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Limits to the precision of gradient sensing with spatial communication and temporal integration.
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Role of spatial averaging in multicellular gradient sensing.
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Gradient sensing via cell communication.
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Cell-cell communication enhances the capacity of cell ensembles to sense shallow gradients during morphogenesis.
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Fundamental Limits to Collective Concentration Sensing in Cell Populations.
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Collective Chemotaxis through Noisy Multicellular Gradient Sensing.
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Energy dissipation and noise correlations in biochemical sensing.
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The role of cell geometry and cell-cell communication in gradient sensing.
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2D effects enhance precision of gradient-based tissue patterning.
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Single-cell directional sensing from just a few receptor binding events.
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The impact of cell size on morphogen gradient precision.
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A Microfluidic Device for Long-Term Maintenance of Organotypic Liver Cultures.
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High-throughput co-culture system for analysis of spatiotemporal cell-cell signaling.
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Deduction of signaling mechanisms from cellular responses to multiple cues.
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The role of cell geometry and cell-cell communication in gradient sensing.
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A single-cell resolved cell-cell communication model explains lineage commitment in hematopoiesis.
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Revising Berg-Purcell for finite receptor kinetics.
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Optimizing information flow in small genetic networks. IV. Spatial coupling.
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Collective cell motility promotes chemotactic prowess and resistance to chemorepulsion.
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The Berg-Purcell limit revisited.
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Directional tissue migration through a self-generated chemokine gradient.
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IP3, a small molecule with a powerful message.
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Diverse sensitivity thresholds in dynamic signaling responses by social amoebae.
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A comparison of mathematical models for polarization of single eukaryotic cells in response to guided cues.
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Pattern, growth, and control.
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