DNA double-strand break repair, immunodeficiency and the RIDDLE syndrome. - Wikidata - awgldk - TriplyDB

DNA double-strand break repair, immunodeficiency and the RIDDLE syndrome.

DNA double-strand break repair, immunodeficiency and the RIDDLE syndrome.

http://www.wikidata.org/entity/Q37855947

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Novel Combined Immune Deficiency and Radiation Sensitivity Blended Phenotype in an Adult with Biallelic Variations in ZAP70 and RNF168.Diagnostics of primary immunodeficiency diseases: a sequencing capture approach USP-11 as a predictive and prognostic factor following neoadjuvant therapy in women with breast cancer Effects of expression level of DNA repair-related genes involved in the NHEJ pathway on radiation-induced cognitive impairment.Role of p97/VCP (Cdc48) in genome stability.Primary immunodeficiency diseases associated with neurologic manifestations.Ubiquitination in disease pathogenesis and treatment.Clinical and Biological Manifestation of RNF168 Deficiency in Two Polish Siblings.Neurological Manifestations of Primary Immunodeficiency Diseases.Neurological Manifestations of Primary Immunodeficiencies

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P2860

DNA double-strand break repair, immunodeficiency and the RIDDLE syndrome.

http://www.wikidata.org/entity/Q37855947

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on March 2011

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

DNA double-strand break repair, immunodeficiency and the RIDDLE syndrome.

@en

DNA double-strand break repair, immunodeficiency and the RIDDLE syndrome.

@nl

type

label

DNA double-strand break repair, immunodeficiency and the RIDDLE syndrome.

@en

DNA double-strand break repair, immunodeficiency and the RIDDLE syndrome.

@nl

prefLabel

DNA double-strand break repair, immunodeficiency and the RIDDLE syndrome.

@en

DNA double-strand break repair, immunodeficiency and the RIDDLE syndrome.

@nl

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P1433

Expert Review of Clinical Immunology

P1476

DNA double-strand break repair, immunodeficiency and the RIDDLE syndrome.

@en

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Rachel M Blundred

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

HERC2 coordinates ubiquitin-dependent assembly of DNA repair factors on damaged chromosomes

Hairpin opening and overhang processing by an Artemis/DNA-dependent protein kinase complex in nonhomologous end joining and V(D)J recombination

MDC1 is a mediator of the mammalian DNA damage checkpoint

MDC1 directly binds phosphorylated histone H2AX to regulate cellular responses to DNA double-strand breaks

RNF8 ubiquitylates histones at DNA double-strand breaks and promotes assembly of repair proteins

RNF8 transduces the DNA-damage signal via histone ubiquitylation and checkpoint protein assembly

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

The Rad50 zinc-hook is a structure joining Mre11 complexes in DNA recombination and repair

P304

169-185

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scholarly article

P356

10.1586/ECI.10.93

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2

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7

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Grant S Stewart

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2011-03-01T00:00:00Z

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P698

21426255

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