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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...

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Detalles Bibliográficos
Autores principales: Sestak, Andrea L, Nath, Swapan K, Sawalha, Amr H, Harley, John B
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
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.
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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
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