(Q51935283)

English

A missense mutation in the coiled-coil motif of the HP1-interacting domain of ATR-X in a family with X-linked mental retardation.

scientific article published in February 2005

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scholarly article

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15565397

A missense mutation in the coiled-coil motif of the HP1-interacting domain of ATR-X in a family with X-linked mental retardation. (English)

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15565397

7

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15565397

Elke Holinski-Feder

8

object named as

Elke Holinski-Feder

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15565397

author name string

Ilse Wieland

1

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15565397

Julia Sabathil

2

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15565397

Anne Ostendorf

3

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15565397

Olaf Rittinger

4

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15565397

Albrecht Röpke

5

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15565397

Birgitta Winnepenninckx

6

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15565397

Peter Wieacker

9

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15565397

publication date

1 February 2005

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15565397

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15565397

6

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15565397

1

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15565397

45-47

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15565397

https://scigraph.springernature.com/pub.10.1007/s10048-004-0190-3

0 references

The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies

1 reference

https://pubmed.ncbi.nlm.nih.gov/15565397

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of the human and murine ATRX gene identifies highly conserved, functionally important domains.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15565397

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determination of the genomic structure of the XNP/ATRX gene encoding a potential zinc finger helicase

1 reference

https://pubmed.ncbi.nlm.nih.gov/15565397

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation: evidence for a recent mutation in a five-generation family (MRX65) linked to the pericentromeric region

1 reference

https://pubmed.ncbi.nlm.nih.gov/15565397

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular-clinical spectrum of the ATR-X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15565397

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation of the XNP/ATR-X gene in a family with severe mental retardation, spastic paraplegia and skewed pattern of X inactivation: demonstration that the mutation is involved in the inactivation bias

1 reference

https://pubmed.ncbi.nlm.nih.gov/15565397

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10048-004-0190-3

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15565397

release_ppjbjeo6kngtfnbyjn5ofxsr4y

1 reference

https://api.fatcat.wiki/v0/release/ppjbjeo6kngtfnbyjn5ofxsr4y

24 November 2022

based on heuristic

mapped directly with Wikidata item

1 reference

Europe PubMed Central

17 April 2018

http://europepmc.org/abstract/MED/15565397

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