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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Suhoski, M.M., Perez, E.E., Heltzer, M.L., Laney, A., Shaffer, L.G., Saitta, S., Nachman, S., Spinner, N., June, C.H., Orange, J.S.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2008
Pynciau:
Article
Mynediad Ar-lein: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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