Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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Materials Map under construction

The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2014Differentially instructive extracellular protein micro-nets38citations

Places of action

Chart of shared publication
Ray, Santanu
1 / 6 shared
Lamarre, Baptiste
1 / 1 shared
Bella, Angelo
1 / 1 shared
Ravi, Jascindra
1 / 1 shared
Ryadnov, Maxim G.
1 / 1 shared
Chart of publication period
2014

Co-Authors (by relevance)

  • Ray, Santanu
  • Lamarre, Baptiste
  • Bella, Angelo
  • Ravi, Jascindra
  • Ryadnov, Maxim G.
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article

Differentially instructive extracellular protein micro-nets

  • Ray, Santanu
  • Lamarre, Baptiste
  • Bella, Angelo
  • Ravi, Jascindra
  • Ryadnov, Maxim G.
  • Faruqui, Nilofar
Abstract

<p>An ability to construct biological matter from the molecule up holds promise for applications ranging from smart materials to integrated biophysical models for synthetic biology. Biomolecular self-assembly is an efficient strategy for biomaterial construction which can be programmed to support desired function. A challenge remains in replicating the strategy synthetically, that is at will, and differentially, that is for a specific function at a given length scale. Here we introduce a self-assembly topology enabling a net-like architectural mimetic of native extracellular matrices capable of differential responses to cell adhesion-enhanced mammalian cell attachment and proliferation, and enhanced resistance to bacterial colonization-at the native sub-millimeter length scales. The biological performance of such protein micro-nets directly correlates with their morphological and chemical properties, offering thus an application model for differential extracellular matrices.</p>

Topics
  • impedance spectroscopy
  • self-assembly