CHD8 interacts with CHD7, a protein which is mutated in CHARGE syndrome (Q24311335)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20453063%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

title

CHD8 interacts with CHD7, a protein which is mutated in CHARGE syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20453063%20AND%20SRC:MED&resulttype=core&format=json

Chromodomain helicase DNA binding protein 7

2 February 2020

main subject

1 reference

Chromodomain helicase DNA binding protein 8

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1 reference

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20453063%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

8

Lies H Hoefsloot

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20453063%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

author name string

Tserendulam Batsukh

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20453063%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Lasse Pieper

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20453063%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Anna M Koszucka

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20453063%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Nina von Velsen

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20453063%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Sigrid Hoyer-Fender

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20453063%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Miriam Elbracht

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20453063%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Silke Pauli

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20453063%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

language of work or name

English

0 references

publication date

7 May 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20453063%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

published in

Human Molecular Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20453063%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

volume

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20453063%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

issue

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20453063%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

page(s)

2858-2866

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20453063%20AND%20SRC:MED&resulttype=core&format=json

Choanal atresia and associated multiple anomalies

2 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

CHARGE syndrome: an update

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

Phenotypic spectrum of CHARGE syndrome with CHD7 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

CHD7 mutation spectrum in 28 Swedish patients diagnosed with CHARGE syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

Molecular implications of evolutionary differences in CHD double chromodomains

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

CHD proteins: a diverse family with strong ties

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

A mammalian DNA-binding protein that contains a chromodomain and an SNF2/SWI2-like helicase domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

Transcription regulation by histone methylation: interplay between different covalent modifications of the core histone tails

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

ATP-dependent nucleosome remodeling

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

CHD8 is an ATP-dependent chromatin remodeling factor that regulates beta-catenin target genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

ZFYVE27 (SPG33), a novel spastin-binding protein, is mutated in hereditary spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

A cDNA library functional screening strategy based on fluorescent protein complementation assays to identify novel components of signaling pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

Chromatin remodelling: the industrial revolution of DNA around histones

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

CHD8 associates with human Staf and contributes to efficient U6 RNA polymerase III transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

The chromatin remodeling factor CHD8 interacts with elongating RNA polymerase II and controls expression of the cyclin E2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

The Drosophila trithorax group protein Kismet facilitates an early step in transcriptional elongation by RNA Polymerase II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

Drosophila Kismet regulates histone H3 lysine 27 methylation and early elongation by RNA polymerase II

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

NURD, a novel complex with both ATP-dependent chromatin-remodeling and histone deacetylase activities

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

Novel deletions of 14q11.2 associated with developmental delay, cognitive impairment and similar minor anomalies in three children

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

The Chd family of chromatin remodelers

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ189

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1093/HMG/DDQ189

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20453063%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

1 reference