Mutations in the bare lymphocyte syndrome define critical steps in the assembly of the regulatory factor X complex

Mutations in the bare lymphocyte syndrome define critical steps in the assembly of the regulatory factor X complex

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http://www.wikidata.org/entity/Q24554195
Identification of the ankyrin repeat proteins ANKRA and RFXANK as novel partners of class IIa histone deacetylasesNew functions of the major histocompatibility complex class II-specific transcription factor RFXANK revealed by a high-resolution mutagenesis studyAnalysis of ankyrin repeats reveals how a single point mutation in RFXANK results in bare lymphocyte syndromeInterferon gamma repression of collagen (COL1A2) transcription is mediated by the RFX5 complexExpression of the three human major histocompatibility complex class II isotypes exhibits a differential dependence on the transcription factor RFXAPA 36-amino-acid region of CIITA is an effective inhibitor of CBP: novel mechanism of gamma interferon-mediated suppression of collagen alpha(2)(I) and other promotersPromoter-specific functions of CIITA and the MHC class II enhanceosome in transcriptional activationPhosphorylation of CIITA directs its oligomerization, accumulation and increased activity on MHCII promoters.Inhibition of proteasome activity impairs centrosome-dependent microtubule nucleation and organization.Differential splicing generates Tvl-1/RFXANK isoforms with different functions.Kaposi's Sarcoma-Associated Herpesvirus Latency-Associated Nuclear Antigen Inhibits Major Histocompatibility Complex Class II Expression by Disrupting Enhanceosome Assembly through Binding with the Regulatory Factor X ComplexMajor histocompatibility complex class II transcriptional platform: assembly of nuclear factor Y and regulatory factor X (RFX) on DNA requires RFX5 dimers.Collagen alpha1(I) gene (COL1A1) is repressed by RFX familySolution structure of the heterotrimeric complex between the interaction domains of RFX5 and RFXAP from the RFX gene regulatory complex.
P2860

Mutations in the bare lymphocyte syndrome define critical steps in the assembly of the regulatory factor X complex

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http://www.wikidata.org/entity/Q24554195
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2000 nî lūn-bûn
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2000 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հունիսին հրատարակված գիտական հոդված
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2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Mutations in the bare lymphocy ...... he regulatory factor X complex
@ast
Mutations in the bare lymphocy ...... he regulatory factor X complex
@en
Mutations in the bare lymphocy ...... he regulatory factor X complex
@nl
type
label
Mutations in the bare lymphocy ...... he regulatory factor X complex
@ast
Mutations in the bare lymphocy ...... he regulatory factor X complex
@en
Mutations in the bare lymphocy ...... he regulatory factor X complex
@nl
prefLabel
Mutations in the bare lymphocy ...... he regulatory factor X complex
@ast
Mutations in the bare lymphocy ...... he regulatory factor X complex
@en
Mutations in the bare lymphocy ...... he regulatory factor X complex
@nl
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698
P932
P356
P1433
P1476
Mutations in the bare lymphocy ...... he regulatory factor X complex
@en
P2093
P2860
P304
P31
P356
10.1128/MCB.20.12.4455-4461.2000
P407
P433
P478
P50
P577
P698
P932