Evolutionary conservation and characterization of the bare lymphocyte syndrome transcription factor RFX-B and its paralogue ANKRA2. (Q40469893)

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7 January 2020

title

Evolutionary conservation and characterization of the bare lymphocyte syndrome transcription factor RFX-B and its paralogue ANKRA2 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15655668%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

main subject

lymphocyte

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Bare lymphocyte syndrome

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1

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7 January 2020

author name string

Jeremy M Boss

series ordinal

2

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7 January 2020

language of work or name

English

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publication date

18 January 2005

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7 January 2020

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15655668%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

volume

56

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7 January 2020

issue

11

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7 January 2020

page(s)

788-797

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https://scigraph.springernature.com/pub.10.1007/s00251-004-0738-2

7 January 2020

exact match

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cites work

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

1 reference

12 December 2020

Genetic complexity of regulatory mutants defective for HLA class II gene expression

1 reference

12 December 2020

Characterization of ANKRA, a novel ankyrin repeat protein that interacts with the cytoplasmic domain of megalin

1 reference

12 December 2020

Insight into the primordial MHC from studies in ectothermic vertebrates

1 reference

12 December 2020

Identification of Gasz, an evolutionarily conserved gene expressed exclusively in germ cells and encoding a protein with four ankyrin repeats, a sterile-alpha motif, and a basic leucine zipper

1 reference

12 December 2020

Birth of the major histocompatibility complex

1 reference

12 December 2020

Associations and interactions between bare lymphocyte syndrome factors

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

RFX-B is the gene responsible for the most common cause of the bare lymphocyte syndrome, an MHC class II immunodeficiency

1 reference

12 December 2020

Isolation of the Promoters of Atlantic Salmon MHCII Genes

1 reference

12 December 2020

Novel mutations in the RFXANK gene: RFX complex containing in-vitro-generated RFXANK mutant binds the promoter without transactivating MHC II.

1 reference

12 December 2020

The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools

1 reference

12 December 2020

Identification and characterization of evolutionarily conserved pufferfish, zebrafish, and frog orthologs of GASZ.

1 reference

12 December 2020

Amino acid sequences common to rapidly degraded proteins: the PEST hypothesis

1 reference

12 December 2020

Regulatory factor X, a bare lymphocyte syndrome transcription factor, is a multimeric phosphoprotein complex

1 reference

12 December 2020

Major histocompatibility complex class II deficiency: a clinical review

1 reference

12 December 2020

Exon shuffling and other ways of module exchange

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12 December 2020

Class II-antigen-negative patient and mutant B-cell lines represent at least three, and probably four, distinct genetic defects defined by complementation analysis

1 reference

12 December 2020

Regulation of MHC class II genes: lessons from a disease

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12 December 2020

Combined immunodeficiency with defective expression in MHC class II genes

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12 December 2020

Major histocompatibility complex class II deficiency: clinical manifestations, immunologic features, and outcome

1 reference

12 December 2020

Genomic organization of the mammalian MHC.

1 reference

12 December 2020

The ankyrin repeat-containing adaptor protein Tvl-1 is a novel substrate and regulator of Raf-1

1 reference

12 December 2020

Evolution of the major histocompatibility complex: a current overview

1 reference

12 December 2020

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

1 reference

12 December 2020

The Draft Genome of Ciona intestinalis: Insights into Chordate and Vertebrate Origins

1 reference

12 December 2020

TreeView: an application to display phylogenetic trees on personal computers

1 reference

12 December 2020

Novel mutations within the RFX-B gene and partial rescue of MHC and related genes through exogenous class II transactivator in RFX-B-deficient cells

1 reference

12 December 2020

1 reference

12 December 2020

Transcriptional regulation of the MHC class II antigen presentation pathway

1 reference

12 December 2020

10.1007/S00251-004-0738-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15655668%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

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