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  • Popat, S (author)

Variation in the CTLA4/CD28 gene region confers an increased risk of coeliac disease.

  • Article/chapterEnglish2002

Publisher, publication year, extent ...

  • 2002

Numbers

  • LIBRIS-ID:oai:gup.ub.gu.se/65509
  • https://gup.ub.gu.se/publication/65509URI
  • https://doi.org/10.1017/S0003480002001021DOI
  • https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-26468URI

Supplementary language notes

  • Language:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Susceptibility to coeliac disease involves HLA and non-HLA-linked genes. The CTLA4/CD28 gene region encodes immune regulatory T-cell surface molecules and is a strong candidate as a susceptibility locus. We evaluated CTLA4/CD28 in coeliac disease by genetic linkage and association and combined our findings with published studies through a meta-analysis. 116 multiplex families were genotyped across CTLA4/CD28 using eight markers. The contribution of CTLA4/CD28 to coeliac disease was assessed by non-parametric linkage and association analyses. Seven studies were identified that had evaluated the relationship between CTLA4/CD28 and coeliac disease and a pooled analysis of data undertaken. In our study there was evidence for a relationship between variation in the CTLA4/CD28 region and coeliac disease by linkage and association analyses. However, the findings did not attain formal statistical significance (p = 0.004 and 0.039, respectively). Pooling findings with published results showed significant evidence for linkage (504 families) and association (940 families): p values, 0.0001 and 0.0014 at D2S2214, respectively, and 0.0008 and 0.0006 at D2S116, respectively. These findings suggest that variation in the CD28/CTLA4 gene region is a determinant of coeliac disease susceptibility. Dissecting the sequence variation underlying this relationship will depend on further analyses utilising denser sets of markers.

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Added entries (persons, corporate bodies, meetings, titles ...)

  • Hearle, N (author)
  • Högberg, LottaLinköpings universitet,Hälsouniversitetet,Pediatrik(Swepub:liu)lotho28 (author)
  • Braegger, C P (author)
  • O'Donoghue, D (author)
  • Fälth-Magnusson, Karin,1949-Östergötlands Läns Landsting,Linköpings universitet,Hälsouniversitetet,Pediatrik,Barn(Swepub:liu)karfa12 (author)
  • Holmes, G K T (author)
  • Howdle, P D (author)
  • Jenkins, H (author)
  • Johnston, S (author)
  • Kennedy, N P (author)
  • Kumar, P J (author)
  • Logan, R F A (author)
  • Marsh, M N (author)
  • Mulder, C J (author)
  • Torinsson Naluai, Åsa,1968Gothenburg University,Göteborgs universitet,Institutionen för kvinnors och barns hälsa,Institute for the Health of Women and Children(Swepub:gu)xnalas (author)
  • Sjoberg, KÖstergötlands Läns Landsting,Barn (author)
  • Stenhammar, Lars,1939-Östergötlands Läns Landsting,Linköpings universitet,Hälsouniversitetet,Pediatrik,Barn(Swepub:liu)larst66 (author)
  • Walters, J R F (author)
  • Jewell, D P (author)
  • Houlston, R S (author)
  • Linköpings universitetHälsouniversitetet (creator_code:org_t)

Related titles

  • In:Annals of human genetics66:Pt 2, s. 125-370003-48001469-1809

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