Human genetic defects in class-switch recombination (hyper-IgM syndromes). (Q34360486)

1 August 2017

1 reference

title

Human genetic defects in class-switch recombination (hyper-IgM syndromes). (English)

1 reference

1 August 2017

Durandy A

1

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PubMed ID

11544001

1 August 2017

Honjo T

series ordinal

2

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1 August 2017

1 October 2001

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Current Opinion in Immunology

1 August 2017

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1 August 2017

13

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1 August 2017

5

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1 August 2017

543-548

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Linking class-switch recombination with somatic hypermutation

1 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Cis-acting sequences that affect somatic hypermutation of Ig genes

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

CD40 ligand gene defects responsible for X-linked hyper-IgM syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

CD40 ligand mutations in X-linked immunodeficiency with hyper-IgM

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Defective expression of the CD40 ligand in X chromosome-linked immunoglobulin deficiency with normal or elevated IgM

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Defective expression of CD40 ligand on T cells causes "X-linked immunodeficiency with hyper-IgM (HIGM1)".

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

CD40-CD40L independent Ig gene hypermutation suggests a second B cell diversification pathway in humans

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

T-Independent immune response: new aspects of B cell biology

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

CD40 ligand expression deficiency in a female carrier of the X-linked hyper-IgM syndrome as a result of X chromosome lyonization

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Specific missense mutations in NEMO result in hyper-IgM syndrome with hypohydrotic ectodermal dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

NF-kappa B and Rel proteins: evolutionarily conserved mediators of immune responses

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

A ubiquitin ligase complex essential for the NF-kappaB, Wnt/Wingless, and Hedgehog signaling pathways

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

TTRAP, a novel protein that associates with CD40, tumor necrosis factor (TNF) receptor-75 and TNF receptor-associated factors (TRAFs), and that inhibits nuclear factor-kappa B activation

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Requirement for NF-kappaB in osteoclast and B-cell development

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2)

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Germinal center founder cells display propensity for apoptosis before onset of somatic mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Isolation, tissue distribution, and chromosomal localization of the human activation-induced cytidine deaminase (AID) gene

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Class switch recombination and hypermutation require activation-induced cytidine deaminase (AID), a potential RNA editing enzyme

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Specific expression of activation-induced cytidine deaminase (AID), a novel member of the RNA-editing deaminase family in germinal center B cells

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Molecular cloning of an apolipoprotein B messenger RNA editing protein

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Molecular cloning of apobec-1 complementation factor, a novel RNA-binding protein involved in the editing of apolipoprotein B mRNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Frequent but biased class switch recombination in the S mu flanking regions.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Asymmetric mutation around the recombination break point of immunoglobulin class switch sequences on extrachromosomal substrates

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Processing of switch transcripts is required for targeting of antibody class switch recombination

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Somatic hypermutation, transcription, and DNA mismatch repair

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

DNA Double-Strand Breaks in Immunoglobulin Genes Undergoing Somatic Hypermutation

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Cell-cycle-regulated DNA double-stranded breaks in somatic hypermutation of immunoglobulin genes

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Hypermutation in antibody affinity maturation

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

The SCID but not the RAG-2 gene product is required for S mu-S epsilon heavy chain class switching.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Ku80 is required for immunoglobulin isotype switching

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Somatic hypermutation in the absence of DNA-dependent protein kinase catalytic subunit (DNA-PK(cs)) or recombination-activating gene (RAG)1 activity

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Mismatch repair co-opted by hypermutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

The liaison of isotype class switch and mismatch repair: an illegitimate affair

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Reduced isotype switching in splenic B cells from mice deficient in mismatch repair enzymes

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Deficiency in Msh2 affects the efficiency and local sequence specificity of immunoglobulin class-switch recombination: parallels with somatic hypermutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Roles for mismatch repair factors in regulating genetic recombination

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Transcription-induced cleavage of immunoglobulin switch regions by nucleotide excision repair nucleases in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Misinsertion and bypass of thymine-thymine dimers by human DNA polymerase iota

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

DNA polymerase mu (Pol mu), homologous to TdT, could act as a DNA mutator in eukaryotic cells

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

The translesion DNA polymerase zeta plays a major role in Ig and bcl-6 somatic hypermutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

DNA polymerase eta is an A-T mutator in somatic hypermutation of immunoglobulin variable genes

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Somatic mutation hotspots correlate with DNA polymerase eta error spectrum.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Towards an understanding of somatic hypermutation

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2800%2900256-9

7 January 2021

10.1016/S0952-7915(00)00256-9

Identifiers

DOI

1 reference

1 August 2017

1 reference

PubMed ID

11544001