<p>(<b>A</b>) Naive branching geometry. The epithelium (black) is undergoing branching. <i>Fgf10</i> expression is restricted to the sub-mesothelial mesenchyme. In the model, only the most distal cells are source of FGF10 (blue). (<b>B</b>) Resolution of Laplace’s equation for FGF10 concentration <i>c</i> in the same geometry using finite elements methods. Near the mesothelium the concentration is maximum (red), while it is minimum on the epithelium (blue). (<b>C</b>) Calculation of the gradient norm of FGF10 concentration in the same geometry. Blue stands for weak gradients while red stands for high gradients. Gradient focuses on distal tips.</p
<p>(A) Geometric representation of cells. Cell <i>a</i>, in isolation, is modeled as a disk. Cell <i...
<p>(A) The geometrical domain considers one-fourth of the real fracture callus geometry of a critica...
<p><b>a</b>) FGF10 is transcribed at high levels in the distal mesenchyme (grey) and experiments sug...
<p>(<b>A</b>) Time lapse sequence of a growth simulation. The simulation relies on the laplacian mod...
<p>Calculation of FGF10 flux in a 3D geometry reconstructed from embryonic mouse right cranial lobe ...
International audienceBranching morphogenesis is a widely spread phenomenon in nature. In organogene...
<p>The steady state pattern of FGF10 on the computational domain has (<b>a</b>) an increased radius ...
<p>(<b>A</b>) <i>Spry2</i> whole mount in situ hybridizations before and after a branching event, co...
In this paper we present a comprehensive computational framework within which the effects of chemica...
Spatial tissue patterning during early morphogenesis depends on the coordinated movement and shape c...
<p><b>A.</b> Model schematic shows cell outline (black) and the potential <i>U</i>(<i>s</i>) defined...
Epithelial branching morphogenesis drives the development of organs such as the lung, salivary gland...
The arborescent architecture of mammalian conductive airways results from the repeated branching of ...
<p>(<b>A</b>) The branching mechanism. Consider any prominence on the epithelium (here displayed in ...
International audienceBranched structures are ubiquitous in nature, both in living and non-living sy...
<p>(A) Geometric representation of cells. Cell <i>a</i>, in isolation, is modeled as a disk. Cell <i...
<p>(A) The geometrical domain considers one-fourth of the real fracture callus geometry of a critica...
<p><b>a</b>) FGF10 is transcribed at high levels in the distal mesenchyme (grey) and experiments sug...
<p>(<b>A</b>) Time lapse sequence of a growth simulation. The simulation relies on the laplacian mod...
<p>Calculation of FGF10 flux in a 3D geometry reconstructed from embryonic mouse right cranial lobe ...
International audienceBranching morphogenesis is a widely spread phenomenon in nature. In organogene...
<p>The steady state pattern of FGF10 on the computational domain has (<b>a</b>) an increased radius ...
<p>(<b>A</b>) <i>Spry2</i> whole mount in situ hybridizations before and after a branching event, co...
In this paper we present a comprehensive computational framework within which the effects of chemica...
Spatial tissue patterning during early morphogenesis depends on the coordinated movement and shape c...
<p><b>A.</b> Model schematic shows cell outline (black) and the potential <i>U</i>(<i>s</i>) defined...
Epithelial branching morphogenesis drives the development of organs such as the lung, salivary gland...
The arborescent architecture of mammalian conductive airways results from the repeated branching of ...
<p>(<b>A</b>) The branching mechanism. Consider any prominence on the epithelium (here displayed in ...
International audienceBranched structures are ubiquitous in nature, both in living and non-living sy...
<p>(A) Geometric representation of cells. Cell <i>a</i>, in isolation, is modeled as a disk. Cell <i...
<p>(A) The geometrical domain considers one-fourth of the real fracture callus geometry of a critica...
<p><b>a</b>) FGF10 is transcribed at high levels in the distal mesenchyme (grey) and experiments sug...