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 (3/3 displayed)

  • 2019Gas-foamed poly(lactide-co-glycolide) and poly(lactide-co-glycolide) with bioactive glass fibres demonstrate insufficient bone repair in lapine osteochondral defects15citations
  • 2006Interrelationships between electrical properties and microstructure of human trabecular bone40citations
  • 2006T2 relaxation time mapping reveals age- and species-related diversity of collagen network architecture in articular cartilage104citations

Places of action

Chart of shared publication
Hannula, M.
1 / 4 shared
Muhonen, V.
1 / 2 shared
Uppstu, P.
1 / 2 shared
Aula, Antti
1 / 3 shared
Haaparanta, Am
1 / 1 shared
Rosling, Ari
1 / 3 shared
Pyhältö, T.
1 / 1 shared
Kellomäki, Minna
1 / 31 shared
Järvinen, E.
1 / 1 shared
Salonius, Eve
1 / 1 shared
Lehto, K.
1 / 1 shared
Day, J. S.
1 / 2 shared
Jurvelin, J. S.
2 / 9 shared
Töyräs, Juha
2 / 28 shared
Hakulinen, M. A.
1 / 4 shared
Weinans, H.
1 / 8 shared
Sierpowska, J.
1 / 3 shared
Lappalainen, R.
1 / 8 shared
Nissi, M. J.
1 / 3 shared
Laasanen, M. S.
1 / 3 shared
Nieminen, M. T.
1 / 2 shared
Rieppo, J.
1 / 3 shared
Chart of publication period
2019
2006

Co-Authors (by relevance)

  • Hannula, M.
  • Muhonen, V.
  • Uppstu, P.
  • Aula, Antti
  • Haaparanta, Am
  • Rosling, Ari
  • Pyhältö, T.
  • Kellomäki, Minna
  • Järvinen, E.
  • Salonius, Eve
  • Lehto, K.
  • Day, J. S.
  • Jurvelin, J. S.
  • Töyräs, Juha
  • Hakulinen, M. A.
  • Weinans, H.
  • Sierpowska, J.
  • Lappalainen, R.
  • Nissi, M. J.
  • Laasanen, M. S.
  • Nieminen, M. T.
  • Rieppo, J.
OrganizationsLocationPeople

article

T2 relaxation time mapping reveals age- and species-related diversity of collagen network architecture in articular cartilage

  • Nissi, M. J.
  • Jurvelin, J. S.
  • Töyräs, Juha
  • Kiviranta, I.
  • Laasanen, M. S.
  • Nieminen, M. T.
  • Rieppo, J.
Abstract

Objective: The magnetic resonance imaging (MRI) parameter T relaxation time has been shown to be sensitive to the collagen network architecture of articular cartilage. The aim of the study was to investigate the agreement of T relaxation time mapping and polarized light microscopy (PLM) for the determination of histological properties (i.e., zone and fibril organization) of articular cartilage. Methods: T relaxation time was determined at 9.4 T field strength in healthy adult human, juvenile bovine and juvenile porcine patellar cartilage, and related to collagen anisotropy and fibril angle as measured by quantitative PLM. Results: Both T and PLM revealed a mutually consistent but varying number of collagen-associated laminae (3, 3-5 or 3-7 laminae in human, porcine and bovine cartilage, respectively). Up to 44% of the depth-wise variation in T was accounted for by the changing anisotropy of collagen fibrils, confirming that T contrast of articular cartilage is strongly affected by the collagen fibril anisotropy. A good correspondence was observed between the thickness of T-laminae and collagenous zones as determined from PLM anisotropy measurements (r = 0.91, r = 0.95 and r = 0.91 for human, bovine and porcine specimens, respectively). Conclusions: According to the present results, T mapping is capable of detecting histological differences in cartilage collagen architecture among species, likely to be strongly related to the differences in maturation of the tissue. This diversity in the MRI appearance of healthy articular cartilage should also be recognized when using juvenile animal tissue as a model for mature human cartilage in experimental studies.

Topics
  • impedance spectroscopy
  • strength
  • Polarized light microscopy