Novel immunodeficiency data servers

Forskningsoutput: TidskriftsbidragÖversiktsartikel

Abstract

The Internet contains scientific information in increasing amounts. It is possible to obtain the latest information, and Web services can easily be maintained and updated. We have set up three Internet ser vices an immunodeficiencies. Immunodeficiency-related mutation information is available in immunodeficiency mutation databases (IDbases). Currently 14 registries are distributed, including information about Bloom syndrome (BLMbase), X-linked agammaglobulinemia (BTKbase), X-linked and autosomal recessive chronic granulomatous diseases (CYBBbase for X-linked CGD, CYBAbase for p22(phox) deficiency NCF1base for p47(phox) deficiency NCF2base for p67(phox) deficiency), CD3 gamma and CD3 epsilon deficiencies (CD3Gbase, CD3Ebase), X-linked hyper-IgM syndrome (CD40Lbase), T-B+ severe combined immunodeficiency (JAK3base), V(D)J recombination defects (RAG1base, RAG2base), X-linked lymphoproliferative syndrome (SH2D1Abase), and ZAP-70 deficiency (ZAP70base). Information on laboratories analysing the genetic defects is collected to IDdiagnostics registry Due to the rareness of immunodeficiencies there are very few laboratories performing genetic diagnostics. Such laboratories are Listed in IDdiagnostics and physicians can use the registry to find a suitable laboratory for their diagnostic needs. Immunodeficiency Resource (IDR) is a comprehensive integrated knowledge base for all the information on immunodeficiencies, including clinical, biochemical, genetic, structural and computational data and analyses. Air three services are available at http: //www.uta.fi/imt/bioinfo/.

Detaljer

Författare
Externa organisationer
  • External Organization - Unknown
Forskningsområden

Ämnesklassifikation (UKÄ) – OBLIGATORISK

  • Immunologi inom det medicinska området
Originalspråkengelska
Sidor (från-till)177-185
TidskriftImmunological Reviews
Volym178
StatusPublished - 2000
PublikationskategoriForskning
Peer review utfördJa
Externt publiceradJa