(Q28205734)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12368908%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

title

Mutation in a winged-helix DNA-binding motif causes atypical bare lymphocyte syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12368908%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

main subject

Bare lymphocyte syndrome

1 reference

inferred from title

author

Nabila Jabrane-Ferrat

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12368908%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

Matthias Geyer

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12368908%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

author name string

Nada Nekrep

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12368908%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

Hermann M Wolf

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12368908%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

Martha M Eibl

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12368908%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

B Matija Peterlin

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12368908%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

language of work or name

English

0 references

publication date

30 September 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12368908%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12368908%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

volume

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12368908%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

issue

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12368908%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

page(s)

1075-1081

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12368908%20AND%20SRC:MED&resulttype=core&format=json

Regulation of major histocompatibility complex class-II genes: X, Y and other letters of the alphabet

13 December 2019

cites work

1 reference

7 January 2021

Regulation of transcription of MHC class II genes

1 reference

7 January 2021

Assembly, transport, and function of MHC class II molecules

1 reference

7 January 2021

Sequences and factors: a guide to MHC class-II transcription

1 reference

7 January 2021

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

1 reference

7 January 2021

A gene encoding a novel RFX-associated transactivator is mutated in the majority of MHC class II deficiency patients

1 reference

7 January 2021

Associations and interactions between bare lymphocyte syndrome factors

1 reference

7 January 2021

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

1 reference

7 January 2021

A novel DNA-binding regulatory factor is mutated in primary MHC class II deficiency (bare lymphocyte syndrome)

1 reference

7 January 2021

Complex architecture of major histocompatibility complex class II promoters: reiterated motifs and conserved protein-protein interactions

1 reference

7 January 2021

Complementation cloning of an MHC class II transactivator mutated in hereditary MHC class II deficiency (or bare lymphocyte syndrome)

1 reference

7 January 2021

The class II transactivator CIITA is a transcriptional integrator

1 reference

7 January 2021

Transcriptional scaffold: CIITA interacts with NF-Y, RFX, and CREB to cause stereospecific regulation of the class II major histocompatibility complex promoter

1 reference

7 January 2021

Regulation of MHC class II genes: lessons from a disease

1 reference

7 January 2021

The bare lymphocyte syndrome and the regulation of MHC expression

1 reference

7 January 2021

MHC class II deficiency: a disease of gene regulation

1 reference

7 January 2021

Molecular characterization of major histocompatibility complex class II gene expression and demonstration of antigen-specific T cell response indicate a new phenotype in class II-deficient patients

1 reference

7 January 2021

Genetic evidence for a new type of major histocompatibility complex class II combined immunodeficiency characterized by a dyscoordinate regulation of HLA-D alpha and beta chains

1 reference

7 January 2021

RFX proteins, a novel family of DNA binding proteins conserved in the eukaryotic kingdom

1 reference

7 January 2021

Structure of the winged-helix protein hRFX1 reveals a new mode of DNA binding

1 reference

7 January 2021

ProMod and Swiss-Model: Internet-based tools for automated comparative protein modelling

1 reference

7 January 2021

Assembly of functional regulatory complexes on MHC class II promoters in vivo

1 reference

7 January 2021

Major histocompatibility complex class II transcriptional platform: assembly of nuclear factor Y and regulatory factor X (RFX) on DNA requires RFX5 dimers

1 reference

7 January 2021

A functionally essential domain of RFX5 mediates activation of major histocompatibility complex class II promoters by promoting cooperative binding between RFX and NF-Y

1 reference

7 January 2021

Expression of the three human major histocompatibility complex class II isotypes exhibits a differential dependence on the transcription factor RFXAP

1 reference

7 January 2021

Two DNA-binding proteins discriminate between the promoters of different members of the major histocompatibility complex class II multigene family

1 reference

7 January 2021

MHC class II-deficient combined immunodeficiency: a disease of gene regulation

1 reference

7 January 2021

Residual MHC class II expression on mature dendritic cells and activated B cells in RFX5-deficient mice.

1 reference

7 January 2021

Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease

1 reference

7 January 2021

Looping versus linking: toward a model for long-distance gene activation

1 reference

7 January 2021

A unified theory of gene expression

1 reference

7 January 2021

Specific complex formation between the type II bare lymphocyte syndrome-associated transactivators CIITA and RFX5

1 reference

7 January 2021

Interactions between the class II transactivator and CREB binding protein increase transcription of major histocompatibility complex class II genes

1 reference

7 January 2021

Involvement of CREB binding protein in expression of major histocompatibility complex class II genes via interaction with the class II transactivator

1 reference

7 January 2021

Acetylation by PCAF enhances CIITA nuclear accumulation and transactivation of major histocompatibility complex class II genes

1 reference

7 January 2021

Transcriptional coactivator, CIITA, is an acetyltransferase that bypasses a promoter requirement for TAF(II)250

1 reference

7 January 2021

Promoter-specific functions of CIITA and the MHC class II enhanceosome in transcriptional activation

1 reference

7 January 2021

Analysis of ankyrin repeats reveals how a single point mutation in RFXANK results in bare lymphocyte syndrome

1 reference

7 January 2021

Protein folding and association: insights from the interfacial and thermodynamic properties of hydrocarbons

1 reference

7 January 2021

Identifiers

DOI

10.1038/NI840

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12368908%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

1 reference