Association of the LILRA3 Deletion with B-NHL and Functional Characterization of the Immunostimulatory Molecule

LILRA3 is the sole soluble member of the LILR family. Previous studies from our group had shown that a 6.7 kb genetic deletion of LILRA3 is associated with MS and Sjögren’s syndrome. An impairment of the immune response leads to a predisposition for B-NHL, so we wanted to study whether the deletion...

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Detalles Bibliográficos
Autores principales: Low, Hui Zhi, Reuter, Sandra, Topperwien, Michael, Dankenbrink, Nadine, Peest, Dietrich, Kabalak, Gamze, Stripecke, Renata, Schmidt, Reinhold E., Matthias, Torsten, Witte, Torsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3867304/
https://www.ncbi.nlm.nih.gov/pubmed/24363809
http://dx.doi.org/10.1371/journal.pone.0081360

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3867304/
https://www.ncbi.nlm.nih.gov/pubmed/24363809
http://dx.doi.org/10.1371/journal.pone.0081360

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