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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1.080 Topics available

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977 Locations available

693.932 PEOPLE
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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (5/5 displayed)

  • 2020Investigating the performance of 410, PH13-8Mo and 300M steels in a turning process with a focus on surface finishcitations
  • 2016Mapping Morphological and Structural Properties of Lead Halide Perovskites by Scanning Nanofocus XRD30citations
  • 2016Thermally stable solution processed vanadium oxide as a hole extraction layer in organic solar cells19citations
  • 2002Tumour necrosis factor receptor II polymorphism and juvenile idiopathic arthritiscitations
  • 2002Lack of association between juvenile idiopathic arthritis and Fas gene polymorphismcitations

Places of action

Chart of shared publication
Díaz, F.
1 / 3 shared
Khan, T.
1 / 10 shared
Arrazola, P.
1 / 1 shared
Taylor, C. M.
1 / 3 shared
Alegre, R.
1 / 1 shared
Turner, S.
1 / 13 shared
Lilliu, S.
1 / 8 shared
Friend, Richard, H.
1 / 549 shared
Macdonald, J. E.
1 / 5 shared
Dane, T. G.
1 / 1 shared
Lidzey, D. G.
1 / 14 shared
Alsari, M.
1 / 7 shared
Barrows, A. T.
1 / 2 shared
Dahlem, M. S.
1 / 1 shared
Iraqi, A.
1 / 12 shared
Alqurashi, R.
1 / 1 shared
Alsulami, A.
1 / 1 shared
Lidzey, D.
1 / 3 shared
Buckley, A.
1 / 2 shared
Yi, H.
1 / 2 shared
Chart of publication period
2020
2016
2002

Co-Authors (by relevance)

  • Díaz, F.
  • Khan, T.
  • Arrazola, P.
  • Taylor, C. M.
  • Alegre, R.
  • Turner, S.
  • Lilliu, S.
  • Friend, Richard, H.
  • Macdonald, J. E.
  • Dane, T. G.
  • Lidzey, D. G.
  • Alsari, M.
  • Barrows, A. T.
  • Dahlem, M. S.
  • Iraqi, A.
  • Alqurashi, R.
  • Alsulami, A.
  • Lidzey, D.
  • Buckley, A.
  • Yi, H.
OrganizationsLocationPeople

article

Lack of association between juvenile idiopathic arthritis and Fas gene polymorphism

  • Holt, L.
  • Abinun, M.
  • Herrick, Ariane
  • Wyatt, S.
  • Zeggini, E.
  • David, J.
  • Crawley, E.
  • Griffin, J.
  • Foster, H.
  • Ryder, C.
  • Stewart, I.
  • Thomson, Wendy
  • Hall, M.
  • Woo, P.
  • Hollingworth, P.
  • Shelley, E.
  • Hall, A.
  • Jones, S.
  • Craft, A.
  • Bell, A.
  • Donn, Rachelle
  • Becker, M.
  • Ollier, William
  • Southwood, T.
  • Venning, H.
  • Gardener-Medwin, J.
  • Pountain, G.
Abstract

Objective. Juvenile idiopathic arthritis (JIA) is a complex genetic disease of autoimmune etiology. Fas is a molecule with a pivotal role in apoptosis and hence in immune regulation. Elevated transcriptional levels of Fas in the synovial fluid of patients with JIA suggest that it might be implicated in disease etiopathogenesis. We investigated whether a polymorphism in the Fas promoter region (-670) confers susceptibility to JIA. Methods. In this association study, 342 UK patients with JIA and 255 healthy individuals were genotyped for the polymorphism using polymerase chain reaction restriction fragment length polymorphism. Comparisons of the genotypic frequencies were made using chi-square analysis. Results. No statistically significant differences were found when the genotype frequencies of the -670 Fas polymorphism were compared between the JIA cases and the control panel. Similarly, no differences were seen between the JIA subgroups, or when the patients were divided on the basis of rheumatoid factor or antinuclear antibody positivity. Conclusion. The -670 polymorphism of Fas does not appear to be associated with susceptibility to JIA.

Topics
  • impedance spectroscopy
  • susceptibility