Functional complementation of major histocompatibility complex class II regulatory mutants by the purified X-box-binding protein RFX.

Major histocompatibility complex (MHC) class II deficiency, or bare lymphocyte syndrome (BLS), is a disease of gene regulation. Patients with BLS have been classified into at least three complementation groups (A, B, and C) believed to correspond to three distinct MHC class II regulatory genes. The...

Täydet tiedot

Bibliografiset tiedot

Julkaisussa:	Mol Cell Biol
Päätekijät:	Durand, B, Kobr, M, Reith, W, Mach, B
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	Taylor & Francis 1994
Aiheet:	Research Article
Linkit:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC359214/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7935401/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/mcb.14.10.6839-6847.1994
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