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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University of Manchester

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (5/5 displayed)

  • 2012The non-synonymous SNP, R1150W, in SCN9A is not associated with chronic widespread pain susceptibility20citations
  • 2002Sequence analysis of MHC DRB alleles in domestic cats from the United Kingdom66citations
  • 2002Tumour necrosis factor receptor II polymorphism and juvenile idiopathic arthritiscitations
  • 2002Lack of association between juvenile idiopathic arthritis and Fas gene polymorphismcitations
  • 2001A novel 5′-flanking region polymorphism of macrophage migration inhibitory factor is associated with systemic-onset juvenile idiopathic arthritiscitations

Places of action

Chart of shared publication
Horan, Michael A.
1 / 1 shared
Macfarlane, Gary J.
1 / 1 shared
Forti, Gianni
1 / 1 shared
Casanueva, Felipe
1 / 1 shared
Wang, Ke
1 / 18 shared
Wu, Frederick C.
1 / 1 shared
Bartfai, Gyorgy
1 / 1 shared
Huhtaniemi, Ilpo T.
1 / 1 shared
Holliday, Kate L.
1 / 1 shared
Felson, David T.
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Neogi, Tuhina
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Pendleton, Neil
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Ollier, William
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Payton, Antony
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Kula, Krzysztof
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Vanderschueren, Dirk
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Punab, Margus
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Mcbeth, John
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Radford, Alan
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Carter, Stuart
1 / 1 shared
Willoughby, Kim
1 / 1 shared
Kennedy, Lorna
1 / 1 shared
Addie, Diane
1 / 1 shared
Gaskell, Rosalind
1 / 2 shared
Ryvar, Ruth
1 / 1 shared
Donn, Rachelle
3 / 3 shared
Shelley, E.
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Chart of publication period
2012
2002
2001

Co-Authors (by relevance)

  • Horan, Michael A.
  • Macfarlane, Gary J.
  • Forti, Gianni
  • Casanueva, Felipe
  • Wang, Ke
  • Wu, Frederick C.
  • Bartfai, Gyorgy
  • Huhtaniemi, Ilpo T.
  • Holliday, Kate L.
  • Felson, David T.
  • Neogi, Tuhina
  • Pendleton, Neil
  • Ollier, William
  • Payton, Antony
  • Kula, Krzysztof
  • Vanderschueren, Dirk
  • Punab, Margus
  • Mcbeth, John
  • Radford, Alan
  • Carter, Stuart
  • Willoughby, Kim
  • Kennedy, Lorna
  • Addie, Diane
  • Gaskell, Rosalind
  • Ryvar, Ruth
  • Donn, Rachelle
  • Shelley, E.
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