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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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)

  • 2019Cortical bone properties in the Brtl/+ mouse model of Osteogenesis imperfecta as evidenced by acoustic transmission microscopy10citations

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Chart of shared publication
Blouin, S.
1 / 2 shared
Klaushofer, K.
1 / 106 shared
Cabral, W. A.
1 / 1 shared
Fratzl-Zelman, N.
1 / 31 shared
Fratzl, P.
1 / 10 shared
Roschger, Andreas
1 / 13 shared
Roschger, P.
1 / 127 shared
Chart of publication period
2019

Co-Authors (by relevance)

  • Blouin, S.
  • Klaushofer, K.
  • Cabral, W. A.
  • Fratzl-Zelman, N.
  • Fratzl, P.
  • Roschger, Andreas
  • Roschger, P.
OrganizationsLocationPeople

article

Cortical bone properties in the Brtl/+ mouse model of Osteogenesis imperfecta as evidenced by acoustic transmission microscopy

  • Blouin, S.
  • Klaushofer, K.
  • Cabral, W. A.
  • Fratzl-Zelman, N.
  • Fratzl, P.
  • Roschger, Andreas
  • Marini, J. C.
  • Roschger, P.
Abstract

<p>Higher skeletal fragility has been established for the Brtl/+ mouse model of osteogenesis imperfecta at the whole bone level, but previous investigations of mechanical properties at the bone material level were inconclusive. Bone material was analyzed separately at endosteal (ER) and periosteal regions (PR) on transverse femoral midshaft sections for 2-month old mice (wild-type n = 6; Brtl/+ n = 6). Quantitative backscattered electron imaging revealed that the mass density computed from mineral density maps was higher in PR than in ER for both wild-type (+2.1%, p &lt; 0.05) and Brtl/+ mice (+1.8%, p &lt; 0.05). Electron induced X-ray fluorescence analysis indicated significantly lower atomic Ca/P ratios and higher Na/Ca, Mg/Ca and K/Ca ratios in PR bone compared to ER independently of genotype. Second harmonic generation microscopy indicated that the occurrence of periodically alternating collagen orientation in ER of Brtl/+ mice was strongly reduced compared to wild-type mice. Scanning acoustic microscopy in time of flight mode revealed that the sound velocity and Young's modulus (estimated based on sound velocity and mass density maps) were significantly greater in PR (respectively +6% and +15%) compared to ER in wild-type mice but not in Brtl/+ mice. ER sound velocity and Young's modulus were significantly increased in Brtl/+ mice (+9.4% and +22%, respectively) compared to wild-type mice. These data demonstrate that the Col1a1 G349C mutation in Brtl/+ mice affects the mechanical behavior of bone material predominantly in the endosteal region by altering the collagen orientation.</p>

Topics
  • density
  • mineral
  • microscopy