The I?BL gene polymorphism influences risk of acquiring systemic lupus erythematosus and Sjögren's syndrome

The human inhibitory ?B-like gene (I?BL) maps to a chromosomal region ?25 kb telomeric of the TNF gene at 6p21.3. I?BL encodes a protein related to I?B? that may interact with members of the NF-?B/Rel family. We evaluated the role of I?BL gene polymorphism in systemic lupus erythematosus (SLE) and p...

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Autores:

Tipo de recurso:

Fecha de publicación:

2008

Institución:

Universidad del Rosario

Repositorio:

Repositorio EdocUR - U. Rosario

Idioma:

eng

OAI Identifier:

oai:repository.urosario.edu.co:10336/24219

Acceso en línea:

https://doi.org/10.1016/j.humimm.2007.11.008
https://repository.urosario.edu.co/handle/10336/24219

Palabra clave:

I kappa B
HLA antigen class 2
Tumor necrosis factor alpha
Unclassified drug
Adolescent
Adult
Aged
Allele
Article
Controlled study
DNA isolation
Female
Genetic polymorphism
Genotype
Haplotype
Human
Major clinical study
Male
Priority journal
Risk factor
School child
Sjoegren syndrome
Systemic lupus erythematosus
Child
Gene frequency
Gene linkage disequilibrium
Genetic polymorphism
Genetic predisposition
Genetics
Middle aged
Adolescent
Adult
Aged
Aged, 80 and over
Child
Female
Gene Frequency
Genetic Predisposition to Disease
Haplotypes
Histocompatibility Antigens Class II
Humans
Linkage Disequilibrium
Male
Middle Aged
Sjogren's Syndrome
Tumor Necrosis Factor-alpha
I?bl
Sjögren's syndrome
Systemic lupus erythematosus
TNF
Systemic
Genetic
human
NFKBIL1 protein
Lupus Erythematosus
Polymorphism

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