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Monosomy 1p36 uncovers a role for OX40 in survival of activated CD4+ T cells
Monosomy 1p36 is a subtelomeric deletion syndrome associated with congenital anomalies presumably due to haploinsufficiency of multiple genes. Although immunodeficiency has not been reported, genes encoding costimulatory molecules of the TNF receptor superfamily (TNFRSF) are within 1p36 and may be a...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2583253/ https://ncbi.nlm.nih.gov/pubmed/18511345 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.clim.2008.03.522 |
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