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Article title
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Abstract
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Keywords
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Introduction
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Aim
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Materials and methods
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Phase 1
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Simultaneous cultivation of periopathogenic flora
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Preparation of prototype extracellular matrix
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Phase 2
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Phase 3
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Results
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Phase 2
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Specimens without prototype extracellular matrix (control group)
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Specimens with prototype extracellular matrix (test group)
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Phase 3
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FRAP microscopy
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Mathematical analysis of the intensity profile and determination of the local diffusion coefficient
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Discussion
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Conclusions
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Acknowledgements
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Author contributions
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References
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