Novel immunodeficiency data servers
Valiaho, L ; Riikonen, P and Vihinen, Mauno LU
(2000)
In Immunological Reviews
178.
p.177-185
- 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... (More)
- 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/. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/3851950
- author
- Valiaho, L
; Riikonen, P
and Vihinen, Mauno
LU
- publishing date
- 2000
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Immunological Reviews
- volume
- 178
- pages
- 177 - 185
- publisher
- Wiley-Blackwell
- external identifiers
-
- wos:000166530000018
- scopus:0034576088
- ISSN
- 1600-065X
- language
- English
- LU publication?
- no
- id
- 1e3408f6-9dbd-4a78-a63f-bc49f901abd8 (old id 3851950)
- date added to LUP
- 2016-04-01 17:03:59
- date last changed
- 2022-02-28 01:36:57
@article{1e3408f6-9dbd-4a78-a63f-bc49f901abd8,
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/.}},
author = {{Valiaho, L and Riikonen, P and Vihinen, Mauno}},
issn = {{1600-065X}},
language = {{eng}},
pages = {{177--185}},
publisher = {{Wiley-Blackwell}},
series = {{Immunological Reviews}},
title = {{Novel immunodeficiency data servers}},
volume = {{178}},
year = {{2000}},
}