CARD15 gene mutations are not associated with ankylosing spondylitis

An insertion mutation at nucleotide 3020 (3020insC) and a missense mutation G2722C in the CARD15 gene on chromosome 16p have been reported to be associated with Crohn's disease (CD). The protein encoded by the CARD15 gene is expressed in peripheral monocytes and regulates apoptosis and NF-κB ac...

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Veröffentlicht in:	Genes and immunity 2003-01, Vol.4 (1), p.77-78
Hauptverfasser:	van der Paardt, M, Crusius, J B A, de Koning, M H M T, Murillo, L S, van de Stadt, R J, Dijkmans, B A C, Peña, A S, van der Horst-Bruinsma, I E
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Aged Aged, 80 and over Ankylosing spondylitis Apoptosis Arthritis Biological and medical sciences Biomedical and Life Sciences Biomedicine brief-communication Cancer Research Carrier Proteins - genetics Chromosome 16 Confidence Intervals Crohn's disease Female Fundamental and applied biological sciences. Psychology Gene Expression Gene Frequency - genetics Genetic aspects Genetic Predisposition to Disease Health aspects Human Genetics Humans Immunology Intracellular Signaling Peptides and Proteins Male Microbiology Middle Aged Missense mutation Monocytes Mutagenesis, Insertional Mutation Mutation, Missense NF-κB protein Nod2 Signaling Adaptor Protein Odds Ratio Spondylitis, Ankylosing - genetics
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