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RFXAP, a novel subunit of the RFX DNA binding complex is mutated in MHC class II deficiency.

Major Histocompatibility Complex class II (MHC-II) deficiency is a disease of gene regulation that provides a unique opportunity for the genetic dissection of the molecular mechanisms controlling transcription of MHC-II genes. Cell lines from MHC-II deficiency patients have been assigned to three co...

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Detaylı Bibliyografya
Asıl Yazarlar: Durand, B, Sperisen, P, Emery, P, Barras, E, Zufferey, M, Mach, B, Reith, W
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1997
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1169704/
https://ncbi.nlm.nih.gov/pubmed/9118943
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/emboj/16.5.1045
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