Mitosis is a highly dynamic and choreographed process in which chromosomes are captured by the mitotic spindle and physically segregated into the two daughter cells to ensure faithful transmission of the genetic material. Live-cell fluorescence microscopy enables these dynamics to be analyzed over diverse temporal scales. Here we present the methodologies to study chromosome segregation at three timescales: we first show how automated tracking of kinetochores enables investigation of mitotic spindle and chromosome dynamics in the seconds-to-minutes timescale; next we highlight how new DNA live dyes allow the study of chromosome segregation over a period of several hours in any cell line; finally, we demonstrate how image sequences acquired ...
Although the dynamic behaviour of chromosomes has been extensively studied in their condensed state ...
Recent studies have suggested that chromosomes are hierarchically organized into topologically assoc...
The extraction of fluorescence time course data is a major bottleneck in high-throughput live-cell m...
Individual chromosomes are not directly visible within the interphase nuclei of most somatic cells; ...
Individual chromosomes are not directly visible within the interphase nuclei of most somatic cells; ...
Recombination in first meiotic prophase is initiated by endogenous breaks in double-stranded DNA (DS...
AbstractWe investigated positioning of chromosomes during the cell cycle in live mammalian cells wit...
In the field of cell biology, there is an increasing use of time-lapse data to understand cellular f...
Asymmetric cell division is an important mechanism for generating cellular diversity, however, techn...
Automated visual-tracking systems of stem cell populations in vitro allow for high-throughput analys...
doi:10.3791/1878 (2010). Changes in cellular organization and chromosome dynamics that occur during ...
Despite the distinctive structure of mitotic chromosomes, it has not been possible to visualise indi...
AbstractHow chromosomes are folded and how this folding relates to function remain fundamental quest...
In this paper we propose a workflow to detect and track mitotic cells in time-lapse microscopy image...
<p>Lineage specification of both mouse and human pluripotent stem cells (PSCs) is accompanied by spa...
Although the dynamic behaviour of chromosomes has been extensively studied in their condensed state ...
Recent studies have suggested that chromosomes are hierarchically organized into topologically assoc...
The extraction of fluorescence time course data is a major bottleneck in high-throughput live-cell m...
Individual chromosomes are not directly visible within the interphase nuclei of most somatic cells; ...
Individual chromosomes are not directly visible within the interphase nuclei of most somatic cells; ...
Recombination in first meiotic prophase is initiated by endogenous breaks in double-stranded DNA (DS...
AbstractWe investigated positioning of chromosomes during the cell cycle in live mammalian cells wit...
In the field of cell biology, there is an increasing use of time-lapse data to understand cellular f...
Asymmetric cell division is an important mechanism for generating cellular diversity, however, techn...
Automated visual-tracking systems of stem cell populations in vitro allow for high-throughput analys...
doi:10.3791/1878 (2010). Changes in cellular organization and chromosome dynamics that occur during ...
Despite the distinctive structure of mitotic chromosomes, it has not been possible to visualise indi...
AbstractHow chromosomes are folded and how this folding relates to function remain fundamental quest...
In this paper we propose a workflow to detect and track mitotic cells in time-lapse microscopy image...
<p>Lineage specification of both mouse and human pluripotent stem cells (PSCs) is accompanied by spa...
Although the dynamic behaviour of chromosomes has been extensively studied in their condensed state ...
Recent studies have suggested that chromosomes are hierarchically organized into topologically assoc...
The extraction of fluorescence time course data is a major bottleneck in high-throughput live-cell m...