Time-lapse optical microscopy datasets from living cells can potentially afford an enormous amount of quantitative information on the relevant structural and dynamic properties of sub-cellular organelles/ structures, provided that both the spatial and temporal dimensions are properly sampled during the experiment. Here we provide exemplary live-cell, time-lapse confocal imaging datasets corresponding to three sub-cellular structures of the endo-lysosomal pathway, i.e. early endosomes, late endosomes and lysosomes, along with detailed guidelines to produce analogous experiments. Validation of the datasets is conducted by means of established analytical tools to extract the structural and dynamic properties at the sub-cellular scale, such as ...
oralInternational audienceWe report a method for combining confocal microscopy with single-cell mech...
Background: The dynamic growing and shortening behaviors of microtubules are central to the fundamen...
We investigated lysosome dynamics during neuronal stem cell (NSC) differentiation by two quantitativ...
Time-lapse optical microscopy datasets from living cells can potentially afford an enormous amount o...
Here we provide demonstration that image mean square displacement (iMSD) analysis is a fast and robu...
International audienceMotivation: Motility is a fundamental cellular attribute, which plays a major ...
This is the author accepted manuscript. The final version is available from the American Association...
In this thesis, we have applied time resolved confocal microscopy to five different processes, - int...
Imaging is a method of choice to investigate the complex spatio-temporal cellular dynamics and the s...
When studying the living endosome one must first recognise that we are not studying a single discret...
<p>(<b>A</b>) Time lapse imaging of a p-body during cell division. A wild type strain expressing Edc...
In the development of multicellular organisms, tissue development and homeostasis require coordinate...
Confocal microscopy offers a mean to extract quantitative data on spatially confined subcellular str...
A biological tissue is an ensemble of soft cells in close physical contact. Events such as cell-shap...
A biological tissue is an ensemble of soft cells in close physical contact. Events such as cell-shap...
oralInternational audienceWe report a method for combining confocal microscopy with single-cell mech...
Background: The dynamic growing and shortening behaviors of microtubules are central to the fundamen...
We investigated lysosome dynamics during neuronal stem cell (NSC) differentiation by two quantitativ...
Time-lapse optical microscopy datasets from living cells can potentially afford an enormous amount o...
Here we provide demonstration that image mean square displacement (iMSD) analysis is a fast and robu...
International audienceMotivation: Motility is a fundamental cellular attribute, which plays a major ...
This is the author accepted manuscript. The final version is available from the American Association...
In this thesis, we have applied time resolved confocal microscopy to five different processes, - int...
Imaging is a method of choice to investigate the complex spatio-temporal cellular dynamics and the s...
When studying the living endosome one must first recognise that we are not studying a single discret...
<p>(<b>A</b>) Time lapse imaging of a p-body during cell division. A wild type strain expressing Edc...
In the development of multicellular organisms, tissue development and homeostasis require coordinate...
Confocal microscopy offers a mean to extract quantitative data on spatially confined subcellular str...
A biological tissue is an ensemble of soft cells in close physical contact. Events such as cell-shap...
A biological tissue is an ensemble of soft cells in close physical contact. Events such as cell-shap...
oralInternational audienceWe report a method for combining confocal microscopy with single-cell mech...
Background: The dynamic growing and shortening behaviors of microtubules are central to the fundamen...
We investigated lysosome dynamics during neuronal stem cell (NSC) differentiation by two quantitativ...