Study of the role of functional variants of SLC22A4, RUNX1 and SUMO4 in systemic lupus erythematosus

Background: Functional polymorphisms of the solute carrier family 22, member 4 (SLC22A4), runt related transcription factor 1 (RUNX1) and small ubiquitin-like modifier 4 (SUMO-4) genes have been shown to be associated with several autoimmune diseases. Objective: To test the possible role of these va...

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Autores:

Tipo de recurso:

Fecha de publicación:

2006

Institución:

Universidad del Rosario

Repositorio:

Repositorio EdocUR - U. Rosario

Idioma:

eng

OAI Identifier:

oai:repository.urosario.edu.co:10336/22345

Acceso en línea:

https://doi.org/10.1136/ard.2005.044891
https://repository.urosario.edu.co/handle/10336/22345

Palabra clave:

Membrane protein
Protein slc22a4
Sumo protein
Transcription factor runx1
Unclassified drug
Adult
Allele
Article
Autoimmune disease
Colombia
Controlled study
Disease severity
Gene linkage disequilibrium
Genetic susceptibility
Genotype
Human
Major clinical study
Nephritis
Priority journal
Single nucleotide polymorphism
Spain
Sweden
Systemic lupus erythematosus
Adult
Alleles
Case-control studies
Chi-square distribution
Core binding factor alpha 2 subunit
Female
Genetic predisposition to disease
Genotype
Humans
Male
Middle aged
Odds ratio
Organic cation transport proteins
Small ubiquitin-related modifier proteins
systemic
genetic
Lupus erythematosus
Polymorphism

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