(Q33640298)

28 July 2017

title

CHD7 targets active gene enhancer elements to modulate ES cell-specific gene expression (English)

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28 July 2017

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8

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28 July 2017

Paul Tesar

11

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Gregory E. Crawford

9

object named as

Gregory E Crawford

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28 July 2017

6

Amanda G Fisher

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28 July 2017

Michael P Schnetz

1

1 reference

28 July 2017

Lusy Handoko

2

1 reference

28 July 2017

Batool Akhtar-Zaidi

3

1 reference

28 July 2017

Cynthia F Bartels

4

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28 July 2017

C Filipe Pereira

5

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28 July 2017

David J Adams

7

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28 July 2017

Thomas Laframboise

10

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28 July 2017

Chia-Lin Wei

12

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28 July 2017

Peter C Scacheri

13

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28 July 2017

publication date

15 July 2010

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28 July 2017

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28 July 2017

volume

6

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28 July 2017

issue

7

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28 July 2017

page(s)

e1001023

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Creative Commons Attribution 4.0 International

28 July 2017

copyright license

start time

15 July 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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21 June 2018

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An embryonic stem cell chromatin remodeling complex, esBAF, is an essential component of the core pluripotency transcriptional network.

21 June 2018

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21 June 2018

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Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns

21 June 2018

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ChIP-seq accurately predicts tissue-specific activity of enhancers

21 June 2018

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CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndrome

21 June 2018

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Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Mutations in CHD7 in patients with CHARGE syndrome cause T-B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Pluripotency governed by Sox2 via regulation of Oct3/4 expression in mouse embryonic stem cells.

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Multiple mutations in mouse Chd7 provide models for CHARGE syndrome

21 June 2018

1 reference

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2904778

Promoter features related to tissue specificity as measured by Shannon entropy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2904778

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21 June 2018

1 reference

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21 June 2018

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2904778

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21 June 2018

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affy--analysis of Affymetrix GeneChip data at the probe level

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2904778

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21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2904778

Formation of pluripotent stem cells in the mammalian embryo depends on the POU transcription factor Oct4

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2904778

Kallmann syndrome phenotype in a female patient with CHARGE syndrome and CHD7 mutation.

21 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001023

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001023

Complete DiGeorge syndrome associated with CHD7 mutation

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20657823

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PGEN.1001023

1 reference

28 July 2017

1 reference

28 July 2017

1 reference