Accurate lineage reconstruction of mammalian pre-implantation development is essential for inferring the earliest cell fate decisions. Lineage tracing using global fluorescence labeling techniques is complicated by increasing cell density and rapid embryo rotation, which hampers automatic alignment and accurate cell tracking of obtained four-dimensional imaging data sets. Here, we exploit the advantageous properties of primed convertible fluorescent proteins (pr-pcFPs) to simultaneously visualize the global green and the photoconverted red population in order to minimize tracking uncertainties over prolonged time windows. Confined primed conversion of H2B-pr-mEosFP-labeled nuclei combined with light-sheet imaging greatly facilitates segment...
The extraction of fluorescence time course data is a major bottleneck in high-throughput live-cell m...
Green Fluorescent Protein (GFP) has rapidly been established as a versatile and powerful cell marker...
Human and mouse embryonic stem cells (ESCs) differ in terms of their pluripotency status, i.e., naiv...
AbstractThe first lineage segregation in the pre-implantation mouse embryo gives rise to cells of th...
Summary: Determining how signaling dynamics relate to gene expression and cell fate is essential to ...
The comprehensive reconstruction of cell lineages in complex multicellular organisms is a central go...
Advances in optical imaging modalities and the continued evolution of genetically-encoded fluorescen...
Single/selective-plane illumination, or light-sheet, systems offer several advantages over other flu...
Abstract We present a method for automated nucleus identification and tracking in time-lapse microsc...
We present a method to automatically identify and track nuclei in time-lapse microscopy recordings o...
Development of quantitative, safe and rapid techniques for assessing embryo quality provides signifi...
Ontogeny describes the emergence of complex multicellular organisms from single totipotent cells. Th...
The extraction of fluorescence time course data is a major bottleneck in high-throughput live-cell m...
Ontogeny describes the emergence of complex multicellular organisms from single totipotent cells. Th...
Understanding the development of complex multicellular organisms as a function of the underlying cel...
The extraction of fluorescence time course data is a major bottleneck in high-throughput live-cell m...
Green Fluorescent Protein (GFP) has rapidly been established as a versatile and powerful cell marker...
Human and mouse embryonic stem cells (ESCs) differ in terms of their pluripotency status, i.e., naiv...
AbstractThe first lineage segregation in the pre-implantation mouse embryo gives rise to cells of th...
Summary: Determining how signaling dynamics relate to gene expression and cell fate is essential to ...
The comprehensive reconstruction of cell lineages in complex multicellular organisms is a central go...
Advances in optical imaging modalities and the continued evolution of genetically-encoded fluorescen...
Single/selective-plane illumination, or light-sheet, systems offer several advantages over other flu...
Abstract We present a method for automated nucleus identification and tracking in time-lapse microsc...
We present a method to automatically identify and track nuclei in time-lapse microscopy recordings o...
Development of quantitative, safe and rapid techniques for assessing embryo quality provides signifi...
Ontogeny describes the emergence of complex multicellular organisms from single totipotent cells. Th...
The extraction of fluorescence time course data is a major bottleneck in high-throughput live-cell m...
Ontogeny describes the emergence of complex multicellular organisms from single totipotent cells. Th...
Understanding the development of complex multicellular organisms as a function of the underlying cel...
The extraction of fluorescence time course data is a major bottleneck in high-throughput live-cell m...
Green Fluorescent Protein (GFP) has rapidly been established as a versatile and powerful cell marker...
Human and mouse embryonic stem cells (ESCs) differ in terms of their pluripotency status, i.e., naiv...