Primary immunodeficiencies associated with DNA-repair disorders. - Wikidata - wikimedia - TriplyDB

Primary immunodeficiencies associated with DNA-repair disorders.

Primary immunodeficiencies associated with DNA-repair disorders.

http://www.wikidata.org/entity/Q37713997

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REPAIRtoire--a database of DNA repair pathways DNA ligase IV syndrome; a review Induced pluripotent stem cells: a novel frontier in the study of human primary immunodeficiencies.Rescue of DNA-PK Signaling and T-Cell Differentiation by Targeted Genome Editing in a prkdc Deficient iPSC Disease Model.TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfism.DNA damage-dependent NF-κB activation: NEMO turns nuclear signaling inside out.Manipulating DNA damage-response signaling for the treatment of immune-mediated diseases.Evaluation of genotoxicity of Trois through Ames and in vitro chromosomal aberration tests.Guidance for submission for food additive evaluations

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Primary immunodeficiencies associated with DNA-repair disorders.

http://www.wikidata.org/entity/Q37713997

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 18 March 2010

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Primary immunodeficiencies associated with DNA-repair disorders.

@en

Primary immunodeficiencies associated with DNA-repair disorders.

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type

label

Primary immunodeficiencies associated with DNA-repair disorders.

@en

Primary immunodeficiencies associated with DNA-repair disorders.

@nl

prefLabel

Primary immunodeficiencies associated with DNA-repair disorders.

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Primary immunodeficiencies associated with DNA-repair disorders.

@nl

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S1462399410001419

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Expert Reviews in Molecular Medicine

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Primary immunodeficiencies associated with DNA-repair disorders.

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Andrew R Gennery

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Mary A Slatter

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

Cernunnos, a novel nonhomologous end-joining factor, is mutated in human immunodeficiency with microcephaly

XLF interacts with the XRCC4-DNA ligase IV complex to promote DNA nonhomologous end-joining

ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage

The RIDDLE syndrome protein mediates a ubiquitin-dependent signaling cascade at sites of DNA damage

Partial V(D)J recombination activity leads to Omenn syndrome

Nonhomologous end joining and V(D)J recombination require an additional factor

Partial T and B lymphocyte immunodeficiency and predisposition to lymphoma in patients with hypomorphic mutations in Artemis

Direct association of Bloom's syndrome gene product with the human mismatch repair protein MLH1

Lymphocyte-specific compensation for XLF/cernunnos end-joining functions in V(D)J recombination

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e9

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scholarly article

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10.1017/S1462399410001419

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12

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2010-03-18T00:00:00Z

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20298636

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