glass). c–d: Cell morphology in a flat silicon region (S)....
<p>Microscopy analysis of SF214 and of its unpigmented mutant (SF214-Mut). For each strain the same ...
<p>Microscopy analysis of cells from different fields observed by phase contrast, DAPI-staining, imm...
<p>Microscopy fields of SF214 cells grown at different conditions and observed by phase contrast and...
<p>The same microscopy field observed by phase contrast (left), autofluorescence (middle). The right...
Using the decomposition of an image field in two spatial components that can be controllably shifted...
Fluorescence microscopy is the standard tool for detection and analysis of cellular phenomena. This ...
<p>The fluorescence analysis was performed to compare the presence of peroxisomes (red) between (A, ...
(A) Optical phase contrast image of cells double-stained with anti-integrin β1 and anti-F-actin anti...
<p>(<b>A–C</b>) Morphological parameters, here major/minor axis and cell area are calculated using o...
<p>A) upper panel overlay of bright field and fluorescence, lower panel fluorrscence, B) left upper ...
<p>(<b>A</b>) Cell diameter (Ø) distribution histogram with a representative bright field image. (<b...
Fluorescence microscopy is the standard tool for detection and analysis of cellular phenomena. This ...
Segmentation of transparent cells in brightfield microscopy images could facilitate the quantitative...
Label-free quantitative measurement of morphological features of cells (e.g., size of nucleus, thick...
<p>a–b: Cell morphology on a glass slide (glass). c–d: Cell morphology in a flat silicon region (S)....
<p>Microscopy analysis of SF214 and of its unpigmented mutant (SF214-Mut). For each strain the same ...
<p>Microscopy analysis of cells from different fields observed by phase contrast, DAPI-staining, imm...
<p>Microscopy fields of SF214 cells grown at different conditions and observed by phase contrast and...
<p>The same microscopy field observed by phase contrast (left), autofluorescence (middle). The right...
Using the decomposition of an image field in two spatial components that can be controllably shifted...
Fluorescence microscopy is the standard tool for detection and analysis of cellular phenomena. This ...
<p>The fluorescence analysis was performed to compare the presence of peroxisomes (red) between (A, ...
(A) Optical phase contrast image of cells double-stained with anti-integrin β1 and anti-F-actin anti...
<p>(<b>A–C</b>) Morphological parameters, here major/minor axis and cell area are calculated using o...
<p>A) upper panel overlay of bright field and fluorescence, lower panel fluorrscence, B) left upper ...
<p>(<b>A</b>) Cell diameter (Ø) distribution histogram with a representative bright field image. (<b...
Fluorescence microscopy is the standard tool for detection and analysis of cellular phenomena. This ...
Segmentation of transparent cells in brightfield microscopy images could facilitate the quantitative...
Label-free quantitative measurement of morphological features of cells (e.g., size of nucleus, thick...
<p>a–b: Cell morphology on a glass slide (glass). c–d: Cell morphology in a flat silicon region (S)....