Associations and Interactions between Bare Lymphocyte Syndrome Factors

The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator...

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Podrobná bibliografie

Vydáno v:	Mol Cell Biol
Hlavní autoři:	DeSandro, Angela M., Nagarajan, Uma M., Boss, Jeremy M.
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Taylor & Francis 2000
Témata:	Transcriptional Regulation
On-line přístup:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC86141/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10938133/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/mcb.20.17.6587-6599.2000
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