Clinical and Biological Manifestation of RNF168 Deficiency in Two Polish Siblings.

about

Clinical and Biological Manifestation of RNF168 Deficiency in Two Polish Siblings.

Item

http://www.wikidata.org/entity/Q47101755

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Clinical and Biological Manifestation of RNF168 Deficiency in Two Polish Siblings.

@en

Clinical and Biological Manifestation of RNF168 Deficiency in Two Polish Siblings.

@nl

type

Item

label

Clinical and Biological Manifestation of RNF168 Deficiency in Two Polish Siblings.

@en

Clinical and Biological Manifestation of RNF168 Deficiency in Two Polish Siblings.

@nl

prefLabel

Clinical and Biological Manifestation of RNF168 Deficiency in Two Polish Siblings.

@en

Clinical and Biological Manifestation of RNF168 Deficiency in Two Polish Siblings.

@nl

P1476

Clinical and Biological Manifestation of RNF168 Deficiency in Two Polish Siblings.

@en

P2093

Britta Wieland

http://www.w3.org/2001/XMLSchema#string

Julia Enßen

http://www.w3.org/2001/XMLSchema#string

Natalia Valerijevna Bogdanova

http://www.w3.org/2001/XMLSchema#string

Robert Geffers

http://www.w3.org/2001/XMLSchema#string

P2860

Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency

RNF168 ubiquitinates K13-15 on H2A/H2AX to drive DNA damage signaling

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

RNF168 binds and amplifies ubiquitin conjugates on damaged chromosomes to allow accumulation of repair proteins

RNF168, a new RING finger, MIU-containing protein that modifies chromatin by ubiquitination of histones H2A and H2AX

Writers, Readers, and Erasers of Histone Ubiquitylation in DNA Double-Strand Break Repair

The structural basis of modified nucleosome recognition by 53BP1

The RNF8/RNF168 ubiquitin ligase cascade facilitates class switch recombination

53BP1 is a reader of the DNA-damage-induced H2A Lys 15 ubiquitin mark.

Novel Combined Immune Deficiency and Radiation Sensitivity Blended Phenotype in an Adult with Biallelic Variations in ZAP70 and RNF168.

P304

1683

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.3389/FIMMU.2017.01683

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Thilo Dörk

Barbara Pietrucha

Edyta Heropolitanska-Pliszka

P577

2017-12-04T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

29255463

http://www.w3.org/2001/XMLSchema#string

P921

sibling

P932

5722808

http://www.w3.org/2001/XMLSchema#string