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Current status of lupus genetics
Over the past 40 years more than 100 genetic risk factors have been defined in systemic lupus erythematosus through a combination of case studies, linkage analyses of multiplex families, and case-control analyses of single genes. Multiple investigators have examined patient cohorts gathered from aro...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2206359/ https://www.ncbi.nlm.nih.gov/pubmed/17509159 http://dx.doi.org/10.1186/ar2176 |
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author | Sestak, Andrea L Nath, Swapan K Sawalha, Amr H Harley, John B |
author_facet | Sestak, Andrea L Nath, Swapan K Sawalha, Amr H Harley, John B |
author_sort | Sestak, Andrea L |
collection | PubMed |
description | Over the past 40 years more than 100 genetic risk factors have been defined in systemic lupus erythematosus through a combination of case studies, linkage analyses of multiplex families, and case-control analyses of single genes. Multiple investigators have examined patient cohorts gathered from around the world, and although we doubt that all of the reported associations will be replicated, we have probably already discovered many of the genes that are important in lupus pathogenesis, including those encoding human leukocyte antigen-DR, Fcγ receptor 3A, protein tyrosine phosphatase nonreceptor 22, cytotoxic T lymphocyte associated antigen 4, and mannose-binding lectin. In this review we will present what is known, what is disputed, and what remains to be discovered in the world of lupus genetics. |
format | Text |
id | pubmed-2206359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22063592008-01-19 Current status of lupus genetics Sestak, Andrea L Nath, Swapan K Sawalha, Amr H Harley, John B Arthritis Res Ther Review Over the past 40 years more than 100 genetic risk factors have been defined in systemic lupus erythematosus through a combination of case studies, linkage analyses of multiplex families, and case-control analyses of single genes. Multiple investigators have examined patient cohorts gathered from around the world, and although we doubt that all of the reported associations will be replicated, we have probably already discovered many of the genes that are important in lupus pathogenesis, including those encoding human leukocyte antigen-DR, Fcγ receptor 3A, protein tyrosine phosphatase nonreceptor 22, cytotoxic T lymphocyte associated antigen 4, and mannose-binding lectin. In this review we will present what is known, what is disputed, and what remains to be discovered in the world of lupus genetics. BioMed Central 2007 2007-05-14 /pmc/articles/PMC2206359/ /pubmed/17509159 http://dx.doi.org/10.1186/ar2176 Text en |
spellingShingle | Review Sestak, Andrea L Nath, Swapan K Sawalha, Amr H Harley, John B Current status of lupus genetics |
title | Current status of lupus genetics |
title_full | Current status of lupus genetics |
title_fullStr | Current status of lupus genetics |
title_full_unstemmed | Current status of lupus genetics |
title_short | Current status of lupus genetics |
title_sort | current status of lupus genetics |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2206359/ https://www.ncbi.nlm.nih.gov/pubmed/17509159 http://dx.doi.org/10.1186/ar2176 |
work_keys_str_mv | AT sestakandreal currentstatusoflupusgenetics AT nathswapank currentstatusoflupusgenetics AT sawalhaamrh currentstatusoflupusgenetics AT harleyjohnb currentstatusoflupusgenetics |